Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 57501 |
|---|---|
| ensemblid | ENSG00000114656.13 |
| hgncid | 29231 |
| symbol | CFAP92 |
| name | cilia and flagella associated protein 92 (putative) |
| refseq_nuc | NM_001394090.1 |
| refseq_prot | NP_001381019.1 |
| ensembl_nuc | ENST00000645291.3 |
| ensembl_prot | ENSP00000496592.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 128909873 |
| end | 128994076 |
| strand | - |
| ver | v1.2 |
| region | chr3:128909873-128994076 |
| region5000 | chr3:128904873-128999076 |
| regionname0 | CFAP92_chr3_128909873_128994076 |
| regionname5000 | CFAP92_chr3_128904873_128999076 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1104 | 292 | 64 | 67 | 115 | 15 | 30 | 86 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0002 | 0/0 | 1104 | 23 | 9 | 0 | 7 | 0 | 7 | 5 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0003 | 0/0 | 1104 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0004 | 0/0 | 1103 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0005 | 0/0 | 1104 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0006 | 0/0 | 1104 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0007 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0008 | 0/0 | 1104 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0009 | 0/0 | 505 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0010 | 0/0 | 1104 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0011 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0012 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0013 | 0/1 | 1104 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0014 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0015 | 0/0 | 1104 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0016 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0017 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0018 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0019 | 0/0 | 1104 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0020 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0021 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 3315 | 210 | 23 | 44 | 107 | 11 | 24 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0002 | 0/0 | 3315 | 45 | 17 | 14 | 7 | 2 | 5 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0003 | 0/0 | 3315 | 24 | 13 | 8 | 0 | 2 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0004 | 0/0 | 3315 | 23 | 9 | 0 | 7 | 0 | 7 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0005 | 0/0 | 3315 | 7 | 6 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0006 | 0/0 | 3315 | 5 | 5 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0007 | 0/0 | 3315 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0008 | 0/0 | 3315 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0009 | 0/0 | 3315 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0010 | 0/0 | 3312 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0011 | 0/0 | 3315 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0012 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0013 | 0/0 | 3315 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0014 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0015 | 0/1 | 3315 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0016 | 0/0 | 3315 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0017 | 0/0 | 3315 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0018 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0019 | 0/0 | 3315 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0020 | 0/0 | 3315 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0021 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0022 | 0/0 | 3315 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0023 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0024 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0025 | 0/0 | 3315 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0026 | 0/0 | 2410 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0027 | 0/0 | 3315 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0028 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0029 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| c0030 | 0/0 | 3312 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| 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 | 556 | 295 | 62 | 64 | 120 | 15 | 32 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| t0002 | 0/0 | 556 | 30 | 16 | 0 | 7 | 0 | 7 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| t0003 | 0/0 | 556 | 7 | 6 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| t0004 | 0/0 | 553 | 5 | 0 | 4 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| t0005 | 0/0 | 556 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| t0006 | 0/0 | 556 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| t0007 | 0/0 | 556 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| t0008 | 0/0 | 556 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| 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 | 1 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0187 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3315 | 210 | 23 | 44 | 107 | 11 | 24 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0001c0002 | 0/0 | 3315 | 45 | 17 | 14 | 7 | 2 | 5 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0001c0003 | 0/0 | 3315 | 24 | 13 | 8 | 0 | 2 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0001c0005 | 0/0 | 3315 | 7 | 6 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0001c0009 | 0/0 | 3315 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0001c0019 | 0/0 | 3315 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0001c0021 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0001c0023 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0001c0024 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0002c0004 | 0/0 | 3315 | 23 | 9 | 0 | 7 | 0 | 7 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0003c0006 | 0/0 | 3315 | 5 | 5 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0004c0010 | 0/0 | 3312 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0004c0030 | 0/0 | 3312 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0005c0008 | 0/0 | 3315 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0006c0007 | 0/0 | 3315 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0007c0028 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0008c0027 | 0/0 | 3315 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0009c0026 | 0/0 | 2410 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0010c0022 | 0/0 | 3315 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0011c0017 | 0/0 | 3315 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0012c0018 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0013c0015 | 0/1 | 3315 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0014c0020 | 0/0 | 3315 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0015c0016 | 0/0 | 3315 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0016c0025 | 0/0 | 3315 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0017c0014 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0018c0029 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0019c0013 | 0/0 | 3315 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0020c0012 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0021c0011 | 0/0 | 3315 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3870 | 200 | 17 | 42 | 106 | 11 | 23 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0001c0001t0003 | 0/0 | 3870 | 7 | 6 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0001c0001t0006 | 0/0 | 3870 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0001c0001t0007 | 0/0 | 3870 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0001c0001t0008 | 0/0 | 3870 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0001c0002t0001 | 0/0 | 3870 | 45 | 17 | 14 | 7 | 2 | 5 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0001c0003t0001 | 0/0 | 3870 | 19 | 13 | 4 | 0 | 1 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0001c0003t0004 | 0/0 | 3867 | 5 | 0 | 4 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0001c0005t0001 | 0/0 | 3870 | 7 | 6 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0001c0009t0001 | 0/0 | 3870 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0001c0019t0001 | 0/0 | 3870 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0001c0021t0001 | 0/0 | 3870 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0001c0023t0005 | 0/0 | 3870 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0001c0024t0005 | 0/0 | 3870 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0002c0004t0002 | 0/0 | 3870 | 23 | 9 | 0 | 7 | 0 | 7 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0003c0006t0002 | 0/0 | 3870 | 5 | 5 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0004c0010t0001 | 0/0 | 3867 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0004c0030t0001 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0005c0008t0001 | 0/0 | 3870 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0006c0007t0001 | 0/0 | 3870 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0007c0028t0002 | 0/0 | 3870 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0008c0027t0001 | 0/0 | 3870 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0009c0026t0001 | 0/0 | 2965 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0010c0022t0001 | 0/0 | 3870 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0011c0017t0001 | 0/0 | 3870 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0012c0018t0002 | 0/0 | 3870 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0013c0015t0001 | 0/1 | 3870 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0014c0020t0001 | 0/0 | 3870 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0015c0016t0001 | 0/0 | 3870 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0016c0025t0001 | 0/0 | 3870 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0017c0014t0001 | 0/0 | 3870 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0018c0029t0001 | 0/0 | 3870 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0019c0013t0001 | 0/0 | 3870 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0020c0012t0001 | 0/0 | 3870 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| a0021c0011t0001 | 0/0 | 3870 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | copy fasta | chr3 | 128904873 | 128999076 |
| 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 | 1 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0006g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0001t0008g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0002t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0003t0004g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0005t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0005t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0005t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0005t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0005t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0005t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0005t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0009t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0009t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0019t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0021t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0023t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0001c0024t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0002c0004t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0003c0006t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0003c0006t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0003c0006t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0003c0006t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0003c0006t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0004c0010t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0004c0010t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0004c0030t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0005c0008t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0005c0008t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0006c0007t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0006c0007t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0007c0028t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0008c0027t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0009c0026t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0010c0022t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0011c0017t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0012c0018t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0013c0015t0001g0187 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0014c0020t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0015c0016t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0016c0025t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0017c0014t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0018c0029t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0019c0013t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0020c0012t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| a0021c0011t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | GBR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | GBR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | FIN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0279 | EUR | FIN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00323 | hp1 | a0015 | c0016 | t0001 | g0176 | EUR | FIN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | FIN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | CHS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00423 | hp2 | a0005 | c0008 | t0001 | g0327 | EAS | CHS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00639 | hp2 | a0001 | c0005 | t0001 | g0211 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00642 | hp1 | a0004 | c0010 | t0001 | g0329 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00642 | hp2 | a0001 | c0003 | t0004 | g0273 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00673 | hp2 | a0001 | c0019 | t0001 | g0069 | EAS | CHS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00733 | hp2 | a0001 | c0003 | t0004 | g0280 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0308 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0304 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0013 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0278 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0277 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01074 | hp2 | a0001 | c0001 | t0006 | g0111 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0295 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01109 | hp2 | a0006 | c0007 | t0001 | g0014 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0299 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0322 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0128 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01192 | hp1 | a0001 | c0003 | t0004 | g0274 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0156 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0306 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01243 | hp2 | a0010 | c0022 | t0001 | g0276 | AMR | PUR | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01261 | hp2 | a0001 | c0003 | t0004 | g0215 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0171 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0178 | EUR | IBS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01515 | hp2 | a0001 | c0003 | t0001 | g0288 | EUR | IBS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0284 | EUR | IBS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01884 | hp2 | a0001 | c0005 | t0001 | g0209 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01891 | hp1 | a0004 | c0030 | t0001 | g0328 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0155 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0157 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02040 | hp1 | a0002 | c0004 | t0002 | g0081 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02055 | hp2 | a0002 | c0004 | t0002 | g0321 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02056 | hp2 | a0002 | c0004 | t0002 | g0301 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02132 | hp2 | a0005 | c0008 | t0001 | g0230 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02135 | hp1 | a0011 | c0017 | t0001 | g0054 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0169 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02145 | hp2 | a0018 | c0029 | t0001 | g0095 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0123 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CDX | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CDX | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0188 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0325 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02258 | hp1 | a0003 | c0006 | t0002 | g0182 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02258 | hp2 | a0002 | c0004 | t0002 | g0323 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02280 | hp2 | a0001 | c0023 | t0005 | g0333 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | PEL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02451 | hp1 | a0001 | c0021 | t0001 | g0198 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02451 | hp2 | a0002 | c0004 | t0002 | g0314 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0195 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02572 | hp2 | a0012 | c0018 | t0002 | g0143 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0194 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0167 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02622 | hp1 | a0001 | c0005 | t0001 | g0206 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02622 | hp2 | a0007 | c0028 | t0002 | g0185 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02630 | hp2 | a0001 | c0024 | t0005 | g0332 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0315 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02683 | hp1 | a0002 | c0004 | t0002 | g0313 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0331 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02698 | hp2 | a0001 | c0001 | t0008 | g0334 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02717 | hp2 | a0020 | c0012 | t0001 | g0048 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02818 | hp1 | a0001 | c0005 | t0001 | g0150 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0166 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0160 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0192 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0309 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02896 | hp1 | a0001 | c0009 | t0001 | g0213 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02897 | hp2 | a0001 | c0009 | t0001 | g0210 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02922 | hp2 | a0002 | c0004 | t0002 | g0318 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02965 | hp2 | a0004 | c0010 | t0001 | g0330 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02970 | hp1 | a0003 | c0006 | t0002 | g0180 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02970 | hp2 | a0002 | c0004 | t0002 | g0320 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0199 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0189 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0154 | AFR | GWD | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0191 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0168 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0307 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03209 | hp1 | a0001 | c0005 | t0001 | g0208 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03209 | hp2 | a0002 | c0004 | t0002 | g0317 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03225 | hp2 | a0006 | c0007 | t0001 | g0015 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03239 | hp1 | a0019 | c0013 | t0001 | g0049 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03239 | hp2 | a0009 | c0026 | t0001 | g0296 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0190 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0130 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0305 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03491 | hp1 | a0002 | c0004 | t0002 | g0298 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03516 | hp1 | a0003 | c0006 | t0002 | g0183 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03579 | hp1 | a0001 | c0005 | t0001 | g0212 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0158 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0282 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | STU | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0172 | SAS | STU | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03704 | hp2 | a0002 | c0004 | t0002 | g0311 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0179 | SAS | BEB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03927 | hp2 | a0002 | c0004 | t0002 | g0326 | SAS | BEB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03942 | hp1 | a0002 | c0004 | t0002 | g0310 | SAS | BEB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | STU | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0174 | SAS | STU | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG04184 | hp1 | a0008 | c0027 | t0001 | g0019 | SAS | BEB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | STU | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | STU | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG04204 | hp2 | a0002 | c0004 | t0002 | g0312 | SAS | STU | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG04228 | hp1 | a0002 | c0004 | t0002 | g0316 | SAS | STU | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | STU | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | YRI | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0196 | AFR | YRI | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18906 | hp2 | a0003 | c0006 | t0002 | g0184 | AFR | YRI | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18950 | hp2 | a0002 | c0004 | t0002 | g0008 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18951 | hp2 | a0016 | c0025 | t0001 | g0077 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18973 | hp2 | a0001 | c0001 | t0007 | g0066 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18984 | hp1 | a0014 | c0020 | t0001 | g0270 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18985 | hp2 | a0002 | c0004 | t0002 | g0303 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19007 | hp2 | a0021 | c0011 | t0001 | g0047 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19030 | hp1 | a0001 | c0005 | t0001 | g0207 | AFR | LWK | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19030 | hp2 | a0002 | c0004 | t0002 | g0324 | AFR | LWK | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19063 | hp1 | a0002 | c0004 | t0002 | g0300 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19066 | hp2 | a0002 | c0004 | t0002 | g0008 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA19091 | hp2 | a0002 | c0004 | t0002 | g0302 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA20129 | hp1 | a0003 | c0006 | t0002 | g0181 | AFR | ASW | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA20129 | hp2 | a0002 | c0004 | t0002 | g0297 | AFR | ASW | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0068 | EUR | TSI | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | TSI | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA20805 | hp2 | a0001 | c0003 | t0004 | g0281 | EUR | TSI | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0148 | AMR | CLM | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0197 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0175 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0145 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0193 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03471 | hp1 | a0017 | c0014 | t0001 | g0205 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | MSL | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0159 | AFR | USA | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| HG06807 | hp2 | a0002 | c0004 | t0002 | g0319 | AFR | USA | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | USA | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | USA | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| homoSapiens_chm13v2 | hp1 | a0013 | c0015 | t0001 | g0187 | REF | REF | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0110 | REF | REF | CFAP92_chr3_128904873_128999076 | CFAP92 | chr3 | 128904873 | 128999076 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:128915125
|
C | T | 1 | a0014 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.3274G>A | p.Val1092Ile | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/16 | 3403/3870 | 3274/3315 | 1092/1104 | chr3 | 128915125 | ||
| chr3:128915194
|
C | T | 1 | a0013 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.3205G>A | p.Val1069Met | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/16 | 3334/3870 | 3205/3315 | 1069/1104 | chr3 | 128915194 | ||
| chr3:128915468
|
TTTC | T | 1 | a0004 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
disruptive_inframe_deletion | MODERATE | c.3009_3011delGAA | p.Lys1004del | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 14/16 | 3140/3870 | 3009/3315 | 1003/1104 | chr3 | 128915468 | ||
| chr3:128916219
|
G | A | 1 | a0015 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.2804C>T | p.Ala935Val | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/16 | 2933/3870 | 2804/3315 | 935/1104 | chr3 | 128916219 | ||
| chr3:128932735
|
T | G | 4 | a0002a0003a0007others(1): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
missense_variant | MODERATE | c.2716A>C | p.Met906Leu | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/16 | 2845/3870 | 2716/3315 | 906/1104 | chr3 | 128932735 | ||
| chr3:128932737
|
A | T | 1 | a0006 | 2 | HG01109.hp2 HG03225.hp2 |
missense_variant | MODERATE | c.2714T>A | p.Leu905His | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/16 | 2843/3870 | 2714/3315 | 905/1104 | chr3 | 128932737 | ||
| chr3:128932953
|
G | A | 1 | a0002 | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
missense_variant | MODERATE | c.2498C>T | p.Thr833Met | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/16 | 2627/3870 | 2498/3315 | 833/1104 | chr3 | 128932953 | ||
| chr3:128932957
|
C | T | 1 | a0011 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.2494G>A | p.Val832Met | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/16 | 2623/3870 | 2494/3315 | 832/1104 | chr3 | 128932957 | ||
| chr3:128944223
|
GCACCTGG others(2064): Show |
G | 1 | a0009 | 1 | HG03239.hp2 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.1354-319_2258+847d others(2): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | chr3 | 128944223 | ||||||
| chr3:128945073
|
G | C | 1 | a0010 | 1 | HG01243.hp2 | missense_variant&splice_region_variant | MODERATE | c.2256C>G | p.Ser752Arg | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 2385/3870 | 2256/3315 | 752/1104 | chr3 | 128945073 | ||
| chr3:128945326
|
T | G | 1 | a0016 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.2003A>C | p.Lys668Thr | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 2132/3870 | 2003/3315 | 668/1104 | chr3 | 128945326 | ||
| chr3:128945612
|
G | A | 1 | a0005 | 2 | HG00423.hp2 HG02132.hp2 |
missense_variant | MODERATE | c.1717C>T | p.Leu573Phe | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 1846/3870 | 1717/3315 | 573/1104 | chr3 | 128945612 | ||
| chr3:128945782
|
C | T | 1 | a0007 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.1547G>A | p.Arg516His | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 1676/3870 | 1547/3315 | 516/1104 | chr3 | 128945782 | ||
| chr3:128945821
|
T | C | 1 | a0002 | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
missense_variant | MODERATE | c.1508A>G | p.Glu503Gly | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 1637/3870 | 1508/3315 | 503/1104 | chr3 | 128945821 | ||
| chr3:128965578
|
G | A | 1 | a0008 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.1286C>T | p.Pro429Leu | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/16 | 1415/3870 | 1286/3315 | 429/1104 | chr3 | 128965578 | ||
| chr3:128975786
|
C | G | 1 | a0017 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1014G>C | p.Arg338Ser | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/16 | 1143/3870 | 1014/3315 | 338/1104 | chr3 | 128975786 | ||
| chr3:128975880
|
G | C | 2 | a0003a0007 | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
missense_variant | MODERATE | c.920C>G | p.Thr307Ser | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/16 | 1049/3870 | 920/3315 | 307/1104 | chr3 | 128975880 | ||
| chr3:128976994
|
T | C | 1 | a0018 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.881A>G | p.Asp294Gly | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 6/16 | 1010/3870 | 881/3315 | 294/1104 | chr3 | 128976994 | ||
| chr3:128993082
|
A | G | 1 | a0019 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.223T>C | p.Cys75Arg | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/16 | 352/3870 | 223/3315 | 75/1104 | chr3 | 128993082 | ||
| chr3:128993103
|
C | T | 1 | a0020 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.202G>A | p.Asp68Asn | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/16 | 331/3870 | 202/3315 | 68/1104 | chr3 | 128993103 | ||
| chr3:128993142
|
T | C | 1 | a0004 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
missense_variant | MODERATE | c.163A>G | p.Ile55Val | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/16 | 292/3870 | 163/3315 | 55/1104 | chr3 | 128993142 | ||
| chr3:128993185
|
C | G | 1 | a0021 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.120G>C | p.Lys40Asn | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/16 | 249/3870 | 120/3315 | 40/1104 | chr3 | 128993185 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:128915120
|
T | G | 1 | a0001c0021 | 1 | HG02451.hp1 | splice_region_variant&synonymous_variant | LOW | c.3279A>C | p.Thr1093Thr | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/16 | 3408/3870 | 3279/3315 | 1093/1104 | chr3 | 128915120 | ||
| chr3:128916212
|
C | T | 1 | a0001c0019 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.2811G>A | p.Val937Val | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/16 | 2940/3870 | 2811/3315 | 937/1104 | chr3 | 128916212 | ||
| chr3:128916227
|
C | T | 1 | a0004c0030 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.2796G>A | p.Lys932Lys | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/16 | 2925/3870 | 2796/3315 | 932/1104 | chr3 | 128916227 | ||
| chr3:128916230
|
C | T | 1 | a0017c0014 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.2793G>A | p.Pro931Pro | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/16 | 2922/3870 | 2793/3315 | 931/1104 | chr3 | 128916230 | ||
| chr3:128932736
|
A | C | 4 | a0002c0004a0003c0006a0007c0028others(1): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
synonymous_variant | LOW | c.2715T>G | p.Leu905Leu | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/16 | 2844/3870 | 2715/3315 | 905/1104 | chr3 | 128932736 | ||
| chr3:128935160
|
G | A | 2 | a0003c0006a0007c0028 | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
synonymous_variant | LOW | c.2418C>T | p.Asp806Asp | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/16 | 2547/3870 | 2418/3315 | 806/1104 | chr3 | 128935160 | ||
| chr3:128945112
|
G | A | 9 | a0001c0003a0001c0005a0001c0009others(6): Show | 41 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(38): Show |
synonymous_variant | LOW | c.2217C>T | p.Ala739Ala | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 2346/3870 | 2217/3315 | 739/1104 | chr3 | 128945112 | ||
| chr3:128945148
|
G | A | 6 | a0001c0002a0001c0024a0013c0015others(3): Show | 50 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(47): Show |
synonymous_variant | LOW | c.2181C>T | p.Asp727Asp | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 2310/3870 | 2181/3315 | 727/1104 | chr3 | 128945148 | ||
| chr3:128945625
|
G | A | 1 | a0001c0009 | 2 | HG02896.hp1 HG02897.hp2 |
synonymous_variant | LOW | c.1704C>T | p.Val568Val | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 1833/3870 | 1704/3315 | 568/1104 | chr3 | 128945625 | ||
| chr3:128945676
|
G | A | 1 | a0015c0016 | 1 | HG00323.hp1 | synonymous_variant | LOW | c.1653C>T | p.Asn551Asn | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 1782/3870 | 1653/3315 | 551/1104 | chr3 | 128945676 | ||
| chr3:128945706
|
G | T | 5 | a0001c0002a0013c0015a0015c0016others(2): Show | 49 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(46): Show |
synonymous_variant | LOW | c.1623C>A | p.Ala541Ala | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 1752/3870 | 1623/3315 | 541/1104 | chr3 | 128945706 | ||
| chr3:128945811
|
G | T | 4 | a0001c0003a0001c0005a0001c0009others(1): Show | 35 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(32): Show |
synonymous_variant | LOW | c.1518C>A | p.Pro506Pro | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/16 | 1647/3870 | 1518/3315 | 506/1104 | chr3 | 128945811 | ||
| chr3:128988764
|
T | C | 2 | a0001c0005a0001c0009 | 9 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
synonymous_variant | LOW | c.417A>G | p.Pro139Pro | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/16 | 546/3870 | 417/3315 | 139/1104 | chr3 | 128988764 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:128909880
|
A | G | 1 | a0001c0001t0006 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*419T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 16/16 | 419 | chr3 | 128909880 | |||||
| chr3:128909966
|
A | G | 4 | a0002c0004t0002a0003c0006t0002a0007c0028t0002others(1): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*333T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 16/16 | 333 | chr3 | 128909966 | |||||
| chr3:128910132
|
C | A | 1 | a0001c0001t0007 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*167G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 16/16 | 167 | chr3 | 128910132 | |||||
| chr3:128910140
|
C | T | 2 | a0001c0023t0005a0001c0024t0005 | 2 | HG02280.hp2 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*159G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 16/16 | 159 | chr3 | 128910140 | |||||
| chr3:128910196
|
CCTG | C | 1 | a0001c0003t0004 | 5 | HG00642.hp2 HG00733.hp2 HG01192.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*100_*102delCAG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 16/16 | 100 | chr3 | 128910196 | |||||
| chr3:128910273
|
G | A | 1 | a0001c0001t0003 | 7 | HG01123.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*26C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 16/16 | 26 | chr3 | 128910273 | |||||
| chr3:128910294
|
G | C | 4 | a0002c0004t0002a0003c0006t0002a0007c0028t0002others(1): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*5C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 16/16 | 5 | chr3 | 128910294 | |||||
| chr3:128993991
|
T | C | 1 | a0001c0001t0008 | 1 | HG02698.hp2 | 5_prime_UTR_variant | MODIFIER | c.-44A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 1/16 | 687 | chr3 | 128993991 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:128910434
|
C | T | 2 | a0001c0002t0001g0006a0001c0002t0001g0295 | 3 | HG01081.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3281-101G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128910434 | ||||||
| chr3:128910489
|
G | A | 45 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0007others(42): Show | 48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.3281-156C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128910489 | ||||||
| chr3:128910575
|
G | C | 2 | a0001c0003t0001g0277a0001c0003t0001g0278 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3281-242C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128910575 | ||||||
| chr3:128910662
|
C | CTGAT | 116 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(113): Show | 118 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.3281-333_3281-330d others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128910662 | ||||||
| chr3:128910891
|
T | C | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG02056.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.3281-558A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128910891 | ||||||
| chr3:128910918
|
C | A | 1 | a0002c0004t0002g0326 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3281-585G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128910918 | ||||||
| chr3:128910939
|
C | T | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3281-606G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128910939 | ||||||
| chr3:128911050
|
T | A | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3281-717A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911050 | ||||||
| chr3:128911118
|
G | A | 1 | a0001c0021t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3281-785C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911118 | ||||||
| chr3:128911202
|
G | A | 6 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0085others(3): Show | 6 | HG00609.hp2 NA18965.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.3281-869C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911202 | ||||||
| chr3:128911206
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3281-873C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911206 | ||||||
| chr3:128911214
|
G | A | 10 | a0001c0002t0001g0158a0001c0002t0001g0159a0001c0002t0001g0160others(7): Show | 10 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.3281-881C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911214 | ||||||
| chr3:128911217
|
C | T | 7 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3281-884G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911217 | ||||||
| chr3:128911275
|
C | G | 1 | a0001c0002t0001g0157 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3281-942G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911275 | ||||||
| chr3:128911278
|
C | G | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.3281-945G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911278 | ||||||
| chr3:128911342
|
G | A | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.3281-1009C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911342 | ||||||
| chr3:128911458
|
T | C | 4 | a0002c0004t0002g0317a0002c0004t0002g0318a0002c0004t0002g0319others(1): Show | 4 | HG02922.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3281-1125A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911458 | ||||||
| chr3:128911654
|
C | G | 4 | a0001c0001t0001g0218a0001c0001t0001g0262a0001c0001t0001g0263others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3281-1321G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911654 | ||||||
| chr3:128911667
|
CCT | C | 4 | a0001c0001t0001g0036a0001c0001t0001g0283a0001c0001t0001g0284others(1): Show | 4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3281-1336_3281-133 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911667 | ||||||
| chr3:128911736
|
C | A | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3281-1403G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911736 | ||||||
| chr3:128911736
|
C | G | 7 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(4): Show | 7 | HG01123.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.3281-1403G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911736 | ||||||
| chr3:128911792
|
T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.3281-1459A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911792 | ||||||
| chr3:128911966
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3281-1633G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911966 | ||||||
| chr3:128911983
|
G | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0331 | 2 | HG01261.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.3281-1650C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128911983 | ||||||
| chr3:128912119
|
T | A | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3281-1786A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912119 | ||||||
| chr3:128912251
|
C | A | 2 | a0006c0007t0001g0014a0006c0007t0001g0015 | 2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3281-1918G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912251 | ||||||
| chr3:128912303
|
G | C | 3 | a0004c0010t0001g0329a0004c0010t0001g0330a0004c0030t0001g0328 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3281-1970C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912303 | ||||||
| chr3:128912334
|
C | T | 7 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3281-2001G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912334 | ||||||
| chr3:128912344
|
C | T | 1 | a0001c0003t0004g0280 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3281-2011G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912344 | ||||||
| chr3:128912448
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0074 | 2 | NA18999.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.3281-2115G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912448 | ||||||
| chr3:128912467
|
T | C | 1 | a0001c0003t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3281-2134A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912467 | ||||||
| chr3:128912598
|
G | A | 1 | a0002c0004t0002g0302 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3281-2265C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912598 | ||||||
| chr3:128912633
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0043 | 2 | HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.3281-2300G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912633 | ||||||
| chr3:128912638
|
G | A | 33 | a0001c0001t0001g0186a0001c0001t0001g0331a0001c0001t0003g0144others(30): Show | 34 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.3281-2305C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912638 | ||||||
| chr3:128912675
|
C | T | 7 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3281-2342G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912675 | ||||||
| chr3:128912829
|
GGA | G | 4 | a0001c0001t0001g0036a0001c0001t0001g0283a0001c0001t0001g0284others(1): Show | 4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3280+2288_3280+228 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912829 | ||||||
| chr3:128912938
|
T | G | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151 | 3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3280+2181A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128912938 | ||||||
| chr3:128913209
|
C | T | 26 | a0001c0001t0001g0186a0001c0001t0001g0331a0001c0003t0001g0004others(23): Show | 27 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.3280+1910G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128913209 | ||||||
| chr3:128913210
|
C | T | 1 | a0002c0004t0002g0302 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3280+1909G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128913210 | ||||||
| chr3:128913309
|
C | G | 1 | a0001c0003t0001g0193 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3280+1810G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128913309 | ||||||
| chr3:128913477
|
T | TTACACCA others(10): Show |
46 | a0001c0001t0001g0132a0001c0002t0001g0002a0001c0002t0001g0006others(43): Show | 49 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.3280+1625_3280+164 others(21): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128913477 | ||||||
| chr3:128913561
|
T | C | 1 | a0002c0004t0002g0326 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3280+1558A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128913561 | ||||||
| chr3:128913596
|
G | A | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3280+1523C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128913596 | ||||||
| chr3:128913611
|
A | G | 33 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(30): Show | 34 | HG01167.hp1 HG01175.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.3280+1508T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128913611 | ||||||
| chr3:128913879
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0021 | 2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3280+1240G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128913879 | ||||||
| chr3:128913926
|
G | A | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3280+1193C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128913926 | ||||||
| chr3:128913964
|
C | T | 1 | a0004c0010t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3280+1155G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128913964 | ||||||
| chr3:128914027
|
T | C | 4 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3280+1092A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128914027 | ||||||
| chr3:128914112
|
C | A | 27 | a0001c0001t0001g0186a0001c0001t0001g0331a0001c0001t0003g0214others(24): Show | 28 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.3280+1007G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128914112 | ||||||
| chr3:128914231
|
A | G | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.3280+888T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128914231 | ||||||
| chr3:128914296
|
A | C | 7 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(4): Show | 7 | HG00423.hp2 HG00558.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.3280+823T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128914296 | ||||||
| chr3:128914537
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3280+582A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128914537 | ||||||
| chr3:128914627
|
CAG | C | 3 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0294 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3280+490_3280+491d others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128914627 | ||||||
| chr3:128914664
|
C | T | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.3280+455G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128914664 | ||||||
| chr3:128914919
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3280+200C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128914919 | ||||||
| chr3:128914965
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(194): Show |
intron_variant | MODIFIER | c.3280+154A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 15/15 | chr3 | 128914965 | ||||||
| chr3:128915319
|
T | G | 2 | a0001c0003t0001g0188a0001c0003t0001g0189 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3123+38A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 14/15 | chr3 | 128915319 | ||||||
| chr3:128915730
|
T | C | 22 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(19): Show | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2917-167A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/15 | chr3 | 128915730 | ||||||
| chr3:128915743
|
G | A | 1 | a0001c0021t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2917-180C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/15 | chr3 | 128915743 | ||||||
| chr3:128915804
|
G | A | 3 | a0004c0010t0001g0329a0004c0010t0001g0330a0004c0030t0001g0328 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2917-241C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/15 | chr3 | 128915804 | ||||||
| chr3:128915830
|
A | G | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2917-267T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/15 | chr3 | 128915830 | ||||||
| chr3:128915930
|
G | A | 22 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(19): Show | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2916+177C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/15 | chr3 | 128915930 | ||||||
| chr3:128916083
|
C | T | 66 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0044others(63): Show | 67 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.2916+24G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/15 | chr3 | 128916083 | ||||||
| chr3:128916095
|
T | C | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2916+12A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 13/15 | chr3 | 128916095 | ||||||
| chr3:128916337
|
G | C | 2 | a0001c0002t0001g0177a0001c0002t0001g0178 | 2 | HG01515.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.2752-66C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128916337 | ||||||
| chr3:128916555
|
A | C | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2752-284T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128916555 | ||||||
| chr3:128916616
|
CA | C | 7 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2752-346delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128916616 | ||||||
| chr3:128916618
|
A | G | 22 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(19): Show | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2752-347T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128916618 | ||||||
| chr3:128916619
|
C | G | 7 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2752-348G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128916619 | ||||||
| chr3:128916720
|
G | A | 4 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0294others(1): Show | 4 | HG02451.hp1 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2752-449C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128916720 | ||||||
| chr3:128916895
|
G | A | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151 | 3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2752-624C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128916895 | ||||||
| chr3:128917105
|
A | G | 2 | a0004c0010t0001g0329a0004c0030t0001g0328 | 2 | HG00642.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.2752-834T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128917105 | ||||||
| chr3:128917156
|
G | T | 1 | a0001c0001t0001g0113 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2752-885C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128917156 | ||||||
| chr3:128917262
|
G | A | 6 | a0001c0001t0001g0071a0001c0001t0001g0222a0001c0001t0001g0225others(3): Show | 6 | HG02040.hp2 HG02293.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.2752-991C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128917262 | ||||||
| chr3:128917444
|
G | A | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2752-1173C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128917444 | ||||||
| chr3:128917757
|
G | A | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2752-1486C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128917757 | ||||||
| chr3:128917791
|
C | A | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2752-1520G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128917791 | ||||||
| chr3:128917872
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.2752-1601T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128917872 | ||||||
| chr3:128917934
|
GAC | G | 7 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(4): Show | 7 | HG01123.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2752-1665_2752-166 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128917934 | ||||||
| chr3:128918118
|
A | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(110): Show | 115 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.2752-1847T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918118 | ||||||
| chr3:128918182
|
T | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.2752-1911A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918182 | ||||||
| chr3:128918212
|
G | A | 1 | a0012c0018t0002g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2752-1941C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918212 | ||||||
| chr3:128918262
|
A | T | 1 | a0001c0002t0001g0167 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2752-1991T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918262 | ||||||
| chr3:128918467
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2752-2196G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918467 | ||||||
| chr3:128918489
|
A | C | 1 | a0001c0001t0001g0265 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2752-2218T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918489 | ||||||
| chr3:128918564
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2752-2293G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918564 | ||||||
| chr3:128918793
|
T | C | 2 | a0001c0002t0001g0164a0021c0011t0001g0047 | 2 | NA19007.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2752-2522A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918793 | ||||||
| chr3:128918851
|
C | T | 1 | a0001c0021t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2752-2580G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918851 | ||||||
| chr3:128918940
|
A | AT | 15 | a0001c0001t0001g0032a0001c0001t0001g0078a0001c0001t0001g0100others(12): Show | 15 | HG00673.hp1 HG00735.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.2752-2670dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918940 | ||||||
| chr3:128918940
|
AT | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.2752-2670delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918940 | ||||||
| chr3:128918940
|
ATT | A | 11 | a0001c0001t0001g0027a0001c0001t0001g0219a0001c0001t0001g0226others(8): Show | 11 | HG00642.hp1 HG01071.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.2752-2671_2752-267 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918940 | ||||||
| chr3:128918940
|
ATTT | A | 34 | a0001c0001t0001g0036a0001c0001t0001g0186a0001c0001t0001g0283others(31): Show | 35 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2752-2672_2752-267 others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918940 | ||||||
| chr3:128918940
|
ATTTTTTT | A | 21 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(18): Show | 22 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.2752-2676_2752-267 others(11): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918940 | ||||||
| chr3:128918972
|
A | C | 1 | a0012c0018t0002g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2752-2701T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918972 | ||||||
| chr3:128918972
|
A | T | 6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2752-2701T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128918972 | ||||||
| chr3:128919009
|
G | A | 8 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(5): Show | 8 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2752-2738C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128919009 | ||||||
| chr3:128919040
|
C | T | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2752-2769G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128919040 | ||||||
| chr3:128919221
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2752-2950C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128919221 | ||||||
| chr3:128919224
|
G | T | 1 | a0001c0002t0001g0172 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2752-2953C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128919224 | ||||||
| chr3:128919247
|
A | AT | 7 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2752-2977dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128919247 | ||||||
| chr3:128919748
|
C | G | 1 | a0001c0001t0001g0012 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2752-3477G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128919748 | ||||||
| chr3:128919783
|
A | G | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2752-3512T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128919783 | ||||||
| chr3:128919926
|
C | G | 11 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(8): Show | 12 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2752-3655G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128919926 | ||||||
| chr3:128919958
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2752-3687G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128919958 | ||||||
| chr3:128919987
|
C | G | 22 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(19): Show | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2752-3716G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128919987 | ||||||
| chr3:128920116
|
A | G | 45 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0007others(42): Show | 48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2752-3845T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128920116 | ||||||
| chr3:128920229
|
C | A | 22 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(19): Show | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2752-3958G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128920229 | ||||||
| chr3:128920262
|
G | C | 33 | a0001c0001t0001g0186a0001c0001t0001g0331a0001c0001t0003g0144others(30): Show | 34 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2752-3991C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128920262 | ||||||
| chr3:128920488
|
A | G | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2752-4217T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128920488 | ||||||
| chr3:128920768
|
C | T | 7 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2752-4497G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128920768 | ||||||
| chr3:128920901
|
C | A | 1 | a0001c0001t0001g0221 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2752-4630G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128920901 | ||||||
| chr3:128920984
|
T | C | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2752-4713A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128920984 | ||||||
| chr3:128921005
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2752-4734T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921005 | ||||||
| chr3:128921068
|
G | A | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2752-4797C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921068 | ||||||
| chr3:128921209
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2752-4938T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921209 | ||||||
| chr3:128921264
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG01257.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.2752-4993G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921264 | ||||||
| chr3:128921287
|
C | T | 3 | a0004c0010t0001g0329a0004c0010t0001g0330a0004c0030t0001g0328 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2752-5016G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921287 | ||||||
| chr3:128921331
|
C | A | 1 | a0004c0010t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2752-5060G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921331 | ||||||
| chr3:128921396
|
C | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(155): Show | 161 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.2752-5125G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921396 | ||||||
| chr3:128921402
|
A | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0216a0001c0001t0001g0253 | 3 | HG01496.hp2 HG01884.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.2752-5131T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921402 | ||||||
| chr3:128921434
|
A | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(114): Show | 119 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.2752-5163T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921434 | ||||||
| chr3:128921541
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2752-5270T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921541 | ||||||
| chr3:128921751
|
C | A | 2 | a0001c0002t0001g0166a0001c0002t0001g0167 | 2 | HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2752-5480G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921751 | ||||||
| chr3:128921770
|
C | T | 1 | a0001c0001t0001g0293 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2752-5499G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128921770 | ||||||
| chr3:128922065
|
C | T | 1 | a0001c0003t0001g0128 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2752-5794G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922065 | ||||||
| chr3:128922136
|
G | C | 1 | a0001c0021t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2752-5865C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922136 | ||||||
| chr3:128922144
|
T | C | 304 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(301): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.2752-5873A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922144 | ||||||
| chr3:128922166
|
C | T | 3 | a0002c0004t0002g0300a0002c0004t0002g0301a0002c0004t0002g0303 | 3 | HG02056.hp2 NA18985.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.2752-5895G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922166 | ||||||
| chr3:128922183
|
C | A | 4 | a0001c0003t0001g0128a0001c0003t0001g0277a0001c0003t0001g0278others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.2752-5912G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922183 | ||||||
| chr3:128922183
|
CA | C | 31 | a0001c0023t0005g0333a0001c0024t0005g0332a0002c0004t0002g0008others(28): Show | 32 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.2752-5913delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922183 | ||||||
| chr3:128922212
|
G | A | 1 | a0014c0020t0001g0270 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2752-5941C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922212 | ||||||
| chr3:128922342
|
C | CA | 6 | a0001c0001t0001g0186a0001c0001t0001g0331a0001c0003t0001g0013others(3): Show | 6 | HG01069.hp1 HG01261.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2752-6072dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922342 | ||||||
| chr3:128922342
|
CA | C | 33 | a0001c0001t0001g0036a0001c0001t0001g0283a0001c0001t0001g0284others(30): Show | 34 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(31): Show |
intron_variant | MODIFIER | c.2752-6072delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922342 | ||||||
| chr3:128922357
|
T | C | 7 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2752-6086A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922357 | ||||||
| chr3:128922437
|
A | G | 17 | a0001c0002t0001g0130a0001c0002t0001g0154a0001c0002t0001g0158others(14): Show | 17 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.2752-6166T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922437 | ||||||
| chr3:128922499
|
G | A | 11 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(8): Show | 12 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2752-6228C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922499 | ||||||
| chr3:128922511
|
G | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0283a0001c0001t0001g0284others(1): Show | 4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2752-6240C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922511 | ||||||
| chr3:128922621
|
A | G | 4 | a0001c0001t0001g0036a0001c0001t0001g0283a0001c0001t0001g0284others(1): Show | 4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2752-6350T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922621 | ||||||
| chr3:128922666
|
C | T | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2752-6395G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128922666 | ||||||
| chr3:128923076
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2752-6805C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128923076 | ||||||
| chr3:128923108
|
G | A | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2752-6837C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128923108 | ||||||
| chr3:128923135
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2752-6864C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128923135 | ||||||
| chr3:128923152
|
CAGG | C | 41 | a0001c0001t0001g0036a0001c0001t0001g0186a0001c0001t0001g0283others(38): Show | 42 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.2752-6884_2752-688 others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128923152 | ||||||
| chr3:128923205
|
A | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(196): Show | 203 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.2752-6934T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128923205 | ||||||
| chr3:128923233
|
G | C | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2752-6962C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128923233 | ||||||
| chr3:128923303
|
T | C | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2752-7032A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128923303 | ||||||
| chr3:128923619
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2752-7348G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128923619 | ||||||
| chr3:128923868
|
T | C | 1 | a0001c0005t0001g0211 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2752-7597A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128923868 | ||||||
| chr3:128924038
|
G | A | 22 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(19): Show | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2752-7767C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924038 | ||||||
| chr3:128924093
|
C | T | 22 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0068others(19): Show | 24 | HG00323.hp1 HG00423.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.2752-7822G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924093 | ||||||
| chr3:128924207
|
G | C | 7 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2752-7936C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924207 | ||||||
| chr3:128924263
|
G | C | 1 | a0001c0001t0007g0066 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2752-7992C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924263 | ||||||
| chr3:128924301
|
G | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(114): Show | 119 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.2752-8030C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924301 | ||||||
| chr3:128924312
|
C | T | 45 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0007others(42): Show | 48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2752-8041G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924312 | ||||||
| chr3:128924432
|
C | CT | 22 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0078others(19): Show | 22 | HG00280.hp2 HG02055.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2752-8162dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924432 | ||||||
| chr3:128924432
|
C | CTT | 37 | a0001c0001t0001g0050a0001c0002t0001g0002a0001c0002t0001g0006others(34): Show | 40 | HG00323.hp1 HG00423.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2752-8163_2752-816 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924432 | ||||||
| chr3:128924432
|
C | CTTT | 9 | a0001c0002t0001g0164a0001c0002t0001g0165a0001c0002t0001g0169others(6): Show | 9 | HG00642.hp1 HG00735.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.2752-8164_2752-816 others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924432 | ||||||
| chr3:128924432
|
CT | C | 16 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0083others(13): Show | 16 | HG00280.hp1 HG01169.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.2752-8162delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924432 | ||||||
| chr3:128924432
|
CTTTT | C | 6 | a0001c0001t0001g0036a0001c0001t0001g0283a0001c0001t0001g0284others(3): Show | 6 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2752-8165_2752-816 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924432 | ||||||
| chr3:128924432
|
CTTTTT | C | 24 | a0001c0001t0001g0238a0001c0001t0001g0252a0001c0001t0001g0255others(21): Show | 25 | HG01928.hp1 HG01981.hp1 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.2752-8166_2752-816 others(9): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924432 | ||||||
| chr3:128924432
|
CTTTTTT | C | 65 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0022others(62): Show | 66 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.2752-8167_2752-816 others(10): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924432 | ||||||
| chr3:128924432
|
CTTTTTTT | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(45): Show | 49 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.2752-8168_2752-816 others(11): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924432 | ||||||
| chr3:128924466
|
CAG | C | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2752-8197_2752-819 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924466 | ||||||
| chr3:128924474
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(119): Show | 124 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.2752-8203G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924474 | ||||||
| chr3:128924505
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0283a0001c0001t0001g0284others(1): Show | 4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2751+8195G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924505 | ||||||
| chr3:128924531
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(186): Show | 193 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.2751+8169T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924531 | ||||||
| chr3:128924532
|
T | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(186): Show | 193 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.2751+8168A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924532 | ||||||
| chr3:128924618
|
A | ATTT | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(152): Show | 158 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.2751+8079_2751+808 others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924618 | ||||||
| chr3:128924710
|
G | A | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2751+7990C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924710 | ||||||
| chr3:128924727
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG01257.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.2751+7973C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924727 | ||||||
| chr3:128924893
|
C | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(107): Show | 112 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.2751+7807G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924893 | ||||||
| chr3:128924900
|
C | G | 1 | a0001c0001t0001g0219 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2751+7800G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924900 | ||||||
| chr3:128924923
|
G | GT | 7 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2751+7776dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924923 | ||||||
| chr3:128924969
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(186): Show | 193 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.2751+7731G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924969 | ||||||
| chr3:128924974
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0216 | 2 | HG01496.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.2751+7726G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128924974 | ||||||
| chr3:128925064
|
T | A | 1 | a0001c0001t0001g0101 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2751+7636A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128925064 | ||||||
| chr3:128925172
|
T | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(186): Show | 193 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.2751+7528A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128925172 | ||||||
| chr3:128925204
|
T | C | 1 | a0001c0024t0005g0332 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2751+7496A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128925204 | ||||||
| chr3:128925524
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0021 | 2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2751+7176G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128925524 | ||||||
| chr3:128925615
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(116): Show | 121 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.2751+7085T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128925615 | ||||||
| chr3:128925752
|
A | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(114): Show | 119 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.2751+6948T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128925752 | ||||||
| chr3:128925769
|
G | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0283a0001c0001t0001g0284others(1): Show | 4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2751+6931C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128925769 | ||||||
| chr3:128925973
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(186): Show | 193 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.2751+6727G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128925973 | ||||||
| chr3:128925997
|
T | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(186): Show | 193 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.2751+6703A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128925997 | ||||||
| chr3:128926077
|
G | A | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2751+6623C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926077 | ||||||
| chr3:128926113
|
G | A | 3 | a0004c0010t0001g0329a0004c0010t0001g0330a0004c0030t0001g0328 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2751+6587C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926113 | ||||||
| chr3:128926180
|
G | C | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | NA19076.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.2751+6520C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926180 | ||||||
| chr3:128926196
|
G | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(185): Show | 192 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.2751+6504C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926196 | ||||||
| chr3:128926206
|
C | G | 22 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(19): Show | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2751+6494G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926206 | ||||||
| chr3:128926246
|
CGCCTGTA | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(186): Show | 193 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.2751+6447_2751+645 others(11): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926246 | ||||||
| chr3:128926369
|
C | G | 1 | a0001c0001t0001g0113 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2751+6331G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926369 | ||||||
| chr3:128926478
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2751+6222C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926478 | ||||||
| chr3:128926586
|
G | C | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2751+6114C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926586 | ||||||
| chr3:128926756
|
C | T | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2751+5944G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926756 | ||||||
| chr3:128926867
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2751+5833C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926867 | ||||||
| chr3:128926891
|
T | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(185): Show | 192 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.2751+5809A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926891 | ||||||
| chr3:128926944
|
A | G | 3 | a0001c0003t0001g0128a0001c0003t0001g0277a0001c0003t0001g0278 | 3 | HG01070.hp2 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.2751+5756T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926944 | ||||||
| chr3:128926990
|
A | G | 1 | a0002c0004t0002g0008 | 2 | NA18950.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2751+5710T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128926990 | ||||||
| chr3:128927066
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2751+5634G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927066 | ||||||
| chr3:128927104
|
A | G | 4 | a0001c0001t0001g0036a0001c0001t0001g0283a0001c0001t0001g0284others(1): Show | 4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2751+5596T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927104 | ||||||
| chr3:128927125
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0283a0001c0001t0001g0284others(1): Show | 4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2751+5575G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927125 | ||||||
| chr3:128927201
|
G | C | 1 | a0001c0003t0001g0188 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2751+5499C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927201 | ||||||
| chr3:128927282
|
T | C | 1 | a0001c0002t0001g0107 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2751+5418A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927282 | ||||||
| chr3:128927321
|
A | AAAGG | 233 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(230): Show | 240 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.2751+5375_2751+537 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927321 | ||||||
| chr3:128927446
|
C | T | 1 | a0002c0004t0002g0320 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2751+5254G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927446 | ||||||
| chr3:128927449
|
G | A | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2751+5251C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927449 | ||||||
| chr3:128927515
|
A | G | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2751+5185T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927515 | ||||||
| chr3:128927640
|
C | T | 45 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0007others(42): Show | 48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2751+5060G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927640 | ||||||
| chr3:128927723
|
C | CA | 88 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(85): Show | 91 | HG00099.hp1 HG00140.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.2751+4976dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927723 | ||||||
| chr3:128927723
|
C | CAA | 17 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0005t0001g0150others(14): Show | 17 | HG00639.hp2 HG01257.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2751+4975_2751+497 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927723 | ||||||
| chr3:128927723
|
CA | C | 9 | a0001c0001t0001g0060a0001c0002t0001g0130a0001c0002t0001g0154others(6): Show | 9 | HG01167.hp2 HG01346.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2751+4976delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927723 | ||||||
| chr3:128927748
|
T | C | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2751+4952A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927748 | ||||||
| chr3:128927904
|
T | C | 1 | a0001c0001t0001g0268 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2751+4796A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128927904 | ||||||
| chr3:128928109
|
C | T | 1 | a0001c0005t0001g0208 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2751+4591G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928109 | ||||||
| chr3:128928122
|
G | A | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2751+4578C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928122 | ||||||
| chr3:128928170
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0201 | 2 | HG00438.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.2751+4530C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928170 | ||||||
| chr3:128928208
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0112 | 2 | NA18969.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.2751+4492C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928208 | ||||||
| chr3:128928247
|
C | T | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2751+4453G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928247 | ||||||
| chr3:128928270
|
A | T | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151 | 3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2751+4430T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928270 | ||||||
| chr3:128928298
|
T | C | 40 | a0001c0001t0001g0036a0001c0001t0001g0186a0001c0001t0001g0283others(37): Show | 41 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.2751+4402A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928298 | ||||||
| chr3:128928518
|
G | C | 22 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(19): Show | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2751+4182C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928518 | ||||||
| chr3:128928636
|
C | A | 1 | a0001c0001t0001g0062 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2751+4064G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928636 | ||||||
| chr3:128928779
|
CAT | C | 26 | a0001c0001t0001g0186a0001c0001t0001g0331a0001c0003t0001g0004others(23): Show | 27 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.2751+3919_2751+392 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928779 | ||||||
| chr3:128928979
|
C | T | 3 | a0004c0010t0001g0329a0004c0010t0001g0330a0004c0030t0001g0328 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2751+3721G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928979 | ||||||
| chr3:128928980
|
A | G | 40 | a0001c0001t0001g0036a0001c0001t0001g0186a0001c0001t0001g0283others(37): Show | 41 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.2751+3720T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128928980 | ||||||
| chr3:128929274
|
T | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(154): Show | 160 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.2751+3426A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128929274 | ||||||
| chr3:128929349
|
G | A | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2751+3351C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128929349 | ||||||
| chr3:128929474
|
A | G | 10 | a0001c0003t0001g0128a0001c0003t0001g0277a0001c0003t0001g0278others(7): Show | 10 | HG00642.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.2751+3226T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128929474 | ||||||
| chr3:128929477
|
G | A | 1 | a0002c0004t0002g0008 | 2 | NA18950.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2751+3223C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128929477 | ||||||
| chr3:128929581
|
T | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(230): Show | 240 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.2751+3119A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128929581 | ||||||
| chr3:128929592
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2751+3108T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128929592 | ||||||
| chr3:128929603
|
C | T | 32 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(29): Show | 33 | HG01255.hp2 HG02040.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.2751+3097G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128929603 | ||||||
| chr3:128929604
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2751+3096C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128929604 | ||||||
| chr3:128929759
|
G | A | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2751+2941C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128929759 | ||||||
| chr3:128929984
|
T | C | 7 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2751+2716A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128929984 | ||||||
| chr3:128930182
|
G | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0283a0001c0001t0001g0284others(1): Show | 4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2751+2518C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930182 | ||||||
| chr3:128930238
|
C | T | 40 | a0001c0001t0001g0036a0001c0001t0001g0186a0001c0001t0001g0283others(37): Show | 41 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.2751+2462G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930238 | ||||||
| chr3:128930307
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2751+2393G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930307 | ||||||
| chr3:128930486
|
C | T | 7 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2751+2214G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930486 | ||||||
| chr3:128930522
|
A | AGGTG | 188 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(185): Show | 192 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.2751+2174_2751+217 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930522 | ||||||
| chr3:128930676
|
G | A | 33 | a0001c0001t0001g0186a0001c0001t0001g0331a0001c0001t0003g0144others(30): Show | 34 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2751+2024C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930676 | ||||||
| chr3:128930696
|
A | T | 70 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0044others(67): Show | 71 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.2751+2004T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930696 | ||||||
| chr3:128930719
|
C | T | 45 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0007others(42): Show | 48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2751+1981G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930719 | ||||||
| chr3:128930743
|
T | C | 4 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(1): Show | 4 | HG01167.hp1 HG01175.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2751+1957A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930743 | ||||||
| chr3:128930803
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2751+1897A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930803 | ||||||
| chr3:128930910
|
G | C | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2751+1790C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128930910 | ||||||
| chr3:128931036
|
G | A | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151 | 3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2751+1664C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931036 | ||||||
| chr3:128931059
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2751+1641G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931059 | ||||||
| chr3:128931107
|
G | C | 7 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2751+1593C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931107 | ||||||
| chr3:128931125
|
G | A | 45 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0007others(42): Show | 48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2751+1575C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931125 | ||||||
| chr3:128931200
|
G | A | 4 | a0001c0001t0001g0247a0001c0001t0001g0252a0001c0001t0001g0256others(1): Show | 4 | HG01255.hp1 HG01433.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.2751+1500C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931200 | ||||||
| chr3:128931336
|
C | T | 7 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2751+1364G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931336 | ||||||
| chr3:128931356
|
C | T | 2 | a0001c0001t0001g0275a0010c0022t0001g0276 | 2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2751+1344G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931356 | ||||||
| chr3:128931412
|
C | T | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2751+1288G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931412 | ||||||
| chr3:128931417
|
C | T | 3 | a0004c0010t0001g0329a0004c0010t0001g0330a0004c0030t0001g0328 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2751+1283G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931417 | ||||||
| chr3:128931432
|
G | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(185): Show | 192 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.2751+1268C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931432 | ||||||
| chr3:128931441
|
A | ATATATAT others(27): Show |
1 | a0001c0002t0001g0157 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2751+1225_2751+125 others(38): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931441 | ||||||
| chr3:128931453
|
G | GTA | 40 | a0001c0001t0001g0036a0001c0001t0001g0186a0001c0001t0001g0283others(37): Show | 41 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.2751+1245_2751+124 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931453 | ||||||
| chr3:128931455
|
A | G | 23 | a0001c0021t0001g0198a0002c0004t0002g0008a0002c0004t0002g0081others(20): Show | 24 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.2751+1245T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931455 | ||||||
| chr3:128931472
|
C | CATATATA others(3): Show |
157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(154): Show | 160 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.2751+1227_2751+122 others(14): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931472 | ||||||
| chr3:128931472
|
C | CATATATA others(13): Show |
29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2751+1227_2751+122 others(24): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931472 | ||||||
| chr3:128931479
|
A | G | 2 | a0001c0003t0004g0273a0001c0003t0004g0274 | 2 | HG00642.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.2751+1221T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931479 | ||||||
| chr3:128931509
|
A | G | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2751+1191T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931509 | ||||||
| chr3:128931513
|
ATATG | A | 6 | a0001c0002t0001g0002a0001c0002t0001g0152a0001c0002t0001g0155others(3): Show | 7 | HG00423.hp1 HG01081.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.2751+1183_2751+118 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931513 | ||||||
| chr3:128931519
|
ATGTATG | A | 37 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0068others(34): Show | 39 | HG00323.hp1 HG00735.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.2751+1175_2751+118 others(10): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931519 | ||||||
| chr3:128931523
|
A | G | 1 | a0001c0002t0001g0161 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2751+1177T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931523 | ||||||
| chr3:128931523
|
ATG | A | 26 | a0001c0001t0001g0186a0001c0001t0001g0331a0001c0003t0001g0004others(23): Show | 27 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.2751+1175_2751+117 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931523 | ||||||
| chr3:128931525
|
G | A | 1 | a0001c0002t0001g0161 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2751+1175C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931525 | ||||||
| chr3:128931527
|
G | A | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2751+1173C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931527 | ||||||
| chr3:128931527
|
G | GTA | 81 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0046others(78): Show | 83 | HG00423.hp2 HG00558.hp2 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.2751+1171_2751+117 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931527 | ||||||
| chr3:128931527
|
GTA | G | 8 | a0001c0001t0001g0036a0001c0001t0001g0137a0001c0001t0001g0283others(5): Show | 8 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.2751+1171_2751+117 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931527 | ||||||
| chr3:128931529
|
A | G | 39 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0068others(36): Show | 41 | HG00323.hp1 HG00642.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.2751+1171T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931529 | ||||||
| chr3:128931531
|
A | G | 1 | a0001c0002t0001g0157 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2751+1169T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931531 | ||||||
| chr3:128931590
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2751+1110A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931590 | ||||||
| chr3:128931857
|
T | TA | 23 | a0001c0003t0001g0193a0002c0004t0002g0008a0002c0004t0002g0081others(20): Show | 24 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.2751+842dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931857 | ||||||
| chr3:128931868
|
T | TA | 6 | a0001c0001t0001g0036a0001c0001t0001g0093a0001c0001t0001g0131others(3): Show | 6 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2751+831dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128931868 | ||||||
| chr3:128932097
|
T | C | 30 | a0001c0001t0003g0144a0002c0004t0002g0008a0002c0004t0002g0081others(27): Show | 31 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(28): Show |
intron_variant | MODIFIER | c.2751+603A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932097 | ||||||
| chr3:128932156
|
A | C | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2751+544T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932156 | ||||||
| chr3:128932332
|
T | C | 4 | a0002c0004t0002g0317a0002c0004t0002g0318a0002c0004t0002g0319others(1): Show | 4 | HG02922.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2751+368A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932332 | ||||||
| chr3:128932342
|
A | T | 9 | a0001c0005t0001g0150a0001c0005t0001g0206a0001c0005t0001g0207others(6): Show | 9 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2751+358T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932342 | ||||||
| chr3:128932352
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2751+348A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932352 | ||||||
| chr3:128932352
|
T | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(154): Show | 160 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.2751+348A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932352 | ||||||
| chr3:128932378
|
T | TAC | 145 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(142): Show | 148 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.2751+320_2751+321d others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932378 | ||||||
| chr3:128932378
|
T | TACAC | 12 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0218others(9): Show | 12 | HG00639.hp1 HG01069.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.2751+318_2751+321d others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932378 | ||||||
| chr3:128932378
|
T | TACACACA others(3): Show |
6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02572.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2751+312_2751+321d others(12): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932378 | ||||||
| chr3:128932378
|
T | TACACACA others(13): Show |
2 | a0002c0004t0002g0081a0002c0004t0002g0311 | 2 | HG02040.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2751+321_2751+322i others(22): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932378 | ||||||
| chr3:128932378
|
T | TACACACA others(17): Show |
9 | a0002c0004t0002g0008a0002c0004t0002g0298a0002c0004t0002g0300others(6): Show | 10 | HG02056.hp2 HG03491.hp1 HG03927.hp2 others(7): Show |
intron_variant | MODIFIER | c.2751+321_2751+322i others(26): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932378 | ||||||
| chr3:128932378
|
T | TACACACA others(19): Show |
2 | a0002c0004t0002g0312a0002c0004t0002g0316 | 2 | HG04204.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2751+321_2751+322i others(28): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932378 | ||||||
| chr3:128932378
|
T | TACACACA others(21): Show |
4 | a0002c0004t0002g0297a0002c0004t0002g0313a0002c0004t0002g0317others(1): Show | 4 | HG02683.hp1 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2751+321_2751+322i others(30): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932378 | ||||||
| chr3:128932378
|
T | TACACACA others(23): Show |
3 | a0002c0004t0002g0321a0002c0004t0002g0323a0002c0004t0002g0324 | 3 | HG02055.hp2 HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2751+321_2751+322i others(32): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932378 | ||||||
| chr3:128932378
|
T | TACACACA others(27): Show |
1 | a0002c0004t0002g0314 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2751+321_2751+322i others(36): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932378 | ||||||
| chr3:128932396
|
CAT | C | 45 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0007others(42): Show | 48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2751+302_2751+303d others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932396 | ||||||
| chr3:128932397
|
A | ACACACAC others(19): Show |
1 | a0002c0004t0002g0320 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2751+302_2751+303i others(28): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932397 | ||||||
| chr3:128932398
|
T | C | 20 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(17): Show | 21 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.2751+302A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932398 | ||||||
| chr3:128932681
|
G | C | 7 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(4): Show | 7 | HG01123.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2751+19C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932681 | ||||||
| chr3:128932693
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(108): Show |
splice_region_variant&intron_variant | LOW | c.2751+7C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 12/15 | chr3 | 128932693 | ||||||
| chr3:128933038
|
T | A | 5 | a0001c0001t0001g0186a0001c0001t0001g0331a0001c0003t0001g0013others(2): Show | 5 | HG01069.hp1 HG01109.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.2454-41A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128933038 | ||||||
| chr3:128933071
|
G | A | 22 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(19): Show | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2454-74C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128933071 | ||||||
| chr3:128933398
|
A | G | 8 | a0001c0002t0001g0171a0003c0006t0002g0180a0003c0006t0002g0181others(5): Show | 8 | HG01346.hp2 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2454-401T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128933398 | ||||||
| chr3:128933441
|
C | T | 13 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(10): Show | 13 | HG00558.hp1 HG02135.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.2454-444G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128933441 | ||||||
| chr3:128933562
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2454-565C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128933562 | ||||||
| chr3:128933579
|
A | G | 33 | a0001c0001t0001g0186a0001c0001t0001g0331a0001c0001t0003g0144others(30): Show | 34 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2454-582T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128933579 | ||||||
| chr3:128933710
|
C | T | 37 | a0001c0001t0001g0036a0001c0001t0001g0186a0001c0001t0001g0283others(34): Show | 38 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.2454-713G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128933710 | ||||||
| chr3:128933793
|
C | T | 1 | a0001c0003t0001g0282 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2454-796G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128933793 | ||||||
| chr3:128933933
|
C | CTAG | 22 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(19): Show | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2454-939_2454-937d others(5): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128933933 | ||||||
| chr3:128933951
|
G | A | 2 | a0001c0002t0001g0006a0001c0002t0001g0295 | 3 | HG01081.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2454-954C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128933951 | ||||||
| chr3:128934134
|
GTTCT | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(155): Show | 161 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.2453+987_2453+990d others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128934134 | ||||||
| chr3:128934142
|
T | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(155): Show | 161 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.2453+983A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128934142 | ||||||
| chr3:128934296
|
T | C | 33 | a0001c0001t0001g0186a0001c0001t0001g0331a0001c0001t0003g0144others(30): Show | 34 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2453+829A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128934296 | ||||||
| chr3:128934466
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2453+659C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128934466 | ||||||
| chr3:128934481
|
A | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.2453+644T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128934481 | ||||||
| chr3:128934786
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2453+339G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128934786 | ||||||
| chr3:128934961
|
G | A | 2 | a0001c0003t0001g0190a0001c0003t0001g0193 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2453+164C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128934961 | ||||||
| chr3:128935011
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2453+114C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128935011 | ||||||
| chr3:128935072
|
G | C | 1 | a0001c0001t0001g0039 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2453+53C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128935072 | ||||||
| chr3:128935107
|
C | G | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2453+18G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128935107 | ||||||
| chr3:128935109
|
A | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(185): Show | 192 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.2453+16T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 11/15 | chr3 | 128935109 | ||||||
| chr3:128935335
|
G | A | 1 | a0014c0020t0001g0270 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2259-16C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128935335 | ||||||
| chr3:128935471
|
G | C | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2259-152C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128935471 | ||||||
| chr3:128935572
|
C | T | 1 | a0001c0003t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2259-253G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128935572 | ||||||
| chr3:128935684
|
C | A | 22 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(19): Show | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2259-365G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128935684 | ||||||
| chr3:128935793
|
C | T | 33 | a0001c0001t0001g0036a0001c0001t0001g0283a0001c0001t0001g0284others(30): Show | 34 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(31): Show |
intron_variant | MODIFIER | c.2259-474G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128935793 | ||||||
| chr3:128936304
|
G | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0283a0001c0001t0001g0284others(1): Show | 4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2259-985C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128936304 | ||||||
| chr3:128936464
|
T | C | 31 | a0001c0023t0005g0333a0001c0024t0005g0332a0002c0004t0002g0008others(28): Show | 32 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.2259-1145A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128936464 | ||||||
| chr3:128936498
|
CAG | C | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2259-1181_2259-118 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128936498 | ||||||
| chr3:128936511
|
C | T | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2259-1192G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128936511 | ||||||
| chr3:128936513
|
G | A | 26 | a0001c0001t0001g0186a0001c0001t0001g0331a0001c0003t0001g0004others(23): Show | 27 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.2259-1194C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128936513 | ||||||
| chr3:128936657
|
C | T | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2259-1338G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128936657 | ||||||
| chr3:128936704
|
A | C | 33 | a0001c0001t0001g0186a0001c0001t0001g0331a0001c0001t0003g0144others(30): Show | 34 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2259-1385T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128936704 | ||||||
| chr3:128936800
|
T | A | 1 | a0001c0001t0001g0076 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2259-1481A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128936800 | ||||||
| chr3:128936922
|
C | T | 45 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0007others(42): Show | 48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2259-1603G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128936922 | ||||||
| chr3:128936927
|
C | A | 7 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2259-1608G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128936927 | ||||||
| chr3:128937053
|
C | T | 1 | a0001c0003t0001g0189 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2259-1734G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937053 | ||||||
| chr3:128937250
|
CT | C | 22 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(19): Show | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2259-1932delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937250 | ||||||
| chr3:128937258
|
G | A | 4 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 4 | NA18941.hp1 NA18968.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.2259-1939C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937258 | ||||||
| chr3:128937303
|
A | G | 1 | a0012c0018t0002g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2259-1984T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937303 | ||||||
| chr3:128937312
|
C | CA | 30 | a0001c0001t0001g0036a0001c0001t0001g0067a0001c0001t0001g0076others(27): Show | 31 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.2259-1994dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937312 | ||||||
| chr3:128937312
|
CA | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(98): Show | 103 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.2259-1994delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937312 | ||||||
| chr3:128937332
|
A | AAC | 9 | a0002c0004t0002g0303a0002c0004t0002g0314a0002c0004t0002g0317others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2259-2014_2259-201 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937332 | ||||||
| chr3:128937332
|
A | AC | 18 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(15): Show | 19 | HG02040.hp1 HG02056.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.2259-2014dupG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937332 | ||||||
| chr3:128937332
|
A | C | 1 | a0007c0028t0002g0185 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2259-2013T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937332 | ||||||
| chr3:128937341
|
A | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(185): Show | 192 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.2259-2022T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937341 | ||||||
| chr3:128937379
|
G | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(151): Show | 157 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.2259-2060C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937379 | ||||||
| chr3:128937383
|
T | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(146): Show | 152 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.2259-2064A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937383 | ||||||
| chr3:128937461
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2259-2142C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937461 | ||||||
| chr3:128937513
|
T | C | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151 | 3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2259-2194A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937513 | ||||||
| chr3:128937542
|
G | A | 1 | a0010c0022t0001g0276 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2259-2223C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937542 | ||||||
| chr3:128937604
|
CA | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(184): Show | 191 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.2259-2286delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937604 | ||||||
| chr3:128937838
|
G | C | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2259-2519C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937838 | ||||||
| chr3:128937861
|
G | A | 22 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(19): Show | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2259-2542C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937861 | ||||||
| chr3:128937938
|
C | T | 45 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0007others(42): Show | 48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2259-2619G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128937938 | ||||||
| chr3:128938072
|
G | GA | 232 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(229): Show | 239 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.2259-2754dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938072 | ||||||
| chr3:128938160
|
G | A | 6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2259-2841C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938160 | ||||||
| chr3:128938161
|
G | T | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2259-2842C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938161 | ||||||
| chr3:128938179
|
T | C | 2 | a0001c0001t0001g0222a0001c0001t0001g0271 | 2 | HG02293.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.2259-2860A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938179 | ||||||
| chr3:128938186
|
C | G | 1 | a0001c0001t0001g0060 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2259-2867G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938186 | ||||||
| chr3:128938236
|
AAAAG | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0283a0001c0001t0001g0284others(1): Show | 4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2259-2921_2259-291 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938236 | ||||||
| chr3:128938263
|
C | A | 22 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0068others(19): Show | 24 | HG00323.hp1 HG00423.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.2259-2944G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938263 | ||||||
| chr3:128938269
|
A | G | 33 | a0001c0001t0001g0186a0001c0001t0001g0331a0001c0001t0003g0144others(30): Show | 34 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2259-2950T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938269 | ||||||
| chr3:128938463
|
C | T | 7 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(4): Show | 7 | HG01123.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2259-3144G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938463 | ||||||
| chr3:128938491
|
CT | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(209): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.2259-3173delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938491 | ||||||
| chr3:128938516
|
T | C | 3 | a0004c0010t0001g0329a0004c0010t0001g0330a0004c0030t0001g0328 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2259-3197A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938516 | ||||||
| chr3:128938533
|
T | G | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2259-3214A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938533 | ||||||
| chr3:128938629
|
G | A | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG02056.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.2259-3310C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938629 | ||||||
| chr3:128938650
|
C | G | 4 | a0001c0001t0001g0036a0001c0001t0001g0283a0001c0001t0001g0284others(1): Show | 4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2259-3331G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938650 | ||||||
| chr3:128938651
|
G | A | 1 | a0001c0021t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2259-3332C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938651 | ||||||
| chr3:128938652
|
C | T | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2259-3333G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938652 | ||||||
| chr3:128938709
|
G | T | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2259-3390C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938709 | ||||||
| chr3:128938734
|
C | T | 22 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(19): Show | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2259-3415G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128938734 | ||||||
| chr3:128939046
|
T | C | 1 | a0002c0004t0002g0313 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2259-3727A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939046 | ||||||
| chr3:128939134
|
T | C | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2259-3815A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939134 | ||||||
| chr3:128939208
|
G | A | 22 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(19): Show | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2259-3889C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939208 | ||||||
| chr3:128939264
|
G | A | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2259-3945C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939264 | ||||||
| chr3:128939287
|
C | T | 24 | a0001c0023t0005g0333a0001c0024t0005g0332a0002c0004t0002g0008others(21): Show | 25 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.2259-3968G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939287 | ||||||
| chr3:128939295
|
C | T | 1 | a0001c0023t0005g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2259-3976G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939295 | ||||||
| chr3:128939354
|
G | T | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2259-4035C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939354 | ||||||
| chr3:128939363
|
T | G | 7 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2259-4044A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939363 | ||||||
| chr3:128939418
|
G | A | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2259-4099C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939418 | ||||||
| chr3:128939420
|
G | A | 22 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(19): Show | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2259-4101C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939420 | ||||||
| chr3:128939541
|
CCAT | C | 3 | a0004c0010t0001g0329a0004c0010t0001g0330a0004c0030t0001g0328 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2259-4225_2259-422 others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939541 | ||||||
| chr3:128939543
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2259-4224T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939543 | ||||||
| chr3:128939649
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(113): Show | 118 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.2259-4330C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939649 | ||||||
| chr3:128939789
|
G | C | 1 | a0001c0001t0001g0140 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2259-4470C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939789 | ||||||
| chr3:128939839
|
A | G | 7 | a0002c0004t0002g0297a0002c0004t0002g0314a0002c0004t0002g0317others(4): Show | 7 | HG02055.hp2 HG02451.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.2259-4520T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939839 | ||||||
| chr3:128939849
|
C | T | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2259-4530G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939849 | ||||||
| chr3:128939872
|
A | G | 146 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(143): Show | 149 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.2259-4553T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939872 | ||||||
| chr3:128939892
|
C | T | 1 | a0015c0016t0001g0176 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2259-4573G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128939892 | ||||||
| chr3:128940119
|
A | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(234): Show | 244 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.2259-4800T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128940119 | ||||||
| chr3:128940217
|
G | C | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151 | 3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2258+4854C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128940217 | ||||||
| chr3:128940401
|
T | G | 46 | a0001c0001t0001g0036a0001c0001t0001g0115a0001c0001t0001g0116others(43): Show | 47 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.2258+4670A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128940401 | ||||||
| chr3:128940737
|
A | G | 22 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(19): Show | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2258+4334T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128940737 | ||||||
| chr3:128940905
|
A | G | 4 | a0001c0001t0001g0036a0001c0001t0001g0283a0001c0001t0001g0284others(1): Show | 4 | HG00639.hp1 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2258+4166T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128940905 | ||||||
| chr3:128940911
|
C | T | 7 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2258+4160G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128940911 | ||||||
| chr3:128941068
|
A | C | 12 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(9): Show | 13 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.2258+4003T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128941068 | ||||||
| chr3:128941209
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2258+3862C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128941209 | ||||||
| chr3:128941209
|
G | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(230): Show | 240 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.2258+3862C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128941209 | ||||||
| chr3:128941376
|
TTA | T | 33 | a0001c0001t0001g0186a0001c0001t0001g0331a0001c0001t0003g0144others(30): Show | 34 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2258+3693_2258+369 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128941376 | ||||||
| chr3:128941550
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0074 | 2 | NA18999.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.2258+3521G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128941550 | ||||||
| chr3:128941633
|
C | T | 9 | a0001c0005t0001g0150a0001c0005t0001g0206a0001c0005t0001g0207others(6): Show | 9 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2258+3438G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128941633 | ||||||
| chr3:128941714
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(114): Show | 119 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.2258+3357G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128941714 | ||||||
| chr3:128941719
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(114): Show | 119 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.2258+3352G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128941719 | ||||||
| chr3:128941939
|
T | C | 1 | a0001c0002t0001g0305 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2258+3132A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128941939 | ||||||
| chr3:128942009
|
A | G | 1 | a0001c0021t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2258+3062T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942009 | ||||||
| chr3:128942076
|
G | A | 7 | a0002c0004t0002g0297a0002c0004t0002g0314a0002c0004t0002g0317others(4): Show | 7 | HG02055.hp2 HG02451.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.2258+2995C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942076 | ||||||
| chr3:128942094
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(171): Show | 177 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.2258+2977T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942094 | ||||||
| chr3:128942139
|
A | G | 29 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(26): Show | 30 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.2258+2932T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942139 | ||||||
| chr3:128942143
|
A | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(230): Show | 240 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.2258+2928T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942143 | ||||||
| chr3:128942165
|
A | G | 9 | a0001c0005t0001g0150a0001c0005t0001g0206a0001c0005t0001g0207others(6): Show | 9 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2258+2906T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942165 | ||||||
| chr3:128942176
|
G | A | 22 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(19): Show | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2258+2895C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942176 | ||||||
| chr3:128942256
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2258+2815C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942256 | ||||||
| chr3:128942298
|
C | T | 1 | a0001c0002t0001g0162 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2258+2773G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942298 | ||||||
| chr3:128942356
|
G | A | 1 | a0001c0003t0001g0192 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2258+2715C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942356 | ||||||
| chr3:128942417
|
G | T | 42 | a0001c0001t0001g0036a0001c0001t0001g0186a0001c0001t0001g0283others(39): Show | 43 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.2258+2654C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942417 | ||||||
| chr3:128942442
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(1): Show | 4 | HG00099.hp1 HG00140.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.2258+2629G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942442 | ||||||
| chr3:128942677
|
A | G | 9 | a0001c0005t0001g0150a0001c0005t0001g0206a0001c0005t0001g0207others(6): Show | 9 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2258+2394T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942677 | ||||||
| chr3:128942679
|
C | CT | 114 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(111): Show | 116 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.2258+2391dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942679 | ||||||
| chr3:128942838
|
C | T | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2258+2233G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942838 | ||||||
| chr3:128942916
|
C | CT | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(105): Show | 110 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.2258+2154dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942916 | ||||||
| chr3:128942916
|
C | CTT | 11 | a0001c0001t0001g0009a0001c0001t0001g0232a0001c0001t0001g0235others(8): Show | 11 | HG00140.hp1 HG01243.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.2258+2153_2258+215 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942916 | ||||||
| chr3:128942916
|
CT | C | 50 | a0001c0001t0001g0064a0001c0001t0001g0094a0001c0001t0001g0134others(47): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.2258+2154delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942916 | ||||||
| chr3:128942916
|
CTTT | C | 21 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(18): Show | 22 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.2258+2152_2258+215 others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128942916 | ||||||
| chr3:128943078
|
GC | G | 26 | a0001c0001t0001g0186a0001c0001t0001g0331a0001c0003t0001g0004others(23): Show | 27 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.2258+1992delG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943078 | ||||||
| chr3:128943373
|
C | CCT | 64 | a0001c0001t0001g0036a0001c0001t0001g0186a0001c0001t0001g0283others(61): Show | 66 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.2258+1697_2258+169 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943373 | ||||||
| chr3:128943537
|
C | CT | 25 | a0001c0001t0001g0080a0001c0001t0001g0234a0001c0002t0001g0171others(22): Show | 26 | HG01346.hp2 HG02040.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.2258+1533dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943537 | ||||||
| chr3:128943557
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2258+1514G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943557 | ||||||
| chr3:128943598
|
C | T | 22 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(19): Show | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.2258+1473G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943598 | ||||||
| chr3:128943699
|
G | C | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2258+1372C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943699 | ||||||
| chr3:128943748
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(181): Show | 189 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.2258+1323T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943748 | ||||||
| chr3:128943914
|
T | TC | 38 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(35): Show | 40 | HG00423.hp1 HG00735.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.2258+1156dupG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943914 | ||||||
| chr3:128943914
|
T | TCC | 129 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(126): Show | 133 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.2258+1155_2258+115 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943914 | ||||||
| chr3:128943919
|
C | CCCCG | 22 | a0001c0001t0001g0036a0001c0003t0001g0013a0001c0003t0001g0189others(19): Show | 22 | HG00642.hp2 HG00733.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.2258+1151_2258+115 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943919 | ||||||
| chr3:128943919
|
C | CCCCGT | 13 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(10): Show | 14 | HG00639.hp1 HG00639.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2258+1151_2258+115 others(9): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943919 | ||||||
| chr3:128943920
|
G | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(174): Show | 183 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.2258+1151C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943920 | ||||||
| chr3:128943920
|
G | T | 49 | a0001c0001t0001g0036a0001c0001t0001g0283a0001c0001t0001g0284others(46): Show | 50 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.2258+1151C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943920 | ||||||
| chr3:128943921
|
T | C | 46 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(43): Show | 48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2258+1150A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943921 | ||||||
| chr3:128943921
|
T | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(128): Show | 135 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.2258+1150A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943921 | ||||||
| chr3:128943922
|
T | C | 7 | a0001c0002t0001g0158a0001c0002t0001g0159a0001c0002t0001g0160others(4): Show | 7 | HG00323.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2258+1149A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943922 | ||||||
| chr3:128943922
|
T | G | 39 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(36): Show | 41 | HG00423.hp1 HG00735.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.2258+1149A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943922 | ||||||
| chr3:128943923
|
T | G | 7 | a0001c0002t0001g0158a0001c0002t0001g0159a0001c0002t0001g0160others(4): Show | 7 | HG00323.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2258+1148A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943923 | ||||||
| chr3:128943931
|
T | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(111): Show | 117 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.2258+1140A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943931 | ||||||
| chr3:128943932
|
T | G | 1 | a0001c0001t0001g0259 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2258+1139A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128943932 | ||||||
| chr3:128944097
|
T | C | 43 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0068others(40): Show | 45 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.2258+974A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128944097 | ||||||
| chr3:128944180
|
AC | A | 3 | a0001c0003t0001g0128a0001c0003t0001g0277a0001c0003t0001g0278 | 3 | HG01070.hp2 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.2258+890delG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128944180 | ||||||
| chr3:128944316
|
T | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(93): Show | 98 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.2258+755A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128944316 | ||||||
| chr3:128944721
|
A | G | 7 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(4): Show | 7 | HG01123.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2258+350T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128944721 | ||||||
| chr3:128944758
|
G | A | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2258+313C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128944758 | ||||||
| chr3:128944875
|
G | A | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151 | 3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2258+196C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128944875 | ||||||
| chr3:128945018
|
C | A | 1 | a0015c0016t0001g0176 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2258+53G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 10/15 | chr3 | 128945018 | ||||||
| chr3:128945979
|
C | T | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | splice_region_variant&intron_variant | LOW | c.1354-4G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128945979 | ||||||
| chr3:128946042
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1354-67C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946042 | ||||||
| chr3:128946064
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1354-89G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946064 | ||||||
| chr3:128946170
|
G | A | 4 | a0004c0010t0001g0329a0004c0010t0001g0330a0004c0030t0001g0328others(1): Show | 4 | HG00642.hp1 HG01891.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354-195C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946170 | ||||||
| chr3:128946176
|
G | A | 6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-201C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946176 | ||||||
| chr3:128946177
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1354-202C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946177 | ||||||
| chr3:128946237
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1354-262T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946237 | ||||||
| chr3:128946261
|
A | G | 1 | a0001c0001t0001g0045 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1354-286T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946261 | ||||||
| chr3:128946326
|
AG | A | 10 | a0001c0001t0001g0036a0001c0001t0001g0275a0001c0001t0001g0283others(7): Show | 10 | HG00639.hp1 HG01243.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.1354-352delC | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946326 | ||||||
| chr3:128946446
|
C | A | 4 | a0004c0010t0001g0329a0004c0010t0001g0330a0004c0030t0001g0328others(1): Show | 4 | HG00642.hp1 HG01891.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354-471G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946446 | ||||||
| chr3:128946642
|
G | A | 1 | a0001c0002t0001g0006 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1354-667C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946642 | ||||||
| chr3:128946665
|
C | T | 45 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0007others(42): Show | 48 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.1354-690G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946665 | ||||||
| chr3:128946838
|
C | A | 4 | a0001c0002t0001g0152a0001c0002t0001g0161a0001c0002t0001g0162others(1): Show | 4 | HG00423.hp1 NA18960.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1354-863G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946838 | ||||||
| chr3:128946841
|
G | C | 22 | a0002c0004t0002g0008a0002c0004t0002g0081a0002c0004t0002g0297others(19): Show | 23 | HG02040.hp1 HG02055.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.1354-866C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946841 | ||||||
| chr3:128946947
|
T | A | 79 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(76): Show | 81 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1354-972A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128946947 | ||||||
| chr3:128947077
|
A | T | 4 | a0001c0002t0001g0299a0001c0002t0001g0304a0001c0002t0001g0305others(1): Show | 4 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354-1102T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947077 | ||||||
| chr3:128947186
|
T | G | 247 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(244): Show | 254 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.1354-1211A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947186 | ||||||
| chr3:128947230
|
G | GA | 6 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0141others(3): Show | 6 | HG00673.hp1 HG01243.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1354-1256dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947230 | ||||||
| chr3:128947230
|
G | GAA | 6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-1257_1354-125 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947230 | ||||||
| chr3:128947286
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(128): Show | 134 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1354-1311C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947286 | ||||||
| chr3:128947340
|
A | G | 1 | a0004c0010t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1354-1365T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947340 | ||||||
| chr3:128947342
|
A | T | 1 | a0004c0010t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1354-1367T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947342 | ||||||
| chr3:128947350
|
C | T | 2 | a0006c0007t0001g0014a0006c0007t0001g0015 | 2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1354-1375G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947350 | ||||||
| chr3:128947588
|
C | T | 1 | a0001c0019t0001g0069 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1354-1613G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947588 | ||||||
| chr3:128947643
|
C | T | 1 | a0012c0018t0002g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1354-1668G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947643 | ||||||
| chr3:128947678
|
A | C | 3 | a0001c0023t0005g0333a0001c0024t0005g0332a0017c0014t0001g0205 | 3 | HG02280.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1354-1703T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947678 | ||||||
| chr3:128947693
|
G | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(11): Show | 14 | HG00642.hp1 HG01255.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1354-1718C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947693 | ||||||
| chr3:128947842
|
GA | G | 6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-1868delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128947842 | ||||||
| chr3:128948037
|
C | T | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1354-2062G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948037 | ||||||
| chr3:128948298
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1354-2323C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948298 | ||||||
| chr3:128948377
|
C | CT | 98 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(95): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.1354-2403dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948377 | ||||||
| chr3:128948377
|
C | CTT | 17 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0046others(14): Show | 17 | HG00423.hp2 HG00438.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.1354-2404_1354-240 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948377 | ||||||
| chr3:128948377
|
CT | C | 98 | a0001c0001t0001g0003a0001c0001t0001g0050a0001c0001t0001g0051others(95): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.1354-2403delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948377 | ||||||
| chr3:128948377
|
CTTTTTTT others(4): Show |
C | 8 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(5): Show | 8 | HG02056.hp2 HG02976.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1354-2413_1354-240 others(15): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948377 | ||||||
| chr3:128948377
|
CTTTTTTT others(5): Show |
C | 61 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(58): Show | 64 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.1354-2414_1354-240 others(16): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948377 | ||||||
| chr3:128948377
|
CTTTTTTT others(12): Show |
C | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-2421_1354-240 others(23): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948377 | ||||||
| chr3:128948406
|
T | G | 1 | a0001c0001t0001g0103 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1354-2431A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948406 | ||||||
| chr3:128948411
|
A | G | 12 | a0001c0001t0001g0279a0001c0002t0001g0006a0001c0002t0001g0295others(9): Show | 13 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-2436T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948411 | ||||||
| chr3:128948513
|
C | T | 1 | a0001c0002t0001g0174 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1354-2538G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948513 | ||||||
| chr3:128948528
|
A | AT | 12 | a0001c0001t0001g0080a0001c0001t0001g0201a0001c0001t0001g0224others(9): Show | 13 | HG00423.hp1 HG01081.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-2554dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948528 | ||||||
| chr3:128948528
|
AT | A | 29 | a0001c0001t0003g0214a0001c0003t0001g0004a0001c0003t0001g0013others(26): Show | 30 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1354-2554delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948528 | ||||||
| chr3:128948711
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0129 | 2 | NA18970.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1354-2736C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948711 | ||||||
| chr3:128948759
|
A | G | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-2784T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948759 | ||||||
| chr3:128948769
|
A | T | 1 | a0001c0003t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1354-2794T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948769 | ||||||
| chr3:128948820
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1354-2845C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948820 | ||||||
| chr3:128948875
|
G | A | 1 | a0012c0018t0002g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1354-2900C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948875 | ||||||
| chr3:128948904
|
A | C | 1 | a0001c0002t0001g0155 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1354-2929T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948904 | ||||||
| chr3:128948926
|
A | C | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG01175.hp2 HG01256.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1354-2951T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948926 | ||||||
| chr3:128948934
|
G | A | 6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-2959C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948934 | ||||||
| chr3:128948981
|
G | A | 1 | a0001c0001t0001g0039 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1354-3006C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128948981 | ||||||
| chr3:128949010
|
A | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(230): Show | 240 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1354-3035T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128949010 | ||||||
| chr3:128949133
|
C | T | 3 | a0004c0010t0001g0329a0004c0010t0001g0330a0004c0030t0001g0328 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1354-3158G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128949133 | ||||||
| chr3:128949164
|
G | C | 23 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0079others(20): Show | 23 | HG00323.hp2 HG00609.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.1354-3189C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128949164 | ||||||
| chr3:128949348
|
C | T | 2 | a0001c0002t0001g0177a0001c0002t0001g0178 | 2 | HG01515.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1354-3373G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128949348 | ||||||
| chr3:128949375
|
T | C | 15 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(12): Show | 16 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1354-3400A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128949375 | ||||||
| chr3:128949403
|
G | A | 3 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285 | 3 | HG00639.hp1 HG01516.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1354-3428C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128949403 | ||||||
| chr3:128949747
|
C | T | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(3): Show | 6 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-3772G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128949747 | ||||||
| chr3:128949833
|
C | T | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1354-3858G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128949833 | ||||||
| chr3:128949836
|
G | A | 1 | a0001c0003t0001g0013 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1354-3861C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128949836 | ||||||
| chr3:128949936
|
C | T | 15 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(12): Show | 16 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1354-3961G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128949936 | ||||||
| chr3:128950021
|
T | C | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(3): Show | 6 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-4046A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128950021 | ||||||
| chr3:128950068
|
T | A | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151 | 3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1354-4093A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128950068 | ||||||
| chr3:128950068
|
T | TA | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1354-4094dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128950068 | ||||||
| chr3:128950344
|
C | T | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1354-4369G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128950344 | ||||||
| chr3:128950421
|
C | A | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1354-4446G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128950421 | ||||||
| chr3:128950464
|
A | T | 1 | a0001c0003t0001g0191 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1354-4489T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128950464 | ||||||
| chr3:128950640
|
G | C | 6 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(3): Show | 6 | HG01123.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-4665C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128950640 | ||||||
| chr3:128950691
|
T | C | 80 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(77): Show | 83 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.1354-4716A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128950691 | ||||||
| chr3:128950809
|
C | T | 29 | a0001c0002t0001g0002a0001c0002t0001g0068a0001c0002t0001g0123others(26): Show | 30 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1354-4834G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128950809 | ||||||
| chr3:128950911
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1354-4936C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128950911 | ||||||
| chr3:128951007
|
C | A | 1 | a0008c0027t0001g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1354-5032G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951007 | ||||||
| chr3:128951020
|
C | T | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-5045G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951020 | ||||||
| chr3:128951125
|
T | C | 80 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(77): Show | 83 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.1354-5150A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951125 | ||||||
| chr3:128951236
|
GA | G | 45 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(42): Show | 47 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.1354-5262delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951236 | ||||||
| chr3:128951324
|
G | A | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1354-5349C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951324 | ||||||
| chr3:128951466
|
G | A | 12 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(9): Show | 12 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1354-5491C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951466 | ||||||
| chr3:128951603
|
A | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(229): Show | 239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1354-5628T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951603 | ||||||
| chr3:128951662
|
A | C | 1 | a0001c0003t0001g0013 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1354-5687T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951662 | ||||||
| chr3:128951734
|
A | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0089 | 2 | NA19002.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1354-5759T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951734 | ||||||
| chr3:128951747
|
C | T | 1 | a0001c0002t0001g0152 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1354-5772G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951747 | ||||||
| chr3:128951766
|
A | G | 12 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(9): Show | 12 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1354-5791T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951766 | ||||||
| chr3:128951878
|
G | T | 1 | a0001c0001t0001g0021 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1354-5903C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128951878 | ||||||
| chr3:128952121
|
TTTC | T | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151 | 3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1354-6149_1354-614 others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952121 | ||||||
| chr3:128952136
|
C | CT | 38 | a0001c0001t0001g0082a0001c0001t0001g0232a0001c0001t0001g0279others(35): Show | 39 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.1354-6162dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952136 | ||||||
| chr3:128952136
|
C | CTT | 5 | a0001c0002t0001g0006a0001c0002t0001g0295a0001c0003t0001g0277others(2): Show | 6 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-6163_1354-616 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952136 | ||||||
| chr3:128952136
|
CT | C | 9 | a0001c0001t0001g0040a0001c0001t0001g0072a0001c0001t0001g0129others(6): Show | 9 | HG01070.hp1 HG01074.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.1354-6162delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952136 | ||||||
| chr3:128952168
|
T | A | 1 | a0001c0001t0007g0066 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1354-6193A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952168 | ||||||
| chr3:128952175
|
G | A | 2 | a0001c0001t0003g0214a0017c0014t0001g0205 | 2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1354-6200C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952175 | ||||||
| chr3:128952180
|
G | T | 29 | a0001c0002t0001g0002a0001c0002t0001g0068a0001c0002t0001g0123others(26): Show | 30 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1354-6205C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952180 | ||||||
| chr3:128952298
|
T | TA | 232 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(229): Show | 239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1354-6324dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952298 | ||||||
| chr3:128952303
|
T | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(229): Show | 239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1354-6328A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952303 | ||||||
| chr3:128952527
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1354-6552A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952527 | ||||||
| chr3:128952572
|
A | G | 1 | a0001c0001t0001g0092 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1354-6597T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952572 | ||||||
| chr3:128952674
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1354-6699C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952674 | ||||||
| chr3:128952738
|
G | A | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1354-6763C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952738 | ||||||
| chr3:128952747
|
C | G | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1354-6772G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952747 | ||||||
| chr3:128952808
|
G | A | 1 | a0019c0013t0001g0049 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1354-6833C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952808 | ||||||
| chr3:128952814
|
G | A | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151 | 3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1354-6839C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952814 | ||||||
| chr3:128952815
|
G | A | 1 | a0002c0004t0002g0320 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1354-6840C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128952815 | ||||||
| chr3:128953079
|
A | C | 1 | a0001c0001t0001g0293 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1354-7104T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953079 | ||||||
| chr3:128953082
|
A | C | 1 | a0012c0018t0002g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1354-7107T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953082 | ||||||
| chr3:128953184
|
G | T | 1 | a0001c0001t0001g0238 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1354-7209C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953184 | ||||||
| chr3:128953303
|
CAGG | C | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1354-7331_1354-732 others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953303 | ||||||
| chr3:128953331
|
C | T | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1354-7356G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953331 | ||||||
| chr3:128953332
|
G | A | 12 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(9): Show | 12 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1354-7357C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953332 | ||||||
| chr3:128953387
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(118): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1354-7412G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953387 | ||||||
| chr3:128953420
|
G | C | 12 | a0001c0003t0001g0013a0001c0005t0001g0150a0001c0005t0001g0206others(9): Show | 12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1354-7445C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953420 | ||||||
| chr3:128953470
|
A | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(227): Show | 237 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1354-7495T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953470 | ||||||
| chr3:128953496
|
C | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(229): Show | 239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1354-7521G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953496 | ||||||
| chr3:128953524
|
AAAAG | A | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(3): Show | 6 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-7553_1354-755 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953524 | ||||||
| chr3:128953526
|
AAGAAAGA others(2701): Show |
A | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1353+9277_1354-755 others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953526 | ||||||
| chr3:128953567
|
G | GTCTCCC | 15 | a0001c0001t0001g0163a0001c0001t0001g0255a0001c0001t0001g0283others(12): Show | 15 | HG00639.hp1 HG00733.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1354-7598_1354-759 others(10): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953567 | ||||||
| chr3:128953567
|
G | GTCTCCCT others(5): Show |
1 | a0001c0001t0001g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1354-7604_1354-759 others(16): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953567 | ||||||
| chr3:128953576
|
TCCCTCTC others(17): Show |
T | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-7625_1354-760 others(28): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953576 | ||||||
| chr3:128953594
|
T | C | 17 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(14): Show | 17 | HG00639.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1354-7619A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953594 | ||||||
| chr3:128953594
|
T | TCCCTCTC others(5): Show |
1 | a0001c0003t0001g0013 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1354-7620_1354-761 others(16): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953594 | ||||||
| chr3:128953600
|
C | T | 10 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(7): Show | 10 | HG01255.hp2 HG02258.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1354-7625G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953600 | ||||||
| chr3:128953600
|
CCCCTCTC others(5): Show |
C | 1 | a0001c0001t0001g0086 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1354-7637_1354-762 others(16): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953600 | ||||||
| chr3:128953600
|
CCCCTCTC others(11): Show |
C | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-7643_1354-762 others(22): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953600 | ||||||
| chr3:128953604
|
TCTCCCTC others(9): Show |
T | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18999.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1354-7645_1354-763 others(20): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953604 | ||||||
| chr3:128953606
|
T | C | 23 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(20): Show | 23 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1354-7631A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953606 | ||||||
| chr3:128953609
|
C | G | 2 | a0001c0009t0001g0210a0001c0009t0001g0213 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1354-7634G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953609 | ||||||
| chr3:128953609
|
CTCTCCCT others(15): Show |
C | 1 | a0001c0001t0001g0052 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1354-7656_1354-763 others(26): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953609 | ||||||
| chr3:128953610
|
TCTCCCTC others(3): Show |
T | 2 | a0001c0009t0001g0210a0001c0009t0001g0213 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1354-7645_1354-763 others(14): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953610 | ||||||
| chr3:128953612
|
T | C | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1354-7637A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953612 | ||||||
| chr3:128953615
|
C | CTCCCTCT others(3): Show |
6 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(3): Show | 6 | HG01123.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-7641_1354-764 others(14): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953615 | ||||||
| chr3:128953615
|
C | G | 1 | a0006c0007t0001g0015 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1354-7640G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953615 | ||||||
| chr3:128953615
|
CTCTCCCT others(9): Show |
C | 1 | a0001c0002t0001g0295 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1354-7656_1354-764 others(20): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953615 | ||||||
| chr3:128953618
|
T | C | 4 | a0001c0001t0003g0214a0004c0010t0001g0329a0004c0010t0001g0330others(1): Show | 4 | HG00642.hp1 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1354-7643A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953618 | ||||||
| chr3:128953620
|
C | CGT | 13 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(10): Show | 13 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-7646_1354-764 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953620 | ||||||
| chr3:128953620
|
C | T | 6 | a0001c0001t0003g0214a0001c0023t0005g0333a0001c0024t0005g0332others(3): Show | 6 | HG00642.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-7645G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953620 | ||||||
| chr3:128953624
|
CCTCTCCG others(9): Show |
C | 1 | a0001c0001t0001g0245 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1354-7665_1354-765 others(20): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953624 | ||||||
| chr3:128953625
|
C | CCCTCTCC others(17): Show |
6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-7651_1354-765 others(28): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953625 | ||||||
| chr3:128953625
|
C | CTCTCCG | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(3): Show | 6 | HG01255.hp2 HG01891.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-7656_1354-765 others(10): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953625 | ||||||
| chr3:128953625
|
C | G | 24 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(21): Show | 24 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.1354-7650G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953625 | ||||||
| chr3:128953631
|
G | C | 2 | a0001c0002t0001g0177a0001c0002t0001g0178 | 2 | HG01515.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1354-7656C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953631 | ||||||
| chr3:128953740
|
C | A | 18 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(15): Show | 18 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1354-7765G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953740 | ||||||
| chr3:128953743
|
GTGCCTGC others(4): Show |
G | 6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-7779_1354-776 others(15): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953743 | ||||||
| chr3:128953768
|
A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(165): Show | 172 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1354-7793T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953768 | ||||||
| chr3:128953790
|
G | A | 1 | a0001c0002t0001g0165 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1354-7815C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953790 | ||||||
| chr3:128953798
|
G | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1354-7823C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953798 | ||||||
| chr3:128953816
|
G | A | 6 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(3): Show | 6 | HG00639.hp1 HG01516.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1354-7841C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953816 | ||||||
| chr3:128953818
|
GC | G | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(3): Show | 6 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-7844delG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953818 | ||||||
| chr3:128953840
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1354-7865G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953840 | ||||||
| chr3:128953854
|
C | A | 47 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(44): Show | 48 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.1354-7879G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953854 | ||||||
| chr3:128953920
|
A | G | 2 | a0001c0002t0001g0130a0012c0018t0002g0143 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1354-7945T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953920 | ||||||
| chr3:128953974
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1354-7999C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128953974 | ||||||
| chr3:128954025
|
A | AC | 10 | a0001c0001t0001g0046a0001c0001t0001g0088a0001c0001t0001g0099others(7): Show | 10 | HG01123.hp1 HG01496.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.1354-8051dupG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954025 | ||||||
| chr3:128954061
|
C | T | 15 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(12): Show | 16 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1354-8086G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954061 | ||||||
| chr3:128954097
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18999.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1354-8122C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954097 | ||||||
| chr3:128954123
|
C | T | 1 | a0001c0002t0001g0171 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1354-8148G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954123 | ||||||
| chr3:128954137
|
C | T | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1354-8162G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954137 | ||||||
| chr3:128954164
|
G | A | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151 | 3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1354-8189C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954164 | ||||||
| chr3:128954178
|
G | A | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-8203C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954178 | ||||||
| chr3:128954242
|
C | T | 6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-8267G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954242 | ||||||
| chr3:128954289
|
C | T | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-8314G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954289 | ||||||
| chr3:128954319
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(118): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1354-8344G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954319 | ||||||
| chr3:128954486
|
C | G | 1 | a0012c0018t0002g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1354-8511G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954486 | ||||||
| chr3:128954486
|
C | T | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1354-8511G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954486 | ||||||
| chr3:128954498
|
T | A | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(3): Show | 6 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-8523A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954498 | ||||||
| chr3:128954498
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(190): Show | 198 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1354-8523A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954498 | ||||||
| chr3:128954502
|
C | G | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG02056.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1354-8527G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954502 | ||||||
| chr3:128954527
|
C | G | 4 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 4 | NA18941.hp1 NA18968.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354-8552G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954527 | ||||||
| chr3:128954527
|
C | T | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-8552G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954527 | ||||||
| chr3:128954537
|
G | A | 29 | a0001c0002t0001g0002a0001c0002t0001g0068a0001c0002t0001g0123others(26): Show | 30 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1354-8562C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954537 | ||||||
| chr3:128954544
|
C | T | 4 | a0001c0002t0001g0158a0001c0002t0001g0159a0001c0002t0001g0160others(1): Show | 4 | HG02109.hp2 HG02886.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354-8569G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954544 | ||||||
| chr3:128954565
|
G | C | 12 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(9): Show | 12 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1354-8590C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954565 | ||||||
| chr3:128954592
|
C | T | 35 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(32): Show | 36 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1354-8617G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954592 | ||||||
| chr3:128954602
|
G | A | 1 | a0001c0003t0001g0013 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1354-8627C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954602 | ||||||
| chr3:128954630
|
G | A | 26 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0072others(23): Show | 26 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1354-8655C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954630 | ||||||
| chr3:128954635
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1354-8660C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954635 | ||||||
| chr3:128954668
|
T | C | 18 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(15): Show | 18 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1354-8693A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954668 | ||||||
| chr3:128954720
|
G | A | 1 | a0001c0001t0001g0256 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1354-8745C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954720 | ||||||
| chr3:128954739
|
T | TGGGGGTG others(43): Show |
12 | a0001c0001t0001g0279a0001c0002t0001g0006a0001c0002t0001g0295others(9): Show | 13 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-8765_1354-876 others(54): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954739 | ||||||
| chr3:128954744
|
G | C | 2 | a0001c0001t0001g0202a0018c0029t0001g0095 | 2 | HG00738.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1354-8769C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954744 | ||||||
| chr3:128954745
|
G | A | 2 | a0001c0001t0001g0202a0018c0029t0001g0095 | 2 | HG00738.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1354-8770C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954745 | ||||||
| chr3:128954749
|
A | G | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8774T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954749 | ||||||
| chr3:128954751
|
CCCTCCGC others(168): Show |
C | 1 | a0001c0001t0001g0112 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1354-8951_1354-877 others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954751 | ||||||
| chr3:128954754
|
T | C | 27 | a0001c0001t0001g0202a0001c0001t0001g0279a0001c0002t0001g0006others(24): Show | 29 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.1354-8779A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954754 | ||||||
| chr3:128954756
|
C | CT | 12 | a0001c0001t0001g0279a0001c0002t0001g0006a0001c0002t0001g0295others(9): Show | 13 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-8782_1354-878 others(5): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954756 | ||||||
| chr3:128954770
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1354-8795G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954770 | ||||||
| chr3:128954777
|
T | C | 25 | a0001c0001t0001g0279a0001c0002t0001g0006a0001c0002t0001g0295others(22): Show | 27 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.1354-8802A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954777 | ||||||
| chr3:128954779
|
G | A | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1354-8804C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954779 | ||||||
| chr3:128954783
|
GT | G | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8809delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954783 | ||||||
| chr3:128954788
|
G | GTGGGGGT others(54): Show |
1 | a0001c0003t0001g0194 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1354-8814_1354-881 others(65): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954788 | ||||||
| chr3:128954788
|
G | GTGGGGGT others(53): Show |
12 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(9): Show | 13 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1354-8814_1354-881 others(64): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954788 | ||||||
| chr3:128954789
|
G | A | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8814C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954789 | ||||||
| chr3:128954792
|
G | C | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8817C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954792 | ||||||
| chr3:128954795
|
T | C | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8820A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954795 | ||||||
| chr3:128954802
|
G | GGCCA | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8828_1354-882 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954802 | ||||||
| chr3:128954806
|
G | A | 12 | a0001c0001t0001g0279a0001c0002t0001g0006a0001c0002t0001g0295others(9): Show | 13 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-8831C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954806 | ||||||
| chr3:128954811
|
T | G | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8836A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954811 | ||||||
| chr3:128954812
|
A | T | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8837T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954812 | ||||||
| chr3:128954814
|
T | C | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8839A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954814 | ||||||
| chr3:128954819
|
A | G | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8844T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954819 | ||||||
| chr3:128954821
|
A | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(57): Show | 63 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1354-8846T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954821 | ||||||
| chr3:128954826
|
A | G | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8851T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954826 | ||||||
| chr3:128954829
|
C | G | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8854G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954829 | ||||||
| chr3:128954834
|
TGCCCGGC others(42): Show |
T | 12 | a0001c0001t0001g0005a0001c0001t0001g0217a0001c0001t0001g0226others(9): Show | 13 | HG01070.hp1 HG01074.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.1354-8908_1354-886 others(53): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954834 | ||||||
| chr3:128954838
|
C | A | 1 | a0001c0005t0001g0208 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1354-8863G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954838 | ||||||
| chr3:128954839
|
G | A | 57 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0046others(54): Show | 57 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.1354-8864C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954839 | ||||||
| chr3:128954840
|
G | A | 20 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(17): Show | 20 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1354-8865C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954840 | ||||||
| chr3:128954844
|
G | C | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8869C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954844 | ||||||
| chr3:128954846
|
C | T | 2 | a0001c0001t0001g0202a0018c0029t0001g0095 | 2 | HG00738.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1354-8871G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954846 | ||||||
| chr3:128954848
|
CCCCGTCC others(41): Show |
C | 1 | a0001c0001t0001g0234 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1354-8921_1354-887 others(52): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954848 | ||||||
| chr3:128954851
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(40): Show | 44 | HG00099.hp1 HG00140.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1354-8876G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954851 | ||||||
| chr3:128954852
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1354-8877C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954852 | ||||||
| chr3:128954857
|
G | C | 60 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(57): Show | 63 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1354-8882C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954857 | ||||||
| chr3:128954872
|
G | T | 63 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0046others(60): Show | 63 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.1354-8897C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954872 | ||||||
| chr3:128954876
|
G | A | 60 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(57): Show | 63 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1354-8901C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954876 | ||||||
| chr3:128954878
|
CCCCCCGC others(41): Show |
C | 4 | a0001c0001t0001g0046a0001c0001t0001g0223a0001c0001t0001g0232others(1): Show | 4 | HG01496.hp2 HG02074.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354-8951_1354-890 others(52): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954878 | ||||||
| chr3:128954888
|
G | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0217a0001c0001t0001g0226others(8): Show | 12 | HG01070.hp1 HG01074.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1354-8913C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954888 | ||||||
| chr3:128954904
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0026others(1): Show | 5 | HG02080.hp1 HG03490.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.1354-8929G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954904 | ||||||
| chr3:128954915
|
T | TG | 11 | a0001c0001t0001g0088a0001c0001t0001g0279a0001c0002t0001g0006others(8): Show | 12 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.1354-8941dupC | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954915 | ||||||
| chr3:128954915
|
TGGGGGTG others(450): Show |
T | 33 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(30): Show | 34 | HG00099.hp1 HG00140.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1354-9397_1354-894 others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954915 | ||||||
| chr3:128954916
|
GGGGGTGT others(41): Show |
G | 64 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0216others(61): Show | 64 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1354-8989_1354-894 others(52): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954916 | ||||||
| chr3:128954916
|
GGGGGTGT others(269): Show |
G | 2 | a0001c0001t0001g0202a0018c0029t0001g0095 | 2 | HG00738.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1354-9217_1354-894 others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954916 | ||||||
| chr3:128954917
|
GGGGTGTC others(40): Show |
G | 2 | a0001c0001t0001g0237a0001c0001t0001g0286 | 2 | HG02895.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1354-8989_1354-894 others(51): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954917 | ||||||
| chr3:128954921
|
T | G | 25 | a0001c0001t0001g0279a0001c0002t0001g0006a0001c0002t0001g0295others(22): Show | 27 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.1354-8946A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954921 | ||||||
| chr3:128954923
|
T | G | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8948A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954923 | ||||||
| chr3:128954924
|
C | CCA | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8950_1354-894 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954924 | ||||||
| chr3:128954925
|
G | A | 12 | a0001c0001t0001g0279a0001c0002t0001g0006a0001c0002t0001g0295others(9): Show | 13 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-8950C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954925 | ||||||
| chr3:128954926
|
G | C | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8951C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954926 | ||||||
| chr3:128954932
|
C | CT | 12 | a0001c0001t0001g0279a0001c0002t0001g0006a0001c0002t0001g0295others(9): Show | 13 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-8958_1354-895 others(5): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954932 | ||||||
| chr3:128954932
|
C | T | 14 | a0001c0001t0001g0112a0001c0003t0001g0004a0001c0003t0001g0188others(11): Show | 15 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1354-8957G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954932 | ||||||
| chr3:128954935
|
C | A | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-8960G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954935 | ||||||
| chr3:128954964
|
T | TG | 80 | a0001c0001t0001g0005a0001c0001t0001g0046a0001c0001t0001g0112others(77): Show | 84 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1354-8990dupC | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954964 | ||||||
| chr3:128954969
|
C | G | 166 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0021others(163): Show | 170 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1354-8994G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954969 | ||||||
| chr3:128954970
|
G | A | 69 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0055others(66): Show | 70 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1354-8995C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954970 | ||||||
| chr3:128954995
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1354-9020C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128954995 | ||||||
| chr3:128955032
|
A | G | 27 | a0001c0001t0001g0112a0001c0001t0001g0279a0001c0001t0001g0294others(24): Show | 29 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.1354-9057T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955032 | ||||||
| chr3:128955033
|
CCCCTACT others(30): Show |
C | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-9095_1354-905 others(41): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955033 | ||||||
| chr3:128955072
|
C | T | 33 | a0001c0001t0001g0112a0001c0001t0001g0279a0001c0001t0001g0294others(30): Show | 35 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.1354-9097G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955072 | ||||||
| chr3:128955077
|
C | T | 1 | a0001c0002t0001g0164 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1354-9102G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955077 | ||||||
| chr3:128955083
|
C | G | 7 | a0001c0001t0001g0061a0001c0001t0001g0141a0001c0001t0001g0142others(4): Show | 7 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1354-9108G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955083 | ||||||
| chr3:128955106
|
C | T | 12 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(9): Show | 12 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1354-9131G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955106 | ||||||
| chr3:128955109
|
C | T | 12 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(9): Show | 12 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1354-9134G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955109 | ||||||
| chr3:128955109
|
CGCCCGGC others(44): Show |
C | 1 | a0001c0001t0001g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1354-9185_1354-913 others(55): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955109 | ||||||
| chr3:128955114
|
G | A | 12 | a0001c0001t0001g0279a0001c0002t0001g0006a0001c0002t0001g0295others(9): Show | 13 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-9139C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955114 | ||||||
| chr3:128955126
|
CG | C | 12 | a0001c0003t0001g0013a0001c0005t0001g0150a0001c0005t0001g0206others(9): Show | 12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1354-9152delC | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955126 | ||||||
| chr3:128955142
|
GGGGGGGG others(43): Show |
G | 24 | a0001c0001t0001g0112a0001c0001t0001g0279a0001c0002t0001g0006others(21): Show | 25 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.1354-9217_1354-916 others(54): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955142 | ||||||
| chr3:128955143
|
GGGGGGGT others(42): Show |
G | 7 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(4): Show | 8 | HG00642.hp2 HG01123.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1354-9217_1354-916 others(53): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955143 | ||||||
| chr3:128955144
|
GGGGGGTC others(41): Show |
G | 1 | a0001c0001t0003g0147 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1354-9217_1354-917 others(52): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955144 | ||||||
| chr3:128955150
|
T | C | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-9175A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955150 | ||||||
| chr3:128955160
|
T | TGCCCGGC others(120): Show |
12 | a0001c0001t0001g0061a0001c0003t0001g0013a0001c0005t0001g0150others(9): Show | 12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1354-9186_1354-918 others(131): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955160 | ||||||
| chr3:128955163
|
C | A | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-9188G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955163 | ||||||
| chr3:128955165
|
G | A | 3 | a0001c0001t0001g0294a0001c0023t0005g0333a0001c0024t0005g0332 | 3 | HG02280.hp2 HG02630.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-9190C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955165 | ||||||
| chr3:128955165
|
G | GGCCAGCC others(120): Show |
2 | a0001c0001t0001g0021a0014c0020t0001g0270 | 2 | HG02717.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1354-9191_1354-919 others(131): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955165 | ||||||
| chr3:128955178
|
G | GTCCGGGA others(120): Show |
1 | a0001c0005t0001g0209 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1354-9204_1354-920 others(131): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955178 | ||||||
| chr3:128955192
|
T | TG | 19 | a0001c0001t0001g0061a0001c0001t0001g0070a0001c0001t0001g0092others(16): Show | 19 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1354-9218dupC | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955192 | ||||||
| chr3:128955192
|
T | TGGGGGGG others(173): Show |
1 | a0001c0001t0001g0132 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1354-9218_1354-921 others(184): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955192 | ||||||
| chr3:128955194
|
G | C | 1 | a0001c0003t0004g0281 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1354-9219C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955194 | ||||||
| chr3:128955229
|
G | A | 1 | a0001c0003t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1354-9254C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955229 | ||||||
| chr3:128955246
|
C | T | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1354-9271G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955246 | ||||||
| chr3:128955275
|
G | T | 12 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(9): Show | 13 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1354-9300C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955275 | ||||||
| chr3:128955301
|
T | C | 57 | a0001c0001t0001g0021a0001c0001t0001g0061a0001c0001t0001g0094others(54): Show | 59 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1354-9326A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955301 | ||||||
| chr3:128955301
|
T | TGCCCCAT others(173): Show |
1 | a0001c0001t0001g0133 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1354-9327_1354-932 others(184): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955301 | ||||||
| chr3:128955301
|
T | TGCCCCGT others(172): Show |
6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-9327_1354-932 others(183): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955301 | ||||||
| chr3:128955306
|
C | T | 16 | a0001c0001t0001g0021a0001c0001t0001g0279a0001c0001t0001g0294others(13): Show | 17 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.1354-9331G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955306 | ||||||
| chr3:128955311
|
G | A | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(2): Show | 5 | HG00642.hp1 HG01255.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1354-9336C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955311 | ||||||
| chr3:128955312
|
CGAGGGAG others(222): Show |
C | 28 | a0001c0002t0001g0002a0001c0002t0001g0068a0001c0002t0001g0123others(25): Show | 29 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.1354-9566_1354-933 others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955312 | ||||||
| chr3:128955322
|
GGGGGGGT others(221): Show |
G | 1 | a0001c0002t0001g0172 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1354-9575_1354-934 others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955322 | ||||||
| chr3:128955332
|
GC | G | 131 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0021others(128): Show | 134 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.1354-9358delG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955332 | ||||||
| chr3:128955333
|
C | CCCCCCAC others(171): Show |
1 | a0001c0001t0001g0120 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1354-9359_1354-935 others(182): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955333 | ||||||
| chr3:128955333
|
C | CCCCCCGC others(171): Show |
7 | a0001c0001t0001g0275a0001c0001t0001g0283a0001c0001t0001g0284others(4): Show | 7 | HG00639.hp1 HG01243.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1354-9359_1354-935 others(182): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955333 | ||||||
| chr3:128955333
|
C | CCCCCCGC others(171): Show |
1 | a0001c0002t0001g0130 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1354-9359_1354-935 others(182): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955333 | ||||||
| chr3:128955333
|
C | CCCCCCGC others(173): Show |
2 | a0001c0001t0001g0186a0001c0003t0001g0128 | 2 | HG01175.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1354-9359_1354-935 others(184): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955333 | ||||||
| chr3:128955333
|
C | CCCCCCGC others(172): Show |
12 | a0001c0001t0001g0050a0001c0001t0001g0059a0001c0001t0001g0078others(9): Show | 12 | HG01255.hp2 HG01934.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1354-9359_1354-935 others(183): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955333 | ||||||
| chr3:128955333
|
C | CCCCCCGC others(171): Show |
1 | a0001c0001t0001g0116 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1354-9359_1354-935 others(182): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955333 | ||||||
| chr3:128955333
|
C | CCCCCCGC others(172): Show |
2 | a0001c0001t0001g0115a0001c0001t0001g0125 | 2 | HG01934.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1354-9359_1354-935 others(183): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955333 | ||||||
| chr3:128955333
|
C | CCCCCCGC others(171): Show |
80 | a0001c0001t0001g0003a0001c0001t0001g0051a0001c0001t0001g0052others(77): Show | 81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1354-9359_1354-935 others(182): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955333 | ||||||
| chr3:128955339
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG01255.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1354-9364G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955339 | ||||||
| chr3:128955340
|
G | A | 6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-9365C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955340 | ||||||
| chr3:128955344
|
G | A | 66 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0046others(63): Show | 67 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1354-9369C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955344 | ||||||
| chr3:128955346
|
C | T | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-9371G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955346 | ||||||
| chr3:128955371
|
TG | T | 165 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0050others(162): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1354-9397delC | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955371 | ||||||
| chr3:128955372
|
G | GGGGGGGG others(171): Show |
1 | a0001c0001t0001g0151 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1354-9398_1354-939 others(182): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955372 | ||||||
| chr3:128955409
|
G | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | NA19076.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1354-9434C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955409 | ||||||
| chr3:128955427
|
G | A | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1354-9452C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955427 | ||||||
| chr3:128955473
|
T | C | 67 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0046others(64): Show | 68 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1354-9498A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955473 | ||||||
| chr3:128955482
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(52): Show | 57 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.1354-9507C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955482 | ||||||
| chr3:128955486
|
C | T | 66 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0046others(63): Show | 67 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1354-9511G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955486 | ||||||
| chr3:128955487
|
G | A | 13 | a0001c0001t0003g0214a0001c0003t0001g0013a0001c0005t0001g0150others(10): Show | 13 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-9512C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955487 | ||||||
| chr3:128955492
|
G | C | 65 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0046others(62): Show | 66 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.1354-9517C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955492 | ||||||
| chr3:128955492
|
G | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0290 | 2 | HG02074.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1354-9517C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955492 | ||||||
| chr3:128955501
|
TG | T | 168 | a0001c0001t0001g0003a0001c0001t0001g0050a0001c0001t0001g0051others(165): Show | 171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.1354-9527delC | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955501 | ||||||
| chr3:128955501
|
TGGGGGGG others(43): Show |
T | 35 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 36 | HG00099.hp1 HG00140.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1354-9576_1354-952 others(54): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955501 | ||||||
| chr3:128955502
|
G | GGGGGGGT others(170): Show |
1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1354-9528_1354-952 others(181): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955502 | ||||||
| chr3:128955519
|
G | A | 1 | a0004c0010t0001g0329 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1354-9544C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955519 | ||||||
| chr3:128955520
|
A | C | 66 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0046others(63): Show | 67 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1354-9545T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955520 | ||||||
| chr3:128955530
|
C | T | 2 | a0004c0010t0001g0329a0004c0030t0001g0328 | 2 | HG00642.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1354-9555G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955530 | ||||||
| chr3:128955531
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1354-9556C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955531 | ||||||
| chr3:128955536
|
A | G | 66 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0046others(63): Show | 67 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1354-9561T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955536 | ||||||
| chr3:128955539
|
C | T | 12 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(9): Show | 12 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1354-9564G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955539 | ||||||
| chr3:128955540
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1354-9565C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955540 | ||||||
| chr3:128955550
|
TG | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0217a0001c0001t0001g0226others(7): Show | 11 | HG01070.hp1 HG01074.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.1354-9576delC | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955550 | ||||||
| chr3:128955551
|
G | GGGGGGGG others(121): Show |
1 | a0001c0001t0001g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1354-9577_1354-957 others(132): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955551 | ||||||
| chr3:128955551
|
G | GGGGGGGG others(121): Show |
53 | a0001c0001t0001g0046a0001c0001t0001g0216a0001c0001t0001g0218others(50): Show | 53 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.1354-9577_1354-957 others(132): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955551 | ||||||
| chr3:128955551
|
G | GGGGGGGT others(171): Show |
1 | a0001c0001t0001g0253 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1354-9577_1354-957 others(182): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955551 | ||||||
| chr3:128955551
|
G | T | 12 | a0001c0003t0001g0013a0001c0005t0001g0150a0001c0005t0001g0206others(9): Show | 12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1354-9576C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955551 | ||||||
| chr3:128955572
|
G | A | 4 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 4 | NA18941.hp1 NA18968.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354-9597C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955572 | ||||||
| chr3:128955580
|
G | A | 1 | a0001c0021t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1354-9605C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955580 | ||||||
| chr3:128955586
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1354-9611G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955586 | ||||||
| chr3:128955589
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1354-9614T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955589 | ||||||
| chr3:128955612
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1354-9637G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955612 | ||||||
| chr3:128955650
|
A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(165): Show | 172 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1354-9675T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955650 | ||||||
| chr3:128955673
|
G | T | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1354-9698C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955673 | ||||||
| chr3:128955696
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1354-9721C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955696 | ||||||
| chr3:128955727
|
T | C | 1 | a0001c0001t0006g0111 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1354-9752A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955727 | ||||||
| chr3:128955735
|
C | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0040 | 2 | HG01167.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.1354-9760G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955735 | ||||||
| chr3:128955913
|
C | T | 3 | a0001c0002t0001g0158a0001c0002t0001g0159a0001c0002t0001g0175 | 3 | HG02109.hp2 HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1353+9598G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955913 | ||||||
| chr3:128955979
|
T | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18999.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1353+9532A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955979 | ||||||
| chr3:128955990
|
A | C | 1 | a0001c0001t0006g0111 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1353+9521T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128955990 | ||||||
| chr3:128956080
|
T | C | 9 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(6): Show | 9 | HG01255.hp1 HG01433.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.1353+9431A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956080 | ||||||
| chr3:128956184
|
T | A | 1 | a0012c0018t0002g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1353+9327A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956184 | ||||||
| chr3:128956184
|
TA | T | 15 | a0001c0001t0001g0051a0001c0001t0001g0101a0001c0001t0001g0279others(12): Show | 16 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.1353+9326delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956184 | ||||||
| chr3:128956192
|
A | T | 16 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(13): Show | 16 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.1353+9319T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956192 | ||||||
| chr3:128956193
|
A | T | 4 | a0001c0003t0001g0004a0001c0003t0001g0191a0001c0003t0001g0192others(1): Show | 5 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1353+9318T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956193 | ||||||
| chr3:128956194
|
AAT | A | 28 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(25): Show | 29 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.1353+9315_1353+931 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956194 | ||||||
| chr3:128956196
|
T | A | 2 | a0001c0001t0003g0214a0017c0014t0001g0205 | 2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1353+9315A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956196 | ||||||
| chr3:128956196
|
TA | T | 29 | a0001c0002t0001g0002a0001c0002t0001g0068a0001c0002t0001g0123others(26): Show | 30 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1353+9314delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956196 | ||||||
| chr3:128956198
|
A | T | 2 | a0001c0001t0003g0214a0017c0014t0001g0205 | 2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1353+9313T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956198 | ||||||
| chr3:128956199
|
A | T | 12 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(9): Show | 13 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1353+9312T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956199 | ||||||
| chr3:128956200
|
A | T | 3 | a0001c0003t0001g0196a0001c0023t0005g0333a0001c0024t0005g0332 | 3 | HG02280.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1353+9311T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956200 | ||||||
| chr3:128956202
|
A | T | 16 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(13): Show | 16 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.1353+9309T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956202 | ||||||
| chr3:128956203
|
A | T | 12 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(9): Show | 13 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1353+9308T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956203 | ||||||
| chr3:128956204
|
A | T | 4 | a0001c0023t0005g0333a0001c0024t0005g0332a0006c0007t0001g0014others(1): Show | 4 | HG01109.hp2 HG02280.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1353+9307T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956204 | ||||||
| chr3:128956207
|
T | A | 25 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(22): Show | 25 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1353+9304A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956207 | ||||||
| chr3:128956211
|
A | T | 16 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(13): Show | 16 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.1353+9300T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956211 | ||||||
| chr3:128956213
|
A | T | 2 | a0006c0007t0001g0014a0006c0007t0001g0015 | 2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1353+9298T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956213 | ||||||
| chr3:128956215
|
T | A | 33 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(30): Show | 34 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1353+9296A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956215 | ||||||
| chr3:128956215
|
T | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(1): Show | 4 | HG00099.hp1 HG00140.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1353+9296A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956215 | ||||||
| chr3:128956215
|
TA | T | 6 | a0001c0001t0001g0056a0001c0001t0001g0223a0001c0002t0001g0002others(3): Show | 7 | HG01081.hp2 HG01192.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.1353+9295delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956215 | ||||||
| chr3:128956217
|
A | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | NA18965.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1353+9294T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956217 | ||||||
| chr3:128956220
|
A | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(1): Show | 4 | HG00099.hp1 HG00140.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1353+9291T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956220 | ||||||
| chr3:128956223
|
A | T | 11 | a0001c0001t0001g0045a0001c0002t0001g0154a0001c0002t0001g0158others(8): Show | 11 | HG01346.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1353+9288T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956223 | ||||||
| chr3:128956224
|
A | G | 33 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(30): Show | 34 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.1353+9287T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956224 | ||||||
| chr3:128956224
|
AAAAAGAA others(3): Show |
A | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(1): Show | 4 | HG00099.hp1 HG00140.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1353+9277_1353+928 others(14): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956224 | ||||||
| chr3:128956225
|
A | G | 2 | a0006c0007t0001g0014a0006c0007t0001g0015 | 2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1353+9286T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956225 | ||||||
| chr3:128956229
|
G | A | 2 | a0006c0007t0001g0014a0006c0007t0001g0015 | 2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1353+9282C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956229 | ||||||
| chr3:128956229
|
G | T | 33 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(30): Show | 34 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.1353+9282C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956229 | ||||||
| chr3:128956230
|
A | T | 2 | a0006c0007t0001g0014a0006c0007t0001g0015 | 2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1353+9281T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956230 | ||||||
| chr3:128956233
|
AT | A | 33 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(30): Show | 34 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.1353+9277delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956233 | ||||||
| chr3:128956234
|
T | A | 2 | a0006c0007t0001g0014a0006c0007t0001g0015 | 2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1353+9277A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956234 | ||||||
| chr3:128956234
|
T | TAAAA | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(155): Show | 162 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1353+9276_1353+927 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956234 | ||||||
| chr3:128956598
|
G | GA | 34 | a0001c0001t0001g0249a0001c0002t0001g0007a0001c0002t0001g0299others(31): Show | 36 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1353+8912dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956598 | ||||||
| chr3:128956746
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1353+8765C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956746 | ||||||
| chr3:128956837
|
A | G | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1353+8674T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956837 | ||||||
| chr3:128956929
|
A | G | 80 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(77): Show | 83 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.1353+8582T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956929 | ||||||
| chr3:128956977
|
C | CAAAA | 15 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(12): Show | 15 | HG00639.hp2 HG01167.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1353+8530_1353+853 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956977 | ||||||
| chr3:128956977
|
C | CAAAAA | 40 | a0001c0001t0003g0144a0001c0001t0003g0146a0001c0001t0003g0147others(37): Show | 42 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.1353+8529_1353+853 others(9): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956977 | ||||||
| chr3:128956977
|
C | CAAAAAA | 19 | a0001c0001t0003g0145a0001c0001t0003g0148a0001c0003t0001g0004others(16): Show | 20 | HG01123.hp2 HG02109.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1353+8528_1353+853 others(10): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956977 | ||||||
| chr3:128956994
|
A | AAAAAG | 6 | a0001c0001t0001g0042a0001c0001t0001g0228a0001c0001t0001g0250others(3): Show | 6 | HG01175.hp1 HG02056.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1353+8516_1353+851 others(9): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956994 | ||||||
| chr3:128956994
|
A | AAAAG | 210 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(207): Show | 214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1353+8513_1353+851 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956994 | ||||||
| chr3:128956994
|
A | AAAG | 22 | a0001c0001t0001g0036a0001c0001t0001g0073a0001c0001t0001g0080others(19): Show | 23 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.1353+8516_1353+851 others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956994 | ||||||
| chr3:128956994
|
A | G | 1 | a0001c0001t0001g0293 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1353+8517T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128956994 | ||||||
| chr3:128957037
|
G | C | 1 | a0001c0001t0001g0071 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1353+8474C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957037 | ||||||
| chr3:128957075
|
T | G | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1353+8436A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957075 | ||||||
| chr3:128957258
|
T | C | 20 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(17): Show | 20 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1353+8253A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957258 | ||||||
| chr3:128957352
|
AC | A | 15 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(12): Show | 16 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1353+8158delG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957352 | ||||||
| chr3:128957355
|
A | T | 15 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(12): Show | 16 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1353+8156T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957355 | ||||||
| chr3:128957423
|
T | C | 2 | a0001c0003t0004g0273a0001c0003t0004g0274 | 2 | HG00642.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1353+8088A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957423 | ||||||
| chr3:128957489
|
A | T | 6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1353+8022T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957489 | ||||||
| chr3:128957797
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1353+7714T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957797 | ||||||
| chr3:128957832
|
TG | T | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(235): Show | 246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1353+7678delC | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957832 | ||||||
| chr3:128957839
|
G | T | 36 | a0001c0001t0001g0003a0001c0001t0001g0153a0001c0001t0001g0163others(33): Show | 38 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.1353+7672C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957839 | ||||||
| chr3:128957915
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1353+7596G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128957915 | ||||||
| chr3:128958064
|
T | C | 5 | a0001c0001t0001g0217a0001c0001t0001g0226a0001c0001t0001g0259others(2): Show | 5 | HG01070.hp1 HG01074.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.1353+7447A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128958064 | ||||||
| chr3:128958255
|
A | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(225): Show | 236 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1353+7256T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128958255 | ||||||
| chr3:128958345
|
T | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(166): Show | 174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.1353+7166A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128958345 | ||||||
| chr3:128958669
|
G | A | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1353+6842C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128958669 | ||||||
| chr3:128958699
|
A | G | 1 | a0009c0026t0001g0296 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1353+6812T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128958699 | ||||||
| chr3:128958748
|
A | G | 9 | a0001c0005t0001g0150a0001c0005t0001g0206a0001c0005t0001g0207others(6): Show | 9 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1353+6763T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128958748 | ||||||
| chr3:128958770
|
G | A | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1353+6741C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128958770 | ||||||
| chr3:128958893
|
CCT | C | 34 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(31): Show | 36 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1353+6616_1353+661 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128958893 | ||||||
| chr3:128958998
|
G | A | 4 | a0001c0003t0001g0004a0001c0003t0001g0191a0001c0003t0001g0192others(1): Show | 5 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1353+6513C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128958998 | ||||||
| chr3:128959124
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1353+6387G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128959124 | ||||||
| chr3:128959128
|
T | G | 3 | a0004c0010t0001g0329a0004c0010t0001g0330a0004c0030t0001g0328 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1353+6383A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128959128 | ||||||
| chr3:128959456
|
A | G | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1353+6055T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128959456 | ||||||
| chr3:128959495
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0114 | 3 | HG02735.hp1 HG04204.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1353+6016T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128959495 | ||||||
| chr3:128959614
|
G | A | 6 | a0001c0002t0001g0006a0001c0002t0001g0295a0001c0003t0001g0277others(3): Show | 7 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1353+5897C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128959614 | ||||||
| chr3:128959628
|
G | T | 61 | a0001c0001t0001g0003a0001c0001t0001g0141a0001c0001t0001g0142others(58): Show | 64 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1353+5883C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128959628 | ||||||
| chr3:128959753
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG00099.hp1 HG00140.hp1 |
intron_variant | MODIFIER | c.1353+5758G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128959753 | ||||||
| chr3:128959834
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1353+5677G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128959834 | ||||||
| chr3:128959902
|
T | C | 20 | a0001c0001t0001g0275a0001c0001t0001g0279a0001c0001t0001g0283others(17): Show | 21 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.1353+5609A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128959902 | ||||||
| chr3:128960144
|
C | T | 34 | a0001c0001t0001g0120a0001c0002t0001g0007a0001c0002t0001g0299others(31): Show | 36 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1353+5367G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128960144 | ||||||
| chr3:128960160
|
G | A | 18 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(15): Show | 18 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1353+5351C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128960160 | ||||||
| chr3:128960193
|
C | T | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1353+5318G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128960193 | ||||||
| chr3:128960406
|
G | C | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1353+5105C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128960406 | ||||||
| chr3:128960439
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(118): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1353+5072T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128960439 | ||||||
| chr3:128960763
|
G | A | 18 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(15): Show | 18 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1353+4748C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128960763 | ||||||
| chr3:128960772
|
C | T | 18 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(15): Show | 18 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1353+4739G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128960772 | ||||||
| chr3:128960851
|
G | A | 2 | a0001c0001t0001g0217a0001c0001t0001g0260 | 2 | HG01070.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1353+4660C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128960851 | ||||||
| chr3:128960876
|
T | C | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1353+4635A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128960876 | ||||||
| chr3:128960890
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1353+4621G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128960890 | ||||||
| chr3:128961036
|
CAAG | C | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1353+4472_1353+447 others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961036 | ||||||
| chr3:128961284
|
A | C | 8 | a0001c0003t0001g0188a0001c0003t0001g0189a0001c0003t0001g0190others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1353+4227T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961284 | ||||||
| chr3:128961312
|
TC | T | 3 | a0004c0010t0001g0329a0004c0010t0001g0330a0004c0030t0001g0328 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1353+4198delG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961312 | ||||||
| chr3:128961410
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1353+4101C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961410 | ||||||
| chr3:128961415
|
A | G | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1353+4096T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961415 | ||||||
| chr3:128961478
|
T | G | 1 | a0001c0002t0001g0162 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1353+4033A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961478 | ||||||
| chr3:128961499
|
GT | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(227): Show | 237 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1353+4011delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961499 | ||||||
| chr3:128961789
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1353+3722G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961789 | ||||||
| chr3:128961793
|
C | T | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1353+3718G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961793 | ||||||
| chr3:128961807
|
A | G | 12 | a0001c0001t0001g0279a0001c0002t0001g0006a0001c0002t0001g0295others(9): Show | 13 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1353+3704T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961807 | ||||||
| chr3:128961924
|
G | A | 3 | a0004c0010t0001g0329a0004c0010t0001g0330a0004c0030t0001g0328 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1353+3587C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961924 | ||||||
| chr3:128961928
|
G | A | 3 | a0004c0010t0001g0329a0004c0010t0001g0330a0004c0030t0001g0328 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1353+3583C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961928 | ||||||
| chr3:128961932
|
C | A | 3 | a0004c0010t0001g0329a0004c0010t0001g0330a0004c0030t0001g0328 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1353+3579G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961932 | ||||||
| chr3:128961959
|
C | A | 1 | a0001c0002t0001g0130 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1353+3552G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961959 | ||||||
| chr3:128961962
|
C | T | 1 | a0001c0002t0001g0130 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1353+3549G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961962 | ||||||
| chr3:128961986
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1353+3525C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128961986 | ||||||
| chr3:128962002
|
C | T | 1 | a0001c0003t0001g0282 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1353+3509G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962002 | ||||||
| chr3:128962019
|
C | T | 2 | a0002c0004t0002g0298a0002c0004t0002g0310 | 2 | HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1353+3492G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962019 | ||||||
| chr3:128962039
|
A | G | 1 | a0003c0006t0002g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1353+3472T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962039 | ||||||
| chr3:128962058
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1353+3453G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962058 | ||||||
| chr3:128962068
|
C | G | 6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1353+3443G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962068 | ||||||
| chr3:128962147
|
T | G | 1 | a0001c0001t0001g0113 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1353+3364A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962147 | ||||||
| chr3:128962259
|
C | T | 30 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(27): Show | 30 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.1353+3252G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962259 | ||||||
| chr3:128962437
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(119): Show | 125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1353+3074G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962437 | ||||||
| chr3:128962442
|
C | A | 52 | a0001c0002t0001g0007a0001c0002t0001g0154a0001c0002t0001g0158others(49): Show | 54 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.1353+3069G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962442 | ||||||
| chr3:128962500
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02165.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1353+3011T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962500 | ||||||
| chr3:128962561
|
G | A | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1353+2950C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962561 | ||||||
| chr3:128962599
|
T | C | 1 | a0001c0002t0001g0174 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1353+2912A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962599 | ||||||
| chr3:128962837
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1353+2674T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962837 | ||||||
| chr3:128962842
|
C | T | 6 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(3): Show | 6 | HG01123.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1353+2669G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962842 | ||||||
| chr3:128962879
|
T | C | 13 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(10): Show | 13 | HG00558.hp1 HG02135.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.1353+2632A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962879 | ||||||
| chr3:128962925
|
T | A | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1353+2586A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962925 | ||||||
| chr3:128962979
|
C | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0153a0001c0001t0001g0163others(31): Show | 36 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.1353+2532G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962979 | ||||||
| chr3:128962982
|
G | T | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1353+2529C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962982 | ||||||
| chr3:128962991
|
G | T | 34 | a0001c0001t0001g0003a0001c0001t0001g0153a0001c0001t0001g0163others(31): Show | 36 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.1353+2520C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128962991 | ||||||
| chr3:128963031
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1353+2480A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963031 | ||||||
| chr3:128963096
|
T | G | 6 | a0001c0001t0001g0254a0001c0001t0003g0214a0002c0004t0002g0298others(3): Show | 6 | HG02129.hp1 HG02280.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.1353+2415A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963096 | ||||||
| chr3:128963214
|
G | C | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0088others(8): Show | 11 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.1353+2297C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963214 | ||||||
| chr3:128963241
|
C | G | 1 | a0001c0001t0001g0042 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1353+2270G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963241 | ||||||
| chr3:128963263
|
A | C | 24 | a0001c0001t0001g0024a0001c0001t0001g0042a0001c0001t0001g0044others(21): Show | 24 | HG00558.hp1 HG02071.hp1 HG02135.hp1 others(21): Show |
intron_variant | MODIFIER | c.1353+2248T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963263 | ||||||
| chr3:128963274
|
G | A | 14 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(11): Show | 14 | HG00558.hp1 HG02135.hp1 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.1353+2237C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963274 | ||||||
| chr3:128963278
|
C | T | 15 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(12): Show | 15 | HG00558.hp1 HG02135.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1353+2233G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963278 | ||||||
| chr3:128963279
|
A | G | 15 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(12): Show | 15 | HG00558.hp1 HG02135.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1353+2232T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963279 | ||||||
| chr3:128963284
|
G | C | 24 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(21): Show | 24 | HG00558.hp1 HG01123.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.1353+2227C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963284 | ||||||
| chr3:128963326
|
C | G | 1 | a0001c0023t0005g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1353+2185G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963326 | ||||||
| chr3:128963329
|
A | G | 1 | a0001c0023t0005g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1353+2182T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963329 | ||||||
| chr3:128963333
|
C | A | 1 | a0001c0023t0005g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1353+2178G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963333 | ||||||
| chr3:128963347
|
C | T | 1 | a0001c0003t0001g0193 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1353+2164G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963347 | ||||||
| chr3:128963355
|
G | A | 3 | a0001c0002t0001g0174a0001c0002t0001g0177a0001c0002t0001g0178 | 3 | HG01515.hp1 HG02300.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1353+2156C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963355 | ||||||
| chr3:128963358
|
G | A | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1353+2153C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963358 | ||||||
| chr3:128963374
|
T | C | 14 | a0001c0001t0001g0331a0001c0003t0001g0004a0001c0003t0001g0188others(11): Show | 15 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1353+2137A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963374 | ||||||
| chr3:128963382
|
C | G | 7 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1353+2129G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963382 | ||||||
| chr3:128963452
|
C | G | 58 | a0001c0001t0001g0003a0001c0001t0001g0141a0001c0001t0001g0142others(55): Show | 61 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.1353+2059G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963452 | ||||||
| chr3:128963528
|
C | T | 1 | a0001c0023t0005g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1353+1983G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963528 | ||||||
| chr3:128963533
|
T | C | 6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1353+1978A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963533 | ||||||
| chr3:128963539
|
C | A | 3 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233 | 3 | NA18946.hp2 NA18965.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1353+1972G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963539 | ||||||
| chr3:128963540
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1353+1971A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963540 | ||||||
| chr3:128963658
|
C | T | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG00558.hp1 HG02523.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1353+1853G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963658 | ||||||
| chr3:128963673
|
C | T | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(232): Show | 243 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1353+1838G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963673 | ||||||
| chr3:128963731
|
C | G | 2 | a0006c0007t0001g0014a0006c0007t0001g0015 | 2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1353+1780G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963731 | ||||||
| chr3:128963751
|
C | T | 5 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(2): Show | 5 | HG01123.hp2 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1353+1760G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963751 | ||||||
| chr3:128963776
|
C | G | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(235): Show | 246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1353+1735G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963776 | ||||||
| chr3:128963860
|
C | T | 7 | a0001c0001t0001g0094a0001c0001t0001g0112a0001c0001t0001g0136others(4): Show | 7 | NA18747.hp2 NA18941.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.1353+1651G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963860 | ||||||
| chr3:128963998
|
T | C | 1 | a0002c0004t0002g0008 | 2 | NA18950.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1353+1513A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128963998 | ||||||
| chr3:128964072
|
C | T | 4 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 4 | NA18941.hp1 NA18968.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1353+1439G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964072 | ||||||
| chr3:128964158
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0044 | 2 | NA19010.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1353+1353G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964158 | ||||||
| chr3:128964239
|
A | C | 1 | a0001c0003t0001g0013 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1353+1272T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964239 | ||||||
| chr3:128964327
|
C | T | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1353+1184G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964327 | ||||||
| chr3:128964450
|
C | T | 9 | a0001c0005t0001g0150a0001c0005t0001g0206a0001c0005t0001g0207others(6): Show | 9 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1353+1061G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964450 | ||||||
| chr3:128964631
|
C | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1353+880G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964631 | ||||||
| chr3:128964641
|
A | T | 1 | a0001c0001t0001g0100 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1353+870T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964641 | ||||||
| chr3:128964642
|
C | T | 34 | a0001c0001t0001g0003a0001c0001t0001g0153a0001c0001t0001g0163others(31): Show | 36 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.1353+869G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964642 | ||||||
| chr3:128964793
|
C | G | 7 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0101others(4): Show | 7 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1353+718G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964793 | ||||||
| chr3:128964820
|
C | T | 1 | a0021c0011t0001g0047 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1353+691G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964820 | ||||||
| chr3:128964823
|
T | C | 6 | a0001c0001t0001g0072a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG01255.hp2 HG01346.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1353+688A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964823 | ||||||
| chr3:128964824
|
G | A | 1 | a0014c0020t0001g0270 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1353+687C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964824 | ||||||
| chr3:128964837
|
C | T | 1 | a0001c0001t0008g0334 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1353+674G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964837 | ||||||
| chr3:128964865
|
G | A | 1 | a0001c0002t0001g0172 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1353+646C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128964865 | ||||||
| chr3:128965010
|
C | T | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1353+501G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128965010 | ||||||
| chr3:128965087
|
C | A | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1353+424G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128965087 | ||||||
| chr3:128965392
|
C | A | 9 | a0001c0005t0001g0150a0001c0005t0001g0206a0001c0005t0001g0207others(6): Show | 9 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1353+119G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128965392 | ||||||
| chr3:128965423
|
G | T | 9 | a0001c0005t0001g0150a0001c0005t0001g0206a0001c0005t0001g0207others(6): Show | 9 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1353+88C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128965423 | ||||||
| chr3:128965475
|
G | A | 2 | a0002c0004t0002g0323a0002c0004t0002g0324 | 2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1353+36C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 9/15 | chr3 | 128965475 | ||||||
| chr3:128965748
|
C | T | 45 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(42): Show | 47 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.1169-53G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128965748 | ||||||
| chr3:128965830
|
A | G | 1 | a0001c0002t0001g0130 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1169-135T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128965830 | ||||||
| chr3:128966099
|
A | G | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1169-404T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966099 | ||||||
| chr3:128966214
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1169-519C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966214 | ||||||
| chr3:128966221
|
A | C | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | NA19076.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1169-526T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966221 | ||||||
| chr3:128966568
|
C | CT | 7 | a0001c0001t0001g0072a0001c0001t0001g0137a0002c0004t0002g0313others(4): Show | 7 | HG02258.hp1 HG02683.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1169-874dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966568 | ||||||
| chr3:128966568
|
CT | C | 14 | a0001c0001t0001g0135a0001c0003t0001g0013a0001c0005t0001g0150others(11): Show | 14 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1169-874delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966568 | ||||||
| chr3:128966571
|
T | TC | 11 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(8): Show | 12 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1169-877_1169-876i others(3): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966571 | ||||||
| chr3:128966572
|
T | C | 4 | a0001c0003t0001g0194a0001c0003t0001g0199a0001c0023t0005g0333others(1): Show | 4 | HG02280.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1169-877A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966572 | ||||||
| chr3:128966573
|
T | TC | 39 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0022others(36): Show | 41 | HG00323.hp1 HG00423.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1169-879_1169-878i others(3): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966573 | ||||||
| chr3:128966574
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(120): Show | 126 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1169-879A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966574 | ||||||
| chr3:128966575
|
T | C | 1 | a0009c0026t0001g0296 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1169-880A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966575 | ||||||
| chr3:128966633
|
C | T | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1169-938G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966633 | ||||||
| chr3:128966738
|
T | C | 1 | a0001c0001t0001g0255 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1169-1043A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966738 | ||||||
| chr3:128966835
|
G | A | 4 | a0001c0005t0001g0211a0001c0005t0001g0212a0001c0009t0001g0210others(1): Show | 4 | HG00639.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1169-1140C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966835 | ||||||
| chr3:128966918
|
A | C | 1 | a0001c0001t0001g0290 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1169-1223T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128966918 | ||||||
| chr3:128967062
|
A | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(232): Show | 243 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1169-1367T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967062 | ||||||
| chr3:128967093
|
T | G | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1169-1398A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967093 | ||||||
| chr3:128967156
|
C | CA | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1169-1462dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967156 | ||||||
| chr3:128967238
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1169-1543G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967238 | ||||||
| chr3:128967657
|
G | A | 1 | a0001c0001t0007g0066 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1169-1962C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967657 | ||||||
| chr3:128967677
|
G | A | 1 | a0001c0001t0001g0256 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1169-1982C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967677 | ||||||
| chr3:128967702
|
C | CA | 69 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0131others(66): Show | 72 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.1169-2008dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967702 | ||||||
| chr3:128967702
|
C | CAA | 34 | a0001c0001t0003g0147a0001c0002t0001g0007a0001c0002t0001g0299others(31): Show | 36 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1169-2009_1169-200 others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967702 | ||||||
| chr3:128967703
|
A | C | 1 | a0001c0003t0001g0013 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1169-2008T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967703 | ||||||
| chr3:128967741
|
C | T | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1169-2046G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967741 | ||||||
| chr3:128967861
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1169-2166T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967861 | ||||||
| chr3:128967978
|
A | G | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1169-2283T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128967978 | ||||||
| chr3:128968069
|
A | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(125): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1169-2374T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968069 | ||||||
| chr3:128968078
|
CA | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(125): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1169-2384delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968078 | ||||||
| chr3:128968156
|
A | G | 1 | a0001c0003t0004g0215 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1169-2461T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968156 | ||||||
| chr3:128968193
|
T | C | 1 | a0009c0026t0001g0296 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1169-2498A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968193 | ||||||
| chr3:128968354
|
A | C | 2 | a0002c0004t0002g0323a0002c0004t0002g0324 | 2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1169-2659T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968354 | ||||||
| chr3:128968597
|
T | TA | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(232): Show | 243 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1168+2689dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968597 | ||||||
| chr3:128968612
|
G | A | 2 | a0002c0004t0002g0314a0002c0004t0002g0321 | 2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1168+2675C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968612 | ||||||
| chr3:128968736
|
A | C | 2 | a0001c0003t0001g0277a0001c0003t0001g0278 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1168+2551T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968736 | ||||||
| chr3:128968765
|
G | A | 45 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(42): Show | 47 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.1168+2522C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968765 | ||||||
| chr3:128968785
|
G | A | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1168+2502C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968785 | ||||||
| chr3:128968810
|
T | A | 45 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(42): Show | 47 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.1168+2477A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968810 | ||||||
| chr3:128968845
|
C | T | 3 | a0001c0001t0003g0145a0001c0001t0003g0146a0001c0001t0003g0147 | 3 | HG02055.hp1 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1168+2442G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968845 | ||||||
| chr3:128968846
|
G | A | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151 | 3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1168+2441C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968846 | ||||||
| chr3:128968901
|
T | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 5 | HG01167.hp1 HG01175.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.1168+2386A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968901 | ||||||
| chr3:128968937
|
G | A | 1 | a0002c0004t0002g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1168+2350C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128968937 | ||||||
| chr3:128969073
|
A | C | 1 | a0001c0001t0001g0070 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1168+2214T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969073 | ||||||
| chr3:128969218
|
A | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1168+2069T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969218 | ||||||
| chr3:128969227
|
T | C | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1168+2060A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969227 | ||||||
| chr3:128969238
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0126 | 2 | NA19077.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1168+2049G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969238 | ||||||
| chr3:128969247
|
GCTGA | G | 6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168+2036_1168+203 others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969247 | ||||||
| chr3:128969370
|
A | G | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1168+1917T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969370 | ||||||
| chr3:128969475
|
A | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(232): Show | 243 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1168+1812T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969475 | ||||||
| chr3:128969522
|
G | A | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1168+1765C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969522 | ||||||
| chr3:128969572
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1168+1715G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969572 | ||||||
| chr3:128969573
|
G | A | 1 | a0003c0006t0002g0180 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1168+1714C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969573 | ||||||
| chr3:128969573
|
GA | G | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1168+1713delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969573 | ||||||
| chr3:128969656
|
C | T | 34 | a0001c0001t0001g0003a0001c0001t0001g0153a0001c0001t0001g0163others(31): Show | 36 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.1168+1631G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969656 | ||||||
| chr3:128969697
|
C | T | 8 | a0001c0001t0001g0052a0001c0001t0001g0094a0001c0001t0001g0112others(5): Show | 8 | HG02602.hp2 NA18747.hp2 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.1168+1590G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969697 | ||||||
| chr3:128969700
|
A | G | 1 | a0001c0001t0007g0066 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1168+1587T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969700 | ||||||
| chr3:128969719
|
G | A | 12 | a0001c0003t0001g0013a0001c0005t0001g0150a0001c0005t0001g0206others(9): Show | 12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1168+1568C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969719 | ||||||
| chr3:128969745
|
T | C | 34 | a0001c0001t0001g0003a0001c0001t0001g0153a0001c0001t0001g0163others(31): Show | 36 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.1168+1542A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969745 | ||||||
| chr3:128969791
|
T | C | 34 | a0001c0001t0001g0003a0001c0001t0001g0153a0001c0001t0001g0163others(31): Show | 36 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.1168+1496A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969791 | ||||||
| chr3:128969805
|
G | A | 9 | a0001c0005t0001g0150a0001c0005t0001g0206a0001c0005t0001g0207others(6): Show | 9 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1168+1482C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128969805 | ||||||
| chr3:128970086
|
C | T | 6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168+1201G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128970086 | ||||||
| chr3:128970241
|
C | CA | 19 | a0001c0001t0001g0258a0001c0001t0003g0144a0001c0001t0003g0145others(16): Show | 19 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1168+1045dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128970241 | ||||||
| chr3:128970474
|
C | CA | 5 | a0001c0001t0001g0258a0001c0001t0003g0145a0001c0002t0001g0157others(2): Show | 5 | HG01433.hp2 HG01978.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1168+812dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128970474 | ||||||
| chr3:128970504
|
T | TA | 3 | a0004c0010t0001g0329a0004c0010t0001g0330a0004c0030t0001g0328 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1168+782dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128970504 | ||||||
| chr3:128970541
|
T | C | 1 | a0001c0024t0005g0332 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1168+746A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128970541 | ||||||
| chr3:128970648
|
A | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(98): Show | 103 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1168+639T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128970648 | ||||||
| chr3:128970811
|
C | T | 3 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233 | 3 | NA18946.hp2 NA18965.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1168+476G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128970811 | ||||||
| chr3:128970870
|
G | A | 6 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(3): Show | 6 | HG01123.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168+417C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128970870 | ||||||
| chr3:128971076
|
C | T | 1 | a0001c0001t0001g0290 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1168+211G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 8/15 | chr3 | 128971076 | ||||||
| chr3:128971584
|
A | G | 2 | a0001c0002t0001g0068a0001c0002t0001g0123 | 2 | HG02148.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1022-151T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128971584 | ||||||
| chr3:128971618
|
C | T | 6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1022-185G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128971618 | ||||||
| chr3:128971870
|
C | A | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1022-437G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128971870 | ||||||
| chr3:128971907
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1022-474G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128971907 | ||||||
| chr3:128971982
|
G | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0096 | 2 | NA18943.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1022-549C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128971982 | ||||||
| chr3:128972105
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG00099.hp1 HG00140.hp1 |
intron_variant | MODIFIER | c.1022-672G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972105 | ||||||
| chr3:128972247
|
C | CTT | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1022-816_1022-815d others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972247 | ||||||
| chr3:128972309
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1022-876C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972309 | ||||||
| chr3:128972414
|
G | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0153a0001c0001t0001g0163others(31): Show | 36 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.1022-981C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972414 | ||||||
| chr3:128972418
|
T | A | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1022-985A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972418 | ||||||
| chr3:128972467
|
C | G | 7 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(4): Show | 7 | HG00423.hp2 HG00558.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.1022-1034G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972467 | ||||||
| chr3:128972521
|
T | C | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1022-1088A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972521 | ||||||
| chr3:128972564
|
G | A | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(234): Show | 245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1022-1131C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972564 | ||||||
| chr3:128972574
|
G | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0153a0001c0001t0001g0163others(31): Show | 36 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.1022-1141C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972574 | ||||||
| chr3:128972636
|
G | A | 112 | a0001c0001t0001g0003a0001c0001t0001g0141a0001c0001t0001g0142others(109): Show | 117 | HG00323.hp1 HG00423.hp1 HG00639.hp2 others(114): Show |
intron_variant | MODIFIER | c.1022-1203C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972636 | ||||||
| chr3:128972749
|
G | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0153a0001c0001t0001g0163others(31): Show | 36 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.1022-1316C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972749 | ||||||
| chr3:128972812
|
G | A | 1 | a0002c0004t0002g0314 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1022-1379C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972812 | ||||||
| chr3:128972936
|
C | T | 12 | a0001c0003t0001g0013a0001c0005t0001g0150a0001c0005t0001g0206others(9): Show | 12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1022-1503G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972936 | ||||||
| chr3:128972973
|
G | A | 1 | a0004c0010t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1022-1540C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128972973 | ||||||
| chr3:128973098
|
T | C | 304 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(301): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.1022-1665A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128973098 | ||||||
| chr3:128973518
|
T | C | 34 | a0001c0001t0001g0003a0001c0001t0001g0153a0001c0001t0001g0163others(31): Show | 36 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.1022-2085A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128973518 | ||||||
| chr3:128973546
|
C | T | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1022-2113G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128973546 | ||||||
| chr3:128973610
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1021+2169G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128973610 | ||||||
| chr3:128973659
|
G | GA | 17 | a0001c0001t0003g0144a0001c0001t0003g0146a0001c0001t0003g0147others(14): Show | 17 | HG00639.hp2 HG01069.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1021+2119dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128973659 | ||||||
| chr3:128973659
|
GA | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(123): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1021+2119delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128973659 | ||||||
| chr3:128973912
|
T | C | 4 | a0001c0001t0001g0218a0001c0001t0001g0262a0001c0001t0001g0263others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021+1867A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128973912 | ||||||
| chr3:128973921
|
T | C | 1 | a0002c0004t0002g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1021+1858A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128973921 | ||||||
| chr3:128974039
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1021+1740C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128974039 | ||||||
| chr3:128974069
|
A | C | 1 | a0001c0019t0001g0069 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1021+1710T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128974069 | ||||||
| chr3:128974350
|
C | T | 1 | a0004c0010t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1021+1429G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128974350 | ||||||
| chr3:128974611
|
AG | A | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1021+1167delC | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128974611 | ||||||
| chr3:128974764
|
T | C | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1021+1015A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128974764 | ||||||
| chr3:128974778
|
G | A | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1021+1001C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128974778 | ||||||
| chr3:128974877
|
T | C | 35 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 36 | HG00099.hp1 HG00140.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1021+902A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128974877 | ||||||
| chr3:128974962
|
C | T | 45 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(42): Show | 47 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.1021+817G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128974962 | ||||||
| chr3:128974976
|
C | G | 3 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0294 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1021+803G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128974976 | ||||||
| chr3:128974989
|
G | A | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1021+790C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128974989 | ||||||
| chr3:128975064
|
G | C | 6 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(3): Show | 6 | HG01123.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1021+715C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975064 | ||||||
| chr3:128975123
|
AAAAAT | A | 12 | a0001c0003t0001g0013a0001c0005t0001g0150a0001c0005t0001g0206others(9): Show | 12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1021+651_1021+655d others(7): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975123 | ||||||
| chr3:128975128
|
T | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0122 | 2 | HG03688.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1021+651A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975128 | ||||||
| chr3:128975231
|
A | G | 2 | a0001c0002t0001g0177a0001c0002t0001g0178 | 2 | HG01515.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1021+548T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975231 | ||||||
| chr3:128975426
|
G | GGGAT | 4 | a0001c0001t0001g0059a0001c0001t0001g0132a0001c0001t0001g0133others(1): Show | 4 | HG01943.hp2 HG02602.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1021+349_1021+352d others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975426 | ||||||
| chr3:128975426
|
GGGAT | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(118): Show | 123 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1021+349_1021+352d others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975426 | ||||||
| chr3:128975426
|
GGGATGGA others(1): Show |
G | 51 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0117others(48): Show | 53 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.1021+345_1021+352d others(10): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975426 | ||||||
| chr3:128975426
|
GGGATGGA others(9): Show |
G | 57 | a0001c0001t0001g0003a0001c0001t0001g0141a0001c0001t0001g0142others(54): Show | 61 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.1021+337_1021+352d others(18): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975426 | ||||||
| chr3:128975426
|
GGGATGGA others(17): Show |
G | 6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1021+329_1021+352d others(26): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975426 | ||||||
| chr3:128975457
|
A | T | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1021+322T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975457 | ||||||
| chr3:128975577
|
T | C | 1 | a0002c0004t0002g0313 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1021+202A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 7/15 | chr3 | 128975577 | ||||||
| chr3:128976190
|
A | C | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.897-287T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 6/15 | chr3 | 128976190 | ||||||
| chr3:128976205
|
T | A | 1 | a0001c0003t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.897-302A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 6/15 | chr3 | 128976205 | ||||||
| chr3:128976253
|
T | G | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01069.hp1 HG01109.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.897-350A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 6/15 | chr3 | 128976253 | ||||||
| chr3:128976788
|
T | C | 21 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(18): Show | 21 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.896+191A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 6/15 | chr3 | 128976788 | ||||||
| chr3:128976869
|
G | A | 2 | a0001c0002t0001g0130a0012c0018t0002g0143 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.896+110C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 6/15 | chr3 | 128976869 | ||||||
| chr3:128976966
|
G | A | 19 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(16): Show | 20 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.896+13C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 6/15 | chr3 | 128976966 | ||||||
| chr3:128977184
|
A | G | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.809-118T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 5/15 | chr3 | 128977184 | ||||||
| chr3:128977355
|
A | G | 1 | a0001c0001t0001g0266 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.809-289T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 5/15 | chr3 | 128977355 | ||||||
| chr3:128977511
|
C | T | 1 | a0012c0018t0002g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.809-445G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 5/15 | chr3 | 128977511 | ||||||
| chr3:128977675
|
A | G | 13 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(10): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.808+370T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 5/15 | chr3 | 128977675 | ||||||
| chr3:128977689
|
T | C | 15 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(12): Show | 15 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.808+356A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 5/15 | chr3 | 128977689 | ||||||
| chr3:128977723
|
G | A | 61 | a0001c0001t0001g0003a0001c0001t0001g0141a0001c0001t0001g0142others(58): Show | 64 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.808+322C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 5/15 | chr3 | 128977723 | ||||||
| chr3:128977732
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.808+313C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 5/15 | chr3 | 128977732 | ||||||
| chr3:128977751
|
C | T | 6 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(3): Show | 6 | HG01123.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.808+294G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 5/15 | chr3 | 128977751 | ||||||
| chr3:128977816
|
G | A | 12 | a0001c0003t0001g0013a0001c0005t0001g0150a0001c0005t0001g0206others(9): Show | 12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.808+229C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 5/15 | chr3 | 128977816 | ||||||
| chr3:128977838
|
G | A | 2 | a0002c0004t0002g0314a0002c0004t0002g0321 | 2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.808+207C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 5/15 | chr3 | 128977838 | ||||||
| chr3:128978242
|
AT | A | 45 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(42): Show | 47 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.668-58delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128978242 | ||||||
| chr3:128978361
|
T | C | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.668-176A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128978361 | ||||||
| chr3:128978470
|
G | A | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(125): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.668-285C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128978470 | ||||||
| chr3:128978565
|
C | G | 34 | a0001c0001t0001g0003a0001c0001t0001g0153a0001c0001t0001g0163others(31): Show | 36 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.668-380G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128978565 | ||||||
| chr3:128978661
|
A | T | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.668-476T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128978661 | ||||||
| chr3:128978832
|
C | G | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.668-647G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128978832 | ||||||
| chr3:128978971
|
A | G | 2 | a0001c0001t0001g0275a0010c0022t0001g0276 | 2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.668-786T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128978971 | ||||||
| chr3:128979408
|
A | T | 1 | a0002c0004t0002g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.668-1223T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979408 | ||||||
| chr3:128979484
|
G | A | 6 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(3): Show | 6 | HG01123.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.668-1299C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979484 | ||||||
| chr3:128979546
|
C | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0096 | 2 | NA18943.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.668-1361G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979546 | ||||||
| chr3:128979718
|
G | C | 1 | a0001c0001t0001g0039 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.668-1533C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979718 | ||||||
| chr3:128979776
|
A | G | 1 | a0001c0001t0001g0227 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.668-1591T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979776 | ||||||
| chr3:128979812
|
G | A | 1 | a0004c0010t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.668-1627C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979812 | ||||||
| chr3:128979836
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.668-1651A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979836 | ||||||
| chr3:128979852
|
C | T | 1 | a0002c0004t0002g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.668-1667G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979852 | ||||||
| chr3:128979866
|
T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(235): Show | 246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.668-1681A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979866 | ||||||
| chr3:128979923
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.668-1738C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979923 | ||||||
| chr3:128979944
|
AATAATAT | A | 4 | a0002c0004t0002g0317a0002c0004t0002g0318a0002c0004t0002g0319others(1): Show | 4 | HG02922.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.668-1766_668-1760d others(9): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979944 | ||||||
| chr3:128979946
|
TA | T | 27 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(24): Show | 29 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.668-1762delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979946 | ||||||
| chr3:128979947
|
A | AAT | 13 | a0001c0001t0001g0098a0001c0001t0001g0115a0001c0001t0001g0116others(10): Show | 13 | HG00642.hp2 HG01069.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.668-1764_668-1763d others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979947 | ||||||
| chr3:128979947
|
A | AATAATAT others(4): Show |
1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.668-1763_668-1762i others(13): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979947 | ||||||
| chr3:128979947
|
A | AATAT | 63 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(60): Show | 64 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.668-1766_668-1763d others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979947 | ||||||
| chr3:128979947
|
A | AATATAT | 18 | a0001c0001t0001g0067a0001c0001t0001g0126a0001c0001t0001g0275others(15): Show | 18 | HG00609.hp2 HG00639.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.668-1768_668-1763d others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979947 | ||||||
| chr3:128979947
|
A | AATATATA others(1): Show |
4 | a0001c0001t0001g0053a0001c0001t0001g0061a0001c0001t0001g0065others(1): Show | 4 | HG01943.hp1 HG02165.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.668-1770_668-1763d others(10): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979947 | ||||||
| chr3:128979947
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0059 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.668-1772_668-1763d others(12): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979947 | ||||||
| chr3:128979947
|
AATAT | A | 36 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(33): Show | 37 | HG00099.hp1 HG00140.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.668-1766_668-1763d others(6): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979947 | ||||||
| chr3:128979947
|
AATATAT | A | 58 | a0001c0001t0001g0003a0001c0001t0001g0153a0001c0001t0001g0163others(55): Show | 61 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.668-1768_668-1763d others(8): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979947 | ||||||
| chr3:128979973
|
A | T | 1 | a0011c0017t0001g0054 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.668-1788T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128979973 | ||||||
| chr3:128980366
|
C | CA | 8 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0113others(5): Show | 8 | HG01175.hp1 HG01928.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.668-2182dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128980366 | ||||||
| chr3:128980366
|
CA | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(137): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.668-2182delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128980366 | ||||||
| chr3:128980366
|
CAA | C | 51 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0040others(48): Show | 53 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.668-2183_668-2182d others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128980366 | ||||||
| chr3:128980366
|
CAAA | C | 44 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(41): Show | 46 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.668-2184_668-2182d others(5): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128980366 | ||||||
| chr3:128980524
|
T | A | 1 | a0001c0001t0001g0269 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.668-2339A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128980524 | ||||||
| chr3:128980563
|
G | A | 2 | a0002c0004t0002g0323a0002c0004t0002g0324 | 2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.668-2378C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128980563 | ||||||
| chr3:128980916
|
T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(235): Show | 246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.668-2731A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128980916 | ||||||
| chr3:128981038
|
C | CT | 9 | a0001c0001t0001g0044a0001c0001t0001g0060a0001c0001t0001g0115others(6): Show | 9 | HG01934.hp2 HG02074.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.668-2854dupA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128981038 | ||||||
| chr3:128981090
|
G | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(124): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.668-2905C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128981090 | ||||||
| chr3:128981181
|
C | T | 34 | a0001c0001t0001g0003a0001c0001t0001g0153a0001c0001t0001g0163others(31): Show | 36 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.668-2996G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128981181 | ||||||
| chr3:128981197
|
C | T | 1 | a0001c0001t0003g0149 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.668-3012G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128981197 | ||||||
| chr3:128981252
|
C | G | 2 | a0001c0003t0001g0194a0001c0003t0001g0197 | 2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.668-3067G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128981252 | ||||||
| chr3:128981274
|
G | A | 1 | a0001c0002t0001g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.668-3089C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128981274 | ||||||
| chr3:128981683
|
C | G | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151 | 3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.668-3498G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128981683 | ||||||
| chr3:128981890
|
C | G | 61 | a0001c0001t0001g0003a0001c0001t0001g0141a0001c0001t0001g0142others(58): Show | 64 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.668-3705G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128981890 | ||||||
| chr3:128982023
|
A | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(125): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.668-3838T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982023 | ||||||
| chr3:128982084
|
G | C | 1 | a0001c0001t0001g0005 | 2 | NA18943.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.668-3899C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982084 | ||||||
| chr3:128982127
|
C | T | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.668-3942G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982127 | ||||||
| chr3:128982222
|
C | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG00558.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.668-4037G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982222 | ||||||
| chr3:128982248
|
C | G | 1 | a0001c0002t0001g0157 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.668-4063G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982248 | ||||||
| chr3:128982287
|
T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(235): Show | 246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.668-4102A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982287 | ||||||
| chr3:128982487
|
G | A | 4 | a0001c0003t0001g0194a0001c0003t0001g0195a0001c0003t0001g0196others(1): Show | 4 | HG02109.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.668-4302C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982487 | ||||||
| chr3:128982531
|
G | A | 6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.668-4346C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982531 | ||||||
| chr3:128982611
|
A | G | 1 | a0008c0027t0001g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.668-4426T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982611 | ||||||
| chr3:128982624
|
G | A | 1 | a0017c0014t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.668-4439C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982624 | ||||||
| chr3:128982645
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.668-4460A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982645 | ||||||
| chr3:128982662
|
T | C | 1 | a0001c0003t0001g0197 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.668-4477A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982662 | ||||||
| chr3:128982797
|
G | A | 2 | a0001c0001t0008g0334a0001c0003t0001g0128 | 2 | HG01175.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.668-4612C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128982797 | ||||||
| chr3:128983030
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.667+4586C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128983030 | ||||||
| chr3:128983038
|
T | C | 4 | a0001c0001t0001g0053a0001c0001t0001g0119a0001c0001t0001g0120others(1): Show | 4 | HG00323.hp2 HG01943.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.667+4578A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128983038 | ||||||
| chr3:128983406
|
C | G | 1 | a0001c0023t0005g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.667+4210G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128983406 | ||||||
| chr3:128983661
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.667+3955A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128983661 | ||||||
| chr3:128983904
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.667+3712G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128983904 | ||||||
| chr3:128983954
|
G | A | 2 | a0001c0002t0001g0177a0001c0002t0001g0178 | 2 | HG01515.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.667+3662C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128983954 | ||||||
| chr3:128984024
|
G | T | 6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.667+3592C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984024 | ||||||
| chr3:128984050
|
CGGGGGAC others(18): Show |
C | 1 | a0001c0001t0001g0122 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.667+3541_667+3565d others(27): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984050 | ||||||
| chr3:128984173
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0040 | 2 | HG01167.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.667+3443G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984173 | ||||||
| chr3:128984425
|
C | T | 1 | a0009c0026t0001g0296 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.667+3191G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984425 | ||||||
| chr3:128984524
|
C | T | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(3): Show | 6 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.667+3092G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984524 | ||||||
| chr3:128984566
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0043 | 2 | HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.667+3050G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984566 | ||||||
| chr3:128984633
|
G | T | 1 | a0001c0001t0001g0058 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.667+2983C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984633 | ||||||
| chr3:128984748
|
A | G | 2 | a0001c0003t0004g0273a0001c0003t0004g0274 | 2 | HG00642.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.667+2868T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984748 | ||||||
| chr3:128984825
|
T | A | 1 | a0001c0001t0001g0045 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.667+2791A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984825 | ||||||
| chr3:128984859
|
G | A | 106 | a0001c0001t0001g0003a0001c0001t0001g0141a0001c0001t0001g0142others(103): Show | 111 | HG00323.hp1 HG00423.hp1 HG00639.hp2 others(108): Show |
intron_variant | MODIFIER | c.667+2757C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984859 | ||||||
| chr3:128984909
|
A | T | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.667+2707T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128984909 | ||||||
| chr3:128985447
|
A | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(119): Show | 125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.667+2169T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128985447 | ||||||
| chr3:128985757
|
C | T | 3 | a0001c0002t0001g0002a0001c0002t0001g0155a0001c0002t0001g0156 | 4 | HG01081.hp2 HG01192.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.667+1859G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128985757 | ||||||
| chr3:128986037
|
C | A | 1 | a0012c0018t0002g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.667+1579G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986037 | ||||||
| chr3:128986048
|
A | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(98): Show | 103 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.667+1568T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986048 | ||||||
| chr3:128986168
|
T | C | 6 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(3): Show | 6 | HG00639.hp1 HG01516.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.667+1448A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986168 | ||||||
| chr3:128986192
|
C | T | 5 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(2): Show | 5 | HG03471.hp1 NA18747.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.667+1424G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986192 | ||||||
| chr3:128986193
|
G | A | 1 | a0015c0016t0001g0176 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.667+1423C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986193 | ||||||
| chr3:128986240
|
CT | C | 61 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0141others(58): Show | 64 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.667+1375delA | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986240 | ||||||
| chr3:128986396
|
T | C | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.667+1220A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986396 | ||||||
| chr3:128986471
|
TC | T | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.667+1144delG | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986471 | ||||||
| chr3:128986724
|
G | A | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(234): Show | 245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.667+892C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986724 | ||||||
| chr3:128986737
|
G | A | 3 | a0001c0001t0001g0271a0001c0023t0005g0333a0001c0024t0005g0332 | 3 | HG02280.hp2 HG02293.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.667+879C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986737 | ||||||
| chr3:128986741
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.667+875C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128986741 | ||||||
| chr3:128987030
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.667+586C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128987030 | ||||||
| chr3:128987161
|
G | A | 6 | a0003c0006t0002g0180a0003c0006t0002g0181a0003c0006t0002g0182others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.667+455C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128987161 | ||||||
| chr3:128987240
|
A | G | 1 | a0001c0024t0005g0332 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.667+376T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128987240 | ||||||
| chr3:128987311
|
T | G | 1 | a0001c0001t0001g0131 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.667+305A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 4/15 | chr3 | 128987311 | ||||||
| chr3:128987861
|
G | A | 1 | a0001c0001t0001g0005 | 2 | NA18943.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.454-32C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128987861 | ||||||
| chr3:128987873
|
G | A | 3 | a0004c0010t0001g0329a0004c0010t0001g0330a0004c0030t0001g0328 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.454-44C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128987873 | ||||||
| chr3:128987882
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.454-53C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128987882 | ||||||
| chr3:128987930
|
G | A | 2 | a0006c0007t0001g0014a0006c0007t0001g0015 | 2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.454-101C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128987930 | ||||||
| chr3:128988139
|
ACACACAT others(15): Show |
A | 1 | a0001c0021t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.454-332_454-311del others(22): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128988139 | ||||||
| chr3:128988157
|
G | A | 3 | a0004c0010t0001g0329a0004c0010t0001g0330a0004c0030t0001g0328 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.454-328C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128988157 | ||||||
| chr3:128988269
|
G | A | 2 | a0001c0002t0001g0177a0001c0002t0001g0178 | 2 | HG01515.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.454-440C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128988269 | ||||||
| chr3:128988279
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(118): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.453+449C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128988279 | ||||||
| chr3:128988517
|
G | A | 20 | a0001c0001t0001g0275a0001c0001t0001g0279a0001c0001t0001g0283others(17): Show | 21 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.453+211C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128988517 | ||||||
| chr3:128988545
|
A | C | 4 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(1): Show | 4 | HG00558.hp1 HG02135.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.453+183T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128988545 | ||||||
| chr3:128988631
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.453+97C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 3/15 | chr3 | 128988631 | ||||||
| chr3:128989289
|
T | TA | 7 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(4): Show | 7 | HG01175.hp1 HG01928.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.263-372dupT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128989289 | ||||||
| chr3:128989289
|
TA | T | 23 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(20): Show | 23 | HG01928.hp1 HG01943.hp1 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.263-372delT | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128989289 | ||||||
| chr3:128989289
|
TAA | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(185): Show | 195 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.263-373_263-372del others(2): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128989289 | ||||||
| chr3:128989289
|
TAAA | T | 22 | a0001c0001t0001g0142a0001c0001t0001g0151a0001c0001t0001g0153others(19): Show | 23 | HG01070.hp1 HG01884.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.263-374_263-372del others(3): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128989289 | ||||||
| chr3:128989289
|
TAAAA | T | 7 | a0001c0001t0001g0141a0001c0001t0003g0144a0001c0001t0003g0145others(4): Show | 7 | HG01123.hp2 HG01255.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.263-375_263-372del others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128989289 | ||||||
| chr3:128989571
|
C | T | 1 | a0001c0003t0004g0215 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.263-653G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128989571 | ||||||
| chr3:128989602
|
C | G | 12 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(9): Show | 13 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.263-684G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128989602 | ||||||
| chr3:128989711
|
G | A | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(234): Show | 245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.263-793C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128989711 | ||||||
| chr3:128989844
|
AGCAT | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0186 | 3 | HG01261.hp1 HG01433.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.263-930_263-927del others(4): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128989844 | ||||||
| chr3:128990280
|
T | C | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.263-1362A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128990280 | ||||||
| chr3:128990465
|
C | A | 1 | a0001c0001t0001g0131 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.263-1547G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128990465 | ||||||
| chr3:128990483
|
A | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(232): Show | 243 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.263-1565T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128990483 | ||||||
| chr3:128990634
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG02602.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.263-1716C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128990634 | ||||||
| chr3:128990714
|
G | C | 1 | a0001c0001t0001g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.263-1796C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128990714 | ||||||
| chr3:128990838
|
A | C | 1 | a0001c0005t0001g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.263-1920T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128990838 | ||||||
| chr3:128990923
|
T | A | 16 | a0001c0003t0001g0004a0001c0003t0001g0188a0001c0003t0001g0189others(13): Show | 17 | HG00642.hp1 HG01891.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.263-2005A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128990923 | ||||||
| chr3:128990963
|
T | C | 1 | a0002c0004t0002g0326 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.263-2045A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128990963 | ||||||
| chr3:128990979
|
T | A | 6 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(3): Show | 6 | HG01123.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.263-2061A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128990979 | ||||||
| chr3:128991120
|
C | A | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151 | 3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.262+1923G>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991120 | ||||||
| chr3:128991137
|
T | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(232): Show | 243 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.262+1906A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991137 | ||||||
| chr3:128991176
|
G | A | 61 | a0001c0001t0001g0003a0001c0001t0001g0141a0001c0001t0001g0142others(58): Show | 64 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.262+1867C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991176 | ||||||
| chr3:128991187
|
A | C | 3 | a0004c0010t0001g0329a0004c0010t0001g0330a0004c0030t0001g0328 | 3 | HG00642.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.262+1856T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991187 | ||||||
| chr3:128991210
|
C | G | 1 | a0001c0001t0001g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.262+1833G>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991210 | ||||||
| chr3:128991228
|
G | C | 2 | a0001c0002t0001g0006a0001c0002t0001g0295 | 3 | HG01081.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.262+1815C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991228 | ||||||
| chr3:128991257
|
G | T | 12 | a0001c0003t0001g0013a0001c0005t0001g0150a0001c0005t0001g0206others(9): Show | 12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.262+1786C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991257 | ||||||
| chr3:128991702
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.262+1341C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991702 | ||||||
| chr3:128991862
|
A | T | 2 | a0001c0005t0001g0150a0001c0005t0001g0206 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.262+1181T>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991862 | ||||||
| chr3:128991870
|
G | A | 1 | a0009c0026t0001g0296 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.262+1173C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991870 | ||||||
| chr3:128991912
|
T | G | 1 | a0001c0001t0001g0135 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.262+1131A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991912 | ||||||
| chr3:128991922
|
A | G | 19 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(16): Show | 20 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.262+1121T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991922 | ||||||
| chr3:128991927
|
G | A | 12 | a0001c0003t0001g0013a0001c0005t0001g0150a0001c0005t0001g0206others(9): Show | 12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.262+1116C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128991927 | ||||||
| chr3:128992175
|
G | A | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.262+868C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992175 | ||||||
| chr3:128992290
|
G | A | 5 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(2): Show | 5 | NA18747.hp2 NA18941.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.262+753C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992290 | ||||||
| chr3:128992353
|
G | A | 1 | a0013c0015t0001g0187 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.262+690C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992353 | ||||||
| chr3:128992445
|
C | T | 48 | a0001c0001t0001g0003a0001c0001t0001g0141a0001c0001t0001g0142others(45): Show | 50 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.262+598G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992445 | ||||||
| chr3:128992487
|
G | A | 12 | a0001c0003t0001g0013a0001c0005t0001g0150a0001c0005t0001g0206others(9): Show | 12 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.262+556C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992487 | ||||||
| chr3:128992571
|
G | T | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151 | 3 | HG01255.hp2 HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.262+472C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992571 | ||||||
| chr3:128992575
|
T | A | 1 | a0001c0001t0001g0151 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.262+468A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992575 | ||||||
| chr3:128992581
|
T | TA | 13 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0151others(10): Show | 13 | HG01123.hp2 HG01255.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.262+461_262+462ins others(1): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992581 | ||||||
| chr3:128992582
|
T | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(224): Show | 235 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.262+461A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992582 | ||||||
| chr3:128992583
|
T | A | 1 | a0001c0001t0003g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.262+460A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992583 | ||||||
| chr3:128992585
|
T | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(118): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.262+458A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992585 | ||||||
| chr3:128992645
|
G | A | 33 | a0001c0002t0001g0007a0001c0002t0001g0299a0001c0002t0001g0304others(30): Show | 35 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.262+398C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992645 | ||||||
| chr3:128992755
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.262+288T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992755 | ||||||
| chr3:128992766
|
T | C | 1 | a0005c0008t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+277A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992766 | ||||||
| chr3:128992768
|
T | A | 1 | a0005c0008t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+275A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992768 | ||||||
| chr3:128992771
|
ATGGTTTT others(6): Show |
A | 1 | a0005c0008t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+259_262+271del others(13): Show |
CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992771 | ||||||
| chr3:128992788
|
T | C | 1 | a0005c0008t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+255A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992788 | ||||||
| chr3:128992789
|
G | T | 1 | a0005c0008t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+254C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992789 | ||||||
| chr3:128992868
|
G | C | 1 | a0005c0008t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+175C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992868 | ||||||
| chr3:128992869
|
C | T | 1 | a0005c0008t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+174G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992869 | ||||||
| chr3:128992870
|
C | T | 1 | a0005c0008t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+173G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992870 | ||||||
| chr3:128992872
|
C | T | 1 | a0005c0008t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+171G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992872 | ||||||
| chr3:128992876
|
T | C | 1 | a0005c0008t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+167A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992876 | ||||||
| chr3:128992878
|
A | C | 1 | a0005c0008t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+165T>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992878 | ||||||
| chr3:128992880
|
A | G | 1 | a0005c0008t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+163T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992880 | ||||||
| chr3:128992881
|
T | C | 1 | a0005c0008t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+162A>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992881 | ||||||
| chr3:128992882
|
T | A | 1 | a0005c0008t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+161A>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992882 | ||||||
| chr3:128992886
|
G | T | 1 | a0005c0008t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+157C>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992886 | ||||||
| chr3:128992887
|
T | G | 1 | a0005c0008t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.262+156A>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992887 | ||||||
| chr3:128992970
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.262+73G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 2/15 | chr3 | 128992970 | ||||||
| chr3:128993368
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-32-32G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 1/15 | chr3 | 128993368 | ||||||
| chr3:128993535
|
A | G | 35 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 36 | HG00099.hp1 HG00140.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.-32-199T>C | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 1/15 | chr3 | 128993535 | ||||||
| chr3:128993587
|
C | T | 3 | a0001c0003t0001g0013a0006c0007t0001g0014a0006c0007t0001g0015 | 3 | HG01069.hp1 HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-32-251G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 1/15 | chr3 | 128993587 | ||||||
| chr3:128993689
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(1): Show | 4 | HG00099.hp1 HG00140.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+291G>A | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 1/15 | chr3 | 128993689 | ||||||
| chr3:128993763
|
G | C | 1 | a0001c0001t0001g0331 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-33+217C>G | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 1/15 | chr3 | 128993763 | ||||||
| chr3:128993931
|
G | A | 2 | a0001c0023t0005g0333a0001c0024t0005g0332 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-33+49C>T | CFAP92 | ENSG00000114656.13 | transcript | ENST00000645291.3 | protein_coding | 1/15 | chr3 | 128993931 |