Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 55081 |
|---|---|
| ensemblid | ENSG00000114446.5 |
| hgncid | 17367 |
| symbol | IFT57 |
| name | intraflagellar transport 57 |
| refseq_nuc | NM_018010.4 |
| refseq_prot | NP_060480.1 |
| ensembl_nuc | ENST00000264538.4 |
| ensembl_prot | ENSP00000264538.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 108160812 |
| end | 108222424 |
| strand | - |
| ver | v1.2 |
| region | chr3:108160812-108222424 |
| region5000 | chr3:108155812-108227424 |
| regionname0 | IFT57_chr3_108160812_108222424 |
| regionname5000 | IFT57_chr3_108155812_108227424 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 429 | 350 | 81 | 65 | 157 | 8 | 37 | 123 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0002 | 0/0 | 429 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0003 | 0/0 | 429 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0004 | 0/0 | 429 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1290 | 296 | 62 | 54 | 134 | 8 | 36 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| c0002 | 0/0 | 1290 | 36 | 6 | 10 | 19 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| c0003 | 0/0 | 1290 | 7 | 7 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| c0004 | 0/0 | 1290 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| c0005 | 0/0 | 1290 | 3 | 3 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| c0006 | 0/0 | 1290 | 2 | 0 | 1 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| c0007 | 0/0 | 1290 | 2 | 1 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| c0008 | 0/0 | 1290 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| c0009 | 0/0 | 1290 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| c0010 | 0/0 | 1290 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| c0011 | 0/0 | 1290 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| c0012 | 0/0 | 1290 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1766 | 97 | 32 | 29 | 19 | 6 | 11 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| t0002 | 0/0 | 1768 | 90 | 11 | 10 | 62 | 0 | 7 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| t0003 | 0/0 | 1767 | 84 | 17 | 4 | 55 | 1 | 7 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| t0004 | 0/0 | 1773 | 31 | 2 | 9 | 19 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| t0005 | 0/1 | 1767 | 26 | 3 | 10 | 1 | 1 | 10 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| t0006 | 1/0 | 1768 | 10 | 9 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| t0007 | 0/0 | 1773 | 4 | 4 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| t0008 | 0/0 | 1766 | 2 | 0 | 2 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| t0009 | 0/0 | 1766 | 2 | 0 | 0 | 0 | 0 | 2 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| t0010 | 0/0 | 1773 | 2 | 2 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| t0011 | 0/0 | 1766 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| t0012 | 0/0 | 1768 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| t0013 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| t0014 | 0/0 | 1767 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| t0015 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| t0016 | 0/0 | 1772 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| 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 | 4 | 4 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0021 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0151 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0230 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1290 | 296 | 62 | 54 | 134 | 8 | 36 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0002 | 0/0 | 1290 | 36 | 6 | 10 | 19 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0003 | 0/0 | 1290 | 7 | 7 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0004 | 0/0 | 1290 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0005 | 0/0 | 1290 | 3 | 3 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0007 | 0/0 | 1290 | 2 | 1 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0008 | 0/0 | 1290 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0009 | 0/0 | 1290 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0012 | 0/0 | 1290 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0002c0006 | 0/0 | 1290 | 2 | 0 | 1 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0003c0011 | 0/0 | 1290 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0004c0010 | 0/0 | 1290 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3055 | 90 | 25 | 29 | 19 | 6 | 11 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0001t0002 | 0/0 | 3057 | 87 | 10 | 9 | 61 | 0 | 7 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0001t0003 | 0/0 | 3056 | 79 | 16 | 4 | 51 | 1 | 7 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0001t0005 | 0/1 | 3056 | 24 | 3 | 9 | 1 | 1 | 9 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0001t0006 | 1/0 | 3057 | 6 | 5 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0001t0008 | 0/0 | 3055 | 2 | 0 | 2 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0001t0009 | 0/0 | 3055 | 2 | 0 | 0 | 0 | 0 | 2 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0001t0010 | 0/0 | 3062 | 2 | 2 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0001t0011 | 0/0 | 3055 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0001t0012 | 0/0 | 3057 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0001t0013 | 0/0 | 3056 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0001t0014 | 0/0 | 3056 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0002t0004 | 0/0 | 3062 | 31 | 2 | 9 | 19 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0002t0007 | 0/0 | 3062 | 4 | 4 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0002t0016 | 0/0 | 3061 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0003t0001 | 0/0 | 3055 | 7 | 7 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0004t0003 | 0/0 | 3056 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0005t0006 | 0/0 | 3057 | 3 | 3 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0007t0002 | 0/0 | 3057 | 2 | 1 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0008t0002 | 0/0 | 3057 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0009t0006 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0001c0012t0015 | 0/0 | 3062 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0002c0006t0005 | 0/0 | 3056 | 2 | 0 | 1 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0003c0011t0003 | 0/0 | 3056 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| a0004c0010t0003 | 0/0 | 3056 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | copy fasta | chr3 | 108155812 | 108227424 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0021 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0230 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0006g0151 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0008g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0009g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0009g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0010g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0010g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0011g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0012g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0013g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0014g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0007g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0007g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0007g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0007g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0016g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0003t0001g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0003t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0003t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0004t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0004t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0004t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0005t0006g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0005t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0007t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0007t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0008t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0009t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0012t0015g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0002c0006t0005g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0002c0006t0005g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0003c0011t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0004c0010t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | GBR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | GBR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | FIN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | FIN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | CHS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00408 | hp2 | a0001 | c0002 | t0004 | g0052 | EAS | CHS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | CHS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | CHS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00558 | hp1 | a0001 | c0002 | t0004 | g0042 | EAS | CHS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0286 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00673 | hp1 | a0001 | c0002 | t0004 | g0043 | EAS | CHS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | CHS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0232 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00738 | hp2 | a0001 | c0002 | t0004 | g0058 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0252 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00741 | hp2 | a0001 | c0001 | t0008 | g0017 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0235 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0248 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01070 | hp2 | a0001 | c0002 | t0004 | g0038 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0247 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01106 | hp1 | a0001 | c0002 | t0004 | g0056 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0245 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0022 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01175 | hp1 | a0001 | c0002 | t0004 | g0034 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01175 | hp2 | a0001 | c0001 | t0014 | g0240 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01192 | hp1 | a0001 | c0007 | t0002 | g0127 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01255 | hp2 | a0001 | c0002 | t0004 | g0057 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0302 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01257 | hp1 | a0001 | c0002 | t0016 | g0036 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01257 | hp2 | a0002 | c0006 | t0005 | g0231 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01258 | hp1 | a0001 | c0002 | t0004 | g0037 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0303 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0236 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01346 | hp2 | a0001 | c0002 | t0004 | g0050 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0229 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0124 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0288 | EUR | IBS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0021 | EUR | IBS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0234 | EUR | IBS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | IBS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01891 | hp2 | a0001 | c0012 | t0015 | g0314 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01981 | hp1 | a0001 | c0002 | t0004 | g0049 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02004 | hp2 | a0001 | c0001 | t0008 | g0017 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02040 | hp2 | a0001 | c0002 | t0004 | g0045 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02055 | hp1 | a0001 | c0002 | t0007 | g0315 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02080 | hp2 | a0001 | c0002 | t0004 | g0033 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02129 | hp2 | a0001 | c0002 | t0004 | g0032 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02132 | hp2 | a0001 | c0002 | t0004 | g0008 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02135 | hp1 | a0001 | c0002 | t0004 | g0047 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0239 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | CDX | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | CDX | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | CDX | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0312 | EAS | CDX | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0224 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02300 | hp2 | a0001 | c0002 | t0004 | g0035 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02451 | hp1 | a0001 | c0002 | t0004 | g0060 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0287 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0237 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02615 | hp1 | a0001 | c0009 | t0006 | g0153 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0309 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0148 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02698 | hp1 | a0001 | c0001 | t0005 | g0250 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02717 | hp2 | a0001 | c0005 | t0006 | g0154 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0233 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0265 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0145 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0225 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0223 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0253 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02922 | hp2 | a0001 | c0002 | t0007 | g0318 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0150 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0149 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0152 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03017 | hp2 | a0001 | c0001 | t0009 | g0221 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03130 | hp1 | a0001 | c0001 | t0010 | g0144 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03139 | hp1 | a0001 | c0002 | t0007 | g0316 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03139 | hp2 | a0001 | c0007 | t0002 | g0126 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03209 | hp2 | a0001 | c0005 | t0006 | g0014 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0021 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0246 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0291 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03579 | hp2 | a0001 | c0005 | t0006 | g0014 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | STU | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0238 | SAS | STU | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03704 | hp1 | a0001 | c0002 | t0004 | g0053 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03710 | hp1 | a0002 | c0006 | t0005 | g0249 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0290 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0022 | SAS | BEB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0275 | SAS | BEB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0285 | SAS | BEB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0228 | SAS | BEB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0304 | SAS | STU | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | STU | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | BEB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG04199 | hp1 | a0001 | c0001 | t0009 | g0214 | SAS | STU | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0289 | SAS | STU | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0254 | SAS | STU | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | STU | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | YRI | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | YRI | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18612 | hp1 | a0001 | c0002 | t0004 | g0039 | EAS | CHB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | CHB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | CHB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | CHB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | YRI | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0147 | AFR | YRI | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0294 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18939 | hp2 | a0001 | c0004 | t0003 | g0143 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18944 | hp1 | a0001 | c0002 | t0004 | g0040 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18957 | hp2 | a0001 | c0004 | t0003 | g0142 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18966 | hp1 | a0001 | c0002 | t0004 | g0054 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18974 | hp2 | a0001 | c0001 | t0012 | g0075 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18983 | hp1 | a0003 | c0011 | t0003 | g0261 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18989 | hp2 | a0001 | c0002 | t0004 | g0048 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18994 | hp2 | a0001 | c0004 | t0003 | g0141 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19002 | hp2 | a0001 | c0002 | t0004 | g0046 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19005 | hp1 | a0001 | c0002 | t0004 | g0055 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19007 | hp1 | a0001 | c0008 | t0002 | g0029 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0273 | AFR | LWK | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | LWK | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19057 | hp1 | a0001 | c0002 | t0004 | g0044 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19058 | hp1 | a0001 | c0002 | t0004 | g0051 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19084 | hp1 | a0001 | c0002 | t0004 | g0061 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19085 | hp2 | a0001 | c0002 | t0004 | g0008 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19091 | hp2 | a0001 | c0002 | t0004 | g0041 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19240 | hp1 | a0004 | c0010 | t0003 | g0242 | AFR | YRI | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19240 | hp2 | a0001 | c0002 | t0004 | g0059 | AFR | YRI | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ASW | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ASW | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | GIH | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0227 | SAS | GIH | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02109 | hp1 | a0001 | c0002 | t0007 | g0317 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0001 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0266 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0001 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0219 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18955 | hp2 | a0001 | c0001 | t0011 | g0277 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA20300 | hp1 | a0001 | c0001 | t0013 | g0243 | AFR | USA | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0264 | AFR | USA | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | LWK | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0244 | AFR | LWK | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0230 | REF | REF | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0006 | g0151 | REF | REF | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:108162535
|
T | C | 1 | a0002 | 2 | HG01257.hp2 HG03710.hp1 |
missense_variant | MODERATE | c.1232A>G | p.Asn411Ser | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1334/3057 | 1232/1290 | 411/429 | chr3 | 108162535 | ||
| chr3:108165477
|
T | C | 1 | a0004 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.998A>G | p.Gln333Arg | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/11 | 1100/3057 | 998/1290 | 333/429 | chr3 | 108165477 | ||
| chr3:108167814
|
T | G | 1 | a0003 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.828A>C | p.Glu276Asp | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 7/11 | 930/3057 | 828/1290 | 276/429 | chr3 | 108167814 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:108165455
|
C | T | 1 | a0001c0003 | 7 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(4): Show |
synonymous_variant | LOW | c.1020G>A | p.Thr340Thr | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/11 | 1122/3057 | 1020/1290 | 340/429 | chr3 | 108165455 | ||
| chr3:108167832
|
C | T | 1 | a0001c0009 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.810G>A | p.Gln270Gln | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 7/11 | 912/3057 | 810/1290 | 270/429 | chr3 | 108167832 | ||
| chr3:108206655
|
G | A | 1 | a0001c0007 | 2 | HG01192.hp1 HG03139.hp2 |
synonymous_variant | LOW | c.627C>T | p.Asn209Asn | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/11 | 729/3057 | 627/1290 | 209/429 | chr3 | 108206655 | ||
| chr3:108218561
|
C | T | 1 | a0001c0002 | 36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
synonymous_variant | LOW | c.468G>A | p.Leu156Leu | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/11 | 570/3057 | 468/1290 | 156/429 | chr3 | 108218561 | ||
| chr3:108219425
|
G | A | 1 | a0001c0005 | 3 | HG02717.hp2 HG03209.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.360C>T | p.Ser120Ser | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/11 | 462/3057 | 360/1290 | 120/429 | chr3 | 108219425 | ||
| chr3:108219425
|
G | C | 1 | a0001c0004 | 3 | NA18939.hp2 NA18957.hp2 NA18994.hp2 |
synonymous_variant | LOW | c.360C>G | p.Ser120Ser | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/11 | 462/3057 | 360/1290 | 120/429 | chr3 | 108219425 | ||
| chr3:108222161
|
G | C | 1 | a0001c0012 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.162C>G | p.Leu54Leu | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/11 | 264/3057 | 162/1290 | 54/429 | chr3 | 108222161 | ||
| chr3:108222227
|
C | G | 1 | a0001c0008 | 1 | NA19007.hp1 | synonymous_variant | LOW | c.96G>C | p.Arg32Arg | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/11 | 198/3057 | 96/1290 | 32/429 | chr3 | 108222227 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:108160883
|
G | C | 5 | a0001c0001t0010a0001c0002t0004a0001c0002t0007others(2): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1594C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1594 | chr3 | 108160883 | |||||
| chr3:108161139
|
T | C | 12 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(9): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*1338A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1338 | chr3 | 108161139 | |||||
| chr3:108161222
|
C | CT | 9 | a0001c0001t0002a0001c0001t0010a0001c0001t0012others(6): Show | 130 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*1254dupA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1254 | chr3 | 108161222 | |||||
| chr3:108161222
|
CT | C | 5 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(2): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1254delA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1254 | chr3 | 108161222 | |||||
| chr3:108161257
|
A | C | 1 | a0001c0012t0015 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1220T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1220 | chr3 | 108161257 | |||||
| chr3:108161265
|
T | C | 1 | a0001c0001t0012 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1212A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1212 | chr3 | 108161265 | |||||
| chr3:108161295
|
T | C | 1 | a0001c0001t0008 | 2 | HG00741.hp2 HG02004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1182A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1182 | chr3 | 108161295 | |||||
| chr3:108161301
|
C | CACTA | 5 | a0001c0001t0010a0001c0002t0004a0001c0002t0007others(2): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1175_*1176insTAGT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1175 | chr3 | 108161301 | |||||
| chr3:108161306
|
T | C | 4 | a0001c0001t0010a0001c0002t0004a0001c0002t0007others(1): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1171A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1171 | chr3 | 108161306 | |||||
| chr3:108161325
|
T | C | 1 | a0001c0001t0013 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1152A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1152 | chr3 | 108161325 | |||||
| chr3:108161536
|
T | TA | 4 | a0001c0001t0010a0001c0002t0004a0001c0002t0007others(1): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*940dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 940 | chr3 | 108161536 | |||||
| chr3:108161536
|
TA | T | 17 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*940delT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 940 | chr3 | 108161536 | |||||
| chr3:108161607
|
C | T | 1 | a0001c0001t0010 | 2 | HG02818.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*870G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 870 | chr3 | 108161607 | |||||
| chr3:108161626
|
T | G | 5 | a0001c0001t0010a0001c0002t0004a0001c0002t0007others(2): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*851A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 851 | chr3 | 108161626 | |||||
| chr3:108161639
|
T | C | 1 | a0001c0001t0014 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*838A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 838 | chr3 | 108161639 | |||||
| chr3:108161673
|
T | C | 1 | a0001c0002t0007 | 4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*804A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 804 | chr3 | 108161673 | |||||
| chr3:108161818
|
T | G | 1 | a0001c0001t0009 | 2 | HG03017.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*659A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 659 | chr3 | 108161818 | |||||
| chr3:108161973
|
GT | G | 5 | a0001c0001t0010a0001c0002t0004a0001c0002t0007others(2): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*503delA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 503 | chr3 | 108161973 | |||||
| chr3:108162072
|
T | C | 5 | a0001c0001t0010a0001c0002t0004a0001c0002t0007others(2): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*405A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 405 | chr3 | 108162072 | |||||
| chr3:108162130
|
G | A | 5 | a0001c0001t0010a0001c0002t0004a0001c0002t0007others(2): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*347C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 347 | chr3 | 108162130 | |||||
| chr3:108162291
|
T | A | 5 | a0001c0001t0010a0001c0002t0004a0001c0002t0007others(2): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*186A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 186 | chr3 | 108162291 | |||||
| chr3:108162305
|
T | C | 4 | a0001c0001t0010a0001c0002t0004a0001c0002t0007others(1): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*172A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 172 | chr3 | 108162305 | |||||
| chr3:108222354
|
G | A | 1 | a0001c0002t0007 | 4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-32C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/11 | chr3 | 108222354 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:108162759
|
G | T | 1 | a0001c0001t0001g0207 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1112-104C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108162759 | ||||||
| chr3:108162854
|
G | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1112-199C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108162854 | ||||||
| chr3:108162864
|
T | C | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.1112-209A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108162864 | ||||||
| chr3:108162949
|
G | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1112-294C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108162949 | ||||||
| chr3:108162983
|
G | A | 2 | a0001c0001t0005g0030a0001c0001t0005g0031 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1112-328C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108162983 | ||||||
| chr3:108163230
|
C | A | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1111+433G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108163230 | ||||||
| chr3:108163329
|
A | C | 1 | a0001c0001t0003g0301 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1111+334T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108163329 | ||||||
| chr3:108163444
|
G | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1111+219C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108163444 | ||||||
| chr3:108163452
|
C | G | 1 | a0001c0001t0002g0071 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1111+211G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108163452 | ||||||
| chr3:108163510
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1111+153G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108163510 | ||||||
| chr3:108163651
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1111+12C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108163651 | ||||||
| chr3:108163796
|
G | A | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1045-67C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108163796 | ||||||
| chr3:108164105
|
T | C | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.1045-376A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108164105 | ||||||
| chr3:108164385
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1045-656A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108164385 | ||||||
| chr3:108164404
|
A | T | 1 | a0001c0002t0004g0045 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1045-675T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108164404 | ||||||
| chr3:108164442
|
G | A | 1 | a0001c0001t0003g0309 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1045-713C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108164442 | ||||||
| chr3:108164561
|
ACTAT | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1045-836_1045-833d others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108164561 | ||||||
| chr3:108164683
|
C | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1044+748G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108164683 | ||||||
| chr3:108164820
|
G | A | 4 | a0001c0001t0005g0247a0001c0001t0005g0248a0002c0006t0005g0231others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1044+611C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108164820 | ||||||
| chr3:108164921
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1044+510T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108164921 | ||||||
| chr3:108165122
|
G | A | 2 | a0001c0001t0005g0229a0001c0001t0005g0230 | 2 | HG01433.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1044+309C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108165122 | ||||||
| chr3:108165161
|
TG | T | 35 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(32): Show | 36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1044+269delC | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108165161 | ||||||
| chr3:108165162
|
GT | G | 3 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0012t0015g0314 | 3 | HG01891.hp2 HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1044+268delA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108165162 | ||||||
| chr3:108165180
|
A | C | 1 | a0001c0001t0003g0278 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1044+251T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108165180 | ||||||
| chr3:108165285
|
T | C | 31 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(28): Show | 32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.1044+146A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108165285 | ||||||
| chr3:108165346
|
T | G | 1 | a0001c0001t0003g0275 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1044+85A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108165346 | ||||||
| chr3:108165364
|
T | C | 315 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(312): Show | 351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.1044+67A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108165364 | ||||||
| chr3:108165373
|
C | T | 1 | a0001c0001t0005g0021 | 2 | HG01515.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1044+58G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108165373 | ||||||
| chr3:108165422
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1044+9T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108165422 | ||||||
| chr3:108165646
|
A | G | 1 | a0001c0001t0002g0116 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.982-153T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 8/10 | chr3 | 108165646 | ||||||
| chr3:108165978
|
A | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.982-485T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 8/10 | chr3 | 108165978 | ||||||
| chr3:108166081
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.982-588T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 8/10 | chr3 | 108166081 | ||||||
| chr3:108166229
|
C | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.981+625G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 8/10 | chr3 | 108166229 | ||||||
| chr3:108166258
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.981+596G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 8/10 | chr3 | 108166258 | ||||||
| chr3:108166284
|
C | T | 11 | a0001c0001t0002g0009a0001c0001t0002g0074a0001c0001t0002g0076others(8): Show | 12 | HG01358.hp1 HG01993.hp1 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.981+570G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 8/10 | chr3 | 108166284 | ||||||
| chr3:108166469
|
CTT | C | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.981+383_981+384del others(2): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 8/10 | chr3 | 108166469 | ||||||
| chr3:108166636
|
G | C | 35 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(32): Show | 36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.981+218C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 8/10 | chr3 | 108166636 | ||||||
| chr3:108166812
|
T | C | 2 | a0002c0006t0005g0231a0002c0006t0005g0249 | 2 | HG01257.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.981+42A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 8/10 | chr3 | 108166812 | ||||||
| chr3:108167028
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.850-43T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 7/10 | chr3 | 108167028 | ||||||
| chr3:108167331
|
T | G | 1 | a0001c0001t0001g0171 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.850-346A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 7/10 | chr3 | 108167331 | ||||||
| chr3:108167461
|
G | C | 1 | a0001c0001t0001g0193 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.849+332C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 7/10 | chr3 | 108167461 | ||||||
| chr3:108167774
|
C | T | 1 | a0001c0001t0003g0259 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.849+19G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 7/10 | chr3 | 108167774 | ||||||
| chr3:108167892
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.778-28A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108167892 | ||||||
| chr3:108167919
|
C | A | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-55G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108167919 | ||||||
| chr3:108168078
|
C | T | 35 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(32): Show | 36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.778-214G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108168078 | ||||||
| chr3:108168245
|
T | G | 1 | a0001c0001t0001g0197 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.778-381A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108168245 | ||||||
| chr3:108168259
|
G | A | 2 | a0001c0005t0006g0014a0001c0005t0006g0154 | 3 | HG02717.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.778-395C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108168259 | ||||||
| chr3:108168521
|
A | C | 1 | a0001c0001t0001g0203 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.778-657T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108168521 | ||||||
| chr3:108168558
|
C | T | 31 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(28): Show | 32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.778-694G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108168558 | ||||||
| chr3:108168741
|
G | A | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-877C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108168741 | ||||||
| chr3:108168863
|
A | G | 3 | a0001c0001t0005g0030a0001c0001t0005g0031a0001c0001t0005g0244 | 3 | HG02615.hp2 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.778-999T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108168863 | ||||||
| chr3:108168866
|
T | C | 3 | a0001c0001t0005g0030a0001c0001t0005g0031a0001c0001t0005g0244 | 3 | HG02615.hp2 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.778-1002A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108168866 | ||||||
| chr3:108168909
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-1045T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108168909 | ||||||
| chr3:108168974
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-1110G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108168974 | ||||||
| chr3:108169059
|
A | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-1195T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169059 | ||||||
| chr3:108169087
|
T | G | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.778-1223A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169087 | ||||||
| chr3:108169230
|
T | C | 308 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(305): Show | 343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.778-1366A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169230 | ||||||
| chr3:108169237
|
T | G | 308 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(305): Show | 343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.778-1373A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169237 | ||||||
| chr3:108169283
|
A | G | 2 | a0001c0002t0004g0057a0001c0002t0004g0058 | 2 | HG00738.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.778-1419T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169283 | ||||||
| chr3:108169401
|
A | G | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.778-1537T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169401 | ||||||
| chr3:108169466
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.778-1602G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169466 | ||||||
| chr3:108169513
|
A | G | 150 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(147): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.778-1649T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169513 | ||||||
| chr3:108169596
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-1732G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169596 | ||||||
| chr3:108169676
|
A | T | 35 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(32): Show | 36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.778-1812T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169676 | ||||||
| chr3:108169821
|
C | G | 1 | a0001c0001t0003g0278 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.778-1957G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169821 | ||||||
| chr3:108169887
|
G | A | 316 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(313): Show | 352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.778-2023C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169887 | ||||||
| chr3:108169910
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-2046G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169910 | ||||||
| chr3:108169994
|
T | G | 16 | a0001c0001t0001g0234a0001c0001t0005g0021a0001c0001t0005g0022others(13): Show | 18 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.778-2130A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169994 | ||||||
| chr3:108170020
|
T | C | 94 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(91): Show | 104 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.778-2156A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108170020 | ||||||
| chr3:108170085
|
G | A | 4 | a0001c0001t0001g0172a0001c0001t0001g0196a0001c0001t0001g0197others(1): Show | 4 | HG01255.hp1 HG01261.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-2221C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108170085 | ||||||
| chr3:108170295
|
G | A | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.778-2431C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108170295 | ||||||
| chr3:108170402
|
G | T | 1 | a0001c0001t0002g0098 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.778-2538C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108170402 | ||||||
| chr3:108170668
|
C | CA | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(78): Show | 96 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.778-2805dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108170668 | ||||||
| chr3:108170900
|
G | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-3036C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108170900 | ||||||
| chr3:108170913
|
A | G | 1 | a0001c0001t0003g0155 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.778-3049T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108170913 | ||||||
| chr3:108170956
|
C | A | 1 | a0001c0001t0001g0307 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.778-3092G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108170956 | ||||||
| chr3:108171116
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-3252A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171116 | ||||||
| chr3:108171132
|
C | G | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-3268G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171132 | ||||||
| chr3:108171214
|
G | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-3350C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171214 | ||||||
| chr3:108171371
|
C | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.778-3507G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171371 | ||||||
| chr3:108171401
|
T | C | 2 | a0001c0003t0001g0223a0001c0003t0001g0224 | 2 | HG02280.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.778-3537A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171401 | ||||||
| chr3:108171421
|
A | C | 1 | a0001c0001t0002g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.778-3557T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171421 | ||||||
| chr3:108171457
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-3593A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171457 | ||||||
| chr3:108171469
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.778-3605C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171469 | ||||||
| chr3:108171483
|
G | A | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-3619C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171483 | ||||||
| chr3:108171548
|
G | A | 1 | a0001c0001t0006g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.778-3684C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171548 | ||||||
| chr3:108171573
|
G | A | 1 | a0001c0001t0003g0260 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.778-3709C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171573 | ||||||
| chr3:108171613
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-3749T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171613 | ||||||
| chr3:108171654
|
G | A | 4 | a0001c0001t0005g0247a0001c0001t0005g0248a0002c0006t0005g0231others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-3790C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171654 | ||||||
| chr3:108171657
|
T | C | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-3793A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171657 | ||||||
| chr3:108171685
|
C | G | 2 | a0001c0001t0001g0200a0001c0001t0001g0203 | 2 | HG01243.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.778-3821G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171685 | ||||||
| chr3:108171716
|
A | G | 2 | a0001c0001t0010g0144a0001c0001t0010g0145 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.778-3852T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171716 | ||||||
| chr3:108171951
|
G | GCATA | 85 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(82): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.778-4091_778-4088d others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171951 | ||||||
| chr3:108172080
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-4216A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108172080 | ||||||
| chr3:108172151
|
T | C | 6 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(3): Show | 6 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-4287A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108172151 | ||||||
| chr3:108172218
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-4354G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108172218 | ||||||
| chr3:108172298
|
C | A | 3 | a0001c0002t0004g0032a0001c0002t0004g0051a0001c0002t0004g0061 | 3 | HG02129.hp2 NA19058.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.778-4434G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108172298 | ||||||
| chr3:108172335
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.778-4471C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108172335 | ||||||
| chr3:108172349
|
A | G | 40 | a0001c0001t0005g0030a0001c0001t0005g0031a0001c0001t0010g0144others(37): Show | 41 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.778-4485T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108172349 | ||||||
| chr3:108172366
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-4502T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108172366 | ||||||
| chr3:108172604
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-4740T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108172604 | ||||||
| chr3:108172726
|
G | A | 3 | a0001c0001t0001g0195a0001c0001t0001g0220a0001c0001t0001g0222 | 3 | HG00280.hp2 HG02451.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.778-4862C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108172726 | ||||||
| chr3:108172923
|
A | G | 2 | a0001c0001t0002g0087a0001c0001t0002g0105 | 2 | NA19084.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.778-5059T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108172923 | ||||||
| chr3:108173186
|
C | A | 1 | a0001c0001t0003g0241 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.778-5322G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173186 | ||||||
| chr3:108173230
|
T | C | 90 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(87): Show | 100 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.778-5366A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173230 | ||||||
| chr3:108173250
|
T | C | 1 | a0001c0002t0004g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.778-5386A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173250 | ||||||
| chr3:108173254
|
A | AAC | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00673.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.778-5392_778-5391d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173254 | ||||||
| chr3:108173728
|
G | A | 1 | a0001c0001t0003g0273 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.778-5864C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173728 | ||||||
| chr3:108173766
|
C | CTG | 38 | a0001c0001t0001g0163a0001c0001t0001g0183a0001c0001t0001g0184others(35): Show | 43 | HG00408.hp1 HG00621.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.778-5904_778-5903d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | ||||||
| chr3:108173766
|
C | CTGTG | 23 | a0001c0001t0002g0003a0001c0001t0002g0067a0001c0001t0002g0068others(20): Show | 25 | HG00558.hp2 HG01192.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.778-5906_778-5903d others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | ||||||
| chr3:108173766
|
C | CTGTGTG | 7 | a0001c0001t0002g0009a0001c0001t0002g0079a0001c0001t0002g0099others(4): Show | 8 | HG02683.hp1 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.778-5908_778-5903d others(8): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | ||||||
| chr3:108173766
|
C | CTGTGTGT others(1): Show |
5 | a0001c0001t0002g0072a0001c0001t0002g0078a0001c0001t0002g0089others(2): Show | 5 | HG00673.hp2 HG01934.hp2 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-5910_778-5903d others(10): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | ||||||
| chr3:108173766
|
C | CTGTGTGT others(3): Show |
4 | a0001c0001t0002g0084a0001c0001t0002g0121a0001c0001t0002g0131others(1): Show | 4 | HG00642.hp2 HG01167.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-5912_778-5903d others(12): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | ||||||
| chr3:108173766
|
C | CTGTGTGT others(5): Show |
3 | a0001c0001t0002g0125a0001c0001t0002g0132a0001c0001t0006g0149 | 3 | HG02257.hp1 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.778-5914_778-5903d others(14): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | ||||||
| chr3:108173766
|
C | CTGTGTGT others(13): Show |
2 | a0001c0001t0003g0302a0001c0001t0003g0303 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.778-5922_778-5903d others(22): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | ||||||
| chr3:108173766
|
CTG | C | 29 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0190others(26): Show | 31 | HG00423.hp2 HG00741.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.778-5904_778-5903d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | ||||||
| chr3:108173766
|
CTGTG | C | 78 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(75): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.778-5906_778-5903d others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | ||||||
| chr3:108173766
|
CTGTGTG | C | 38 | a0001c0001t0001g0200a0001c0001t0003g0309a0001c0001t0005g0232others(35): Show | 43 | HG00408.hp2 HG00558.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.778-5908_778-5903d others(8): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | ||||||
| chr3:108173766
|
CTGTGTGT others(1): Show |
C | 5 | a0001c0001t0001g0164a0001c0001t0001g0203a0001c0001t0002g0111others(2): Show | 5 | HG01070.hp2 NA18951.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-5910_778-5903d others(10): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | ||||||
| chr3:108173798
|
GTGTGTGT others(7): Show |
G | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-5948_778-5935d others(16): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173798 | ||||||
| chr3:108173806
|
G | A | 33 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(30): Show | 34 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.778-5942C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173806 | ||||||
| chr3:108173808
|
G | A | 66 | a0001c0001t0001g0234a0001c0001t0001g0251a0001c0001t0003g0241others(63): Show | 70 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.778-5944C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173808 | ||||||
| chr3:108173808
|
G | GTA | 13 | a0001c0001t0003g0023a0001c0001t0003g0225a0001c0001t0003g0226others(10): Show | 14 | HG00423.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.778-5946_778-5945d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173808 | ||||||
| chr3:108173808
|
G | GTGTA | 5 | a0001c0001t0003g0253a0001c0001t0003g0270a0001c0001t0003g0272others(2): Show | 5 | HG02080.hp1 HG02922.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-5945_778-5944i others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173808 | ||||||
| chr3:108173808
|
G | GTGTGTA | 16 | a0001c0001t0003g0007a0001c0001t0003g0155a0001c0001t0003g0260others(13): Show | 18 | HG02155.hp2 HG02165.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.778-5945_778-5944i others(8): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173808 | ||||||
| chr3:108173808
|
G | GTGTGTGT others(1): Show |
26 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(23): Show | 30 | HG00642.hp1 HG01515.hp1 HG02071.hp1 others(27): Show |
intron_variant | MODIFIER | c.778-5945_778-5944i others(10): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173808 | ||||||
| chr3:108173808
|
G | GTGTGTGT others(3): Show |
5 | a0001c0001t0003g0062a0001c0001t0003g0273a0001c0001t0003g0289others(2): Show | 5 | HG03041.hp1 HG04199.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-5945_778-5944i others(12): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173808 | ||||||
| chr3:108173808
|
G | GTGTGTGT others(11): Show |
1 | a0001c0001t0003g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.778-5945_778-5944i others(20): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173808 | ||||||
| chr3:108173810
|
A | G | 5 | a0001c0001t0002g0087a0001c0001t0002g0089a0001c0001t0002g0105others(2): Show | 5 | HG02074.hp2 NA18991.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-5946T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173810 | ||||||
| chr3:108173870
|
C | CA | 6 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(3): Show | 7 | HG00408.hp2 HG02080.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.778-6007dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173870 | ||||||
| chr3:108173871
|
A | G | 1 | a0001c0001t0003g0289 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.778-6007T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173871 | ||||||
| chr3:108173934
|
T | C | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.778-6070A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173934 | ||||||
| chr3:108173997
|
A | AAT | 78 | a0001c0001t0001g0158a0001c0001t0001g0161a0001c0001t0001g0165others(75): Show | 82 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.778-6134_778-6133i others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173997 | ||||||
| chr3:108173997
|
A | AATGT | 84 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0002g0002others(81): Show | 98 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.778-6134_778-6133i others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173997 | ||||||
| chr3:108173997
|
A | AATGTGT | 22 | a0001c0001t0001g0217a0001c0001t0002g0067a0001c0001t0002g0079others(19): Show | 22 | HG01891.hp1 HG02135.hp1 HG02155.hp2 others(19): Show |
intron_variant | MODIFIER | c.778-6134_778-6133i others(8): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173997 | ||||||
| chr3:108173997
|
A | AATGTGTG others(1): Show |
7 | a0001c0001t0003g0264a0001c0001t0003g0265a0001c0001t0003g0266others(4): Show | 7 | HG02165.hp1 HG02165.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.778-6134_778-6133i others(10): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173997 | ||||||
| chr3:108173997
|
AGT | A | 20 | a0001c0001t0001g0019a0001c0001t0001g0168a0001c0001t0001g0170others(17): Show | 21 | HG00738.hp2 HG01099.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.778-6135_778-6134d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173997 | ||||||
| chr3:108173997
|
AGTGT | A | 3 | a0001c0001t0001g0171a0001c0001t0003g0062a0001c0003t0001g0223 | 3 | HG01192.hp2 HG02896.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.778-6137_778-6134d others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173997 | ||||||
| chr3:108173997
|
AGTGTGT | A | 3 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0306 | 3 | HG01069.hp2 HG01071.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.778-6139_778-6134d others(8): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173997 | ||||||
| chr3:108173997
|
AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0001g0307 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.778-6145_778-6134d others(14): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173997 | ||||||
| chr3:108173997
|
AGTGTGTG others(13): Show |
A | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-6153_778-6134d others(22): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173997 | ||||||
| chr3:108173998
|
G | A | 95 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(92): Show | 112 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.778-6134C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173998 | ||||||
| chr3:108174000
|
G | A | 20 | a0001c0001t0001g0019a0001c0001t0001g0168a0001c0001t0001g0170others(17): Show | 21 | HG00738.hp2 HG01099.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.778-6136C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174000 | ||||||
| chr3:108174002
|
G | A | 3 | a0001c0001t0001g0171a0001c0001t0003g0062a0001c0003t0001g0223 | 3 | HG01192.hp2 HG02896.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.778-6138C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174002 | ||||||
| chr3:108174004
|
G | A | 3 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0306 | 3 | HG01069.hp2 HG01071.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.778-6140C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174004 | ||||||
| chr3:108174006
|
G | A | 2 | a0001c0001t0001g0305a0001c0001t0003g0155 | 2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.778-6142C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174006 | ||||||
| chr3:108174010
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.778-6146C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174010 | ||||||
| chr3:108174018
|
G | A | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-6154C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174018 | ||||||
| chr3:108174019
|
T | C | 2 | a0001c0001t0003g0225a0001c0001t0003g0226 | 2 | HG02145.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.778-6155A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174019 | ||||||
| chr3:108174045
|
T | TGTG | 4 | a0001c0001t0003g0287a0001c0001t0005g0233a0001c0001t0005g0304others(1): Show | 4 | HG02602.hp1 HG02738.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.778-6182_778-6181i others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174045 | ||||||
| chr3:108174045
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0218 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.778-6182_778-6181i others(13): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174045 | ||||||
| chr3:108174046
|
T | G | 1 | a0001c0003t0001g0219 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.778-6182A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174046 | ||||||
| chr3:108174155
|
G | T | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-6291C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174155 | ||||||
| chr3:108174194
|
G | T | 59 | a0001c0001t0003g0007a0001c0001t0003g0023a0001c0001t0003g0024others(56): Show | 66 | HG00423.hp1 HG00642.hp1 HG01256.hp1 others(63): Show |
intron_variant | MODIFIER | c.778-6330C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174194 | ||||||
| chr3:108174211
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-6347T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174211 | ||||||
| chr3:108174302
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-6438A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174302 | ||||||
| chr3:108174314
|
T | C | 1 | a0001c0001t0002g0110 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.778-6450A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174314 | ||||||
| chr3:108174344
|
TGAA | T | 122 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(119): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.778-6483_778-6481d others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174344 | ||||||
| chr3:108174393
|
C | T | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-6529G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174393 | ||||||
| chr3:108174414
|
C | T | 1 | a0001c0002t0004g0049 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.778-6550G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174414 | ||||||
| chr3:108174457
|
G | A | 1 | a0001c0001t0002g0092 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.778-6593C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174457 | ||||||
| chr3:108174474
|
T | TTACAATG others(313): Show |
2 | a0001c0002t0007g0316a0001c0002t0007g0318 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.778-6611_778-6610i others(322): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174474 | ||||||
| chr3:108174474
|
T | TTACAATG others(314): Show |
2 | a0001c0002t0007g0315a0001c0002t0007g0317 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.778-6611_778-6610i others(323): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174474 | ||||||
| chr3:108174474
|
T | TTACAATG others(319): Show |
9 | a0001c0002t0004g0032a0001c0002t0004g0033a0001c0002t0004g0040others(6): Show | 9 | HG00408.hp2 HG00558.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.778-6611_778-6610i others(328): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174474 | ||||||
| chr3:108174474
|
T | TTACAATG others(320): Show |
8 | a0001c0002t0004g0008a0001c0002t0004g0039a0001c0002t0004g0041others(5): Show | 9 | HG00673.hp1 HG01346.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.778-6611_778-6610i others(329): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174474 | ||||||
| chr3:108174474
|
T | TTACAATG others(321): Show |
8 | a0001c0002t0004g0037a0001c0002t0004g0044a0001c0002t0004g0045others(5): Show | 8 | HG00738.hp2 HG01255.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.778-6611_778-6610i others(330): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174474 | ||||||
| chr3:108174474
|
T | TTACAATG others(322): Show |
2 | a0001c0002t0004g0048a0001c0002t0004g0054 | 2 | NA18966.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.778-6611_778-6610i others(331): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174474 | ||||||
| chr3:108174474
|
T | TTACAATG others(323): Show |
2 | a0001c0002t0004g0034a0001c0002t0004g0056 | 2 | HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.778-6611_778-6610i others(332): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174474 | ||||||
| chr3:108174474
|
T | TTACAATG others(324): Show |
1 | a0001c0002t0004g0035 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.778-6611_778-6610i others(333): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174474 | ||||||
| chr3:108174474
|
T | TTACAATG others(325): Show |
1 | a0001c0002t0004g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.778-6611_778-6610i others(334): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174474 | ||||||
| chr3:108174581
|
T | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-6717A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174581 | ||||||
| chr3:108174620
|
T | A | 1 | a0001c0001t0013g0243 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.778-6756A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174620 | ||||||
| chr3:108174630
|
A | T | 1 | a0001c0001t0013g0243 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.778-6766T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174630 | ||||||
| chr3:108174669
|
T | C | 1 | a0001c0001t0013g0243 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.778-6805A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174669 | ||||||
| chr3:108174732
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-6868A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174732 | ||||||
| chr3:108174790
|
C | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-6926G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174790 | ||||||
| chr3:108174893
|
A | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.778-7029T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174893 | ||||||
| chr3:108174924
|
G | A | 1 | a0001c0001t0005g0239 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.778-7060C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174924 | ||||||
| chr3:108174927
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.778-7063A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174927 | ||||||
| chr3:108174944
|
A | G | 1 | a0001c0001t0002g0086 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.778-7080T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174944 | ||||||
| chr3:108174979
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.778-7115T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174979 | ||||||
| chr3:108175003
|
A | G | 65 | a0001c0001t0003g0007a0001c0001t0003g0023a0001c0001t0003g0024others(62): Show | 72 | HG00423.hp1 HG00642.hp1 HG01256.hp1 others(69): Show |
intron_variant | MODIFIER | c.778-7139T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175003 | ||||||
| chr3:108175054
|
T | C | 1 | a0001c0001t0002g0120 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.778-7190A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175054 | ||||||
| chr3:108175125
|
G | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-7261C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175125 | ||||||
| chr3:108175160
|
G | T | 1 | a0001c0001t0001g0171 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.778-7296C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175160 | ||||||
| chr3:108175195
|
G | A | 1 | a0001c0001t0001g0308 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.778-7331C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175195 | ||||||
| chr3:108175257
|
T | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-7393A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175257 | ||||||
| chr3:108175270
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-7406A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175270 | ||||||
| chr3:108175386
|
G | A | 4 | a0001c0001t0003g0062a0001c0001t0003g0063a0001c0001t0003g0064others(1): Show | 4 | HG02622.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-7522C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175386 | ||||||
| chr3:108175504
|
A | T | 1 | a0001c0001t0001g0167 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.778-7640T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175504 | ||||||
| chr3:108175539
|
T | C | 85 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(82): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.778-7675A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175539 | ||||||
| chr3:108175558
|
G | A | 2 | a0001c0001t0003g0146a0001c0001t0006g0149 | 2 | HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.778-7694C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175558 | ||||||
| chr3:108175645
|
C | A | 35 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(32): Show | 36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.778-7781G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175645 | ||||||
| chr3:108175722
|
A | G | 2 | a0001c0001t0003g0146a0001c0001t0006g0149 | 2 | HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.778-7858T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175722 | ||||||
| chr3:108175745
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-7881A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175745 | ||||||
| chr3:108175802
|
TA | T | 25 | a0001c0001t0001g0234a0001c0001t0001g0251a0001c0001t0002g0133others(22): Show | 27 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.778-7939delT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175802 | ||||||
| chr3:108175832
|
G | A | 85 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(82): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.778-7968C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175832 | ||||||
| chr3:108175972
|
C | A | 3 | a0001c0001t0003g0225a0001c0001t0003g0226a0001c0001t0003g0246 | 3 | HG02145.hp2 HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.778-8108G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175972 | ||||||
| chr3:108175993
|
C | A | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.778-8129G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175993 | ||||||
| chr3:108176063
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.778-8199G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176063 | ||||||
| chr3:108176142
|
G | A | 31 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(28): Show | 32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.778-8278C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176142 | ||||||
| chr3:108176191
|
T | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-8327A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176191 | ||||||
| chr3:108176211
|
G | A | 1 | a0001c0001t0014g0240 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.778-8347C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176211 | ||||||
| chr3:108176212
|
C | A | 1 | a0001c0001t0014g0240 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.778-8348G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176212 | ||||||
| chr3:108176280
|
T | C | 1 | a0001c0001t0006g0147 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.778-8416A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176280 | ||||||
| chr3:108176360
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-8496G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176360 | ||||||
| chr3:108176361
|
A | G | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.778-8497T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176361 | ||||||
| chr3:108176479
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-8615T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176479 | ||||||
| chr3:108176550
|
A | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0172others(12): Show | 18 | HG00099.hp2 HG00738.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.778-8686T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176550 | ||||||
| chr3:108176649
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-8785A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176649 | ||||||
| chr3:108176670
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.778-8806C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176670 | ||||||
| chr3:108176695
|
C | T | 1 | a0001c0001t0003g0241 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.778-8831G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176695 | ||||||
| chr3:108176697
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.778-8833G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176697 | ||||||
| chr3:108176732
|
T | C | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.778-8868A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176732 | ||||||
| chr3:108176736
|
C | T | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.778-8872G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176736 | ||||||
| chr3:108176746
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-8882G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176746 | ||||||
| chr3:108176887
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-9023A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176887 | ||||||
| chr3:108176914
|
A | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-9050T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176914 | ||||||
| chr3:108177027
|
T | C | 6 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(3): Show | 6 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-9163A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177027 | ||||||
| chr3:108177044
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-9180A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177044 | ||||||
| chr3:108177054
|
T | C | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-9190A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177054 | ||||||
| chr3:108177228
|
T | C | 31 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(28): Show | 32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.778-9364A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177228 | ||||||
| chr3:108177261
|
C | T | 24 | a0001c0001t0001g0234a0001c0001t0001g0251a0001c0001t0005g0021others(21): Show | 26 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.778-9397G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177261 | ||||||
| chr3:108177275
|
C | T | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0176 | 3 | HG01099.hp1 HG01109.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.778-9411G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177275 | ||||||
| chr3:108177319
|
T | C | 1 | a0001c0001t0005g0235 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.778-9455A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177319 | ||||||
| chr3:108177324
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-9460A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177324 | ||||||
| chr3:108177334
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.778-9470G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177334 | ||||||
| chr3:108177421
|
C | A | 90 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(87): Show | 100 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.778-9557G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177421 | ||||||
| chr3:108177617
|
T | C | 1 | a0001c0001t0002g0128 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.778-9753A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177617 | ||||||
| chr3:108177639
|
A | AT | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-9776_778-9775i others(3): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177639 | ||||||
| chr3:108177715
|
T | C | 31 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(28): Show | 32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.778-9851A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177715 | ||||||
| chr3:108177722
|
G | A | 5 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(2): Show | 6 | HG00741.hp2 HG01099.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-9858C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177722 | ||||||
| chr3:108177770
|
T | G | 1 | a0001c0001t0001g0174 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.778-9906A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177770 | ||||||
| chr3:108177864
|
C | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-10000G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177864 | ||||||
| chr3:108177937
|
T | C | 2 | a0001c0001t0005g0030a0001c0001t0005g0031 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.778-10073A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177937 | ||||||
| chr3:108177955
|
T | C | 1 | a0001c0001t0009g0221 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.778-10091A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177955 | ||||||
| chr3:108178030
|
T | C | 5 | a0001c0001t0003g0146a0001c0001t0006g0147a0001c0001t0006g0148others(2): Show | 5 | HG02647.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-10166A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178030 | ||||||
| chr3:108178125
|
A | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-10261T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178125 | ||||||
| chr3:108178137
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-10273A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178137 | ||||||
| chr3:108178365
|
T | G | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-10501A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178365 | ||||||
| chr3:108178392
|
A | G | 39 | a0001c0001t0003g0275a0001c0001t0010g0144a0001c0001t0010g0145others(36): Show | 40 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.778-10528T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178392 | ||||||
| chr3:108178447
|
G | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-10583C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178447 | ||||||
| chr3:108178660
|
C | T | 1 | a0001c0001t0003g0274 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.778-10796G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178660 | ||||||
| chr3:108178698
|
C | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-10834G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178698 | ||||||
| chr3:108178807
|
T | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-10943A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178807 | ||||||
| chr3:108178841
|
C | T | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-10977G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178841 | ||||||
| chr3:108178859
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-10995G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178859 | ||||||
| chr3:108178891
|
AATTCCAG others(13): Show |
A | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.778-11047_778-1102 others(24): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178891 | ||||||
| chr3:108178906
|
G | A | 1 | a0001c0001t0005g0236 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.778-11042C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178906 | ||||||
| chr3:108179073
|
C | T | 2 | a0001c0001t0001g0251a0001c0001t0005g0252 | 2 | HG00280.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.778-11209G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179073 | ||||||
| chr3:108179089
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.778-11225C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179089 | ||||||
| chr3:108179289
|
G | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-11425C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179289 | ||||||
| chr3:108179424
|
C | T | 2 | a0001c0001t0002g0087a0001c0012t0015g0314 | 2 | HG01891.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.778-11560G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179424 | ||||||
| chr3:108179425
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.778-11561C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179425 | ||||||
| chr3:108179584
|
C | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0177a0001c0001t0001g0178others(1): Show | 6 | HG02040.hp1 HG02074.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-11720G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179584 | ||||||
| chr3:108179682
|
G | A | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.778-11818C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179682 | ||||||
| chr3:108179701
|
T | C | 1 | a0001c0001t0005g0244 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.777+11820A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179701 | ||||||
| chr3:108179716
|
T | C | 1 | a0001c0001t0002g0072 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.777+11805A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179716 | ||||||
| chr3:108179746
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+11775G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179746 | ||||||
| chr3:108179771
|
G | A | 1 | a0001c0001t0003g0288 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.777+11750C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179771 | ||||||
| chr3:108179786
|
T | G | 4 | a0001c0001t0002g0082a0001c0001t0002g0083a0001c0001t0002g0100others(1): Show | 4 | HG02523.hp1 NA18943.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+11735A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179786 | ||||||
| chr3:108179880
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+11641G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179880 | ||||||
| chr3:108179881
|
G | A | 1 | a0001c0001t0002g0089 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.777+11640C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179881 | ||||||
| chr3:108179905
|
T | TA | 315 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(312): Show | 351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.777+11615dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179905 | ||||||
| chr3:108180156
|
G | C | 1 | a0001c0001t0002g0079 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.777+11365C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108180156 | ||||||
| chr3:108180242
|
A | G | 1 | a0001c0001t0002g0105 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.777+11279T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108180242 | ||||||
| chr3:108180475
|
C | A | 1 | a0001c0002t0004g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.777+11046G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108180475 | ||||||
| chr3:108180491
|
C | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+11030G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108180491 | ||||||
| chr3:108180666
|
T | C | 24 | a0001c0001t0001g0234a0001c0001t0001g0251a0001c0001t0005g0021others(21): Show | 26 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.777+10855A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108180666 | ||||||
| chr3:108180670
|
C | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+10851G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108180670 | ||||||
| chr3:108180733
|
T | C | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+10788A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108180733 | ||||||
| chr3:108180801
|
C | T | 1 | a0001c0001t0003g0256 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.777+10720G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108180801 | ||||||
| chr3:108180811
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+10710G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108180811 | ||||||
| chr3:108180985
|
A | G | 5 | a0001c0001t0003g0146a0001c0001t0006g0147a0001c0001t0006g0148others(2): Show | 5 | HG02647.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.777+10536T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108180985 | ||||||
| chr3:108181009
|
T | C | 4 | a0001c0002t0007g0315a0001c0002t0007g0316a0001c0002t0007g0317others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+10512A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181009 | ||||||
| chr3:108181064
|
C | T | 64 | a0001c0001t0003g0007a0001c0001t0003g0023a0001c0001t0003g0024others(61): Show | 71 | HG00423.hp1 HG00642.hp1 HG01256.hp1 others(68): Show |
intron_variant | MODIFIER | c.777+10457G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181064 | ||||||
| chr3:108181114
|
A | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+10407T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181114 | ||||||
| chr3:108181117
|
G | A | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.777+10404C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181117 | ||||||
| chr3:108181173
|
C | A | 308 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(305): Show | 343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.777+10348G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181173 | ||||||
| chr3:108181255
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+10266T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181255 | ||||||
| chr3:108181260
|
C | CT | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+10260dupA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181260 | ||||||
| chr3:108181471
|
A | C | 6 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(3): Show | 6 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+10050T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181471 | ||||||
| chr3:108181515
|
G | A | 1 | a0001c0002t0004g0056 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.777+10006C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181515 | ||||||
| chr3:108181577
|
C | T | 80 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(77): Show | 90 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.777+9944G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181577 | ||||||
| chr3:108181604
|
T | C | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+9917A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181604 | ||||||
| chr3:108181655
|
G | A | 1 | a0001c0001t0005g0237 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.777+9866C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181655 | ||||||
| chr3:108181795
|
G | A | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.777+9726C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181795 | ||||||
| chr3:108181892
|
G | A | 39 | a0001c0001t0003g0241a0001c0001t0010g0144a0001c0001t0010g0145others(36): Show | 40 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.777+9629C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181892 | ||||||
| chr3:108182032
|
T | A | 308 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(305): Show | 343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.777+9489A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182032 | ||||||
| chr3:108182218
|
G | A | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+9303C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182218 | ||||||
| chr3:108182313
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.777+9208G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182313 | ||||||
| chr3:108182337
|
G | A | 27 | a0001c0001t0001g0234a0001c0001t0001g0251a0001c0001t0005g0021others(24): Show | 29 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.777+9184C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182337 | ||||||
| chr3:108182375
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+9146A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182375 | ||||||
| chr3:108182397
|
G | C | 1 | a0001c0001t0005g0244 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.777+9124C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182397 | ||||||
| chr3:108182409
|
T | G | 1 | a0001c0002t0004g0046 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.777+9112A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182409 | ||||||
| chr3:108182410
|
G | A | 1 | a0001c0001t0002g0129 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.777+9111C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182410 | ||||||
| chr3:108182758
|
C | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+8763G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182758 | ||||||
| chr3:108182796
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+8725A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182796 | ||||||
| chr3:108182834
|
A | T | 80 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(77): Show | 90 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.777+8687T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182834 | ||||||
| chr3:108182901
|
T | C | 1 | a0001c0001t0013g0243 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.777+8620A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182901 | ||||||
| chr3:108182975
|
G | C | 31 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(28): Show | 32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.777+8546C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182975 | ||||||
| chr3:108183021
|
A | G | 85 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(82): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.777+8500T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183021 | ||||||
| chr3:108183212
|
C | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+8309G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183212 | ||||||
| chr3:108183236
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+8285G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183236 | ||||||
| chr3:108183253
|
C | G | 1 | a0001c0001t0012g0075 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.777+8268G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183253 | ||||||
| chr3:108183312
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.777+8209G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183312 | ||||||
| chr3:108183381
|
C | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+8140G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183381 | ||||||
| chr3:108183542
|
C | A | 1 | a0001c0001t0002g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.777+7979G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183542 | ||||||
| chr3:108183609
|
T | C | 2 | a0001c0001t0005g0030a0001c0001t0005g0031 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.777+7912A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183609 | ||||||
| chr3:108183617
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+7904A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183617 | ||||||
| chr3:108183631
|
G | C | 1 | a0001c0002t0004g0047 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.777+7890C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183631 | ||||||
| chr3:108183646
|
A | C | 90 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(87): Show | 100 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.777+7875T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183646 | ||||||
| chr3:108183655
|
G | A | 3 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134 | 3 | HG02257.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.777+7866C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183655 | ||||||
| chr3:108183665
|
A | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+7856T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183665 | ||||||
| chr3:108183686
|
T | C | 317 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(314): Show | 353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.777+7835A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183686 | ||||||
| chr3:108183746
|
T | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+7775A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183746 | ||||||
| chr3:108183877
|
C | G | 1 | a0001c0001t0002g0120 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.777+7644G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183877 | ||||||
| chr3:108184036
|
A | G | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+7485T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184036 | ||||||
| chr3:108184052
|
A | T | 4 | a0001c0002t0007g0315a0001c0002t0007g0316a0001c0002t0007g0317others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+7469T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184052 | ||||||
| chr3:108184100
|
G | A | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.777+7421C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184100 | ||||||
| chr3:108184101
|
T | G | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.777+7420A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184101 | ||||||
| chr3:108184119
|
C | T | 9 | a0001c0001t0002g0010a0001c0001t0002g0080a0001c0001t0002g0088others(6): Show | 10 | HG01361.hp1 HG02132.hp1 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.777+7402G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184119 | ||||||
| chr3:108184154
|
G | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+7367C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184154 | ||||||
| chr3:108184228
|
A | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+7293T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184228 | ||||||
| chr3:108184306
|
C | T | 1 | a0001c0001t0002g0086 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.777+7215G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184306 | ||||||
| chr3:108184335
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.777+7186A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184335 | ||||||
| chr3:108184369
|
T | A | 27 | a0001c0001t0001g0234a0001c0001t0001g0251a0001c0001t0005g0021others(24): Show | 29 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.777+7152A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184369 | ||||||
| chr3:108184515
|
T | C | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.777+7006A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184515 | ||||||
| chr3:108184517
|
C | CA | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+7003dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184517 | ||||||
| chr3:108184582
|
T | C | 4 | a0001c0001t0003g0062a0001c0001t0003g0063a0001c0001t0003g0064others(1): Show | 4 | HG02622.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+6939A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184582 | ||||||
| chr3:108184639
|
A | G | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+6882T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184639 | ||||||
| chr3:108184668
|
T | C | 1 | a0001c0001t0002g0111 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.777+6853A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184668 | ||||||
| chr3:108184734
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+6787A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184734 | ||||||
| chr3:108184941
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+6580A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184941 | ||||||
| chr3:108185137
|
T | C | 4 | a0001c0001t0003g0062a0001c0001t0003g0063a0001c0001t0003g0064others(1): Show | 4 | HG02622.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+6384A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185137 | ||||||
| chr3:108185200
|
A | G | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+6321T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185200 | ||||||
| chr3:108185223
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+6298T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185223 | ||||||
| chr3:108185255
|
C | T | 7 | a0001c0001t0002g0003a0001c0001t0002g0097a0001c0001t0002g0098others(4): Show | 9 | HG00558.hp2 HG01496.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.777+6266G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185255 | ||||||
| chr3:108185258
|
C | G | 4 | a0001c0002t0007g0315a0001c0002t0007g0316a0001c0002t0007g0317others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+6263G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185258 | ||||||
| chr3:108185374
|
G | A | 1 | a0001c0002t0004g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.777+6147C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185374 | ||||||
| chr3:108185474
|
C | T | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188 | 3 | HG03130.hp2 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.777+6047G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185474 | ||||||
| chr3:108185551
|
A | AT | 95 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0020others(92): Show | 107 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.777+5969dupA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185551 | ||||||
| chr3:108185551
|
A | ATT | 29 | a0001c0001t0001g0018a0001c0001t0001g0159a0001c0001t0001g0178others(26): Show | 32 | HG00423.hp1 HG01071.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.777+5968_777+5969d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185551 | ||||||
| chr3:108185551
|
AT | A | 74 | a0001c0001t0001g0170a0001c0001t0002g0002a0001c0001t0002g0003others(71): Show | 84 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.777+5969delA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185551 | ||||||
| chr3:108185591
|
G | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+5930C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185591 | ||||||
| chr3:108185595
|
G | T | 65 | a0001c0001t0003g0007a0001c0001t0003g0023a0001c0001t0003g0024others(62): Show | 72 | HG00423.hp1 HG00642.hp1 HG01256.hp1 others(69): Show |
intron_variant | MODIFIER | c.777+5926C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185595 | ||||||
| chr3:108185619
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.777+5902G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185619 | ||||||
| chr3:108185636
|
G | A | 1 | a0001c0001t0003g0146 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.777+5885C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185636 | ||||||
| chr3:108185780
|
G | C | 1 | a0001c0001t0001g0204 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.777+5741C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185780 | ||||||
| chr3:108185821
|
T | C | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.777+5700A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185821 | ||||||
| chr3:108185834
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.777+5687T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185834 | ||||||
| chr3:108185925
|
G | A | 1 | a0001c0001t0001g0019 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.777+5596C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185925 | ||||||
| chr3:108186000
|
G | A | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.777+5521C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186000 | ||||||
| chr3:108186182
|
T | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.777+5339A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186182 | ||||||
| chr3:108186257
|
C | T | 1 | a0001c0001t0013g0243 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.777+5264G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186257 | ||||||
| chr3:108186321
|
C | CA | 87 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(84): Show | 98 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.777+5199dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186321 | ||||||
| chr3:108186321
|
C | CAA | 39 | a0001c0001t0001g0015a0001c0001t0001g0159a0001c0001t0001g0160others(36): Show | 42 | HG00280.hp1 HG00735.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.777+5198_777+5199d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186321 | ||||||
| chr3:108186321
|
C | CAAA | 140 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(137): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.777+5197_777+5199d others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186321 | ||||||
| chr3:108186321
|
C | CAAAA | 6 | a0001c0001t0001g0178a0001c0001t0001g0180a0001c0001t0003g0226others(3): Show | 6 | HG02145.hp2 HG02738.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+5196_777+5199d others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186321 | ||||||
| chr3:108186321
|
CAAA | C | 35 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(32): Show | 36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.777+5197_777+5199d others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186321 | ||||||
| chr3:108186469
|
G | A | 2 | a0001c0001t0006g0147a0001c0001t0006g0148 | 2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.777+5052C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186469 | ||||||
| chr3:108186492
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+5029T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186492 | ||||||
| chr3:108186534
|
G | A | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+4987C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186534 | ||||||
| chr3:108186581
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.777+4940T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186581 | ||||||
| chr3:108186913
|
A | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+4608T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186913 | ||||||
| chr3:108187190
|
T | A | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.777+4331A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187190 | ||||||
| chr3:108187335
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.777+4186C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187335 | ||||||
| chr3:108187395
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+4126G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187395 | ||||||
| chr3:108187519
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.777+4002G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187519 | ||||||
| chr3:108187587
|
T | TA | 6 | a0001c0001t0001g0004a0001c0001t0001g0177a0001c0001t0001g0178others(3): Show | 8 | HG02040.hp1 HG02074.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.777+3933dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187587 | ||||||
| chr3:108187590
|
A | G | 2 | a0001c0001t0003g0257a0001c0001t0003g0263 | 2 | NA18969.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.777+3931T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187590 | ||||||
| chr3:108187597
|
A | AG | 35 | a0001c0001t0005g0304a0001c0001t0010g0144a0001c0001t0010g0145others(32): Show | 36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.777+3923dupC | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187597 | ||||||
| chr3:108187643
|
T | TA | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+3877dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187643 | ||||||
| chr3:108187791
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+3730T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187791 | ||||||
| chr3:108187829
|
ATTTCT | A | 5 | a0001c0001t0002g0128a0001c0001t0003g0062a0001c0001t0003g0063others(2): Show | 5 | HG02622.hp2 HG03041.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.777+3687_777+3691d others(7): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187829 | ||||||
| chr3:108187886
|
T | C | 1 | a0001c0001t0001g0205 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.777+3635A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187886 | ||||||
| chr3:108187941
|
TG | T | 5 | a0001c0002t0004g0034a0001c0002t0007g0315a0001c0002t0007g0316others(2): Show | 5 | HG01175.hp1 HG02055.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.777+3579delC | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187941 | ||||||
| chr3:108187942
|
G | T | 33 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(30): Show | 34 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.777+3579C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187942 | ||||||
| chr3:108187952
|
T | A | 35 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(32): Show | 36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.777+3569A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187952 | ||||||
| chr3:108188008
|
A | AT | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+3512_777+3513i others(3): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108188008 | ||||||
| chr3:108188038
|
C | T | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.777+3483G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108188038 | ||||||
| chr3:108188099
|
C | A | 2 | a0001c0001t0003g0302a0001c0001t0003g0303 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.777+3422G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108188099 | ||||||
| chr3:108188328
|
T | C | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+3193A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108188328 | ||||||
| chr3:108188394
|
C | T | 317 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(314): Show | 353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.777+3127G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108188394 | ||||||
| chr3:108188576
|
T | G | 1 | a0001c0001t0001g0178 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.777+2945A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108188576 | ||||||
| chr3:108188679
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+2842A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108188679 | ||||||
| chr3:108188753
|
G | C | 2 | a0001c0001t0002g0068a0001c0001t0002g0139 | 2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.777+2768C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108188753 | ||||||
| chr3:108188761
|
G | C | 1 | a0001c0001t0003g0283 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.777+2760C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108188761 | ||||||
| chr3:108188971
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+2550A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108188971 | ||||||
| chr3:108189016
|
A | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+2505T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189016 | ||||||
| chr3:108189077
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+2444G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189077 | ||||||
| chr3:108189078
|
C | A | 1 | a0001c0002t0004g0041 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.777+2443G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189078 | ||||||
| chr3:108189127
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+2394A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189127 | ||||||
| chr3:108189153
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+2368A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189153 | ||||||
| chr3:108189334
|
C | T | 31 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(28): Show | 32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.777+2187G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189334 | ||||||
| chr3:108189468
|
G | T | 1 | a0001c0001t0001g0192 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.777+2053C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189468 | ||||||
| chr3:108189544
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+1977T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189544 | ||||||
| chr3:108189556
|
T | C | 3 | a0001c0001t0005g0030a0001c0001t0005g0031a0001c0001t0005g0244 | 3 | HG02615.hp2 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.777+1965A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189556 | ||||||
| chr3:108189573
|
G | C | 2 | a0001c0001t0010g0144a0001c0001t0010g0145 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.777+1948C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189573 | ||||||
| chr3:108189736
|
C | A | 1 | a0001c0001t0006g0147 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.777+1785G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189736 | ||||||
| chr3:108189753
|
T | TAGAAAAT others(9): Show |
38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+1767_777+1768i others(18): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189753 | ||||||
| chr3:108189887
|
A | ATGT | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+1633_777+1634i others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189887 | ||||||
| chr3:108189941
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0199a0001c0001t0008g0017 | 4 | HG00741.hp2 HG01099.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+1580C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189941 | ||||||
| chr3:108189958
|
T | C | 1 | a0001c0001t0010g0145 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.777+1563A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189958 | ||||||
| chr3:108190067
|
A | C | 1 | a0001c0001t0001g0180 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.777+1454T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190067 | ||||||
| chr3:108190187
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+1334A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190187 | ||||||
| chr3:108190264
|
T | G | 1 | a0001c0001t0002g0083 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.777+1257A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190264 | ||||||
| chr3:108190321
|
C | T | 1 | a0004c0010t0003g0242 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.777+1200G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190321 | ||||||
| chr3:108190402
|
A | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+1119T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190402 | ||||||
| chr3:108190452
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+1069T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190452 | ||||||
| chr3:108190489
|
T | C | 1 | a0001c0001t0003g0266 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.777+1032A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190489 | ||||||
| chr3:108190507
|
C | T | 1 | a0001c0001t0006g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.777+1014G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190507 | ||||||
| chr3:108190615
|
T | C | 5 | a0001c0001t0003g0146a0001c0001t0006g0147a0001c0001t0006g0148others(2): Show | 5 | HG02647.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.777+906A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190615 | ||||||
| chr3:108190913
|
C | T | 4 | a0001c0001t0002g0067a0001c0001t0002g0125a0001c0007t0002g0126others(1): Show | 4 | HG01192.hp1 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.777+608G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190913 | ||||||
| chr3:108190941
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+580A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190941 | ||||||
| chr3:108191093
|
C | T | 24 | a0001c0001t0001g0234a0001c0001t0001g0251a0001c0001t0005g0021others(21): Show | 26 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.777+428G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108191093 | ||||||
| chr3:108191228
|
A | G | 4 | a0001c0003t0001g0001a0001c0003t0001g0219a0001c0003t0001g0223others(1): Show | 7 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.777+293T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108191228 | ||||||
| chr3:108191457
|
CT | C | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0009g0214 | 3 | HG02683.hp2 HG04199.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.777+63delA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108191457 | ||||||
| chr3:108191480
|
C | CTT | 35 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(32): Show | 36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.777+39_777+40dupAA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108191480 | ||||||
| chr3:108191844
|
A | T | 1 | a0001c0001t0005g0250 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.655-201T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108191844 | ||||||
| chr3:108191910
|
A | T | 1 | a0001c0001t0005g0238 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.655-267T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108191910 | ||||||
| chr3:108192045
|
G | A | 1 | a0001c0001t0003g0262 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.655-402C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192045 | ||||||
| chr3:108192125
|
T | C | 2 | a0001c0001t0010g0144a0001c0001t0010g0145 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.655-482A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192125 | ||||||
| chr3:108192137
|
A | G | 1 | a0001c0001t0001g0005 | 3 | NA18947.hp1 NA18988.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.655-494T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192137 | ||||||
| chr3:108192174
|
CA | C | 255 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(252): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.655-532delT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192174 | ||||||
| chr3:108192174
|
CAA | C | 9 | a0001c0001t0001g0169a0001c0001t0001g0199a0001c0001t0002g0073others(6): Show | 9 | HG01099.hp2 HG01167.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.655-533_655-532del others(2): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192174 | ||||||
| chr3:108192196
|
A | G | 2 | a0001c0001t0010g0144a0001c0001t0010g0145 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.655-553T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192196 | ||||||
| chr3:108192197
|
G | A | 2 | a0001c0001t0010g0144a0001c0001t0010g0145 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.655-554C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192197 | ||||||
| chr3:108192197
|
G | GA | 36 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(33): Show | 37 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.655-555_655-554ins others(1): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192197 | ||||||
| chr3:108192199
|
G | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-556C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192199 | ||||||
| chr3:108192255
|
T | C | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.655-612A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192255 | ||||||
| chr3:108192317
|
AATTT | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-678_655-675del others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192317 | ||||||
| chr3:108192336
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-693G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192336 | ||||||
| chr3:108192351
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-708G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192351 | ||||||
| chr3:108192352
|
G | A | 2 | a0001c0005t0006g0014a0001c0005t0006g0154 | 3 | HG02717.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.655-709C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192352 | ||||||
| chr3:108192382
|
T | A | 316 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(313): Show | 352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.655-739A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192382 | ||||||
| chr3:108192503
|
T | C | 1 | a0001c0002t0004g0042 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.655-860A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192503 | ||||||
| chr3:108192537
|
G | A | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.655-894C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192537 | ||||||
| chr3:108192571
|
T | G | 94 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(91): Show | 104 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.655-928A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192571 | ||||||
| chr3:108192676
|
T | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-1033A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192676 | ||||||
| chr3:108192698
|
T | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-1055A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192698 | ||||||
| chr3:108192761
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-1118G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192761 | ||||||
| chr3:108192812
|
T | G | 1 | a0001c0001t0001g0206 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.655-1169A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192812 | ||||||
| chr3:108192823
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-1180T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192823 | ||||||
| chr3:108192847
|
A | T | 1 | a0001c0001t0002g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.655-1204T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192847 | ||||||
| chr3:108192892
|
T | A | 1 | a0001c0001t0002g0012 | 2 | NA18971.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.655-1249A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192892 | ||||||
| chr3:108192908
|
CT | C | 85 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(82): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.655-1266delA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192908 | ||||||
| chr3:108193042
|
A | G | 2 | a0001c0001t0010g0144a0001c0001t0010g0145 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.655-1399T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193042 | ||||||
| chr3:108193100
|
C | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0177a0001c0001t0001g0178others(1): Show | 6 | HG02040.hp1 HG02074.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-1457G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193100 | ||||||
| chr3:108193118
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-1475A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193118 | ||||||
| chr3:108193361
|
C | G | 39 | a0001c0001t0002g0122a0001c0001t0010g0144a0001c0001t0010g0145others(36): Show | 40 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.655-1718G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193361 | ||||||
| chr3:108193504
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-1861G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193504 | ||||||
| chr3:108193518
|
A | C | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.655-1875T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193518 | ||||||
| chr3:108193551
|
C | T | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.655-1908G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193551 | ||||||
| chr3:108193588
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-1945A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193588 | ||||||
| chr3:108193641
|
G | A | 1 | a0001c0001t0005g0239 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.655-1998C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193641 | ||||||
| chr3:108193827
|
T | A | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.655-2184A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193827 | ||||||
| chr3:108193968
|
G | T | 94 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(91): Show | 104 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.655-2325C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193968 | ||||||
| chr3:108194212
|
C | A | 24 | a0001c0001t0001g0234a0001c0001t0001g0251a0001c0001t0005g0021others(21): Show | 26 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.655-2569G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108194212 | ||||||
| chr3:108194260
|
A | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-2617T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108194260 | ||||||
| chr3:108194286
|
C | T | 3 | a0001c0001t0005g0030a0001c0001t0005g0031a0001c0001t0005g0244 | 3 | HG02615.hp2 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.655-2643G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108194286 | ||||||
| chr3:108194438
|
C | T | 2 | a0001c0003t0001g0223a0001c0003t0001g0224 | 2 | HG02280.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.655-2795G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108194438 | ||||||
| chr3:108194477
|
T | TA | 27 | a0001c0001t0001g0234a0001c0001t0001g0251a0001c0001t0005g0021others(24): Show | 29 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.655-2835dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108194477 | ||||||
| chr3:108194477
|
TAA | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-2836_655-2835d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108194477 | ||||||
| chr3:108194565
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.655-2922G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108194565 | ||||||
| chr3:108194620
|
T | C | 1 | a0001c0001t0002g0113 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.655-2977A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108194620 | ||||||
| chr3:108195002
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-3359T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195002 | ||||||
| chr3:108195024
|
G | A | 2 | a0001c0001t0002g0078a0001c0001t0002g0079 | 2 | HG00673.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.655-3381C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195024 | ||||||
| chr3:108195149
|
A | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0156a0001c0001t0001g0159others(3): Show | 7 | HG01934.hp1 HG01978.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-3506T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195149 | ||||||
| chr3:108195196
|
C | T | 2 | a0001c0001t0010g0144a0001c0001t0010g0145 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.655-3553G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195196 | ||||||
| chr3:108195215
|
C | T | 7 | a0001c0001t0001g0158a0001c0001t0002g0130a0001c0001t0002g0131others(4): Show | 7 | HG00099.hp1 HG02257.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-3572G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195215 | ||||||
| chr3:108195278
|
C | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.655-3635G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195278 | ||||||
| chr3:108195298
|
G | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-3655C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195298 | ||||||
| chr3:108195358
|
CT | C | 90 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(87): Show | 100 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.655-3716delA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195358 | ||||||
| chr3:108195394
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-3751A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195394 | ||||||
| chr3:108195466
|
G | A | 24 | a0001c0001t0001g0234a0001c0001t0001g0251a0001c0001t0005g0021others(21): Show | 26 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.655-3823C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195466 | ||||||
| chr3:108195547
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.655-3904A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195547 | ||||||
| chr3:108195827
|
C | T | 2 | a0001c0001t0010g0144a0001c0001t0010g0145 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.655-4184G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195827 | ||||||
| chr3:108195920
|
T | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-4277A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195920 | ||||||
| chr3:108195947
|
T | A | 1 | a0001c0002t0004g0043 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.655-4304A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195947 | ||||||
| chr3:108195994
|
G | A | 4 | a0001c0001t0003g0062a0001c0001t0003g0063a0001c0001t0003g0064others(1): Show | 4 | HG02622.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.655-4351C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195994 | ||||||
| chr3:108196078
|
T | C | 4 | a0001c0002t0007g0315a0001c0002t0007g0316a0001c0002t0007g0317others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.655-4435A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108196078 | ||||||
| chr3:108196164
|
A | T | 6 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(3): Show | 6 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-4521T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108196164 | ||||||
| chr3:108196258
|
C | CACCCTCA others(6): Show |
38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-4628_655-4616d others(15): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108196258 | ||||||
| chr3:108196341
|
G | A | 1 | a0001c0001t0002g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.655-4698C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108196341 | ||||||
| chr3:108196350
|
A | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-4707T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108196350 | ||||||
| chr3:108196374
|
A | T | 1 | a0001c0001t0001g0157 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.655-4731T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108196374 | ||||||
| chr3:108196667
|
T | G | 1 | a0001c0002t0004g0052 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.655-5024A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108196667 | ||||||
| chr3:108196709
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0192others(2): Show | 9 | HG00621.hp2 NA18943.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.655-5066C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108196709 | ||||||
| chr3:108196848
|
C | T | 1 | a0001c0001t0003g0268 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.655-5205G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108196848 | ||||||
| chr3:108196909
|
T | C | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG02896.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.655-5266A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108196909 | ||||||
| chr3:108197108
|
G | A | 1 | a0001c0001t0005g0250 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.655-5465C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197108 | ||||||
| chr3:108197211
|
A | G | 41 | a0001c0001t0002g0097a0001c0001t0002g0098a0001c0001t0002g0117others(38): Show | 42 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.655-5568T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197211 | ||||||
| chr3:108197279
|
C | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.655-5636G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197279 | ||||||
| chr3:108197314
|
G | A | 2 | a0001c0002t0004g0044a0001c0002t0004g0055 | 2 | NA19005.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.655-5671C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197314 | ||||||
| chr3:108197341
|
T | A | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.655-5698A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197341 | ||||||
| chr3:108197407
|
C | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-5764G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197407 | ||||||
| chr3:108197415
|
A | C | 1 | a0001c0001t0002g0081 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.655-5772T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197415 | ||||||
| chr3:108197419
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-5776G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197419 | ||||||
| chr3:108197483
|
C | G | 3 | a0001c0001t0005g0030a0001c0001t0005g0031a0001c0001t0005g0244 | 3 | HG02615.hp2 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.655-5840G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197483 | ||||||
| chr3:108197570
|
G | A | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.655-5927C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197570 | ||||||
| chr3:108197572
|
T | C | 31 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(28): Show | 32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.655-5929A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197572 | ||||||
| chr3:108197778
|
G | A | 4 | a0001c0001t0002g0067a0001c0001t0002g0125a0001c0007t0002g0126others(1): Show | 4 | HG01192.hp1 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.655-6135C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197778 | ||||||
| chr3:108197900
|
A | G | 2 | a0001c0001t0010g0144a0001c0001t0010g0145 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.655-6257T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197900 | ||||||
| chr3:108198072
|
T | C | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.655-6429A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108198072 | ||||||
| chr3:108198078
|
A | G | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.655-6435T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108198078 | ||||||
| chr3:108198156
|
T | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-6513A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108198156 | ||||||
| chr3:108198385
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-6742G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108198385 | ||||||
| chr3:108198397
|
T | C | 1 | a0001c0001t0002g0138 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.655-6754A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108198397 | ||||||
| chr3:108198471
|
T | C | 1 | a0004c0010t0003g0242 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.655-6828A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108198471 | ||||||
| chr3:108198484
|
C | G | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.655-6841G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108198484 | ||||||
| chr3:108198556
|
C | T | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.655-6913G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108198556 | ||||||
| chr3:108198958
|
A | AT | 31 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(28): Show | 32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.655-7316dupA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108198958 | ||||||
| chr3:108198977
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-7334A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108198977 | ||||||
| chr3:108199003
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-7360T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199003 | ||||||
| chr3:108199113
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.655-7470C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199113 | ||||||
| chr3:108199372
|
T | C | 90 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(87): Show | 100 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.654+7256A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199372 | ||||||
| chr3:108199453
|
G | A | 1 | a0001c0001t0002g0072 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.654+7175C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199453 | ||||||
| chr3:108199632
|
T | C | 2 | a0001c0001t0002g0115a0001c0001t0002g0116 | 2 | HG04184.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.654+6996A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199632 | ||||||
| chr3:108199683
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0189others(7): Show | 14 | HG00621.hp2 HG01516.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.654+6945A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199683 | ||||||
| chr3:108199787
|
TTGGGTTT others(4): Show |
T | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.654+6830_654+6840d others(13): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199787 | ||||||
| chr3:108199794
|
T | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+6834A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199794 | ||||||
| chr3:108199799
|
TGGG | T | 3 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0310 | 3 | NA19010.hp2 NA19056.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.654+6826_654+6828d others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199799 | ||||||
| chr3:108199830
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.654+6798C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199830 | ||||||
| chr3:108199901
|
T | G | 1 | a0001c0001t0005g0252 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.654+6727A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199901 | ||||||
| chr3:108199931
|
G | A | 1 | a0001c0001t0002g0117 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.654+6697C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199931 | ||||||
| chr3:108200277
|
A | T | 7 | a0001c0001t0002g0080a0001c0001t0002g0088a0001c0001t0002g0093others(4): Show | 7 | HG01361.hp1 NA18957.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.654+6351T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200277 | ||||||
| chr3:108200293
|
T | C | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.654+6335A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200293 | ||||||
| chr3:108200382
|
C | T | 1 | a0001c0001t0005g0227 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.654+6246G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200382 | ||||||
| chr3:108200414
|
A | G | 1 | a0001c0001t0002g0093 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.654+6214T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200414 | ||||||
| chr3:108200444
|
G | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+6184C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200444 | ||||||
| chr3:108200501
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+6127A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200501 | ||||||
| chr3:108200556
|
T | C | 1 | a0001c0001t0003g0064 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.654+6072A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200556 | ||||||
| chr3:108200633
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+5995G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200633 | ||||||
| chr3:108200693
|
A | T | 4 | a0001c0002t0007g0315a0001c0002t0007g0316a0001c0002t0007g0317others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.654+5935T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200693 | ||||||
| chr3:108200731
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+5897T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200731 | ||||||
| chr3:108200738
|
T | C | 85 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(82): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.654+5890A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200738 | ||||||
| chr3:108200768
|
T | C | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.654+5860A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200768 | ||||||
| chr3:108200921
|
G | C | 1 | a0001c0001t0002g0118 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.654+5707C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200921 | ||||||
| chr3:108200925
|
G | A | 7 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+5703C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200925 | ||||||
| chr3:108201014
|
C | T | 85 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(82): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.654+5614G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108201014 | ||||||
| chr3:108201083
|
C | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+5545G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108201083 | ||||||
| chr3:108201156
|
G | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.654+5472C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108201156 | ||||||
| chr3:108201274
|
C | T | 2 | a0001c0001t0005g0030a0001c0001t0005g0031 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.654+5354G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108201274 | ||||||
| chr3:108201292
|
C | T | 2 | a0001c0001t0003g0024a0001c0001t0003g0267 | 3 | NA18951.hp1 NA18968.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.654+5336G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108201292 | ||||||
| chr3:108201772
|
T | C | 6 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(3): Show | 6 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+4856A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108201772 | ||||||
| chr3:108201973
|
T | C | 1 | a0001c0007t0002g0127 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.654+4655A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108201973 | ||||||
| chr3:108202076
|
G | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+4552C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202076 | ||||||
| chr3:108202091
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+4537A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202091 | ||||||
| chr3:108202096
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+4532A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202096 | ||||||
| chr3:108202132
|
T | C | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.654+4496A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202132 | ||||||
| chr3:108202158
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.654+4470G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202158 | ||||||
| chr3:108202233
|
G | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+4395C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202233 | ||||||
| chr3:108202241
|
G | A | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.654+4387C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202241 | ||||||
| chr3:108202404
|
C | T | 4 | a0001c0001t0001g0195a0001c0001t0001g0220a0001c0001t0001g0222others(1): Show | 4 | HG00280.hp2 HG02451.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+4224G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202404 | ||||||
| chr3:108202454
|
C | G | 3 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134 | 3 | HG02257.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.654+4174G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202454 | ||||||
| chr3:108202590
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+4038A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202590 | ||||||
| chr3:108202869
|
G | A | 2 | a0001c0001t0010g0144a0001c0001t0010g0145 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.654+3759C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202869 | ||||||
| chr3:108202944
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.654+3684G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202944 | ||||||
| chr3:108203008
|
G | A | 33 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(30): Show | 34 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.654+3620C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203008 | ||||||
| chr3:108203015
|
T | C | 34 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(31): Show | 35 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.654+3613A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203015 | ||||||
| chr3:108203269
|
C | T | 24 | a0001c0001t0001g0234a0001c0001t0001g0251a0001c0001t0005g0021others(21): Show | 26 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.654+3359G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203269 | ||||||
| chr3:108203320
|
T | C | 1 | a0001c0001t0003g0299 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.654+3308A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203320 | ||||||
| chr3:108203425
|
A | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+3203T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203425 | ||||||
| chr3:108203563
|
TGTCA | T | 31 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(28): Show | 32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.654+3061_654+3064d others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203563 | ||||||
| chr3:108203613
|
A | G | 1 | a0001c0001t0002g0070 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.654+3015T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203613 | ||||||
| chr3:108203660
|
T | C | 2 | a0001c0005t0006g0014a0001c0005t0006g0154 | 3 | HG02717.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.654+2968A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203660 | ||||||
| chr3:108203716
|
T | G | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.654+2912A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203716 | ||||||
| chr3:108203724
|
A | G | 35 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(32): Show | 36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.654+2904T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203724 | ||||||
| chr3:108203852
|
T | A | 4 | a0001c0002t0007g0315a0001c0002t0007g0316a0001c0002t0007g0317others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.654+2776A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203852 | ||||||
| chr3:108203887
|
G | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+2741C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203887 | ||||||
| chr3:108203960
|
T | C | 1 | a0001c0001t0002g0119 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.654+2668A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203960 | ||||||
| chr3:108204008
|
A | G | 1 | a0001c0002t0007g0315 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.654+2620T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108204008 | ||||||
| chr3:108204313
|
AGTTAT | A | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.654+2310_654+2314d others(7): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108204313 | ||||||
| chr3:108204404
|
G | A | 31 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(28): Show | 32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.654+2224C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108204404 | ||||||
| chr3:108204440
|
T | C | 2 | a0001c0001t0010g0144a0001c0001t0010g0145 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.654+2188A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108204440 | ||||||
| chr3:108204444
|
C | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+2184G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108204444 | ||||||
| chr3:108204486
|
C | A | 1 | a0001c0001t0001g0020 | 2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.654+2142G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108204486 | ||||||
| chr3:108204685
|
T | G | 1 | a0004c0010t0003g0242 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.654+1943A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108204685 | ||||||
| chr3:108204749
|
T | C | 2 | a0001c0001t0003g0289a0001c0001t0003g0290 | 2 | HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.654+1879A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108204749 | ||||||
| chr3:108204853
|
A | G | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.654+1775T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108204853 | ||||||
| chr3:108204893
|
C | G | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.654+1735G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108204893 | ||||||
| chr3:108205254
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+1374T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205254 | ||||||
| chr3:108205303
|
T | C | 1 | a0001c0002t0004g0053 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.654+1325A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205303 | ||||||
| chr3:108205372
|
G | GT | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+1255dupA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205372 | ||||||
| chr3:108205386
|
A | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+1242T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205386 | ||||||
| chr3:108205415
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+1213T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205415 | ||||||
| chr3:108205417
|
C | T | 1 | a0001c0001t0002g0131 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.654+1211G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205417 | ||||||
| chr3:108205493
|
T | C | 85 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(82): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.654+1135A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205493 | ||||||
| chr3:108205495
|
T | A | 308 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(305): Show | 343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.654+1133A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205495 | ||||||
| chr3:108205650
|
GAGGATTC others(5): Show |
G | 4 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0140others(1): Show | 4 | NA18972.hp1 NA18995.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+966_654+977del others(12): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205650 | ||||||
| chr3:108205677
|
A | T | 1 | a0001c0001t0001g0209 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.654+951T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205677 | ||||||
| chr3:108205678
|
AGGACTAA others(378): Show |
A | 1 | a0001c0001t0001g0209 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.654+565_654+949del | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205678 | ||||||
| chr3:108205802
|
ATAT | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+823_654+825del others(3): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205802 | ||||||
| chr3:108205808
|
T | C | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.654+820A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205808 | ||||||
| chr3:108205811
|
CAT | C | 6 | a0001c0001t0003g0225a0001c0001t0003g0226a0001c0001t0003g0241others(3): Show | 6 | HG02145.hp2 HG02895.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+815_654+816del others(2): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205811 | ||||||
| chr3:108205814
|
ATTATATA others(4): Show |
A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+803_654+813del others(11): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205814 | ||||||
| chr3:108205836
|
TTTAA | T | 27 | a0001c0001t0001g0234a0001c0001t0001g0251a0001c0001t0005g0021others(24): Show | 29 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.654+788_654+791del others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205836 | ||||||
| chr3:108205910
|
T | C | 1 | a0001c0001t0002g0080 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.654+718A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205910 | ||||||
| chr3:108205942
|
TA | T | 80 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(77): Show | 90 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.654+685delT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205942 | ||||||
| chr3:108205946
|
T | TTATAATA others(23): Show |
6 | a0001c0001t0003g0285a0001c0001t0003g0286a0001c0001t0003g0287others(3): Show | 6 | HG00642.hp1 HG01515.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.654+652_654+681dup others(30): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205946 | ||||||
| chr3:108205946
|
T | TTATAATA others(53): Show |
1 | a0001c0001t0003g0291 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.654+681_654+682ins others(60): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205946 | ||||||
| chr3:108205954
|
TATAA | T | 25 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0156others(22): Show | 28 | HG00099.hp1 HG00741.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.654+670_654+673del others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205954 | ||||||
| chr3:108205956
|
TA | T | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+671delT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205956 | ||||||
| chr3:108205957
|
A | AAATATAT others(22): Show |
1 | a0001c0001t0003g0264 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.654+642_654+670dup others(29): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205957 | ||||||
| chr3:108205963
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+665T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205963 | ||||||
| chr3:108205966
|
ATATAT | A | 34 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(31): Show | 35 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.654+657_654+661del others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205966 | ||||||
| chr3:108205966
|
ATATATTT others(25): Show |
A | 1 | a0001c0002t0004g0045 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.654+630_654+661del others(32): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205966 | ||||||
| chr3:108205972
|
T | A | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.654+656A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205972 | ||||||
| chr3:108205976
|
A | T | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.654+652T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205976 | ||||||
| chr3:108205977
|
T | A | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.654+651A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205977 | ||||||
| chr3:108205978
|
A | T | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.654+650T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205978 | ||||||
| chr3:108205980
|
A | T | 35 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(32): Show | 36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.654+648T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205980 | ||||||
| chr3:108205983
|
A | T | 34 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(31): Show | 35 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.654+645T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205983 | ||||||
| chr3:108205986
|
TA | T | 34 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(31): Show | 35 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.654+641delT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205986 | ||||||
| chr3:108205994
|
T | TAA | 35 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(32): Show | 36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.654+633_654+634ins others(2): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205994 | ||||||
| chr3:108205994
|
T | TTA | 110 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.654+632_654+633dup others(2): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205994 | ||||||
| chr3:108205998
|
G | A | 35 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(32): Show | 36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.654+630C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205998 | ||||||
| chr3:108206004
|
T | A | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.654+624A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206004 | ||||||
| chr3:108206009
|
C | T | 1 | a0001c0002t0004g0045 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.654+619G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206009 | ||||||
| chr3:108206013
|
TATATA | T | 34 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(31): Show | 35 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.654+610_654+614del others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206013 | ||||||
| chr3:108206026
|
G | A | 35 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(32): Show | 36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.654+602C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206026 | ||||||
| chr3:108206028
|
ATAT | A | 6 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(3): Show | 6 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+597_654+599del others(3): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206028 | ||||||
| chr3:108206029
|
T | A | 1 | a0001c0002t0004g0045 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.654+599A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206029 | ||||||
| chr3:108206034
|
T | C | 1 | a0001c0002t0004g0045 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.654+594A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206034 | ||||||
| chr3:108206035
|
TTATAA | T | 34 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(31): Show | 35 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.654+588_654+592del others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206035 | ||||||
| chr3:108206046
|
ATT | A | 9 | a0001c0001t0003g0026a0001c0001t0003g0292a0001c0001t0003g0293others(6): Show | 10 | NA18939.hp1 NA18945.hp2 NA18971.hp2 others(7): Show |
intron_variant | MODIFIER | c.654+580_654+581del others(2): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206046 | ||||||
| chr3:108206048
|
T | A | 34 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(31): Show | 35 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.654+580A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206048 | ||||||
| chr3:108206057
|
TTTATATA others(3): Show |
T | 34 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(31): Show | 35 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.654+561_654+570del others(10): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206057 | ||||||
| chr3:108206067
|
A | T | 1 | a0001c0002t0004g0045 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.654+561T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206067 | ||||||
| chr3:108206068
|
T | A | 35 | a0001c0001t0001g0209a0001c0002t0004g0008a0001c0002t0004g0032others(32): Show | 36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.654+560A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206068 | ||||||
| chr3:108206068
|
TA | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0183others(11): Show | 18 | HG00621.hp2 HG00735.hp1 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.654+559delT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206068 | ||||||
| chr3:108206069
|
A | T | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.654+559T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206069 | ||||||
| chr3:108206069
|
AATATATT | A | 4 | a0001c0001t0002g0012a0001c0001t0002g0136a0001c0001t0002g0137others(1): Show | 5 | NA18971.hp1 NA18979.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.654+552_654+558del others(7): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206069 | ||||||
| chr3:108206072
|
A | T | 1 | a0001c0001t0001g0209 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.654+556T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206072 | ||||||
| chr3:108206075
|
T | A | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.654+553A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206075 | ||||||
| chr3:108206076
|
T | A | 1 | a0001c0001t0001g0209 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.654+552A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206076 | ||||||
| chr3:108206111
|
A | T | 1 | a0001c0001t0003g0309 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.654+517T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206111 | ||||||
| chr3:108206125
|
A | AAT | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+501_654+502dup others(2): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206125 | ||||||
| chr3:108206147
|
T | A | 6 | a0001c0001t0003g0225a0001c0001t0003g0226a0001c0001t0003g0241others(3): Show | 6 | HG02145.hp2 HG02895.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+481A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206147 | ||||||
| chr3:108206316
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.654+312C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206316 | ||||||
| chr3:108206361
|
T | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+267A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206361 | ||||||
| chr3:108206419
|
A | G | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+209T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206419 | ||||||
| chr3:108206476
|
A | G | 1 | a0001c0001t0003g0253 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.654+152T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206476 | ||||||
| chr3:108206507
|
A | G | 1 | a0001c0001t0003g0246 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.654+121T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206507 | ||||||
| chr3:108206545
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.654+83G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206545 | ||||||
| chr3:108206549
|
G | A | 90 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(87): Show | 100 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.654+79C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206549 | ||||||
| chr3:108206601
|
G | A | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.654+27C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206601 | ||||||
| chr3:108206839
|
G | A | 175 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(172): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.586-143C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108206839 | ||||||
| chr3:108206962
|
G | C | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.586-266C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108206962 | ||||||
| chr3:108207147
|
A | G | 6 | a0001c0001t0003g0225a0001c0001t0003g0226a0001c0001t0003g0241others(3): Show | 6 | HG02145.hp2 HG02895.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.586-451T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207147 | ||||||
| chr3:108207250
|
A | G | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.586-554T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207250 | ||||||
| chr3:108207253
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.586-557C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207253 | ||||||
| chr3:108207279
|
T | A | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.586-583A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207279 | ||||||
| chr3:108207298
|
T | A | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.586-602A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207298 | ||||||
| chr3:108207379
|
TC | T | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188 | 3 | HG03130.hp2 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.586-684delG | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207379 | ||||||
| chr3:108207411
|
C | T | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.586-715G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207411 | ||||||
| chr3:108207415
|
T | C | 2 | a0001c0001t0010g0144a0001c0001t0010g0145 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.586-719A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207415 | ||||||
| chr3:108207493
|
C | T | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.586-797G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207493 | ||||||
| chr3:108207570
|
T | C | 3 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212 | 3 | HG00099.hp2 HG00738.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.586-874A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207570 | ||||||
| chr3:108207671
|
C | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.586-975G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207671 | ||||||
| chr3:108207781
|
C | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.586-1085G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207781 | ||||||
| chr3:108207912
|
G | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.586-1216C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207912 | ||||||
| chr3:108207936
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.586-1240C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207936 | ||||||
| chr3:108207974
|
C | T | 4 | a0001c0001t0003g0155a0001c0001t0003g0264a0001c0001t0003g0265others(1): Show | 4 | HG02486.hp1 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-1278G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207974 | ||||||
| chr3:108208038
|
G | A | 1 | a0001c0003t0001g0224 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.586-1342C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208038 | ||||||
| chr3:108208047
|
G | GA | 61 | a0001c0001t0001g0166a0001c0001t0003g0007a0001c0001t0003g0024others(58): Show | 68 | HG00642.hp1 HG01256.hp1 HG01258.hp2 others(65): Show |
intron_variant | MODIFIER | c.586-1352dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208047 | ||||||
| chr3:108208047
|
GA | G | 39 | a0001c0001t0002g0088a0001c0001t0010g0144a0001c0001t0010g0145others(36): Show | 40 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.586-1352delT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208047 | ||||||
| chr3:108208163
|
G | A | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0176 | 3 | HG01099.hp1 HG01109.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.586-1467C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208163 | ||||||
| chr3:108208170
|
T | C | 4 | a0001c0002t0007g0315a0001c0002t0007g0316a0001c0002t0007g0317others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.586-1474A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208170 | ||||||
| chr3:108208277
|
T | A | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.586-1581A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208277 | ||||||
| chr3:108208307
|
C | T | 1 | a0001c0001t0003g0256 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.586-1611G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208307 | ||||||
| chr3:108208397
|
T | C | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.586-1701A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208397 | ||||||
| chr3:108208421
|
T | C | 38 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(35): Show | 39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.586-1725A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208421 | ||||||
| chr3:108208442
|
C | T | 1 | a0001c0001t0002g0087 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.586-1746G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208442 | ||||||
| chr3:108208573
|
T | C | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.586-1877A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208573 | ||||||
| chr3:108208653
|
G | A | 4 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-1957C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208653 | ||||||
| chr3:108208747
|
C | G | 1 | a0001c0001t0002g0086 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.586-2051G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208747 | ||||||
| chr3:108208793
|
A | G | 6 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(3): Show | 6 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.586-2097T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208793 | ||||||
| chr3:108208794
|
A | C | 6 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(3): Show | 6 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.586-2098T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208794 | ||||||
| chr3:108208913
|
C | G | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.586-2217G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208913 | ||||||
| chr3:108209178
|
G | A | 1 | a0001c0001t0002g0120 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.586-2482C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209178 | ||||||
| chr3:108209183
|
T | C | 2 | a0001c0001t0003g0027a0001c0001t0003g0300 | 3 | NA18941.hp2 NA19007.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.586-2487A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209183 | ||||||
| chr3:108209193
|
T | C | 39 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0001t0013g0243others(36): Show | 40 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.586-2497A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209193 | ||||||
| chr3:108209288
|
T | G | 1 | a0001c0001t0014g0240 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.586-2592A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209288 | ||||||
| chr3:108209477
|
G | A | 2 | a0001c0001t0002g0084a0001c0001t0002g0121 | 2 | HG00642.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.586-2781C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209477 | ||||||
| chr3:108209566
|
T | C | 4 | a0001c0001t0002g0003a0001c0001t0002g0122a0001c0001t0002g0123others(1): Show | 6 | HG00558.hp2 HG01496.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.586-2870A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209566 | ||||||
| chr3:108209585
|
G | A | 1 | a0001c0001t0003g0301 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.586-2889C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209585 | ||||||
| chr3:108209593
|
A | G | 1 | a0001c0002t0004g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.586-2897T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209593 | ||||||
| chr3:108209649
|
T | C | 1 | a0001c0001t0003g0226 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.586-2953A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209649 | ||||||
| chr3:108209710
|
C | T | 27 | a0001c0001t0001g0234a0001c0001t0001g0251a0001c0001t0005g0021others(24): Show | 29 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.586-3014G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209710 | ||||||
| chr3:108209715
|
T | C | 1 | a0001c0002t0004g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.586-3019A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209715 | ||||||
| chr3:108209725
|
A | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG01192.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.586-3029T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209725 | ||||||
| chr3:108209823
|
T | C | 4 | a0001c0002t0007g0315a0001c0002t0007g0316a0001c0002t0007g0317others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.586-3127A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209823 | ||||||
| chr3:108209916
|
A | ATG | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(78): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.586-3222_586-3221d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209916 | ||||||
| chr3:108209916
|
A | ATGTG | 32 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(29): Show | 33 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.586-3224_586-3221d others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209916 | ||||||
| chr3:108209916
|
A | ATGTGTG | 4 | a0001c0002t0004g0034a0001c0002t0004g0056a0001c0002t0004g0057others(1): Show | 4 | HG00738.hp2 HG01106.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-3226_586-3221d others(8): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209916 | ||||||
| chr3:108209916
|
ATG | A | 7 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0007g0315others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.586-3222_586-3221d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209916 | ||||||
| chr3:108210061
|
T | C | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.586-3365A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210061 | ||||||
| chr3:108210073
|
G | T | 1 | a0001c0003t0001g0223 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.586-3377C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210073 | ||||||
| chr3:108210187
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.586-3491G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210187 | ||||||
| chr3:108210194
|
C | T | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.586-3498G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210194 | ||||||
| chr3:108210246
|
G | A | 6 | a0001c0001t0003g0225a0001c0001t0003g0226a0001c0001t0003g0241others(3): Show | 6 | HG02145.hp2 HG02895.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.586-3550C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210246 | ||||||
| chr3:108210255
|
C | G | 80 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(77): Show | 90 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.586-3559G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210255 | ||||||
| chr3:108210293
|
C | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.586-3597G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210293 | ||||||
| chr3:108210299
|
G | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.586-3603C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210299 | ||||||
| chr3:108210304
|
T | C | 1 | a0001c0001t0002g0128 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.586-3608A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210304 | ||||||
| chr3:108210332
|
C | CT | 11 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(8): Show | 11 | HG00408.hp1 HG00642.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.585+3598dupA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210332 | ||||||
| chr3:108210332
|
C | CTT | 24 | a0001c0001t0001g0234a0001c0001t0001g0251a0001c0001t0005g0021others(21): Show | 26 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.585+3597_585+3598d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210332 | ||||||
| chr3:108210332
|
C | CTTTTTTT | 22 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(19): Show | 23 | HG00408.hp2 HG00738.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.585+3592_585+3598d others(9): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210332 | ||||||
| chr3:108210332
|
C | CTTTTTTT others(1): Show |
7 | a0001c0002t0004g0035a0001c0002t0004g0039a0001c0002t0004g0040others(4): Show | 7 | HG00558.hp1 HG00673.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.585+3591_585+3598d others(10): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210332 | ||||||
| chr3:108210332
|
C | CTTTTTTT others(3): Show |
4 | a0001c0002t0007g0315a0001c0002t0007g0316a0001c0002t0007g0317others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.585+3589_585+3598d others(12): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210332 | ||||||
| chr3:108210332
|
CT | C | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(78): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.585+3598delA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210332 | ||||||
| chr3:108210381
|
C | T | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.585+3550G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210381 | ||||||
| chr3:108210418
|
C | T | 6 | a0001c0001t0003g0225a0001c0001t0003g0226a0001c0001t0003g0241others(3): Show | 6 | HG02145.hp2 HG02895.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+3513G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210418 | ||||||
| chr3:108210438
|
G | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+3493C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210438 | ||||||
| chr3:108210492
|
CCTGT | C | 6 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(3): Show | 6 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+3435_585+3438d others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210492 | ||||||
| chr3:108210671
|
A | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0177a0001c0001t0001g0178others(1): Show | 6 | HG02040.hp1 HG02074.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+3260T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210671 | ||||||
| chr3:108210741
|
A | T | 2 | a0001c0001t0010g0144a0001c0001t0010g0145 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.585+3190T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210741 | ||||||
| chr3:108210852
|
G | A | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+3079C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210852 | ||||||
| chr3:108210960
|
C | A | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.585+2971G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210960 | ||||||
| chr3:108210974
|
C | A | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.585+2957G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210974 | ||||||
| chr3:108211158
|
C | T | 213 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(210): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.585+2773G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108211158 | ||||||
| chr3:108211295
|
G | A | 2 | a0001c0001t0010g0144a0001c0001t0010g0145 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.585+2636C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108211295 | ||||||
| chr3:108211362
|
C | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+2569G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108211362 | ||||||
| chr3:108211363
|
G | T | 24 | a0001c0001t0001g0234a0001c0001t0001g0251a0001c0001t0005g0021others(21): Show | 26 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.585+2568C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108211363 | ||||||
| chr3:108211514
|
T | C | 1 | a0001c0003t0001g0219 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.585+2417A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108211514 | ||||||
| chr3:108211631
|
T | A | 1 | a0001c0001t0003g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.585+2300A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108211631 | ||||||
| chr3:108211666
|
C | T | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.585+2265G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108211666 | ||||||
| chr3:108211731
|
T | A | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.585+2200A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108211731 | ||||||
| chr3:108212050
|
A | G | 1 | a0001c0001t0002g0080 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.585+1881T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212050 | ||||||
| chr3:108212177
|
T | G | 1 | a0001c0001t0006g0152 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.585+1754A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212177 | ||||||
| chr3:108212239
|
T | A | 3 | a0001c0001t0003g0225a0001c0001t0003g0226a0001c0001t0003g0246 | 3 | HG02145.hp2 HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.585+1692A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212239 | ||||||
| chr3:108212243
|
T | C | 2 | a0001c0001t0006g0147a0001c0001t0006g0148 | 2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.585+1688A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212243 | ||||||
| chr3:108212331
|
C | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+1600G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212331 | ||||||
| chr3:108212385
|
A | G | 4 | a0001c0001t0002g0069a0001c0001t0002g0077a0001c0001t0002g0078others(1): Show | 4 | HG00673.hp2 NA18995.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.585+1546T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212385 | ||||||
| chr3:108212524
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.585+1407T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212524 | ||||||
| chr3:108212592
|
TA | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+1338delT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212592 | ||||||
| chr3:108212727
|
T | C | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+1204A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212727 | ||||||
| chr3:108212774
|
C | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0177a0001c0001t0001g0178others(1): Show | 6 | HG02040.hp1 HG02074.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+1157G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212774 | ||||||
| chr3:108212832
|
A | T | 119 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(116): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.585+1099T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212832 | ||||||
| chr3:108212886
|
T | C | 4 | a0001c0001t0002g0012a0001c0001t0002g0136a0001c0001t0002g0137others(1): Show | 5 | NA18971.hp1 NA18979.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.585+1045A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212886 | ||||||
| chr3:108213036
|
T | C | 10 | a0001c0002t0004g0034a0001c0002t0004g0035a0001c0002t0004g0037others(7): Show | 10 | HG00738.hp2 HG01070.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.585+895A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213036 | ||||||
| chr3:108213063
|
G | T | 1 | a0001c0001t0003g0254 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.585+868C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213063 | ||||||
| chr3:108213066
|
T | G | 5 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(2): Show | 6 | HG00741.hp2 HG01099.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+865A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213066 | ||||||
| chr3:108213130
|
G | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+801C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213130 | ||||||
| chr3:108213153
|
A | G | 1 | a0001c0001t0003g0253 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.585+778T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213153 | ||||||
| chr3:108213185
|
G | A | 1 | a0001c0001t0005g0245 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.585+746C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213185 | ||||||
| chr3:108213294
|
G | GT | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+636dupA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213294 | ||||||
| chr3:108213298
|
G | T | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.585+633C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213298 | ||||||
| chr3:108213310
|
A | G | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+621T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213310 | ||||||
| chr3:108213333
|
A | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+598T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213333 | ||||||
| chr3:108213458
|
T | G | 213 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(210): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.585+473A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213458 | ||||||
| chr3:108213571
|
C | T | 4 | a0001c0002t0007g0315a0001c0002t0007g0316a0001c0002t0007g0317others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.585+360G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213571 | ||||||
| chr3:108213573
|
T | C | 2 | a0001c0001t0002g0068a0001c0001t0002g0139 | 2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.585+358A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213573 | ||||||
| chr3:108213774
|
G | A | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+157C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213774 | ||||||
| chr3:108213890
|
C | A | 4 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0175others(1): Show | 4 | HG01109.hp2 HG01433.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.585+41G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213890 | ||||||
| chr3:108214292
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.495-271A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214292 | ||||||
| chr3:108214323
|
C | T | 1 | a0001c0001t0005g0030 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.495-302G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214323 | ||||||
| chr3:108214483
|
G | T | 2 | a0001c0001t0005g0030a0001c0001t0005g0031 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.495-462C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214483 | ||||||
| chr3:108214503
|
C | T | 1 | a0001c0001t0006g0147 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.495-482G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214503 | ||||||
| chr3:108214586
|
A | G | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-565T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214586 | ||||||
| chr3:108214606
|
A | G | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.495-585T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214606 | ||||||
| chr3:108214620
|
T | C | 2 | a0001c0001t0010g0144a0001c0001t0010g0145 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.495-599A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214620 | ||||||
| chr3:108214630
|
T | C | 1 | a0001c0009t0006g0153 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.495-609A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214630 | ||||||
| chr3:108214751
|
A | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-730T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214751 | ||||||
| chr3:108214756
|
A | AC | 5 | a0001c0001t0002g0009a0001c0001t0002g0073a0001c0001t0002g0074others(2): Show | 6 | HG02523.hp2 NA18953.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.495-736_495-735ins others(1): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214756 | ||||||
| chr3:108214757
|
A | C | 5 | a0001c0001t0002g0009a0001c0001t0002g0073a0001c0001t0002g0074others(2): Show | 6 | HG02523.hp2 NA18953.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.495-736T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214757 | ||||||
| chr3:108214765
|
T | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.495-744A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214765 | ||||||
| chr3:108214946
|
A | G | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-925T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214946 | ||||||
| chr3:108215199
|
A | G | 4 | a0001c0001t0003g0062a0001c0001t0003g0063a0001c0001t0003g0064others(1): Show | 4 | HG02622.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.495-1178T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215199 | ||||||
| chr3:108215213
|
AT | A | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-1193delA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215213 | ||||||
| chr3:108215267
|
A | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-1246T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215267 | ||||||
| chr3:108215356
|
G | A | 1 | a0001c0012t0015g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.495-1335C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215356 | ||||||
| chr3:108215455
|
C | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-1434G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215455 | ||||||
| chr3:108215514
|
G | A | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-1493C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215514 | ||||||
| chr3:108215543
|
C | T | 2 | a0001c0001t0006g0147a0001c0001t0006g0148 | 2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.495-1522G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215543 | ||||||
| chr3:108215565
|
G | A | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-1544C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215565 | ||||||
| chr3:108215567
|
T | TA | 5 | a0001c0001t0003g0225a0001c0001t0003g0226a0001c0001t0003g0246others(2): Show | 5 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.495-1547dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215567 | ||||||
| chr3:108215610
|
A | G | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-1589T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215610 | ||||||
| chr3:108215622
|
AATC | A | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-1604_495-1602d others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215622 | ||||||
| chr3:108215627
|
T | C | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-1606A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215627 | ||||||
| chr3:108215663
|
G | T | 4 | a0001c0002t0004g0035a0001c0002t0004g0037a0001c0002t0004g0038others(1): Show | 4 | HG01070.hp2 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.495-1642C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215663 | ||||||
| chr3:108215702
|
T | A | 2 | a0001c0002t0004g0032a0001c0002t0004g0061 | 2 | HG02129.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.495-1681A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215702 | ||||||
| chr3:108215739
|
A | C | 2 | a0001c0001t0005g0247a0001c0001t0005g0248 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.495-1718T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215739 | ||||||
| chr3:108215910
|
C | T | 3 | a0001c0001t0002g0070a0001c0001t0002g0071a0001c0001t0002g0072 | 3 | HG01243.hp2 HG01934.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.495-1889G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215910 | ||||||
| chr3:108215915
|
G | A | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.495-1894C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215915 | ||||||
| chr3:108216039
|
T | C | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-2018A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108216039 | ||||||
| chr3:108216131
|
T | C | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-2110A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108216131 | ||||||
| chr3:108216253
|
C | T | 1 | a0001c0002t0004g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.495-2232G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108216253 | ||||||
| chr3:108216307
|
A | G | 213 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(210): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.494+2228T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108216307 | ||||||
| chr3:108216351
|
G | A | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.494+2184C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108216351 | ||||||
| chr3:108216438
|
G | A | 2 | a0001c0001t0005g0247a0001c0001t0005g0248 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.494+2097C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108216438 | ||||||
| chr3:108216696
|
T | C | 31 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(28): Show | 32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.494+1839A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108216696 | ||||||
| chr3:108216704
|
A | G | 1 | a0001c0001t0002g0013 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.494+1831T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108216704 | ||||||
| chr3:108216852
|
A | G | 1 | a0001c0001t0002g0069 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.494+1683T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108216852 | ||||||
| chr3:108217288
|
T | C | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.494+1247A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217288 | ||||||
| chr3:108217403
|
C | T | 1 | a0001c0001t0003g0146 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.494+1132G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217403 | ||||||
| chr3:108217426
|
C | T | 1 | a0001c0001t0002g0068 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.494+1109G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217426 | ||||||
| chr3:108217478
|
T | G | 1 | a0001c0001t0002g0140 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.494+1057A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217478 | ||||||
| chr3:108217521
|
A | G | 1 | a0001c0001t0002g0067 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.494+1014T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217521 | ||||||
| chr3:108217648
|
T | C | 1 | a0002c0006t0005g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.494+887A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217648 | ||||||
| chr3:108217671
|
AAT | A | 3 | a0001c0001t0001g0222a0001c0001t0005g0250a0001c0001t0009g0221 | 3 | HG02698.hp1 HG03017.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.494+862_494+863del others(2): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217671 | ||||||
| chr3:108217711
|
C | A | 213 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(210): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.494+824G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217711 | ||||||
| chr3:108217727
|
T | TA | 34 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0034others(31): Show | 35 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.494+807dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217727 | ||||||
| chr3:108217728
|
A | T | 83 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(80): Show | 97 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.494+807T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217728 | ||||||
| chr3:108217769
|
G | C | 1 | a0001c0001t0002g0013 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.494+766C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217769 | ||||||
| chr3:108217794
|
G | A | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.494+741C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217794 | ||||||
| chr3:108217851
|
T | C | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.494+684A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217851 | ||||||
| chr3:108218003
|
A | AAATAT | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.494+527_494+531dup others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218003 | ||||||
| chr3:108218147
|
T | G | 2 | a0001c0001t0001g0251a0001c0001t0005g0252 | 2 | HG00280.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.494+388A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218147 | ||||||
| chr3:108218233
|
A | G | 1 | a0001c0001t0003g0062 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.494+302T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218233 | ||||||
| chr3:108218241
|
TA | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.494+293delT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218241 | ||||||
| chr3:108218243
|
A | T | 4 | a0001c0002t0007g0315a0001c0002t0007g0316a0001c0002t0007g0317others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+292T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218243 | ||||||
| chr3:108218318
|
C | G | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.494+217G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218318 | ||||||
| chr3:108218318
|
C | T | 1 | a0001c0001t0003g0146 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.494+217G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218318 | ||||||
| chr3:108218384
|
T | C | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.494+151A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218384 | ||||||
| chr3:108218439
|
A | G | 213 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(210): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.494+96T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218439 | ||||||
| chr3:108218455
|
GTTCAATT others(42): Show |
G | 1 | a0001c0002t0004g0032 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.494+31_494+79delTT others(47): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218455 | ||||||
| chr3:108218513
|
C | T | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.494+22G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218513 | ||||||
| chr3:108218697
|
C | T | 25 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0156others(22): Show | 28 | HG00099.hp1 HG00741.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.376-44G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108218697 | ||||||
| chr3:108218724
|
G | A | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.376-71C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108218724 | ||||||
| chr3:108218755
|
C | T | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.376-102G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108218755 | ||||||
| chr3:108219095
|
G | A | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.375+315C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108219095 | ||||||
| chr3:108219106
|
G | C | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.375+304C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108219106 | ||||||
| chr3:108219116
|
A | AT | 174 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(171): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.375+293dupA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108219116 | ||||||
| chr3:108219194
|
T | A | 59 | a0001c0001t0003g0007a0001c0001t0003g0023a0001c0001t0003g0024others(56): Show | 66 | HG00423.hp1 HG00642.hp1 HG01256.hp1 others(63): Show |
intron_variant | MODIFIER | c.375+216A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108219194 | ||||||
| chr3:108219195
|
A | T | 2 | a0001c0001t0003g0225a0001c0001t0003g0226 | 2 | HG02145.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.375+215T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108219195 | ||||||
| chr3:108219213
|
A | G | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.375+197T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108219213 | ||||||
| chr3:108219364
|
A | C | 4 | a0001c0001t0003g0062a0001c0001t0003g0063a0001c0001t0003g0064others(1): Show | 4 | HG02622.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.375+46T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108219364 | ||||||
| chr3:108219393
|
G | C | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.375+17C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108219393 | ||||||
| chr3:108219594
|
T | C | 2 | a0001c0003t0001g0223a0001c0003t0001g0224 | 2 | HG02280.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.213-22A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108219594 | ||||||
| chr3:108219696
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.213-124T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108219696 | ||||||
| chr3:108219737
|
C | A | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.213-165G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108219737 | ||||||
| chr3:108219737
|
C | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.213-165G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108219737 | ||||||
| chr3:108219965
|
C | T | 4 | a0001c0001t0003g0062a0001c0001t0003g0063a0001c0001t0003g0064others(1): Show | 4 | HG02622.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.213-393G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108219965 | ||||||
| chr3:108220025
|
G | A | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.213-453C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108220025 | ||||||
| chr3:108220218
|
A | T | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.213-646T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108220218 | ||||||
| chr3:108220239
|
A | C | 1 | a0001c0001t0003g0155 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.213-667T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108220239 | ||||||
| chr3:108220378
|
C | G | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.213-806G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108220378 | ||||||
| chr3:108220714
|
A | AC | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.213-1143_213-1142i others(3): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108220714 | ||||||
| chr3:108220828
|
T | C | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.213-1256A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108220828 | ||||||
| chr3:108220937
|
A | C | 37 | a0001c0001t0010g0144a0001c0001t0010g0145a0001c0002t0004g0008others(34): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.212+1174T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108220937 | ||||||
| chr3:108221184
|
G | A | 1 | a0001c0001t0005g0304 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.212+927C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221184 | ||||||
| chr3:108221245
|
T | C | 2 | a0001c0001t0010g0144a0001c0001t0010g0145 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.212+866A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221245 | ||||||
| chr3:108221287
|
A | G | 35 | a0001c0002t0004g0008a0001c0002t0004g0032a0001c0002t0004g0033others(32): Show | 36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.212+824T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221287 | ||||||
| chr3:108221611
|
A | G | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.212+500T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221611 | ||||||
| chr3:108221722
|
A | AG | 308 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(305): Show | 343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.212+388_212+389ins others(1): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221722 | ||||||
| chr3:108221759
|
T | C | 4 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(1): Show | 4 | HG01106.hp2 HG02895.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.212+352A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221759 | ||||||
| chr3:108221768
|
T | C | 1 | a0001c0001t0003g0309 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.212+343A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221768 | ||||||
| chr3:108221789
|
ATT | A | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.212+320_212+321del others(2): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221789 | ||||||
| chr3:108221926
|
A | G | 1 | a0001c0001t0002g0310 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.212+185T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221926 | ||||||
| chr3:108221927
|
G | C | 1 | a0001c0001t0002g0310 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.212+184C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221927 | ||||||
| chr3:108221934
|
C | A | 1 | a0001c0001t0001g0311 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.212+177G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221934 | ||||||
| chr3:108222076
|
C | T | 2 | a0001c0001t0005g0030a0001c0001t0005g0031 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.212+35G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108222076 | ||||||
| chr3:108222077
|
AGGCACCC others(17): Show |
A | 3 | a0001c0001t0003g0028a0001c0001t0003g0312a0001c0001t0003g0313 | 4 | HG02165.hp2 NA18747.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.212+10_212+33delGG others(22): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108222077 |