Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 144406 |
|---|---|
| ensemblid | ENSG00000158023.10 |
| hgncid | 28506 |
| symbol | CFAP251 |
| name | cilia and flagella associated protein 251 |
| refseq_nuc | NM_144668.6 |
| refseq_prot | NP_653269.3 |
| ensembl_nuc | ENST00000288912.9 |
| ensembl_prot | ENSP00000288912.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 121918592 |
| end | 122003919 |
| strand | + |
| ver | v1.2 |
| region | chr12:121918592-122003919 |
| region5000 | chr12:121913592-122008919 |
| regionname0 | CFAP251_chr12_121918592_122003919 |
| regionname5000 | CFAP251_chr12_121913592_122008919 |
| 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 | 0/0 | 1154 | 108 | 0 | 27 | 61 | 7 | 13 | 43 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0002 | 0/0 | 1154 | 50 | 6 | 0 | 39 | 0 | 5 | 29 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0003 | 0/1 | 1154 | 50 | 16 | 16 | 6 | 5 | 6 | 6 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0004 | 1/0 | 1149 | 48 | 6 | 14 | 20 | 2 | 5 | 16 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0005 | 0/0 | 1154 | 34 | 12 | 2 | 11 | 0 | 9 | 7 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0006 | 0/0 | 1154 | 34 | 31 | 3 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0007 | 0/0 | 1154 | 17 | 0 | 3 | 11 | 0 | 3 | 10 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0008 | 0/0 | 1154 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0009 | 0/0 | 1154 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0010 | 0/0 | 323 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0011 | 0/0 | 1161 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0012 | 0/0 | 1154 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0013 | 0/0 | 1154 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0014 | 0/0 | 1154 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0015 | 0/0 | 1149 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0016 | 0/0 | 1149 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3465 | 107 | 0 | 27 | 61 | 6 | 13 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0002 | 1/0 | 3450 | 46 | 6 | 14 | 20 | 2 | 3 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0003 | 0/1 | 3465 | 40 | 12 | 16 | 0 | 5 | 6 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0004 | 0/0 | 3465 | 39 | 6 | 0 | 28 | 0 | 5 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0005 | 0/0 | 3465 | 33 | 11 | 2 | 11 | 0 | 9 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0006 | 0/0 | 3465 | 30 | 28 | 2 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0007 | 0/0 | 3465 | 17 | 0 | 3 | 11 | 0 | 3 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0008 | 0/0 | 3465 | 11 | 0 | 0 | 11 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0009 | 0/0 | 3465 | 6 | 0 | 0 | 6 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0010 | 0/0 | 3465 | 4 | 3 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0011 | 0/0 | 3465 | 3 | 2 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0012 | 0/0 | 3465 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0013 | 0/0 | 3465 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0014 | 0/0 | 3450 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0015 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0016 | 0/0 | 3465 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0017 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0018 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0019 | 0/0 | 3486 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0020 | 0/0 | 3465 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0021 | 0/0 | 3465 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0022 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0023 | 0/0 | 3465 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0024 | 0/0 | 3450 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| c0025 | 0/0 | 3450 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| 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 | 1/1 | 280 | 352 | 74 | 67 | 152 | 14 | 43 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| t0002 | 0/0 | 280 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| t0003 | 0/0 | 280 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0023 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0104 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| 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 | 0/0 | 3465 | 107 | 0 | 27 | 61 | 6 | 13 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0001c0021 | 0/0 | 3465 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0002c0004 | 0/0 | 3465 | 39 | 6 | 0 | 28 | 0 | 5 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0002c0008 | 0/0 | 3465 | 11 | 0 | 0 | 11 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0003c0003 | 0/1 | 3465 | 40 | 12 | 16 | 0 | 5 | 6 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0003c0009 | 0/0 | 3465 | 6 | 0 | 0 | 6 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0003c0012 | 0/0 | 3465 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0003c0017 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0004c0002 | 1/0 | 3450 | 46 | 6 | 14 | 20 | 2 | 3 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0004c0014 | 0/0 | 3450 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0005c0005 | 0/0 | 3465 | 33 | 11 | 2 | 11 | 0 | 9 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0005c0015 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0006c0006 | 0/0 | 3465 | 30 | 28 | 2 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0006c0011 | 0/0 | 3465 | 3 | 2 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0006c0018 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0007c0007 | 0/0 | 3465 | 17 | 0 | 3 | 11 | 0 | 3 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0008c0010 | 0/0 | 3465 | 4 | 3 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0009c0013 | 0/0 | 3465 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0010c0022 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0011c0019 | 0/0 | 3486 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0012c0020 | 0/0 | 3465 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0013c0016 | 0/0 | 3465 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0014c0023 | 0/0 | 3465 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0015c0025 | 0/0 | 3450 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0016c0024 | 0/0 | 3450 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3744 | 107 | 0 | 27 | 61 | 6 | 13 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0001c0021t0001 | 0/0 | 3744 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0002c0004t0001 | 0/0 | 3744 | 39 | 6 | 0 | 28 | 0 | 5 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0002c0008t0001 | 0/0 | 3744 | 11 | 0 | 0 | 11 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0003c0003t0001 | 0/1 | 3744 | 40 | 12 | 16 | 0 | 5 | 6 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0003c0009t0001 | 0/0 | 3744 | 6 | 0 | 0 | 6 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0003c0012t0001 | 0/0 | 3744 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0003c0017t0001 | 0/0 | 3744 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0004c0002t0001 | 1/0 | 3729 | 46 | 6 | 14 | 20 | 2 | 3 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0004c0014t0001 | 0/0 | 3729 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0005c0005t0001 | 0/0 | 3744 | 32 | 11 | 2 | 11 | 0 | 8 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0005c0005t0003 | 0/0 | 3744 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0005c0015t0001 | 0/0 | 3744 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0006c0006t0001 | 0/0 | 3744 | 30 | 28 | 2 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0006c0011t0001 | 0/0 | 3744 | 3 | 2 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0006c0018t0001 | 0/0 | 3744 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0007c0007t0001 | 0/0 | 3744 | 17 | 0 | 3 | 11 | 0 | 3 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0008c0010t0001 | 0/0 | 3744 | 4 | 3 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0009c0013t0001 | 0/0 | 3744 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0010c0022t0001 | 0/0 | 3744 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0011c0019t0002 | 0/0 | 3765 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0012c0020t0001 | 0/0 | 3744 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0013c0016t0001 | 0/0 | 3744 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0014c0023t0001 | 0/0 | 3744 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0015c0025t0001 | 0/0 | 3729 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| a0016c0024t0001 | 0/0 | 3729 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | copy fasta | chr12 | 121913592 | 122008919 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0001c0021t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0004t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0008t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0008t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0008t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0008t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0008t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0008t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0008t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0008t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0008t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0002c0008t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0104 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0003t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0009t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0009t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0009t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0009t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0009t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0009t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0012t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0012t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0012t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0003c0017t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0023 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0014t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0004c0014t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0005t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0005c0015t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0006t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0011t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0011t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0011t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0006c0018t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0007c0007t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0007c0007t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0007c0007t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0007c0007t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0007c0007t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0007c0007t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0007c0007t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0007c0007t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0007c0007t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0007c0007t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0007c0007t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0007c0007t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0007c0007t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0007c0007t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0007c0007t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0007c0007t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0007c0007t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0008c0010t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0008c0010t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0008c0010t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0008c0010t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0009c0013t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0009c0013t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0010c0022t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0011c0019t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0012c0020t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0013c0016t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0014c0023t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0015c0025t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| a0016c0024t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | GBR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00099 | hp2 | a0003 | c0003 | t0001 | g0095 | EUR | GBR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | GBR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00140 | hp2 | a0004 | c0002 | t0001 | g0047 | EUR | GBR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | FIN | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00280 | hp2 | a0003 | c0003 | t0001 | g0097 | EUR | FIN | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00323 | hp1 | a0003 | c0003 | t0001 | g0091 | EUR | FIN | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | FIN | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00423 | hp1 | a0005 | c0005 | t0001 | g0241 | EAS | CHS | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00438 | hp1 | a0002 | c0004 | t0001 | g0309 | EAS | CHS | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00597 | hp2 | a0002 | c0004 | t0001 | g0314 | EAS | CHS | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00609 | hp1 | a0004 | c0002 | t0001 | g0012 | EAS | CHS | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00609 | hp2 | a0009 | c0013 | t0001 | g0299 | EAS | CHS | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00621 | hp2 | a0002 | c0004 | t0001 | g0298 | EAS | CHS | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0108 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00642 | hp1 | a0013 | c0016 | t0001 | g0098 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00642 | hp2 | a0006 | c0011 | t0001 | g0283 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00673 | hp2 | a0004 | c0002 | t0001 | g0022 | EAS | CHS | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00738 | hp1 | a0004 | c0002 | t0001 | g0026 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG00741 | hp2 | a0003 | c0003 | t0001 | g0102 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01070 | hp1 | a0004 | c0002 | t0001 | g0005 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01071 | hp1 | a0004 | c0002 | t0001 | g0017 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01081 | hp1 | a0003 | c0003 | t0001 | g0096 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01099 | hp2 | a0008 | c0010 | t0001 | g0217 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01106 | hp1 | a0003 | c0003 | t0001 | g0100 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0106 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01109 | hp2 | a0003 | c0003 | t0001 | g0331 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01167 | hp1 | a0003 | c0003 | t0001 | g0093 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01168 | hp1 | a0005 | c0005 | t0001 | g0221 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01168 | hp2 | a0007 | c0007 | t0001 | g0082 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01169 | hp2 | a0005 | c0005 | t0001 | g0222 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0092 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01243 | hp1 | a0003 | c0003 | t0001 | g0330 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01243 | hp2 | a0006 | c0006 | t0001 | g0342 | AMR | PUR | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01255 | hp1 | a0007 | c0007 | t0001 | g0078 | AMR | CLM | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01256 | hp2 | a0003 | c0003 | t0001 | g0090 | AMR | CLM | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01257 | hp2 | a0006 | c0006 | t0001 | g0340 | AMR | CLM | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01258 | hp2 | a0011 | c0019 | t0002 | g0338 | AMR | CLM | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01261 | hp1 | a0007 | c0007 | t0001 | g0077 | AMR | CLM | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01261 | hp2 | a0003 | c0003 | t0001 | g0325 | AMR | CLM | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01346 | hp1 | a0003 | c0003 | t0001 | g0110 | AMR | CLM | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01358 | hp1 | a0004 | c0002 | t0001 | g0033 | AMR | CLM | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01361 | hp1 | a0004 | c0002 | t0001 | g0008 | AMR | CLM | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01433 | hp2 | a0004 | c0002 | t0001 | g0048 | AMR | CLM | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01515 | hp1 | a0001 | c0021 | t0001 | g0202 | EUR | IBS | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01515 | hp2 | a0003 | c0003 | t0001 | g0322 | EUR | IBS | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | IBS | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01517 | hp2 | a0003 | c0003 | t0001 | g0323 | EUR | IBS | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01884 | hp1 | a0006 | c0006 | t0001 | g0249 | AFR | ACB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01884 | hp2 | a0006 | c0006 | t0001 | g0255 | AFR | ACB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01891 | hp1 | a0002 | c0004 | t0001 | g0300 | AFR | ACB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01891 | hp2 | a0006 | c0018 | t0001 | g0252 | AFR | ACB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01928 | hp2 | a0004 | c0002 | t0001 | g0028 | AMR | PEL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01934 | hp1 | a0003 | c0003 | t0001 | g0109 | AMR | PEL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01934 | hp2 | a0004 | c0002 | t0001 | g0032 | AMR | PEL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01943 | hp1 | a0003 | c0003 | t0001 | g0087 | AMR | PEL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01952 | hp2 | a0004 | c0002 | t0001 | g0030 | AMR | PEL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01975 | hp2 | a0003 | c0003 | t0001 | g0094 | AMR | PEL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG01981 | hp2 | a0004 | c0002 | t0001 | g0046 | AMR | PEL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02015 | hp2 | a0005 | c0005 | t0001 | g0229 | EAS | KHV | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02027 | hp1 | a0005 | c0005 | t0001 | g0235 | EAS | KHV | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02040 | hp1 | a0002 | c0004 | t0001 | g0291 | EAS | KHV | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02040 | hp2 | a0002 | c0004 | t0001 | g0289 | EAS | KHV | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02056 | hp2 | a0002 | c0004 | t0001 | g0316 | EAS | KHV | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02071 | hp1 | a0002 | c0004 | t0001 | g0297 | EAS | KHV | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02080 | hp1 | a0002 | c0008 | t0001 | g0311 | EAS | KHV | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02083 | hp2 | a0002 | c0004 | t0001 | g0302 | EAS | KHV | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02135 | hp2 | a0004 | c0002 | t0001 | g0044 | EAS | KHV | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02145 | hp1 | a0006 | c0006 | t0001 | g0263 | AFR | ACB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02145 | hp2 | a0006 | c0011 | t0001 | g0347 | AFR | ACB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02148 | hp1 | a0003 | c0003 | t0001 | g0057 | AMR | PEL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02148 | hp2 | a0004 | c0002 | t0001 | g0029 | AMR | PEL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CDX | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02155 | hp2 | a0004 | c0002 | t0001 | g0014 | EAS | CDX | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02257 | hp1 | a0005 | c0005 | t0001 | g0240 | AFR | ACB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02257 | hp2 | a0003 | c0003 | t0001 | g0350 | AFR | ACB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02258 | hp1 | a0002 | c0004 | t0001 | g0296 | AFR | ACB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02258 | hp2 | a0003 | c0003 | t0001 | g0271 | AFR | ACB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02273 | hp2 | a0004 | c0002 | t0001 | g0031 | AMR | PEL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02280 | hp1 | a0006 | c0006 | t0001 | g0248 | AFR | ACB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0348 | AFR | ACB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02293 | hp1 | a0004 | c0002 | t0001 | g0015 | AMR | PEL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02300 | hp1 | a0004 | c0002 | t0001 | g0052 | AMR | PEL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02451 | hp1 | a0003 | c0003 | t0001 | g0088 | AFR | ACB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02451 | hp2 | a0003 | c0003 | t0001 | g0264 | AFR | ACB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02523 | hp1 | a0007 | c0007 | t0001 | g0076 | EAS | KHV | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02572 | hp1 | a0006 | c0006 | t0001 | g0268 | AFR | GWD | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02572 | hp2 | a0008 | c0010 | t0001 | g0329 | AFR | GWD | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02602 | hp1 | a0003 | c0003 | t0001 | g0101 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02615 | hp1 | a0006 | c0006 | t0001 | g0258 | AFR | GWD | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02615 | hp2 | a0002 | c0004 | t0001 | g0055 | AFR | GWD | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02647 | hp1 | a0002 | c0004 | t0001 | g0056 | AFR | GWD | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02647 | hp2 | a0006 | c0006 | t0001 | g0262 | AFR | GWD | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02683 | hp1 | a0005 | c0005 | t0001 | g0230 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02683 | hp2 | a0003 | c0003 | t0001 | g0320 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02698 | hp2 | a0014 | c0023 | t0001 | g0225 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02723 | hp1 | a0006 | c0006 | t0001 | g0261 | AFR | GWD | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02723 | hp2 | a0005 | c0005 | t0001 | g0219 | AFR | GWD | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02735 | hp1 | a0015 | c0025 | t0001 | g0027 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02738 | hp1 | a0004 | c0002 | t0001 | g0053 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02738 | hp2 | a0005 | c0005 | t0003 | g0270 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02809 | hp1 | a0006 | c0006 | t0001 | g0337 | AFR | GWD | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02809 | hp2 | a0003 | c0003 | t0001 | g0352 | AFR | GWD | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02895 | hp1 | a0004 | c0002 | t0001 | g0034 | AFR | GWD | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02895 | hp2 | a0003 | c0003 | t0001 | g0334 | AFR | GWD | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02897 | hp1 | a0004 | c0002 | t0001 | g0035 | AFR | GWD | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02897 | hp2 | a0006 | c0006 | t0001 | g0064 | AFR | GWD | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02922 | hp1 | a0006 | c0006 | t0001 | g0250 | AFR | ESN | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02922 | hp2 | a0005 | c0005 | t0001 | g0218 | AFR | ESN | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02970 | hp1 | a0003 | c0003 | t0001 | g0349 | AFR | ESN | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02970 | hp2 | a0002 | c0004 | t0001 | g0315 | AFR | ESN | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02976 | hp1 | a0006 | c0006 | t0001 | g0345 | AFR | ESN | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02976 | hp2 | a0006 | c0006 | t0001 | g0344 | AFR | ESN | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03017 | hp2 | a0007 | c0007 | t0001 | g0079 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03098 | hp1 | a0006 | c0006 | t0001 | g0341 | AFR | MSL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03098 | hp2 | a0003 | c0003 | t0001 | g0099 | AFR | MSL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03139 | hp1 | a0005 | c0005 | t0001 | g0239 | AFR | ESN | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03139 | hp2 | a0006 | c0011 | t0001 | g0306 | AFR | ESN | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03195 | hp1 | a0005 | c0005 | t0001 | g0335 | AFR | ESN | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03195 | hp2 | a0004 | c0002 | t0001 | g0006 | AFR | ESN | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03209 | hp1 | a0006 | c0006 | t0001 | g0351 | AFR | MSL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03209 | hp2 | a0006 | c0006 | t0001 | g0253 | AFR | MSL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03225 | hp1 | a0006 | c0006 | t0001 | g0260 | AFR | MSL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03225 | hp2 | a0008 | c0010 | t0001 | g0066 | AFR | MSL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03239 | hp1 | a0002 | c0004 | t0001 | g0086 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03239 | hp2 | a0007 | c0007 | t0001 | g0080 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03453 | hp1 | a0003 | c0003 | t0001 | g0333 | AFR | MSL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03453 | hp2 | a0003 | c0017 | t0001 | g0216 | AFR | MSL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03486 | hp1 | a0006 | c0006 | t0001 | g0343 | AFR | MSL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03486 | hp2 | a0006 | c0006 | t0001 | g0267 | AFR | MSL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03490 | hp1 | a0005 | c0005 | t0001 | g0228 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03490 | hp2 | a0003 | c0003 | t0001 | g0319 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03491 | hp1 | a0004 | c0014 | t0001 | g0019 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03491 | hp2 | a0005 | c0005 | t0001 | g0244 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03492 | hp1 | a0004 | c0014 | t0001 | g0018 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03492 | hp2 | a0003 | c0003 | t0001 | g0321 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03516 | hp1 | a0006 | c0006 | t0001 | g0251 | AFR | ESN | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03516 | hp2 | a0005 | c0005 | t0001 | g0243 | AFR | ESN | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03540 | hp1 | a0002 | c0004 | t0001 | g0295 | AFR | GWD | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03540 | hp2 | a0005 | c0005 | t0001 | g0245 | AFR | GWD | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03654 | hp2 | a0005 | c0005 | t0001 | g0238 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03669 | hp2 | a0002 | c0004 | t0001 | g0305 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03688 | hp1 | a0005 | c0005 | t0001 | g0336 | SAS | STU | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | STU | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03704 | hp1 | a0003 | c0003 | t0001 | g0103 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03704 | hp2 | a0012 | c0020 | t0001 | g0136 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03710 | hp2 | a0004 | c0002 | t0001 | g0041 | SAS | PJL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03834 | hp1 | a0002 | c0004 | t0001 | g0303 | SAS | BEB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03834 | hp2 | a0005 | c0005 | t0001 | g0233 | SAS | BEB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03927 | hp2 | a0007 | c0007 | t0001 | g0081 | SAS | BEB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03942 | hp1 | a0004 | c0002 | t0001 | g0045 | SAS | BEB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG04184 | hp2 | a0002 | c0004 | t0001 | g0317 | SAS | BEB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG04199 | hp1 | a0002 | c0004 | t0001 | g0304 | SAS | STU | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG04199 | hp2 | a0005 | c0005 | t0001 | g0236 | SAS | STU | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | STU | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG04204 | hp2 | a0003 | c0003 | t0001 | g0107 | SAS | STU | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | STU | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG04228 | hp2 | a0005 | c0005 | t0001 | g0346 | SAS | STU | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18522 | hp1 | a0006 | c0006 | t0001 | g0246 | AFR | YRI | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18522 | hp2 | a0005 | c0005 | t0001 | g0242 | AFR | YRI | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18612 | hp1 | a0005 | c0005 | t0001 | g0234 | EAS | CHB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18747 | hp2 | a0002 | c0004 | t0001 | g0292 | EAS | CHB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18906 | hp1 | a0005 | c0005 | t0001 | g0220 | AFR | YRI | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18906 | hp2 | a0008 | c0010 | t0001 | g0065 | AFR | YRI | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18939 | hp1 | a0004 | c0002 | t0001 | g0042 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18940 | hp2 | a0007 | c0007 | t0001 | g0069 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18942 | hp1 | a0003 | c0009 | t0001 | g0062 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18944 | hp1 | a0002 | c0004 | t0001 | g0279 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18945 | hp2 | a0002 | c0004 | t0001 | g0275 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18948 | hp2 | a0002 | c0004 | t0001 | g0282 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18950 | hp2 | a0002 | c0008 | t0001 | g0280 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18951 | hp1 | a0005 | c0005 | t0001 | g0232 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18956 | hp1 | a0002 | c0004 | t0001 | g0003 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18956 | hp2 | a0007 | c0007 | t0001 | g0070 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18957 | hp2 | a0002 | c0008 | t0001 | g0285 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18959 | hp1 | a0002 | c0004 | t0001 | g0281 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18960 | hp2 | a0002 | c0004 | t0001 | g0278 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18961 | hp2 | a0004 | c0002 | t0001 | g0049 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18962 | hp1 | a0002 | c0008 | t0001 | g0313 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18963 | hp2 | a0004 | c0002 | t0001 | g0043 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18964 | hp1 | a0002 | c0008 | t0001 | g0277 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18964 | hp2 | a0007 | c0007 | t0001 | g0073 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18966 | hp2 | a0002 | c0008 | t0001 | g0002 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18969 | hp2 | a0005 | c0005 | t0001 | g0223 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18970 | hp1 | a0002 | c0008 | t0001 | g0002 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18970 | hp2 | a0004 | c0002 | t0001 | g0024 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18971 | hp1 | a0016 | c0024 | t0001 | g0010 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18971 | hp2 | a0004 | c0002 | t0001 | g0039 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18975 | hp2 | a0005 | c0005 | t0001 | g0231 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18978 | hp1 | a0003 | c0009 | t0001 | g0063 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18980 | hp1 | a0007 | c0007 | t0001 | g0074 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18981 | hp1 | a0003 | c0009 | t0001 | g0060 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18981 | hp2 | a0004 | c0002 | t0001 | g0037 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18982 | hp2 | a0002 | c0004 | t0001 | g0284 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18984 | hp1 | a0004 | c0002 | t0001 | g0009 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18984 | hp2 | a0002 | c0004 | t0001 | g0287 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18985 | hp2 | a0002 | c0004 | t0001 | g0308 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18986 | hp2 | a0002 | c0004 | t0001 | g0276 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18990 | hp1 | a0004 | c0002 | t0001 | g0007 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18992 | hp2 | a0007 | c0007 | t0001 | g0072 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18993 | hp1 | a0002 | c0004 | t0001 | g0294 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18994 | hp2 | a0002 | c0008 | t0001 | g0307 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18998 | hp1 | a0004 | c0002 | t0001 | g0051 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18998 | hp2 | a0005 | c0005 | t0001 | g0226 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18999 | hp1 | a0003 | c0009 | t0001 | g0061 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18999 | hp2 | a0002 | c0008 | t0001 | g0288 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19000 | hp1 | a0002 | c0004 | t0001 | g0318 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19002 | hp1 | a0007 | c0007 | t0001 | g0068 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19004 | hp1 | a0002 | c0008 | t0001 | g0286 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19004 | hp2 | a0007 | c0007 | t0001 | g0071 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19011 | hp1 | a0005 | c0005 | t0001 | g0237 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19030 | hp1 | a0006 | c0006 | t0001 | g0269 | AFR | LWK | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19030 | hp2 | a0004 | c0002 | t0001 | g0054 | AFR | LWK | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19043 | hp1 | a0004 | c0002 | t0001 | g0040 | AFR | LWK | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19043 | hp2 | a0006 | c0006 | t0001 | g0247 | AFR | LWK | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19054 | hp1 | a0004 | c0002 | t0001 | g0020 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19055 | hp2 | a0003 | c0009 | t0001 | g0058 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19058 | hp1 | a0002 | c0004 | t0001 | g0273 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19060 | hp1 | a0007 | c0007 | t0001 | g0067 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19060 | hp2 | a0010 | c0022 | t0001 | g0115 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19064 | hp1 | a0004 | c0002 | t0001 | g0021 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19064 | hp2 | a0002 | c0004 | t0001 | g0004 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19065 | hp1 | a0004 | c0002 | t0001 | g0038 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19065 | hp2 | a0002 | c0004 | t0001 | g0274 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19066 | hp2 | a0002 | c0004 | t0001 | g0310 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19067 | hp2 | a0009 | c0013 | t0001 | g0324 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19068 | hp2 | a0002 | c0004 | t0001 | g0312 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19070 | hp2 | a0007 | c0007 | t0001 | g0075 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19079 | hp1 | a0004 | c0002 | t0001 | g0011 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19080 | hp2 | a0002 | c0004 | t0001 | g0301 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19081 | hp1 | a0004 | c0002 | t0001 | g0013 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19082 | hp1 | a0003 | c0009 | t0001 | g0059 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19083 | hp1 | a0005 | c0005 | t0001 | g0266 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19083 | hp2 | a0004 | c0002 | t0001 | g0036 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19090 | hp1 | a0005 | c0005 | t0001 | g0224 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19090 | hp2 | a0002 | c0004 | t0001 | g0293 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA19091 | hp2 | a0002 | c0008 | t0001 | g0290 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA20129 | hp1 | a0006 | c0006 | t0001 | g0259 | AFR | ASW | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA20129 | hp2 | a0003 | c0003 | t0001 | g0089 | AFR | ASW | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | TSI | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA20805 | hp2 | a0004 | c0002 | t0001 | g0050 | EUR | TSI | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02109 | hp1 | a0006 | c0006 | t0001 | g0254 | AFR | ACB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02109 | hp2 | a0003 | c0012 | t0001 | g0084 | AFR | ACB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02486 | hp1 | a0003 | c0012 | t0001 | g0083 | AFR | ACB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG02486 | hp2 | a0005 | c0005 | t0001 | g0265 | AFR | ACB | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03471 | hp1 | a0003 | c0003 | t0001 | g0332 | AFR | MSL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG03471 | hp2 | a0005 | c0015 | t0001 | g0105 | AFR | MSL | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG06807 | hp1 | a0006 | c0006 | t0001 | g0257 | AFR | USA | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| HG06807 | hp2 | a0006 | c0006 | t0001 | g0339 | AFR | USA | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18955 | hp1 | a0004 | c0002 | t0001 | g0025 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA18955 | hp2 | a0007 | c0007 | t0001 | g0085 | EAS | JPT | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA20300 | hp1 | a0004 | c0002 | t0001 | g0016 | AFR | USA | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA20300 | hp2 | a0005 | c0005 | t0001 | g0227 | AFR | USA | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA21309 | hp1 | a0003 | c0012 | t0001 | g0272 | AFR | LWK | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| NA21309 | hp2 | a0006 | c0006 | t0001 | g0256 | AFR | LWK | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0001 | g0104 | REF | REF | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| homoSapiens_grch38 | hp1 | a0004 | c0002 | t0001 | g0023 | REF | REF | CFAP251_chr12_121913592_122008919 | CFAP251 | chr12 | 121913592 | 122008919 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121921491
|
G | GGAGGAGG others(8): Show |
13 | a0001a0002a0003others(10): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
disruptive_inframe_insertion | MODERATE | c.196_197insAGAAAGAG others(7): Show |
p.Glu65_Gly66insGluL others(11): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/22 | 321/3729 | 197/3450 | 66/1149 | INFO_REALIGN_3_PRIME | chr12 | 121921491 | |
| chr12:121923624
|
A | C | 1 | a0014 | 1 | HG02698.hp2 | missense_variant&splice_region_variant | MODERATE | c.381A>C | p.Lys127Asn | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/22 | 505/3729 | 381/3450 | 127/1149 | chr12 | 121923624 | ||
| chr12:121934277
|
G | A | 1 | a0007 | 17 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(14): Show |
missense_variant | MODERATE | c.919G>A | p.Val307Ile | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/22 | 1043/3729 | 919/3450 | 307/1149 | chr12 | 121934277 | ||
| chr12:121934313
|
A | T | 1 | a0010 | 1 | NA19060.hp2 | stop_gained | HIGH | c.955A>T | p.Lys319* | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/22 | 1079/3729 | 955/3450 | 319/1149 | chr12 | 121934313 | ||
| chr12:121942932
|
C | T | 2 | a0005a0014 | 35 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(32): Show |
missense_variant | MODERATE | c.1148C>T | p.Thr383Met | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/22 | 1272/3729 | 1148/3450 | 383/1149 | chr12 | 121942932 | ||
| chr12:121949042
|
G | A | 1 | a0007 | 17 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(14): Show |
missense_variant | MODERATE | c.1250G>A | p.Arg417Gln | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/22 | 1374/3729 | 1250/3450 | 417/1149 | chr12 | 121949042 | ||
| chr12:121954132
|
C | T | 6 | a0002a0005a0006others(3): Show | 122 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(119): Show |
missense_variant | MODERATE | c.1333C>T | p.Leu445Phe | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/22 | 1457/3729 | 1333/3450 | 445/1149 | chr12 | 121954132 | ||
| chr12:121957265
|
T | C | 1 | a0016 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.1727T>C | p.Leu576Ser | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 11/22 | 1851/3729 | 1727/3450 | 576/1149 | chr12 | 121957265 | ||
| chr12:121958489
|
C | T | 3 | a0001a0010a0012 | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
missense_variant | MODERATE | c.1948C>T | p.Leu650Phe | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 12/22 | 2072/3729 | 1948/3450 | 650/1149 | chr12 | 121958489 | ||
| chr12:121959084
|
T | C | 1 | a0013 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.2123T>C | p.Met708Thr | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/22 | 2247/3729 | 2123/3450 | 708/1149 | chr12 | 121959084 | ||
| chr12:121962081
|
C | A | 1 | a0009 | 2 | HG00609.hp2 NA19067.hp2 |
missense_variant | MODERATE | c.2411C>A | p.Pro804Gln | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/22 | 2535/3729 | 2411/3450 | 804/1149 | chr12 | 121962081 | ||
| chr12:121968006
|
G | T | 3 | a0001a0008a0010 | 113 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(110): Show |
missense_variant&splice_region_variant | MODERATE | c.2608G>T | p.Val870Leu | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/22 | 2732/3729 | 2608/3450 | 870/1149 | chr12 | 121968006 | ||
| chr12:121975290
|
T | C | 4 | a0002a0009a0012others(1): Show | 54 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(51): Show |
missense_variant | MODERATE | c.2818T>C | p.Phe940Leu | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 18/22 | 2942/3729 | 2818/3450 | 940/1149 | chr12 | 121975290 | ||
| chr12:121999733
|
C | CGAAATCA others(14): Show |
1 | a0011 | 1 | HG01258.hp2 | disruptive_inframe_insertion | MODERATE | c.3026_3046dupAAATCA others(15): Show |
p.Glu1009_Tyr1015dup | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 20/22 | 3171/3729 | 3047/3450 | 1016/1149 | INFO_REALIGN_3_PRIME | chr12 | 121999733 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121923864
|
G | A | 1 | a0005c0015 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.621G>A | p.Glu207Glu | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/22 | 745/3729 | 621/3450 | 207/1149 | chr12 | 121923864 | ||
| chr12:121931856
|
C | T | 4 | a0001c0001a0001c0021a0010c0022others(1): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
synonymous_variant | LOW | c.858C>T | p.Asn286Asn | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/22 | 982/3729 | 858/3450 | 286/1149 | chr12 | 121931856 | ||
| chr12:121934270
|
C | T | 2 | a0003c0012a0007c0007 | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
synonymous_variant | LOW | c.912C>T | p.Cys304Cys | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/22 | 1036/3729 | 912/3450 | 304/1149 | chr12 | 121934270 | ||
| chr12:121934354
|
A | G | 1 | a0003c0009 | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.996A>G | p.Thr332Thr | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/22 | 1120/3729 | 996/3450 | 332/1149 | chr12 | 121934354 | ||
| chr12:121958518
|
C | A | 4 | a0004c0014a0006c0006a0006c0018others(1): Show | 34 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(31): Show |
synonymous_variant | LOW | c.1977C>A | p.Pro659Pro | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 12/22 | 2101/3729 | 1977/3450 | 659/1149 | chr12 | 121958518 | ||
| chr12:121960671
|
T | C | 1 | a0003c0017 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.2220T>C | p.His740His | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 14/22 | 2344/3729 | 2220/3450 | 740/1149 | chr12 | 121960671 | ||
| chr12:121966961
|
G | A | 1 | a0006c0018 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.2499G>A | p.Thr833Thr | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 16/22 | 2623/3729 | 2499/3450 | 833/1149 | chr12 | 121966961 | ||
| chr12:121975589
|
C | T | 1 | a0001c0021 | 1 | HG01515.hp1 | synonymous_variant | LOW | c.2910C>T | p.Ile970Ile | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/22 | 3034/3729 | 2910/3450 | 970/1149 | chr12 | 121975589 | ||
| chr12:122003680
|
T | C | 1 | a0002c0008 | 11 | HG02080.hp1 NA18950.hp2 NA18957.hp2 others(8): Show |
synonymous_variant | LOW | c.3366T>C | p.Leu1122Leu | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 22/22 | 3490/3729 | 3366/3450 | 1122/1149 | chr12 | 122003680 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:122003811
|
A | G | 1 | a0005c0005t0003 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*47A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 22/22 | 47 | chr12 | 122003811 | |||||
| chr12:122003914
|
A | T | 1 | a0011c0019t0002 | 1 | HG01258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*150A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 22/22 | 150 | chr12 | 122003914 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121919007
|
T | C | 2 | a0002c0004t0001g0003a0002c0004t0001g0004 | 2 | NA18956.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-21+312T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121919007 | ||||||
| chr12:121919124
|
A | AT | 227 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(224): Show | 228 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.-21+432dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 121919124 | |||||
| chr12:121919125
|
T | TTTTA | 75 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(72): Show | 76 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.-21+432_-21+433ins others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 121919125 | |||||
| chr12:121919140
|
A | AT | 22 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0328others(19): Show | 22 | HG00741.hp1 HG01081.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-21+447dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 121919140 | |||||
| chr12:121919140
|
A | ATT | 5 | a0003c0003t0001g0348a0003c0003t0001g0349a0003c0003t0001g0350others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+446_-21+447dup others(2): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 121919140 | |||||
| chr12:121919143
|
A | AT | 180 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.-21+458dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 121919143 | |||||
| chr12:121919143
|
A | ATTTT | 6 | a0003c0003t0001g0319a0003c0003t0001g0320a0003c0003t0001g0321others(3): Show | 6 | HG01515.hp2 HG01517.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21+455_-21+458dup others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 121919143 | |||||
| chr12:121919143
|
A | T | 78 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0328others(75): Show | 79 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.-21+448A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121919143 | ||||||
| chr12:121919144
|
T | TTA | 18 | a0007c0007t0001g0067a0007c0007t0001g0068a0007c0007t0001g0069others(15): Show | 18 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.-21+450_-21+451ins others(2): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 121919144 | |||||
| chr12:121919145
|
T | TA | 8 | a0003c0003t0001g0057a0003c0009t0001g0058a0003c0009t0001g0059others(5): Show | 8 | HG02148.hp1 HG02897.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.-21+450_-21+451ins others(1): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121919145 | ||||||
| chr12:121919146
|
T | A | 2 | a0002c0004t0001g0055a0002c0004t0001g0056 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-21+451T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121919146 | ||||||
| chr12:121919503
|
G | A | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21+808G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121919503 | ||||||
| chr12:121919849
|
A | C | 1 | a0003c0003t0001g0271 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-21+1154A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121919849 | ||||||
| chr12:121919974
|
G | A | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21+1279G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121919974 | ||||||
| chr12:121920190
|
A | G | 52 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(49): Show | 53 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.-20-1096A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121920190 | ||||||
| chr12:121920222
|
C | CT | 8 | a0004c0002t0001g0046a0004c0002t0001g0047a0004c0002t0001g0048others(5): Show | 8 | HG00140.hp2 HG01433.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20-1041dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 121920222 | |||||
| chr12:121920222
|
CT | C | 143 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(140): Show | 144 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.-20-1041delT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 121920222 | |||||
| chr12:121920222
|
CTT | C | 31 | a0002c0004t0001g0274a0002c0004t0001g0275a0003c0003t0001g0330others(28): Show | 31 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.-20-1042_-20-1041d others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 121920222 | |||||
| chr12:121920222
|
CTTT | C | 16 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(13): Show | 16 | HG00621.hp1 HG01106.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.-20-1043_-20-1041d others(5): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 121920222 | |||||
| chr12:121920222
|
CTTTT | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(96): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.-20-1044_-20-1041d others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 121920222 | |||||
| chr12:121920273
|
G | C | 4 | a0003c0012t0001g0083a0003c0012t0001g0084a0003c0012t0001g0272others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-1013G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121920273 | ||||||
| chr12:121920308
|
A | T | 1 | a0003c0003t0001g0104 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-20-978A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121920308 | ||||||
| chr12:121920313
|
C | T | 4 | a0003c0009t0001g0060a0003c0009t0001g0061a0003c0009t0001g0062others(1): Show | 4 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-973C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121920313 | ||||||
| chr12:121920398
|
A | AT | 53 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0056others(50): Show | 54 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.-20-872dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 121920398 | |||||
| chr12:121920398
|
A | ATT | 24 | a0002c0004t0001g0273a0002c0004t0001g0308a0002c0004t0001g0309others(21): Show | 24 | HG00438.hp1 HG01168.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.-20-873_-20-872dup others(2): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 121920398 | |||||
| chr12:121920398
|
AT | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(118): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.-20-872delT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 121920398 | |||||
| chr12:121920460
|
G | A | 53 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(50): Show | 54 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.-20-826G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121920460 | ||||||
| chr12:121920490
|
G | A | 4 | a0003c0009t0001g0060a0003c0009t0001g0061a0003c0009t0001g0062others(1): Show | 4 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-796G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121920490 | ||||||
| chr12:121920558
|
G | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(122): Show | 126 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.-20-728G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121920558 | ||||||
| chr12:121920579
|
G | T | 1 | a0002c0008t0001g0307 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-20-707G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121920579 | ||||||
| chr12:121920643
|
G | A | 53 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(50): Show | 54 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.-20-643G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121920643 | ||||||
| chr12:121920691
|
C | T | 1 | a0003c0009t0001g0059 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-20-595C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121920691 | ||||||
| chr12:121920871
|
A | G | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20-415A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121920871 | ||||||
| chr12:121920896
|
TG | T | 35 | a0005c0005t0001g0218a0005c0005t0001g0219a0005c0005t0001g0220others(32): Show | 35 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.-20-388delG | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 121920896 | |||||
| chr12:121920910
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(299): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.-20-376A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121920910 | ||||||
| chr12:121920984
|
G | A | 11 | a0003c0003t0001g0330a0003c0003t0001g0331a0003c0003t0001g0332others(8): Show | 11 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.-20-302G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121920984 | ||||||
| chr12:121921135
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-20-151C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121921135 | ||||||
| chr12:121921139
|
G | A | 17 | a0007c0007t0001g0067a0007c0007t0001g0068a0007c0007t0001g0069others(14): Show | 17 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.-20-147G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121921139 | ||||||
| chr12:121921155
|
A | T | 21 | a0003c0012t0001g0083a0003c0012t0001g0084a0003c0012t0001g0272others(18): Show | 21 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.-20-131A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121921155 | ||||||
| chr12:121921163
|
C | G | 2 | a0003c0003t0001g0322a0003c0003t0001g0323 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-20-123C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121921163 | ||||||
| chr12:121921266
|
T | C | 177 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(174): Show | 178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.-20-20T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121921266 | ||||||
| chr12:121921285
|
G | C | 1 | a0004c0002t0001g0046 | 1 | HG01981.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.-20-1G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 1/21 | chr12 | 121921285 | ||||||
| chr12:121921701
|
T | G | 1 | a0001c0001t0001g0111 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.378+18T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121921701 | ||||||
| chr12:121921792
|
C | CTT | 140 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(137): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.378+123_378+124dup others(2): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr12 | 121921792 | |||||
| chr12:121921792
|
C | CTTT | 160 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0213others(157): Show | 161 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.378+122_378+124dup others(3): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr12 | 121921792 | |||||
| chr12:121921872
|
C | G | 20 | a0003c0012t0001g0083a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.378+189C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121921872 | ||||||
| chr12:121922090
|
C | T | 1 | a0005c0005t0001g0245 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.378+407C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121922090 | ||||||
| chr12:121922105
|
C | CT | 6 | a0003c0003t0001g0331a0003c0009t0001g0059a0004c0002t0001g0052others(3): Show | 6 | HG01109.hp2 HG02300.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+441dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr12 | 121922105 | |||||
| chr12:121922105
|
CT | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(105): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.378+441delT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr12 | 121922105 | |||||
| chr12:121922200
|
T | C | 26 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(23): Show | 26 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.378+517T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121922200 | ||||||
| chr12:121922252
|
G | A | 53 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(50): Show | 54 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.378+569G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121922252 | ||||||
| chr12:121922263
|
C | T | 4 | a0003c0003t0001g0348a0003c0003t0001g0349a0003c0003t0001g0350others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+580C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121922263 | ||||||
| chr12:121922341
|
C | T | 2 | a0008c0010t0001g0065a0008c0010t0001g0066 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.378+658C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121922341 | ||||||
| chr12:121922560
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.378+877G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121922560 | ||||||
| chr12:121922662
|
G | A | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.379-960G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121922662 | ||||||
| chr12:121922683
|
C | CA | 151 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(148): Show | 152 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.379-938dupA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr12 | 121922683 | |||||
| chr12:121922686
|
G | A | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.379-936G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121922686 | ||||||
| chr12:121922769
|
GTTCTT | G | 151 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(148): Show | 152 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.379-843_379-839del others(5): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr12 | 121922769 | |||||
| chr12:121922812
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.379-810C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121922812 | ||||||
| chr12:121922843
|
A | G | 1 | a0005c0005t0001g0244 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.379-779A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121922843 | ||||||
| chr12:121922875
|
C | T | 1 | a0007c0007t0001g0081 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.379-747C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121922875 | ||||||
| chr12:121922919
|
A | T | 2 | a0003c0003t0001g0264a0003c0003t0001g0271 | 2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.379-703A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121922919 | ||||||
| chr12:121922927
|
C | T | 1 | a0003c0003t0001g0352 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.379-695C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121922927 | ||||||
| chr12:121922985
|
T | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0113 | 2 | HG00099.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.379-637T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121922985 | ||||||
| chr12:121922997
|
A | G | 2 | a0001c0001t0001g0111a0001c0001t0001g0113 | 2 | HG00099.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.379-625A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121922997 | ||||||
| chr12:121923042
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.379-580G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121923042 | ||||||
| chr12:121923046
|
C | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(121): Show | 125 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.379-576C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121923046 | ||||||
| chr12:121923063
|
G | A | 1 | a0004c0002t0001g0008 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.379-559G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121923063 | ||||||
| chr12:121923084
|
C | T | 1 | a0004c0002t0001g0042 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.379-538C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121923084 | ||||||
| chr12:121923086
|
T | C | 1 | a0010c0022t0001g0115 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.379-536T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121923086 | ||||||
| chr12:121923120
|
C | T | 26 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(23): Show | 26 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.379-502C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121923120 | ||||||
| chr12:121923499
|
A | G | 1 | a0002c0004t0001g0318 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.379-123A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121923499 | ||||||
| chr12:121923506
|
A | G | 177 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(174): Show | 178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.379-116A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 2/21 | chr12 | 121923506 | ||||||
| chr12:121924023
|
CT | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(299): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.747+37delT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121924023 | |||||
| chr12:121924118
|
G | GT | 7 | a0003c0003t0001g0271a0003c0009t0001g0058a0003c0009t0001g0059others(4): Show | 7 | HG02258.hp2 NA18942.hp1 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.747+139dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121924118 | |||||
| chr12:121924118
|
G | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(106): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.747+128G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121924118 | ||||||
| chr12:121924385
|
G | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(106): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.747+395G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121924385 | ||||||
| chr12:121924410
|
C | T | 151 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(148): Show | 152 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.747+420C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121924410 | ||||||
| chr12:121924426
|
C | CT | 31 | a0004c0002t0001g0041a0004c0002t0001g0045a0005c0005t0001g0243others(28): Show | 31 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.747+458dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121924426 | |||||
| chr12:121924426
|
CT | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(182): Show | 187 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.747+458delT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121924426 | |||||
| chr12:121924426
|
CTT | C | 7 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(4): Show | 7 | HG01255.hp2 HG03017.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.747+457_747+458del others(2): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121924426 | |||||
| chr12:121924426
|
CTTTTTTT others(2): Show |
C | 30 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.747+450_747+458del others(9): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121924426 | |||||
| chr12:121924518
|
C | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(122): Show | 126 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.747+528C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121924518 | ||||||
| chr12:121924526
|
G | A | 177 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(174): Show | 178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.747+536G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121924526 | ||||||
| chr12:121924536
|
G | A | 30 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.747+546G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121924536 | ||||||
| chr12:121924693
|
G | C | 4 | a0004c0002t0001g0009a0004c0002t0001g0011a0004c0002t0001g0012others(1): Show | 4 | HG00609.hp1 NA18971.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.747+703G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121924693 | ||||||
| chr12:121924696
|
C | T | 1 | a0007c0007t0001g0069 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.747+706C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121924696 | ||||||
| chr12:121924710
|
G | A | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.747+720G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121924710 | ||||||
| chr12:121924714
|
G | A | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.747+724G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121924714 | ||||||
| chr12:121924777
|
G | A | 3 | a0002c0004t0001g0278a0002c0004t0001g0279a0002c0004t0001g0308 | 3 | NA18944.hp1 NA18960.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.747+787G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121924777 | ||||||
| chr12:121924880
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.747+890C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121924880 | ||||||
| chr12:121925039
|
C | T | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.747+1049C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121925039 | ||||||
| chr12:121925183
|
A | G | 1 | a0003c0003t0001g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.747+1193A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121925183 | ||||||
| chr12:121925192
|
C | G | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.747+1202C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121925192 | ||||||
| chr12:121925364
|
CT | C | 26 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(23): Show | 26 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.747+1375delT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121925364 | ||||||
| chr12:121925682
|
A | AAGG | 302 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(299): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.747+1694_747+1695i others(5): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121925682 | |||||
| chr12:121925789
|
C | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(121): Show | 125 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.747+1799C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121925789 | ||||||
| chr12:121925875
|
T | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(299): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.747+1885T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121925875 | ||||||
| chr12:121925916
|
A | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0328 | 2 | HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.747+1926A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121925916 | ||||||
| chr12:121926021
|
AT | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(108): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.747+2056delT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121926021 | |||||
| chr12:121926021
|
ATT | A | 168 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(165): Show | 169 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.747+2055_747+2056d others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121926021 | |||||
| chr12:121926021
|
ATTT | A | 12 | a0002c0004t0001g0281a0002c0008t0001g0280a0002c0008t0001g0313others(9): Show | 12 | HG01943.hp1 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.747+2054_747+2056d others(5): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121926021 | |||||
| chr12:121926021
|
ATTTTTTT others(8): Show |
A | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.747+2042_747+2056d others(17): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121926021 | |||||
| chr12:121926056
|
G | A | 3 | a0003c0012t0001g0083a0003c0012t0001g0084a0003c0012t0001g0272 | 3 | HG02109.hp2 HG02486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.747+2066G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121926056 | ||||||
| chr12:121926076
|
C | A | 125 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(122): Show | 126 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.747+2086C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121926076 | ||||||
| chr12:121926088
|
A | C | 1 | a0004c0002t0001g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.747+2098A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121926088 | ||||||
| chr12:121926160
|
C | T | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.747+2170C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121926160 | ||||||
| chr12:121926184
|
C | T | 2 | a0003c0003t0001g0264a0003c0003t0001g0271 | 2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.747+2194C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121926184 | ||||||
| chr12:121926389
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.747+2399C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121926389 | ||||||
| chr12:121926505
|
T | G | 20 | a0003c0012t0001g0083a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.747+2515T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121926505 | ||||||
| chr12:121926584
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.747+2594T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121926584 | ||||||
| chr12:121926585
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.747+2595C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121926585 | ||||||
| chr12:121926621
|
C | A | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.747+2631C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121926621 | ||||||
| chr12:121926670
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0184 | 2 | HG00597.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.747+2680C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121926670 | ||||||
| chr12:121926918
|
T | C | 11 | a0003c0003t0001g0330a0003c0003t0001g0331a0003c0003t0001g0332others(8): Show | 11 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.747+2928T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121926918 | ||||||
| chr12:121927120
|
T | C | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.747+3130T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121927120 | ||||||
| chr12:121927128
|
AT | A | 4 | a0006c0006t0001g0064a0006c0006t0001g0247a0006c0006t0001g0248others(1): Show | 4 | HG02280.hp1 HG02647.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+3139delT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121927128 | ||||||
| chr12:121927188
|
G | GT | 152 | a0001c0001t0001g0189a0001c0001t0001g0193a0002c0004t0001g0003others(149): Show | 153 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.747+3213dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121927188 | |||||
| chr12:121927677
|
C | T | 2 | a0003c0003t0001g0102a0003c0003t0001g0103 | 2 | HG00741.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.747+3687C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121927677 | ||||||
| chr12:121927724
|
C | A | 1 | a0002c0004t0001g0282 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.747+3734C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121927724 | ||||||
| chr12:121927889
|
G | C | 121 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(118): Show | 122 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.748-3857G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121927889 | ||||||
| chr12:121927934
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(106): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.748-3812T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121927934 | ||||||
| chr12:121928040
|
C | T | 1 | a0003c0003t0001g0101 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.748-3706C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928040 | ||||||
| chr12:121928338
|
A | G | 2 | a0002c0004t0001g0274a0002c0004t0001g0275 | 2 | NA18945.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.748-3408A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928338 | ||||||
| chr12:121928477
|
A | G | 1 | a0005c0005t0001g0242 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.748-3269A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928477 | ||||||
| chr12:121928506
|
A | G | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.748-3240A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928506 | ||||||
| chr12:121928625
|
T | TGTATATA others(23): Show |
2 | a0004c0002t0001g0047a0004c0002t0001g0053 | 2 | HG00140.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.748-3092_748-3091i others(32): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928625 | |||||
| chr12:121928625
|
T | TGTGTATA others(75): Show |
1 | a0003c0003t0001g0271 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.748-3119_748-3118i others(84): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928625 | |||||
| chr12:121928625
|
TGTATATA others(5): Show |
T | 12 | a0006c0006t0001g0253a0006c0006t0001g0254a0006c0006t0001g0255others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.748-3109_748-3098d others(14): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928625 | |||||
| chr12:121928626
|
G | GTATA | 3 | a0003c0012t0001g0083a0003c0012t0001g0084a0003c0012t0001g0272 | 3 | HG02109.hp2 HG02486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.748-3113_748-3110d others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928626 | |||||
| chr12:121928626
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0125 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.748-3119_748-3110d others(12): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928626 | |||||
| chr12:121928626
|
G | GTGTATAT others(1): Show |
29 | a0002c0004t0001g0276a0002c0004t0001g0278a0002c0004t0001g0279others(26): Show | 30 | HG00438.hp1 HG00597.hp2 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.748-3119_748-3118i others(10): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928626 | |||||
| chr12:121928626
|
G | GTGTGTAT others(3): Show |
4 | a0002c0004t0001g0086a0002c0004t0001g0303a0002c0004t0001g0304others(1): Show | 4 | HG03239.hp1 HG03834.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.748-3119_748-3118i others(12): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928626 | |||||
| chr12:121928626
|
GTATATAT others(7): Show |
G | 47 | a0005c0005t0001g0218a0005c0005t0001g0219a0005c0005t0001g0220others(44): Show | 47 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(44): Show |
intron_variant | MODIFIER | c.748-3109_748-3096d others(16): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928626 | |||||
| chr12:121928627
|
TATATATA others(3): Show |
T | 6 | a0003c0017t0001g0216a0006c0006t0001g0064a0006c0006t0001g0247others(3): Show | 6 | HG02280.hp1 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-3118_748-3109d others(12): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928627 | ||||||
| chr12:121928628
|
A | G | 26 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(23): Show | 26 | HG00609.hp2 HG00621.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.748-3118A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928628 | ||||||
| chr12:121928628
|
ATATATAT others(3): Show |
A | 8 | a0001c0001t0001g0124a0001c0001t0001g0177a0001c0001t0001g0178others(5): Show | 8 | HG02027.hp2 HG02056.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.748-3109_748-3100d others(12): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928628 | |||||
| chr12:121928630
|
ATATATAC others(1): Show |
A | 8 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(5): Show | 8 | HG01081.hp2 HG02080.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.748-3109_748-3102d others(10): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928630 | |||||
| chr12:121928634
|
ATACG | A | 3 | a0003c0003t0001g0323a0008c0010t0001g0217a0008c0010t0001g0329 | 3 | HG01099.hp2 HG01517.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.748-3109_748-3106d others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928634 | |||||
| chr12:121928636
|
ACG | A | 27 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(24): Show | 27 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.748-3109_748-3108d others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928636 | ||||||
| chr12:121928636
|
ACGTATAT others(15): Show |
A | 88 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.748-3109_748-3088d others(24): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928636 | ||||||
| chr12:121928636
|
ACGTATAT others(27): Show |
A | 4 | a0003c0003t0001g0348a0003c0003t0001g0349a0003c0003t0001g0350others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.748-3109_748-3076d others(36): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928636 | ||||||
| chr12:121928637
|
C | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0175a0001c0001t0001g0176others(57): Show | 61 | HG00280.hp2 HG00609.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.748-3109C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928637 | ||||||
| chr12:121928638
|
G | A | 60 | a0001c0001t0001g0001a0001c0001t0001g0175a0001c0001t0001g0176others(57): Show | 61 | HG00280.hp2 HG00609.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.748-3108G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928638 | ||||||
| chr12:121928638
|
G | GTA | 3 | a0004c0002t0001g0038a0004c0002t0001g0039a0004c0002t0001g0051 | 3 | NA18971.hp2 NA18998.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.748-3091_748-3090d others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928638 | |||||
| chr12:121928640
|
A | ATACG | 16 | a0007c0007t0001g0067a0007c0007t0001g0068a0007c0007t0001g0069others(13): Show | 16 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.748-3104_748-3103i others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928640 | |||||
| chr12:121928640
|
A | G | 13 | a0003c0003t0001g0271a0006c0006t0001g0253a0006c0006t0001g0254others(10): Show | 13 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.748-3106A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928640 | ||||||
| chr12:121928642
|
A | ATATATAC others(1): Show |
36 | a0002c0004t0001g0086a0002c0004t0001g0276a0002c0004t0001g0278others(33): Show | 37 | HG00438.hp1 HG00597.hp2 HG02040.hp1 others(34): Show |
intron_variant | MODIFIER | c.748-3098_748-3097i others(10): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928642 | |||||
| chr12:121928642
|
A | G | 47 | a0005c0005t0001g0218a0005c0005t0001g0219a0005c0005t0001g0220others(44): Show | 47 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(44): Show |
intron_variant | MODIFIER | c.748-3104A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928642 | ||||||
| chr12:121928645
|
T | C | 23 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(20): Show | 23 | HG00609.hp2 HG00621.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.748-3101T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928645 | ||||||
| chr12:121928646
|
A | ATACG | 5 | a0003c0009t0001g0058a0003c0009t0001g0060a0003c0009t0001g0061others(2): Show | 5 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-3098_748-3097i others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928646 | |||||
| chr12:121928646
|
A | G | 23 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(20): Show | 23 | HG00609.hp2 HG00621.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.748-3100A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928646 | ||||||
| chr12:121928647
|
T | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 5 | NA18960.hp1 NA18962.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-3099T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928647 | ||||||
| chr12:121928648
|
A | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 5 | NA18960.hp1 NA18962.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-3098A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928648 | ||||||
| chr12:121928649
|
T | C | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | HG00738.hp2 HG01071.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.748-3097T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928649 | ||||||
| chr12:121928650
|
A | G | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | HG00738.hp2 HG01071.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.748-3096A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928650 | ||||||
| chr12:121928653
|
TATAC | T | 5 | a0006c0006t0001g0064a0006c0006t0001g0247a0006c0006t0001g0248others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-3092_748-3089d others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928653 | ||||||
| chr12:121928657
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0126a0001c0001t0001g0127others(4): Show | 8 | HG00738.hp2 HG01071.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.748-3089C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928657 | ||||||
| chr12:121928657
|
CGTATATA others(31): Show |
C | 1 | a0003c0003t0001g0332 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.748-3088_748-3051d others(40): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928657 | ||||||
| chr12:121928658
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0126a0001c0001t0001g0127others(5): Show | 9 | HG00738.hp2 HG01071.hp2 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.748-3088G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928658 | ||||||
| chr12:121928658
|
G | GTATA | 28 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(25): Show | 28 | HG00609.hp2 HG00621.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.748-3081_748-3078d others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928658 | |||||
| chr12:121928658
|
GTATATAT others(31): Show |
G | 5 | a0003c0003t0001g0330a0003c0003t0001g0333a0003c0003t0001g0334others(2): Show | 5 | HG01099.hp2 HG01243.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-3078_748-3041d others(40): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928658 | |||||
| chr12:121928660
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0001g0208 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.748-3077_748-3068d others(12): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928660 | |||||
| chr12:121928662
|
ATATATAC others(1): Show |
A | 8 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(5): Show | 8 | HG01081.hp2 HG02080.hp2 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.748-3077_748-3070d others(10): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928662 | |||||
| chr12:121928664
|
ATATACG | A | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0207 | 3 | HG02056.hp1 HG03710.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.748-3077_748-3072d others(8): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928664 | |||||
| chr12:121928668
|
ACGTATAT others(31): Show |
A | 31 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(28): Show | 31 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.748-3077_748-3040d others(40): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928668 | ||||||
| chr12:121928669
|
C | T | 20 | a0003c0012t0001g0083a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.748-3077C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928669 | ||||||
| chr12:121928670
|
G | A | 20 | a0003c0012t0001g0083a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.748-3076G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928670 | ||||||
| chr12:121928670
|
G | GTATATAT others(1): Show |
4 | a0003c0009t0001g0060a0003c0009t0001g0061a0003c0009t0001g0062others(1): Show | 4 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.748-3065_748-3058d others(10): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928670 | |||||
| chr12:121928670
|
G | GTATATAT others(13): Show |
1 | a0002c0004t0001g0291 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.748-3062_748-3061i others(22): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928670 | |||||
| chr12:121928670
|
GTATA | G | 69 | a0002c0004t0001g0086a0002c0004t0001g0303a0002c0004t0001g0304others(66): Show | 69 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(66): Show |
intron_variant | MODIFIER | c.748-3061_748-3058d others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928670 | |||||
| chr12:121928672
|
A | ACG | 3 | a0007c0007t0001g0067a0007c0007t0001g0071a0007c0007t0001g0081 | 3 | HG03927.hp2 NA19004.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.748-3074_748-3073i others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928672 | ||||||
| chr12:121928672
|
A | ATACG | 13 | a0007c0007t0001g0068a0007c0007t0001g0069a0007c0007t0001g0070others(10): Show | 13 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.748-3072_748-3071i others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928672 | |||||
| chr12:121928672
|
A | ATATACG | 4 | a0003c0012t0001g0083a0003c0012t0001g0084a0003c0012t0001g0272others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.748-3070_748-3069i others(8): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928672 | |||||
| chr12:121928672
|
A | G | 1 | a0003c0003t0001g0271 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.748-3074A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928672 | ||||||
| chr12:121928674
|
A | ATATATAC others(1): Show |
23 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(20): Show | 23 | HG00609.hp2 HG00621.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.748-3066_748-3065i others(10): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928674 | |||||
| chr12:121928674
|
A | ATATATAT others(17): Show |
16 | a0002c0004t0001g0276a0002c0004t0001g0278a0002c0004t0001g0279others(13): Show | 17 | HG00597.hp2 HG02040.hp2 NA18944.hp1 others(14): Show |
intron_variant | MODIFIER | c.748-3062_748-3061i others(26): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928674 | |||||
| chr12:121928674
|
A | ATATATAT others(45): Show |
3 | a0002c0004t0001g0302a0002c0008t0001g0280a0002c0008t0001g0311 | 3 | HG02080.hp1 HG02083.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.748-3062_748-3061i others(54): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928674 | |||||
| chr12:121928683
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.748-3063T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928683 | ||||||
| chr12:121928684
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.748-3062A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928684 | ||||||
| chr12:121928685
|
T | C | 18 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(15): Show | 18 | HG00438.hp1 HG01081.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.748-3061T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928685 | ||||||
| chr12:121928686
|
A | G | 19 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(16): Show | 19 | HG00438.hp1 HG01081.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.748-3060A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928686 | ||||||
| chr12:121928688
|
ACG | A | 24 | a0001c0001t0001g0124a0001c0001t0001g0177a0001c0001t0001g0178others(21): Show | 24 | HG00438.hp1 HG01081.hp2 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.748-3057_748-3056d others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928688 | ||||||
| chr12:121928689
|
C | T | 1 | a0002c0004t0001g0291 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.748-3057C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928689 | ||||||
| chr12:121928690
|
G | A | 1 | a0002c0004t0001g0291 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.748-3056G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928690 | ||||||
| chr12:121928690
|
G | GTA | 82 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.748-3042_748-3041d others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928690 | |||||
| chr12:121928695
|
T | C | 4 | a0003c0003t0001g0348a0003c0003t0001g0349a0003c0003t0001g0350others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.748-3051T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928695 | ||||||
| chr12:121928696
|
A | G | 4 | a0003c0003t0001g0348a0003c0003t0001g0349a0003c0003t0001g0350others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.748-3050A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928696 | ||||||
| chr12:121928702
|
A | AT | 44 | a0002c0004t0001g0055a0002c0004t0001g0056a0002c0004t0001g0086others(41): Show | 44 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.748-3043dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928702 | |||||
| chr12:121928702
|
A | T | 2 | a0002c0004t0001g0316a0006c0011t0001g0347 | 2 | HG02056.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.748-3044A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928702 | ||||||
| chr12:121928704
|
A | ACGTATAT others(10): Show |
7 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(4): Show | 7 | HG03139.hp2 NA18942.hp1 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.748-3042_748-3041i others(19): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928704 | ||||||
| chr12:121928704
|
A | AT | 54 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0274others(51): Show | 55 | HG00597.hp2 HG02015.hp2 HG02027.hp1 others(52): Show |
intron_variant | MODIFIER | c.748-3032dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928704 | |||||
| chr12:121928704
|
A | ATT | 15 | a0001c0001t0001g0001a0001c0001t0001g0122a0001c0001t0001g0123others(12): Show | 16 | HG00597.hp1 HG01256.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.748-3033_748-3032d others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121928704 | |||||
| chr12:121928704
|
A | T | 46 | a0002c0004t0001g0055a0002c0004t0001g0056a0002c0004t0001g0086others(43): Show | 46 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.748-3042A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928704 | ||||||
| chr12:121928705
|
T | TA | 32 | a0001c0001t0001g0212a0002c0004t0001g0303a0003c0012t0001g0083others(29): Show | 32 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.748-3041_748-3040i others(3): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928705 | ||||||
| chr12:121928706
|
T | A | 8 | a0001c0001t0001g0116a0001c0001t0001g0129a0001c0001t0001g0199others(5): Show | 8 | HG01070.hp1 HG01071.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.748-3040T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928706 | ||||||
| chr12:121928707
|
T | A | 9 | a0001c0001t0001g0211a0005c0005t0001g0219a0005c0005t0001g0220others(6): Show | 9 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.748-3039T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928707 | ||||||
| chr12:121928816
|
C | T | 20 | a0003c0012t0001g0083a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.748-2930C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121928816 | ||||||
| chr12:121929042
|
G | T | 4 | a0006c0006t0001g0246a0006c0006t0001g0251a0006c0006t0001g0267others(1): Show | 4 | HG01891.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.748-2704G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121929042 | ||||||
| chr12:121929266
|
A | G | 1 | a0005c0005t0001g0244 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.748-2480A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121929266 | ||||||
| chr12:121929316
|
T | C | 3 | a0007c0007t0001g0077a0007c0007t0001g0078a0007c0007t0001g0082 | 3 | HG01168.hp2 HG01255.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.748-2430T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121929316 | ||||||
| chr12:121929319
|
C | CA | 27 | a0001c0001t0001g0206a0002c0004t0001g0281a0003c0009t0001g0058others(24): Show | 27 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.748-2412dupA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121929319 | |||||
| chr12:121929357
|
C | G | 35 | a0005c0005t0001g0218a0005c0005t0001g0219a0005c0005t0001g0220others(32): Show | 35 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.748-2389C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121929357 | ||||||
| chr12:121929408
|
CTTTT | C | 148 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(145): Show | 149 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.748-2336_748-2333d others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121929408 | |||||
| chr12:121929415
|
A | C | 148 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(145): Show | 149 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.748-2331A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121929415 | ||||||
| chr12:121929557
|
G | A | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-2189G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121929557 | ||||||
| chr12:121929681
|
C | CT | 20 | a0003c0012t0001g0083a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.748-2051dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121929681 | |||||
| chr12:121929973
|
G | A | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.748-1773G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121929973 | ||||||
| chr12:121930001
|
A | AT | 191 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(188): Show | 192 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.748-1745_748-1744i others(3): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121930001 | ||||||
| chr12:121930126
|
T | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(108): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.748-1620T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121930126 | ||||||
| chr12:121930195
|
A | G | 121 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(118): Show | 122 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.748-1551A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121930195 | ||||||
| chr12:121930379
|
C | T | 35 | a0005c0005t0001g0218a0005c0005t0001g0219a0005c0005t0001g0220others(32): Show | 35 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.748-1367C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121930379 | ||||||
| chr12:121930476
|
ACT | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(108): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.748-1267_748-1266d others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121930476 | |||||
| chr12:121930487
|
T | C | 148 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(145): Show | 149 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.748-1259T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121930487 | ||||||
| chr12:121930630
|
T | C | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-1116T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121930630 | ||||||
| chr12:121930646
|
T | G | 20 | a0003c0012t0001g0083a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.748-1100T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121930646 | ||||||
| chr12:121930734
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(106): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.748-1012A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121930734 | ||||||
| chr12:121930748
|
CT | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.748-980delT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121930748 | |||||
| chr12:121930748
|
CTT | C | 136 | a0001c0001t0001g0130a0001c0001t0001g0170a0001c0001t0001g0212others(133): Show | 137 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.748-981_748-980del others(2): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121930748 | |||||
| chr12:121930829
|
A | ACCT | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-914_748-912dup others(3): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121930829 | |||||
| chr12:121931038
|
G | A | 41 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(38): Show | 41 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.748-708G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121931038 | ||||||
| chr12:121931203
|
G | C | 10 | a0006c0006t0001g0253a0006c0006t0001g0254a0006c0006t0001g0255others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.748-543G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121931203 | ||||||
| chr12:121931247
|
A | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(108): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.748-499A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121931247 | ||||||
| chr12:121931279
|
AT | A | 53 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(50): Show | 54 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.748-458delT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 121931279 | |||||
| chr12:121931370
|
T | C | 2 | a0004c0014t0001g0018a0004c0014t0001g0019 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.748-376T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121931370 | ||||||
| chr12:121931370
|
TGGCGCGA others(17): Show |
T | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.748-375_748-352del others(24): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121931370 | ||||||
| chr12:121931381
|
C | T | 20 | a0003c0012t0001g0083a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.748-365C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121931381 | ||||||
| chr12:121931394
|
C | A | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-352C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121931394 | ||||||
| chr12:121931540
|
C | T | 121 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(118): Show | 122 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.748-206C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121931540 | ||||||
| chr12:121931579
|
C | T | 1 | a0004c0002t0001g0008 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.748-167C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 3/21 | chr12 | 121931579 | ||||||
| chr12:121932005
|
TG | T | 3 | a0002c0004t0001g0292a0002c0004t0001g0293a0002c0004t0001g0312 | 3 | NA18747.hp2 NA19068.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.888+121delG | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 121932005 | |||||
| chr12:121932225
|
C | T | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.888+339C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/21 | chr12 | 121932225 | ||||||
| chr12:121932300
|
T | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(299): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.888+414T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/21 | chr12 | 121932300 | ||||||
| chr12:121932542
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.888+656C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/21 | chr12 | 121932542 | ||||||
| chr12:121932741
|
G | A | 4 | a0003c0003t0001g0348a0003c0003t0001g0349a0003c0003t0001g0350others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.888+855G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/21 | chr12 | 121932741 | ||||||
| chr12:121932799
|
C | T | 2 | a0008c0010t0001g0065a0008c0010t0001g0066 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.888+913C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/21 | chr12 | 121932799 | ||||||
| chr12:121932930
|
C | T | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.888+1044C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/21 | chr12 | 121932930 | ||||||
| chr12:121932943
|
G | A | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.888+1057G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/21 | chr12 | 121932943 | ||||||
| chr12:121932954
|
G | A | 1 | a0004c0002t0001g0053 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.888+1068G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/21 | chr12 | 121932954 | ||||||
| chr12:121933123
|
G | A | 3 | a0002c0004t0001g0303a0002c0004t0001g0304a0002c0004t0001g0317 | 3 | HG03834.hp1 HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.889-1124G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/21 | chr12 | 121933123 | ||||||
| chr12:121933157
|
G | T | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.889-1090G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/21 | chr12 | 121933157 | ||||||
| chr12:121933192
|
T | C | 1 | a0002c0008t0001g0280 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.889-1055T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/21 | chr12 | 121933192 | ||||||
| chr12:121933491
|
A | C | 1 | a0004c0002t0001g0042 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.889-756A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/21 | chr12 | 121933491 | ||||||
| chr12:121933528
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.889-719G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/21 | chr12 | 121933528 | ||||||
| chr12:121933568
|
T | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(299): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.889-679T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/21 | chr12 | 121933568 | ||||||
| chr12:121933569
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.889-678G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/21 | chr12 | 121933569 | ||||||
| chr12:121933687
|
C | T | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.889-560C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/21 | chr12 | 121933687 | ||||||
| chr12:121933794
|
G | C | 17 | a0007c0007t0001g0067a0007c0007t0001g0068a0007c0007t0001g0069others(14): Show | 17 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.889-453G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/21 | chr12 | 121933794 | ||||||
| chr12:121934035
|
T | A | 1 | a0003c0003t0001g0271 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.889-212T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/21 | chr12 | 121934035 | ||||||
| chr12:121934103
|
G | A | 1 | a0004c0002t0001g0008 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.889-144G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/21 | chr12 | 121934103 | ||||||
| chr12:121934140
|
G | A | 2 | a0004c0002t0001g0006a0004c0002t0001g0054 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.889-107G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 4/21 | chr12 | 121934140 | ||||||
| chr12:121934655
|
T | TATCGCTG others(11): Show |
1 | a0001c0001t0001g0169 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.998+302_998+319dup others(18): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr12 | 121934655 | |||||
| chr12:121934659
|
G | A | 1 | a0003c0003t0001g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.998+303G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121934659 | ||||||
| chr12:121934661
|
T | G | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.998+305T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121934661 | ||||||
| chr12:121934781
|
C | G | 86 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(83): Show | 87 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.998+425C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121934781 | ||||||
| chr12:121934867
|
C | T | 1 | a0004c0002t0001g0012 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.998+511C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121934867 | ||||||
| chr12:121934909
|
A | C | 148 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(145): Show | 149 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.998+553A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121934909 | ||||||
| chr12:121935136
|
T | G | 4 | a0003c0003t0001g0348a0003c0003t0001g0349a0003c0003t0001g0350others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.998+780T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121935136 | ||||||
| chr12:121935247
|
G | A | 1 | a0002c0008t0001g0280 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.998+891G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121935247 | ||||||
| chr12:121935252
|
C | T | 1 | a0003c0003t0001g0109 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.998+896C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121935252 | ||||||
| chr12:121935260
|
C | T | 1 | a0006c0006t0001g0259 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.998+904C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121935260 | ||||||
| chr12:121935373
|
C | T | 30 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.998+1017C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121935373 | ||||||
| chr12:121935730
|
G | A | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.998+1374G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121935730 | ||||||
| chr12:121935822
|
C | G | 1 | a0002c0004t0001g0281 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.998+1466C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121935822 | ||||||
| chr12:121935823
|
C | T | 30 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.998+1467C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121935823 | ||||||
| chr12:121935892
|
C | T | 54 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(51): Show | 55 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.998+1536C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121935892 | ||||||
| chr12:121935916
|
G | A | 121 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(118): Show | 122 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.998+1560G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121935916 | ||||||
| chr12:121936002
|
G | A | 1 | a0006c0006t0001g0342 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.998+1646G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121936002 | ||||||
| chr12:121936172
|
G | A | 1 | a0006c0006t0001g0267 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.998+1816G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121936172 | ||||||
| chr12:121936202
|
G | A | 30 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.998+1846G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121936202 | ||||||
| chr12:121936282
|
T | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(107): Show | 111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.998+1926T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121936282 | ||||||
| chr12:121936447
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.998+2091A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121936447 | ||||||
| chr12:121936550
|
TG | T | 121 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(118): Show | 122 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.998+2199delG | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr12 | 121936550 | |||||
| chr12:121936607
|
C | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(107): Show | 111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.998+2251C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121936607 | ||||||
| chr12:121936621
|
G | A | 10 | a0006c0006t0001g0253a0006c0006t0001g0254a0006c0006t0001g0255others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.998+2265G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121936621 | ||||||
| chr12:121936677
|
C | G | 54 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(51): Show | 55 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.998+2321C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121936677 | ||||||
| chr12:121936949
|
G | T | 12 | a0005c0005t0001g0218a0005c0005t0001g0219a0005c0005t0001g0220others(9): Show | 12 | HG01168.hp1 HG01169.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.998+2593G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121936949 | ||||||
| chr12:121936960
|
C | T | 1 | a0004c0002t0001g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.998+2604C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121936960 | ||||||
| chr12:121936982
|
C | T | 43 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(40): Show | 43 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.998+2626C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121936982 | ||||||
| chr12:121936991
|
G | A | 53 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(50): Show | 54 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.998+2635G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121936991 | ||||||
| chr12:121937162
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.998+2806G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121937162 | ||||||
| chr12:121937182
|
G | A | 2 | a0006c0006t0001g0343a0006c0006t0001g0344 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.998+2826G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121937182 | ||||||
| chr12:121937234
|
G | A | 32 | a0006c0006t0001g0064a0006c0006t0001g0246a0006c0006t0001g0247others(29): Show | 32 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.998+2878G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121937234 | ||||||
| chr12:121937254
|
T | C | 3 | a0002c0004t0001g0303a0002c0004t0001g0304a0002c0004t0001g0317 | 3 | HG03834.hp1 HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.998+2898T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121937254 | ||||||
| chr12:121937267
|
G | A | 121 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(118): Show | 122 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.998+2911G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121937267 | ||||||
| chr12:121937270
|
T | A | 53 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(50): Show | 54 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.998+2914T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121937270 | ||||||
| chr12:121937316
|
A | C | 1 | a0006c0006t0001g0341 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.998+2960A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121937316 | ||||||
| chr12:121937318
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.998+2962C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121937318 | ||||||
| chr12:121937357
|
G | C | 1 | a0001c0001t0001g0111 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.998+3001G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121937357 | ||||||
| chr12:121937520
|
G | A | 1 | a0007c0007t0001g0069 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.998+3164G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121937520 | ||||||
| chr12:121937554
|
G | A | 30 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.998+3198G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121937554 | ||||||
| chr12:121937941
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.998+3585G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121937941 | ||||||
| chr12:121938142
|
C | A | 1 | a0001c0001t0001g0111 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.998+3786C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121938142 | ||||||
| chr12:121938171
|
A | AT | 20 | a0003c0012t0001g0083a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.998+3828dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr12 | 121938171 | |||||
| chr12:121938284
|
A | T | 1 | a0001c0001t0001g0183 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.998+3928A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121938284 | ||||||
| chr12:121938416
|
G | T | 1 | a0003c0003t0001g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.998+4060G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121938416 | ||||||
| chr12:121938626
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.999-3908G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121938626 | ||||||
| chr12:121938748
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.999-3786C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121938748 | ||||||
| chr12:121938797
|
A | G | 1 | a0007c0007t0001g0076 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.999-3737A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121938797 | ||||||
| chr12:121938834
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.999-3700C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121938834 | ||||||
| chr12:121938851
|
A | G | 121 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(118): Show | 122 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.999-3683A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121938851 | ||||||
| chr12:121938874
|
C | T | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.999-3660C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121938874 | ||||||
| chr12:121938879
|
A | T | 1 | a0003c0003t0001g0271 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.999-3655A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121938879 | ||||||
| chr12:121938901
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.999-3633C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121938901 | ||||||
| chr12:121938985
|
TA | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(109): Show | 113 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.999-3536delA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr12 | 121938985 | |||||
| chr12:121939081
|
G | A | 86 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(83): Show | 87 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.999-3453G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121939081 | ||||||
| chr12:121939123
|
G | A | 1 | a0003c0003t0001g0330 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.999-3411G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121939123 | ||||||
| chr12:121939173
|
G | A | 1 | a0006c0006t0001g0064 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.999-3361G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121939173 | ||||||
| chr12:121939182
|
G | A | 302 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(299): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.999-3352G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121939182 | ||||||
| chr12:121939186
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.999-3348A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121939186 | ||||||
| chr12:121939265
|
G | A | 2 | a0002c0004t0001g0318a0003c0003t0001g0271 | 2 | HG02258.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.999-3269G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121939265 | ||||||
| chr12:121939291
|
A | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(106): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.999-3243A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121939291 | ||||||
| chr12:121939479
|
C | T | 1 | a0004c0002t0001g0008 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.999-3055C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121939479 | ||||||
| chr12:121939547
|
ATTTGTGA others(65): Show |
A | 3 | a0003c0003t0001g0332a0003c0003t0001g0333a0003c0003t0001g0334 | 3 | HG02895.hp2 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.999-2986_999-2915d others(74): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121939547 | ||||||
| chr12:121939604
|
T | A | 18 | a0002c0004t0001g0056a0007c0007t0001g0067a0007c0007t0001g0068others(15): Show | 18 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.999-2930T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121939604 | ||||||
| chr12:121939605
|
A | T | 30 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.999-2929A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121939605 | ||||||
| chr12:121939623
|
G | A | 1 | a0004c0002t0001g0049 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.999-2911G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121939623 | ||||||
| chr12:121939772
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.999-2762A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121939772 | ||||||
| chr12:121939792
|
G | A | 3 | a0003c0003t0001g0332a0003c0003t0001g0333a0003c0003t0001g0334 | 3 | HG02895.hp2 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.999-2742G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121939792 | ||||||
| chr12:121940089
|
C | T | 53 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(50): Show | 54 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.999-2445C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121940089 | ||||||
| chr12:121940184
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.999-2350C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121940184 | ||||||
| chr12:121940300
|
G | A | 301 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(298): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.999-2234G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121940300 | ||||||
| chr12:121940504
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.999-2030T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121940504 | ||||||
| chr12:121940544
|
A | T | 1 | a0003c0009t0001g0058 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.999-1990A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121940544 | ||||||
| chr12:121940649
|
C | T | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.999-1885C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121940649 | ||||||
| chr12:121940723
|
A | G | 1 | a0007c0007t0001g0078 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.999-1811A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121940723 | ||||||
| chr12:121940736
|
G | T | 1 | a0001c0001t0001g0169 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.999-1798G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121940736 | ||||||
| chr12:121940921
|
G | A | 4 | a0003c0003t0001g0348a0003c0003t0001g0349a0003c0003t0001g0350others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.999-1613G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121940921 | ||||||
| chr12:121940932
|
G | C | 6 | a0003c0003t0001g0106a0003c0003t0001g0107a0003c0003t0001g0108others(3): Show | 6 | HG00639.hp1 HG01109.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.999-1602G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121940932 | ||||||
| chr12:121941029
|
T | C | 4 | a0003c0003t0001g0348a0003c0003t0001g0349a0003c0003t0001g0350others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.999-1505T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121941029 | ||||||
| chr12:121941061
|
C | A | 2 | a0003c0012t0001g0083a0003c0012t0001g0084 | 2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.999-1473C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121941061 | ||||||
| chr12:121941285
|
G | A | 85 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(82): Show | 86 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.999-1249G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121941285 | ||||||
| chr12:121941330
|
C | CT | 125 | a0001c0001t0001g0116a0001c0001t0001g0122a0001c0001t0001g0132others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.999-1183dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr12 | 121941330 | |||||
| chr12:121941330
|
C | CTT | 34 | a0002c0004t0001g0004a0002c0004t0001g0055a0002c0004t0001g0289others(31): Show | 34 | HG00438.hp1 HG00597.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.999-1184_999-1183d others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr12 | 121941330 | |||||
| chr12:121941330
|
C | CTTT | 28 | a0005c0005t0001g0218a0005c0005t0001g0219a0005c0005t0001g0220others(25): Show | 28 | HG01168.hp1 HG01169.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.999-1185_999-1183d others(5): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr12 | 121941330 | |||||
| chr12:121941330
|
C | CTTTT | 7 | a0005c0005t0001g0235a0005c0005t0001g0236a0005c0005t0001g0237others(4): Show | 7 | HG00423.hp1 HG02027.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.999-1186_999-1183d others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr12 | 121941330 | |||||
| chr12:121941436
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.999-1098C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121941436 | ||||||
| chr12:121941440
|
A | G | 4 | a0003c0003t0001g0104a0003c0003t0001g0320a0003c0003t0001g0322others(1): Show | 4 | HG01515.hp2 HG01517.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.999-1094A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121941440 | ||||||
| chr12:121941854
|
G | C | 2 | a0005c0005t0001g0336a0005c0005t0001g0346 | 2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.999-680G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121941854 | ||||||
| chr12:121941861
|
C | G | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.999-673C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121941861 | ||||||
| chr12:121941940
|
C | T | 2 | a0008c0010t0001g0065a0008c0010t0001g0066 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.999-594C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121941940 | ||||||
| chr12:121941963
|
A | G | 32 | a0006c0006t0001g0064a0006c0006t0001g0246a0006c0006t0001g0247others(29): Show | 32 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.999-571A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121941963 | ||||||
| chr12:121942047
|
G | T | 10 | a0002c0004t0001g0281a0002c0004t0001g0282a0002c0004t0001g0284others(7): Show | 10 | HG00438.hp1 HG02040.hp1 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.999-487G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121942047 | ||||||
| chr12:121942077
|
G | C | 3 | a0001c0001t0001g0133a0001c0001t0001g0163a0001c0001t0001g0193 | 3 | NA18945.hp1 NA18953.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.999-457G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121942077 | ||||||
| chr12:121942295
|
A | G | 35 | a0005c0005t0001g0218a0005c0005t0001g0219a0005c0005t0001g0220others(32): Show | 35 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.999-239A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121942295 | ||||||
| chr12:121942343
|
G | A | 1 | a0006c0011t0001g0283 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.999-191G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121942343 | ||||||
| chr12:121942368
|
A | G | 299 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.999-166A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121942368 | ||||||
| chr12:121942421
|
C | A | 1 | a0002c0008t0001g0311 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.999-113C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121942421 | ||||||
| chr12:121942469
|
C | T | 1 | a0002c0004t0001g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.999-65C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121942469 | ||||||
| chr12:121942513
|
C | T | 13 | a0003c0003t0001g0352a0006c0006t0001g0249a0006c0006t0001g0250others(10): Show | 13 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.999-21C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 5/21 | chr12 | 121942513 | ||||||
| chr12:121942672
|
C | T | 21 | a0003c0003t0001g0057a0003c0012t0001g0083a0003c0012t0001g0084others(18): Show | 21 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.1110+27C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 6/21 | chr12 | 121942672 | ||||||
| chr12:121942787
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0001g0203 | 2 | HG02071.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.1111-108G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 6/21 | chr12 | 121942787 | ||||||
| chr12:121943178
|
T | G | 1 | a0001c0001t0001g0201 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1191+203T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121943178 | ||||||
| chr12:121943182
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(150): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1191+207A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121943182 | ||||||
| chr12:121943228
|
T | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(150): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1191+253T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121943228 | ||||||
| chr12:121943261
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1191+286C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121943261 | ||||||
| chr12:121943288
|
C | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(150): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1191+313C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121943288 | ||||||
| chr12:121943521
|
C | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0326a0001c0001t0001g0327 | 3 | HG00741.hp1 HG01081.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1191+546C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121943521 | ||||||
| chr12:121943666
|
C | T | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1191+691C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121943666 | ||||||
| chr12:121943678
|
T | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(150): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1191+703T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121943678 | ||||||
| chr12:121943693
|
G | A | 1 | a0002c0008t0001g0307 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1191+718G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121943693 | ||||||
| chr12:121943936
|
T | G | 121 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(118): Show | 122 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.1191+961T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121943936 | ||||||
| chr12:121943938
|
G | A | 35 | a0005c0005t0001g0218a0005c0005t0001g0219a0005c0005t0001g0220others(32): Show | 35 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.1191+963G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121943938 | ||||||
| chr12:121944178
|
G | GTGCCAGG others(21): Show |
1 | a0001c0001t0001g0201 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1191+1204_1191+123 others(32): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr12 | 121944178 | |||||
| chr12:121944273
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(150): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1191+1298A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121944273 | ||||||
| chr12:121944323
|
T | G | 40 | a0003c0003t0001g0087a0003c0003t0001g0088a0003c0003t0001g0089others(37): Show | 40 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.1191+1348T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121944323 | ||||||
| chr12:121944686
|
T | C | 1 | a0003c0009t0001g0060 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1191+1711T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121944686 | ||||||
| chr12:121944795
|
T | A | 1 | a0001c0001t0001g0201 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1191+1820T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121944795 | ||||||
| chr12:121944796
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1191+1821C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121944796 | ||||||
| chr12:121944797
|
T | C | 1 | a0001c0001t0001g0201 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1191+1822T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121944797 | ||||||
| chr12:121944803
|
G | A | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1191+1828G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121944803 | ||||||
| chr12:121944810
|
G | T | 18 | a0003c0003t0001g0057a0007c0007t0001g0067a0007c0007t0001g0068others(15): Show | 18 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.1191+1835G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121944810 | ||||||
| chr12:121944955
|
T | A | 121 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(118): Show | 122 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.1191+1980T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121944955 | ||||||
| chr12:121945046
|
G | A | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1191+2071G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121945046 | ||||||
| chr12:121945241
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1191+2266C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121945241 | ||||||
| chr12:121945327
|
G | C | 4 | a0003c0003t0001g0264a0004c0002t0001g0038a0004c0002t0001g0039others(1): Show | 4 | HG02451.hp2 NA18971.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1191+2352G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121945327 | ||||||
| chr12:121945327
|
GTTTTC | G | 31 | a0003c0003t0001g0087a0003c0003t0001g0088a0003c0003t0001g0089others(28): Show | 31 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1191+2377_1191+238 others(9): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr12 | 121945327 | |||||
| chr12:121945327
|
GTTTTCTT others(3): Show |
G | 2 | a0004c0002t0001g0034a0004c0002t0001g0035 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1191+2372_1191+238 others(14): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr12 | 121945327 | |||||
| chr12:121945332
|
C | G | 153 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0132others(150): Show | 154 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(151): Show |
intron_variant | MODIFIER | c.1191+2357C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121945332 | ||||||
| chr12:121945337
|
C | G | 38 | a0002c0004t0001g0274a0002c0004t0001g0275a0005c0005t0001g0218others(35): Show | 38 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(35): Show |
intron_variant | MODIFIER | c.1191+2362C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121945337 | ||||||
| chr12:121945354
|
T | C | 1 | a0001c0001t0001g0201 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1191+2379T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121945354 | ||||||
| chr12:121945529
|
C | G | 2 | a0008c0010t0001g0065a0008c0010t0001g0066 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1191+2554C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121945529 | ||||||
| chr12:121945545
|
A | G | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1191+2570A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121945545 | ||||||
| chr12:121945586
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1191+2611G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121945586 | ||||||
| chr12:121945708
|
T | C | 300 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(297): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1191+2733T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121945708 | ||||||
| chr12:121945760
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(106): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1191+2785G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121945760 | ||||||
| chr12:121945932
|
C | T | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1191+2957C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121945932 | ||||||
| chr12:121946282
|
T | C | 1 | a0002c0004t0001g0293 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1192-2702T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121946282 | ||||||
| chr12:121946394
|
G | A | 2 | a0006c0006t0001g0343a0006c0006t0001g0344 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1192-2590G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121946394 | ||||||
| chr12:121946438
|
A | G | 42 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(39): Show | 42 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.1192-2546A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121946438 | ||||||
| chr12:121946530
|
T | G | 4 | a0002c0004t0001g0295a0002c0004t0001g0296a0002c0004t0001g0300others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1192-2454T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121946530 | ||||||
| chr12:121946551
|
A | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1192-2433A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121946551 | ||||||
| chr12:121946554
|
T | C | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1192-2430T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121946554 | ||||||
| chr12:121946779
|
G | A | 5 | a0004c0002t0001g0007a0004c0002t0001g0013a0004c0002t0001g0021others(2): Show | 5 | HG00673.hp2 NA18939.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.1192-2205G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121946779 | ||||||
| chr12:121946859
|
A | G | 351 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(348): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1192-2125A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121946859 | ||||||
| chr12:121947053
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1192-1931T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121947053 | ||||||
| chr12:121947217
|
G | T | 1 | a0002c0004t0001g0282 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1192-1767G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121947217 | ||||||
| chr12:121947245
|
C | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1192-1739C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121947245 | ||||||
| chr12:121947247
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1192-1737A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121947247 | ||||||
| chr12:121947307
|
G | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1192-1677G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121947307 | ||||||
| chr12:121947396
|
G | A | 2 | a0004c0002t0001g0034a0004c0002t0001g0035 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1192-1588G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121947396 | ||||||
| chr12:121947580
|
C | T | 4 | a0003c0003t0001g0348a0003c0003t0001g0349a0003c0003t0001g0350others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1192-1404C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121947580 | ||||||
| chr12:121947784
|
C | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1192-1200C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121947784 | ||||||
| chr12:121947805
|
C | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1192-1179C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121947805 | ||||||
| chr12:121947948
|
G | A | 1 | a0004c0002t0001g0015 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1192-1036G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121947948 | ||||||
| chr12:121947958
|
G | A | 1 | a0003c0003t0001g0320 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1192-1026G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121947958 | ||||||
| chr12:121948195
|
G | A | 20 | a0003c0012t0001g0083a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.1192-789G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121948195 | ||||||
| chr12:121948271
|
T | G | 2 | a0005c0005t0001g0219a0005c0005t0001g0220 | 2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1192-713T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121948271 | ||||||
| chr12:121948306
|
G | A | 1 | a0002c0004t0001g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1192-678G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121948306 | ||||||
| chr12:121948394
|
T | G | 121 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(118): Show | 122 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.1192-590T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121948394 | ||||||
| chr12:121948609
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1192-375A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121948609 | ||||||
| chr12:121948677
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0328 | 2 | HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1192-307G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121948677 | ||||||
| chr12:121948698
|
C | T | 33 | a0002c0004t0001g0274a0002c0004t0001g0275a0003c0003t0001g0057others(30): Show | 33 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.1192-286C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121948698 | ||||||
| chr12:121948852
|
G | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1192-132G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121948852 | ||||||
| chr12:121948859
|
G | C | 338 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(335): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1192-125G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121948859 | ||||||
| chr12:121948901
|
A | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(108): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1192-83A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 7/21 | chr12 | 121948901 | ||||||
| chr12:121949256
|
C | T | 4 | a0001c0001t0001g0131a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | NA18966.hp1 NA18969.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1269+195C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/21 | chr12 | 121949256 | ||||||
| chr12:121949283
|
G | C | 1 | a0001c0001t0001g0213 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1269+222G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/21 | chr12 | 121949283 | ||||||
| chr12:121949431
|
G | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(108): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1269+370G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/21 | chr12 | 121949431 | ||||||
| chr12:121949481
|
G | GT | 77 | a0001c0001t0001g0124a0001c0001t0001g0159a0001c0001t0001g0165others(74): Show | 77 | HG00423.hp1 HG00741.hp2 HG01168.hp1 others(74): Show |
intron_variant | MODIFIER | c.1269+440dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr12 | 121949481 | |||||
| chr12:121949481
|
G | GTT | 51 | a0001c0001t0001g0214a0002c0004t0001g0003a0002c0004t0001g0004others(48): Show | 52 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.1269+439_1269+440d others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr12 | 121949481 | |||||
| chr12:121949481
|
GT | G | 12 | a0003c0003t0001g0091a0003c0003t0001g0330a0003c0003t0001g0332others(9): Show | 12 | HG00323.hp1 HG01099.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1269+440delT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr12 | 121949481 | |||||
| chr12:121949831
|
A | G | 303 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1269+770A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/21 | chr12 | 121949831 | ||||||
| chr12:121949966
|
C | G | 31 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(28): Show | 31 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.1269+905C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/21 | chr12 | 121949966 | ||||||
| chr12:121950408
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1270-1072A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/21 | chr12 | 121950408 | ||||||
| chr12:121950425
|
A | G | 1 | a0004c0002t0001g0035 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1270-1055A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/21 | chr12 | 121950425 | ||||||
| chr12:121950429
|
T | C | 1 | a0004c0002t0001g0035 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1270-1051T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/21 | chr12 | 121950429 | ||||||
| chr12:121950461
|
T | C | 20 | a0003c0012t0001g0083a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.1270-1019T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/21 | chr12 | 121950461 | ||||||
| chr12:121950490
|
A | G | 303 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1270-990A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/21 | chr12 | 121950490 | ||||||
| chr12:121950941
|
G | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1270-539G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/21 | chr12 | 121950941 | ||||||
| chr12:121951033
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1270-447A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/21 | chr12 | 121951033 | ||||||
| chr12:121951044
|
C | T | 1 | a0007c0007t0001g0071 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1270-436C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/21 | chr12 | 121951044 | ||||||
| chr12:121951047
|
C | T | 1 | a0006c0006t0001g0261 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1270-433C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/21 | chr12 | 121951047 | ||||||
| chr12:121951111
|
C | T | 4 | a0004c0002t0001g0006a0004c0002t0001g0034a0004c0002t0001g0035others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1270-369C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/21 | chr12 | 121951111 | ||||||
| chr12:121951115
|
G | A | 2 | a0007c0007t0001g0079a0007c0007t0001g0080 | 2 | HG03017.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1270-365G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/21 | chr12 | 121951115 | ||||||
| chr12:121951261
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1270-219A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/21 | chr12 | 121951261 | ||||||
| chr12:121951342
|
A | G | 303 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1270-138A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 8/21 | chr12 | 121951342 | ||||||
| chr12:121951558
|
A | G | 1 | a0003c0003t0001g0095 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1320+28A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121951558 | ||||||
| chr12:121951586
|
T | C | 1 | a0004c0002t0001g0024 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1320+56T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121951586 | ||||||
| chr12:121951668
|
G | T | 1 | a0002c0004t0001g0281 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1320+138G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121951668 | ||||||
| chr12:121951706
|
G | A | 1 | a0003c0003t0001g0096 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1320+176G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121951706 | ||||||
| chr12:121951741
|
C | A | 35 | a0005c0005t0001g0218a0005c0005t0001g0219a0005c0005t0001g0220others(32): Show | 35 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.1320+211C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121951741 | ||||||
| chr12:121951757
|
C | T | 35 | a0005c0005t0001g0218a0005c0005t0001g0219a0005c0005t0001g0220others(32): Show | 35 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.1320+227C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121951757 | ||||||
| chr12:121951859
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(106): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1320+329C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121951859 | ||||||
| chr12:121952013
|
C | T | 42 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(39): Show | 42 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.1320+483C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121952013 | ||||||
| chr12:121952070
|
C | T | 20 | a0003c0012t0001g0083a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.1320+540C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121952070 | ||||||
| chr12:121952153
|
A | G | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1320+623A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121952153 | ||||||
| chr12:121952178
|
G | T | 42 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(39): Show | 42 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.1320+648G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121952178 | ||||||
| chr12:121952208
|
C | T | 17 | a0007c0007t0001g0067a0007c0007t0001g0068a0007c0007t0001g0069others(14): Show | 17 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.1320+678C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121952208 | ||||||
| chr12:121952240
|
T | TA | 28 | a0002c0004t0001g0276a0004c0002t0001g0028a0004c0002t0001g0032others(25): Show | 28 | HG01258.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1320+741dupA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 121952240 | |||||
| chr12:121952240
|
T | TAA | 70 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(67): Show | 71 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.1320+740_1320+741d others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 121952240 | |||||
| chr12:121952240
|
T | TAAA | 25 | a0002c0004t0001g0086a0002c0004t0001g0273a0002c0004t0001g0300others(22): Show | 25 | HG00423.hp1 HG00642.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.1320+739_1320+741d others(5): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 121952240 | |||||
| chr12:121952240
|
T | TAAAAA | 6 | a0002c0004t0001g0304a0002c0004t0001g0317a0003c0009t0001g0059others(3): Show | 6 | HG04184.hp2 HG04199.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1320+737_1320+741d others(7): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 121952240 | |||||
| chr12:121952240
|
T | TAAAAAAA others(4): Show |
2 | a0004c0002t0001g0034a0004c0002t0001g0035 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1320+731_1320+741d others(13): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 121952240 | |||||
| chr12:121952240
|
T | TAAAAAAA others(5): Show |
1 | a0004c0002t0001g0013 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1320+730_1320+741d others(14): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 121952240 | |||||
| chr12:121952240
|
T | TAAAAAAA others(6): Show |
8 | a0004c0002t0001g0009a0004c0002t0001g0012a0004c0002t0001g0026others(5): Show | 8 | HG00609.hp1 HG00738.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1320+729_1320+741d others(15): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 121952240 | |||||
| chr12:121952240
|
T | TAAAAAAA others(7): Show |
10 | a0004c0002t0001g0007a0004c0002t0001g0011a0004c0002t0001g0014others(7): Show | 10 | HG00673.hp2 HG02155.hp2 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.1320+728_1320+741d others(16): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 121952240 | |||||
| chr12:121952240
|
T | TAAAAAAA others(8): Show |
4 | a0004c0002t0001g0036a0004c0002t0001g0044a0004c0002t0001g0049others(1): Show | 4 | HG02135.hp2 HG02738.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.1320+727_1320+741d others(17): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 121952240 | |||||
| chr12:121952240
|
T | TAAAAAAA others(9): Show |
1 | a0004c0002t0001g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1320+726_1320+741d others(18): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 121952240 | |||||
| chr12:121952240
|
T | TAAAAAAA others(11): Show |
2 | a0004c0002t0001g0020a0004c0002t0001g0047 | 2 | HG00140.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1320+724_1320+741d others(20): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 121952240 | |||||
| chr12:121952240
|
T | TAAAAAAA others(12): Show |
1 | a0004c0002t0001g0006 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1320+723_1320+741d others(21): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 121952240 | |||||
| chr12:121952240
|
TAAAAAAA others(4): Show |
T | 35 | a0001c0001t0001g0135a0001c0001t0001g0185a0001c0001t0001g0200others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.1320+731_1320+741d others(13): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 121952240 | |||||
| chr12:121952240
|
TAAAAAAA others(5): Show |
T | 117 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(114): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.1320+730_1320+741d others(14): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 121952240 | |||||
| chr12:121952240
|
TAAAAAAA others(6): Show |
T | 3 | a0001c0001t0001g0131a0001c0001t0001g0162a0001c0021t0001g0202 | 3 | HG01515.hp1 HG02293.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1320+729_1320+741d others(15): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 121952240 | |||||
| chr12:121952418
|
T | TA | 3 | a0001c0001t0001g0126a0001c0001t0001g0134a0001c0001t0001g0215 | 3 | HG02071.hp2 HG03927.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1320+889dupA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 121952418 | |||||
| chr12:121952420
|
T | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(150): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1320+890T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121952420 | ||||||
| chr12:121952420
|
T | TAA | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1320+903_1320+904d others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 121952420 | |||||
| chr12:121952420
|
TA | T | 37 | a0002c0004t0001g0003a0004c0002t0001g0028a0005c0005t0001g0218others(34): Show | 37 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.1320+904delA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 121952420 | |||||
| chr12:121952445
|
A | G | 1 | a0004c0002t0001g0043 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1320+915A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121952445 | ||||||
| chr12:121953051
|
A | G | 3 | a0002c0004t0001g0292a0002c0004t0001g0293a0002c0004t0001g0312 | 3 | NA18747.hp2 NA19068.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1321-1069A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121953051 | ||||||
| chr12:121953148
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG00738.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1321-972G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121953148 | ||||||
| chr12:121953219
|
A | G | 32 | a0006c0006t0001g0064a0006c0006t0001g0246a0006c0006t0001g0247others(29): Show | 32 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.1321-901A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121953219 | ||||||
| chr12:121953230
|
A | G | 1 | a0003c0003t0001g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1321-890A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121953230 | ||||||
| chr12:121953328
|
G | A | 1 | a0004c0002t0001g0007 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1321-792G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121953328 | ||||||
| chr12:121953353
|
C | G | 1 | a0002c0004t0001g0317 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1321-767C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121953353 | ||||||
| chr12:121953510
|
A | G | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1321-610A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121953510 | ||||||
| chr12:121953673
|
A | G | 2 | a0001c0001t0001g0156a0001c0001t0001g0196 | 2 | HG00423.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1321-447A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121953673 | ||||||
| chr12:121953850
|
A | T | 1 | a0004c0002t0001g0024 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1321-270A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121953850 | ||||||
| chr12:121953910
|
A | G | 1 | a0006c0006t0001g0341 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1321-210A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121953910 | ||||||
| chr12:121954040
|
G | A | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1321-80G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121954040 | ||||||
| chr12:121954057
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(299): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1321-63A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 9/21 | chr12 | 121954057 | ||||||
| chr12:121954631
|
T | C | 1 | a0006c0006t0001g0254 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1535+297T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121954631 | ||||||
| chr12:121954636
|
T | TA | 44 | a0003c0009t0001g0061a0003c0012t0001g0083a0003c0012t0001g0272others(41): Show | 44 | HG00423.hp1 HG00673.hp2 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.1535+334dupA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 121954636 | |||||
| chr12:121954636
|
T | TAA | 18 | a0003c0003t0001g0271a0003c0003t0001g0348a0003c0003t0001g0349others(15): Show | 18 | HG01168.hp2 HG02135.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1535+333_1535+334d others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 121954636 | |||||
| chr12:121954636
|
T | TAAAA | 8 | a0001c0001t0001g0119a0001c0001t0001g0131a0001c0001t0001g0152others(5): Show | 8 | HG01169.hp1 HG01255.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.1535+331_1535+334d others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 121954636 | |||||
| chr12:121954636
|
T | TAAAAA | 53 | a0001c0001t0001g0001a0001c0001t0001g0116a0001c0001t0001g0117others(50): Show | 54 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.1535+330_1535+334d others(7): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 121954636 | |||||
| chr12:121954636
|
T | TAAAAAA | 41 | a0001c0001t0001g0114a0001c0001t0001g0118a0001c0001t0001g0127others(38): Show | 41 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.1535+329_1535+334d others(8): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 121954636 | |||||
| chr12:121954636
|
T | TAAAAAAA | 24 | a0001c0001t0001g0112a0001c0001t0001g0137a0001c0001t0001g0138others(21): Show | 24 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(21): Show |
intron_variant | MODIFIER | c.1535+328_1535+334d others(9): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 121954636 | |||||
| chr12:121954636
|
T | TAAAAAAA others(1): Show |
10 | a0001c0001t0001g0165a0001c0001t0001g0191a0003c0003t0001g0092others(7): Show | 10 | HG00741.hp2 HG01109.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1535+327_1535+334d others(10): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 121954636 | |||||
| chr12:121954636
|
TA | T | 36 | a0002c0004t0001g0055a0002c0004t0001g0056a0002c0004t0001g0278others(33): Show | 36 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1535+334delA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 121954636 | |||||
| chr12:121954636
|
TAA | T | 49 | a0002c0004t0001g0004a0002c0004t0001g0086a0002c0004t0001g0273others(46): Show | 50 | HG00609.hp2 HG00642.hp2 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.1535+333_1535+334d others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 121954636 | |||||
| chr12:121954636
|
TAAAAAAA others(4): Show |
T | 2 | a0001c0001t0001g0130a0001c0001t0001g0155 | 2 | HG00323.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1535+324_1535+334d others(13): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 121954636 | |||||
| chr12:121954636
|
TAAAAAAA others(5): Show |
T | 2 | a0001c0001t0001g0111a0001c0001t0001g0113 | 2 | HG00099.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.1535+323_1535+334d others(14): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 121954636 | |||||
| chr12:121954657
|
A | AC | 4 | a0003c0003t0001g0332a0003c0003t0001g0333a0008c0010t0001g0217others(1): Show | 4 | HG01099.hp2 HG02572.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1535+323_1535+324i others(3): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121954657 | ||||||
| chr12:121954657
|
A | C | 3 | a0003c0003t0001g0330a0003c0003t0001g0331a0003c0003t0001g0334 | 3 | HG01109.hp2 HG01243.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1535+323A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121954657 | ||||||
| chr12:121954789
|
G | A | 2 | a0003c0003t0001g0264a0003c0003t0001g0271 | 2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1535+455G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121954789 | ||||||
| chr12:121954882
|
C | T | 1 | a0002c0004t0001g0316 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1535+548C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121954882 | ||||||
| chr12:121954897
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1535+563G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121954897 | ||||||
| chr12:121955011
|
T | G | 1 | a0001c0001t0001g0143 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1535+677T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121955011 | ||||||
| chr12:121955041
|
G | A | 35 | a0005c0005t0001g0218a0005c0005t0001g0219a0005c0005t0001g0220others(32): Show | 35 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.1535+707G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121955041 | ||||||
| chr12:121955197
|
G | A | 119 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(116): Show | 120 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.1535+863G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121955197 | ||||||
| chr12:121955204
|
G | C | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1535+870G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121955204 | ||||||
| chr12:121955211
|
T | G | 1 | a0001c0021t0001g0202 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1535+877T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121955211 | ||||||
| chr12:121955240
|
G | T | 1 | a0002c0004t0001g0304 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1535+906G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121955240 | ||||||
| chr12:121955434
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0162 | 2 | HG01928.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1535+1100G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121955434 | ||||||
| chr12:121955529
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1535+1195G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121955529 | ||||||
| chr12:121955692
|
G | A | 1 | a0007c0007t0001g0081 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1535+1358G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121955692 | ||||||
| chr12:121955824
|
A | T | 18 | a0003c0003t0001g0057a0007c0007t0001g0067a0007c0007t0001g0068others(15): Show | 18 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.1536-1250A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121955824 | ||||||
| chr12:121956020
|
T | G | 2 | a0008c0010t0001g0065a0008c0010t0001g0066 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1536-1054T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121956020 | ||||||
| chr12:121956086
|
T | C | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1536-988T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121956086 | ||||||
| chr12:121956092
|
G | C | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1536-982G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121956092 | ||||||
| chr12:121956170
|
A | G | 119 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(116): Show | 120 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.1536-904A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121956170 | ||||||
| chr12:121956221
|
T | C | 3 | a0003c0012t0001g0083a0003c0012t0001g0084a0003c0012t0001g0272 | 3 | HG02109.hp2 HG02486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1536-853T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121956221 | ||||||
| chr12:121956299
|
G | A | 3 | a0001c0001t0001g0139a0001c0001t0001g0144a0001c0001t0001g0152 | 3 | HG00639.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1536-775G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121956299 | ||||||
| chr12:121956383
|
GATATACC others(31): Show |
G | 1 | a0003c0009t0001g0060 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1536-690_1536-653d others(40): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121956383 | ||||||
| chr12:121956599
|
G | A | 1 | a0006c0006t0001g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1536-475G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121956599 | ||||||
| chr12:121956797
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1536-277C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121956797 | ||||||
| chr12:121957015
|
A | C | 31 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(28): Show | 31 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.1536-59A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 10/21 | chr12 | 121957015 | ||||||
| chr12:121957350
|
G | A | 1 | a0006c0006t0001g0269 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1730+82G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 11/21 | chr12 | 121957350 | ||||||
| chr12:121957508
|
T | A | 4 | a0003c0003t0001g0348a0003c0003t0001g0349a0003c0003t0001g0350others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1730+240T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 11/21 | chr12 | 121957508 | ||||||
| chr12:121957595
|
T | C | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1730+327T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 11/21 | chr12 | 121957595 | ||||||
| chr12:121957683
|
G | A | 3 | a0002c0004t0001g0278a0002c0004t0001g0279a0002c0004t0001g0308 | 3 | NA18944.hp1 NA18960.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1730+415G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 11/21 | chr12 | 121957683 | ||||||
| chr12:121957691
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1730+423G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 11/21 | chr12 | 121957691 | ||||||
| chr12:121957703
|
C | CA | 269 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(266): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1730+455dupA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr12 | 121957703 | |||||
| chr12:121957703
|
C | CAA | 16 | a0001c0001t0001g0169a0001c0001t0001g0179a0001c0001t0001g0186others(13): Show | 16 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(13): Show |
intron_variant | MODIFIER | c.1730+454_1730+455d others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr12 | 121957703 | |||||
| chr12:121957703
|
CA | C | 7 | a0003c0003t0001g0271a0003c0009t0001g0058a0003c0009t0001g0059others(4): Show | 7 | HG02258.hp2 HG03491.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.1730+455delA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr12 | 121957703 | |||||
| chr12:121957811
|
T | A | 2 | a0009c0013t0001g0299a0009c0013t0001g0324 | 2 | HG00609.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1731-461T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 11/21 | chr12 | 121957811 | ||||||
| chr12:121957823
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1731-449C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 11/21 | chr12 | 121957823 | ||||||
| chr12:121957871
|
A | G | 290 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(287): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.1731-401A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 11/21 | chr12 | 121957871 | ||||||
| chr12:121958538
|
C | T | 1 | a0005c0015t0001g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1981+16C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 12/21 | chr12 | 121958538 | ||||||
| chr12:121958667
|
C | T | 119 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(116): Show | 120 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.1981+145C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 12/21 | chr12 | 121958667 | ||||||
| chr12:121958782
|
G | C | 1 | a0003c0003t0001g0271 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1982-161G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 12/21 | chr12 | 121958782 | ||||||
| chr12:121958786
|
A | G | 2 | a0003c0003t0001g0348a0003c0003t0001g0349 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1982-157A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 12/21 | chr12 | 121958786 | ||||||
| chr12:121959184
|
C | T | 1 | a0005c0005t0001g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2133+90C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | chr12 | 121959184 | ||||||
| chr12:121959414
|
T | G | 2 | a0006c0006t0001g0253a0006c0006t0001g0255 | 2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2133+320T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | chr12 | 121959414 | ||||||
| chr12:121959422
|
G | A | 1 | a0006c0006t0001g0251 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2133+328G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | chr12 | 121959422 | ||||||
| chr12:121959445
|
G | A | 119 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(116): Show | 120 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.2133+351G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | chr12 | 121959445 | ||||||
| chr12:121959464
|
C | T | 3 | a0003c0003t0001g0320a0003c0003t0001g0322a0003c0003t0001g0323 | 3 | HG01515.hp2 HG01517.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.2133+370C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | chr12 | 121959464 | ||||||
| chr12:121959570
|
T | C | 301 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(298): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.2133+476T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | chr12 | 121959570 | ||||||
| chr12:121959739
|
C | CTGGAAAG others(10): Show |
1 | a0003c0009t0001g0060 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2133+646_2133+662d others(19): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr12 | 121959739 | |||||
| chr12:121959862
|
T | A | 119 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(116): Show | 120 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.2134-723T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | chr12 | 121959862 | ||||||
| chr12:121959948
|
A | AC | 48 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(45): Show | 49 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.2134-636dupC | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr12 | 121959948 | |||||
| chr12:121959949
|
C | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(156): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.2134-636C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | chr12 | 121959949 | ||||||
| chr12:121959950
|
A | C | 301 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(298): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.2134-635A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | chr12 | 121959950 | ||||||
| chr12:121959955
|
C | T | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2134-630C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | chr12 | 121959955 | ||||||
| chr12:121960003
|
T | C | 28 | a0003c0003t0001g0330a0003c0003t0001g0331a0003c0003t0001g0332others(25): Show | 28 | HG01099.hp2 HG01109.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.2134-582T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | chr12 | 121960003 | ||||||
| chr12:121960022
|
A | G | 1 | a0003c0012t0001g0272 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2134-563A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | chr12 | 121960022 | ||||||
| chr12:121960050
|
TTGAGCCC others(18): Show |
T | 1 | a0015c0025t0001g0027 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2134-528_2134-504d others(27): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr12 | 121960050 | |||||
| chr12:121960082
|
G | A | 1 | a0004c0002t0001g0032 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2134-503G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | chr12 | 121960082 | ||||||
| chr12:121960094
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.2134-491C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | chr12 | 121960094 | ||||||
| chr12:121960133
|
C | CA | 5 | a0001c0001t0001g0132a0001c0001t0001g0177a0003c0003t0001g0325others(2): Show | 5 | HG01261.hp2 HG02056.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.2134-444dupA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr12 | 121960133 | |||||
| chr12:121960142
|
C | T | 5 | a0005c0005t0001g0223a0005c0005t0001g0233a0005c0005t0001g0234others(2): Show | 5 | HG03834.hp2 NA18612.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.2134-443C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | chr12 | 121960142 | ||||||
| chr12:121960217
|
A | G | 301 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(298): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.2134-368A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | chr12 | 121960217 | ||||||
| chr12:121960477
|
C | T | 2 | a0003c0003t0001g0089a0003c0003t0001g0091 | 2 | HG00323.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2134-108C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | chr12 | 121960477 | ||||||
| chr12:121960511
|
C | T | 1 | a0015c0025t0001g0027 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2134-74C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 13/21 | chr12 | 121960511 | ||||||
| chr12:121960979
|
A | C | 2 | a0002c0004t0001g0300a0002c0004t0001g0315 | 2 | HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2307+221A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 14/21 | chr12 | 121960979 | ||||||
| chr12:121960994
|
G | A | 21 | a0005c0005t0001g0223a0005c0005t0001g0224a0005c0005t0001g0226others(18): Show | 21 | HG00423.hp1 HG02015.hp2 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.2307+236G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 14/21 | chr12 | 121960994 | ||||||
| chr12:121961036
|
C | T | 1 | a0005c0005t0001g0244 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2307+278C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 14/21 | chr12 | 121961036 | ||||||
| chr12:121961047
|
A | C | 48 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(45): Show | 49 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.2307+289A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 14/21 | chr12 | 121961047 | ||||||
| chr12:121961119
|
A | T | 2 | a0004c0002t0001g0005a0004c0002t0001g0017 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2307+361A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 14/21 | chr12 | 121961119 | ||||||
| chr12:121961267
|
C | A | 4 | a0003c0003t0001g0102a0003c0003t0001g0103a0003c0003t0001g0319others(1): Show | 4 | HG00741.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.2307+509C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 14/21 | chr12 | 121961267 | ||||||
| chr12:121961322
|
C | T | 1 | a0003c0012t0001g0272 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2307+564C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 14/21 | chr12 | 121961322 | ||||||
| chr12:121961442
|
G | A | 11 | a0006c0006t0001g0253a0006c0006t0001g0254a0006c0006t0001g0255others(8): Show | 11 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2308-536G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 14/21 | chr12 | 121961442 | ||||||
| chr12:121961643
|
T | G | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2308-335T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 14/21 | chr12 | 121961643 | ||||||
| chr12:121962267
|
T | A | 1 | a0002c0004t0001g0289 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2492+105T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121962267 | ||||||
| chr12:121962279
|
TGCTTTGC others(7): Show |
T | 1 | a0003c0009t0001g0060 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2492+119_2492+132d others(16): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121962279 | |||||
| chr12:121962637
|
A | G | 1 | a0007c0007t0001g0069 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2492+475A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121962637 | ||||||
| chr12:121962699
|
GA | G | 45 | a0001c0001t0001g0114a0001c0001t0001g0140a0001c0001t0001g0157others(42): Show | 45 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.2492+550delA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121962699 | |||||
| chr12:121962699
|
GAA | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(102): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.2492+549_2492+550d others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121962699 | |||||
| chr12:121962708
|
A | AAAAAGG | 60 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(57): Show | 60 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.2492+559_2492+564d others(8): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121962708 | |||||
| chr12:121962737
|
A | G | 1 | a0002c0004t0001g0003 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2492+575A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121962737 | ||||||
| chr12:121962853
|
G | T | 3 | a0006c0006t0001g0246a0006c0006t0001g0267a0006c0018t0001g0252 | 3 | HG01891.hp2 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2492+691G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121962853 | ||||||
| chr12:121962887
|
G | A | 11 | a0003c0003t0001g0330a0003c0003t0001g0331a0003c0003t0001g0332others(8): Show | 11 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.2492+725G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121962887 | ||||||
| chr12:121962907
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(107): Show | 111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.2492+745C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121962907 | ||||||
| chr12:121962908
|
G | A | 14 | a0007c0007t0001g0067a0007c0007t0001g0068a0007c0007t0001g0069others(11): Show | 14 | HG02523.hp1 HG03017.hp2 HG03239.hp2 others(11): Show |
intron_variant | MODIFIER | c.2492+746G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121962908 | ||||||
| chr12:121962956
|
A | G | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2492+794A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121962956 | ||||||
| chr12:121963174
|
G | T | 1 | a0006c0006t0001g0351 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2492+1012G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121963174 | ||||||
| chr12:121963232
|
C | T | 1 | a0003c0003t0001g0271 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2492+1070C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121963232 | ||||||
| chr12:121963445
|
G | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(105): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.2492+1283G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121963445 | ||||||
| chr12:121963450
|
A | G | 1 | a0003c0009t0001g0060 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2492+1288A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121963450 | ||||||
| chr12:121963452
|
G | T | 1 | a0003c0009t0001g0060 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2492+1290G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121963452 | ||||||
| chr12:121963471
|
C | A | 1 | a0003c0009t0001g0060 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2492+1309C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121963471 | ||||||
| chr12:121963496
|
G | A | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2492+1334G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121963496 | ||||||
| chr12:121963517
|
G | C | 2 | a0004c0002t0001g0006a0004c0002t0001g0054 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2492+1355G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121963517 | ||||||
| chr12:121963528
|
G | A | 1 | a0003c0009t0001g0059 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2492+1366G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121963528 | ||||||
| chr12:121963537
|
G | C | 34 | a0003c0003t0001g0271a0003c0012t0001g0083a0003c0012t0001g0084others(31): Show | 34 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(31): Show |
intron_variant | MODIFIER | c.2492+1375G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121963537 | ||||||
| chr12:121963595
|
A | G | 193 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(190): Show | 194 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.2492+1433A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121963595 | ||||||
| chr12:121963849
|
G | T | 1 | a0003c0009t0001g0060 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2492+1687G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121963849 | ||||||
| chr12:121963870
|
G | A | 1 | a0005c0005t0001g0229 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2492+1708G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121963870 | ||||||
| chr12:121964145
|
T | TTTG | 84 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(81): Show | 85 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.2492+2015_2492+201 others(7): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121964145 | |||||
| chr12:121964145
|
T | TTTGTTG | 11 | a0003c0003t0001g0348a0003c0003t0001g0349a0003c0003t0001g0350others(8): Show | 11 | HG02257.hp2 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2492+2012_2492+201 others(10): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121964145 | |||||
| chr12:121964145
|
TTTG | T | 161 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.2492+2015_2492+201 others(7): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121964145 | |||||
| chr12:121964145
|
TTTGTTG | T | 4 | a0003c0003t0001g0271a0003c0012t0001g0083a0003c0012t0001g0084others(1): Show | 4 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2492+2012_2492+201 others(10): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121964145 | |||||
| chr12:121964177
|
T | A | 1 | a0001c0001t0001g0188 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2492+2015T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121964177 | ||||||
| chr12:121964632
|
G | A | 36 | a0001c0001t0001g0194a0005c0005t0001g0218a0005c0005t0001g0219others(33): Show | 36 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.2493-2323G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121964632 | ||||||
| chr12:121964708
|
T | A | 1 | a0003c0009t0001g0060 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2493-2247T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121964708 | ||||||
| chr12:121964817
|
T | C | 58 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(55): Show | 58 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.2493-2138T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121964817 | ||||||
| chr12:121964882
|
G | A | 1 | a0003c0003t0001g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2493-2073G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121964882 | ||||||
| chr12:121964965
|
G | C | 53 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(50): Show | 54 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.2493-1990G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121964965 | ||||||
| chr12:121965163
|
C | CAGTTCAC others(30): Show |
1 | a0001c0001t0001g0204 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2493-1791_2493-175 others(41): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121965163 | |||||
| chr12:121965257
|
A | C | 9 | a0003c0003t0001g0330a0003c0003t0001g0331a0003c0003t0001g0332others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2493-1698A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121965257 | ||||||
| chr12:121965402
|
A | G | 3 | a0003c0003t0001g0332a0003c0003t0001g0333a0003c0003t0001g0334 | 3 | HG02895.hp2 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2493-1553A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121965402 | ||||||
| chr12:121965495
|
A | T | 5 | a0006c0006t0001g0253a0006c0006t0001g0255a0006c0006t0001g0256others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2493-1460A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121965495 | ||||||
| chr12:121965524
|
A | G | 2 | a0008c0010t0001g0065a0008c0010t0001g0066 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2493-1431A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121965524 | ||||||
| chr12:121965532
|
T | C | 26 | a0003c0003t0001g0330a0003c0003t0001g0331a0003c0003t0001g0332others(23): Show | 26 | HG01109.hp2 HG01168.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.2493-1423T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121965532 | ||||||
| chr12:121965807
|
C | CCTT | 12 | a0001c0001t0001g0119a0001c0001t0001g0162a0001c0001t0001g0169others(9): Show | 12 | HG00639.hp1 HG01255.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.2493-1135_2493-113 others(7): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121965807 | |||||
| chr12:121965821
|
T | TTC | 279 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(276): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.2493-1133_2493-113 others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121965821 | |||||
| chr12:121965822
|
T | TC | 6 | a0001c0001t0001g0120a0001c0001t0001g0157a0001c0001t0001g0174others(3): Show | 6 | HG01168.hp1 HG01256.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.2493-1133_2493-113 others(5): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121965822 | ||||||
| chr12:121965823
|
T | C | 1 | a0003c0009t0001g0063 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2493-1132T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121965823 | ||||||
| chr12:121965905
|
G | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(150): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.2493-1050G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121965905 | ||||||
| chr12:121966027
|
A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.2493-928A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966027 | ||||||
| chr12:121966079
|
C | T | 2 | a0006c0006t0001g0340a0011c0019t0002g0338 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2493-876C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966079 | ||||||
| chr12:121966106
|
A | G | 1 | a0003c0012t0001g0084 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2493-849A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966106 | ||||||
| chr12:121966118
|
A | G | 26 | a0003c0003t0001g0330a0003c0003t0001g0331a0003c0003t0001g0332others(23): Show | 26 | HG01109.hp2 HG01168.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.2493-837A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966118 | ||||||
| chr12:121966141
|
T | TCCCTTCC others(18): Show |
1 | a0006c0006t0001g0064 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2493-788_2493-764d others(27): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121966141 | |||||
| chr12:121966151
|
C | CCCCCTCC others(14): Show |
1 | a0001c0001t0001g0120 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2493-801_2493-800i others(23): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121966151 | |||||
| chr12:121966151
|
C | CCCCTCCC others(13): Show |
121 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0114others(118): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.2493-784_2493-765d others(22): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121966151 | |||||
| chr12:121966151
|
C | CCCCTCCC others(33): Show |
11 | a0001c0001t0001g0116a0001c0001t0001g0125a0001c0001t0001g0129others(8): Show | 11 | HG00741.hp1 HG01081.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.2493-765_2493-764i others(42): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121966151 | |||||
| chr12:121966155
|
T | TCCCCTCC others(14): Show |
1 | a0001c0001t0001g0204 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2493-796_2493-776d others(23): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121966155 | |||||
| chr12:121966161
|
C | CCCCTCCC others(48): Show |
1 | a0001c0001t0001g0178 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2493-765_2493-764i others(57): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121966161 | |||||
| chr12:121966171
|
T | TCCCTCCC others(28): Show |
1 | a0008c0010t0001g0065 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2493-765_2493-764i others(37): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121966171 | |||||
| chr12:121966171
|
T | TCCCTCCC others(53): Show |
1 | a0008c0010t0001g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2493-765_2493-764i others(62): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121966171 | |||||
| chr12:121966176
|
C | CCCCTCCC others(8): Show |
6 | a0003c0003t0001g0089a0003c0003t0001g0100a0003c0003t0001g0102others(3): Show | 6 | HG00741.hp2 HG01106.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.2493-765_2493-764i others(17): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121966176 | |||||
| chr12:121966191
|
C | T | 25 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(22): Show | 25 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.2493-764C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966191 | ||||||
| chr12:121966192
|
T | C | 34 | a0001c0001t0001g0111a0001c0001t0001g0113a0002c0008t0001g0311others(31): Show | 34 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.2493-763T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966192 | ||||||
| chr12:121966196
|
T | C | 27 | a0001c0001t0001g0111a0001c0001t0001g0113a0003c0003t0001g0057others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.2493-759T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966196 | ||||||
| chr12:121966196
|
T | TCCCTCCC others(43): Show |
1 | a0006c0006t0001g0250 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2493-750_2493-701d others(52): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121966196 | |||||
| chr12:121966206
|
T | C | 31 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(28): Show | 31 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.2493-749T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966206 | ||||||
| chr12:121966206
|
T | TCCCTC | 5 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0061others(2): Show | 5 | NA18942.hp1 NA18978.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.2493-739_2493-735d others(7): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121966206 | |||||
| chr12:121966207
|
C | CCCTCCCC others(12): Show |
1 | a0003c0009t0001g0060 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2493-735_2493-734i others(21): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121966207 | |||||
| chr12:121966211
|
C | T | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2493-744C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966211 | ||||||
| chr12:121966212
|
C | T | 24 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(21): Show | 24 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.2493-743C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966212 | ||||||
| chr12:121966216
|
C | T | 24 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(21): Show | 24 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.2493-739C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966216 | ||||||
| chr12:121966217
|
C | T | 6 | a0003c0003t0001g0089a0003c0003t0001g0100a0003c0003t0001g0102others(3): Show | 6 | HG00741.hp2 HG01106.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.2493-738C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966217 | ||||||
| chr12:121966221
|
T | C | 25 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(22): Show | 25 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.2493-734T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966221 | ||||||
| chr12:121966226
|
C | CCCCTCCC others(8): Show |
5 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0061others(2): Show | 5 | NA18942.hp1 NA18978.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.2493-715_2493-701d others(17): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121966226 | |||||
| chr12:121966226
|
C | CCCCTT | 6 | a0003c0003t0001g0089a0003c0003t0001g0100a0003c0003t0001g0102others(3): Show | 6 | HG00741.hp2 HG01106.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.2493-725_2493-724i others(7): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121966226 | |||||
| chr12:121966226
|
C | T | 25 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(22): Show | 25 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.2493-729C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966226 | ||||||
| chr12:121966231
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2493-724C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966231 | ||||||
| chr12:121966236
|
C | T | 1 | a0003c0003t0001g0332 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2493-719C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966236 | ||||||
| chr12:121966237
|
C | A | 1 | a0004c0002t0001g0033 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2493-718C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966237 | ||||||
| chr12:121966237
|
C | CCCTTCCC others(13): Show |
30 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.2493-701_2493-700i others(22): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121966237 | |||||
| chr12:121966241
|
T | C | 1 | a0003c0003t0001g0332 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2493-714T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966241 | ||||||
| chr12:121966250
|
T | TC | 8 | a0001c0001t0001g0120a0001c0001t0001g0171a0001c0001t0001g0184others(5): Show | 8 | HG00597.hp1 HG02155.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.2493-700dupC | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121966250 | |||||
| chr12:121966255
|
C | T | 1 | a0003c0003t0001g0332 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2493-700C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966255 | ||||||
| chr12:121966322
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0162 | 2 | HG01928.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.2493-633G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966322 | ||||||
| chr12:121966423
|
G | T | 58 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(55): Show | 58 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.2493-532G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966423 | ||||||
| chr12:121966427
|
A | AT | 35 | a0001c0001t0001g0001a0001c0001t0001g0118a0001c0001t0001g0120others(32): Show | 36 | HG00323.hp1 HG01257.hp1 HG01515.hp2 others(33): Show |
intron_variant | MODIFIER | c.2493-504dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121966427 | |||||
| chr12:121966427
|
A | ATT | 101 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.2493-505_2493-504d others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121966427 | |||||
| chr12:121966427
|
A | ATTT | 50 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0126others(47): Show | 50 | HG00597.hp1 HG00621.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.2493-506_2493-504d others(5): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121966427 | |||||
| chr12:121966427
|
AT | A | 16 | a0002c0004t0001g0003a0002c0004t0001g0274a0002c0004t0001g0282others(13): Show | 16 | HG01070.hp1 HG01168.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.2493-504delT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121966427 | |||||
| chr12:121966587
|
CT | C | 9 | a0001c0001t0001g0157a0001c0001t0001g0163a0001c0001t0001g0189others(6): Show | 9 | HG01168.hp1 HG01256.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2493-352delT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 121966587 | |||||
| chr12:121966591
|
T | C | 2 | a0008c0010t0001g0217a0008c0010t0001g0329 | 2 | HG01099.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2493-364T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966591 | ||||||
| chr12:121966854
|
G | A | 1 | a0014c0023t0001g0225 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2493-101G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966854 | ||||||
| chr12:121966935
|
C | G | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.2493-20C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 15/21 | chr12 | 121966935 | ||||||
| chr12:121967294
|
T | C | 2 | a0006c0006t0001g0340a0011c0019t0002g0338 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2607+225T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 16/21 | chr12 | 121967294 | ||||||
| chr12:121967441
|
G | A | 4 | a0004c0002t0001g0041a0004c0002t0001g0045a0004c0014t0001g0018others(1): Show | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.2607+372G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 16/21 | chr12 | 121967441 | ||||||
| chr12:121967513
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2607+444T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 16/21 | chr12 | 121967513 | ||||||
| chr12:121967529
|
C | T | 301 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(298): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.2607+460C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 16/21 | chr12 | 121967529 | ||||||
| chr12:121967574
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0213 | 2 | HG00408.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.2608-432C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 16/21 | chr12 | 121967574 | ||||||
| chr12:121967696
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2608-310C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 16/21 | chr12 | 121967696 | ||||||
| chr12:121968530
|
G | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.2771+361G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121968530 | ||||||
| chr12:121968541
|
C | CA | 29 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0089others(26): Show | 29 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.2771+373dupA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr12 | 121968541 | |||||
| chr12:121968641
|
AAT | A | 4 | a0003c0003t0001g0271a0003c0012t0001g0083a0003c0012t0001g0084others(1): Show | 4 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2771+475_2771+476d others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr12 | 121968641 | |||||
| chr12:121968643
|
T | C | 1 | a0005c0005t0001g0238 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2771+474T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121968643 | ||||||
| chr12:121968846
|
G | A | 121 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(118): Show | 122 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.2771+677G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121968846 | ||||||
| chr12:121968934
|
C | G | 2 | a0002c0004t0001g0055a0002c0004t0001g0056 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2771+765C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121968934 | ||||||
| chr12:121969053
|
C | T | 1 | a0006c0006t0001g0268 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2771+884C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121969053 | ||||||
| chr12:121969277
|
G | A | 1 | a0002c0004t0001g0308 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2771+1108G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121969277 | ||||||
| chr12:121969297
|
G | A | 4 | a0003c0003t0001g0271a0003c0012t0001g0083a0003c0012t0001g0084others(1): Show | 4 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2771+1128G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121969297 | ||||||
| chr12:121969624
|
C | A | 1 | a0004c0002t0001g0007 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2771+1455C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121969624 | ||||||
| chr12:121969653
|
C | A | 26 | a0003c0003t0001g0330a0003c0003t0001g0331a0003c0003t0001g0332others(23): Show | 26 | HG01109.hp2 HG01168.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.2771+1484C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121969653 | ||||||
| chr12:121969664
|
T | A | 35 | a0005c0005t0001g0218a0005c0005t0001g0219a0005c0005t0001g0220others(32): Show | 35 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.2771+1495T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121969664 | ||||||
| chr12:121969722
|
A | C | 1 | a0006c0006t0001g0351 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2771+1553A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121969722 | ||||||
| chr12:121969895
|
T | C | 1 | a0003c0003t0001g0350 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2771+1726T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121969895 | ||||||
| chr12:121970122
|
T | C | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.2771+1953T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121970122 | ||||||
| chr12:121970154
|
C | T | 1 | a0005c0005t0001g0238 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2771+1985C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121970154 | ||||||
| chr12:121970199
|
C | T | 2 | a0003c0003t0001g0088a0003c0003t0001g0099 | 2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2771+2030C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121970199 | ||||||
| chr12:121970415
|
C | T | 1 | a0005c0005t0001g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2771+2246C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121970415 | ||||||
| chr12:121970573
|
T | G | 1 | a0006c0006t0001g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2771+2404T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121970573 | ||||||
| chr12:121970747
|
C | T | 1 | a0007c0007t0001g0069 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2771+2578C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121970747 | ||||||
| chr12:121970906
|
T | A | 2 | a0003c0012t0001g0083a0003c0012t0001g0084 | 2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2771+2737T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121970906 | ||||||
| chr12:121970917
|
G | C | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2771+2748G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121970917 | ||||||
| chr12:121970949
|
T | A | 302 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(299): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.2771+2780T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121970949 | ||||||
| chr12:121971019
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2771+2850G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121971019 | ||||||
| chr12:121971155
|
G | T | 1 | a0003c0003t0001g0090 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2771+2986G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121971155 | ||||||
| chr12:121971183
|
A | T | 6 | a0002c0004t0001g0281a0002c0004t0001g0284a0002c0004t0001g0291others(3): Show | 6 | HG00438.hp1 HG02040.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.2771+3014A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121971183 | ||||||
| chr12:121971468
|
G | A | 4 | a0003c0003t0001g0271a0003c0012t0001g0083a0003c0012t0001g0084others(1): Show | 4 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2771+3299G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121971468 | ||||||
| chr12:121971507
|
C | T | 1 | a0006c0006t0001g0262 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2771+3338C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121971507 | ||||||
| chr12:121971700
|
C | T | 1 | a0006c0006t0001g0351 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2771+3531C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121971700 | ||||||
| chr12:121971758
|
T | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(166): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.2772-3486T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121971758 | ||||||
| chr12:121971982
|
T | C | 17 | a0007c0007t0001g0067a0007c0007t0001g0068a0007c0007t0001g0069others(14): Show | 17 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.2772-3262T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121971982 | ||||||
| chr12:121972123
|
T | C | 1 | a0003c0003t0001g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2772-3121T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121972123 | ||||||
| chr12:121972143
|
G | A | 1 | a0007c0007t0001g0082 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2772-3101G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121972143 | ||||||
| chr12:121972254
|
G | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(178): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.2772-2990G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121972254 | ||||||
| chr12:121972307
|
T | G | 1 | a0003c0003t0001g0271 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2772-2937T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121972307 | ||||||
| chr12:121972415
|
G | A | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.2772-2829G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121972415 | ||||||
| chr12:121972486
|
G | A | 11 | a0003c0003t0001g0271a0003c0009t0001g0058a0003c0009t0001g0059others(8): Show | 11 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2772-2758G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121972486 | ||||||
| chr12:121972489
|
A | ATT | 9 | a0003c0003t0001g0271a0003c0009t0001g0058a0003c0009t0001g0059others(6): Show | 9 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2772-2740_2772-273 others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr12 | 121972489 | |||||
| chr12:121972511
|
G | A | 1 | a0004c0002t0001g0033 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2772-2733G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121972511 | ||||||
| chr12:121972551
|
C | T | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2772-2693C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121972551 | ||||||
| chr12:121972690
|
G | T | 1 | a0004c0002t0001g0024 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2772-2554G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121972690 | ||||||
| chr12:121972964
|
G | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(299): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.2772-2280G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121972964 | ||||||
| chr12:121973021
|
C | T | 4 | a0003c0003t0001g0271a0003c0012t0001g0083a0003c0012t0001g0084others(1): Show | 4 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2772-2223C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121973021 | ||||||
| chr12:121973079
|
G | A | 4 | a0003c0009t0001g0060a0003c0009t0001g0061a0003c0009t0001g0062others(1): Show | 4 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.2772-2165G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121973079 | ||||||
| chr12:121973145
|
C | T | 2 | a0007c0007t0001g0067a0007c0007t0001g0071 | 2 | NA19004.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2772-2099C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121973145 | ||||||
| chr12:121973194
|
C | G | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.2772-2050C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121973194 | ||||||
| chr12:121973195
|
A | G | 35 | a0005c0005t0001g0218a0005c0005t0001g0219a0005c0005t0001g0220others(32): Show | 35 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.2772-2049A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121973195 | ||||||
| chr12:121973389
|
G | A | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.2772-1855G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121973389 | ||||||
| chr12:121973500
|
A | G | 1 | a0002c0004t0001g0302 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2772-1744A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121973500 | ||||||
| chr12:121973639
|
G | A | 4 | a0003c0003t0001g0271a0003c0012t0001g0083a0003c0012t0001g0084others(1): Show | 4 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2772-1605G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121973639 | ||||||
| chr12:121973728
|
G | T | 1 | a0001c0001t0001g0178 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2772-1516G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121973728 | ||||||
| chr12:121973793
|
A | G | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2772-1451A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121973793 | ||||||
| chr12:121973993
|
G | A | 4 | a0003c0003t0001g0348a0003c0003t0001g0349a0003c0003t0001g0350others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2772-1251G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121973993 | ||||||
| chr12:121974014
|
G | A | 173 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(170): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.2772-1230G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121974014 | ||||||
| chr12:121974239
|
C | T | 31 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(28): Show | 31 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.2772-1005C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121974239 | ||||||
| chr12:121974240
|
G | A | 7 | a0003c0003t0001g0264a0003c0009t0001g0058a0003c0009t0001g0059others(4): Show | 7 | HG02451.hp2 NA18942.hp1 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.2772-1004G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121974240 | ||||||
| chr12:121974319
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(171): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.2772-925G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121974319 | ||||||
| chr12:121974323
|
A | C | 4 | a0003c0003t0001g0348a0003c0003t0001g0349a0003c0003t0001g0350others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2772-921A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121974323 | ||||||
| chr12:121974410
|
C | T | 2 | a0008c0010t0001g0217a0008c0010t0001g0329 | 2 | HG01099.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2772-834C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121974410 | ||||||
| chr12:121974683
|
A | G | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2772-561A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121974683 | ||||||
| chr12:121974691
|
AGGTTTTC others(8): Show |
A | 1 | a0001c0001t0001g0174 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2772-551_2772-537d others(17): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr12 | 121974691 | |||||
| chr12:121974926
|
A | G | 303 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.2772-318A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 17/21 | chr12 | 121974926 | ||||||
| chr12:121975482
|
C | G | 3 | a0001c0001t0001g0140a0001c0001t0001g0204a0001c0001t0001g0213 | 3 | HG00408.hp1 NA18963.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.2863-60C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 18/21 | chr12 | 121975482 | ||||||
| chr12:121975525
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2863-17G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 18/21 | chr12 | 121975525 | ||||||
| chr12:121976011
|
C | CT | 6 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0204others(3): Show | 6 | HG01099.hp2 NA18961.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3006+341dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121976011 | |||||
| chr12:121976134
|
G | A | 7 | a0003c0003t0001g0271a0003c0003t0001g0332a0003c0003t0001g0333others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.3006+449G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121976134 | ||||||
| chr12:121976167
|
C | G | 1 | a0003c0003t0001g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3006+482C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121976167 | ||||||
| chr12:121976197
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(107): Show | 111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.3006+512C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121976197 | ||||||
| chr12:121976203
|
T | C | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3006+518T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121976203 | ||||||
| chr12:121976208
|
G | A | 1 | a0006c0006t0001g0262 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3006+523G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121976208 | ||||||
| chr12:121976284
|
C | T | 1 | a0008c0010t0001g0329 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3006+599C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121976284 | ||||||
| chr12:121976427
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3006+742G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121976427 | ||||||
| chr12:121976474
|
G | A | 1 | a0002c0004t0001g0273 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3006+789G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121976474 | ||||||
| chr12:121976511
|
G | A | 1 | a0006c0006t0001g0262 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3006+826G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121976511 | ||||||
| chr12:121976733
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3006+1048C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121976733 | ||||||
| chr12:121976754
|
C | A | 18 | a0003c0017t0001g0216a0004c0002t0001g0007a0004c0002t0001g0013others(15): Show | 18 | HG00673.hp2 HG02135.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.3006+1069C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121976754 | ||||||
| chr12:121976840
|
T | G | 54 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(51): Show | 55 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.3006+1155T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121976840 | ||||||
| chr12:121977006
|
A | C | 1 | a0005c0005t0001g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3006+1321A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121977006 | ||||||
| chr12:121977007
|
A | C | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3006+1322A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121977007 | ||||||
| chr12:121977137
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3006+1452A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121977137 | ||||||
| chr12:121977206
|
T | C | 35 | a0005c0005t0001g0218a0005c0005t0001g0219a0005c0005t0001g0220others(32): Show | 35 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.3006+1521T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121977206 | ||||||
| chr12:121977308
|
A | G | 1 | a0003c0003t0001g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3006+1623A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121977308 | ||||||
| chr12:121977533
|
G | A | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3006+1848G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121977533 | ||||||
| chr12:121977596
|
G | T | 2 | a0004c0014t0001g0018a0004c0014t0001g0019 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3006+1911G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121977596 | ||||||
| chr12:121977638
|
CGACAGAG others(292): Show |
C | 2 | a0008c0010t0001g0065a0008c0010t0001g0066 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3006+1964_3006+226 others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121977638 | |||||
| chr12:121977647
|
G | A | 1 | a0004c0002t0001g0045 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3006+1962G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121977647 | ||||||
| chr12:121977682
|
G | A | 1 | a0002c0004t0001g0305 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3006+1997G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121977682 | ||||||
| chr12:121977683
|
T | C | 3 | a0002c0004t0001g0305a0005c0005t0001g0336a0005c0005t0001g0346 | 3 | HG03669.hp2 HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3006+1998T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121977683 | ||||||
| chr12:121977737
|
C | G | 1 | a0006c0006t0001g0261 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3006+2052C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121977737 | ||||||
| chr12:121977761
|
C | G | 1 | a0002c0004t0001g0298 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3006+2076C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121977761 | ||||||
| chr12:121977766
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3006+2081T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121977766 | ||||||
| chr12:121977771
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0175a0001c0001t0001g0176others(2): Show | 6 | HG01975.hp1 NA18960.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.3006+2086C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121977771 | ||||||
| chr12:121977783
|
A | G | 3 | a0003c0012t0001g0083a0003c0012t0001g0084a0003c0012t0001g0272 | 3 | HG02109.hp2 HG02486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3006+2098A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121977783 | ||||||
| chr12:121977818
|
G | T | 7 | a0005c0005t0001g0218a0005c0005t0001g0219a0005c0005t0001g0220others(4): Show | 7 | HG02257.hp1 HG02723.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.3006+2133G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121977818 | ||||||
| chr12:121977819
|
C | T | 7 | a0005c0005t0001g0218a0005c0005t0001g0219a0005c0005t0001g0220others(4): Show | 7 | HG02257.hp1 HG02723.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.3006+2134C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121977819 | ||||||
| chr12:121977827
|
T | C | 1 | a0004c0002t0001g0026 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3006+2142T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121977827 | ||||||
| chr12:121977864
|
G | C | 3 | a0007c0007t0001g0077a0007c0007t0001g0078a0007c0007t0001g0082 | 3 | HG01168.hp2 HG01255.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.3006+2179G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121977864 | ||||||
| chr12:121977926
|
T | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 5 | NA18960.hp1 NA18962.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.3006+2241T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121977926 | ||||||
| chr12:121978158
|
C | T | 30 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0089others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.3006+2473C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121978158 | ||||||
| chr12:121978205
|
A | C | 2 | a0001c0001t0001g0165a0001c0001t0001g0191 | 2 | HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.3006+2520A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121978205 | ||||||
| chr12:121978266
|
T | C | 4 | a0003c0003t0001g0271a0003c0012t0001g0083a0003c0012t0001g0084others(1): Show | 4 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3006+2581T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121978266 | ||||||
| chr12:121978348
|
C | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(155): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.3006+2663C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121978348 | ||||||
| chr12:121978350
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3006+2665T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121978350 | ||||||
| chr12:121978367
|
C | A | 1 | a0003c0003t0001g0271 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3006+2682C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121978367 | ||||||
| chr12:121978372
|
C | T | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3006+2687C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121978372 | ||||||
| chr12:121978381
|
A | G | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3006+2696A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121978381 | ||||||
| chr12:121978388
|
T | C | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3006+2703T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121978388 | ||||||
| chr12:121978389
|
G | A | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3006+2704G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121978389 | ||||||
| chr12:121978393
|
C | CA | 41 | a0002c0004t0001g0086a0002c0004t0001g0273a0002c0004t0001g0276others(38): Show | 42 | HG00609.hp2 HG01952.hp2 HG01981.hp2 others(39): Show |
intron_variant | MODIFIER | c.3006+2736dupA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
C | CAA | 26 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0274others(23): Show | 26 | HG00621.hp2 HG00673.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.3006+2735_3006+273 others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
C | CAAA | 7 | a0002c0004t0001g0310a0002c0004t0001g0314a0003c0012t0001g0084others(4): Show | 7 | HG00597.hp2 HG00642.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.3006+2734_3006+273 others(7): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
C | CAAAA | 20 | a0002c0004t0001g0284a0002c0004t0001g0289a0002c0004t0001g0291others(17): Show | 20 | HG02015.hp2 HG02027.hp1 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.3006+2733_3006+273 others(8): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
C | CAAAAA | 15 | a0002c0004t0001g0281a0002c0004t0001g0282a0002c0004t0001g0309others(12): Show | 15 | HG00438.hp1 HG01891.hp2 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.3006+2732_3006+273 others(9): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
C | CAAAAAA | 17 | a0002c0004t0001g0292a0002c0004t0001g0293a0002c0004t0001g0294others(14): Show | 17 | HG01257.hp2 HG01258.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.3006+2731_3006+273 others(10): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
C | CAAAAAAA others(3): Show |
2 | a0005c0005t0001g0218a0005c0005t0001g0243 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3006+2727_3006+273 others(14): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
C | CAAAAAAA others(4): Show |
8 | a0003c0003t0001g0330a0003c0003t0001g0334a0005c0005t0001g0221others(5): Show | 8 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.3006+2726_3006+273 others(15): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
C | CAAAAAAA others(5): Show |
27 | a0003c0003t0001g0092a0003c0003t0001g0332a0003c0003t0001g0333others(24): Show | 27 | HG01168.hp2 HG01175.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.3006+2725_3006+273 others(16): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
C | CAAAAAAA others(6): Show |
3 | a0003c0003t0001g0090a0007c0007t0001g0073a0007c0007t0001g0078 | 3 | HG01255.hp1 HG01256.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.3006+2724_3006+273 others(17): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
C | CAAAAAAA others(7): Show |
11 | a0003c0003t0001g0089a0003c0003t0001g0091a0003c0003t0001g0101others(8): Show | 11 | HG00323.hp1 HG00639.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.3006+2723_3006+273 others(18): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
C | CAAAAAAA others(8): Show |
9 | a0003c0003t0001g0057a0003c0003t0001g0093a0003c0003t0001g0095others(6): Show | 9 | HG00099.hp2 HG00280.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.3006+2722_3006+273 others(19): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
C | CAAAAAAA others(9): Show |
8 | a0003c0003t0001g0094a0003c0003t0001g0102a0003c0003t0001g0103others(5): Show | 8 | HG00741.hp2 HG01109.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.3006+2721_3006+273 others(20): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
C | CAAAAAAA others(10): Show |
3 | a0003c0009t0001g0060a0003c0009t0001g0061a0003c0009t0001g0063 | 3 | NA18978.hp1 NA18981.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3006+2720_3006+273 others(21): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
C | CAAAAAAA others(11): Show |
2 | a0003c0003t0001g0350a0003c0009t0001g0062 | 2 | HG02257.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.3006+2719_3006+273 others(22): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
C | CAAAAAAA others(12): Show |
3 | a0003c0003t0001g0087a0003c0003t0001g0320a0008c0010t0001g0065 | 3 | HG01943.hp1 HG02683.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3006+2718_3006+273 others(23): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
C | CAAAAAAA others(13): Show |
1 | a0008c0010t0001g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3006+2717_3006+273 others(24): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
C | CAAAAAAA others(14): Show |
2 | a0003c0003t0001g0349a0008c0010t0001g0217 | 2 | HG01099.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3006+2716_3006+273 others(25): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
C | CAAAAAAA others(15): Show |
1 | a0003c0009t0001g0059 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.3006+2715_3006+273 others(26): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
C | CAAAAAAA others(23): Show |
1 | a0003c0009t0001g0058 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3006+2736_3006+273 others(34): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
CAAAA | C | 17 | a0001c0001t0001g0113a0001c0001t0001g0120a0001c0001t0001g0130others(14): Show | 17 | HG00099.hp1 HG00323.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.3006+2733_3006+273 others(8): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
CAAAAA | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(88): Show | 92 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.3006+2732_3006+273 others(9): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
CAAAAAAA others(4): Show |
C | 2 | a0003c0003t0001g0100a0013c0016t0001g0098 | 2 | HG00642.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.3006+2726_3006+273 others(15): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978393
|
CAAAAAAA others(5): Show |
C | 1 | a0005c0005t0001g0346 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3006+2725_3006+273 others(16): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121978393 | |||||
| chr12:121978395
|
A | G | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3006+2710A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121978395 | ||||||
| chr12:121978400
|
A | ATAAAAAT others(421): Show |
1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3006+2715_3006+271 others(432): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121978400 | ||||||
| chr12:121978427
|
C | T | 4 | a0001c0001t0001g0165a0001c0001t0001g0191a0003c0003t0001g0095others(1): Show | 4 | HG00099.hp2 HG00280.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.3006+2742C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121978427 | ||||||
| chr12:121978428
|
G | A | 1 | a0006c0006t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3006+2743G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121978428 | ||||||
| chr12:121978488
|
G | C | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3006+2803G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121978488 | ||||||
| chr12:121978684
|
G | A | 1 | a0006c0006t0001g0342 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3006+2999G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121978684 | ||||||
| chr12:121978749
|
G | C | 2 | a0003c0003t0001g0319a0003c0003t0001g0321 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3006+3064G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121978749 | ||||||
| chr12:121978761
|
A | G | 32 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(29): Show | 32 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.3006+3076A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121978761 | ||||||
| chr12:121978824
|
G | A | 31 | a0006c0006t0001g0064a0006c0006t0001g0246a0006c0006t0001g0247others(28): Show | 31 | HG01257.hp2 HG01258.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.3006+3139G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121978824 | ||||||
| chr12:121978971
|
C | G | 1 | a0009c0013t0001g0324 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.3006+3286C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121978971 | ||||||
| chr12:121979123
|
G | C | 2 | a0008c0010t0001g0065a0008c0010t0001g0066 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3006+3438G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121979123 | ||||||
| chr12:121979563
|
C | CTTCTTTT others(2): Show |
6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3006+3880_3006+388 others(13): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121979563 | |||||
| chr12:121979563
|
C | CTTTTTTT | 18 | a0003c0003t0001g0090a0003c0003t0001g0101a0003c0003t0001g0271others(15): Show | 18 | HG01168.hp2 HG01255.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.3006+3891_3006+389 others(11): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121979563 | |||||
| chr12:121979563
|
C | CTTTTTTT others(1): Show |
45 | a0001c0001t0001g0113a0001c0001t0001g0139a0001c0001t0001g0143others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.3006+3890_3006+389 others(12): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121979563 | |||||
| chr12:121979563
|
C | CTTTTTTT others(2): Show |
123 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(120): Show | 124 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.3006+3889_3006+389 others(13): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121979563 | |||||
| chr12:121979563
|
C | CTTTTTTT others(3): Show |
59 | a0001c0001t0001g0140a0001c0001t0001g0160a0001c0001t0001g0167others(56): Show | 60 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.3006+3888_3006+389 others(14): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121979563 | |||||
| chr12:121979563
|
C | CTTTTTTT others(4): Show |
7 | a0001c0001t0001g0179a0002c0004t0001g0055a0002c0004t0001g0293others(4): Show | 7 | HG01891.hp1 HG02080.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3006+3887_3006+389 others(15): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121979563 | |||||
| chr12:121979563
|
C | CTTTTTTT others(5): Show |
1 | a0002c0004t0001g0056 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3006+3886_3006+389 others(16): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121979563 | |||||
| chr12:121979690
|
G | A | 2 | a0004c0002t0001g0034a0004c0002t0001g0035 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3006+4005G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121979690 | ||||||
| chr12:121979736
|
T | A | 5 | a0005c0005t0001g0224a0005c0005t0001g0226a0005c0005t0001g0231others(2): Show | 5 | HG00423.hp1 NA18951.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.3006+4051T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121979736 | ||||||
| chr12:121979846
|
G | A | 1 | a0004c0002t0001g0024 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3006+4161G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121979846 | ||||||
| chr12:121979917
|
C | G | 2 | a0008c0010t0001g0065a0008c0010t0001g0066 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3006+4232C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121979917 | ||||||
| chr12:121980046
|
T | C | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3006+4361T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121980046 | ||||||
| chr12:121980060
|
T | C | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3006+4375T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121980060 | ||||||
| chr12:121980225
|
T | C | 2 | a0003c0003t0001g0087a0003c0003t0001g0093 | 2 | HG01167.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.3006+4540T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121980225 | ||||||
| chr12:121980254
|
C | T | 20 | a0003c0003t0001g0271a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.3006+4569C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121980254 | ||||||
| chr12:121980339
|
C | T | 15 | a0004c0002t0001g0007a0004c0002t0001g0013a0004c0002t0001g0014others(12): Show | 15 | HG00673.hp2 HG02135.hp2 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.3006+4654C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121980339 | ||||||
| chr12:121980408
|
C | CT | 57 | a0001c0001t0001g0164a0001c0001t0001g0178a0002c0004t0001g0293others(54): Show | 57 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(54): Show |
intron_variant | MODIFIER | c.3006+4740dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121980408 | |||||
| chr12:121980408
|
CT | C | 8 | a0001c0001t0001g0141a0001c0001t0001g0192a0003c0003t0001g0094others(5): Show | 8 | HG01070.hp1 HG01975.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.3006+4740delT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121980408 | |||||
| chr12:121980434
|
G | T | 14 | a0001c0001t0001g0118a0001c0001t0001g0131a0001c0001t0001g0141others(11): Show | 14 | HG02080.hp2 NA18747.hp1 NA18939.hp2 others(11): Show |
intron_variant | MODIFIER | c.3006+4749G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121980434 | ||||||
| chr12:121980594
|
C | T | 2 | a0002c0004t0001g0304a0002c0004t0001g0317 | 2 | HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.3006+4909C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121980594 | ||||||
| chr12:121980637
|
C | T | 1 | a0003c0003t0001g0096 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3006+4952C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121980637 | ||||||
| chr12:121981255
|
T | C | 1 | a0003c0003t0001g0352 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3006+5570T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121981255 | ||||||
| chr12:121981308
|
C | CA | 141 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.3006+5629dupA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121981308 | |||||
| chr12:121981314
|
A | G | 8 | a0003c0003t0001g0330a0003c0003t0001g0331a0003c0003t0001g0348others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3006+5629A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121981314 | ||||||
| chr12:121981321
|
A | T | 3 | a0001c0001t0001g0140a0001c0001t0001g0204a0001c0001t0001g0213 | 3 | HG00408.hp1 NA18963.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.3006+5636A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121981321 | ||||||
| chr12:121981571
|
T | G | 1 | a0001c0001t0001g0131 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.3006+5886T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121981571 | ||||||
| chr12:121981604
|
T | C | 49 | a0003c0003t0001g0332a0003c0003t0001g0333a0003c0003t0001g0334others(46): Show | 49 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.3006+5919T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121981604 | ||||||
| chr12:121981883
|
C | G | 1 | a0004c0002t0001g0014 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3006+6198C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121981883 | ||||||
| chr12:121981912
|
AC | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.3006+6229delC | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121981912 | |||||
| chr12:121982122
|
T | C | 20 | a0003c0003t0001g0271a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.3006+6437T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121982122 | ||||||
| chr12:121982381
|
A | AT | 25 | a0001c0001t0001g0134a0002c0004t0001g0287a0002c0004t0001g0293others(22): Show | 25 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.3006+6711dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121982381 | |||||
| chr12:121982399
|
G | A | 8 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0132others(5): Show | 8 | HG01361.hp2 HG01928.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.3006+6714G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121982399 | ||||||
| chr12:121982402
|
G | A | 30 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.3006+6717G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121982402 | ||||||
| chr12:121982457
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3006+6772G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121982457 | ||||||
| chr12:121982472
|
G | A | 20 | a0003c0003t0001g0271a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.3006+6787G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121982472 | ||||||
| chr12:121982531
|
A | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(246): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.3006+6846A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121982531 | ||||||
| chr12:121982553
|
T | G | 4 | a0003c0003t0001g0102a0003c0003t0001g0103a0003c0003t0001g0319others(1): Show | 4 | HG00741.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.3006+6868T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121982553 | ||||||
| chr12:121982718
|
G | A | 1 | a0006c0006t0001g0345 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3006+7033G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121982718 | ||||||
| chr12:121983107
|
G | C | 1 | a0001c0001t0001g0131 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.3006+7422G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121983107 | ||||||
| chr12:121983135
|
G | A | 2 | a0005c0005t0001g0221a0005c0005t0001g0222 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3006+7450G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121983135 | ||||||
| chr12:121983156
|
C | A | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3006+7471C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121983156 | ||||||
| chr12:121983265
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.3006+7580G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121983265 | ||||||
| chr12:121983270
|
C | T | 1 | a0003c0012t0001g0272 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3006+7585C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121983270 | ||||||
| chr12:121983291
|
G | T | 1 | a0003c0003t0001g0331 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3006+7606G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121983291 | ||||||
| chr12:121983292
|
G | T | 1 | a0003c0003t0001g0331 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3006+7607G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121983292 | ||||||
| chr12:121983326
|
G | A | 1 | a0001c0021t0001g0202 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3006+7641G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121983326 | ||||||
| chr12:121983351
|
G | GC | 30 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.3006+7668dupC | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121983351 | |||||
| chr12:121983396
|
C | CA | 14 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0127others(11): Show | 15 | HG00738.hp2 HG01361.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.3006+7727dupA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121983396 | |||||
| chr12:121983396
|
CA | C | 28 | a0002c0004t0001g0298a0002c0004t0001g0301a0003c0003t0001g0271others(25): Show | 28 | HG00621.hp2 HG01168.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.3006+7727delA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121983396 | |||||
| chr12:121983428
|
A | G | 2 | a0003c0012t0001g0084a0003c0012t0001g0272 | 2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3006+7743A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121983428 | ||||||
| chr12:121983665
|
C | A | 1 | a0001c0001t0001g0156 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3006+7980C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121983665 | ||||||
| chr12:121983740
|
T | TA | 38 | a0001c0001t0001g0191a0001c0001t0001g0200a0002c0008t0001g0307others(35): Show | 38 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.3006+8068dupA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121983740 | |||||
| chr12:121983784
|
C | T | 1 | a0006c0006t0001g0268 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3006+8099C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121983784 | ||||||
| chr12:121984003
|
G | T | 1 | a0007c0007t0001g0077 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3006+8318G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121984003 | ||||||
| chr12:121984016
|
G | T | 2 | a0005c0005t0001g0219a0005c0005t0001g0220 | 2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3006+8331G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121984016 | ||||||
| chr12:121984276
|
G | C | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3006+8591G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121984276 | ||||||
| chr12:121984521
|
A | T | 20 | a0003c0003t0001g0271a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.3006+8836A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121984521 | ||||||
| chr12:121984548
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3006+8863C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121984548 | ||||||
| chr12:121984885
|
A | G | 1 | a0003c0003t0001g0330 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3006+9200A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121984885 | ||||||
| chr12:121985012
|
A | G | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3006+9327A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121985012 | ||||||
| chr12:121985041
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.3006+9356C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121985041 | ||||||
| chr12:121985123
|
C | T | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3006+9438C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121985123 | ||||||
| chr12:121985273
|
C | A | 2 | a0002c0004t0001g0276a0002c0004t0001g0287 | 2 | NA18984.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.3006+9588C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121985273 | ||||||
| chr12:121985497
|
A | C | 1 | a0005c0005t0001g0241 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3006+9812A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121985497 | ||||||
| chr12:121985526
|
A | T | 1 | a0001c0001t0001g0167 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3006+9841A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121985526 | ||||||
| chr12:121985535
|
C | CA | 37 | a0001c0001t0001g0169a0001c0001t0001g0203a0002c0004t0001g0314others(34): Show | 37 | HG00597.hp2 HG01109.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.3006+9869dupA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121985535 | |||||
| chr12:121985535
|
CA | C | 67 | a0001c0001t0001g0118a0001c0001t0001g0152a0003c0003t0001g0271others(64): Show | 67 | HG00423.hp1 HG01168.hp1 HG01168.hp2 others(64): Show |
intron_variant | MODIFIER | c.3006+9869delA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121985535 | |||||
| chr12:121985933
|
A | AC | 3 | a0001c0001t0001g0213a0002c0008t0001g0288a0003c0003t0001g0349 | 3 | HG02970.hp1 NA18999.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.3006+10250dupC | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121985933 | |||||
| chr12:121986061
|
G | A | 20 | a0003c0003t0001g0271a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.3006+10376G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121986061 | ||||||
| chr12:121986296
|
A | AT | 11 | a0001c0001t0001g0179a0001c0001t0001g0208a0001c0001t0001g0212others(8): Show | 11 | HG01109.hp2 HG01981.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.3006+10629dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121986296 | |||||
| chr12:121986321
|
C | G | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3006+10636C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121986321 | ||||||
| chr12:121986464
|
A | AT | 58 | a0001c0001t0001g0200a0002c0004t0001g0003a0002c0004t0001g0004others(55): Show | 59 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.3006+10789dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121986464 | |||||
| chr12:121986478
|
T | C | 1 | a0006c0006t0001g0256 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3006+10793T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121986478 | ||||||
| chr12:121986512
|
G | A | 3 | a0006c0006t0001g0064a0006c0006t0001g0247a0006c0006t0001g0248 | 3 | HG02280.hp1 HG02897.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3006+10827G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121986512 | ||||||
| chr12:121986591
|
G | A | 20 | a0003c0003t0001g0271a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.3006+10906G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121986591 | ||||||
| chr12:121986625
|
T | G | 6 | a0003c0003t0001g0330a0003c0003t0001g0331a0003c0003t0001g0348others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3006+10940T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121986625 | ||||||
| chr12:121986637
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3006+10952C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121986637 | ||||||
| chr12:121986773
|
G | GA | 8 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0142others(5): Show | 8 | HG02145.hp1 HG03098.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.3006+11102dupA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121986773 | |||||
| chr12:121986773
|
GA | G | 14 | a0001c0001t0001g0138a0001c0001t0001g0149a0001c0001t0001g0151others(11): Show | 14 | HG00140.hp1 HG01109.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.3006+11102delA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121986773 | |||||
| chr12:121986791
|
C | T | 7 | a0003c0003t0001g0330a0003c0003t0001g0331a0003c0003t0001g0348others(4): Show | 7 | HG01109.hp2 HG01243.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.3006+11106C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121986791 | ||||||
| chr12:121986816
|
G | C | 1 | a0004c0002t0001g0046 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3006+11131G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121986816 | ||||||
| chr12:121986819
|
G | A | 1 | a0006c0006t0001g0261 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3006+11134G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121986819 | ||||||
| chr12:121986883
|
G | A | 1 | a0004c0002t0001g0030 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3006+11198G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121986883 | ||||||
| chr12:121987001
|
T | C | 26 | a0003c0003t0001g0271a0003c0009t0001g0058a0003c0009t0001g0059others(23): Show | 26 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.3006+11316T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121987001 | ||||||
| chr12:121987084
|
G | A | 1 | a0007c0007t0001g0076 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3006+11399G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121987084 | ||||||
| chr12:121987106
|
A | G | 301 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(298): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.3006+11421A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121987106 | ||||||
| chr12:121987145
|
T | A | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3006+11460T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121987145 | ||||||
| chr12:121987292
|
AG | A | 30 | a0003c0003t0001g0264a0003c0003t0001g0330a0003c0003t0001g0331others(27): Show | 30 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.3006+11609delG | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121987292 | |||||
| chr12:121987365
|
A | T | 1 | a0001c0001t0001g0189 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3006+11680A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121987365 | ||||||
| chr12:121987646
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3006+11961C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121987646 | ||||||
| chr12:121987715
|
CA | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(113): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.3007-11983delA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121987715 | |||||
| chr12:121987881
|
G | A | 16 | a0004c0002t0001g0007a0004c0002t0001g0013a0004c0002t0001g0014others(13): Show | 16 | HG00673.hp2 HG02135.hp2 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.3007-11835G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121987881 | ||||||
| chr12:121987957
|
G | A | 1 | a0004c0002t0001g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3007-11759G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121987957 | ||||||
| chr12:121988072
|
A | T | 1 | a0001c0001t0001g0157 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3007-11644A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121988072 | ||||||
| chr12:121988124
|
T | A | 1 | a0007c0007t0001g0071 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.3007-11592T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121988124 | ||||||
| chr12:121988165
|
G | A | 1 | a0002c0004t0001g0297 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3007-11551G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121988165 | ||||||
| chr12:121988311
|
A | G | 246 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.3007-11405A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121988311 | ||||||
| chr12:121988323
|
A | G | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-11393A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121988323 | ||||||
| chr12:121988330
|
C | T | 301 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(298): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.3007-11386C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121988330 | ||||||
| chr12:121988500
|
TTTCACTC others(22): Show |
T | 1 | a0001c0001t0001g0157 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3007-11211_3007-11 others(35): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121988500 | |||||
| chr12:121988563
|
T | G | 2 | a0008c0010t0001g0065a0008c0010t0001g0066 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3007-11153T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121988563 | ||||||
| chr12:121988734
|
TTCTTTTT others(4): Show |
T | 1 | a0001c0001t0001g0178 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3007-10971_3007-10 others(17): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121988734 | |||||
| chr12:121988737
|
T | C | 30 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.3007-10979T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121988737 | ||||||
| chr12:121988747
|
CT | C | 26 | a0001c0001t0001g0199a0002c0008t0001g0288a0003c0003t0001g0271others(23): Show | 26 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.3007-10955delT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121988747 | |||||
| chr12:121989255
|
C | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(107): Show | 111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.3007-10461C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121989255 | ||||||
| chr12:121989261
|
T | C | 1 | a0003c0003t0001g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3007-10455T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121989261 | ||||||
| chr12:121989285
|
T | C | 2 | a0008c0010t0001g0065a0008c0010t0001g0066 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3007-10431T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121989285 | ||||||
| chr12:121989404
|
A | G | 37 | a0001c0001t0001g0214a0003c0003t0001g0057a0003c0003t0001g0087others(34): Show | 37 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.3007-10312A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121989404 | ||||||
| chr12:121989430
|
G | C | 1 | a0001c0001t0001g0187 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3007-10286G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121989430 | ||||||
| chr12:121989432
|
C | A | 49 | a0003c0003t0001g0332a0003c0003t0001g0333a0003c0003t0001g0334others(46): Show | 49 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.3007-10284C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121989432 | ||||||
| chr12:121989572
|
G | A | 1 | a0005c0005t0001g0236 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3007-10144G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121989572 | ||||||
| chr12:121989748
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.3007-9968T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121989748 | ||||||
| chr12:121989755
|
T | C | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3007-9961T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121989755 | ||||||
| chr12:121989936
|
C | T | 1 | a0004c0002t0001g0008 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3007-9780C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121989936 | ||||||
| chr12:121989947
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3007-9769C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121989947 | ||||||
| chr12:121989980
|
C | G | 2 | a0008c0010t0001g0065a0008c0010t0001g0066 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3007-9736C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121989980 | ||||||
| chr12:121989989
|
G | C | 1 | a0005c0005t0001g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3007-9727G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121989989 | ||||||
| chr12:121990060
|
C | T | 55 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(52): Show | 56 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.3007-9656C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121990060 | ||||||
| chr12:121990193
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0155 | 2 | HG00323.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.3007-9523G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121990193 | ||||||
| chr12:121990281
|
C | G | 3 | a0003c0003t0001g0271a0003c0012t0001g0084a0003c0012t0001g0272 | 3 | HG02109.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3007-9435C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121990281 | ||||||
| chr12:121990353
|
G | T | 24 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0126others(21): Show | 24 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.3007-9363G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121990353 | ||||||
| chr12:121990426
|
G | A | 19 | a0006c0006t0001g0064a0006c0006t0001g0246a0006c0006t0001g0247others(16): Show | 19 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.3007-9290G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121990426 | ||||||
| chr12:121990523
|
C | G | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-9193C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121990523 | ||||||
| chr12:121990569
|
G | A | 27 | a0003c0003t0001g0330a0003c0003t0001g0331a0003c0003t0001g0348others(24): Show | 27 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.3007-9147G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121990569 | ||||||
| chr12:121990572
|
G | A | 20 | a0003c0003t0001g0271a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.3007-9144G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121990572 | ||||||
| chr12:121990584
|
C | T | 2 | a0002c0004t0001g0274a0002c0004t0001g0275 | 2 | NA18945.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.3007-9132C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121990584 | ||||||
| chr12:121990754
|
C | T | 3 | a0006c0006t0001g0267a0006c0006t0001g0337a0006c0006t0001g0344 | 3 | HG02809.hp1 HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3007-8962C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121990754 | ||||||
| chr12:121991077
|
A | C | 1 | a0004c0002t0001g0026 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3007-8639A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121991077 | ||||||
| chr12:121991324
|
C | T | 1 | a0003c0003t0001g0332 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3007-8392C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121991324 | ||||||
| chr12:121991522
|
C | A | 1 | a0001c0001t0001g0145 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3007-8194C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121991522 | ||||||
| chr12:121991578
|
G | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(137): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.3007-8138G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121991578 | ||||||
| chr12:121991745
|
G | T | 1 | a0002c0004t0001g0004 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3007-7971G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121991745 | ||||||
| chr12:121991748
|
A | C | 305 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(302): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.3007-7968A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121991748 | ||||||
| chr12:121991866
|
G | A | 19 | a0002c0004t0001g0276a0002c0004t0001g0278a0002c0004t0001g0279others(16): Show | 20 | HG00597.hp2 HG02040.hp2 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.3007-7850G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121991866 | ||||||
| chr12:121991882
|
A | G | 2 | a0008c0010t0001g0065a0008c0010t0001g0066 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3007-7834A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121991882 | ||||||
| chr12:121991940
|
C | G | 1 | a0003c0003t0001g0330 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3007-7776C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121991940 | ||||||
| chr12:121991949
|
C | T | 1 | a0005c0015t0001g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3007-7767C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121991949 | ||||||
| chr12:121992223
|
C | G | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-7493C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121992223 | ||||||
| chr12:121992284
|
G | C | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-7432G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121992284 | ||||||
| chr12:121992536
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-7180C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121992536 | ||||||
| chr12:121992728
|
C | T | 2 | a0008c0010t0001g0065a0008c0010t0001g0066 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3007-6988C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121992728 | ||||||
| chr12:121992741
|
A | G | 20 | a0003c0003t0001g0271a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.3007-6975A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121992741 | ||||||
| chr12:121992749
|
T | A | 1 | a0003c0003t0001g0106 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3007-6967T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121992749 | ||||||
| chr12:121992800
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-6916C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121992800 | ||||||
| chr12:121992931
|
T | TATA | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-6782_3007-678 others(7): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121992931 | |||||
| chr12:121992952
|
TCTCCCTC others(5): Show |
T | 2 | a0002c0004t0001g0304a0002c0004t0001g0317 | 2 | HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.3007-6752_3007-674 others(16): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121992952 | |||||
| chr12:121992958
|
TCTCCCA | T | 134 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(131): Show | 135 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.3007-6752_3007-674 others(10): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121992958 | |||||
| chr12:121992964
|
A | C | 1 | a0001c0001t0001g0157 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3007-6752A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121992964 | ||||||
| chr12:121992964
|
A | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(161): Show | 165 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.3007-6752A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121992964 | ||||||
| chr12:121992965
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3007-6751C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121992965 | ||||||
| chr12:121992966
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3007-6750T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121992966 | ||||||
| chr12:121992981
|
GTCTCCC | G | 24 | a0003c0003t0001g0271a0003c0012t0001g0084a0003c0012t0001g0272others(21): Show | 24 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.3007-6716_3007-671 others(10): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121992981 | |||||
| chr12:121992997
|
C | T | 4 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | HG02080.hp2 NA18747.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.3007-6719C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121992997 | ||||||
| chr12:121993129
|
C | T | 2 | a0005c0005t0001g0221a0005c0005t0001g0222 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3007-6587C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993129 | ||||||
| chr12:121993158
|
C | G | 23 | a0005c0005t0001g0221a0005c0005t0001g0222a0005c0005t0001g0265others(20): Show | 23 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.3007-6558C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993158 | ||||||
| chr12:121993264
|
C | T | 1 | a0003c0012t0001g0083 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3007-6452C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993264 | ||||||
| chr12:121993326
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3007-6390C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993326 | ||||||
| chr12:121993379
|
C | T | 58 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(55): Show | 59 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.3007-6337C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993379 | ||||||
| chr12:121993387
|
A | AC | 12 | a0001c0001t0001g0157a0001c0001t0001g0178a0001c0001t0001g0182others(9): Show | 12 | HG01175.hp1 HG01934.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.3007-6325dupC | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121993387 | |||||
| chr12:121993434
|
G | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-6282G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993434 | ||||||
| chr12:121993444
|
G | C | 1 | a0005c0005t0001g0266 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.3007-6272G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993444 | ||||||
| chr12:121993491
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-6225C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993491 | ||||||
| chr12:121993492
|
A | G | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-6224A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993492 | ||||||
| chr12:121993496
|
G | C | 1 | a0001c0001t0001g0157 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3007-6220G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993496 | ||||||
| chr12:121993506
|
C | CCATCTAG others(33): Show |
1 | a0001c0001t0001g0146 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3007-6189_3007-615 others(44): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121993506 | |||||
| chr12:121993551
|
T | C | 3 | a0007c0007t0001g0077a0007c0007t0001g0078a0007c0007t0001g0082 | 3 | HG01168.hp2 HG01255.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.3007-6165T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993551 | ||||||
| chr12:121993580
|
G | C | 1 | a0001c0001t0001g0157 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3007-6136G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993580 | ||||||
| chr12:121993615
|
C | T | 1 | a0002c0004t0001g0287 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3007-6101C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993615 | ||||||
| chr12:121993618
|
C | T | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3007-6098C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993618 | ||||||
| chr12:121993619
|
G | A | 1 | a0002c0004t0001g0287 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3007-6097G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993619 | ||||||
| chr12:121993641
|
T | C | 9 | a0002c0004t0001g0274a0002c0004t0001g0275a0002c0004t0001g0287others(6): Show | 9 | NA18942.hp1 NA18945.hp2 NA18978.hp1 others(6): Show |
intron_variant | MODIFIER | c.3007-6075T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993641 | ||||||
| chr12:121993643
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-6073C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993643 | ||||||
| chr12:121993648
|
G | A | 1 | a0002c0004t0001g0273 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3007-6068G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993648 | ||||||
| chr12:121993656
|
GAGA | G | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-6059_3007-605 others(7): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993656 | ||||||
| chr12:121993669
|
G | A | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-6047G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993669 | ||||||
| chr12:121993672
|
G | A | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-6044G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993672 | ||||||
| chr12:121993681
|
C | A | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-6035C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993681 | ||||||
| chr12:121993682
|
G | C | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-6034G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993682 | ||||||
| chr12:121993683
|
T | C | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-6033T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993683 | ||||||
| chr12:121993691
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-6025C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993691 | ||||||
| chr12:121993693
|
G | GCAA | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-6022_3007-602 others(7): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121993693 | |||||
| chr12:121993696
|
G | A | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-6020G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993696 | ||||||
| chr12:121993718
|
A | C | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-5998A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993718 | ||||||
| chr12:121993722
|
T | C | 1 | a0002c0004t0001g0291 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3007-5994T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993722 | ||||||
| chr12:121993724
|
T | C | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-5992T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993724 | ||||||
| chr12:121993728
|
T | C | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-5988T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993728 | ||||||
| chr12:121993733
|
A | G | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-5983A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993733 | ||||||
| chr12:121993735
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-5981C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993735 | ||||||
| chr12:121993736
|
A | G | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-5980A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993736 | ||||||
| chr12:121993760
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-5956C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993760 | ||||||
| chr12:121993764
|
T | C | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-5952T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993764 | ||||||
| chr12:121993765
|
G | GCCCGGCA others(308): Show |
6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-5945_3007-594 others(319): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121993765 | |||||
| chr12:121993774
|
G | GC | 8 | a0003c0003t0001g0088a0003c0003t0001g0099a0003c0009t0001g0058others(5): Show | 8 | HG02451.hp1 HG03098.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.3007-5941dupC | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121993774 | |||||
| chr12:121993776
|
A | G | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-5940A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993776 | ||||||
| chr12:121993808
|
C | T | 1 | a0003c0003t0001g0271 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3007-5908C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993808 | ||||||
| chr12:121993812
|
CGCCCGGC others(301): Show |
C | 1 | a0001c0001t0001g0326 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3007-5763_3007-545 others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121993812 | |||||
| chr12:121993817
|
G | A | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-5899G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993817 | ||||||
| chr12:121993829
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-5887C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993829 | ||||||
| chr12:121993846
|
G | C | 1 | a0003c0003t0001g0110 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3007-5870G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993846 | ||||||
| chr12:121993861
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-5855C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993861 | ||||||
| chr12:121993863
|
CGCCCGGC others(480): Show |
C | 1 | a0003c0003t0001g0104 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3007-5765_3007-527 others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121993863 | |||||
| chr12:121993884
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-5832C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993884 | ||||||
| chr12:121993909
|
G | A | 30 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.3007-5807G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121993909 | ||||||
| chr12:121993953
|
ACCCCGTC others(42): Show |
A | 2 | a0003c0003t0001g0109a0003c0003t0001g0325 | 2 | HG01261.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.3007-5736_3007-568 others(53): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121993953 | |||||
| chr12:121993972
|
TGGGGGGG others(43): Show |
T | 28 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.3007-5736_3007-568 others(54): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121993972 | |||||
| chr12:121994021
|
TG | T | 240 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(237): Show | 242 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.3007-5685delG | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121994021 | |||||
| chr12:121994021
|
TGG | T | 23 | a0003c0003t0001g0271a0003c0003t0001g0331a0003c0012t0001g0084others(20): Show | 23 | HG01109.hp2 HG01168.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.3007-5686_3007-568 others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121994021 | |||||
| chr12:121994022
|
GGGGGGGG others(123): Show |
G | 1 | a0002c0004t0001g0305 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3007-5685_3007-555 others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121994022 | |||||
| chr12:121994040
|
C | T | 1 | a0006c0006t0001g0261 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3007-5676C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994040 | ||||||
| chr12:121994046
|
T | C | 1 | a0003c0003t0001g0331 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3007-5670T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994046 | ||||||
| chr12:121994065
|
G | GGAGGT | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-5646_3007-564 others(9): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121994065 | |||||
| chr12:121994090
|
C | T | 1 | a0005c0005t0001g0266 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.3007-5626C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994090 | ||||||
| chr12:121994091
|
G | C | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-5625G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994091 | ||||||
| chr12:121994091
|
GGCCCCTA others(122): Show |
G | 1 | a0006c0006t0001g0064 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3007-5556_3007-542 others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121994091 | |||||
| chr12:121994152
|
T | TG | 52 | a0001c0001t0001g0157a0002c0004t0001g0003a0002c0004t0001g0004others(49): Show | 53 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.3007-5556dupG | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121994152 | |||||
| chr12:121994152
|
TG | T | 20 | a0003c0003t0001g0271a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.3007-5556delG | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121994152 | |||||
| chr12:121994170
|
C | T | 18 | a0006c0006t0001g0246a0006c0006t0001g0247a0006c0006t0001g0248others(15): Show | 18 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.3007-5546C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994170 | ||||||
| chr12:121994176
|
G | C | 1 | a0001c0001t0001g0157 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3007-5540G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994176 | ||||||
| chr12:121994183
|
C | T | 1 | a0005c0005t0001g0266 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.3007-5533C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994183 | ||||||
| chr12:121994191
|
C | T | 30 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.3007-5525C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994191 | ||||||
| chr12:121994252
|
CCGGCCAG others(43): Show |
C | 2 | a0005c0005t0001g0236a0005c0005t0001g0241 | 2 | HG00423.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.3007-5427_3007-537 others(54): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121994252 | |||||
| chr12:121994281
|
T | G | 1 | a0001c0001t0001g0182 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3007-5435T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994281 | ||||||
| chr12:121994292
|
GC | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(240): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.3007-5417delC | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121994292 | |||||
| chr12:121994332
|
G | C | 1 | a0003c0003t0001g0271 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3007-5384G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994332 | ||||||
| chr12:121994350
|
T | C | 2 | a0002c0004t0001g0274a0002c0004t0001g0275 | 2 | NA18945.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.3007-5366T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994350 | ||||||
| chr12:121994369
|
T | C | 30 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.3007-5347T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994369 | ||||||
| chr12:121994371
|
C | T | 30 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.3007-5345C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994371 | ||||||
| chr12:121994400
|
G | C | 1 | a0002c0004t0001g0293 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3007-5316G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994400 | ||||||
| chr12:121994401
|
C | T | 1 | a0007c0007t0001g0077 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3007-5315C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994401 | ||||||
| chr12:121994451
|
G | GA | 110 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(107): Show | 111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.3007-5264dupA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121994451 | |||||
| chr12:121994453
|
C | G | 26 | a0003c0003t0001g0271a0003c0009t0001g0058a0003c0009t0001g0059others(23): Show | 26 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.3007-5263C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994453 | ||||||
| chr12:121994500
|
C | T | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3007-5216C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994500 | ||||||
| chr12:121994507
|
G | A | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-5209G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994507 | ||||||
| chr12:121994561
|
G | A | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-5155G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994561 | ||||||
| chr12:121994608
|
C | T | 1 | a0006c0006t0001g0259 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3007-5108C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994608 | ||||||
| chr12:121994623
|
C | T | 1 | a0006c0006t0001g0259 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3007-5093C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994623 | ||||||
| chr12:121994762
|
T | C | 18 | a0003c0003t0001g0332a0003c0003t0001g0333a0003c0003t0001g0334others(15): Show | 18 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3007-4954T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994762 | ||||||
| chr12:121994930
|
T | C | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-4786T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994930 | ||||||
| chr12:121994967
|
TA | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(110): Show | 114 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.3007-4739delA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121994967 | |||||
| chr12:121994977
|
AT | A | 3 | a0003c0012t0001g0084a0003c0012t0001g0272a0007c0007t0001g0081 | 3 | HG02109.hp2 HG03927.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3007-4738delT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994977 | ||||||
| chr12:121994978
|
T | A | 16 | a0003c0003t0001g0264a0003c0003t0001g0271a0007c0007t0001g0067others(13): Show | 16 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.3007-4738T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994978 | ||||||
| chr12:121994985
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-4731C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121994985 | ||||||
| chr12:121995016
|
G | C | 1 | a0004c0002t0001g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3007-4700G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121995016 | ||||||
| chr12:121995048
|
C | A | 1 | a0003c0003t0001g0330 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3007-4668C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121995048 | ||||||
| chr12:121995084
|
G | T | 49 | a0003c0003t0001g0332a0003c0003t0001g0333a0003c0003t0001g0334others(46): Show | 49 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.3007-4632G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121995084 | ||||||
| chr12:121995093
|
T | A | 1 | a0007c0007t0001g0077 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3007-4623T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121995093 | ||||||
| chr12:121995123
|
G | A | 2 | a0008c0010t0001g0065a0008c0010t0001g0066 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3007-4593G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121995123 | ||||||
| chr12:121995159
|
G | A | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-4557G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121995159 | ||||||
| chr12:121995311
|
A | G | 6 | a0001c0001t0001g0121a0001c0001t0001g0133a0001c0001t0001g0151others(3): Show | 6 | HG00673.hp1 HG02523.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-4405A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121995311 | ||||||
| chr12:121995365
|
C | T | 1 | a0014c0023t0001g0225 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3007-4351C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121995365 | ||||||
| chr12:121995679
|
T | G | 1 | a0001c0001t0001g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3007-4037T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121995679 | ||||||
| chr12:121996148
|
C | T | 20 | a0001c0001t0001g0196a0006c0006t0001g0064a0006c0006t0001g0246others(17): Show | 20 | HG00423.hp2 HG01243.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.3007-3568C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121996148 | ||||||
| chr12:121996270
|
C | G | 2 | a0002c0004t0001g0055a0002c0004t0001g0056 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.3007-3446C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121996270 | ||||||
| chr12:121996490
|
T | A | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-3226T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121996490 | ||||||
| chr12:121996536
|
G | A | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-3180G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121996536 | ||||||
| chr12:121996678
|
T | C | 17 | a0007c0007t0001g0067a0007c0007t0001g0068a0007c0007t0001g0069others(14): Show | 17 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.3007-3038T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121996678 | ||||||
| chr12:121997028
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-2688C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121997028 | ||||||
| chr12:121997039
|
A | G | 1 | a0002c0004t0001g0295 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3007-2677A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121997039 | ||||||
| chr12:121997114
|
G | A | 1 | a0005c0005t0001g0228 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3007-2602G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121997114 | ||||||
| chr12:121997236
|
G | A | 17 | a0007c0007t0001g0067a0007c0007t0001g0068a0007c0007t0001g0069others(14): Show | 17 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.3007-2480G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121997236 | ||||||
| chr12:121997401
|
C | CA | 226 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.3007-2295dupA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121997401 | |||||
| chr12:121997401
|
C | CAA | 13 | a0001c0001t0001g0121a0001c0001t0001g0148a0001c0001t0001g0197others(10): Show | 13 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.3007-2296_3007-229 others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121997401 | |||||
| chr12:121997401
|
CA | C | 10 | a0002c0004t0001g0274a0002c0008t0001g0002a0002c0008t0001g0277others(7): Show | 11 | HG02080.hp1 NA18957.hp2 NA18962.hp1 others(8): Show |
intron_variant | MODIFIER | c.3007-2295delA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121997401 | |||||
| chr12:121997464
|
G | T | 1 | a0001c0001t0001g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3007-2252G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121997464 | ||||||
| chr12:121997580
|
G | GT | 41 | a0001c0001t0001g0200a0002c0004t0001g0293a0003c0003t0001g0332others(38): Show | 41 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(38): Show |
intron_variant | MODIFIER | c.3007-2122dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121997580 | |||||
| chr12:121997580
|
G | GTT | 16 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(13): Show | 16 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.3007-2123_3007-212 others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121997580 | |||||
| chr12:121997750
|
AGTTT | A | 4 | a0005c0005t0001g0239a0005c0005t0001g0240a0005c0005t0001g0242others(1): Show | 4 | HG02257.hp1 HG03139.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.3007-1961_3007-195 others(8): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121997750 | |||||
| chr12:121997751
|
G | GTTTTT | 4 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0061others(1): Show | 4 | NA18942.hp1 NA18999.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.3007-1962_3007-196 others(9): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121997751 | |||||
| chr12:121997755
|
G | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-1961G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121997755 | ||||||
| chr12:121997756
|
T | G | 1 | a0005c0005t0001g0226 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3007-1960T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121997756 | ||||||
| chr12:121997910
|
C | T | 1 | a0002c0004t0001g0289 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3007-1806C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121997910 | ||||||
| chr12:121997911
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0213 | 2 | HG00408.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.3007-1805C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121997911 | ||||||
| chr12:121997950
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3007-1766C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121997950 | ||||||
| chr12:121998137
|
G | A | 23 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(20): Show | 23 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.3007-1579G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121998137 | ||||||
| chr12:121998180
|
T | C | 1 | a0003c0003t0001g0271 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3007-1536T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121998180 | ||||||
| chr12:121998300
|
C | T | 30 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.3007-1416C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121998300 | ||||||
| chr12:121998306
|
C | G | 2 | a0004c0002t0001g0034a0004c0002t0001g0035 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3007-1410C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121998306 | ||||||
| chr12:121998432
|
A | AATAT | 7 | a0002c0004t0001g0312a0003c0003t0001g0057a0003c0003t0001g0103others(4): Show | 7 | HG02148.hp1 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.3007-1231_3007-122 others(8): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998432 | |||||
| chr12:121998432
|
A | AATATATA others(3): Show |
1 | a0006c0006t0001g0248 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3007-1237_3007-122 others(14): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998432 | |||||
| chr12:121998432
|
A | AATATATA others(19): Show |
1 | a0002c0004t0001g0295 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3007-1253_3007-122 others(30): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998432 | |||||
| chr12:121998432
|
AAT | A | 32 | a0002c0004t0001g0056a0002c0004t0001g0086a0002c0004t0001g0274others(29): Show | 32 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.3007-1229_3007-122 others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998432 | |||||
| chr12:121998432
|
AATAT | A | 41 | a0002c0004t0001g0279a0002c0004t0001g0284a0002c0004t0001g0287others(38): Show | 41 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.3007-1231_3007-122 others(8): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998432 | |||||
| chr12:121998432
|
AATATAT | A | 18 | a0002c0004t0001g0003a0002c0004t0001g0276a0002c0004t0001g0300others(15): Show | 18 | HG00609.hp2 HG01358.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.3007-1233_3007-122 others(10): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998432 | |||||
| chr12:121998432
|
AATATATA others(1): Show |
A | 11 | a0002c0004t0001g0004a0002c0004t0001g0055a0002c0008t0001g0002others(8): Show | 12 | HG00642.hp2 HG02293.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.3007-1235_3007-122 others(12): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998432 | |||||
| chr12:121998432
|
AATATATA others(3): Show |
A | 30 | a0002c0004t0001g0273a0002c0004t0001g0296a0002c0004t0001g0298others(27): Show | 30 | HG00140.hp2 HG00621.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.3007-1237_3007-122 others(14): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998432 | |||||
| chr12:121998432
|
AATATATA others(5): Show |
A | 12 | a0002c0004t0001g0303a0002c0004t0001g0304a0002c0008t0001g0280others(9): Show | 12 | HG01361.hp1 HG02135.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.3007-1239_3007-122 others(16): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998432 | |||||
| chr12:121998432
|
AATATATA others(7): Show |
A | 3 | a0002c0008t0001g0286a0002c0008t0001g0290a0004c0002t0001g0048 | 3 | HG01433.hp2 NA19004.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.3007-1241_3007-122 others(18): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998432 | |||||
| chr12:121998432
|
AATATATA others(9): Show |
A | 1 | a0007c0007t0001g0076 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3007-1243_3007-122 others(20): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998432 | |||||
| chr12:121998432
|
AATATATA others(13): Show |
A | 4 | a0004c0002t0001g0006a0004c0002t0001g0038a0004c0002t0001g0054others(1): Show | 4 | HG03195.hp2 NA19030.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.3007-1247_3007-122 others(24): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998432 | |||||
| chr12:121998432
|
AATATATA others(15): Show |
A | 5 | a0007c0007t0001g0071a0007c0007t0001g0072a0007c0007t0001g0075others(2): Show | 5 | HG01261.hp1 NA18971.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.3007-1249_3007-122 others(26): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998432 | |||||
| chr12:121998432
|
AATATATA others(17): Show |
A | 11 | a0003c0003t0001g0330a0007c0007t0001g0068a0007c0007t0001g0069others(8): Show | 11 | HG01168.hp2 HG01243.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.3007-1251_3007-122 others(28): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998432 | |||||
| chr12:121998432
|
AATATATA others(19): Show |
A | 3 | a0005c0005t0001g0234a0005c0005t0001g0265a0006c0006t0001g0269 | 3 | HG02486.hp2 NA18612.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3007-1253_3007-122 others(30): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998432 | |||||
| chr12:121998432
|
AATATATA others(21): Show |
A | 6 | a0005c0005t0001g0221a0005c0005t0001g0222a0005c0005t0001g0230others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-1255_3007-122 others(32): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998432 | |||||
| chr12:121998432
|
AATATATA others(23): Show |
A | 38 | a0003c0012t0001g0083a0005c0005t0001g0218a0005c0005t0001g0219others(35): Show | 38 | HG00423.hp1 HG01884.hp2 HG02015.hp2 others(35): Show |
intron_variant | MODIFIER | c.3007-1257_3007-122 others(34): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998432 | |||||
| chr12:121998432
|
AATATATA others(25): Show |
A | 3 | a0003c0003t0001g0332a0003c0003t0001g0333a0003c0003t0001g0334 | 3 | HG02895.hp2 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3007-1259_3007-122 others(36): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998432 | |||||
| chr12:121998432
|
AATATATA others(27): Show |
A | 1 | a0001c0001t0001g0131 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.3007-1261_3007-122 others(38): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998432 | |||||
| chr12:121998432
|
AATATATA others(29): Show |
A | 111 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(108): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.3007-1263_3007-122 others(40): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998432 | |||||
| chr12:121998717
|
C | T | 1 | a0006c0006t0001g0343 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3007-999C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121998717 | ||||||
| chr12:121998723
|
T | TA | 31 | a0002c0008t0001g0307a0003c0003t0001g0057a0003c0003t0001g0087others(28): Show | 31 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.3007-984dupA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998723 | |||||
| chr12:121998836
|
G | A | 2 | a0008c0010t0001g0065a0008c0010t0001g0066 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3007-880G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121998836 | ||||||
| chr12:121998855
|
A | C | 1 | a0003c0003t0001g0091 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3007-861A>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121998855 | ||||||
| chr12:121998881
|
C | A | 1 | a0001c0001t0001g0211 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3007-835C>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121998881 | ||||||
| chr12:121998889
|
C | CA | 83 | a0001c0001t0001g0114a0001c0001t0001g0123a0001c0001t0001g0125others(80): Show | 84 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.3007-798dupA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998889 | |||||
| chr12:121998889
|
C | CAA | 16 | a0001c0001t0001g0112a0002c0004t0001g0273a0002c0004t0001g0275others(13): Show | 16 | HG00438.hp1 HG01169.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.3007-799_3007-798d others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998889 | |||||
| chr12:121998889
|
C | CAAA | 37 | a0002c0004t0001g0055a0002c0004t0001g0056a0002c0004t0001g0304others(34): Show | 37 | HG00423.hp1 HG01168.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.3007-800_3007-798d others(5): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998889 | |||||
| chr12:121998889
|
C | CAAAA | 10 | a0003c0012t0001g0083a0005c0005t0001g0219a0005c0005t0001g0226others(7): Show | 10 | HG02027.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.3007-801_3007-798d others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998889 | |||||
| chr12:121998889
|
CA | C | 27 | a0001c0001t0001g0121a0001c0001t0001g0188a0003c0003t0001g0091others(24): Show | 27 | HG00323.hp1 HG01109.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.3007-798delA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998889 | |||||
| chr12:121998889
|
CAA | C | 18 | a0003c0003t0001g0271a0003c0009t0001g0060a0003c0009t0001g0063others(15): Show | 18 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.3007-799_3007-798d others(4): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 121998889 | |||||
| chr12:121998933
|
G | A | 1 | a0005c0005t0001g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3007-783G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121998933 | ||||||
| chr12:121998940
|
CATCCTTG others(6): Show |
C | 2 | a0005c0005t0001g0219a0005c0005t0001g0220 | 2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3007-775_3007-763d others(15): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121998940 | ||||||
| chr12:121999032
|
C | T | 20 | a0003c0003t0001g0271a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.3007-684C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121999032 | ||||||
| chr12:121999235
|
C | G | 2 | a0001c0001t0001g0185a0001c0001t0001g0210 | 2 | HG01070.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.3007-481C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121999235 | ||||||
| chr12:121999384
|
T | C | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-332T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121999384 | ||||||
| chr12:121999390
|
C | T | 30 | a0003c0003t0001g0264a0003c0003t0001g0330a0003c0003t0001g0331others(27): Show | 30 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.3007-326C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121999390 | ||||||
| chr12:121999394
|
G | A | 2 | a0008c0010t0001g0065a0008c0010t0001g0066 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3007-322G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121999394 | ||||||
| chr12:121999509
|
T | C | 2 | a0008c0010t0001g0065a0008c0010t0001g0066 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3007-207T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 19/21 | chr12 | 121999509 | ||||||
| chr12:122000216
|
G | T | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3235+272G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 20/21 | chr12 | 122000216 | ||||||
| chr12:122000281
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(107): Show | 111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.3235+337G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 20/21 | chr12 | 122000281 | ||||||
| chr12:122000318
|
G | A | 2 | a0004c0002t0001g0009a0016c0024t0001g0010 | 2 | NA18971.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.3235+374G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 20/21 | chr12 | 122000318 | ||||||
| chr12:122000320
|
G | C | 1 | a0003c0003t0001g0096 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3235+376G>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 20/21 | chr12 | 122000320 | ||||||
| chr12:122000326
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0200 | 2 | HG02083.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.3235+382C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 20/21 | chr12 | 122000326 | ||||||
| chr12:122000429
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3235+485G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 20/21 | chr12 | 122000429 | ||||||
| chr12:122000504
|
A | T | 1 | a0003c0003t0001g0092 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3235+560A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 20/21 | chr12 | 122000504 | ||||||
| chr12:122000547
|
C | CA | 30 | a0003c0003t0001g0057a0003c0003t0001g0087a0003c0003t0001g0088others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.3235+617dupA | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 122000547 | |||||
| chr12:122000566
|
G | A | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3235+622G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 20/21 | chr12 | 122000566 | ||||||
| chr12:122000570
|
AAAAG | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 5 | NA18960.hp1 NA18962.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.3235+630_3235+633d others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 122000570 | |||||
| chr12:122001055
|
C | CT | 16 | a0002c0004t0001g0273a0002c0004t0001g0304a0003c0003t0001g0271others(13): Show | 16 | HG00642.hp2 HG01358.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.3236-423dupT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 122001055 | |||||
| chr12:122001055
|
CT | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(103): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.3236-423delT | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 122001055 | |||||
| chr12:122001190
|
G | A | 1 | a0003c0012t0001g0083 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3236-307G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 20/21 | chr12 | 122001190 | ||||||
| chr12:122001202
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3236-295C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 20/21 | chr12 | 122001202 | ||||||
| chr12:122001248
|
G | A | 1 | a0003c0017t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3236-249G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 20/21 | chr12 | 122001248 | ||||||
| chr12:122001354
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3236-143C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 20/21 | chr12 | 122001354 | ||||||
| chr12:122001368
|
T | A | 20 | a0003c0003t0001g0271a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.3236-129T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 20/21 | chr12 | 122001368 | ||||||
| chr12:122001419
|
T | C | 2 | a0004c0002t0001g0006a0004c0002t0001g0054 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3236-78T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 20/21 | chr12 | 122001419 | ||||||
| chr12:122001463
|
T | C | 301 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(298): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.3236-34T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 20/21 | chr12 | 122001463 | ||||||
| chr12:122001750
|
T | G | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3337+152T>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | chr12 | 122001750 | ||||||
| chr12:122001795
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0155 | 2 | HG00323.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.3337+197C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | chr12 | 122001795 | ||||||
| chr12:122001824
|
C | T | 29 | a0003c0003t0001g0264a0003c0003t0001g0330a0003c0003t0001g0331others(26): Show | 29 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.3337+226C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | chr12 | 122001824 | ||||||
| chr12:122001828
|
T | A | 1 | a0003c0003t0001g0331 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3337+230T>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | chr12 | 122001828 | ||||||
| chr12:122001854
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3337+256G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | chr12 | 122001854 | ||||||
| chr12:122002002
|
C | T | 1 | a0003c0003t0001g0100 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3337+404C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | chr12 | 122002002 | ||||||
| chr12:122002121
|
G | A | 23 | a0003c0003t0001g0271a0003c0012t0001g0083a0003c0012t0001g0084others(20): Show | 23 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.3337+523G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | chr12 | 122002121 | ||||||
| chr12:122002172
|
T | C | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3337+574T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | chr12 | 122002172 | ||||||
| chr12:122002228
|
A | T | 1 | a0004c0002t0001g0024 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3337+630A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | chr12 | 122002228 | ||||||
| chr12:122002453
|
T | C | 1 | a0002c0004t0001g0316 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3337+855T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | chr12 | 122002453 | ||||||
| chr12:122002548
|
AAGAG | A | 6 | a0003c0003t0001g0330a0003c0003t0001g0331a0003c0003t0001g0348others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3337+964_3337+967d others(6): Show |
CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr12 | 122002548 | |||||
| chr12:122002660
|
G | T | 1 | a0006c0011t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3338-992G>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | chr12 | 122002660 | ||||||
| chr12:122002972
|
C | G | 1 | a0001c0001t0001g0328 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3338-680C>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | chr12 | 122002972 | ||||||
| chr12:122002983
|
C | T | 1 | a0003c0003t0001g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3338-669C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | chr12 | 122002983 | ||||||
| chr12:122002989
|
C | T | 1 | a0006c0006t0001g0251 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3338-663C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | chr12 | 122002989 | ||||||
| chr12:122003012
|
T | C | 2 | a0003c0012t0001g0084a0003c0012t0001g0272 | 2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3338-640T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | chr12 | 122003012 | ||||||
| chr12:122003031
|
T | C | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3338-621T>C | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | chr12 | 122003031 | ||||||
| chr12:122003092
|
A | T | 1 | a0003c0003t0001g0097 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3338-560A>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | chr12 | 122003092 | ||||||
| chr12:122003143
|
C | T | 6 | a0003c0009t0001g0058a0003c0009t0001g0059a0003c0009t0001g0060others(3): Show | 6 | NA18942.hp1 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3338-509C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | chr12 | 122003143 | ||||||
| chr12:122003325
|
G | A | 56 | a0002c0004t0001g0003a0002c0004t0001g0004a0002c0004t0001g0055others(53): Show | 57 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.3338-327G>A | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | chr12 | 122003325 | ||||||
| chr12:122003392
|
C | T | 20 | a0003c0003t0001g0271a0003c0012t0001g0084a0003c0012t0001g0272others(17): Show | 20 | HG01168.hp2 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.3338-260C>T | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | chr12 | 122003392 | ||||||
| chr12:122003401
|
A | G | 49 | a0003c0003t0001g0332a0003c0003t0001g0333a0003c0003t0001g0334others(46): Show | 49 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.3338-251A>G | CFAP251 | ENSG00000158023.10 | transcript | ENST00000288912.9 | protein_coding | 21/21 | chr12 | 122003401 |