Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9742 |
|---|---|
| ensemblid | ENSG00000187535.14 |
| hgncid | 29077 |
| symbol | IFT140 |
| name | intraflagellar transport 140 |
| refseq_nuc | NM_014714.4 |
| refseq_prot | NP_055529.2 |
| ensembl_nuc | ENST00000426508.7 |
| ensembl_prot | ENSP00000406012.2 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 1510427 |
| end | 1612072 |
| strand | - |
| ver | v1.2 |
| region | chr16:1510427-1612072 |
| region5000 | chr16:1505427-1617072 |
| regionname0 | IFT140_chr16_1510427_1612072 |
| regionname5000 | IFT140_chr16_1505427_1617072 |
| 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 | 1462 | 212 | 54 | 31 | 87 | 6 | 32 | 60 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0002 | 0/0 | 1462 | 29 | 0 | 7 | 19 | 1 | 2 | 16 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0003 | 0/0 | 1462 | 27 | 7 | 2 | 10 | 2 | 6 | 7 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0004 | 0/0 | 1462 | 9 | 0 | 9 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0005 | 0/0 | 1462 | 8 | 6 | 1 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0006 | 0/0 | 1462 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0007 | 0/0 | 1462 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0008 | 0/0 | 1462 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0009 | 0/0 | 1462 | 4 | 0 | 3 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0010 | 0/0 | 1462 | 4 | 0 | 1 | 3 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0011 | 0/0 | 1462 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0012 | 0/0 | 1462 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0013 | 0/0 | 1462 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0014 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0015 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0016 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0017 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0018 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0019 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0020 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0021 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0022 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0023 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0024 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0025 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0026 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0027 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0028 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0029 | 0/0 | 1462 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0030 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0031 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| 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 | 4389 | 103 | 20 | 19 | 40 | 5 | 17 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0002 | 0/0 | 4389 | 64 | 23 | 7 | 20 | 1 | 13 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0003 | 0/0 | 4389 | 29 | 0 | 7 | 19 | 1 | 2 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0004 | 0/0 | 4389 | 21 | 9 | 2 | 9 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0005 | 0/0 | 4389 | 18 | 3 | 1 | 9 | 2 | 3 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0006 | 0/0 | 4389 | 7 | 0 | 7 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0007 | 0/0 | 4389 | 6 | 6 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0008 | 0/0 | 4389 | 5 | 0 | 0 | 5 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0009 | 0/0 | 4389 | 5 | 4 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0010 | 0/0 | 4389 | 5 | 0 | 0 | 5 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0011 | 0/0 | 4389 | 4 | 0 | 3 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0012 | 0/0 | 4389 | 4 | 4 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0013 | 0/0 | 4389 | 4 | 3 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0014 | 0/0 | 4389 | 3 | 0 | 0 | 3 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0015 | 0/0 | 4389 | 2 | 2 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0016 | 0/0 | 4389 | 2 | 2 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0017 | 0/0 | 4389 | 2 | 1 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0018 | 0/0 | 4389 | 2 | 0 | 0 | 1 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0019 | 0/0 | 4389 | 2 | 2 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0020 | 0/0 | 4389 | 2 | 0 | 2 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0021 | 0/0 | 4389 | 2 | 0 | 0 | 2 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0022 | 0/0 | 4389 | 2 | 0 | 2 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0023 | 0/0 | 4389 | 2 | 0 | 0 | 2 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0024 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0025 | 0/0 | 4389 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0026 | 0/0 | 4389 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0027 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0028 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0029 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0030 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0031 | 0/0 | 4389 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0032 | 0/0 | 4389 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0033 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0034 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0035 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0036 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0037 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0038 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0039 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0040 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0041 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0042 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0043 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0044 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0045 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0046 | 0/0 | 4389 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0047 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0048 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0049 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0050 | 0/0 | 4389 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0051 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0052 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0053 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0054 | 0/0 | 4389 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0055 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0056 | 0/0 | 4389 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0057 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0058 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0059 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0060 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| c0061 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| 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 | 844 | 110 | 39 | 12 | 43 | 1 | 15 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| t0002 | 1/1 | 844 | 110 | 15 | 28 | 44 | 4 | 17 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| t0003 | 0/0 | 844 | 84 | 25 | 15 | 37 | 4 | 3 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| t0004 | 0/0 | 844 | 21 | 13 | 3 | 5 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| t0005 | 0/0 | 844 | 2 | 0 | 0 | 0 | 0 | 2 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| t0006 | 0/0 | 844 | 2 | 0 | 0 | 2 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| t0007 | 0/0 | 844 | 2 | 0 | 0 | 0 | 1 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| t0008 | 0/0 | 844 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| t0009 | 0/0 | 844 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| t0010 | 0/0 | 844 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| 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 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0286 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0292 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| 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 | 4389 | 103 | 20 | 19 | 40 | 5 | 17 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0002 | 0/0 | 4389 | 64 | 23 | 7 | 20 | 1 | 13 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0004 | 0/0 | 4389 | 21 | 9 | 2 | 9 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0008 | 0/0 | 4389 | 5 | 0 | 0 | 5 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0010 | 0/0 | 4389 | 5 | 0 | 0 | 5 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0014 | 0/0 | 4389 | 3 | 0 | 0 | 3 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0020 | 0/0 | 4389 | 2 | 0 | 2 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0037 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0043 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0045 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0048 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0050 | 0/0 | 4389 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0052 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0053 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0054 | 0/0 | 4389 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0057 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0002c0003 | 0/0 | 4389 | 29 | 0 | 7 | 19 | 1 | 2 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0003c0005 | 0/0 | 4389 | 18 | 3 | 1 | 9 | 2 | 3 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0003c0017 | 0/0 | 4389 | 2 | 1 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0003c0018 | 0/0 | 4389 | 2 | 0 | 0 | 1 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0003c0019 | 0/0 | 4389 | 2 | 2 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0003c0031 | 0/0 | 4389 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0003c0032 | 0/0 | 4389 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0003c0059 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0004c0006 | 0/0 | 4389 | 7 | 0 | 7 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0004c0025 | 0/0 | 4389 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0004c0026 | 0/0 | 4389 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0005c0009 | 0/0 | 4389 | 5 | 4 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0005c0039 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0005c0044 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0005c0049 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0006c0007 | 0/0 | 4389 | 6 | 6 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0007c0013 | 0/0 | 4389 | 4 | 3 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0007c0060 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0008c0015 | 0/0 | 4389 | 2 | 2 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0008c0016 | 0/0 | 4389 | 2 | 2 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0009c0011 | 0/0 | 4389 | 4 | 0 | 3 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0010c0021 | 0/0 | 4389 | 2 | 0 | 0 | 2 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0010c0040 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0010c0046 | 0/0 | 4389 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0011c0012 | 0/0 | 4389 | 4 | 4 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0012c0023 | 0/0 | 4389 | 2 | 0 | 0 | 2 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0013c0022 | 0/0 | 4389 | 2 | 0 | 2 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0014c0061 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0015c0028 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0016c0027 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0017c0029 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0018c0030 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0019c0033 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0020c0035 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0021c0034 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0022c0038 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0023c0051 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0024c0042 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0025c0041 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0026c0047 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0027c0036 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0028c0055 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0029c0056 | 0/0 | 4389 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0030c0058 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0031c0024 | 0/0 | 4389 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 1/1 | 5232 | 92 | 13 | 18 | 39 | 4 | 16 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0001t0003 | 0/0 | 5232 | 2 | 1 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0001t0004 | 0/0 | 5232 | 7 | 6 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0001t0007 | 0/0 | 5232 | 2 | 0 | 0 | 0 | 1 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0002t0001 | 0/0 | 5232 | 57 | 21 | 6 | 19 | 1 | 10 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0002t0003 | 0/0 | 5232 | 4 | 2 | 1 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0002t0005 | 0/0 | 5232 | 2 | 0 | 0 | 0 | 0 | 2 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0002t0010 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0004t0001 | 0/0 | 5232 | 8 | 5 | 1 | 1 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0004t0003 | 0/0 | 5232 | 13 | 4 | 1 | 8 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0008t0001 | 0/0 | 5232 | 5 | 0 | 0 | 5 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0010t0001 | 0/0 | 5232 | 2 | 0 | 0 | 2 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0010t0002 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0010t0004 | 0/0 | 5232 | 2 | 0 | 0 | 2 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0014t0003 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0014t0006 | 0/0 | 5232 | 2 | 0 | 0 | 2 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0020t0003 | 0/0 | 5232 | 2 | 0 | 2 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0037t0001 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0043t0001 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0045t0002 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0048t0002 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0050t0002 | 0/0 | 5232 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0052t0004 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0053t0002 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0054t0001 | 0/0 | 5232 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0001c0057t0003 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0002c0003t0003 | 0/0 | 5232 | 29 | 0 | 7 | 19 | 1 | 2 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0003c0005t0001 | 0/0 | 5232 | 12 | 1 | 1 | 7 | 0 | 3 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0003c0005t0003 | 0/0 | 5232 | 6 | 2 | 0 | 2 | 2 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0003c0017t0001 | 0/0 | 5232 | 2 | 1 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0003c0018t0001 | 0/0 | 5232 | 2 | 0 | 0 | 1 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0003c0019t0003 | 0/0 | 5232 | 2 | 2 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0003c0031t0009 | 0/0 | 5232 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0003c0032t0008 | 0/0 | 5232 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0003c0059t0001 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0004c0006t0002 | 0/0 | 5232 | 7 | 0 | 7 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0004c0025t0002 | 0/0 | 5232 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0004c0026t0004 | 0/0 | 5232 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0005c0009t0004 | 0/0 | 5232 | 5 | 4 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0005c0039t0001 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0005c0044t0004 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0005c0049t0004 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0006c0007t0003 | 0/0 | 5232 | 6 | 6 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0007c0013t0001 | 0/0 | 5232 | 4 | 3 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0007c0060t0001 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0008c0015t0003 | 0/0 | 5232 | 2 | 2 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0008c0016t0001 | 0/0 | 5232 | 2 | 2 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0009c0011t0003 | 0/0 | 5232 | 4 | 0 | 3 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0010c0021t0002 | 0/0 | 5232 | 2 | 0 | 0 | 2 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0010c0040t0003 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0010c0046t0004 | 0/0 | 5232 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0011c0012t0003 | 0/0 | 5232 | 4 | 4 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0012c0023t0001 | 0/0 | 5232 | 2 | 0 | 0 | 2 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0013c0022t0002 | 0/0 | 5232 | 2 | 0 | 2 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0014c0061t0001 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0015c0028t0001 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0016c0027t0003 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0017c0029t0003 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0018c0030t0003 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0019c0033t0003 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0020c0035t0003 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0021c0034t0003 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0022c0038t0001 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0023c0051t0004 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0024c0042t0001 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0025c0041t0001 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0026c0047t0002 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0027c0036t0003 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0028c0055t0004 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0029c0056t0001 | 0/0 | 5232 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0030c0058t0001 | 0/0 | 5232 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| a0031c0024t0001 | 0/0 | 5232 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | copy fasta | chr16 | 1505427 | 1617072 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0286 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0292 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0007g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0001t0007g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0005g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0005g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0002t0010g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0004t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0004t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0004t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0004t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0004t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0004t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0004t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0004t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0004t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0004t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0004t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0004t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0004t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0004t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0004t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0004t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0004t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0004t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0004t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0004t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0004t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0008t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0008t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0008t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0008t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0008t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0010t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0010t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0010t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0010t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0010t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0014t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0014t0006g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0014t0006g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0020t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0020t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0037t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0043t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0045t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0048t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0050t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0052t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0053t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0054t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0001c0057t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0002c0003t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0005t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0005t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0005t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0005t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0005t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0005t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0005t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0005t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0005t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0005t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0005t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0005t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0005t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0005t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0005t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0005t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0005t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0017t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0017t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0018t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0018t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0019t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0019t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0031t0009g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0032t0008g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0003c0059t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0004c0006t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0004c0006t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0004c0006t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0004c0006t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0004c0006t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0004c0006t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0004c0006t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0004c0025t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0004c0026t0004g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0005c0009t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0005c0009t0004g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0005c0009t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0005c0009t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0005c0009t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0005c0039t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0005c0044t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0005c0049t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0006c0007t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0006c0007t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0006c0007t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0006c0007t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0006c0007t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0006c0007t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0007c0013t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0007c0013t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0007c0013t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0007c0013t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0007c0060t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0008c0015t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0008c0015t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0008c0016t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0008c0016t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0009c0011t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0009c0011t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0009c0011t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0009c0011t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0010c0021t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0010c0021t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0010c0040t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0010c0046t0004g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0011c0012t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0011c0012t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0011c0012t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0011c0012t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0012c0023t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0012c0023t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0013c0022t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0013c0022t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0014c0061t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0015c0028t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0016c0027t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0017c0029t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0018c0030t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0019c0033t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0020c0035t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0021c0034t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0022c0038t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0023c0051t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0024c0042t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0025c0041t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0026c0047t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0027c0036t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0028c0055t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0029c0056t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0030c0058t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| a0031c0024t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0305 | EUR | GBR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00099 | hp2 | a0003 | c0005 | t0003 | g0149 | EUR | GBR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00280 | hp1 | a0003 | c0005 | t0003 | g0153 | EUR | FIN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0071 | EUR | FIN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00323 | hp1 | a0001 | c0001 | t0007 | g0275 | EUR | FIN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0285 | EUR | FIN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00408 | hp1 | a0002 | c0003 | t0003 | g0021 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00544 | hp1 | a0002 | c0003 | t0003 | g0026 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00544 | hp2 | a0001 | c0004 | t0003 | g0185 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00609 | hp1 | a0001 | c0048 | t0002 | g0265 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00609 | hp2 | a0003 | c0005 | t0003 | g0151 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00639 | hp1 | a0001 | c0054 | t0001 | g0119 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00639 | hp2 | a0001 | c0004 | t0003 | g0101 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00642 | hp1 | a0013 | c0022 | t0002 | g0227 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00642 | hp2 | a0002 | c0003 | t0003 | g0020 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00673 | hp1 | a0024 | c0042 | t0001 | g0109 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | CHS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00733 | hp1 | a0004 | c0026 | t0004 | g0312 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00741 | hp1 | a0001 | c0002 | t0003 | g0208 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG00741 | hp2 | a0004 | c0006 | t0002 | g0240 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01069 | hp1 | a0001 | c0020 | t0003 | g0139 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01070 | hp1 | a0005 | c0009 | t0004 | g0167 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01070 | hp2 | a0002 | c0003 | t0003 | g0028 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01071 | hp1 | a0002 | c0003 | t0003 | g0027 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01071 | hp2 | a0001 | c0020 | t0003 | g0138 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0309 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0073 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0300 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0291 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01099 | hp2 | a0013 | c0022 | t0002 | g0230 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01109 | hp2 | a0007 | c0013 | t0001 | g0191 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01175 | hp1 | a0029 | c0056 | t0001 | g0068 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01175 | hp2 | a0004 | c0006 | t0002 | g0313 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01192 | hp1 | a0003 | c0005 | t0001 | g0147 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01192 | hp2 | a0010 | c0046 | t0004 | g0267 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01243 | hp2 | a0003 | c0017 | t0001 | g0058 | AMR | PUR | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01256 | hp1 | a0004 | c0006 | t0002 | g0204 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0212 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0330 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01257 | hp2 | a0009 | c0011 | t0003 | g0044 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0331 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0213 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01261 | hp1 | a0009 | c0011 | t0003 | g0042 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01261 | hp2 | a0002 | c0003 | t0003 | g0034 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01346 | hp1 | a0009 | c0011 | t0003 | g0043 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01346 | hp2 | a0004 | c0006 | t0002 | g0237 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0299 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0084 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0218 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0329 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01496 | hp1 | a0004 | c0006 | t0002 | g0235 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01516 | hp1 | a0009 | c0011 | t0003 | g0045 | EUR | IBS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0307 | EUR | IBS | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01884 | hp1 | a0005 | c0009 | t0004 | g0177 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0196 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01891 | hp1 | a0007 | c0013 | t0001 | g0194 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01928 | hp1 | a0002 | c0003 | t0003 | g0016 | AMR | PEL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0310 | AMR | PEL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01978 | hp2 | a0004 | c0006 | t0002 | g0327 | AMR | PEL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01993 | hp1 | a0002 | c0003 | t0003 | g0011 | AMR | PEL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PEL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | PEL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02004 | hp2 | a0004 | c0006 | t0002 | g0233 | AMR | PEL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02015 | hp1 | a0003 | c0005 | t0001 | g0155 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02015 | hp2 | a0022 | c0038 | t0001 | g0094 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02055 | hp2 | a0007 | c0060 | t0001 | g0195 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02056 | hp1 | a0001 | c0004 | t0001 | g0095 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02056 | hp2 | a0010 | c0021 | t0002 | g0316 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02071 | hp1 | a0001 | c0043 | t0001 | g0219 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02074 | hp2 | a0010 | c0021 | t0002 | g0315 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02080 | hp1 | a0001 | c0014 | t0003 | g0103 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02080 | hp2 | a0001 | c0057 | t0003 | g0214 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02083 | hp2 | a0001 | c0004 | t0003 | g0124 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02129 | hp2 | a0003 | c0005 | t0001 | g0146 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02132 | hp2 | a0001 | c0052 | t0004 | g0234 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02135 | hp1 | a0001 | c0010 | t0004 | g0232 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02145 | hp1 | a0001 | c0004 | t0001 | g0075 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0251 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02148 | hp2 | a0002 | c0003 | t0003 | g0022 | AMR | PEL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | CDX | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | CDX | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | CDX | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02165 | hp2 | a0005 | c0039 | t0001 | g0158 | EAS | CDX | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0301 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0131 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02258 | hp1 | a0028 | c0055 | t0004 | g0165 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02280 | hp2 | a0003 | c0017 | t0001 | g0059 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02523 | hp1 | a0002 | c0003 | t0003 | g0015 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02523 | hp2 | a0001 | c0014 | t0006 | g0209 | EAS | KHV | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02572 | hp1 | a0005 | c0044 | t0004 | g0168 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02572 | hp2 | a0007 | c0013 | t0001 | g0193 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0243 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0087 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02615 | hp1 | a0014 | c0061 | t0001 | g0116 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0298 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02622 | hp2 | a0001 | c0002 | t0003 | g0106 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02630 | hp2 | a0005 | c0009 | t0004 | g0173 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0254 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02647 | hp2 | a0003 | c0005 | t0001 | g0150 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02683 | hp1 | a0001 | c0001 | t0007 | g0270 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02683 | hp2 | a0003 | c0032 | t0008 | g0003 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0236 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0061 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0272 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0223 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02809 | hp2 | a0030 | c0058 | t0001 | g0163 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0260 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02818 | hp2 | a0001 | c0037 | t0001 | g0127 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0047 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02895 | hp2 | a0006 | c0007 | t0003 | g0162 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0333 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02896 | hp2 | a0003 | c0019 | t0003 | g0137 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0334 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02897 | hp2 | a0006 | c0007 | t0003 | g0161 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0175 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0097 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02965 | hp1 | a0005 | c0049 | t0004 | g0171 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0077 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02970 | hp1 | a0001 | c0004 | t0001 | g0105 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02970 | hp2 | a0008 | c0016 | t0001 | g0056 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02976 | hp1 | a0003 | c0005 | t0003 | g0135 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02976 | hp2 | a0001 | c0045 | t0002 | g0176 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03017 | hp2 | a0003 | c0005 | t0001 | g0148 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03041 | hp1 | a0007 | c0013 | t0001 | g0192 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0190 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03098 | hp1 | a0027 | c0036 | t0003 | g0132 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03130 | hp1 | a0001 | c0004 | t0003 | g0115 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03130 | hp2 | a0008 | c0015 | t0003 | g0053 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03139 | hp1 | a0006 | c0007 | t0003 | g0164 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03139 | hp2 | a0001 | c0002 | t0003 | g0090 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0268 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03209 | hp1 | a0011 | c0012 | t0003 | g0051 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03209 | hp2 | a0006 | c0007 | t0003 | g0160 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03225 | hp1 | a0005 | c0009 | t0004 | g0166 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03225 | hp2 | a0026 | c0047 | t0002 | g0289 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0326 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03453 | hp2 | a0001 | c0004 | t0003 | g0079 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03486 | hp2 | a0001 | c0004 | t0003 | g0088 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03490 | hp2 | a0001 | c0002 | t0005 | g0001 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0322 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03491 | hp2 | a0003 | c0005 | t0001 | g0142 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03492 | hp1 | a0003 | c0005 | t0001 | g0141 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03492 | hp2 | a0001 | c0002 | t0005 | g0002 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0076 | AFR | ESN | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03540 | hp2 | a0015 | c0028 | t0001 | g0057 | AFR | GWD | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03579 | hp1 | a0003 | c0059 | t0001 | g0050 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0128 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0274 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0311 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0282 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03704 | hp2 | a0001 | c0050 | t0002 | g0328 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03710 | hp1 | a0002 | c0003 | t0003 | g0031 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03710 | hp2 | a0001 | c0002 | t0003 | g0064 | SAS | PJL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0281 | SAS | BEB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0224 | SAS | BEB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0207 | SAS | BEB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03927 | hp2 | a0003 | c0031 | t0009 | g0140 | SAS | BEB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0217 | SAS | BEB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03942 | hp2 | a0002 | c0003 | t0003 | g0032 | SAS | BEB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0129 | SAS | STU | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0308 | SAS | STU | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0122 | SAS | STU | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0263 | SAS | STU | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG04204 | hp1 | a0003 | c0018 | t0001 | g0133 | SAS | STU | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0273 | SAS | STU | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | STU | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | STU | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18522 | hp1 | a0006 | c0007 | t0003 | g0199 | AFR | YRI | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0121 | AFR | YRI | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0170 | AFR | YRI | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | YRI | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18941 | hp1 | a0002 | c0003 | t0003 | g0007 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18941 | hp2 | a0018 | c0030 | t0003 | g0198 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18943 | hp2 | a0001 | c0008 | t0001 | g0222 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18945 | hp1 | a0001 | c0004 | t0003 | g0112 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18948 | hp1 | a0012 | c0023 | t0001 | g0048 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18948 | hp2 | a0003 | c0005 | t0001 | g0144 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18949 | hp1 | a0002 | c0003 | t0003 | g0037 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18950 | hp2 | a0002 | c0003 | t0003 | g0040 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18953 | hp1 | a0002 | c0003 | t0003 | g0008 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18959 | hp2 | a0019 | c0033 | t0003 | g0018 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18961 | hp1 | a0002 | c0003 | t0003 | g0030 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18961 | hp2 | a0001 | c0004 | t0003 | g0082 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18962 | hp1 | a0001 | c0002 | t0010 | g0186 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18964 | hp2 | a0002 | c0003 | t0003 | g0036 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18970 | hp2 | a0001 | c0010 | t0002 | g0321 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18971 | hp1 | a0001 | c0010 | t0001 | g0125 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18971 | hp2 | a0001 | c0010 | t0004 | g0225 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18973 | hp2 | a0031 | c0024 | t0001 | g0111 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18979 | hp1 | a0001 | c0010 | t0001 | g0126 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18980 | hp1 | a0001 | c0053 | t0002 | g0288 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18983 | hp1 | a0001 | c0004 | t0003 | g0108 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18983 | hp2 | a0001 | c0008 | t0001 | g0216 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18990 | hp1 | a0002 | c0003 | t0003 | g0039 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18990 | hp2 | a0001 | c0004 | t0003 | g0130 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18991 | hp1 | a0012 | c0023 | t0001 | g0060 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA18993 | hp2 | a0001 | c0014 | t0006 | g0215 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19003 | hp1 | a0002 | c0003 | t0003 | g0006 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19007 | hp2 | a0003 | c0005 | t0001 | g0143 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19010 | hp1 | a0002 | c0003 | t0003 | g0017 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19043 | hp1 | a0016 | c0027 | t0003 | g0134 | AFR | LWK | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19043 | hp2 | a0003 | c0005 | t0003 | g0063 | AFR | LWK | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19055 | hp2 | a0002 | c0003 | t0003 | g0019 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19056 | hp1 | a0002 | c0003 | t0003 | g0025 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19056 | hp2 | a0001 | c0008 | t0001 | g0221 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19057 | hp2 | a0003 | c0005 | t0001 | g0156 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19063 | hp1 | a0025 | c0041 | t0001 | g0062 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19063 | hp2 | a0002 | c0003 | t0003 | g0029 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19064 | hp1 | a0002 | c0003 | t0003 | g0023 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19064 | hp2 | a0001 | c0004 | t0003 | g0014 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19065 | hp2 | a0003 | c0005 | t0001 | g0157 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19066 | hp2 | a0003 | c0005 | t0001 | g0145 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19067 | hp1 | a0003 | c0018 | t0001 | g0152 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19074 | hp1 | a0017 | c0029 | t0003 | g0188 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19074 | hp2 | a0002 | c0003 | t0003 | g0024 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19079 | hp1 | a0002 | c0003 | t0003 | g0009 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19081 | hp2 | a0023 | c0051 | t0004 | g0249 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19085 | hp2 | a0002 | c0003 | t0003 | g0033 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19086 | hp1 | a0021 | c0034 | t0003 | g0010 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19086 | hp2 | a0003 | c0005 | t0003 | g0154 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19087 | hp1 | a0010 | c0040 | t0003 | g0187 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19087 | hp2 | a0020 | c0035 | t0003 | g0012 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19088 | hp1 | a0001 | c0008 | t0001 | g0211 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19088 | hp2 | a0001 | c0004 | t0003 | g0114 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19091 | hp1 | a0001 | c0008 | t0001 | g0203 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19240 | hp1 | a0011 | c0012 | t0003 | g0201 | AFR | YRI | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | YRI | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA20129 | hp1 | a0008 | c0016 | t0001 | g0054 | AFR | ASW | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA20129 | hp2 | a0001 | c0004 | t0001 | g0117 | AFR | ASW | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0304 | EUR | TSI | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA20752 | hp2 | a0002 | c0003 | t0003 | g0035 | EUR | TSI | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA20905 | hp1 | a0001 | c0004 | t0001 | g0092 | SAS | GIH | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0096 | SAS | GIH | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01123 | hp1 | a0004 | c0025 | t0002 | g0238 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG01123 | hp2 | a0001 | c0004 | t0001 | g0066 | AMR | CLM | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02486 | hp1 | a0005 | c0009 | t0004 | g0183 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02486 | hp2 | a0008 | c0015 | t0003 | g0055 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0098 | AFR | ACB | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03471 | hp1 | a0003 | c0019 | t0003 | g0136 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG03471 | hp2 | a0001 | c0004 | t0003 | g0189 | AFR | MSL | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG06807 | hp1 | a0011 | c0012 | t0003 | g0052 | AFR | USA | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| HG06807 | hp2 | a0006 | c0007 | t0003 | g0159 | AFR | USA | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | USA | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0290 | AFR | USA | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0069 | AFR | LWK | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| NA21309 | hp2 | a0011 | c0012 | t0003 | g0202 | AFR | LWK | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0286 | REF | REF | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0292 | REF | REF | IFT140_chr16_1505427_1617072 | IFT140 | chr16 | 1505427 | 1617072 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:1511024
|
C | T | 1 | a0023 | 1 | NA19081.hp2 | missense_variant | MODERATE | c.4309G>A | p.Glu1437Lys | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 31/31 | 4635/5232 | 4309/4389 | 1437/1462 | chr16 | 1511024 | ||
| chr16:1511069
|
C | T | 1 | a0016 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.4264G>A | p.Ala1422Thr | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 31/31 | 4590/5232 | 4264/4389 | 1422/1462 | chr16 | 1511069 | ||
| chr16:1519933
|
C | T | 1 | a0024 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.3988G>A | p.Ala1330Thr | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/31 | 4314/5232 | 3988/4389 | 1330/1462 | chr16 | 1519933 | ||
| chr16:1520261
|
A | G | 1 | a0005 | 8 | HG01070.hp1 HG01884.hp1 HG02165.hp2 others(5): Show |
missense_variant | MODERATE | c.3743T>C | p.Ile1248Thr | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 28/31 | 4069/5232 | 3743/4389 | 1248/1462 | chr16 | 1520261 | ||
| chr16:1520660
|
C | T | 1 | a0021 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.3602G>A | p.Arg1201His | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 27/31 | 3928/5232 | 3602/4389 | 1201/1462 | chr16 | 1520660 | ||
| chr16:1523889
|
G | A | 6 | a0002a0010a0018others(3): Show | 37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
missense_variant | MODERATE | c.3209C>T | p.Ala1070Val | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 25/31 | 3535/5232 | 3209/4389 | 1070/1462 | chr16 | 1523889 | ||
| chr16:1524614
|
C | T | 1 | a0025 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.3079G>A | p.Gly1027Arg | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 24/31 | 3405/5232 | 3079/4389 | 1027/1462 | chr16 | 1524614 | ||
| chr16:1525900
|
G | C | 1 | a0020 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.2755C>G | p.Arg919Gly | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/31 | 3081/5232 | 2755/4389 | 919/1462 | chr16 | 1525900 | ||
| chr16:1525909
|
C | T | 1 | a0026 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.2746G>A | p.Asp916Asn | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/31 | 3072/5232 | 2746/4389 | 916/1462 | chr16 | 1525909 | ||
| chr16:1557974
|
T | C | 1 | a0013 | 2 | HG00642.hp1 HG01099.hp2 |
missense_variant | MODERATE | c.2360A>G | p.Asp787Gly | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/31 | 2686/5232 | 2360/4389 | 787/1462 | chr16 | 1557974 | ||
| chr16:1558004
|
A | C | 1 | a0008 | 4 | HG02486.hp2 HG02970.hp2 HG03130.hp2 others(1): Show |
missense_variant | MODERATE | c.2330T>G | p.Leu777Arg | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/31 | 2656/5232 | 2330/4389 | 777/1462 | chr16 | 1558004 | ||
| chr16:1558016
|
C | T | 1 | a0022 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.2318G>A | p.Arg773Gln | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/31 | 2644/5232 | 2318/4389 | 773/1462 | chr16 | 1558016 | ||
| chr16:1562046
|
C | T | 1 | a0017 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.2138G>A | p.Arg713Gln | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/31 | 2464/5232 | 2138/4389 | 713/1462 | chr16 | 1562046 | ||
| chr16:1564007
|
G | C | 1 | a0027 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.2057C>G | p.Ala686Gly | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/31 | 2383/5232 | 2057/4389 | 686/1462 | chr16 | 1564007 | ||
| chr16:1564056
|
G | A | 1 | a0007 | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
missense_variant | MODERATE | c.2008C>T | p.Pro670Ser | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/31 | 2334/5232 | 2008/4389 | 670/1462 | chr16 | 1564056 | ||
| chr16:1564146
|
C | T | 2 | a0007a0027 | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
missense_variant | MODERATE | c.1918G>A | p.Asp640Asn | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/31 | 2244/5232 | 1918/4389 | 640/1462 | chr16 | 1564146 | ||
| chr16:1566200
|
C | T | 5 | a0002a0009a0019others(2): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
missense_variant | MODERATE | c.1862G>A | p.Arg621Gln | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/31 | 2188/5232 | 1862/4389 | 621/1462 | chr16 | 1566200 | ||
| chr16:1566231
|
C | T | 2 | a0015a0016 | 2 | HG03540.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.1831G>A | p.Val611Ile | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/31 | 2157/5232 | 1831/4389 | 611/1462 | chr16 | 1566231 | ||
| chr16:1568305
|
C | T | 2 | a0006a0011 | 10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
missense_variant | MODERATE | c.1682G>A | p.Ser561Asn | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/31 | 2008/5232 | 1682/4389 | 561/1462 | chr16 | 1568305 | ||
| chr16:1568320
|
T | C | 1 | a0028 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.1667A>G | p.His556Arg | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/31 | 1993/5232 | 1667/4389 | 556/1462 | chr16 | 1568320 | ||
| chr16:1583341
|
G | T | 1 | a0019 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.1405C>A | p.Leu469Ile | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/31 | 1731/5232 | 1405/4389 | 469/1462 | chr16 | 1583341 | ||
| chr16:1584224
|
G | A | 2 | a0006a0011 | 10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
missense_variant | MODERATE | c.1352C>T | p.Ala451Val | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/31 | 1678/5232 | 1352/4389 | 451/1462 | chr16 | 1584224 | ||
| chr16:1584240
|
T | C | 1 | a0029 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.1336A>G | p.Ile446Val | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/31 | 1662/5232 | 1336/4389 | 446/1462 | chr16 | 1584240 | ||
| chr16:1584384
|
C | T | 6 | a0003a0008a0015others(3): Show | 35 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(32): Show |
missense_variant | MODERATE | c.1192G>A | p.Val398Ile | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/31 | 1518/5232 | 1192/4389 | 398/1462 | chr16 | 1584384 | ||
| chr16:1587996
|
C | T | 1 | a0007 | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
missense_variant | MODERATE | c.839G>A | p.Arg280Gln | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 8/31 | 1165/5232 | 839/4389 | 280/1462 | chr16 | 1587996 | ||
| chr16:1587997
|
G | A | 2 | a0006a0030 | 7 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
missense_variant | MODERATE | c.838C>T | p.Arg280Trp | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 8/31 | 1164/5232 | 838/4389 | 280/1462 | chr16 | 1587997 | ||
| chr16:1587999
|
C | G | 1 | a0004 | 9 | HG00733.hp1 HG00741.hp2 HG01123.hp1 others(6): Show |
missense_variant | MODERATE | c.836G>C | p.Arg279Pro | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 8/31 | 1162/5232 | 836/4389 | 279/1462 | chr16 | 1587999 | ||
| chr16:1589643
|
T | A | 1 | a0012 | 2 | NA18948.hp1 NA18991.hp1 |
missense_variant | MODERATE | c.772A>T | p.Thr258Ser | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/31 | 1098/5232 | 772/4389 | 258/1462 | chr16 | 1589643 | ||
| chr16:1592284
|
C | T | 1 | a0031 | 1 | NA18973.hp2 | missense_variant | MODERATE | c.526G>A | p.Gly176Ser | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/31 | 852/5232 | 526/4389 | 176/1462 | chr16 | 1592284 | ||
| chr16:1592500
|
G | A | 1 | a0014 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.458C>T | p.Thr153Met | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 5/31 | 784/5232 | 458/4389 | 153/1462 | chr16 | 1592500 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:1510953
|
G | A | 4 | a0003c0017a0003c0059a0008c0016others(1): Show | 6 | HG01243.hp2 HG02280.hp2 HG02970.hp2 others(3): Show |
synonymous_variant | LOW | c.4380C>T | p.Asp1460Asp | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 31/31 | 4706/5232 | 4380/4389 | 1460/1462 | chr16 | 1510953 | ||
| chr16:1518234
|
C | T | 1 | a0001c0050 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.4164G>A | p.Arg1388Arg | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/31 | 4490/5232 | 4164/4389 | 1388/1462 | chr16 | 1518234 | ||
| chr16:1519931
|
C | T | 2 | a0003c0031a0005c0049 | 2 | HG02965.hp1 HG03927.hp2 |
synonymous_variant | LOW | c.3990G>A | p.Ala1330Ala | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/31 | 4316/5232 | 3990/4389 | 1330/1462 | chr16 | 1519931 | ||
| chr16:1520194
|
G | A | 1 | a0001c0043 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.3810C>T | p.Ile1270Ile | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 28/31 | 4136/5232 | 3810/4389 | 1270/1462 | chr16 | 1520194 | ||
| chr16:1523951
|
G | A | 1 | a0001c0052 | 1 | HG02132.hp2 | synonymous_variant | LOW | c.3147C>T | p.Asn1049Asn | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 25/31 | 3473/5232 | 3147/4389 | 1049/1462 | chr16 | 1523951 | ||
| chr16:1524859
|
C | T | 1 | a0001c0048 | 1 | HG00609.hp1 | synonymous_variant | LOW | c.2922G>A | p.Ala974Ala | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 23/31 | 3248/5232 | 2922/4389 | 974/1462 | chr16 | 1524859 | ||
| chr16:1524862
|
G | A | 17 | a0001c0002a0001c0008a0001c0010others(14): Show | 92 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(89): Show |
synonymous_variant | LOW | c.2919C>T | p.Ala973Ala | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 23/31 | 3245/5232 | 2919/4389 | 973/1462 | chr16 | 1524862 | ||
| chr16:1526036
|
G | A | 1 | a0001c0053 | 1 | NA18980.hp1 | synonymous_variant | LOW | c.2619C>T | p.Asp873Asp | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/31 | 2945/5232 | 2619/4389 | 873/1462 | chr16 | 1526036 | ||
| chr16:1526742
|
G | A | 3 | a0003c0031a0003c0032a0007c0013 | 6 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(3): Show |
synonymous_variant | LOW | c.2454C>T | p.Asp818Asp | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 20/31 | 2780/5232 | 2454/4389 | 818/1462 | chr16 | 1526742 | ||
| chr16:1558039
|
C | T | 1 | a0001c0037 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.2295G>A | p.Leu765Leu | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/31 | 2621/5232 | 2295/4389 | 765/1462 | chr16 | 1558039 | ||
| chr16:1558081
|
A | G | 23 | a0001c0002a0001c0004a0001c0008others(20): Show | 124 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
synonymous_variant | LOW | c.2253T>C | p.Pro751Pro | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/31 | 2579/5232 | 2253/4389 | 751/1462 | chr16 | 1558081 | ||
| chr16:1558087
|
G | A | 3 | a0001c0020a0003c0019a0027c0036 | 5 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(2): Show |
synonymous_variant | LOW | c.2247C>T | p.His749His | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/31 | 2573/5232 | 2247/4389 | 749/1462 | chr16 | 1558087 | ||
| chr16:1564096
|
A | G | 45 | a0001c0002a0001c0004a0001c0008others(42): Show | 200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
synonymous_variant | LOW | c.1968T>C | p.Ser656Ser | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/31 | 2294/5232 | 1968/4389 | 656/1462 | chr16 | 1564096 | ||
| chr16:1566238
|
T | C | 1 | a0001c0054 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.1824A>G | p.Thr608Thr | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/31 | 2150/5232 | 1824/4389 | 608/1462 | chr16 | 1566238 | ||
| chr16:1584346
|
C | T | 1 | a0001c0008 | 5 | NA18943.hp2 NA18983.hp2 NA19056.hp2 others(2): Show |
synonymous_variant | LOW | c.1230G>A | p.Ser410Ser | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/31 | 1556/5232 | 1230/4389 | 410/1462 | chr16 | 1584346 | ||
| chr16:1586202
|
G | A | 2 | a0001c0014a0001c0057 | 4 | HG02080.hp1 HG02080.hp2 HG02523.hp2 others(1): Show |
synonymous_variant | LOW | c.1083C>T | p.Pro361Pro | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/31 | 1409/5232 | 1083/4389 | 361/1462 | chr16 | 1586202 | ||
| chr16:1588007
|
T | C | 1 | a0003c0059 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.828A>G | p.Lys276Lys | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 8/31 | 1154/5232 | 828/4389 | 276/1462 | chr16 | 1588007 | ||
| chr16:1592499
|
C | A | 2 | a0007c0013a0007c0060 | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
synonymous_variant | LOW | c.459G>T | p.Thr153Thr | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 5/31 | 785/5232 | 459/4389 | 153/1462 | chr16 | 1592499 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:1510541
|
C | T | 1 | a0001c0014t0006 | 2 | HG02523.hp2 NA18993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*403G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 31/31 | 403 | chr16 | 1510541 | |||||
| chr16:1510709
|
G | T | 1 | a0001c0014t0006 | 2 | HG02523.hp2 NA18993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*235C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 31/31 | 235 | chr16 | 1510709 | |||||
| chr16:1510881
|
T | C | 1 | a0001c0001t0007 | 2 | HG00323.hp1 HG02683.hp1 |
3_prime_UTR_variant | MODIFIER | c.*63A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 31/31 | 63 | chr16 | 1510881 | |||||
| chr16:1510885
|
A | G | 38 | a0001c0001t0004a0001c0002t0001a0001c0002t0005others(35): Show | 137 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*59T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 31/31 | 59 | chr16 | 1510885 | |||||
| chr16:1510932
|
G | A | 1 | a0003c0031t0009 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 31/31 | 12 | chr16 | 1510932 | |||||
| chr16:1510942
|
C | T | 1 | a0001c0002t0005 | 2 | HG03490.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 31/31 | 2 | chr16 | 1510942 | |||||
| chr16:1607283
|
C | G | 50 | a0001c0001t0003a0001c0002t0001a0001c0002t0003others(47): Show | 201 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
5_prime_UTR_variant | MODIFIER | c.-17G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/31 | 17 | chr16 | 1607283 | |||||
| chr16:1610755
|
G | A | 1 | a0001c0002t0010 | 1 | NA18962.hp1 | 5_prime_UTR_variant | MODIFIER | c.-123C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/31 | 3489 | chr16 | 1610755 | |||||
| chr16:1612013
|
C | G | 1 | a0003c0032t0008 | 1 | HG02683.hp2 | 5_prime_UTR_variant | MODIFIER | c.-267G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/31 | 4747 | chr16 | 1612013 | |||||
| chr16:1612063
|
A | T | 1 | a0001c0002t0005 | 2 | HG03490.hp2 HG03492.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-317T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/31 | chr16 | 1612063 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:1511322
|
G | A | 32 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(29): Show | 32 | HG01192.hp1 HG01192.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.4183-172C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511322 | ||||||
| chr16:1511338
|
C | A | 32 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(29): Show | 32 | HG01192.hp1 HG01192.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.4183-188G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511338 | ||||||
| chr16:1511416
|
C | G | 1 | a0001c0002t0001g0210 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4183-266G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511416 | ||||||
| chr16:1511445
|
A | G | 158 | a0001c0001t0002g0169a0001c0001t0002g0180a0001c0001t0002g0181others(155): Show | 158 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.4183-295T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511445 | ||||||
| chr16:1511487
|
G | C | 2 | a0013c0022t0002g0227a0013c0022t0002g0230 | 2 | HG00642.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.4183-337C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511487 | ||||||
| chr16:1511581
|
G | C | 1 | a0001c0001t0002g0046 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4183-431C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511581 | ||||||
| chr16:1511696
|
G | T | 4 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(1): Show | 4 | HG02258.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.4183-546C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511696 | ||||||
| chr16:1511734
|
C | CGA | 31 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(28): Show | 31 | HG01192.hp1 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.4183-586_4183-585d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511734 | ||||||
| chr16:1511756
|
C | G | 1 | a0001c0001t0002g0242 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.4183-606G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511756 | ||||||
| chr16:1511827
|
CAG | C | 13 | a0001c0002t0001g0113a0001c0002t0001g0210a0001c0002t0001g0218others(10): Show | 13 | HG01433.hp1 HG02071.hp1 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.4183-679_4183-678d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511827 | ||||||
| chr16:1511964
|
A | G | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4183-814T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1511964 | ||||||
| chr16:1512025
|
T | C | 144 | a0001c0001t0002g0262a0001c0001t0004g0170a0001c0001t0004g0172others(141): Show | 144 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.4183-875A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512025 | ||||||
| chr16:1512122
|
G | GTGGGGGG others(44): Show |
5 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0005t0003g0135others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.4183-1023_4183-973 others(54): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512122 | ||||||
| chr16:1512140
|
G | A | 2 | a0001c0002t0001g0210a0001c0043t0001g0219 | 2 | HG02071.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.4183-990C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512140 | ||||||
| chr16:1512159
|
TGGTGGGG others(34): Show |
T | 7 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(4): Show | 7 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.4183-1050_4183-101 others(45): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512159 | ||||||
| chr16:1512194
|
A | G | 108 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(105): Show | 108 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.4183-1044T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512194 | ||||||
| chr16:1512200
|
G | GGGTGAGG others(3): Show |
1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4183-1051_4183-105 others(14): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512200 | ||||||
| chr16:1512202
|
GTGGGGGG others(5): Show |
G | 1 | a0001c0001t0002g0302 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.4183-1064_4183-105 others(16): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512202 | ||||||
| chr16:1512251
|
C | T | 101 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(98): Show | 101 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.4183-1101G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512251 | ||||||
| chr16:1512398
|
C | T | 3 | a0001c0002t0001g0061a0001c0002t0001g0071a0004c0026t0004g0312 | 3 | HG00280.hp2 HG00733.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.4183-1248G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512398 | ||||||
| chr16:1512427
|
C | T | 2 | a0001c0001t0002g0271a0001c0001t0002g0272 | 2 | HG02738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.4183-1277G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512427 | ||||||
| chr16:1512459
|
T | C | 111 | a0001c0001t0002g0246a0001c0001t0002g0263a0001c0001t0002g0264others(108): Show | 111 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.4183-1309A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512459 | ||||||
| chr16:1512485
|
C | G | 1 | a0005c0039t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4183-1335G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512485 | ||||||
| chr16:1512488
|
G | C | 5 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(2): Show | 5 | HG02809.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.4183-1338C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512488 | ||||||
| chr16:1512565
|
C | T | 4 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0019t0003g0136others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.4183-1415G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512565 | ||||||
| chr16:1512625
|
C | T | 1 | a0001c0001t0002g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4183-1475G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512625 | ||||||
| chr16:1512721
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4183-1571G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512721 | ||||||
| chr16:1512753
|
G | A | 30 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(27): Show | 30 | HG01192.hp1 HG01192.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.4183-1603C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512753 | ||||||
| chr16:1512803
|
G | A | 200 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0180others(197): Show | 200 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.4183-1653C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512803 | ||||||
| chr16:1512818
|
A | G | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4183-1668T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512818 | ||||||
| chr16:1512821
|
C | T | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4183-1671G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512821 | ||||||
| chr16:1512914
|
C | G | 36 | a0001c0014t0003g0103a0002c0003t0003g0006a0002c0003t0003g0007others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.4183-1764G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512914 | ||||||
| chr16:1512934
|
G | C | 5 | a0001c0004t0003g0189a0008c0015t0003g0053a0008c0015t0003g0055others(2): Show | 5 | HG02486.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.4183-1784C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512934 | ||||||
| chr16:1512956
|
G | C | 7 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(4): Show | 7 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.4183-1806C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1512956 | ||||||
| chr16:1513073
|
C | T | 1 | a0004c0006t0002g0237 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4183-1923G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513073 | ||||||
| chr16:1513114
|
G | A | 7 | a0001c0004t0001g0075a0001c0004t0001g0076a0006c0007t0003g0159others(4): Show | 7 | HG02145.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.4183-1964C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513114 | ||||||
| chr16:1513167
|
A | G | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4183-2017T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513167 | ||||||
| chr16:1513211
|
C | G | 1 | a0019c0033t0003g0018 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.4183-2061G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513211 | ||||||
| chr16:1513215
|
C | T | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4183-2065G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513215 | ||||||
| chr16:1513217
|
C | T | 1 | a0019c0033t0003g0018 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.4183-2067G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513217 | ||||||
| chr16:1513227
|
C | T | 2 | a0001c0004t0001g0077a0003c0031t0009g0140 | 2 | HG02965.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.4183-2077G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513227 | ||||||
| chr16:1513280
|
G | A | 1 | a0001c0001t0002g0231 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4183-2130C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513280 | ||||||
| chr16:1513295
|
C | G | 1 | a0001c0004t0001g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4183-2145G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513295 | ||||||
| chr16:1513305
|
C | T | 2 | a0001c0001t0002g0245a0001c0004t0001g0117 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4183-2155G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513305 | ||||||
| chr16:1513310
|
A | C | 1 | a0001c0001t0002g0245 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4183-2160T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513310 | ||||||
| chr16:1513313
|
C | T | 2 | a0001c0001t0002g0306a0001c0001t0002g0309 | 2 | HG01074.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.4183-2163G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513313 | ||||||
| chr16:1513316
|
C | T | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4183-2166G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513316 | ||||||
| chr16:1513418
|
T | C | 4 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(1): Show | 4 | HG02258.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.4183-2268A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513418 | ||||||
| chr16:1513516
|
A | G | 2 | a0001c0002t0005g0001a0001c0002t0005g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.4183-2366T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513516 | ||||||
| chr16:1513581
|
G | A | 97 | a0001c0001t0004g0254a0001c0002t0001g0005a0001c0002t0001g0013others(94): Show | 97 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.4183-2431C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513581 | ||||||
| chr16:1513609
|
C | A | 1 | a0001c0001t0002g0306 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4183-2459G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513609 | ||||||
| chr16:1513632
|
T | C | 2 | a0001c0004t0001g0077a0003c0031t0009g0140 | 2 | HG02965.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.4183-2482A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513632 | ||||||
| chr16:1513666
|
ACTTT | A | 101 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(98): Show | 101 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.4183-2520_4183-251 others(8): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513666 | ||||||
| chr16:1513671
|
C | CT | 38 | a0001c0001t0002g0169a0001c0001t0002g0184a0001c0001t0002g0200others(35): Show | 38 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.4183-2522dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513671 | ||||||
| chr16:1513704
|
T | C | 203 | a0001c0001t0002g0004a0001c0001t0002g0169a0001c0001t0002g0174others(200): Show | 203 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.4183-2554A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513704 | ||||||
| chr16:1513707
|
T | C | 1 | a0016c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4183-2557A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513707 | ||||||
| chr16:1513708
|
G | C | 1 | a0016c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4183-2558C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513708 | ||||||
| chr16:1513712
|
C | G | 1 | a0016c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4183-2562G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513712 | ||||||
| chr16:1513743
|
T | G | 7 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(4): Show | 7 | HG02109.hp1 HG02145.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.4183-2593A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513743 | ||||||
| chr16:1513753
|
A | C | 1 | a0002c0003t0003g0033 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.4183-2603T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513753 | ||||||
| chr16:1513798
|
C | T | 103 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(100): Show | 103 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.4183-2648G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513798 | ||||||
| chr16:1513799
|
A | G | 199 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0180others(196): Show | 199 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.4183-2649T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513799 | ||||||
| chr16:1513823
|
A | G | 8 | a0001c0001t0002g0169a0001c0001t0002g0184a0001c0001t0002g0200others(5): Show | 8 | HG01175.hp1 HG01891.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.4183-2673T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513823 | ||||||
| chr16:1513824
|
C | T | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4183-2674G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513824 | ||||||
| chr16:1513831
|
A | G | 6 | a0001c0001t0002g0169a0001c0001t0002g0184a0001c0001t0002g0200others(3): Show | 6 | HG01891.hp2 HG02622.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.4183-2681T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513831 | ||||||
| chr16:1513862
|
A | C | 4 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(1): Show | 4 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.4183-2712T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513862 | ||||||
| chr16:1513863
|
C | T | 1 | a0002c0003t0003g0034 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4183-2713G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513863 | ||||||
| chr16:1513864
|
G | A | 152 | a0001c0001t0002g0205a0001c0001t0002g0229a0001c0001t0004g0260others(149): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.4183-2714C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513864 | ||||||
| chr16:1513875
|
G | A | 3 | a0002c0003t0003g0031a0011c0012t0003g0201a0011c0012t0003g0202 | 3 | HG03710.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.4183-2725C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513875 | ||||||
| chr16:1513875
|
G | C | 3 | a0001c0001t0002g0200a0001c0001t0002g0298a0027c0036t0003g0132 | 3 | HG02622.hp1 HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4183-2725C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513875 | ||||||
| chr16:1513885
|
A | G | 211 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0180others(208): Show | 211 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.4183-2735T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513885 | ||||||
| chr16:1513894
|
C | T | 60 | a0001c0001t0002g0169a0001c0001t0002g0184a0001c0001t0002g0200others(57): Show | 60 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.4183-2744G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513894 | ||||||
| chr16:1513895
|
C | G | 209 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0180others(206): Show | 209 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.4183-2745G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513895 | ||||||
| chr16:1513909
|
A | G | 18 | a0001c0001t0002g0324a0001c0001t0002g0325a0001c0004t0003g0189others(15): Show | 18 | HG02056.hp2 HG02074.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.4183-2759T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513909 | ||||||
| chr16:1513915
|
T | C | 143 | a0001c0001t0002g0247a0001c0001t0002g0248a0001c0001t0002g0324others(140): Show | 143 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.4183-2765A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513915 | ||||||
| chr16:1513916
|
G | A | 2 | a0001c0001t0002g0324a0001c0001t0002g0325 | 2 | NA18945.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.4183-2766C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513916 | ||||||
| chr16:1513919
|
C | T | 127 | a0001c0001t0002g0244a0001c0001t0002g0247a0001c0001t0002g0248others(124): Show | 127 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.4183-2769G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513919 | ||||||
| chr16:1513920
|
G | A | 13 | a0001c0001t0002g0324a0001c0001t0002g0325a0002c0003t0003g0006others(10): Show | 13 | HG02056.hp2 HG02074.hp2 NA18945.hp2 others(10): Show |
intron_variant | MODIFIER | c.4183-2770C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513920 | ||||||
| chr16:1513924
|
T | C | 11 | a0002c0003t0003g0006a0002c0003t0003g0023a0002c0003t0003g0025others(8): Show | 11 | HG02056.hp2 HG02074.hp2 NA18949.hp1 others(8): Show |
intron_variant | MODIFIER | c.4183-2774A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513924 | ||||||
| chr16:1513958
|
C | T | 6 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4183-2808G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513958 | ||||||
| chr16:1513962
|
T | C | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4183-2812A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513962 | ||||||
| chr16:1513965
|
A | G | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4183-2815T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513965 | ||||||
| chr16:1513968
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4183-2818G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1513968 | ||||||
| chr16:1514135
|
A | G | 4 | a0002c0003t0003g0021a0002c0003t0003g0026a0019c0033t0003g0018others(1): Show | 4 | HG00408.hp1 HG00544.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.4183-2985T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514135 | ||||||
| chr16:1514143
|
T | C | 4 | a0002c0003t0003g0021a0002c0003t0003g0026a0019c0033t0003g0018others(1): Show | 4 | HG00408.hp1 HG00544.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.4183-2993A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514143 | ||||||
| chr16:1514151
|
G | A | 1 | a0005c0039t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4183-3001C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514151 | ||||||
| chr16:1514164
|
C | G | 10 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0184others(7): Show | 10 | HG01891.hp2 HG02055.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4183-3014G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514164 | ||||||
| chr16:1514164
|
C | T | 1 | a0001c0004t0001g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4183-3014G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514164 | ||||||
| chr16:1514165
|
G | A | 1 | a0006c0007t0003g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4183-3015C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514165 | ||||||
| chr16:1514185
|
G | A | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4183-3035C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514185 | ||||||
| chr16:1514238
|
C | T | 2 | a0001c0001t0002g0174a0002c0003t0003g0007 | 2 | NA18941.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4183-3088G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514238 | ||||||
| chr16:1514301
|
C | T | 1 | a0001c0002t0001g0102 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4183-3151G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514301 | ||||||
| chr16:1514349
|
G | A | 53 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0180others(50): Show | 53 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(50): Show |
intron_variant | MODIFIER | c.4183-3199C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514349 | ||||||
| chr16:1514351
|
T | C | 2 | a0001c0004t0001g0077a0003c0031t0009g0140 | 2 | HG02965.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.4183-3201A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514351 | ||||||
| chr16:1514356
|
C | T | 2 | a0001c0004t0001g0077a0003c0031t0009g0140 | 2 | HG02965.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.4183-3206G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514356 | ||||||
| chr16:1514369
|
C | CAAATAAA others(5): Show |
1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4183-3231_4183-322 others(16): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514369 | ||||||
| chr16:1514369
|
C | CAAATAAA others(13): Show |
1 | a0001c0004t0001g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4183-3239_4183-322 others(24): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514369 | ||||||
| chr16:1514369
|
CAAATAAA others(5): Show |
C | 1 | a0001c0001t0002g0291 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4183-3231_4183-322 others(16): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514369 | ||||||
| chr16:1514533
|
G | A | 1 | a0001c0001t0003g0038 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.4183-3383C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514533 | ||||||
| chr16:1514692
|
T | C | 1 | a0001c0001t0004g0277 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.4182+3524A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514692 | ||||||
| chr16:1514750
|
A | G | 4 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0019t0003g0136others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.4182+3466T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514750 | ||||||
| chr16:1514822
|
G | A | 96 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0180others(93): Show | 96 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.4182+3394C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1514822 | ||||||
| chr16:1515115
|
C | A | 37 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(34): Show | 37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.4182+3101G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1515115 | ||||||
| chr16:1515407
|
C | G | 1 | a0001c0002t0001g0217 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4182+2809G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1515407 | ||||||
| chr16:1515425
|
G | T | 2 | a0001c0004t0001g0077a0003c0031t0009g0140 | 2 | HG02965.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.4182+2791C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1515425 | ||||||
| chr16:1515539
|
C | T | 196 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0184others(193): Show | 196 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.4182+2677G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1515539 | ||||||
| chr16:1515844
|
C | T | 3 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182 | 3 | HG02109.hp1 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4182+2372G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1515844 | ||||||
| chr16:1515892
|
A | T | 35 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(32): Show | 35 | HG00544.hp1 HG00642.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.4182+2324T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1515892 | ||||||
| chr16:1516019
|
A | C | 1 | a0001c0001t0002g0266 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.4182+2197T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516019 | ||||||
| chr16:1516033
|
C | T | 1 | a0001c0004t0001g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4182+2183G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516033 | ||||||
| chr16:1516036
|
A | G | 1 | a0001c0010t0001g0125 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4182+2180T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516036 | ||||||
| chr16:1516139
|
C | CA | 7 | a0001c0001t0002g0206a0001c0001t0002g0264a0001c0001t0002g0271others(4): Show | 7 | HG00673.hp2 HG01516.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.4182+2076dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516139 | ||||||
| chr16:1516139
|
C | CAA | 41 | a0001c0001t0002g0243a0001c0001t0002g0246a0001c0001t0002g0250others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(38): Show |
intron_variant | MODIFIER | c.4182+2075_4182+207 others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516139 | ||||||
| chr16:1516139
|
C | CAAA | 38 | a0001c0001t0002g0004a0001c0001t0002g0046a0001c0001t0002g0179others(35): Show | 38 | HG00544.hp2 HG01081.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.4182+2074_4182+207 others(7): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516139 | ||||||
| chr16:1516139
|
C | CAAAA | 25 | a0001c0001t0002g0178a0001c0001t0002g0205a0001c0001t0002g0228others(22): Show | 25 | HG00733.hp2 HG00741.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.4182+2073_4182+207 others(8): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516139 | ||||||
| chr16:1516139
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0002g0304a0001c0001t0002g0307 | 2 | HG01516.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.4182+2066_4182+207 others(15): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516139 | ||||||
| chr16:1516139
|
CAAAAAAA others(5): Show |
C | 16 | a0001c0001t0002g0252a0001c0001t0002g0255a0001c0002t0001g0013others(13): Show | 16 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.4182+2065_4182+207 others(16): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516139 | ||||||
| chr16:1516139
|
CAAAAAAA others(6): Show |
C | 103 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0004g0251others(100): Show | 103 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.4182+2064_4182+207 others(17): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516139 | ||||||
| chr16:1516139
|
CAAAAAAA others(7): Show |
C | 78 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0180others(75): Show | 78 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.4182+2063_4182+207 others(18): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516139 | ||||||
| chr16:1516139
|
CAAAAAAA others(8): Show |
C | 3 | a0002c0003t0003g0006a0002c0003t0003g0029a0003c0005t0001g0142 | 3 | HG03491.hp2 NA19003.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.4182+2062_4182+207 others(19): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516139 | ||||||
| chr16:1516139
|
CAAAAAAA others(16): Show |
C | 3 | a0001c0001t0002g0247a0001c0001t0002g0248a0001c0004t0003g0082 | 3 | HG00423.hp2 NA18961.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.4182+2054_4182+207 others(27): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516139 | ||||||
| chr16:1516169
|
A | C | 1 | a0001c0004t0001g0066 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4182+2047T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516169 | ||||||
| chr16:1516174
|
A | C | 1 | a0003c0005t0001g0156 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.4182+2042T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516174 | ||||||
| chr16:1516176
|
A | C | 198 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0180others(195): Show | 198 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.4182+2040T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516176 | ||||||
| chr16:1516177
|
A | C | 198 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0180others(195): Show | 198 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.4182+2039T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516177 | ||||||
| chr16:1516198
|
A | G | 4 | a0001c0004t0003g0189a0008c0015t0003g0053a0011c0012t0003g0051others(1): Show | 4 | HG03130.hp2 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.4182+2018T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516198 | ||||||
| chr16:1516283
|
T | C | 195 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0184others(192): Show | 195 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.4182+1933A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516283 | ||||||
| chr16:1516381
|
A | G | 55 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0184others(52): Show | 55 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(52): Show |
intron_variant | MODIFIER | c.4182+1835T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516381 | ||||||
| chr16:1516498
|
G | GGTGGCTC others(126): Show |
1 | a0001c0001t0002g0308 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4182+1717_4182+171 others(137): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516498 | ||||||
| chr16:1516540
|
C | T | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4182+1676G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516540 | ||||||
| chr16:1516541
|
G | A | 2 | a0001c0001t0002g0263a0001c0001t0002g0264 | 2 | HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.4182+1675C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516541 | ||||||
| chr16:1516568
|
G | A | 1 | a0001c0001t0002g0278 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4182+1648C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516568 | ||||||
| chr16:1516585
|
C | T | 104 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(101): Show | 104 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.4182+1631G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516585 | ||||||
| chr16:1516596
|
T | C | 199 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0184others(196): Show | 199 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.4182+1620A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516596 | ||||||
| chr16:1516631
|
G | A | 5 | a0001c0001t0004g0251a0001c0002t0001g0013a0003c0005t0001g0141others(2): Show | 5 | HG02145.hp2 HG02809.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.4182+1585C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516631 | ||||||
| chr16:1516638
|
C | T | 4 | a0001c0001t0004g0251a0003c0005t0001g0141a0003c0005t0001g0142others(1): Show | 4 | HG02145.hp2 HG03017.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.4182+1578G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516638 | ||||||
| chr16:1516680
|
G | A | 1 | a0021c0034t0003g0010 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.4182+1536C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516680 | ||||||
| chr16:1516722
|
A | G | 33 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(30): Show | 33 | HG01192.hp1 HG01192.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.4182+1494T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516722 | ||||||
| chr16:1516769
|
C | CA | 22 | a0001c0001t0002g0180a0001c0001t0002g0226a0001c0001t0002g0231others(19): Show | 22 | HG01192.hp2 HG01361.hp2 HG01978.hp1 others(19): Show |
intron_variant | MODIFIER | c.4182+1446dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516769 | ||||||
| chr16:1516769
|
CA | C | 23 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0184others(20): Show | 23 | HG00621.hp2 HG01070.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.4182+1446delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516769 | ||||||
| chr16:1516825
|
G | A | 105 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(102): Show | 105 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.4182+1391C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1516825 | ||||||
| chr16:1517049
|
A | G | 1 | a0001c0001t0002g0293 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.4182+1167T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517049 | ||||||
| chr16:1517089
|
G | A | 1 | a0007c0060t0001g0195 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4182+1127C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517089 | ||||||
| chr16:1517109
|
G | T | 3 | a0006c0007t0003g0159a0006c0007t0003g0161a0006c0007t0003g0162 | 3 | HG02895.hp2 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4182+1107C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517109 | ||||||
| chr16:1517366
|
AAG | A | 93 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0184others(90): Show | 93 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.4182+848_4182+849d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517366 | ||||||
| chr16:1517367
|
AG | A | 99 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(96): Show | 99 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.4182+848delC | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517367 | ||||||
| chr16:1517368
|
G | A | 5 | a0001c0002t0001g0049a0001c0002t0001g0223a0003c0018t0001g0152others(2): Show | 5 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.4182+848C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517368 | ||||||
| chr16:1517452
|
GAGA | G | 80 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0184others(77): Show | 80 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.4182+761_4182+763d others(5): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517452 | ||||||
| chr16:1517589
|
G | A | 1 | a0001c0002t0001g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4182+627C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517589 | ||||||
| chr16:1517650
|
A | G | 196 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0184others(193): Show | 196 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.4182+566T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517650 | ||||||
| chr16:1517693
|
G | A | 196 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0184others(193): Show | 196 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.4182+523C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517693 | ||||||
| chr16:1517772
|
C | T | 1 | a0001c0004t0001g0092 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4182+444G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517772 | ||||||
| chr16:1517787
|
C | T | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4182+429G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517787 | ||||||
| chr16:1517869
|
G | A | 2 | a0001c0004t0001g0075a0001c0004t0001g0076 | 2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4182+347C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517869 | ||||||
| chr16:1517973
|
G | C | 1 | a0001c0010t0001g0125 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4182+243C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517973 | ||||||
| chr16:1517987
|
G | C | 11 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0019t0003g0136others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.4182+229C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1517987 | ||||||
| chr16:1518150
|
G | A | 1 | a0001c0001t0002g0231 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4182+66C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 30/30 | chr16 | 1518150 | ||||||
| chr16:1518401
|
A | G | 106 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.4041-44T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1518401 | ||||||
| chr16:1518448
|
G | T | 1 | a0016c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4041-91C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1518448 | ||||||
| chr16:1518534
|
G | T | 1 | a0006c0007t0003g0164 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4041-177C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1518534 | ||||||
| chr16:1518578
|
A | G | 2 | a0001c0001t0002g0284a0001c0001t0002g0287 | 2 | HG02155.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.4041-221T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1518578 | ||||||
| chr16:1518692
|
G | C | 7 | a0002c0003t0003g0007a0002c0003t0003g0008a0002c0003t0003g0009others(4): Show | 7 | HG00408.hp1 HG00544.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.4041-335C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1518692 | ||||||
| chr16:1518706
|
G | A | 1 | a0003c0018t0001g0152 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.4041-349C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1518706 | ||||||
| chr16:1518790
|
C | T | 1 | a0001c0001t0002g0262 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4041-433G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1518790 | ||||||
| chr16:1519002
|
A | T | 6 | a0001c0002t0001g0212a0001c0002t0001g0213a0001c0002t0001g0217others(3): Show | 6 | HG01256.hp2 HG01258.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.4041-645T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519002 | ||||||
| chr16:1519137
|
C | T | 1 | a0001c0001t0002g0256 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.4040+744G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519137 | ||||||
| chr16:1519160
|
G | A | 4 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(1): Show | 4 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.4040+721C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519160 | ||||||
| chr16:1519185
|
G | A | 2 | a0001c0001t0002g0304a0001c0001t0002g0307 | 2 | HG01516.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.4040+696C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519185 | ||||||
| chr16:1519201
|
C | T | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.4040+680G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519201 | ||||||
| chr16:1519217
|
A | C | 1 | a0001c0001t0002g0252 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.4040+664T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519217 | ||||||
| chr16:1519251
|
G | A | 106 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.4040+630C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519251 | ||||||
| chr16:1519300
|
G | A | 37 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(34): Show | 37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.4040+581C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519300 | ||||||
| chr16:1519307
|
C | T | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.4040+574G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519307 | ||||||
| chr16:1519351
|
G | A | 1 | a0004c0006t0002g0233 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.4040+530C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519351 | ||||||
| chr16:1519404
|
T | C | 61 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0180others(58): Show | 61 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(58): Show |
intron_variant | MODIFIER | c.4040+477A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519404 | ||||||
| chr16:1519523
|
A | C | 202 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0180others(199): Show | 202 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.4040+358T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519523 | ||||||
| chr16:1519566
|
C | T | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4040+315G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519566 | ||||||
| chr16:1519710
|
G | A | 30 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(27): Show | 30 | HG01192.hp1 HG01192.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.4040+171C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519710 | ||||||
| chr16:1519828
|
G | A | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4040+53C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519828 | ||||||
| chr16:1519830
|
C | G | 1 | a0014c0061t0001g0116 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4040+51G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519830 | ||||||
| chr16:1519871
|
G | A | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4040+10C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519871 | ||||||
| chr16:1519875
|
G | A | 1 | a0001c0010t0001g0125 | 1 | NA18971.hp1 | splice_region_variant&intron_variant | LOW | c.4040+6C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 29/30 | chr16 | 1519875 | ||||||
| chr16:1520058
|
G | A | 2 | a0013c0022t0002g0227a0013c0022t0002g0230 | 2 | HG00642.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.3874-11C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 28/30 | chr16 | 1520058 | ||||||
| chr16:1520075
|
G | T | 1 | a0006c0007t0003g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3874-28C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 28/30 | chr16 | 1520075 | ||||||
| chr16:1520096
|
C | T | 1 | a0008c0016t0001g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3873+35G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 28/30 | chr16 | 1520096 | ||||||
| chr16:1520107
|
T | C | 1 | a0008c0016t0001g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3873+24A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 28/30 | chr16 | 1520107 | ||||||
| chr16:1520387
|
C | T | 1 | a0003c0018t0001g0133 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3661-44G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 27/30 | chr16 | 1520387 | ||||||
| chr16:1520448
|
C | T | 1 | a0001c0004t0001g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3661-105G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 27/30 | chr16 | 1520448 | ||||||
| chr16:1520537
|
G | A | 2 | a0001c0001t0002g0169a0001c0001t0002g0184 | 2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3660+65C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 27/30 | chr16 | 1520537 | ||||||
| chr16:1520856
|
T | C | 208 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0180others(205): Show | 208 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.3454-48A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1520856 | ||||||
| chr16:1521119
|
T | G | 112 | a0001c0001t0002g0226a0001c0001t0002g0239a0001c0001t0002g0299others(109): Show | 112 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.3454-311A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521119 | ||||||
| chr16:1521273
|
C | T | 1 | a0006c0007t0003g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3454-465G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521273 | ||||||
| chr16:1521328
|
A | G | 1 | a0001c0001t0002g0239 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3454-520T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521328 | ||||||
| chr16:1521355
|
C | T | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3454-547G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521355 | ||||||
| chr16:1521360
|
C | T | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3454-552G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521360 | ||||||
| chr16:1521810
|
T | C | 201 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0180others(198): Show | 201 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.3454-1002A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521810 | ||||||
| chr16:1521861
|
G | GA | 42 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0181others(39): Show | 42 | HG01192.hp1 HG01243.hp2 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.3454-1054dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521861 | ||||||
| chr16:1521868
|
A | C | 9 | a0001c0001t0002g0180a0001c0002t0001g0098a0006c0007t0003g0159others(6): Show | 9 | HG02109.hp1 HG02559.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.3454-1060T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521868 | ||||||
| chr16:1521917
|
T | A | 6 | a0001c0001t0002g0262a0001c0002t0001g0129a0001c0020t0003g0138others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3454-1109A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521917 | ||||||
| chr16:1521917
|
TA | T | 62 | a0001c0001t0002g0169a0001c0001t0002g0181a0001c0001t0002g0182others(59): Show | 62 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.3454-1110delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521917 | ||||||
| chr16:1521917
|
TAAA | T | 6 | a0001c0004t0003g0189a0003c0005t0003g0063a0008c0015t0003g0053others(3): Show | 6 | HG02486.hp2 HG03130.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.3454-1112_3454-111 others(7): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521917 | ||||||
| chr16:1521953
|
T | G | 1 | a0001c0001t0002g0205 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3454-1145A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521953 | ||||||
| chr16:1521954
|
G | T | 1 | a0001c0001t0002g0205 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3454-1146C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1521954 | ||||||
| chr16:1522040
|
T | G | 1 | a0001c0002t0001g0100 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3454-1232A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522040 | ||||||
| chr16:1522139
|
A | C | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3454-1331T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522139 | ||||||
| chr16:1522218
|
G | T | 1 | a0001c0001t0002g0205 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3453+1300C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522218 | ||||||
| chr16:1522281
|
C | T | 103 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(100): Show | 103 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.3453+1237G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522281 | ||||||
| chr16:1522313
|
T | C | 201 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0180others(198): Show | 201 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.3453+1205A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522313 | ||||||
| chr16:1522348
|
C | G | 1 | a0001c0004t0001g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3453+1170G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522348 | ||||||
| chr16:1522362
|
A | T | 1 | a0001c0001t0002g0205 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3453+1156T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522362 | ||||||
| chr16:1522392
|
G | A | 104 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(101): Show | 104 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.3453+1126C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522392 | ||||||
| chr16:1522568
|
T | C | 201 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0180others(198): Show | 201 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.3453+950A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522568 | ||||||
| chr16:1522593
|
C | T | 37 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(34): Show | 37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.3453+925G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522593 | ||||||
| chr16:1522764
|
G | A | 4 | a0001c0001t0002g0169a0001c0001t0002g0184a0001c0001t0002g0200others(1): Show | 4 | HG01891.hp2 HG02622.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3453+754C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522764 | ||||||
| chr16:1522773
|
G | C | 4 | a0001c0001t0002g0250a0001c0001t0002g0294a0001c0001t0002g0296others(1): Show | 4 | NA18962.hp2 NA18991.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.3453+745C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522773 | ||||||
| chr16:1522850
|
G | A | 5 | a0001c0004t0003g0189a0008c0015t0003g0053a0008c0015t0003g0055others(2): Show | 5 | HG02486.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.3453+668C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1522850 | ||||||
| chr16:1523159
|
C | T | 1 | a0001c0002t0001g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3453+359G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1523159 | ||||||
| chr16:1523168
|
A | C | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3453+350T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1523168 | ||||||
| chr16:1523218
|
C | CA | 10 | a0001c0001t0002g0205a0001c0001t0002g0274a0001c0001t0002g0323others(7): Show | 10 | HG01109.hp2 HG01192.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.3453+299dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1523218 | ||||||
| chr16:1523218
|
CA | C | 105 | a0001c0001t0003g0038a0001c0001t0007g0270a0001c0001t0007g0275others(102): Show | 105 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.3453+299delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1523218 | ||||||
| chr16:1523234
|
A | G | 4 | a0001c0004t0003g0189a0008c0015t0003g0053a0008c0015t0003g0055others(1): Show | 4 | HG02486.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.3453+284T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1523234 | ||||||
| chr16:1523245
|
G | A | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3453+273C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1523245 | ||||||
| chr16:1523283
|
T | G | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3453+235A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1523283 | ||||||
| chr16:1523484
|
G | A | 79 | a0001c0001t0002g0169a0001c0001t0002g0180a0001c0001t0002g0181others(76): Show | 79 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.3453+34C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 26/30 | chr16 | 1523484 | ||||||
| chr16:1523738
|
C | T | 1 | a0001c0001t0002g0323 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3271-38G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 25/30 | chr16 | 1523738 | ||||||
| chr16:1523753
|
C | T | 68 | a0001c0001t0002g0284a0001c0001t0002g0287a0001c0002t0001g0005others(65): Show | 68 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.3271-53G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 25/30 | chr16 | 1523753 | ||||||
| chr16:1523796
|
C | T | 1 | a0001c0001t0002g0323 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3270+32G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 25/30 | chr16 | 1523796 | ||||||
| chr16:1523809
|
A | G | 333 | a0001c0001t0002g0004a0001c0001t0002g0046a0001c0001t0002g0169others(330): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.3270+19T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 25/30 | chr16 | 1523809 | ||||||
| chr16:1524029
|
G | C | 22 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0205others(19): Show | 22 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.3142-73C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 24/30 | chr16 | 1524029 | ||||||
| chr16:1524032
|
C | T | 4 | a0009c0011t0003g0042a0009c0011t0003g0043a0009c0011t0003g0044others(1): Show | 4 | HG01257.hp2 HG01261.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.3142-76G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 24/30 | chr16 | 1524032 | ||||||
| chr16:1524033
|
G | A | 1 | a0014c0061t0001g0116 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3142-77C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 24/30 | chr16 | 1524033 | ||||||
| chr16:1524169
|
A | G | 1 | a0001c0001t0002g0285 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3142-213T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 24/30 | chr16 | 1524169 | ||||||
| chr16:1524251
|
A | G | 254 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0180others(251): Show | 254 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(251): Show |
intron_variant | MODIFIER | c.3142-295T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 24/30 | chr16 | 1524251 | ||||||
| chr16:1524407
|
G | A | 2 | a0001c0001t0002g0301a0001c0045t0002g0176 | 2 | HG02257.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3141+145C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 24/30 | chr16 | 1524407 | ||||||
| chr16:1524422
|
T | C | 1 | a0005c0039t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3141+130A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 24/30 | chr16 | 1524422 | ||||||
| chr16:1524448
|
G | A | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3141+104C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 24/30 | chr16 | 1524448 | ||||||
| chr16:1524761
|
C | T | 1 | a0005c0009t0004g0183 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2997+23G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 23/30 | chr16 | 1524761 | ||||||
| chr16:1524772
|
C | T | 1 | a0001c0001t0002g0320 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2997+12G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 23/30 | chr16 | 1524772 | ||||||
| chr16:1524773
|
G | A | 1 | a0001c0014t0003g0103 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2997+11C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 23/30 | chr16 | 1524773 | ||||||
| chr16:1524967
|
C | T | 14 | a0001c0001t0004g0251a0001c0001t0004g0277a0001c0004t0001g0095others(11): Show | 14 | HG01192.hp1 HG02015.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.2865-51G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 22/30 | chr16 | 1524967 | ||||||
| chr16:1525154
|
C | T | 1 | a0001c0001t0002g0256 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2864+77G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 22/30 | chr16 | 1525154 | ||||||
| chr16:1525200
|
C | T | 2 | a0001c0020t0003g0138a0001c0020t0003g0139 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2864+31G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 22/30 | chr16 | 1525200 | ||||||
| chr16:1525201
|
G | A | 4 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(1): Show | 4 | HG02109.hp1 HG02886.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2864+30C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 22/30 | chr16 | 1525201 | ||||||
| chr16:1525434
|
G | A | 1 | a0005c0044t0004g0168 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2769-108C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525434 | ||||||
| chr16:1525445
|
TC | T | 4 | a0008c0015t0003g0053a0008c0015t0003g0055a0011c0012t0003g0051others(1): Show | 4 | HG02486.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2769-120delG | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525445 | ||||||
| chr16:1525449
|
G | GCA | 4 | a0008c0015t0003g0053a0008c0015t0003g0055a0011c0012t0003g0051others(1): Show | 4 | HG02486.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2769-124_2769-123i others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525449 | ||||||
| chr16:1525450
|
G | C | 4 | a0008c0015t0003g0053a0008c0015t0003g0055a0011c0012t0003g0051others(1): Show | 4 | HG02486.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2769-124C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525450 | ||||||
| chr16:1525547
|
C | T | 6 | a0001c0001t0002g0258a0001c0001t0002g0318a0001c0001t0002g0319others(3): Show | 6 | HG03491.hp1 NA18945.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.2769-221G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525547 | ||||||
| chr16:1525581
|
G | C | 4 | a0001c0001t0002g0174a0001c0004t0001g0077a0003c0031t0009g0140others(1): Show | 4 | HG02965.hp2 HG03098.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.2769-255C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525581 | ||||||
| chr16:1525601
|
C | T | 1 | a0003c0018t0001g0133 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2769-275G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525601 | ||||||
| chr16:1525636
|
G | C | 1 | a0001c0050t0002g0328 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2768+251C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525636 | ||||||
| chr16:1525649
|
C | T | 2 | a0001c0001t0002g0174a0001c0004t0001g0077 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2768+238G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525649 | ||||||
| chr16:1525684
|
G | A | 1 | a0001c0004t0001g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2768+203C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525684 | ||||||
| chr16:1525703
|
T | C | 333 | a0001c0001t0002g0004a0001c0001t0002g0046a0001c0001t0002g0169others(330): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.2768+184A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525703 | ||||||
| chr16:1525756
|
G | A | 1 | a0007c0013t0001g0193 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2768+131C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525756 | ||||||
| chr16:1525838
|
C | A | 2 | a0001c0004t0003g0088a0001c0004t0003g0101 | 2 | HG00639.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2768+49G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525838 | ||||||
| chr16:1525859
|
G | A | 1 | a0001c0001t0002g0303 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2768+28C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525859 | ||||||
| chr16:1525869
|
C | T | 1 | a0001c0001t0002g0228 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2768+18G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 21/30 | chr16 | 1525869 | ||||||
| chr16:1526156
|
C | T | 1 | a0001c0001t0002g0256 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2578-79G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 20/30 | chr16 | 1526156 | ||||||
| chr16:1526216
|
G | A | 4 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(1): Show | 4 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2578-139C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 20/30 | chr16 | 1526216 | ||||||
| chr16:1526234
|
C | T | 6 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(3): Show | 6 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2578-157G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 20/30 | chr16 | 1526234 | ||||||
| chr16:1526235
|
G | A | 1 | a0001c0001t0004g0170 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2578-158C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 20/30 | chr16 | 1526235 | ||||||
| chr16:1526426
|
C | G | 31 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(28): Show | 31 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.2577+193G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 20/30 | chr16 | 1526426 | ||||||
| chr16:1526435
|
G | A | 34 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(31): Show | 34 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.2577+184C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 20/30 | chr16 | 1526435 | ||||||
| chr16:1526610
|
G | A | 1 | a0001c0004t0003g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2577+9C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 20/30 | chr16 | 1526610 | ||||||
| chr16:1526981
|
G | A | 2 | a0001c0001t0002g0286a0001c0001t0002g0304 | 2 | NA20752.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2400-185C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1526981 | ||||||
| chr16:1527055
|
A | G | 217 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0178others(214): Show | 217 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.2400-259T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1527055 | ||||||
| chr16:1527183
|
A | G | 92 | a0001c0001t0002g0174a0001c0001t0004g0170a0001c0001t0004g0172others(89): Show | 92 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.2400-387T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1527183 | ||||||
| chr16:1527229
|
C | T | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2400-433G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1527229 | ||||||
| chr16:1527234
|
G | A | 1 | a0001c0004t0001g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2400-438C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1527234 | ||||||
| chr16:1527391
|
G | C | 1 | a0001c0001t0004g0254 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2400-595C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1527391 | ||||||
| chr16:1527457
|
C | T | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2400-661G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1527457 | ||||||
| chr16:1527534
|
G | A | 3 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175 | 3 | HG02922.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2400-738C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1527534 | ||||||
| chr16:1527745
|
G | C | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-949C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1527745 | ||||||
| chr16:1527815
|
C | T | 2 | a0007c0013t0001g0191a0007c0013t0001g0193 | 2 | HG01109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2400-1019G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1527815 | ||||||
| chr16:1527962
|
A | G | 220 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0178others(217): Show | 220 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.2400-1166T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1527962 | ||||||
| chr16:1528009
|
C | G | 1 | a0001c0002t0001g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2400-1213G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528009 | ||||||
| chr16:1528251
|
C | G | 34 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(31): Show | 34 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.2400-1455G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528251 | ||||||
| chr16:1528294
|
C | T | 1 | a0001c0004t0001g0066 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2400-1498G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528294 | ||||||
| chr16:1528303
|
CCA | C | 24 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(21): Show | 24 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.2400-1509_2400-150 others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528303 | ||||||
| chr16:1528307
|
ACACACAC others(21): Show |
A | 8 | a0003c0005t0001g0143a0003c0005t0001g0144a0003c0005t0001g0145others(5): Show | 8 | HG02486.hp2 HG02970.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.2400-1539_2400-151 others(32): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528307 | ||||||
| chr16:1528314
|
CGCACGCA others(27): Show |
C | 1 | a0011c0012t0003g0051 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2400-1552_2400-151 others(38): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528314 | ||||||
| chr16:1528315
|
G | GCACGCAT others(19): Show |
1 | a0003c0005t0003g0151 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2400-1545_2400-152 others(30): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528315 | ||||||
| chr16:1528315
|
GCACGCAT others(19): Show |
G | 37 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(34): Show | 37 | HG00099.hp2 HG00639.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.2400-1545_2400-152 others(30): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528315 | ||||||
| chr16:1528318
|
CGCATGCA others(49): Show |
C | 1 | a0020c0035t0003g0012 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2400-1578_2400-152 others(60): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528318 | ||||||
| chr16:1528328
|
CACGTGTG others(23): Show |
C | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2400-1562_2400-153 others(34): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528328 | ||||||
| chr16:1528334
|
T | C | 9 | a0001c0001t0002g0174a0006c0007t0003g0159a0006c0007t0003g0160others(6): Show | 9 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.2400-1538A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528334 | ||||||
| chr16:1528341
|
A | G | 8 | a0003c0005t0001g0143a0003c0005t0001g0144a0003c0005t0001g0145others(5): Show | 8 | HG02486.hp2 HG02970.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.2400-1545T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528341 | ||||||
| chr16:1528345
|
G | A | 13 | a0001c0001t0002g0174a0001c0001t0002g0317a0001c0001t0002g0320others(10): Show | 13 | HG02056.hp2 HG02074.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.2400-1549C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528345 | ||||||
| chr16:1528346
|
CATGCACG others(45): Show |
C | 1 | a0001c0014t0006g0209 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2400-1602_2400-155 others(56): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528346 | ||||||
| chr16:1528352
|
C | G | 3 | a0008c0015t0003g0053a0008c0015t0003g0055a0008c0016t0001g0056 | 3 | HG02486.hp2 HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2400-1556G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528352 | ||||||
| chr16:1528360
|
T | C | 4 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0019t0003g0136others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-1564A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528360 | ||||||
| chr16:1528370
|
C | T | 4 | a0001c0002t0001g0107a0001c0004t0003g0112a0001c0004t0003g0114others(1): Show | 4 | HG00408.hp2 NA18945.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-1574G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528370 | ||||||
| chr16:1528372
|
C | G | 7 | a0001c0001t0002g0256a0003c0031t0009g0140a0003c0032t0008g0003others(4): Show | 7 | HG02055.hp2 HG02630.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.2400-1576G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528372 | ||||||
| chr16:1528374
|
T | C | 2 | a0001c0001t0002g0243a0001c0050t0002g0328 | 2 | HG02602.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2400-1578A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528374 | ||||||
| chr16:1528382
|
C | T | 6 | a0001c0045t0002g0176a0005c0009t0004g0166a0005c0009t0004g0173others(3): Show | 6 | HG02486.hp1 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2400-1586G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528382 | ||||||
| chr16:1528383
|
G | A | 1 | a0005c0039t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2400-1587C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528383 | ||||||
| chr16:1528386
|
T | C | 1 | a0026c0047t0002g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2400-1590A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528386 | ||||||
| chr16:1528398
|
G | C | 3 | a0001c0001t0002g0271a0001c0001t0002g0272a0005c0009t0004g0167 | 3 | HG01070.hp1 HG02738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2400-1602C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528398 | ||||||
| chr16:1528433
|
G | GCA | 213 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0178others(210): Show | 213 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.2400-1639_2400-163 others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528433 | ||||||
| chr16:1528492
|
CACAT | C | 5 | a0001c0004t0001g0105a0001c0014t0003g0103a0001c0014t0006g0209others(2): Show | 5 | HG02080.hp1 HG02523.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2400-1700_2400-169 others(8): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528492 | ||||||
| chr16:1528513
|
A | C | 38 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(35): Show | 38 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2400-1717T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528513 | ||||||
| chr16:1528543
|
G | A | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-1747C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528543 | ||||||
| chr16:1528595
|
G | A | 1 | a0001c0001t0002g0297 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2400-1799C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528595 | ||||||
| chr16:1528618
|
C | T | 1 | a0005c0009t0004g0167 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2400-1822G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528618 | ||||||
| chr16:1528724
|
G | A | 39 | a0001c0004t0001g0066a0002c0003t0003g0006a0002c0003t0003g0007others(36): Show | 39 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.2400-1928C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528724 | ||||||
| chr16:1528796
|
G | A | 1 | a0001c0002t0001g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2400-2000C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528796 | ||||||
| chr16:1528820
|
G | C | 3 | a0011c0012t0003g0051a0011c0012t0003g0052a0027c0036t0003g0132 | 3 | HG03098.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2400-2024C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528820 | ||||||
| chr16:1528858
|
A | C | 1 | a0004c0025t0002g0238 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2400-2062T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528858 | ||||||
| chr16:1528912
|
C | T | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-2116G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528912 | ||||||
| chr16:1528913
|
A | G | 89 | a0001c0001t0002g0174a0001c0001t0004g0170a0001c0001t0004g0172others(86): Show | 89 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.2400-2117T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528913 | ||||||
| chr16:1528983
|
C | T | 34 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(31): Show | 34 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.2400-2187G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1528983 | ||||||
| chr16:1529010
|
T | C | 88 | a0001c0001t0002g0174a0001c0001t0004g0170a0001c0001t0004g0172others(85): Show | 88 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.2400-2214A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529010 | ||||||
| chr16:1529142
|
C | T | 1 | a0001c0001t0002g0248 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2400-2346G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529142 | ||||||
| chr16:1529150
|
C | T | 87 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(84): Show | 87 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.2400-2354G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529150 | ||||||
| chr16:1529187
|
C | T | 4 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0019t0003g0136others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-2391G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529187 | ||||||
| chr16:1529203
|
G | A | 1 | a0001c0010t0002g0321 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2400-2407C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529203 | ||||||
| chr16:1529231
|
C | T | 1 | a0028c0055t0004g0165 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2400-2435G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529231 | ||||||
| chr16:1529243
|
T | C | 2 | a0001c0002t0001g0073a0001c0002t0001g0096 | 2 | HG01081.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2400-2447A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529243 | ||||||
| chr16:1529330
|
C | T | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-2534G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529330 | ||||||
| chr16:1529458
|
G | A | 1 | a0001c0001t0004g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2400-2662C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529458 | ||||||
| chr16:1529482
|
C | T | 111 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0285others(108): Show | 111 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.2400-2686G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529482 | ||||||
| chr16:1529581
|
G | A | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-2785C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529581 | ||||||
| chr16:1529740
|
G | A | 1 | a0001c0001t0002g0253 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2400-2944C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529740 | ||||||
| chr16:1529890
|
C | T | 4 | a0001c0001t0002g0169a0001c0001t0002g0184a0001c0001t0002g0200others(1): Show | 4 | HG01891.hp2 HG02622.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2400-3094G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529890 | ||||||
| chr16:1529910
|
C | T | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-3114G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1529910 | ||||||
| chr16:1530011
|
T | C | 3 | a0011c0012t0003g0051a0011c0012t0003g0052a0027c0036t0003g0132 | 3 | HG03098.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2400-3215A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530011 | ||||||
| chr16:1530018
|
G | A | 7 | a0002c0003t0003g0006a0002c0003t0003g0030a0002c0003t0003g0036others(4): Show | 7 | NA18949.hp1 NA18950.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.2400-3222C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530018 | ||||||
| chr16:1530024
|
A | G | 80 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(77): Show | 80 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.2400-3228T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530024 | ||||||
| chr16:1530074
|
C | T | 4 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(1): Show | 4 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-3278G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530074 | ||||||
| chr16:1530119
|
T | C | 4 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(1): Show | 4 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-3323A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530119 | ||||||
| chr16:1530133
|
C | CT | 15 | a0001c0001t0002g0229a0001c0001t0002g0236a0001c0001t0002g0239others(12): Show | 15 | HG00621.hp2 HG01123.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.2400-3338dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | ||||||
| chr16:1530133
|
C | CTTTTTTT others(4): Show |
2 | a0006c0007t0003g0160a0006c0007t0003g0164 | 2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2400-3348_2400-333 others(15): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | ||||||
| chr16:1530133
|
C | CTTTTTTT others(5): Show |
2 | a0006c0007t0003g0162a0011c0012t0003g0202 | 2 | HG02895.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2400-3349_2400-333 others(16): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | ||||||
| chr16:1530133
|
C | CTTTTTTT others(6): Show |
4 | a0006c0007t0003g0159a0006c0007t0003g0161a0006c0007t0003g0199others(1): Show | 4 | HG02897.hp2 HG06807.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2400-3350_2400-333 others(17): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | ||||||
| chr16:1530133
|
C | CTTTTTTT others(7): Show |
1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2400-3351_2400-333 others(18): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | ||||||
| chr16:1530133
|
C | CTTTTTTT others(9): Show |
7 | a0001c0001t0004g0172a0001c0001t0004g0175a0001c0001t0004g0254others(4): Show | 7 | HG02647.hp1 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2400-3353_2400-333 others(20): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | ||||||
| chr16:1530133
|
C | CTTTTTTT others(10): Show |
12 | a0001c0001t0004g0170a0003c0005t0001g0142a0003c0005t0001g0143others(9): Show | 12 | HG01192.hp1 HG02015.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.2400-3354_2400-333 others(21): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | ||||||
| chr16:1530133
|
C | CTTTTTTT others(11): Show |
7 | a0001c0004t0001g0095a0003c0005t0001g0141a0003c0005t0001g0145others(4): Show | 7 | HG00099.hp2 HG02056.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.2400-3355_2400-333 others(22): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | ||||||
| chr16:1530133
|
C | CTTTTTTT others(12): Show |
2 | a0003c0017t0001g0058a0003c0018t0001g0133 | 2 | HG01243.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2400-3356_2400-333 others(23): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | ||||||
| chr16:1530133
|
C | CTTTTTTT others(13): Show |
2 | a0007c0013t0001g0191a0007c0013t0001g0192 | 2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2400-3357_2400-333 others(24): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | ||||||
| chr16:1530133
|
C | CTTTTTTT others(14): Show |
1 | a0007c0013t0001g0193 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2400-3358_2400-333 others(25): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | ||||||
| chr16:1530133
|
C | CTTTTTTT others(15): Show |
1 | a0007c0013t0001g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2400-3359_2400-333 others(26): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | ||||||
| chr16:1530133
|
C | CTTTTTTT others(16): Show |
5 | a0003c0005t0001g0148a0003c0005t0001g0156a0003c0005t0001g0157others(2): Show | 5 | HG02976.hp1 HG03017.hp2 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.2400-3360_2400-333 others(27): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | ||||||
| chr16:1530133
|
CT | C | 43 | a0001c0001t0002g0307a0001c0001t0002g0322a0001c0002t0001g0197others(40): Show | 43 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.2400-3338delA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | ||||||
| chr16:1530133
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0004t0003g0115 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2400-3349_2400-333 others(16): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530133 | ||||||
| chr16:1530529
|
C | T | 1 | a0001c0002t0001g0065 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2400-3733G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530529 | ||||||
| chr16:1530530
|
G | A | 1 | a0001c0002t0001g0207 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2400-3734C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530530 | ||||||
| chr16:1530532
|
G | A | 1 | a0024c0042t0001g0109 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2400-3736C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530532 | ||||||
| chr16:1530579
|
T | C | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-3783A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530579 | ||||||
| chr16:1530694
|
A | ACCCGTGG others(18): Show |
1 | a0030c0058t0001g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2400-3923_2400-389 others(29): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530694 | ||||||
| chr16:1530694
|
A | ACCCGTGG others(43): Show |
3 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175 | 3 | HG02922.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2400-3948_2400-389 others(54): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530694 | ||||||
| chr16:1530694
|
ACCCGTGG others(18): Show |
A | 2 | a0001c0002t0001g0069a0001c0004t0003g0189 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2400-3923_2400-389 others(29): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530694 | ||||||
| chr16:1530698
|
G | A | 1 | a0001c0001t0002g0280 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2400-3902C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530698 | ||||||
| chr16:1530722
|
C | T | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2400-3926G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530722 | ||||||
| chr16:1530822
|
C | T | 1 | a0001c0001t0002g0332 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2400-4026G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530822 | ||||||
| chr16:1530823
|
G | T | 1 | a0001c0002t0001g0197 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2400-4027C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530823 | ||||||
| chr16:1530843
|
C | G | 1 | a0001c0001t0002g0263 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2400-4047G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530843 | ||||||
| chr16:1530991
|
C | T | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2400-4195G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1530991 | ||||||
| chr16:1531129
|
G | A | 1 | a0001c0002t0001g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2400-4333C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1531129 | ||||||
| chr16:1531337
|
C | T | 1 | a0001c0002t0001g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2400-4541G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1531337 | ||||||
| chr16:1531347
|
CTG | C | 4 | a0001c0020t0003g0138a0001c0020t0003g0139a0006c0007t0003g0164others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2400-4553_2400-455 others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1531347 | ||||||
| chr16:1531506
|
C | T | 2 | a0010c0021t0002g0315a0010c0021t0002g0316 | 2 | HG02056.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.2400-4710G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1531506 | ||||||
| chr16:1531519
|
C | G | 8 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(5): Show | 8 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.2400-4723G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1531519 | ||||||
| chr16:1531769
|
A | G | 94 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(91): Show | 94 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.2400-4973T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1531769 | ||||||
| chr16:1531940
|
T | C | 1 | a0001c0004t0001g0105 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2400-5144A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1531940 | ||||||
| chr16:1531959
|
C | T | 2 | a0007c0013t0001g0191a0007c0013t0001g0193 | 2 | HG01109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2400-5163G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1531959 | ||||||
| chr16:1532087
|
G | A | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-5291C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532087 | ||||||
| chr16:1532094
|
C | T | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2400-5298G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532094 | ||||||
| chr16:1532199
|
C | T | 1 | a0005c0049t0004g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2400-5403G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532199 | ||||||
| chr16:1532308
|
C | T | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2400-5512G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532308 | ||||||
| chr16:1532319
|
C | T | 4 | a0001c0001t0004g0251a0003c0005t0001g0141a0003c0005t0001g0142others(1): Show | 4 | HG02145.hp2 HG03017.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-5523G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532319 | ||||||
| chr16:1532394
|
G | C | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2400-5598C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532394 | ||||||
| chr16:1532455
|
T | C | 2 | a0001c0001t0002g0174a0003c0005t0003g0063 | 2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2400-5659A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532455 | ||||||
| chr16:1532470
|
A | G | 1 | a0001c0002t0001g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2400-5674T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532470 | ||||||
| chr16:1532645
|
G | A | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-5849C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532645 | ||||||
| chr16:1532768
|
C | T | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2400-5972G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532768 | ||||||
| chr16:1532857
|
C | T | 1 | a0001c0001t0002g0264 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2400-6061G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532857 | ||||||
| chr16:1532869
|
C | T | 39 | a0001c0001t0002g0174a0001c0001t0004g0170a0001c0001t0004g0172others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.2400-6073G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532869 | ||||||
| chr16:1532980
|
G | A | 1 | a0010c0040t0003g0187 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2400-6184C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1532980 | ||||||
| chr16:1533015
|
C | T | 1 | a0016c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2400-6219G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533015 | ||||||
| chr16:1533050
|
TCCTCCAA others(53): Show |
T | 4 | a0001c0002t0001g0104a0001c0002t0001g0333a0001c0002t0001g0334others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-6314_2400-625 others(64): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533050 | ||||||
| chr16:1533058
|
G | T | 9 | a0001c0001t0002g0295a0001c0001t0003g0038a0004c0006t0002g0204others(6): Show | 9 | HG00733.hp2 HG01123.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.2400-6262C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533058 | ||||||
| chr16:1533059
|
T | A | 9 | a0001c0001t0002g0295a0001c0001t0003g0038a0004c0006t0002g0204others(6): Show | 9 | HG00733.hp2 HG01123.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.2400-6263A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533059 | ||||||
| chr16:1533075
|
C | T | 2 | a0001c0001t0002g0174a0003c0005t0003g0063 | 2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2400-6279G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533075 | ||||||
| chr16:1533200
|
C | T | 38 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(35): Show | 38 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2400-6404G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533200 | ||||||
| chr16:1533228
|
T | G | 1 | a0002c0003t0003g0030 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2400-6432A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533228 | ||||||
| chr16:1533237
|
C | A | 2 | a0001c0001t0007g0270a0001c0001t0007g0275 | 2 | HG00323.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2400-6441G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533237 | ||||||
| chr16:1533309
|
TCCTATGG others(11): Show |
T | 3 | a0001c0002t0001g0086a0001c0002t0001g0089a0001c0002t0001g0091 | 3 | HG00423.hp1 NA18980.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2400-6531_2400-651 others(22): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533309 | ||||||
| chr16:1533443
|
C | T | 1 | a0001c0001t0002g0169 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2400-6647G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533443 | ||||||
| chr16:1533463
|
G | T | 2 | a0001c0001t0002g0258a0001c0001t0002g0319 | 2 | NA18957.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.2400-6667C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533463 | ||||||
| chr16:1533480
|
CCT | C | 4 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(1): Show | 4 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-6686_2400-668 others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533480 | ||||||
| chr16:1533492
|
G | A | 1 | a0001c0004t0003g0088 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2400-6696C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533492 | ||||||
| chr16:1533598
|
C | T | 3 | a0001c0002t0001g0196a0001c0004t0001g0117a0014c0061t0001g0116 | 3 | HG01884.hp2 HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2400-6802G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533598 | ||||||
| chr16:1533633
|
T | C | 93 | a0001c0001t0002g0174a0001c0001t0004g0170a0001c0001t0004g0172others(90): Show | 93 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.2400-6837A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533633 | ||||||
| chr16:1533668
|
T | C | 1 | a0004c0006t0002g0235 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2400-6872A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533668 | ||||||
| chr16:1533819
|
C | T | 1 | a0001c0004t0003g0108 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2400-7023G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533819 | ||||||
| chr16:1533876
|
C | T | 13 | a0001c0001t0002g0169a0001c0001t0002g0184a0001c0001t0002g0200others(10): Show | 13 | HG01070.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.2400-7080G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1533876 | ||||||
| chr16:1534248
|
C | T | 1 | a0001c0001t0003g0123 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2400-7452G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534248 | ||||||
| chr16:1534265
|
C | A | 1 | a0001c0001t0002g0261 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2400-7469G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534265 | ||||||
| chr16:1534275
|
G | T | 1 | a0001c0001t0002g0303 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2400-7479C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534275 | ||||||
| chr16:1534293
|
C | T | 8 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(5): Show | 8 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.2400-7497G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534293 | ||||||
| chr16:1534437
|
G | C | 4 | a0001c0002t0001g0081a0001c0002t0001g0107a0001c0004t0003g0082others(1): Show | 4 | HG00408.hp2 NA18961.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.2400-7641C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534437 | ||||||
| chr16:1534445
|
G | C | 39 | a0001c0001t0002g0174a0001c0001t0004g0170a0001c0001t0004g0172others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.2400-7649C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534445 | ||||||
| chr16:1534515
|
C | T | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2400-7719G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534515 | ||||||
| chr16:1534590
|
G | C | 2 | a0001c0002t0001g0128a0001c0037t0001g0127 | 2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2400-7794C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534590 | ||||||
| chr16:1534593
|
C | T | 2 | a0006c0007t0003g0161a0006c0007t0003g0162 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2400-7797G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534593 | ||||||
| chr16:1534617
|
T | C | 201 | a0001c0001t0002g0174a0001c0001t0002g0285a0001c0001t0004g0170others(198): Show | 201 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.2400-7821A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534617 | ||||||
| chr16:1534627
|
G | A | 38 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(35): Show | 38 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2400-7831C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534627 | ||||||
| chr16:1534674
|
C | T | 1 | a0003c0005t0001g0147 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2400-7878G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534674 | ||||||
| chr16:1534691
|
C | T | 7 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0020others(4): Show | 7 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2400-7895G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534691 | ||||||
| chr16:1534846
|
G | A | 2 | a0001c0001t0002g0290a0001c0001t0002g0291 | 2 | HG01099.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2400-8050C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534846 | ||||||
| chr16:1534865
|
T | C | 203 | a0001c0001t0002g0174a0001c0001t0002g0285a0001c0001t0004g0170others(200): Show | 203 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.2400-8069A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534865 | ||||||
| chr16:1534866
|
G | A | 2 | a0001c0002t0001g0061a0001c0002t0001g0071 | 2 | HG00280.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2400-8070C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534866 | ||||||
| chr16:1534900
|
C | T | 1 | a0001c0002t0001g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2400-8104G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534900 | ||||||
| chr16:1534942
|
C | T | 1 | a0001c0002t0001g0080 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2400-8146G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534942 | ||||||
| chr16:1534976
|
G | A | 1 | a0002c0003t0003g0007 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2400-8180C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534976 | ||||||
| chr16:1534983
|
C | T | 8 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(5): Show | 8 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.2400-8187G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1534983 | ||||||
| chr16:1535100
|
G | A | 4 | a0001c0001t0004g0251a0003c0005t0001g0141a0003c0005t0001g0142others(1): Show | 4 | HG02145.hp2 HG03017.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-8304C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535100 | ||||||
| chr16:1535113
|
C | T | 1 | a0002c0003t0003g0035 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2400-8317G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535113 | ||||||
| chr16:1535114
|
G | A | 104 | a0001c0001t0002g0285a0001c0002t0001g0005a0001c0002t0001g0013others(101): Show | 104 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.2400-8318C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535114 | ||||||
| chr16:1535138
|
C | T | 1 | a0001c0002t0003g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2400-8342G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535138 | ||||||
| chr16:1535380
|
G | A | 1 | a0001c0004t0001g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2400-8584C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535380 | ||||||
| chr16:1535438
|
G | A | 1 | a0001c0004t0003g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2400-8642C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535438 | ||||||
| chr16:1535455
|
A | G | 35 | a0001c0001t0002g0174a0003c0005t0001g0141a0003c0005t0001g0142others(32): Show | 35 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.2400-8659T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535455 | ||||||
| chr16:1535553
|
G | A | 1 | a0001c0002t0001g0220 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2400-8757C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535553 | ||||||
| chr16:1535625
|
C | T | 1 | a0001c0001t0002g0323 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2400-8829G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535625 | ||||||
| chr16:1535627
|
C | T | 3 | a0001c0001t0002g0169a0001c0001t0002g0184a0001c0001t0002g0200 | 3 | HG01891.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2400-8831G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535627 | ||||||
| chr16:1535649
|
A | G | 1 | a0001c0001t0002g0259 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2400-8853T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535649 | ||||||
| chr16:1535891
|
T | C | 2 | a0001c0002t0001g0041a0001c0054t0001g0119 | 2 | HG00639.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.2400-9095A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535891 | ||||||
| chr16:1535927
|
C | T | 29 | a0003c0005t0001g0141a0003c0005t0001g0142a0003c0005t0001g0143others(26): Show | 29 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.2400-9131G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1535927 | ||||||
| chr16:1536007
|
C | CG | 5 | a0001c0001t0002g0273a0001c0002t0001g0080a0001c0004t0001g0095others(2): Show | 5 | HG02055.hp2 HG02056.hp1 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.2400-9212dupC | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1536007 | ||||||
| chr16:1536153
|
A | G | 4 | a0001c0001t0002g0250a0001c0001t0002g0294a0001c0001t0002g0296others(1): Show | 4 | NA18962.hp2 NA18991.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.2400-9357T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1536153 | ||||||
| chr16:1536220
|
G | A | 2 | a0001c0001t0002g0242a0002c0003t0003g0034 | 2 | HG01261.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.2400-9424C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1536220 | ||||||
| chr16:1536254
|
G | A | 69 | a0001c0001t0002g0174a0002c0003t0003g0006a0002c0003t0003g0007others(66): Show | 69 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.2400-9458C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1536254 | ||||||
| chr16:1536274
|
C | T | 1 | a0001c0002t0001g0073 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2400-9478G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1536274 | ||||||
| chr16:1536308
|
C | T | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-9512G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1536308 | ||||||
| chr16:1536405
|
G | A | 1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2400-9609C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1536405 | ||||||
| chr16:1536595
|
C | T | 38 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(35): Show | 38 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2400-9799G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1536595 | ||||||
| chr16:1536716
|
C | G | 120 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(117): Show | 120 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2400-9920G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1536716 | ||||||
| chr16:1536820
|
G | A | 38 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(35): Show | 38 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2400-10024C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1536820 | ||||||
| chr16:1537028
|
C | T | 2 | a0001c0020t0003g0138a0001c0020t0003g0139 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2400-10232G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537028 | ||||||
| chr16:1537066
|
T | C | 1 | a0001c0001t0002g0329 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2400-10270A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537066 | ||||||
| chr16:1537150
|
A | G | 1 | a0001c0001t0002g0278 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2400-10354T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537150 | ||||||
| chr16:1537184
|
AGCCAGGG others(34): Show |
A | 1 | a0008c0015t0003g0055 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2400-10429_2400-10 others(47): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537184 | ||||||
| chr16:1537210
|
G | A | 2 | a0001c0001t0002g0174a0003c0005t0003g0063 | 2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2400-10414C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537210 | ||||||
| chr16:1537214
|
C | T | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2400-10418G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537214 | ||||||
| chr16:1537232
|
G | T | 2 | a0001c0010t0001g0126a0001c0010t0002g0321 | 2 | NA18970.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.2400-10436C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537232 | ||||||
| chr16:1537276
|
C | T | 191 | a0001c0001t0002g0174a0001c0002t0001g0005a0001c0002t0001g0013others(188): Show | 191 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.2400-10480G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537276 | ||||||
| chr16:1537321
|
G | A | 189 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(186): Show | 189 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.2400-10525C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537321 | ||||||
| chr16:1537510
|
G | A | 114 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(111): Show | 114 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.2400-10714C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537510 | ||||||
| chr16:1537725
|
C | T | 4 | a0001c0002t0001g0069a0001c0002t0001g0074a0001c0004t0003g0189others(1): Show | 4 | HG02630.hp1 HG03139.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-10929G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537725 | ||||||
| chr16:1537841
|
C | T | 2 | a0001c0002t0001g0061a0001c0002t0001g0071 | 2 | HG00280.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2400-11045G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537841 | ||||||
| chr16:1537937
|
C | T | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00544.hp1 HG00642.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.2400-11141G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537937 | ||||||
| chr16:1537978
|
G | A | 3 | a0001c0002t0001g0086a0001c0002t0001g0089a0001c0002t0001g0091 | 3 | HG00423.hp1 NA18980.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2400-11182C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537978 | ||||||
| chr16:1537992
|
C | T | 1 | a0003c0005t0001g0155 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2400-11196G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1537992 | ||||||
| chr16:1538071
|
G | A | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2400-11275C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538071 | ||||||
| chr16:1538086
|
A | G | 201 | a0001c0001t0002g0174a0001c0001t0002g0252a0001c0001t0002g0255others(198): Show | 201 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.2400-11290T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538086 | ||||||
| chr16:1538088
|
T | C | 3 | a0001c0004t0003g0079a0001c0004t0003g0088a0001c0004t0003g0101 | 3 | HG00639.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2400-11292A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538088 | ||||||
| chr16:1538112
|
C | T | 2 | a0001c0002t0001g0072a0001c0002t0001g0080 | 2 | NA19010.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.2400-11316G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538112 | ||||||
| chr16:1538113
|
T | C | 3 | a0001c0001t0002g0258a0001c0001t0002g0319a0001c0001t0002g0322 | 3 | HG03491.hp1 NA18957.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.2400-11317A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538113 | ||||||
| chr16:1538127
|
A | G | 1 | a0001c0001t0002g0310 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2400-11331T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538127 | ||||||
| chr16:1538165
|
C | T | 8 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(5): Show | 8 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.2400-11369G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538165 | ||||||
| chr16:1538179
|
C | T | 3 | a0003c0005t0001g0143a0003c0005t0001g0144a0003c0005t0001g0145 | 3 | NA18948.hp2 NA19007.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2400-11383G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538179 | ||||||
| chr16:1538314
|
C | T | 1 | a0001c0001t0002g0314 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2400-11518G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538314 | ||||||
| chr16:1538438
|
C | T | 1 | a0001c0001t0002g0304 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2400-11642G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538438 | ||||||
| chr16:1538446
|
T | C | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-11650A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538446 | ||||||
| chr16:1538708
|
C | T | 1 | a0001c0002t0001g0224 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2400-11912G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538708 | ||||||
| chr16:1538799
|
G | A | 106 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.2400-12003C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538799 | ||||||
| chr16:1538848
|
C | T | 106 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.2400-12052G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1538848 | ||||||
| chr16:1539004
|
C | T | 1 | a0001c0002t0001g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2400-12208G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539004 | ||||||
| chr16:1539082
|
G | C | 4 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(1): Show | 4 | HG02258.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2400-12286C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539082 | ||||||
| chr16:1539187
|
T | C | 2 | a0003c0005t0003g0151a0017c0029t0003g0188 | 2 | HG00609.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2400-12391A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539187 | ||||||
| chr16:1539220
|
A | C | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2400-12424T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539220 | ||||||
| chr16:1539225
|
A | C | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2400-12429T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539225 | ||||||
| chr16:1539230
|
C | T | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2400-12434G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539230 | ||||||
| chr16:1539231
|
A | G | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2400-12435T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539231 | ||||||
| chr16:1539234
|
A | C | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2400-12438T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539234 | ||||||
| chr16:1539571
|
C | T | 3 | a0001c0004t0003g0088a0001c0004t0003g0101a0003c0059t0001g0050 | 3 | HG00639.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2400-12775G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539571 | ||||||
| chr16:1539792
|
G | A | 4 | a0005c0009t0004g0166a0005c0009t0004g0173a0005c0049t0004g0171others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2400-12996C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539792 | ||||||
| chr16:1539902
|
G | A | 1 | a0001c0001t0002g0182 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2400-13106C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1539902 | ||||||
| chr16:1540088
|
G | C | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2400-13292C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540088 | ||||||
| chr16:1540110
|
C | T | 1 | a0001c0002t0001g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2400-13314G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540110 | ||||||
| chr16:1540117
|
G | A | 1 | a0001c0057t0003g0214 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2400-13321C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540117 | ||||||
| chr16:1540167
|
G | A | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2400-13371C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540167 | ||||||
| chr16:1540181
|
C | A | 1 | a0001c0004t0003g0115 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2400-13385G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540181 | ||||||
| chr16:1540436
|
C | G | 1 | a0001c0002t0001g0061 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2400-13640G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540436 | ||||||
| chr16:1540513
|
C | T | 1 | a0001c0001t0002g0319 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2400-13717G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540513 | ||||||
| chr16:1540575
|
C | G | 193 | a0001c0001t0002g0279a0001c0001t0002g0290a0001c0001t0002g0291others(190): Show | 193 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.2400-13779G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540575 | ||||||
| chr16:1540666
|
C | T | 2 | a0001c0002t0001g0013a0001c0002t0001g0084 | 2 | HG01361.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2400-13870G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540666 | ||||||
| chr16:1540670
|
C | T | 1 | a0014c0061t0001g0116 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2400-13874G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540670 | ||||||
| chr16:1540671
|
G | A | 68 | a0001c0001t0002g0279a0002c0003t0003g0006a0002c0003t0003g0007others(65): Show | 68 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.2400-13875C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540671 | ||||||
| chr16:1540680
|
C | T | 1 | a0015c0028t0001g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2400-13884G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540680 | ||||||
| chr16:1540788
|
C | T | 1 | a0001c0004t0003g0014 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2400-13992G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1540788 | ||||||
| chr16:1541013
|
G | A | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2400-14217C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1541013 | ||||||
| chr16:1541111
|
G | T | 191 | a0001c0001t0002g0279a0001c0002t0001g0005a0001c0002t0001g0013others(188): Show | 191 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.2400-14315C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1541111 | ||||||
| chr16:1541283
|
G | A | 2 | a0001c0001t0002g0304a0001c0001t0002g0307 | 2 | HG01516.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2400-14487C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1541283 | ||||||
| chr16:1541448
|
C | T | 1 | a0001c0002t0001g0061 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2400-14652G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1541448 | ||||||
| chr16:1541591
|
G | A | 107 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(104): Show | 107 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.2400-14795C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1541591 | ||||||
| chr16:1541749
|
G | A | 3 | a0011c0012t0003g0051a0011c0012t0003g0052a0027c0036t0003g0132 | 3 | HG03098.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2400-14953C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1541749 | ||||||
| chr16:1541861
|
C | T | 1 | a0017c0029t0003g0188 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2400-15065G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1541861 | ||||||
| chr16:1541961
|
G | A | 116 | a0001c0001t0002g0282a0001c0002t0001g0005a0001c0002t0001g0013others(113): Show | 116 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.2400-15165C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1541961 | ||||||
| chr16:1542086
|
T | C | 123 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(120): Show | 123 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.2400-15290A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542086 | ||||||
| chr16:1542265
|
A | T | 195 | a0001c0001t0002g0279a0001c0002t0001g0005a0001c0002t0001g0013others(192): Show | 195 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.2400-15469T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542265 | ||||||
| chr16:1542314
|
C | T | 1 | a0006c0007t0003g0164 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2400-15518G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542314 | ||||||
| chr16:1542366
|
G | A | 68 | a0001c0001t0002g0279a0002c0003t0003g0006a0002c0003t0003g0007others(65): Show | 68 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.2399+15569C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542366 | ||||||
| chr16:1542384
|
T | G | 1 | a0020c0035t0003g0012 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2399+15551A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542384 | ||||||
| chr16:1542523
|
C | T | 115 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(112): Show | 115 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.2399+15412G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542523 | ||||||
| chr16:1542634
|
G | A | 1 | a0020c0035t0003g0012 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2399+15301C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542634 | ||||||
| chr16:1542778
|
C | T | 7 | a0001c0002t0001g0113a0001c0004t0001g0095a0001c0004t0003g0112others(4): Show | 7 | HG02056.hp1 HG02083.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2399+15157G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542778 | ||||||
| chr16:1542789
|
T | C | 1 | a0001c0004t0001g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2399+15146A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542789 | ||||||
| chr16:1542850
|
G | A | 1 | a0001c0001t0002g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2399+15085C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542850 | ||||||
| chr16:1542856
|
G | C | 68 | a0001c0001t0002g0279a0002c0003t0003g0006a0002c0003t0003g0007others(65): Show | 68 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.2399+15079C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1542856 | ||||||
| chr16:1543003
|
G | A | 115 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(112): Show | 115 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.2399+14932C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543003 | ||||||
| chr16:1543107
|
G | C | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+14828C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543107 | ||||||
| chr16:1543110
|
C | T | 1 | a0001c0002t0001g0217 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2399+14825G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543110 | ||||||
| chr16:1543170
|
A | G | 190 | a0001c0001t0002g0279a0001c0002t0001g0005a0001c0002t0001g0013others(187): Show | 190 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.2399+14765T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543170 | ||||||
| chr16:1543238
|
T | C | 1 | a0001c0002t0001g0102 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2399+14697A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543238 | ||||||
| chr16:1543279
|
T | C | 1 | a0001c0002t0001g0100 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2399+14656A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543279 | ||||||
| chr16:1543353
|
G | A | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2399+14582C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543353 | ||||||
| chr16:1543432
|
G | A | 2 | a0003c0019t0003g0136a0003c0019t0003g0137 | 2 | HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2399+14503C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543432 | ||||||
| chr16:1543488
|
G | A | 1 | a0001c0001t0002g0269 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2399+14447C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543488 | ||||||
| chr16:1543605
|
C | T | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+14330G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543605 | ||||||
| chr16:1543619
|
G | A | 1 | a0001c0048t0002g0265 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2399+14316C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543619 | ||||||
| chr16:1543644
|
C | T | 263 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0180others(260): Show | 263 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.2399+14291G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543644 | ||||||
| chr16:1543689
|
C | T | 1 | a0001c0001t0002g0280 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2399+14246G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543689 | ||||||
| chr16:1543842
|
G | A | 108 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(105): Show | 108 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.2399+14093C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543842 | ||||||
| chr16:1543862
|
C | T | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+14073G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543862 | ||||||
| chr16:1543958
|
A | C | 1 | a0001c0050t0002g0328 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2399+13977T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1543958 | ||||||
| chr16:1544019
|
C | CT | 11 | a0001c0001t0002g0242a0001c0001t0002g0246a0001c0001t0002g0247others(8): Show | 11 | HG00423.hp2 HG01069.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.2399+13915dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544019 | ||||||
| chr16:1544157
|
G | A | 190 | a0001c0001t0002g0279a0001c0002t0001g0005a0001c0002t0001g0013others(187): Show | 190 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.2399+13778C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544157 | ||||||
| chr16:1544160
|
G | T | 117 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(114): Show | 117 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.2399+13775C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544160 | ||||||
| chr16:1544161
|
GCACCTGC | G | 5 | a0009c0011t0003g0042a0009c0011t0003g0043a0009c0011t0003g0044others(2): Show | 5 | HG01192.hp2 HG01257.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.2399+13767_2399+13 others(13): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544161 | ||||||
| chr16:1544184
|
AT | A | 7 | a0001c0001t0002g0256a0001c0001t0002g0264a0001c0002t0001g0190others(4): Show | 7 | HG03017.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.2399+13750delA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544184 | ||||||
| chr16:1544217
|
T | A | 28 | a0001c0001t0002g0279a0003c0005t0001g0141a0003c0005t0001g0142others(25): Show | 28 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.2399+13718A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544217 | ||||||
| chr16:1544247
|
A | G | 124 | a0001c0001t0002g0231a0001c0002t0001g0005a0001c0002t0001g0013others(121): Show | 124 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.2399+13688T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544247 | ||||||
| chr16:1544276
|
C | T | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2399+13659G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544276 | ||||||
| chr16:1544313
|
A | G | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+13622T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544313 | ||||||
| chr16:1544338
|
C | A | 1 | a0001c0002t0001g0091 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2399+13597G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544338 | ||||||
| chr16:1544340
|
T | C | 6 | a0001c0002t0001g0047a0001c0002t0001g0083a0001c0002t0001g0097others(3): Show | 6 | HG02258.hp2 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2399+13595A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544340 | ||||||
| chr16:1544350
|
A | AT | 10 | a0001c0001t0002g0295a0001c0001t0003g0038a0004c0006t0002g0204others(7): Show | 10 | HG00733.hp2 HG00741.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.2399+13584dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544350 | ||||||
| chr16:1544375
|
T | C | 33 | a0001c0001t0002g0279a0003c0005t0001g0141a0003c0005t0001g0142others(30): Show | 33 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.2399+13560A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544375 | ||||||
| chr16:1544407
|
G | C | 1 | a0002c0003t0003g0026 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2399+13528C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544407 | ||||||
| chr16:1544420
|
C | T | 1 | a0001c0014t0003g0103 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2399+13515G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544420 | ||||||
| chr16:1544475
|
G | A | 1 | a0001c0001t0002g0244 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2399+13460C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544475 | ||||||
| chr16:1544671
|
T | C | 3 | a0001c0001t0002g0259a0001c0001t0002g0286a0004c0026t0004g0312 | 3 | HG00733.hp1 HG01496.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2399+13264A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544671 | ||||||
| chr16:1544682
|
C | T | 3 | a0001c0001t0002g0259a0001c0001t0002g0286a0004c0026t0004g0312 | 3 | HG00733.hp1 HG01496.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2399+13253G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544682 | ||||||
| chr16:1544687
|
G | C | 3 | a0001c0001t0002g0259a0001c0001t0002g0286a0004c0026t0004g0312 | 3 | HG00733.hp1 HG01496.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2399+13248C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544687 | ||||||
| chr16:1544718
|
G | A | 5 | a0001c0002t0001g0005a0001c0002t0001g0067a0001c0002t0001g0072others(2): Show | 5 | NA18966.hp2 NA18970.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+13217C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544718 | ||||||
| chr16:1544734
|
C | T | 1 | a0020c0035t0003g0012 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2399+13201G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544734 | ||||||
| chr16:1544738
|
T | A | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2399+13197A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544738 | ||||||
| chr16:1544741
|
C | T | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2399+13194G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544741 | ||||||
| chr16:1544766
|
A | C | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2399+13169T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544766 | ||||||
| chr16:1544794
|
A | G | 2 | a0003c0005t0003g0063a0003c0018t0001g0133 | 2 | HG04204.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2399+13141T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544794 | ||||||
| chr16:1544800
|
C | T | 1 | a0003c0018t0001g0133 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2399+13135G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544800 | ||||||
| chr16:1544807
|
CCTGG | C | 6 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2399+13124_2399+13 others(10): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544807 | ||||||
| chr16:1544809
|
T | C | 2 | a0001c0001t0002g0228a0003c0018t0001g0133 | 2 | HG04204.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.2399+13126A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544809 | ||||||
| chr16:1544895
|
G | A | 1 | a0001c0001t0007g0270 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2399+13040C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544895 | ||||||
| chr16:1544899
|
C | T | 1 | a0018c0030t0003g0198 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2399+13036G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544899 | ||||||
| chr16:1544925
|
A | G | 19 | a0001c0001t0002g0279a0003c0005t0001g0141a0003c0005t0001g0142others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.2399+13010T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544925 | ||||||
| chr16:1544936
|
C | T | 1 | a0001c0001t0002g0263 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2399+12999G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544936 | ||||||
| chr16:1544943
|
C | T | 35 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(32): Show | 35 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.2399+12992G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1544943 | ||||||
| chr16:1545026
|
G | A | 1 | a0001c0001t0002g0266 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2399+12909C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1545026 | ||||||
| chr16:1545072
|
A | C | 2 | a0001c0002t0001g0333a0001c0002t0001g0334 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2399+12863T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1545072 | ||||||
| chr16:1545124
|
G | A | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+12811C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1545124 | ||||||
| chr16:1545504
|
T | C | 2 | a0001c0001t0002g0273a0001c0001t0002g0274 | 2 | HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2399+12431A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1545504 | ||||||
| chr16:1545514
|
GT | G | 9 | a0002c0003t0003g0008a0006c0007t0003g0159a0006c0007t0003g0160others(6): Show | 9 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.2399+12420delA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1545514 | ||||||
| chr16:1545530
|
T | C | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2399+12405A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1545530 | ||||||
| chr16:1545532
|
G | A | 3 | a0002c0003t0003g0007a0002c0003t0003g0008a0002c0003t0003g0009 | 3 | NA18941.hp1 NA18953.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2399+12403C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1545532 | ||||||
| chr16:1545599
|
C | T | 26 | a0001c0001t0002g0279a0003c0005t0001g0141a0003c0005t0001g0142others(23): Show | 26 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.2399+12336G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1545599 | ||||||
| chr16:1545815
|
T | G | 1 | a0005c0039t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2399+12120A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1545815 | ||||||
| chr16:1546122
|
G | A | 5 | a0001c0002t0001g0086a0001c0002t0001g0089a0001c0002t0001g0091others(2): Show | 5 | HG00423.hp1 HG00673.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+11813C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1546122 | ||||||
| chr16:1546226
|
C | G | 1 | a0001c0001t0002g0279 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2399+11709G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1546226 | ||||||
| chr16:1546258
|
C | T | 34 | a0001c0002t0001g0005a0001c0002t0001g0061a0001c0002t0001g0067others(31): Show | 34 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.2399+11677G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1546258 | ||||||
| chr16:1546515
|
G | A | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+11420C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1546515 | ||||||
| chr16:1546532
|
G | T | 1 | a0001c0004t0003g0101 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2399+11403C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1546532 | ||||||
| chr16:1546559
|
T | C | 2 | a0003c0019t0003g0136a0003c0019t0003g0137 | 2 | HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2399+11376A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1546559 | ||||||
| chr16:1546885
|
G | A | 1 | a0016c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2399+11050C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1546885 | ||||||
| chr16:1547209
|
C | T | 63 | a0001c0001t0002g0279a0002c0003t0003g0006a0002c0003t0003g0007others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.2399+10726G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547209 | ||||||
| chr16:1547271
|
C | T | 2 | a0001c0002t0001g0128a0001c0037t0001g0127 | 2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2399+10664G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547271 | ||||||
| chr16:1547272
|
G | A | 2 | a0001c0001t0002g0180a0001c0001t0002g0181 | 2 | HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2399+10663C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547272 | ||||||
| chr16:1547278
|
A | G | 6 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2399+10657T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547278 | ||||||
| chr16:1547375
|
C | T | 3 | a0003c0005t0001g0143a0003c0005t0001g0144a0003c0005t0001g0145 | 3 | NA18948.hp2 NA19007.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2399+10560G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547375 | ||||||
| chr16:1547376
|
G | A | 1 | a0001c0002t0001g0311 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2399+10559C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547376 | ||||||
| chr16:1547575
|
T | C | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+10360A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547575 | ||||||
| chr16:1547624
|
C | T | 1 | a0002c0003t0003g0030 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2399+10311G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547624 | ||||||
| chr16:1547759
|
C | A | 1 | a0001c0002t0001g0085 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2399+10176G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547759 | ||||||
| chr16:1547800
|
C | T | 1 | a0001c0001t0002g0283 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2399+10135G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547800 | ||||||
| chr16:1547813
|
G | A | 63 | a0001c0001t0002g0279a0002c0003t0003g0006a0002c0003t0003g0007others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.2399+10122C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547813 | ||||||
| chr16:1547876
|
C | T | 28 | a0001c0001t0002g0279a0003c0005t0001g0141a0003c0005t0001g0142others(25): Show | 28 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.2399+10059G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547876 | ||||||
| chr16:1547923
|
C | T | 111 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(108): Show | 111 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.2399+10012G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1547923 | ||||||
| chr16:1548090
|
C | A | 1 | a0001c0001t0002g0263 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2399+9845G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1548090 | ||||||
| chr16:1548090
|
C | T | 1 | a0001c0001t0002g0319 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2399+9845G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1548090 | ||||||
| chr16:1548270
|
G | A | 1 | a0001c0002t0001g0218 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2399+9665C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1548270 | ||||||
| chr16:1548318
|
G | A | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+9617C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1548318 | ||||||
| chr16:1548719
|
C | G | 1 | a0001c0001t0002g0241 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2399+9216G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1548719 | ||||||
| chr16:1548762
|
C | T | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2399+9173G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1548762 | ||||||
| chr16:1548775
|
G | A | 1 | a0001c0002t0001g0086 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2399+9160C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1548775 | ||||||
| chr16:1548779
|
T | C | 1 | a0010c0046t0004g0267 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2399+9156A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1548779 | ||||||
| chr16:1548814
|
C | T | 4 | a0001c0001t0002g0284a0001c0001t0002g0287a0001c0001t0002g0332others(1): Show | 4 | HG02155.hp1 HG02165.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.2399+9121G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1548814 | ||||||
| chr16:1549145
|
C | T | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2399+8790G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1549145 | ||||||
| chr16:1549480
|
G | A | 14 | a0002c0003t0003g0006a0002c0003t0003g0017a0002c0003t0003g0019others(11): Show | 14 | NA18949.hp1 NA18950.hp2 NA18961.hp1 others(11): Show |
intron_variant | MODIFIER | c.2399+8455C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1549480 | ||||||
| chr16:1549489
|
T | C | 6 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2399+8446A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1549489 | ||||||
| chr16:1549498
|
G | A | 1 | a0002c0003t0003g0032 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2399+8437C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1549498 | ||||||
| chr16:1549574
|
G | A | 2 | a0001c0001t0002g0271a0001c0001t0002g0272 | 2 | HG02738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2399+8361C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1549574 | ||||||
| chr16:1549589
|
G | A | 2 | a0001c0001t0002g0253a0026c0047t0002g0289 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2399+8346C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1549589 | ||||||
| chr16:1549912
|
G | A | 117 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(114): Show | 117 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.2399+8023C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1549912 | ||||||
| chr16:1550025
|
G | A | 2 | a0001c0002t0001g0081a0001c0004t0003g0082 | 2 | NA18961.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.2399+7910C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1550025 | ||||||
| chr16:1550136
|
C | T | 107 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(104): Show | 107 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.2399+7799G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1550136 | ||||||
| chr16:1550141
|
T | C | 4 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(1): Show | 4 | HG02258.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2399+7794A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1550141 | ||||||
| chr16:1550251
|
A | G | 4 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0019t0003g0136others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2399+7684T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1550251 | ||||||
| chr16:1550271
|
T | C | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+7664A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1550271 | ||||||
| chr16:1550338
|
A | T | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+7597T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1550338 | ||||||
| chr16:1550737
|
G | A | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+7198C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1550737 | ||||||
| chr16:1550844
|
C | T | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2399+7091G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1550844 | ||||||
| chr16:1550881
|
G | A | 1 | a0001c0001t0002g0279 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2399+7054C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1550881 | ||||||
| chr16:1551286
|
A | G | 193 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(190): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.2399+6649T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551286 | ||||||
| chr16:1551330
|
C | A | 157 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(154): Show | 157 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.2399+6605G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551330 | ||||||
| chr16:1551457
|
A | G | 333 | a0001c0001t0002g0004a0001c0001t0002g0046a0001c0001t0002g0169others(330): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.2399+6478T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551457 | ||||||
| chr16:1551461
|
C | T | 1 | a0002c0003t0003g0021 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2399+6474G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551461 | ||||||
| chr16:1551494
|
T | C | 1 | a0001c0001t0002g0303 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2399+6441A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551494 | ||||||
| chr16:1551682
|
C | T | 1 | a0001c0002t0003g0064 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2399+6253G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551682 | ||||||
| chr16:1551701
|
C | T | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2399+6234G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551701 | ||||||
| chr16:1551766
|
T | C | 157 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(154): Show | 157 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.2399+6169A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551766 | ||||||
| chr16:1551769
|
G | A | 1 | a0001c0002t0001g0100 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2399+6166C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551769 | ||||||
| chr16:1551799
|
T | C | 1 | a0001c0002t0001g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2399+6136A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551799 | ||||||
| chr16:1551815
|
C | T | 33 | a0003c0005t0001g0141a0003c0005t0001g0142a0003c0005t0001g0143others(30): Show | 33 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.2399+6120G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551815 | ||||||
| chr16:1551816
|
G | A | 1 | a0001c0004t0003g0108 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2399+6119C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551816 | ||||||
| chr16:1551853
|
C | T | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2399+6082G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551853 | ||||||
| chr16:1551878
|
A | G | 194 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(191): Show | 194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.2399+6057T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1551878 | ||||||
| chr16:1552034
|
C | T | 15 | a0001c0001t0002g0179a0001c0001t0002g0257a0001c0001t0002g0276others(12): Show | 15 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.2399+5901G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552034 | ||||||
| chr16:1552035
|
G | A | 1 | a0001c0002t0001g0081 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2399+5900C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552035 | ||||||
| chr16:1552113
|
C | A | 34 | a0003c0005t0001g0141a0003c0005t0001g0142a0003c0005t0001g0143others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.2399+5822G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552113 | ||||||
| chr16:1552259
|
C | T | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+5676G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552259 | ||||||
| chr16:1552322
|
T | C | 76 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.2399+5613A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552322 | ||||||
| chr16:1552426
|
A | C | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+5509T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552426 | ||||||
| chr16:1552577
|
G | A | 1 | a0001c0002t0001g0102 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2399+5358C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552577 | ||||||
| chr16:1552593
|
G | A | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+5342C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552593 | ||||||
| chr16:1552607
|
G | A | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+5328C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552607 | ||||||
| chr16:1552648
|
C | CT | 152 | a0001c0001t0002g0282a0001c0001t0007g0270a0001c0002t0001g0005others(149): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.2399+5286dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552648 | ||||||
| chr16:1552709
|
C | T | 1 | a0001c0002t0001g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2399+5226G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552709 | ||||||
| chr16:1552737
|
C | T | 1 | a0001c0002t0001g0073 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2399+5198G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552737 | ||||||
| chr16:1552810
|
A | G | 193 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(190): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.2399+5125T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552810 | ||||||
| chr16:1552844
|
A | G | 197 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(194): Show | 197 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.2399+5091T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552844 | ||||||
| chr16:1552937
|
A | G | 193 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(190): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.2399+4998T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1552937 | ||||||
| chr16:1553013
|
A | C | 1 | a0001c0001t0007g0270 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2399+4922T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553013 | ||||||
| chr16:1553041
|
A | G | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2399+4894T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553041 | ||||||
| chr16:1553068
|
A | T | 1 | a0011c0012t0003g0051 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2399+4867T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553068 | ||||||
| chr16:1553330
|
G | A | 1 | a0001c0002t0001g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2399+4605C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553330 | ||||||
| chr16:1553495
|
C | T | 4 | a0001c0001t0002g0317a0001c0001t0002g0320a0010c0021t0002g0315others(1): Show | 4 | HG02056.hp2 HG02074.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.2399+4440G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553495 | ||||||
| chr16:1553517
|
G | C | 1 | a0001c0004t0001g0095 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2399+4418C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553517 | ||||||
| chr16:1553534
|
T | C | 194 | a0001c0001t0002g0282a0001c0002t0001g0005a0001c0002t0001g0013others(191): Show | 194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.2399+4401A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553534 | ||||||
| chr16:1553575
|
G | A | 194 | a0001c0001t0002g0282a0001c0002t0001g0005a0001c0002t0001g0013others(191): Show | 194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.2399+4360C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553575 | ||||||
| chr16:1553715
|
C | A | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+4220G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553715 | ||||||
| chr16:1553887
|
T | C | 1 | a0001c0002t0001g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2399+4048A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553887 | ||||||
| chr16:1553953
|
C | T | 1 | a0001c0004t0003g0088 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2399+3982G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1553953 | ||||||
| chr16:1554051
|
A | G | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2399+3884T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1554051 | ||||||
| chr16:1554387
|
G | A | 117 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(114): Show | 117 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.2399+3548C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1554387 | ||||||
| chr16:1554526
|
C | T | 3 | a0001c0014t0003g0103a0001c0014t0006g0209a0001c0014t0006g0215 | 3 | HG02080.hp1 HG02523.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.2399+3409G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1554526 | ||||||
| chr16:1554655
|
C | T | 2 | a0001c0002t0001g0333a0001c0002t0001g0334 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2399+3280G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1554655 | ||||||
| chr16:1554700
|
T | C | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+3235A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1554700 | ||||||
| chr16:1555008
|
C | T | 1 | a0001c0001t0002g0273 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2399+2927G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555008 | ||||||
| chr16:1555043
|
C | T | 31 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(28): Show | 31 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.2399+2892G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555043 | ||||||
| chr16:1555049
|
C | T | 1 | a0006c0007t0003g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2399+2886G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555049 | ||||||
| chr16:1555050
|
A | G | 198 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(195): Show | 198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.2399+2885T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555050 | ||||||
| chr16:1555052
|
C | T | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+2883G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555052 | ||||||
| chr16:1555162
|
C | A | 108 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(105): Show | 108 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.2399+2773G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555162 | ||||||
| chr16:1555216
|
G | A | 1 | a0001c0001t0002g0278 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2399+2719C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555216 | ||||||
| chr16:1555233
|
T | C | 1 | a0001c0004t0001g0105 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2399+2702A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555233 | ||||||
| chr16:1555270
|
C | T | 1 | a0001c0002t0001g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2399+2665G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555270 | ||||||
| chr16:1555384
|
G | A | 1 | a0002c0003t0003g0022 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2399+2551C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555384 | ||||||
| chr16:1555536
|
T | C | 194 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(191): Show | 194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.2399+2399A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555536 | ||||||
| chr16:1555605
|
C | T | 118 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(115): Show | 118 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.2399+2330G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555605 | ||||||
| chr16:1555866
|
G | A | 1 | a0006c0007t0003g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2399+2069C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555866 | ||||||
| chr16:1555974
|
C | T | 34 | a0003c0005t0001g0141a0003c0005t0001g0142a0003c0005t0001g0143others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.2399+1961G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1555974 | ||||||
| chr16:1556129
|
A | T | 1 | a0006c0007t0003g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2399+1806T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556129 | ||||||
| chr16:1556148
|
C | T | 3 | a0001c0002t0001g0196a0001c0004t0001g0117a0014c0061t0001g0116 | 3 | HG01884.hp2 HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2399+1787G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556148 | ||||||
| chr16:1556160
|
T | A | 1 | a0001c0001t0002g0317 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2399+1775A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556160 | ||||||
| chr16:1556166
|
A | G | 34 | a0003c0005t0001g0141a0003c0005t0001g0142a0003c0005t0001g0143others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.2399+1769T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556166 | ||||||
| chr16:1556335
|
C | T | 4 | a0001c0002t0001g0070a0001c0002t0001g0197a0001c0002t0010g0186others(1): Show | 4 | HG00621.hp2 NA18962.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.2399+1600G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556335 | ||||||
| chr16:1556443
|
A | G | 193 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(190): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.2399+1492T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556443 | ||||||
| chr16:1556444
|
A | G | 193 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(190): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.2399+1491T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556444 | ||||||
| chr16:1556478
|
C | T | 34 | a0003c0005t0001g0141a0003c0005t0001g0142a0003c0005t0001g0143others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.2399+1457G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556478 | ||||||
| chr16:1556479
|
C | T | 1 | a0003c0005t0001g0155 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2399+1456G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556479 | ||||||
| chr16:1556608
|
A | G | 1 | a0001c0002t0001g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2399+1327T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556608 | ||||||
| chr16:1556731
|
CT | C | 3 | a0001c0004t0003g0079a0001c0004t0003g0088a0001c0004t0003g0101 | 3 | HG00639.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2399+1203delA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556731 | ||||||
| chr16:1556731
|
CTTTTTTA others(16): Show |
C | 1 | a0002c0003t0003g0032 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2399+1181_2399+120 others(27): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556731 | ||||||
| chr16:1556733
|
T | A | 3 | a0001c0004t0003g0079a0001c0004t0003g0088a0001c0004t0003g0101 | 3 | HG00639.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2399+1202A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556733 | ||||||
| chr16:1556738
|
A | G | 107 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(104): Show | 107 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.2399+1197T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556738 | ||||||
| chr16:1556786
|
C | T | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2399+1149G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556786 | ||||||
| chr16:1556803
|
T | G | 1 | a0001c0002t0001g0084 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2399+1132A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556803 | ||||||
| chr16:1556844
|
C | T | 5 | a0001c0001t0002g0206a0001c0001t0002g0271a0001c0001t0002g0272others(2): Show | 5 | HG02738.hp1 HG03239.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+1091G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1556844 | ||||||
| chr16:1557112
|
GC | G | 70 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(67): Show | 70 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.2399+822delG | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557112 | ||||||
| chr16:1557164
|
G | A | 1 | a0001c0001t0002g0264 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2399+771C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557164 | ||||||
| chr16:1557241
|
C | T | 1 | a0001c0001t0002g0285 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2399+694G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557241 | ||||||
| chr16:1557283
|
G | T | 35 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(32): Show | 35 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.2399+652C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557283 | ||||||
| chr16:1557285
|
G | C | 36 | a0001c0001t0002g0291a0001c0002t0001g0128a0001c0037t0001g0127others(33): Show | 36 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+650C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557285 | ||||||
| chr16:1557382
|
G | A | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+553C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557382 | ||||||
| chr16:1557449
|
C | G | 6 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2399+486G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557449 | ||||||
| chr16:1557454
|
T | G | 1 | a0001c0002t0001g0089 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2399+481A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557454 | ||||||
| chr16:1557528
|
G | A | 1 | a0001c0002t0001g0089 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2399+407C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557528 | ||||||
| chr16:1557548
|
A | G | 1 | a0014c0061t0001g0116 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2399+387T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557548 | ||||||
| chr16:1557563
|
T | C | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2399+372A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557563 | ||||||
| chr16:1557573
|
C | T | 194 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(191): Show | 194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.2399+362G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557573 | ||||||
| chr16:1557703
|
G | A | 1 | a0005c0039t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2399+232C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557703 | ||||||
| chr16:1557826
|
C | G | 1 | a0022c0038t0001g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2399+109G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 19/30 | chr16 | 1557826 | ||||||
| chr16:1558176
|
A | G | 160 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(157): Show | 160 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.2200-42T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1558176 | ||||||
| chr16:1558201
|
G | A | 1 | a0006c0007t0003g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2200-67C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1558201 | ||||||
| chr16:1558363
|
G | A | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2200-229C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1558363 | ||||||
| chr16:1558706
|
G | C | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2200-572C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1558706 | ||||||
| chr16:1558728
|
G | A | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2200-594C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1558728 | ||||||
| chr16:1558845
|
G | C | 2 | a0001c0002t0003g0090a0001c0002t0003g0106 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2200-711C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1558845 | ||||||
| chr16:1558885
|
C | G | 3 | a0002c0003t0003g0007a0002c0003t0003g0008a0002c0003t0003g0009 | 3 | NA18941.hp1 NA18953.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2200-751G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1558885 | ||||||
| chr16:1558904
|
G | A | 1 | a0001c0001t0002g0179 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2200-770C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1558904 | ||||||
| chr16:1558933
|
A | G | 194 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(191): Show | 194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.2200-799T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1558933 | ||||||
| chr16:1559115
|
C | T | 2 | a0001c0002t0001g0085a0031c0024t0001g0111 | 2 | NA18973.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2200-981G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559115 | ||||||
| chr16:1559134
|
T | C | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2200-1000A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559134 | ||||||
| chr16:1559205
|
C | T | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2200-1071G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559205 | ||||||
| chr16:1559506
|
G | A | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2200-1372C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559506 | ||||||
| chr16:1559539
|
G | A | 6 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2200-1405C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559539 | ||||||
| chr16:1559623
|
C | A | 1 | a0001c0002t0010g0186 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2200-1489G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559623 | ||||||
| chr16:1559754
|
G | C | 1 | a0002c0003t0003g0015 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2200-1620C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559754 | ||||||
| chr16:1559794
|
C | T | 1 | a0030c0058t0001g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2200-1660G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559794 | ||||||
| chr16:1559842
|
G | C | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2200-1708C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559842 | ||||||
| chr16:1559852
|
C | T | 2 | a0001c0020t0003g0138a0001c0020t0003g0139 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2200-1718G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559852 | ||||||
| chr16:1559907
|
C | T | 1 | a0002c0003t0003g0023 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2200-1773G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559907 | ||||||
| chr16:1559940
|
G | A | 1 | a0006c0007t0003g0164 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2200-1806C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559940 | ||||||
| chr16:1559943
|
C | T | 4 | a0001c0001t0002g0290a0001c0001t0002g0291a0001c0001t0002g0302others(1): Show | 4 | HG01099.hp1 HG01433.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2200-1809G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1559943 | ||||||
| chr16:1560008
|
C | T | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2200-1874G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560008 | ||||||
| chr16:1560175
|
G | A | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2199+1810C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560175 | ||||||
| chr16:1560214
|
C | G | 70 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(67): Show | 70 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.2199+1771G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560214 | ||||||
| chr16:1560366
|
C | T | 7 | a0001c0002t0001g0113a0001c0004t0001g0095a0001c0004t0003g0112others(4): Show | 7 | HG02056.hp1 HG02083.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2199+1619G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560366 | ||||||
| chr16:1560380
|
C | T | 1 | a0016c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2199+1605G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560380 | ||||||
| chr16:1560497
|
C | T | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2199+1488G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560497 | ||||||
| chr16:1560577
|
G | A | 2 | a0001c0001t0007g0270a0001c0001t0007g0275 | 2 | HG00323.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2199+1408C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560577 | ||||||
| chr16:1560718
|
C | A | 2 | a0011c0012t0003g0201a0011c0012t0003g0202 | 2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2199+1267G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560718 | ||||||
| chr16:1560783
|
A | G | 1 | a0001c0002t0001g0190 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2199+1202T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560783 | ||||||
| chr16:1560884
|
A | G | 86 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.2199+1101T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560884 | ||||||
| chr16:1560985
|
T | C | 5 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(2): Show | 5 | HG01884.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2199+1000A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1560985 | ||||||
| chr16:1561053
|
G | A | 1 | a0001c0001t0004g0254 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2199+932C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1561053 | ||||||
| chr16:1561067
|
G | A | 1 | a0001c0002t0001g0311 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2199+918C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1561067 | ||||||
| chr16:1561154
|
G | A | 1 | a0001c0010t0004g0232 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2199+831C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1561154 | ||||||
| chr16:1561187
|
C | T | 1 | a0001c0002t0001g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2199+798G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1561187 | ||||||
| chr16:1561273
|
C | A | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2199+712G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1561273 | ||||||
| chr16:1561362
|
T | A | 2 | a0011c0012t0003g0201a0011c0012t0003g0202 | 2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2199+623A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1561362 | ||||||
| chr16:1561497
|
G | A | 4 | a0006c0007t0003g0159a0006c0007t0003g0161a0006c0007t0003g0162others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2199+488C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1561497 | ||||||
| chr16:1561825
|
C | T | 1 | a0001c0002t0001g0061 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2199+160G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1561825 | ||||||
| chr16:1561949
|
T | A | 3 | a0001c0002t0001g0196a0001c0004t0001g0117a0014c0061t0001g0116 | 3 | HG01884.hp2 HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2199+36A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 18/30 | chr16 | 1561949 | ||||||
| chr16:1562144
|
G | GT | 6 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2068-29dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1562144 | ||||||
| chr16:1562205
|
C | T | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2068-89G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1562205 | ||||||
| chr16:1562219
|
C | T | 1 | a0001c0002t0001g0067 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2068-103G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1562219 | ||||||
| chr16:1562379
|
A | G | 1 | a0001c0001t0002g0248 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2068-263T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1562379 | ||||||
| chr16:1562458
|
C | T | 2 | a0001c0001t0002g0253a0026c0047t0002g0289 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2068-342G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1562458 | ||||||
| chr16:1562492
|
G | A | 4 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0019t0003g0136others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068-376C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1562492 | ||||||
| chr16:1562497
|
C | G | 34 | a0003c0005t0001g0141a0003c0005t0001g0142a0003c0005t0001g0143others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.2068-381G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1562497 | ||||||
| chr16:1562623
|
T | A | 2 | a0001c0001t0002g0243a0001c0050t0002g0328 | 2 | HG02602.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2068-507A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1562623 | ||||||
| chr16:1562639
|
G | A | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2068-523C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1562639 | ||||||
| chr16:1562881
|
T | C | 1 | a0005c0049t0004g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2068-765A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1562881 | ||||||
| chr16:1563038
|
A | G | 10 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(7): Show | 10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.2068-922T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563038 | ||||||
| chr16:1563296
|
CT | C | 31 | a0002c0003t0003g0007a0002c0003t0003g0008a0002c0003t0003g0009others(28): Show | 31 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.2067+700delA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563296 | ||||||
| chr16:1563308
|
C | T | 1 | a0002c0003t0003g0006 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2067+689G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563308 | ||||||
| chr16:1563309
|
T | C | 1 | a0002c0003t0003g0006 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2067+688A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563309 | ||||||
| chr16:1563347
|
A | G | 86 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.2067+650T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563347 | ||||||
| chr16:1563364
|
G | A | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2067+633C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563364 | ||||||
| chr16:1563374
|
G | A | 4 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0019t0003g0136others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2067+623C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563374 | ||||||
| chr16:1563407
|
T | C | 1 | a0002c0003t0003g0035 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2067+590A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563407 | ||||||
| chr16:1563423
|
A | C | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+574T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563423 | ||||||
| chr16:1563427
|
T | C | 5 | a0001c0001t0002g0253a0001c0001t0002g0262a0001c0001t0002g0301others(2): Show | 5 | HG02257.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2067+570A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563427 | ||||||
| chr16:1563431
|
C | T | 1 | a0001c0002t0001g0049 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2067+566G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563431 | ||||||
| chr16:1563432
|
G | C | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+565C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563432 | ||||||
| chr16:1563439
|
A | C | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+558T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563439 | ||||||
| chr16:1563450
|
A | C | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+547T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563450 | ||||||
| chr16:1563451
|
A | G | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+546T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563451 | ||||||
| chr16:1563452
|
A | T | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+545T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563452 | ||||||
| chr16:1563454
|
A | T | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+543T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563454 | ||||||
| chr16:1563455
|
A | C | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+542T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563455 | ||||||
| chr16:1563457
|
C | A | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+540G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563457 | ||||||
| chr16:1563462
|
C | A | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+535G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563462 | ||||||
| chr16:1563466
|
C | A | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+531G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563466 | ||||||
| chr16:1563470
|
C | A | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+527G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563470 | ||||||
| chr16:1563585
|
A | G | 1 | a0021c0034t0003g0010 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2067+412T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563585 | ||||||
| chr16:1563749
|
T | C | 1 | a0002c0003t0003g0006 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2067+248A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563749 | ||||||
| chr16:1563752
|
C | T | 1 | a0002c0003t0003g0006 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2067+245G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563752 | ||||||
| chr16:1563792
|
A | C | 110 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0041others(107): Show | 110 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.2067+205T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563792 | ||||||
| chr16:1563845
|
C | T | 1 | a0001c0002t0001g0084 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2067+152G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563845 | ||||||
| chr16:1563923
|
A | G | 1 | a0002c0003t0003g0006 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2067+74T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563923 | ||||||
| chr16:1563933
|
G | C | 4 | a0006c0007t0003g0159a0006c0007t0003g0161a0006c0007t0003g0162others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2067+64C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 17/30 | chr16 | 1563933 | ||||||
| chr16:1564183
|
C | A | 1 | a0001c0001t0002g0285 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1902-21G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564183 | ||||||
| chr16:1564191
|
C | T | 1 | a0003c0005t0001g0143 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1902-29G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564191 | ||||||
| chr16:1564239
|
C | G | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1902-77G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564239 | ||||||
| chr16:1564255
|
T | C | 4 | a0002c0003t0003g0021a0002c0003t0003g0026a0019c0033t0003g0018others(1): Show | 4 | HG00408.hp1 HG00544.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.1902-93A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564255 | ||||||
| chr16:1564258
|
C | G | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1902-96G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564258 | ||||||
| chr16:1564355
|
G | C | 1 | a0006c0007t0003g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1902-193C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564355 | ||||||
| chr16:1564366
|
C | T | 1 | a0001c0004t0003g0088 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1902-204G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564366 | ||||||
| chr16:1564521
|
C | T | 3 | a0003c0005t0003g0063a0011c0012t0003g0201a0011c0012t0003g0202 | 3 | NA19043.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1902-359G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564521 | ||||||
| chr16:1564524
|
G | C | 1 | a0003c0005t0001g0150 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1902-362C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564524 | ||||||
| chr16:1564568
|
A | C | 1 | a0002c0003t0003g0006 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1902-406T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564568 | ||||||
| chr16:1564569
|
C | A | 1 | a0002c0003t0003g0006 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1902-407G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564569 | ||||||
| chr16:1564610
|
C | A | 1 | a0001c0001t0002g0307 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1902-448G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564610 | ||||||
| chr16:1564688
|
C | T | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1902-526G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564688 | ||||||
| chr16:1564725
|
G | GT | 10 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(7): Show | 10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1902-564dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564725 | ||||||
| chr16:1564754
|
C | G | 1 | a0001c0001t0002g0303 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1902-592G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564754 | ||||||
| chr16:1564762
|
G | A | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1902-600C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564762 | ||||||
| chr16:1564822
|
A | T | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1902-660T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564822 | ||||||
| chr16:1564860
|
C | T | 2 | a0015c0028t0001g0057a0016c0027t0003g0134 | 2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1902-698G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1564860 | ||||||
| chr16:1565029
|
C | T | 1 | a0001c0004t0001g0092 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1902-867G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565029 | ||||||
| chr16:1565067
|
G | A | 2 | a0001c0004t0003g0088a0001c0004t0003g0101 | 2 | HG00639.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1902-905C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565067 | ||||||
| chr16:1565088
|
G | A | 1 | a0001c0001t0002g0286 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1902-926C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565088 | ||||||
| chr16:1565120
|
G | T | 1 | a0002c0003t0003g0006 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1902-958C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565120 | ||||||
| chr16:1565121
|
C | G | 1 | a0002c0003t0003g0006 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1902-959G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565121 | ||||||
| chr16:1565188
|
G | A | 26 | a0003c0005t0001g0141a0003c0005t0001g0142a0003c0005t0001g0143others(23): Show | 26 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1901+973C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565188 | ||||||
| chr16:1565472
|
A | G | 6 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(3): Show | 6 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1901+689T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565472 | ||||||
| chr16:1565489
|
G | A | 1 | a0003c0059t0001g0050 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1901+672C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565489 | ||||||
| chr16:1565785
|
C | T | 1 | a0030c0058t0001g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1901+376G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565785 | ||||||
| chr16:1565827
|
C | G | 2 | a0001c0001t0002g0169a0001c0001t0002g0184 | 2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1901+334G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565827 | ||||||
| chr16:1565831
|
C | G | 3 | a0001c0002t0001g0113a0001c0004t0003g0112a0001c0004t0003g0130 | 3 | NA18945.hp1 NA18975.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1901+330G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565831 | ||||||
| chr16:1565847
|
G | T | 1 | a0001c0004t0001g0092 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1901+314C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 16/30 | chr16 | 1565847 | ||||||
| chr16:1566419
|
C | T | 1 | a0001c0004t0001g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1771-128G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1566419 | ||||||
| chr16:1566527
|
T | A | 7 | a0001c0001t0002g0236a0001c0001t0002g0241a0001c0001t0002g0243others(4): Show | 7 | HG01109.hp1 HG01255.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1771-236A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1566527 | ||||||
| chr16:1566547
|
C | T | 1 | a0001c0052t0004g0234 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1771-256G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1566547 | ||||||
| chr16:1566662
|
C | T | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1771-371G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1566662 | ||||||
| chr16:1566721
|
G | A | 6 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(3): Show | 6 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1771-430C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1566721 | ||||||
| chr16:1566837
|
C | T | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1771-546G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1566837 | ||||||
| chr16:1566959
|
C | T | 3 | a0001c0004t0003g0079a0001c0004t0003g0088a0001c0004t0003g0101 | 3 | HG00639.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1771-668G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1566959 | ||||||
| chr16:1567004
|
T | G | 1 | a0016c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1771-713A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567004 | ||||||
| chr16:1567016
|
C | T | 3 | a0003c0005t0001g0143a0003c0005t0001g0144a0003c0005t0001g0145 | 3 | NA18948.hp2 NA19007.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1771-725G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567016 | ||||||
| chr16:1567075
|
C | T | 1 | a0002c0003t0003g0009 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1771-784G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567075 | ||||||
| chr16:1567177
|
C | G | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1771-886G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567177 | ||||||
| chr16:1567240
|
G | A | 8 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(5): Show | 8 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1771-949C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567240 | ||||||
| chr16:1567362
|
C | T | 1 | a0016c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1770+855G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567362 | ||||||
| chr16:1567392
|
GCCTCTGC | G | 11 | a0001c0008t0001g0203a0006c0007t0003g0159a0006c0007t0003g0160others(8): Show | 11 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(8): Show |
intron_variant | MODIFIER | c.1770+818_1770+824d others(9): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567392 | ||||||
| chr16:1567430
|
C | CACCCGCT others(13): Show |
1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1770+767_1770+786d others(22): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567430 | ||||||
| chr16:1567539
|
C | T | 1 | a0001c0001t0002g0299 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1770+678G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567539 | ||||||
| chr16:1567627
|
G | A | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1770+590C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567627 | ||||||
| chr16:1567687
|
C | G | 85 | a0001c0020t0003g0138a0001c0020t0003g0139a0002c0003t0003g0006others(82): Show | 85 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1770+530G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567687 | ||||||
| chr16:1567688
|
G | A | 3 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175 | 3 | HG02922.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1770+529C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567688 | ||||||
| chr16:1567886
|
T | C | 1 | a0016c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1770+331A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567886 | ||||||
| chr16:1567994
|
G | A | 1 | a0001c0004t0001g0095 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1770+223C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1567994 | ||||||
| chr16:1568006
|
C | A | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1770+211G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1568006 | ||||||
| chr16:1568042
|
G | A | 7 | a0001c0002t0001g0047a0001c0002t0001g0083a0001c0002t0001g0097others(4): Show | 7 | HG02258.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1770+175C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1568042 | ||||||
| chr16:1568091
|
G | A | 1 | a0010c0040t0003g0187 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1770+126C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1568091 | ||||||
| chr16:1568111
|
A | C | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1770+106T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 15/30 | chr16 | 1568111 | ||||||
| chr16:1568348
|
G | A | 1 | a0001c0001t0002g0283 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1653-14C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1568348 | ||||||
| chr16:1568361
|
G | A | 3 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182 | 3 | HG02109.hp1 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1653-27C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1568361 | ||||||
| chr16:1568555
|
G | A | 1 | a0001c0004t0003g0114 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1653-221C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1568555 | ||||||
| chr16:1568704
|
A | G | 1 | a0001c0002t0001g0098 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1653-370T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1568704 | ||||||
| chr16:1568757
|
A | G | 1 | a0001c0001t0002g0263 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1653-423T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1568757 | ||||||
| chr16:1568771
|
A | C | 1 | a0003c0059t0001g0050 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1653-437T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1568771 | ||||||
| chr16:1568835
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1653-501G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1568835 | ||||||
| chr16:1568853
|
G | A | 8 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(5): Show | 8 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1653-519C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1568853 | ||||||
| chr16:1568914
|
G | C | 1 | a0001c0001t0002g0307 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1653-580C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1568914 | ||||||
| chr16:1568994
|
T | C | 3 | a0001c0001t0002g0241a0001c0001t0002g0244a0001c0001t0002g0245 | 3 | HG01109.hp1 HG01255.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1653-660A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1568994 | ||||||
| chr16:1569003
|
G | GT | 13 | a0001c0001t0002g0184a0001c0001t0002g0266a0001c0001t0002g0272others(10): Show | 13 | HG00621.hp1 HG01070.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.1653-670dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569003 | ||||||
| chr16:1569003
|
GT | G | 32 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(29): Show | 32 | HG00408.hp1 HG00642.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.1653-670delA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569003 | ||||||
| chr16:1569003
|
GTT | G | 11 | a0002c0003t0003g0026a0006c0007t0003g0159a0006c0007t0003g0160others(8): Show | 11 | HG00544.hp1 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.1653-671_1653-670d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569003 | ||||||
| chr16:1569038
|
C | T | 11 | a0002c0003t0003g0015a0006c0007t0003g0159a0006c0007t0003g0160others(8): Show | 11 | HG02523.hp1 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.1653-704G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569038 | ||||||
| chr16:1569043
|
T | C | 1 | a0002c0003t0003g0015 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1653-709A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569043 | ||||||
| chr16:1569043
|
T | G | 1 | a0016c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1653-709A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569043 | ||||||
| chr16:1569045
|
C | G | 1 | a0001c0001t0002g0302 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1653-711G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569045 | ||||||
| chr16:1569060
|
A | G | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1653-726T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569060 | ||||||
| chr16:1569065
|
C | T | 2 | a0001c0001t0002g0259a0001c0001t0002g0295 | 2 | HG00733.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1653-731G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569065 | ||||||
| chr16:1569066
|
G | A | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1653-732C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569066 | ||||||
| chr16:1569073
|
C | T | 89 | a0001c0020t0003g0138a0001c0020t0003g0139a0002c0003t0003g0006others(86): Show | 89 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.1653-739G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569073 | ||||||
| chr16:1569081
|
T | C | 90 | a0001c0020t0003g0138a0001c0020t0003g0139a0002c0003t0003g0006others(87): Show | 90 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1653-747A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569081 | ||||||
| chr16:1569228
|
C | T | 3 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182 | 3 | HG02109.hp1 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1653-894G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569228 | ||||||
| chr16:1569251
|
G | A | 1 | a0001c0001t0002g0263 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1653-917C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569251 | ||||||
| chr16:1569255
|
G | A | 1 | a0001c0001t0002g0263 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1653-921C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569255 | ||||||
| chr16:1569260
|
A | C | 1 | a0001c0001t0002g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1653-926T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569260 | ||||||
| chr16:1569320
|
T | C | 1 | a0001c0002t0001g0086 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1653-986A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569320 | ||||||
| chr16:1569363
|
C | T | 7 | a0003c0017t0001g0058a0003c0017t0001g0059a0008c0015t0003g0053others(4): Show | 7 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1653-1029G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569363 | ||||||
| chr16:1569375
|
A | G | 2 | a0001c0001t0002g0174a0005c0009t0004g0167 | 2 | HG01070.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1653-1041T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569375 | ||||||
| chr16:1569430
|
C | T | 90 | a0001c0020t0003g0138a0001c0020t0003g0139a0002c0003t0003g0006others(87): Show | 90 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1653-1096G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569430 | ||||||
| chr16:1569487
|
C | T | 186 | a0001c0001t0002g0169a0001c0001t0002g0184a0001c0001t0002g0200others(183): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1653-1153G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569487 | ||||||
| chr16:1569675
|
T | A | 1 | a0001c0001t0002g0296 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1653-1341A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569675 | ||||||
| chr16:1569702
|
T | A | 2 | a0001c0002t0001g0120a0001c0002t0001g0121 | 2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1653-1368A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569702 | ||||||
| chr16:1569740
|
G | C | 1 | a0007c0013t0001g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1653-1406C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569740 | ||||||
| chr16:1569757
|
A | AT | 45 | a0001c0020t0003g0138a0003c0005t0001g0141a0003c0005t0001g0142others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1653-1424dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569757 | ||||||
| chr16:1569757
|
A | ATT | 41 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(38): Show | 41 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1653-1425_1653-142 others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569757 | ||||||
| chr16:1569788
|
A | T | 2 | a0001c0001t0002g0169a0001c0001t0002g0184 | 2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1653-1454T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569788 | ||||||
| chr16:1569824
|
G | C | 4 | a0001c0002t0001g0070a0001c0002t0001g0197a0001c0002t0010g0186others(1): Show | 4 | HG00621.hp2 NA18962.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1653-1490C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569824 | ||||||
| chr16:1569895
|
A | T | 48 | a0001c0001t0002g0298a0001c0020t0003g0138a0001c0020t0003g0139others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1652+1512T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569895 | ||||||
| chr16:1569961
|
T | C | 1 | a0001c0001t0002g0332 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1652+1446A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1569961 | ||||||
| chr16:1570025
|
G | T | 1 | a0001c0004t0001g0075 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1652+1382C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570025 | ||||||
| chr16:1570306
|
C | T | 1 | a0001c0001t0002g0278 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1652+1101G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570306 | ||||||
| chr16:1570383
|
C | T | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1652+1024G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570383 | ||||||
| chr16:1570467
|
G | C | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1652+940C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570467 | ||||||
| chr16:1570517
|
C | T | 1 | a0022c0038t0001g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1652+890G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570517 | ||||||
| chr16:1570520
|
A | G | 1 | a0001c0001t0002g0268 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1652+887T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570520 | ||||||
| chr16:1570549
|
C | T | 31 | a0003c0005t0001g0141a0003c0005t0001g0142a0003c0005t0001g0143others(28): Show | 31 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1652+858G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570549 | ||||||
| chr16:1570818
|
C | T | 1 | a0003c0059t0001g0050 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1652+589G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570818 | ||||||
| chr16:1570889
|
G | A | 1 | a0001c0002t0001g0217 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1652+518C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570889 | ||||||
| chr16:1570924
|
T | G | 1 | a0001c0002t0001g0089 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1652+483A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570924 | ||||||
| chr16:1570948
|
G | C | 1 | a0011c0012t0003g0051 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1652+459C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1570948 | ||||||
| chr16:1571011
|
C | A | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1652+396G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1571011 | ||||||
| chr16:1571097
|
CTT | C | 4 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(1): Show | 4 | HG02109.hp1 HG02486.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1652+308_1652+309d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1571097 | ||||||
| chr16:1571118
|
G | C | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1652+289C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1571118 | ||||||
| chr16:1571152
|
C | G | 1 | a0001c0001t0002g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1652+255G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1571152 | ||||||
| chr16:1571157
|
A | G | 1 | a0003c0005t0001g0150 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1652+250T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1571157 | ||||||
| chr16:1571332
|
T | C | 1 | a0001c0010t0004g0225 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1652+75A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 14/30 | chr16 | 1571332 | ||||||
| chr16:1571701
|
C | T | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1525-167G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1571701 | ||||||
| chr16:1571719
|
G | A | 6 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1525-185C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1571719 | ||||||
| chr16:1571748
|
G | C | 1 | a0001c0002t0001g0118 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1525-214C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1571748 | ||||||
| chr16:1571927
|
G | A | 2 | a0002c0003t0003g0007a0002c0003t0003g0009 | 2 | NA18941.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1525-393C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1571927 | ||||||
| chr16:1571966
|
T | C | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1525-432A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1571966 | ||||||
| chr16:1572007
|
A | G | 86 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1525-473T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572007 | ||||||
| chr16:1572036
|
G | A | 1 | a0003c0005t0001g0150 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1525-502C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572036 | ||||||
| chr16:1572091
|
C | T | 80 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(77): Show | 80 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1525-557G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572091 | ||||||
| chr16:1572107
|
G | A | 86 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1525-573C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572107 | ||||||
| chr16:1572110
|
G | A | 1 | a0001c0002t0001g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1525-576C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572110 | ||||||
| chr16:1572246
|
C | T | 2 | a0001c0001t0002g0205a0001c0001t0002g0229 | 2 | NA19055.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1525-712G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572246 | ||||||
| chr16:1572259
|
T | C | 4 | a0002c0003t0003g0021a0002c0003t0003g0026a0019c0033t0003g0018others(1): Show | 4 | HG00408.hp1 HG00544.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525-725A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572259 | ||||||
| chr16:1572273
|
G | A | 1 | a0001c0010t0001g0125 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1525-739C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572273 | ||||||
| chr16:1572372
|
C | A | 3 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182 | 3 | HG02109.hp1 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1525-838G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572372 | ||||||
| chr16:1572538
|
C | T | 2 | a0001c0001t0002g0290a0001c0001t0002g0291 | 2 | HG01099.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1525-1004G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572538 | ||||||
| chr16:1572725
|
G | T | 1 | a0001c0002t0003g0208 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1525-1191C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572725 | ||||||
| chr16:1572900
|
C | G | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-1366G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572900 | ||||||
| chr16:1572900
|
C | T | 10 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(7): Show | 10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1525-1366G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572900 | ||||||
| chr16:1572917
|
C | G | 10 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(7): Show | 10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1525-1383G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1572917 | ||||||
| chr16:1573250
|
G | A | 86 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1525-1716C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573250 | ||||||
| chr16:1573358
|
C | T | 1 | a0001c0002t0001g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1525-1824G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573358 | ||||||
| chr16:1573472
|
CTTGTATT | C | 86 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1525-1945_1525-193 others(11): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573472 | ||||||
| chr16:1573630
|
G | C | 1 | a0001c0001t0002g0263 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1525-2096C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573630 | ||||||
| chr16:1573637
|
C | T | 5 | a0001c0001t0002g0253a0001c0001t0002g0262a0001c0001t0002g0301others(2): Show | 5 | HG02257.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-2103G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573637 | ||||||
| chr16:1573745
|
A | AGGCT | 5 | a0001c0008t0001g0203a0001c0008t0001g0211a0001c0008t0001g0216others(2): Show | 5 | NA18943.hp2 NA18983.hp2 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-2215_1525-221 others(8): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573745 | ||||||
| chr16:1573851
|
A | G | 86 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1525-2317T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573851 | ||||||
| chr16:1573879
|
T | C | 8 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(5): Show | 8 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1525-2345A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573879 | ||||||
| chr16:1573911
|
G | A | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-2377C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573911 | ||||||
| chr16:1573935
|
C | A | 5 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(2): Show | 5 | HG01884.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1525-2401G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573935 | ||||||
| chr16:1573990
|
T | C | 2 | a0001c0004t0001g0075a0001c0004t0001g0076 | 2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1525-2456A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1573990 | ||||||
| chr16:1574141
|
T | C | 86 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1525-2607A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1574141 | ||||||
| chr16:1574476
|
T | C | 1 | a0001c0002t0001g0087 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1525-2942A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1574476 | ||||||
| chr16:1574492
|
G | A | 80 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(77): Show | 80 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1525-2958C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1574492 | ||||||
| chr16:1574527
|
C | T | 34 | a0003c0005t0001g0141a0003c0005t0001g0142a0003c0005t0001g0143others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1525-2993G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1574527 | ||||||
| chr16:1574770
|
CCCCT | C | 86 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1525-3240_1525-323 others(8): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1574770 | ||||||
| chr16:1574783
|
T | G | 115 | a0001c0001t0002g0169a0001c0001t0002g0184a0001c0001t0002g0200others(112): Show | 115 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1525-3249A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1574783 | ||||||
| chr16:1574942
|
T | C | 1 | a0001c0004t0001g0095 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1525-3408A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1574942 | ||||||
| chr16:1575142
|
G | A | 14 | a0001c0002t0001g0047a0001c0002t0001g0049a0001c0002t0001g0069others(11): Show | 14 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1525-3608C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575142 | ||||||
| chr16:1575184
|
A | T | 1 | a0001c0001t0002g0266 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1525-3650T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575184 | ||||||
| chr16:1575243
|
T | G | 116 | a0001c0001t0002g0169a0001c0001t0002g0184a0001c0001t0002g0200others(113): Show | 116 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1525-3709A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575243 | ||||||
| chr16:1575289
|
G | A | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-3755C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575289 | ||||||
| chr16:1575299
|
C | T | 1 | a0001c0001t0002g0308 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1525-3765G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575299 | ||||||
| chr16:1575345
|
A | T | 1 | a0001c0010t0002g0321 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1525-3811T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575345 | ||||||
| chr16:1575350
|
G | C | 1 | a0001c0010t0002g0321 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1525-3816C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575350 | ||||||
| chr16:1575445
|
C | T | 1 | a0001c0004t0003g0115 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1525-3911G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575445 | ||||||
| chr16:1575812
|
C | T | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1525-4278G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575812 | ||||||
| chr16:1575889
|
T | C | 86 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1525-4355A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575889 | ||||||
| chr16:1575936
|
G | C | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-4402C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575936 | ||||||
| chr16:1575960
|
G | A | 1 | a0001c0001t0002g0296 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1525-4426C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1575960 | ||||||
| chr16:1576057
|
G | A | 34 | a0003c0005t0001g0141a0003c0005t0001g0142a0003c0005t0001g0143others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1525-4523C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576057 | ||||||
| chr16:1576072
|
G | C | 1 | a0001c0054t0001g0119 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1525-4538C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576072 | ||||||
| chr16:1576078
|
A | G | 86 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1525-4544T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576078 | ||||||
| chr16:1576286
|
T | TA | 83 | a0001c0001t0002g0179a0001c0001t0002g0299a0001c0001t0002g0319others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1524+4472dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576286 | ||||||
| chr16:1576286
|
TA | T | 21 | a0001c0001t0002g0205a0001c0001t0002g0255a0001c0001t0002g0287others(18): Show | 21 | HG01256.hp2 HG01433.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1524+4472delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576286 | ||||||
| chr16:1576287
|
A | T | 1 | a0001c0001t0002g0322 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1524+4472T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576287 | ||||||
| chr16:1576317
|
T | C | 86 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1524+4442A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576317 | ||||||
| chr16:1576358
|
G | A | 1 | a0001c0002t0003g0064 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1524+4401C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576358 | ||||||
| chr16:1576363
|
G | A | 1 | a0001c0002t0001g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1524+4396C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576363 | ||||||
| chr16:1576465
|
G | A | 10 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(7): Show | 10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1524+4294C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576465 | ||||||
| chr16:1576490
|
G | A | 6 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1524+4269C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576490 | ||||||
| chr16:1576523
|
C | T | 1 | a0001c0004t0003g0014 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1524+4236G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576523 | ||||||
| chr16:1576547
|
G | A | 1 | a0001c0001t0002g0285 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1524+4212C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576547 | ||||||
| chr16:1576591
|
C | CA | 128 | a0001c0001t0002g0169a0001c0001t0002g0179a0001c0001t0002g0184others(125): Show | 128 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.1524+4167dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576591 | ||||||
| chr16:1576605
|
AC | A | 4 | a0003c0005t0001g0148a0006c0007t0003g0161a0011c0012t0003g0051others(1): Show | 4 | HG02897.hp2 HG03017.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1524+4153delG | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576605 | ||||||
| chr16:1576606
|
C | A | 82 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1524+4153G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576606 | ||||||
| chr16:1576651
|
TCAGA | T | 77 | a0001c0002t0001g0005a0001c0002t0001g0041a0001c0002t0001g0047others(74): Show | 77 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1524+4104_1524+410 others(8): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576651 | ||||||
| chr16:1576704
|
T | A | 86 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1524+4055A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576704 | ||||||
| chr16:1576831
|
C | T | 3 | a0001c0002t0001g0086a0001c0002t0001g0089a0001c0002t0001g0091 | 3 | HG00423.hp1 NA18980.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1524+3928G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576831 | ||||||
| chr16:1576888
|
C | A | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1524+3871G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576888 | ||||||
| chr16:1576981
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1524+3778C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1576981 | ||||||
| chr16:1577437
|
G | A | 2 | a0001c0002t0001g0041a0001c0054t0001g0119 | 2 | HG00639.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1524+3322C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1577437 | ||||||
| chr16:1577507
|
A | G | 86 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1524+3252T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1577507 | ||||||
| chr16:1577617
|
G | A | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1524+3142C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1577617 | ||||||
| chr16:1577724
|
G | C | 1 | a0001c0001t0004g0251 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1524+3035C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1577724 | ||||||
| chr16:1577754
|
C | T | 86 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1524+3005G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1577754 | ||||||
| chr16:1577972
|
C | CAA | 88 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(85): Show | 88 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1524+2785_1524+278 others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1577972 | ||||||
| chr16:1577994
|
G | C | 10 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(7): Show | 10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1524+2765C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1577994 | ||||||
| chr16:1577997
|
A | G | 7 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0020others(4): Show | 7 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1524+2762T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1577997 | ||||||
| chr16:1578078
|
C | T | 2 | a0011c0012t0003g0201a0011c0012t0003g0202 | 2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1524+2681G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578078 | ||||||
| chr16:1578130
|
C | T | 10 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(7): Show | 10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1524+2629G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578130 | ||||||
| chr16:1578176
|
T | C | 1 | a0001c0001t0002g0269 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1524+2583A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578176 | ||||||
| chr16:1578224
|
T | G | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1524+2535A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578224 | ||||||
| chr16:1578294
|
G | A | 36 | a0002c0003t0003g0006a0002c0003t0003g0007a0002c0003t0003g0008others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1524+2465C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578294 | ||||||
| chr16:1578333
|
C | T | 1 | a0005c0009t0004g0173 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1524+2426G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578333 | ||||||
| chr16:1578578
|
TA | T | 151 | a0001c0001t0002g0169a0001c0001t0002g0184a0001c0001t0002g0200others(148): Show | 151 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.1524+2180delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578578 | ||||||
| chr16:1578603
|
C | T | 1 | a0001c0004t0001g0066 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1524+2156G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578603 | ||||||
| chr16:1578857
|
G | A | 3 | a0003c0019t0003g0136a0003c0019t0003g0137a0016c0027t0003g0134 | 3 | HG02896.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1524+1902C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578857 | ||||||
| chr16:1578878
|
A | AT | 6 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1524+1880dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578878 | ||||||
| chr16:1578964
|
G | A | 2 | a0001c0004t0001g0075a0001c0004t0001g0076 | 2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1524+1795C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1578964 | ||||||
| chr16:1579060
|
T | C | 1 | a0001c0002t0010g0186 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1524+1699A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1579060 | ||||||
| chr16:1579191
|
G | T | 1 | a0001c0001t0002g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1524+1568C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1579191 | ||||||
| chr16:1579257
|
C | T | 10 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(7): Show | 10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1524+1502G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1579257 | ||||||
| chr16:1579280
|
G | A | 1 | a0001c0004t0003g0108 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1524+1479C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1579280 | ||||||
| chr16:1579297
|
G | T | 1 | a0001c0002t0001g0311 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1524+1462C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1579297 | ||||||
| chr16:1579624
|
AGT | A | 3 | a0001c0004t0003g0079a0001c0004t0003g0088a0001c0004t0003g0101 | 3 | HG00639.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1524+1133_1524+113 others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1579624 | ||||||
| chr16:1579748
|
C | G | 1 | a0005c0049t0004g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1524+1011G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1579748 | ||||||
| chr16:1579773
|
T | G | 1 | a0001c0001t0002g0324 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1524+986A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1579773 | ||||||
| chr16:1579963
|
C | CA | 49 | a0001c0001t0002g0257a0001c0001t0002g0271a0001c0001t0002g0272others(46): Show | 49 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.1524+795dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1579963 | ||||||
| chr16:1579963
|
CA | C | 37 | a0001c0001t0002g0236a0001c0002t0001g0212a0003c0005t0001g0141others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.1524+795delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1579963 | ||||||
| chr16:1580129
|
C | T | 1 | a0010c0021t0002g0316 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1524+630G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580129 | ||||||
| chr16:1580184
|
T | C | 52 | a0003c0005t0001g0141a0003c0005t0001g0142a0003c0005t0001g0143others(49): Show | 52 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.1524+575A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580184 | ||||||
| chr16:1580262
|
G | A | 6 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(3): Show | 6 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1524+497C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580262 | ||||||
| chr16:1580263
|
C | T | 1 | a0001c0001t0002g0307 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1524+496G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580263 | ||||||
| chr16:1580287
|
A | G | 1 | a0001c0002t0001g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1524+472T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580287 | ||||||
| chr16:1580323
|
G | A | 1 | a0001c0010t0004g0232 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1524+436C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580323 | ||||||
| chr16:1580347
|
G | C | 1 | a0002c0003t0003g0025 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1524+412C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580347 | ||||||
| chr16:1580380
|
G | A | 116 | a0001c0001t0002g0169a0001c0001t0002g0184a0001c0001t0002g0200others(113): Show | 116 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1524+379C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580380 | ||||||
| chr16:1580452
|
G | T | 2 | a0012c0023t0001g0048a0012c0023t0001g0060 | 2 | NA18948.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1524+307C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580452 | ||||||
| chr16:1580554
|
G | A | 1 | a0001c0004t0001g0066 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1524+205C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580554 | ||||||
| chr16:1580745
|
G | C | 1 | a0001c0004t0003g0088 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1524+14C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 13/30 | chr16 | 1580745 | ||||||
| chr16:1580885
|
C | A | 3 | a0001c0002t0001g0104a0001c0002t0001g0333a0001c0002t0001g0334 | 3 | HG02896.hp1 HG02897.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1433-35G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1580885 | ||||||
| chr16:1580988
|
C | T | 5 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(2): Show | 5 | HG01884.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1433-138G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1580988 | ||||||
| chr16:1581013
|
A | G | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1433-163T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581013 | ||||||
| chr16:1581231
|
T | C | 1 | a0003c0005t0003g0153 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1433-381A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581231 | ||||||
| chr16:1581238
|
A | C | 1 | a0001c0001t0002g0244 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1433-388T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581238 | ||||||
| chr16:1581281
|
A | C | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1433-431T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581281 | ||||||
| chr16:1581293
|
A | G | 8 | a0001c0001t0002g0236a0001c0001t0002g0241a0001c0001t0002g0243others(5): Show | 8 | HG01109.hp1 HG01255.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1433-443T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581293 | ||||||
| chr16:1581514
|
C | T | 2 | a0001c0001t0004g0172a0001c0001t0004g0175 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1433-664G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581514 | ||||||
| chr16:1581521
|
G | A | 1 | a0008c0015t0003g0055 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1433-671C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581521 | ||||||
| chr16:1581535
|
G | A | 31 | a0003c0005t0001g0141a0003c0005t0001g0142a0003c0005t0001g0143others(28): Show | 31 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1433-685C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581535 | ||||||
| chr16:1581590
|
A | ACT | 91 | a0001c0001t0003g0038a0001c0020t0003g0138a0001c0020t0003g0139others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1433-742_1433-741d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581590 | ||||||
| chr16:1581653
|
A | C | 1 | a0001c0001t0002g0326 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1433-803T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581653 | ||||||
| chr16:1581727
|
A | AGGGGAGG others(4): Show |
1 | a0001c0001t0003g0123 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1433-888_1433-878d others(13): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581727 | ||||||
| chr16:1581738
|
GGGGGAGG others(17): Show |
G | 2 | a0001c0002t0001g0223a0001c0002t0001g0224 | 2 | HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1433-912_1433-889d others(26): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581738 | ||||||
| chr16:1581755
|
C | CG | 13 | a0001c0001t0002g0226a0001c0001t0002g0257a0001c0001t0002g0330others(10): Show | 13 | HG01123.hp2 HG01175.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1433-906dupC | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581755 | ||||||
| chr16:1581755
|
C | T | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1433-905G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581755 | ||||||
| chr16:1581758
|
G | T | 1 | a0001c0001t0002g0169 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1433-908C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581758 | ||||||
| chr16:1581761
|
G | A | 32 | a0003c0005t0001g0141a0003c0005t0001g0142a0003c0005t0001g0143others(29): Show | 32 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.1433-911C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581761 | ||||||
| chr16:1581784
|
G | T | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1433-934C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581784 | ||||||
| chr16:1581808
|
T | G | 91 | a0001c0001t0003g0038a0001c0020t0003g0138a0001c0020t0003g0139others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1433-958A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581808 | ||||||
| chr16:1581814
|
T | G | 10 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(7): Show | 10 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1433-964A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581814 | ||||||
| chr16:1581849
|
G | A | 11 | a0001c0002t0001g0049a0006c0007t0003g0159a0006c0007t0003g0160others(8): Show | 11 | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.1433-999C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581849 | ||||||
| chr16:1581881
|
A | G | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1433-1031T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581881 | ||||||
| chr16:1581998
|
C | T | 2 | a0001c0002t0005g0001a0001c0002t0005g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1433-1148G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1581998 | ||||||
| chr16:1582085
|
C | A | 1 | a0001c0001t0004g0251 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1432+1229G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1582085 | ||||||
| chr16:1582124
|
G | A | 2 | a0001c0045t0002g0176a0005c0044t0004g0168 | 2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1432+1190C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1582124 | ||||||
| chr16:1582270
|
C | T | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1432+1044G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1582270 | ||||||
| chr16:1582447
|
C | T | 30 | a0003c0005t0001g0141a0003c0005t0001g0142a0003c0005t0001g0143others(27): Show | 30 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.1432+867G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1582447 | ||||||
| chr16:1582688
|
G | A | 2 | a0001c0004t0003g0014a0024c0042t0001g0109 | 2 | HG00673.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1432+626C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1582688 | ||||||
| chr16:1582693
|
C | G | 5 | a0001c0008t0001g0203a0001c0008t0001g0211a0001c0008t0001g0216others(2): Show | 5 | NA18943.hp2 NA18983.hp2 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.1432+621G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1582693 | ||||||
| chr16:1582699
|
T | C | 1 | a0001c0002t0003g0208 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1432+615A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1582699 | ||||||
| chr16:1582900
|
C | T | 5 | a0001c0001t0002g0253a0001c0001t0002g0262a0001c0001t0002g0301others(2): Show | 5 | HG02257.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1432+414G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1582900 | ||||||
| chr16:1582904
|
G | A | 2 | a0001c0014t0006g0209a0001c0014t0006g0215 | 2 | HG02523.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1432+410C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1582904 | ||||||
| chr16:1582964
|
G | A | 90 | a0001c0020t0003g0138a0001c0020t0003g0139a0002c0003t0003g0006others(87): Show | 90 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1432+350C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1582964 | ||||||
| chr16:1583099
|
A | G | 44 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0005t0001g0141others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.1432+215T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1583099 | ||||||
| chr16:1583136
|
T | G | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1432+178A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 12/30 | chr16 | 1583136 | ||||||
| chr16:1583421
|
G | A | 1 | a0005c0009t0004g0167 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1360-35C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583421 | ||||||
| chr16:1583445
|
A | C | 3 | a0001c0001t0002g0259a0001c0001t0002g0286a0001c0001t0002g0295 | 3 | HG00733.hp2 HG01496.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1360-59T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583445 | ||||||
| chr16:1583557
|
C | T | 3 | a0001c0002t0001g0210a0001c0002t0001g0220a0001c0043t0001g0219 | 3 | HG02071.hp1 HG02129.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1360-171G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583557 | ||||||
| chr16:1583664
|
T | C | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1360-278A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583664 | ||||||
| chr16:1583757
|
T | G | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1360-371A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583757 | ||||||
| chr16:1583784
|
G | A | 1 | a0005c0009t0004g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1360-398C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583784 | ||||||
| chr16:1583849
|
A | G | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1359+368T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583849 | ||||||
| chr16:1583854
|
C | T | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1359+363G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583854 | ||||||
| chr16:1583871
|
G | A | 91 | a0001c0001t0003g0038a0001c0020t0003g0138a0001c0020t0003g0139others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1359+346C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583871 | ||||||
| chr16:1583890
|
A | G | 5 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0175others(2): Show | 5 | HG01884.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1359+327T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583890 | ||||||
| chr16:1583945
|
G | C | 43 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0005t0001g0141others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1359+272C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583945 | ||||||
| chr16:1583978
|
G | C | 3 | a0003c0019t0003g0136a0003c0019t0003g0137a0016c0027t0003g0134 | 3 | HG02896.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1359+239C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 11/30 | chr16 | 1583978 | ||||||
| chr16:1584505
|
G | A | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1156-85C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1584505 | ||||||
| chr16:1584556
|
T | C | 1 | a0001c0010t0004g0225 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1156-136A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1584556 | ||||||
| chr16:1584603
|
T | A | 11 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(8): Show | 11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.1156-183A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1584603 | ||||||
| chr16:1584837
|
A | G | 1 | a0001c0001t0002g0310 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1156-417T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1584837 | ||||||
| chr16:1585136
|
G | A | 58 | a0001c0002t0001g0005a0001c0002t0001g0041a0001c0002t0001g0061others(55): Show | 58 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1156-716C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585136 | ||||||
| chr16:1585160
|
A | G | 11 | a0003c0005t0001g0141a0003c0005t0001g0142a0003c0005t0001g0146others(8): Show | 11 | HG00099.hp2 HG01192.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.1156-740T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585160 | ||||||
| chr16:1585375
|
A | T | 1 | a0001c0002t0001g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1155+755T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585375 | ||||||
| chr16:1585399
|
TGCCAAGG others(8): Show |
T | 1 | a0006c0007t0003g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1155+716_1155+730d others(17): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585399 | ||||||
| chr16:1585751
|
T | C | 43 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0005t0001g0141others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1155+379A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585751 | ||||||
| chr16:1585766
|
C | CT | 30 | a0001c0001t0002g0184a0001c0001t0002g0239a0001c0001t0002g0255others(27): Show | 30 | HG00673.hp2 HG01069.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1155+363dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585766 | ||||||
| chr16:1585766
|
CT | C | 11 | a0001c0001t0002g0236a0001c0001t0002g0317a0001c0001t0002g0320others(8): Show | 11 | HG00099.hp2 HG01070.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1155+363delA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585766 | ||||||
| chr16:1585775
|
T | C | 1 | a0001c0001t0002g0325 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1155+355A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585775 | ||||||
| chr16:1585822
|
G | A | 1 | a0001c0002t0001g0220 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1155+308C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585822 | ||||||
| chr16:1585871
|
C | T | 33 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0005t0001g0141others(30): Show | 33 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1155+259G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585871 | ||||||
| chr16:1585907
|
G | A | 333 | a0001c0001t0002g0004a0001c0001t0002g0046a0001c0001t0002g0169others(330): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.1155+223C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585907 | ||||||
| chr16:1585916
|
G | T | 1 | a0001c0002t0001g0091 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1155+214C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585916 | ||||||
| chr16:1585993
|
G | A | 1 | a0002c0003t0003g0020 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1155+137C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1585993 | ||||||
| chr16:1586027
|
T | C | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | NA18975.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1155+103A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1586027 | ||||||
| chr16:1586034
|
G | A | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1155+96C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1586034 | ||||||
| chr16:1586073
|
G | T | 1 | a0002c0003t0003g0008 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1155+57C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 10/30 | chr16 | 1586073 | ||||||
| chr16:1586404
|
C | A | 1 | a0001c0010t0002g0321 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1010-129G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586404 | ||||||
| chr16:1586548
|
C | A | 43 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0005t0001g0141others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1010-273G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586548 | ||||||
| chr16:1586557
|
C | T | 1 | a0001c0001t0002g0318 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1010-282G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586557 | ||||||
| chr16:1586627
|
G | GCA | 5 | a0001c0001t0002g0174a0001c0001t0002g0301a0001c0004t0003g0079others(2): Show | 5 | HG02257.hp1 HG03453.hp2 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.1010-354_1010-353d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586627 | ||||||
| chr16:1586627
|
GCA | G | 165 | a0001c0001t0003g0038a0001c0002t0001g0005a0001c0002t0001g0013others(162): Show | 165 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1010-354_1010-353d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586627 | ||||||
| chr16:1586629
|
A | G | 1 | a0001c0004t0001g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1010-354T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586629 | ||||||
| chr16:1586718
|
T | C | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1010-443A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586718 | ||||||
| chr16:1586826
|
C | A | 8 | a0003c0017t0001g0058a0003c0017t0001g0059a0003c0059t0001g0050others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1009+372G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586826 | ||||||
| chr16:1586829
|
C | G | 1 | a0001c0001t0002g0169 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1009+369G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586829 | ||||||
| chr16:1586895
|
C | T | 37 | a0001c0001t0003g0038a0002c0003t0003g0006a0002c0003t0003g0007others(34): Show | 37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1009+303G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586895 | ||||||
| chr16:1586907
|
A | G | 43 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0005t0001g0141others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1009+291T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586907 | ||||||
| chr16:1586934
|
T | G | 37 | a0001c0001t0003g0038a0002c0003t0003g0006a0002c0003t0003g0007others(34): Show | 37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1009+264A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1586934 | ||||||
| chr16:1587140
|
C | T | 11 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(8): Show | 11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.1009+58G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1587140 | ||||||
| chr16:1587180
|
C | G | 1 | a0001c0001t0002g0262 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1009+18G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 9/30 | chr16 | 1587180 | ||||||
| chr16:1587464
|
T | C | 1 | a0001c0002t0001g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.903-160A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 8/30 | chr16 | 1587464 | ||||||
| chr16:1587521
|
T | C | 1 | a0001c0004t0003g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.903-217A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 8/30 | chr16 | 1587521 | ||||||
| chr16:1587705
|
G | A | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.902+228C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 8/30 | chr16 | 1587705 | ||||||
| chr16:1587740
|
G | A | 1 | a0001c0004t0001g0092 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.902+193C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 8/30 | chr16 | 1587740 | ||||||
| chr16:1587797
|
T | C | 1 | a0001c0001t0002g0253 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.902+136A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 8/30 | chr16 | 1587797 | ||||||
| chr16:1588070
|
G | A | 1 | a0005c0009t0004g0166 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.811-46C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588070 | ||||||
| chr16:1588159
|
T | C | 11 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(8): Show | 11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.811-135A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588159 | ||||||
| chr16:1588322
|
A | G | 38 | a0001c0001t0002g0264a0001c0001t0003g0038a0002c0003t0003g0006others(35): Show | 38 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.811-298T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588322 | ||||||
| chr16:1588527
|
A | AAATAATA others(5): Show |
16 | a0001c0002t0003g0090a0001c0004t0001g0117a0001c0020t0003g0138others(13): Show | 16 | HG01069.hp1 HG01071.hp2 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.811-515_811-504dup others(12): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588527 | ||||||
| chr16:1588527
|
A | AAATAATA others(8): Show |
10 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(7): Show | 10 | HG00408.hp1 HG00621.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.811-518_811-504dup others(15): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588527 | ||||||
| chr16:1588527
|
A | AAATAATA others(11): Show |
116 | a0001c0001t0002g0169a0001c0001t0002g0184a0001c0001t0002g0200others(113): Show | 116 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.811-521_811-504dup others(18): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588527 | ||||||
| chr16:1588527
|
A | AAATAATA others(14): Show |
57 | a0001c0001t0003g0038a0001c0001t0004g0170a0001c0001t0004g0172others(54): Show | 57 | HG00544.hp1 HG00544.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.811-524_811-504dup others(21): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588527 | ||||||
| chr16:1588527
|
A | AAATAATA others(17): Show |
10 | a0002c0003t0003g0006a0002c0003t0003g0023a0002c0003t0003g0039others(7): Show | 10 | HG00099.hp2 HG01109.hp2 HG03927.hp2 others(7): Show |
intron_variant | MODIFIER | c.811-504_811-503ins others(24): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588527 | ||||||
| chr16:1588527
|
A | AAATAATA others(20): Show |
3 | a0003c0005t0001g0141a0003c0005t0001g0142a0003c0005t0001g0156 | 3 | HG03491.hp2 HG03492.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.811-504_811-503ins others(27): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588527 | ||||||
| chr16:1588614
|
T | TA | 4 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0019t0003g0136others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.811-591_811-590ins others(1): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588614 | ||||||
| chr16:1588615
|
C | G | 4 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0019t0003g0136others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.811-591G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588615 | ||||||
| chr16:1588735
|
G | A | 1 | a0001c0001t0002g0263 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.811-711C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588735 | ||||||
| chr16:1588819
|
C | T | 31 | a0003c0005t0001g0141a0003c0005t0001g0142a0003c0005t0001g0143others(28): Show | 31 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.810+786G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588819 | ||||||
| chr16:1588846
|
A | C | 1 | a0001c0001t0003g0038 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.810+759T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588846 | ||||||
| chr16:1588988
|
T | C | 54 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0005t0001g0141others(51): Show | 54 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.810+617A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1588988 | ||||||
| chr16:1589102
|
G | A | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.810+503C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1589102 | ||||||
| chr16:1589127
|
G | C | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.810+478C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1589127 | ||||||
| chr16:1589217
|
T | C | 1 | a0003c0005t0001g0155 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.810+388A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1589217 | ||||||
| chr16:1589277
|
G | A | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.810+328C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 7/30 | chr16 | 1589277 | ||||||
| chr16:1589792
|
C | G | 91 | a0001c0001t0003g0038a0001c0004t0003g0115a0001c0020t0003g0138others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.635-12G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1589792 | ||||||
| chr16:1589807
|
T | C | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.635-27A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1589807 | ||||||
| chr16:1589836
|
G | A | 1 | a0001c0001t0002g0181 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.635-56C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1589836 | ||||||
| chr16:1589844
|
C | G | 1 | a0001c0001t0004g0254 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.635-64G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1589844 | ||||||
| chr16:1589940
|
T | C | 1 | a0001c0004t0003g0079 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.635-160A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1589940 | ||||||
| chr16:1589963
|
G | A | 8 | a0003c0017t0001g0058a0003c0017t0001g0059a0003c0059t0001g0050others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.635-183C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1589963 | ||||||
| chr16:1590034
|
T | C | 31 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0005t0001g0141others(28): Show | 31 | HG00099.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.635-254A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590034 | ||||||
| chr16:1590062
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.635-282C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590062 | ||||||
| chr16:1590200
|
C | CA | 108 | a0001c0001t0002g0247a0001c0001t0002g0248a0001c0001t0002g0272others(105): Show | 108 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.635-421dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590200 | ||||||
| chr16:1590200
|
C | CAA | 13 | a0001c0002t0001g0065a0001c0002t0001g0070a0001c0002t0001g0080others(10): Show | 13 | HG00621.hp2 HG02040.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.635-422_635-421dup others(2): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590200 | ||||||
| chr16:1590200
|
CA | C | 17 | a0001c0001t0002g0309a0001c0001t0002g0318a0001c0020t0003g0138others(14): Show | 17 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.635-421delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590200 | ||||||
| chr16:1590200
|
CAA | C | 31 | a0003c0005t0001g0141a0003c0005t0001g0143a0003c0005t0001g0144others(28): Show | 31 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.635-422_635-421del others(2): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590200 | ||||||
| chr16:1590248
|
C | G | 1 | a0001c0004t0001g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.635-468G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590248 | ||||||
| chr16:1590300
|
C | G | 37 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0005t0001g0141others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.635-520G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590300 | ||||||
| chr16:1590332
|
G | A | 2 | a0001c0020t0003g0138a0001c0020t0003g0139 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.635-552C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590332 | ||||||
| chr16:1590438
|
G | A | 5 | a0001c0008t0001g0203a0001c0008t0001g0211a0001c0008t0001g0216others(2): Show | 5 | NA18943.hp2 NA18983.hp2 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.635-658C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590438 | ||||||
| chr16:1590614
|
C | T | 2 | a0001c0001t0002g0271a0001c0001t0002g0272 | 2 | HG02738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.635-834G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590614 | ||||||
| chr16:1590712
|
C | T | 1 | a0001c0002t0001g0061 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.635-932G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590712 | ||||||
| chr16:1590994
|
A | G | 2 | a0001c0002t0001g0041a0001c0054t0001g0119 | 2 | HG00639.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.634+1182T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1590994 | ||||||
| chr16:1591008
|
C | T | 2 | a0001c0001t0002g0273a0001c0001t0002g0274 | 2 | HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.634+1168G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591008 | ||||||
| chr16:1591071
|
T | C | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.634+1105A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591071 | ||||||
| chr16:1591092
|
C | T | 5 | a0002c0003t0003g0035a0009c0011t0003g0042a0009c0011t0003g0043others(2): Show | 5 | HG01257.hp2 HG01261.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.634+1084G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591092 | ||||||
| chr16:1591117
|
T | C | 4 | a0001c0002t0001g0065a0001c0002t0001g0085a0001c0002t0001g0102others(1): Show | 4 | HG02040.hp1 HG02155.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+1059A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591117 | ||||||
| chr16:1591210
|
C | T | 1 | a0004c0006t0002g0204 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.634+966G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591210 | ||||||
| chr16:1591281
|
C | T | 6 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.634+895G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591281 | ||||||
| chr16:1591354
|
T | C | 1 | a0003c0005t0001g0150 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.634+822A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591354 | ||||||
| chr16:1591550
|
C | T | 32 | a0001c0001t0003g0038a0002c0003t0003g0006a0002c0003t0003g0007others(29): Show | 32 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.634+626G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591550 | ||||||
| chr16:1591571
|
G | A | 2 | a0001c0020t0003g0138a0001c0020t0003g0139 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.634+605C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591571 | ||||||
| chr16:1591713
|
A | T | 1 | a0001c0004t0003g0115 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.634+463T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591713 | ||||||
| chr16:1591770
|
T | C | 3 | a0003c0019t0003g0136a0003c0019t0003g0137a0016c0027t0003g0134 | 3 | HG02896.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.634+406A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591770 | ||||||
| chr16:1591977
|
C | T | 6 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.634+199G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591977 | ||||||
| chr16:1591982
|
G | A | 1 | a0001c0004t0001g0066 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.634+194C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591982 | ||||||
| chr16:1591994
|
C | T | 11 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(8): Show | 11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.634+182G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1591994 | ||||||
| chr16:1592025
|
G | A | 3 | a0001c0001t0002g0259a0001c0001t0002g0286a0001c0001t0002g0295 | 3 | HG00733.hp2 HG01496.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.634+151C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1592025 | ||||||
| chr16:1592073
|
A | G | 3 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182 | 3 | HG02109.hp1 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.634+103T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 6/30 | chr16 | 1592073 | ||||||
| chr16:1592332
|
C | T | 6 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.492-14G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 5/30 | chr16 | 1592332 | ||||||
| chr16:1592338
|
G | A | 1 | a0001c0001t0002g0281 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.492-20C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 5/30 | chr16 | 1592338 | ||||||
| chr16:1592422
|
C | T | 92 | a0001c0001t0003g0038a0001c0020t0003g0138a0001c0020t0003g0139others(89): Show | 92 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.491+45G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 5/30 | chr16 | 1592422 | ||||||
| chr16:1592460
|
C | T | 4 | a0001c0001t0002g0250a0001c0001t0002g0296a0001c0001t0002g0297others(1): Show | 4 | NA18962.hp2 NA18991.hp2 NA19081.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.491+7G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 5/30 | chr16 | 1592460 | ||||||
| chr16:1592614
|
A | AGGACAGG others(25): Show |
17 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(14): Show | 17 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.370-58_370-27dupCT others(30): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1592614 | ||||||
| chr16:1592614
|
AGGACAGG others(57): Show |
A | 38 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0005t0001g0141others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.370-90_370-27delCA others(62): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1592614 | ||||||
| chr16:1592635
|
C | T | 1 | a0001c0002t0001g0061 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.370-47G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1592635 | ||||||
| chr16:1592659
|
T | C | 54 | a0001c0001t0003g0038a0002c0003t0003g0006a0002c0003t0003g0007others(51): Show | 54 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.370-71A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1592659 | ||||||
| chr16:1592755
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.370-167G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1592755 | ||||||
| chr16:1592845
|
G | A | 2 | a0001c0002t0001g0110a0001c0002t0001g0118 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.370-257C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1592845 | ||||||
| chr16:1592892
|
A | AGGACAGG others(153): Show |
2 | a0001c0002t0005g0001a0001c0002t0005g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.370-464_370-305dup others(160): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1592892 | ||||||
| chr16:1592905
|
T | C | 40 | a0001c0001t0002g0182a0001c0001t0002g0259a0001c0001t0003g0038others(37): Show | 40 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.370-317A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1592905 | ||||||
| chr16:1592969
|
C | CGGCAGAG others(25): Show |
11 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(8): Show | 11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.370-413_370-382dup others(32): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1592969 | ||||||
| chr16:1593246
|
C | T | 9 | a0004c0006t0002g0204a0004c0006t0002g0233a0004c0006t0002g0235others(6): Show | 9 | HG00733.hp1 HG00741.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.370-658G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593246 | ||||||
| chr16:1593315
|
CT | C | 8 | a0001c0001t0002g0242a0001c0002t0001g0047a0001c0002t0001g0083others(5): Show | 8 | HG02258.hp2 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.370-728delA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593315 | ||||||
| chr16:1593397
|
C | T | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.370-809G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593397 | ||||||
| chr16:1593551
|
C | T | 37 | a0001c0001t0003g0038a0002c0003t0003g0006a0002c0003t0003g0007others(34): Show | 37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.370-963G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593551 | ||||||
| chr16:1593605
|
A | T | 37 | a0001c0001t0003g0038a0002c0003t0003g0006a0002c0003t0003g0007others(34): Show | 37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.370-1017T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593605 | ||||||
| chr16:1593635
|
G | A | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.370-1047C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593635 | ||||||
| chr16:1593636
|
G | A | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.370-1048C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593636 | ||||||
| chr16:1593675
|
G | A | 1 | a0002c0003t0003g0040 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.370-1087C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593675 | ||||||
| chr16:1593819
|
T | C | 1 | a0030c0058t0001g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.370-1231A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593819 | ||||||
| chr16:1593855
|
G | A | 1 | a0003c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.370-1267C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593855 | ||||||
| chr16:1593949
|
C | T | 1 | a0001c0001t0002g0283 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.370-1361G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1593949 | ||||||
| chr16:1594031
|
C | T | 2 | a0001c0001t0007g0270a0001c0001t0007g0275 | 2 | HG00323.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.370-1443G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594031 | ||||||
| chr16:1594178
|
T | C | 1 | a0003c0005t0001g0150 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.370-1590A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594178 | ||||||
| chr16:1594221
|
T | G | 1 | a0031c0024t0001g0111 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.370-1633A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594221 | ||||||
| chr16:1594226
|
G | GT | 41 | a0001c0001t0002g0205a0001c0001t0002g0226a0001c0001t0002g0228others(38): Show | 41 | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.370-1639dupA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594226 | ||||||
| chr16:1594311
|
C | G | 49 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0005t0001g0141others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.370-1723G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594311 | ||||||
| chr16:1594368
|
T | A | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.370-1780A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594368 | ||||||
| chr16:1594477
|
T | C | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.370-1889A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594477 | ||||||
| chr16:1594596
|
G | A | 2 | a0001c0002t0001g0110a0001c0002t0001g0118 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.370-2008C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594596 | ||||||
| chr16:1594656
|
G | A | 1 | a0005c0039t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.370-2068C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594656 | ||||||
| chr16:1594710
|
C | G | 2 | a0001c0001t0002g0293a0001c0001t0002g0294 | 2 | NA19005.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.370-2122G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594710 | ||||||
| chr16:1594763
|
A | G | 55 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0005t0001g0141others(52): Show | 55 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.370-2175T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594763 | ||||||
| chr16:1594807
|
C | G | 40 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0005t0001g0141others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.370-2219G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594807 | ||||||
| chr16:1594847
|
C | A | 1 | a0007c0013t0001g0193 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.370-2259G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594847 | ||||||
| chr16:1594870
|
C | T | 1 | a0007c0013t0001g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.370-2282G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594870 | ||||||
| chr16:1594898
|
T | C | 12 | a0001c0001t0002g0314a0001c0001t0002g0317a0001c0001t0002g0318others(9): Show | 12 | HG02056.hp2 HG02074.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.370-2310A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594898 | ||||||
| chr16:1594917
|
C | CAATCTCC others(3): Show |
1 | a0001c0001t0002g0242 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.370-2339_370-2330d others(12): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1594917 | ||||||
| chr16:1595056
|
C | T | 4 | a0001c0001t0002g0317a0001c0001t0002g0320a0010c0021t0002g0315others(1): Show | 4 | HG02056.hp2 HG02074.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-2468G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595056 | ||||||
| chr16:1595057
|
G | A | 39 | a0001c0002t0001g0065a0001c0020t0003g0138a0001c0020t0003g0139others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.370-2469C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595057 | ||||||
| chr16:1595059
|
G | T | 1 | a0001c0002t0001g0217 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.370-2471C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595059 | ||||||
| chr16:1595079
|
A | G | 1 | a0001c0002t0001g0218 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.370-2491T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595079 | ||||||
| chr16:1595242
|
G | C | 6 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.370-2654C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595242 | ||||||
| chr16:1595263
|
T | C | 199 | a0001c0001t0003g0038a0001c0001t0003g0123a0001c0002t0001g0005others(196): Show | 199 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.370-2675A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595263 | ||||||
| chr16:1595603
|
G | GA | 56 | a0001c0001t0003g0038a0001c0002t0001g0065a0001c0002t0001g0085others(53): Show | 56 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.370-3016dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595603 | ||||||
| chr16:1595658
|
G | T | 1 | a0002c0003t0003g0022 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.370-3070C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595658 | ||||||
| chr16:1595691
|
A | G | 2 | a0001c0002t0001g0081a0001c0004t0003g0082 | 2 | NA18961.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.370-3103T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595691 | ||||||
| chr16:1595744
|
T | C | 38 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0005t0001g0141others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.370-3156A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595744 | ||||||
| chr16:1595818
|
C | T | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.370-3230G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595818 | ||||||
| chr16:1595824
|
G | T | 6 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.370-3236C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595824 | ||||||
| chr16:1595826
|
A | G | 199 | a0001c0001t0003g0038a0001c0001t0003g0123a0001c0002t0001g0005others(196): Show | 199 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.370-3238T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595826 | ||||||
| chr16:1595874
|
G | A | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.370-3286C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1595874 | ||||||
| chr16:1596010
|
C | A | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.370-3422G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596010 | ||||||
| chr16:1596012
|
C | T | 2 | a0001c0001t0002g0273a0001c0001t0002g0274 | 2 | HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.370-3424G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596012 | ||||||
| chr16:1596017
|
C | T | 107 | a0001c0001t0003g0123a0001c0002t0001g0005a0001c0002t0001g0013others(104): Show | 107 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.370-3429G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596017 | ||||||
| chr16:1596050
|
C | T | 7 | a0001c0002t0001g0047a0001c0002t0001g0083a0001c0002t0001g0097others(4): Show | 7 | HG02258.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.370-3462G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596050 | ||||||
| chr16:1596193
|
C | G | 3 | a0001c0010t0004g0225a0001c0010t0004g0232a0001c0052t0004g0234 | 3 | HG02132.hp2 HG02135.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.370-3605G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596193 | ||||||
| chr16:1596426
|
A | C | 1 | a0001c0004t0003g0185 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.370-3838T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596426 | ||||||
| chr16:1596486
|
C | T | 1 | a0001c0001t0002g0282 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.370-3898G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596486 | ||||||
| chr16:1596517
|
G | A | 1 | a0022c0038t0001g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.370-3929C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596517 | ||||||
| chr16:1596542
|
G | A | 55 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0005t0001g0141others(52): Show | 55 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.370-3954C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596542 | ||||||
| chr16:1596578
|
G | T | 1 | a0001c0001t0002g0263 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.370-3990C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596578 | ||||||
| chr16:1596655
|
C | T | 9 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(6): Show | 9 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.370-4067G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596655 | ||||||
| chr16:1596874
|
AG | A | 8 | a0003c0017t0001g0058a0003c0017t0001g0059a0003c0059t0001g0050others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.370-4287delC | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596874 | ||||||
| chr16:1596878
|
G | A | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.370-4290C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596878 | ||||||
| chr16:1596933
|
A | C | 30 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0005t0001g0141others(27): Show | 30 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.370-4345T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596933 | ||||||
| chr16:1596942
|
G | A | 7 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(4): Show | 7 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.370-4354C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596942 | ||||||
| chr16:1596972
|
C | A | 1 | a0001c0001t0002g0278 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.370-4384G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1596972 | ||||||
| chr16:1597056
|
T | C | 1 | a0001c0004t0003g0115 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.370-4468A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1597056 | ||||||
| chr16:1597120
|
T | C | 1 | a0001c0001t0002g0308 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.370-4532A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1597120 | ||||||
| chr16:1597201
|
T | TTCCCCAG others(3): Show |
1 | a0001c0001t0002g0294 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.370-4623_370-4614d others(12): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1597201 | ||||||
| chr16:1597334
|
C | T | 1 | a0001c0001t0002g0304 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.370-4746G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1597334 | ||||||
| chr16:1597409
|
G | C | 1 | a0001c0002t0001g0217 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.370-4821C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1597409 | ||||||
| chr16:1597689
|
T | C | 1 | a0001c0001t0002g0307 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.369+4681A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1597689 | ||||||
| chr16:1597772
|
T | C | 2 | a0001c0004t0001g0075a0001c0004t0001g0076 | 2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.369+4598A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1597772 | ||||||
| chr16:1597812
|
G | C | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+4558C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1597812 | ||||||
| chr16:1597827
|
G | A | 1 | a0005c0009t0004g0183 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.369+4543C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1597827 | ||||||
| chr16:1598125
|
A | C | 151 | a0001c0001t0002g0174a0001c0001t0003g0123a0001c0002t0001g0005others(148): Show | 151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.369+4245T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598125 | ||||||
| chr16:1598161
|
T | C | 200 | a0001c0001t0002g0174a0001c0001t0003g0038a0001c0001t0003g0123others(197): Show | 200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.369+4209A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598161 | ||||||
| chr16:1598319
|
G | A | 1 | a0002c0003t0003g0031 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.369+4051C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598319 | ||||||
| chr16:1598407
|
G | A | 1 | a0001c0002t0001g0311 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.369+3963C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598407 | ||||||
| chr16:1598436
|
C | T | 1 | a0003c0005t0003g0151 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.369+3934G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598436 | ||||||
| chr16:1598544
|
A | T | 1 | a0001c0002t0001g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.369+3826T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598544 | ||||||
| chr16:1598566
|
T | C | 1 | a0001c0001t0002g0280 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.369+3804A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598566 | ||||||
| chr16:1598637
|
G | C | 215 | a0001c0001t0002g0174a0001c0001t0002g0205a0001c0001t0002g0226others(212): Show | 215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.369+3733C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598637 | ||||||
| chr16:1598684
|
G | C | 37 | a0001c0001t0003g0038a0002c0003t0003g0006a0002c0003t0003g0007others(34): Show | 37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.369+3686C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598684 | ||||||
| chr16:1598717
|
C | T | 2 | a0001c0004t0001g0075a0001c0004t0001g0076 | 2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.369+3653G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598717 | ||||||
| chr16:1598827
|
G | A | 5 | a0001c0045t0002g0176a0005c0009t0004g0166a0005c0009t0004g0173others(2): Show | 5 | HG02572.hp1 HG02630.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.369+3543C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598827 | ||||||
| chr16:1598834
|
A | AC | 10 | a0001c0001t0002g0294a0001c0001t0002g0310a0001c0002t0001g0086others(7): Show | 10 | HG00544.hp2 HG01978.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.369+3535dupG | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598834 | ||||||
| chr16:1598879
|
T | A | 2 | a0001c0002t0001g0061a0001c0002t0001g0071 | 2 | HG00280.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.369+3491A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598879 | ||||||
| chr16:1598953
|
C | CCATCTAG others(11): Show |
1 | a0001c0002t0001g0085 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.369+3399_369+3416d others(20): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598953 | ||||||
| chr16:1598972
|
C | T | 1 | a0003c0059t0001g0050 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.369+3398G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1598972 | ||||||
| chr16:1599040
|
G | C | 1 | a0001c0001t0002g0302 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.369+3330C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599040 | ||||||
| chr16:1599065
|
C | T | 1 | a0001c0001t0002g0259 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.369+3305G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599065 | ||||||
| chr16:1599105
|
G | C | 4 | a0001c0002t0001g0113a0001c0004t0003g0112a0001c0004t0003g0114others(1): Show | 4 | NA18945.hp1 NA18975.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.369+3265C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599105 | ||||||
| chr16:1599107
|
C | A | 11 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(8): Show | 11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.369+3263G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599107 | ||||||
| chr16:1599128
|
C | T | 1 | a0001c0001t0002g0326 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.369+3242G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599128 | ||||||
| chr16:1599188
|
A | G | 188 | a0001c0001t0002g0174a0001c0001t0003g0038a0001c0001t0003g0123others(185): Show | 188 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.369+3182T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599188 | ||||||
| chr16:1599216
|
G | A | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.369+3154C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599216 | ||||||
| chr16:1599252
|
G | A | 6 | a0003c0005t0003g0063a0007c0013t0001g0191a0007c0013t0001g0192others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+3118C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599252 | ||||||
| chr16:1599286
|
A | G | 200 | a0001c0001t0002g0174a0001c0001t0003g0038a0001c0001t0003g0123others(197): Show | 200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.369+3084T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599286 | ||||||
| chr16:1599309
|
T | C | 1 | a0028c0055t0004g0165 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.369+3061A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599309 | ||||||
| chr16:1599325
|
G | T | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.369+3045C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599325 | ||||||
| chr16:1599337
|
C | T | 1 | a0001c0001t0002g0281 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.369+3033G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599337 | ||||||
| chr16:1599357
|
A | G | 3 | a0001c0001t0002g0243a0001c0002t0001g0041a0001c0054t0001g0119 | 3 | HG00639.hp1 HG01074.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.369+3013T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599357 | ||||||
| chr16:1599392
|
T | A | 1 | a0001c0001t0002g0243 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.369+2978A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599392 | ||||||
| chr16:1599402
|
T | C | 38 | a0001c0001t0002g0243a0001c0001t0003g0038a0002c0003t0003g0006others(35): Show | 38 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.369+2968A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599402 | ||||||
| chr16:1599403
|
G | C | 1 | a0001c0001t0002g0243 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.369+2967C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599403 | ||||||
| chr16:1599403
|
G | GCCGTCCG others(172): Show |
1 | a0003c0031t0009g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.369+2966_369+2967i others(181): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599403 | ||||||
| chr16:1599403
|
G | GCCGTCCG others(170): Show |
136 | a0001c0001t0003g0123a0001c0002t0001g0013a0001c0002t0001g0041others(133): Show | 136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.369+2966_369+2967i others(179): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599403 | ||||||
| chr16:1599403
|
G | GCCGTCCG others(171): Show |
4 | a0001c0002t0001g0005a0001c0002t0001g0207a0001c0002t0001g0223others(1): Show | 4 | HG00544.hp2 HG02738.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+2966_369+2967i others(180): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599403 | ||||||
| chr16:1599403
|
G | GTCGTCCG others(170): Show |
2 | a0001c0002t0001g0073a0001c0002t0001g0096 | 2 | HG01081.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.369+2966_369+2967i others(179): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599403 | ||||||
| chr16:1599406
|
G | A | 1 | a0001c0001t0002g0243 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.369+2964C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599406 | ||||||
| chr16:1599420
|
T | TGGGGGGG others(171): Show |
1 | a0001c0002t0001g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.369+2949_369+2950i others(180): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599420 | ||||||
| chr16:1599420
|
T | TGGGGGGG others(172): Show |
1 | a0001c0002t0001g0080 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.369+2949_369+2950i others(181): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599420 | ||||||
| chr16:1599421
|
G | GGGGGGGT others(169): Show |
1 | a0001c0002t0001g0085 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.369+2948_369+2949i others(178): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599421 | ||||||
| chr16:1599430
|
A | AGCCCCCC others(395): Show |
2 | a0001c0002t0005g0001a0001c0002t0005g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.369+2939_369+2940i others(404): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599430 | ||||||
| chr16:1599441
|
T | C | 6 | a0001c0001t0002g0174a0001c0001t0002g0307a0001c0002t0001g0129others(3): Show | 6 | HG01192.hp1 HG01516.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+2929A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599441 | ||||||
| chr16:1599451
|
T | C | 152 | a0001c0001t0002g0174a0001c0001t0002g0307a0001c0001t0003g0123others(149): Show | 152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.369+2919A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599451 | ||||||
| chr16:1599452
|
G | C | 152 | a0001c0001t0002g0174a0001c0001t0002g0307a0001c0001t0003g0123others(149): Show | 152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.369+2918C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | ||||||
| chr16:1599452
|
G | GCCGTCCG others(493): Show |
2 | a0001c0010t0001g0125a0001c0010t0001g0126 | 2 | NA18971.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.369+2917_369+2918i others(502): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | ||||||
| chr16:1599452
|
G | GCCGTCCG others(925): Show |
1 | a0002c0003t0003g0034 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.369+2917_369+2918i others(934): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | ||||||
| chr16:1599452
|
G | GCCGTCCG others(727): Show |
1 | a0002c0003t0003g0026 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.369+2917_369+2918i others(736): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | ||||||
| chr16:1599452
|
G | GCCGTCCG others(920): Show |
1 | a0002c0003t0003g0006 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.369+2917_369+2918i others(929): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | ||||||
| chr16:1599452
|
G | GCCGTCCG others(919): Show |
1 | a0002c0003t0003g0036 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.369+2917_369+2918i others(928): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | ||||||
| chr16:1599452
|
G | GCCGTCCG others(493): Show |
1 | a0002c0003t0003g0031 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.369+2917_369+2918i others(502): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | ||||||
| chr16:1599452
|
G | GCCGTCCG others(920): Show |
1 | a0002c0003t0003g0029 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.369+2917_369+2918i others(929): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | ||||||
| chr16:1599452
|
G | GCCGTCCG others(722): Show |
4 | a0002c0003t0003g0007a0002c0003t0003g0009a0019c0033t0003g0018others(1): Show | 4 | NA18941.hp1 NA18959.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+2917_369+2918i others(731): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | ||||||
| chr16:1599452
|
G | GCCGTCCG others(820): Show |
1 | a0009c0011t0003g0044 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.369+2917_369+2918i others(829): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | ||||||
| chr16:1599452
|
G | GCCGTCCG others(918): Show |
11 | a0002c0003t0003g0017a0002c0003t0003g0019a0002c0003t0003g0022others(8): Show | 11 | HG01071.hp1 HG02148.hp2 NA18949.hp1 others(8): Show |
intron_variant | MODIFIER | c.369+2917_369+2918i others(927): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | ||||||
| chr16:1599452
|
G | GCCGTCCG others(821): Show |
1 | a0009c0011t0003g0043 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.369+2917_369+2918i others(830): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | ||||||
| chr16:1599452
|
G | GCCGTCCG others(920): Show |
1 | a0002c0003t0003g0025 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.369+2917_369+2918i others(929): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | ||||||
| chr16:1599452
|
G | GCCGTCCG others(920): Show |
1 | a0002c0003t0003g0016 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.369+2917_369+2918i others(929): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | ||||||
| chr16:1599452
|
G | GCCGTCCG others(919): Show |
6 | a0001c0001t0003g0038a0002c0003t0003g0011a0002c0003t0003g0015others(3): Show | 6 | HG00642.hp2 HG01070.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+2917_369+2918i others(928): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | ||||||
| chr16:1599452
|
G | GCCGTCCG others(922): Show |
1 | a0002c0003t0003g0032 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.369+2917_369+2918i others(931): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | ||||||
| chr16:1599452
|
G | GCCGTCCG others(822): Show |
1 | a0009c0011t0003g0045 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.369+2917_369+2918i others(831): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | ||||||
| chr16:1599452
|
G | GCCGTCCG others(490): Show |
1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+2917_369+2918i others(499): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599452 | ||||||
| chr16:1599456
|
T | TCCGGGAG others(706): Show |
1 | a0001c0001t0002g0307 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.369+2913_369+2914i others(715): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599456 | ||||||
| chr16:1599464
|
G | GT | 3 | a0001c0001t0002g0174a0001c0002t0001g0129a0003c0005t0001g0147 | 3 | HG01192.hp1 HG04115.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2905_369+2906i others(3): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599464 | ||||||
| chr16:1599468
|
G | A | 146 | a0001c0001t0003g0123a0001c0002t0001g0005a0001c0002t0001g0013others(143): Show | 146 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.369+2902C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599468 | ||||||
| chr16:1599469
|
T | TGGGGGGG others(829): Show |
1 | a0009c0011t0003g0042 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.369+2900_369+2901i others(838): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599469 | ||||||
| chr16:1599469
|
T | TGGGGGGG others(725): Show |
1 | a0002c0003t0003g0021 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.369+2900_369+2901i others(734): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599469 | ||||||
| chr16:1599469
|
T | TGGGGGGG others(926): Show |
1 | a0002c0003t0003g0030 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.369+2900_369+2901i others(935): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599469 | ||||||
| chr16:1599473
|
G | C | 3 | a0001c0001t0002g0174a0001c0002t0001g0129a0003c0005t0001g0147 | 3 | HG01192.hp1 HG04115.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2897C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599473 | ||||||
| chr16:1599475
|
G | C | 3 | a0001c0001t0002g0174a0001c0002t0001g0129a0003c0005t0001g0147 | 3 | HG01192.hp1 HG04115.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2895C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGGTCAGC others(812): Show |
1 | a0010c0021t0002g0316 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(821): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGGTCAGC others(809): Show |
1 | a0001c0001t0002g0280 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(818): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(805): Show |
1 | a0001c0001t0002g0242 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(807): Show |
1 | a0001c0001t0002g0281 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(816): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(804): Show |
1 | a0001c0001t0002g0330 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(805): Show |
1 | a0001c0001t0002g0331 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(807): Show |
1 | a0001c0001t0002g0272 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(816): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(806): Show |
1 | a0005c0009t0004g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(806): Show |
1 | a0010c0021t0002g0315 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(806): Show |
1 | a0004c0006t0002g0235 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(805): Show |
1 | a0001c0001t0002g0283 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(758): Show |
1 | a0001c0001t0002g0310 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(767): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(806): Show |
1 | a0028c0055t0004g0165 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(805): Show |
1 | a0001c0001t0002g0179 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(810): Show |
1 | a0001c0001t0002g0294 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(819): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(807): Show |
1 | a0001c0001t0002g0291 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(816): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(806): Show |
1 | a0001c0001t0002g0206 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(808): Show |
1 | a0010c0046t0004g0267 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(817): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(804): Show |
1 | a0001c0050t0002g0328 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(755): Show |
3 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182 | 3 | HG02109.hp1 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.369+2894_369+2895i others(764): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(805): Show |
1 | a0001c0001t0004g0254 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(806): Show |
1 | a0004c0006t0002g0327 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(805): Show |
1 | a0001c0001t0002g0245 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(756): Show |
1 | a0001c0001t0002g0302 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(765): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(805): Show |
1 | a0004c0006t0002g0313 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(806): Show |
1 | a0004c0006t0002g0240 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(757): Show |
1 | a0001c0001t0002g0308 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(766): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(806): Show |
1 | a0001c0001t0002g0257 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(804): Show |
1 | a0001c0001t0002g0200 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(804): Show |
2 | a0013c0022t0002g0227a0013c0022t0002g0230 | 2 | HG00642.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(804): Show |
28 | a0001c0001t0002g0169a0001c0001t0002g0178a0001c0001t0002g0184others(25): Show | 28 | HG00733.hp1 HG01123.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(804): Show |
1 | a0001c0001t0002g0236 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(806): Show |
1 | a0001c0001t0002g0297 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(806): Show |
1 | a0001c0001t0002g0229 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(807): Show |
1 | a0005c0009t0004g0183 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(816): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(806): Show |
1 | a0001c0001t0004g0251 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(805): Show |
4 | a0001c0001t0002g0226a0001c0001t0002g0228a0001c0001t0002g0248others(1): Show | 4 | HG00423.hp2 HG01081.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(755): Show |
3 | a0001c0001t0002g0269a0001c0001t0002g0305a0001c0001t0002g0306 | 3 | HG00099.hp1 HG01069.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.369+2894_369+2895i others(764): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(804): Show |
2 | a0001c0001t0002g0273a0001c0001t0002g0274 | 2 | HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(805): Show |
1 | a0001c0001t0002g0268 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(804): Show |
31 | a0001c0001t0002g0046a0001c0001t0002g0243a0001c0001t0002g0252others(28): Show | 31 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(804): Show |
1 | a0001c0001t0002g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(756): Show |
2 | a0001c0001t0002g0304a0001c0001t0002g0309 | 2 | HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.369+2894_369+2895i others(765): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(805): Show |
8 | a0001c0001t0002g0258a0001c0001t0002g0262a0001c0001t0002g0279others(5): Show | 8 | HG02071.hp2 HG02083.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(804): Show |
1 | a0001c0001t0002g0256 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(804): Show |
1 | a0005c0009t0004g0167 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(804): Show |
1 | a0001c0001t0002g0295 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(813): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(882): Show |
1 | a0004c0006t0002g0204 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(891): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(806): Show |
1 | a0001c0001t0002g0332 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.369+2894_369+2895i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(805): Show |
1 | a0023c0051t0004g0249 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | GGTCAGCC others(805): Show |
1 | a0001c0001t0002g0266 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.369+2894_369+2895i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599475
|
G | T | 1 | a0001c0001t0002g0307 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.369+2895C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599475 | ||||||
| chr16:1599476
|
G | C | 3 | a0001c0001t0002g0174a0001c0002t0001g0129a0003c0005t0001g0147 | 3 | HG01192.hp1 HG04115.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2894C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599476 | ||||||
| chr16:1599478
|
C | CAGCCCCC others(805): Show |
1 | a0001c0010t0004g0232 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.369+2891_369+2892i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599478 | ||||||
| chr16:1599478
|
C | CAGCCCCC others(806): Show |
1 | a0001c0001t0002g0319 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.369+2891_369+2892i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599478 | ||||||
| chr16:1599478
|
C | CAGCCCCC others(806): Show |
1 | a0001c0001t0002g0303 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.369+2891_369+2892i others(815): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599478 | ||||||
| chr16:1599478
|
C | CAGCCCCC others(807): Show |
1 | a0001c0001t0002g0231 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.369+2891_369+2892i others(816): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599478 | ||||||
| chr16:1599478
|
C | CAGCCCCC others(805): Show |
1 | a0001c0001t0002g0326 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.369+2891_369+2892i others(814): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599478 | ||||||
| chr16:1599478
|
C | CAGCCCCC others(723): Show |
1 | a0002c0003t0003g0008 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.369+2891_369+2892i others(732): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599478 | ||||||
| chr16:1599479
|
G | A | 157 | a0001c0001t0003g0123a0001c0002t0001g0005a0001c0002t0001g0013others(154): Show | 157 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.369+2891C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599479 | ||||||
| chr16:1599479
|
G | T | 3 | a0001c0001t0002g0174a0001c0002t0001g0129a0003c0005t0001g0147 | 3 | HG01192.hp1 HG04115.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2891C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599479 | ||||||
| chr16:1599480
|
G | C | 6 | a0001c0001t0002g0231a0001c0001t0002g0303a0001c0001t0002g0319others(3): Show | 6 | HG02135.hp1 HG02135.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+2890C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599480 | ||||||
| chr16:1599482
|
C | CCGGCCGC others(20): Show |
2 | a0001c0001t0002g0174a0003c0005t0001g0147 | 2 | HG01192.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2887_369+2888i others(29): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599482 | ||||||
| chr16:1599484
|
C | A | 1 | a0001c0004t0003g0185 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.369+2886G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599484 | ||||||
| chr16:1599484
|
C | G | 1 | a0001c0002t0001g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.369+2886G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599484 | ||||||
| chr16:1599487
|
G | A | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.369+2883C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599487 | ||||||
| chr16:1599487
|
G | GCCCCTAC others(23): Show |
1 | a0001c0002t0001g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.369+2882_369+2883i others(32): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599487 | ||||||
| chr16:1599499
|
G | A | 3 | a0001c0001t0002g0174a0001c0002t0001g0129a0003c0005t0001g0147 | 3 | HG01192.hp1 HG04115.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2871C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599499 | ||||||
| chr16:1599503
|
C | T | 146 | a0001c0001t0003g0123a0001c0002t0001g0005a0001c0002t0001g0013others(143): Show | 146 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.369+2867G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599503 | ||||||
| chr16:1599504
|
G | GTCCGGGA others(923): Show |
1 | a0011c0012t0003g0051 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.369+2865_369+2866i others(932): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599504 | ||||||
| chr16:1599504
|
G | GTCCGGGA others(919): Show |
1 | a0006c0007t0003g0164 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.369+2865_369+2866i others(928): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599504 | ||||||
| chr16:1599504
|
G | GTCCGGGA others(920): Show |
1 | a0006c0007t0003g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.369+2865_369+2866i others(929): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599504 | ||||||
| chr16:1599504
|
G | GTCCGGGA others(868): Show |
1 | a0011c0012t0003g0052 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.369+2865_369+2866i others(877): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599504 | ||||||
| chr16:1599504
|
G | GTCCGGGA others(918): Show |
4 | a0006c0007t0003g0161a0006c0007t0003g0162a0006c0007t0003g0199others(1): Show | 4 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.369+2865_369+2866i others(927): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599504 | ||||||
| chr16:1599504
|
G | GTCCGGGA others(918): Show |
2 | a0011c0012t0003g0201a0011c0012t0003g0202 | 2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.369+2865_369+2866i others(927): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599504 | ||||||
| chr16:1599504
|
G | GTCCGGGA others(919): Show |
1 | a0006c0007t0003g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.369+2865_369+2866i others(928): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599504 | ||||||
| chr16:1599510
|
G | T | 2 | a0001c0002t0001g0067a0012c0023t0001g0060 | 2 | NA18970.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.369+2860C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599510 | ||||||
| chr16:1599517
|
G | A | 3 | a0001c0001t0002g0174a0001c0002t0001g0129a0003c0005t0001g0147 | 3 | HG01192.hp1 HG04115.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2853C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599517 | ||||||
| chr16:1599518
|
T | TG | 44 | a0001c0001t0002g0206a0001c0001t0002g0245a0001c0001t0002g0257others(41): Show | 44 | HG00544.hp1 HG00642.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.369+2851dupC | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599518 | ||||||
| chr16:1599518
|
TG | T | 20 | a0001c0001t0002g0264a0001c0001t0002g0301a0004c0006t0002g0204others(17): Show | 20 | HG00733.hp1 HG00741.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.369+2851delC | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599518 | ||||||
| chr16:1599518
|
TGGG | T | 148 | a0001c0001t0002g0174a0001c0001t0003g0123a0001c0002t0001g0005others(145): Show | 148 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.369+2849_369+2851d others(5): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599518 | ||||||
| chr16:1599529
|
T | C | 3 | a0001c0010t0001g0125a0001c0010t0001g0126a0027c0036t0003g0132 | 3 | HG03098.hp1 NA18971.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.369+2841A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599529 | ||||||
| chr16:1599531
|
A | G | 2 | a0001c0002t0005g0001a0001c0002t0005g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.369+2839T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599531 | ||||||
| chr16:1599536
|
C | T | 146 | a0001c0001t0003g0123a0001c0002t0001g0005a0001c0002t0001g0013others(143): Show | 146 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.369+2834G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599536 | ||||||
| chr16:1599538
|
CT | C | 148 | a0001c0001t0003g0123a0001c0002t0001g0005a0001c0002t0001g0013others(145): Show | 148 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.369+2831delA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599538 | ||||||
| chr16:1599539
|
T | C | 3 | a0001c0001t0002g0174a0001c0002t0001g0129a0003c0005t0001g0147 | 3 | HG01192.hp1 HG04115.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2831A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599539 | ||||||
| chr16:1599540
|
G | A | 3 | a0001c0001t0002g0174a0001c0002t0001g0129a0003c0005t0001g0147 | 3 | HG01192.hp1 HG04115.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2830C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599540 | ||||||
| chr16:1599541
|
C | T | 146 | a0001c0001t0003g0123a0001c0002t0001g0005a0001c0002t0001g0013others(143): Show | 146 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.369+2829G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599541 | ||||||
| chr16:1599542
|
C | T | 1 | a0001c0001t0002g0269 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.369+2828G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599542 | ||||||
| chr16:1599557
|
G | A | 39 | a0001c0001t0003g0038a0001c0002t0005g0001a0001c0002t0005g0002others(36): Show | 39 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.369+2813C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599557 | ||||||
| chr16:1599560
|
C | T | 146 | a0001c0001t0003g0123a0001c0002t0001g0005a0001c0002t0001g0013others(143): Show | 146 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.369+2810G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599560 | ||||||
| chr16:1599561
|
G | A | 2 | a0001c0002t0005g0001a0001c0002t0005g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.369+2809C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599561 | ||||||
| chr16:1599569
|
A | G | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2801T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599569 | ||||||
| chr16:1599572
|
G | T | 2 | a0001c0002t0001g0129a0003c0005t0001g0147 | 2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.369+2798C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599572 | ||||||
| chr16:1599573
|
GCGCCTCT others(17): Show |
G | 2 | a0001c0002t0001g0129a0003c0005t0001g0147 | 2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.369+2773_369+2796d others(26): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599573 | ||||||
| chr16:1599575
|
G | C | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2795C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599575 | ||||||
| chr16:1599577
|
C | G | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2793G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599577 | ||||||
| chr16:1599578
|
T | C | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2792A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599578 | ||||||
| chr16:1599582
|
C | G | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2788G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599582 | ||||||
| chr16:1599585
|
G | A | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2785C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599585 | ||||||
| chr16:1599594
|
T | G | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2776A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599594 | ||||||
| chr16:1599595
|
A | T | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2775T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599595 | ||||||
| chr16:1599597
|
T | C | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2773A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599597 | ||||||
| chr16:1599601
|
A | G | 2 | a0001c0002t0001g0129a0003c0005t0001g0147 | 2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.369+2769T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599601 | ||||||
| chr16:1599602
|
A | G | 3 | a0001c0001t0002g0174a0001c0002t0001g0129a0003c0005t0001g0147 | 3 | HG01192.hp1 HG04115.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.369+2768T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599602 | ||||||
| chr16:1599605
|
G | C | 2 | a0001c0002t0001g0129a0003c0005t0001g0147 | 2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.369+2765C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599605 | ||||||
| chr16:1599606
|
A | G | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2764T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599606 | ||||||
| chr16:1599611
|
C | CCCCCCCG others(91): Show |
2 | a0003c0005t0003g0149a0007c0060t0001g0195 | 2 | HG00099.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.369+2758_369+2759i others(100): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599611 | ||||||
| chr16:1599615
|
T | C | 148 | a0001c0001t0003g0123a0001c0002t0001g0005a0001c0002t0001g0013others(145): Show | 148 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.369+2755A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599615 | ||||||
| chr16:1599617
|
T | C | 149 | a0001c0001t0002g0174a0001c0001t0003g0123a0001c0002t0001g0005others(146): Show | 149 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.369+2753A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599617 | ||||||
| chr16:1599618
|
G | GCCCGGCC others(42): Show |
2 | a0001c0002t0005g0001a0001c0002t0005g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.369+2751_369+2752i others(51): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599618 | ||||||
| chr16:1599621
|
C | T | 2 | a0001c0002t0001g0129a0003c0005t0001g0147 | 2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.369+2749G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599621 | ||||||
| chr16:1599634
|
C | T | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2736G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599634 | ||||||
| chr16:1599638
|
C | T | 1 | a0016c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.369+2732G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599638 | ||||||
| chr16:1599648
|
G | A | 2 | a0001c0002t0001g0129a0003c0005t0001g0147 | 2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.369+2722C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599648 | ||||||
| chr16:1599649
|
T | TGGGGGGG others(175): Show |
1 | a0001c0010t0001g0125 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.369+2720_369+2721i others(184): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599649 | ||||||
| chr16:1599649
|
T | TGGGGGGG others(176): Show |
1 | a0001c0010t0001g0126 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.369+2720_369+2721i others(185): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599649 | ||||||
| chr16:1599649
|
T | TGGGGGGG others(565): Show |
1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+2720_369+2721i others(574): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599649 | ||||||
| chr16:1599649
|
TG | T | 11 | a0001c0001t0002g0174a0001c0002t0001g0074a0001c0002t0001g0100others(8): Show | 11 | HG01192.hp1 HG02056.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.369+2720delC | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599649 | ||||||
| chr16:1599650
|
G | GGGGGTGT others(91): Show |
3 | a0001c0002t0001g0073a0001c0002t0001g0223a0003c0031t0009g0140 | 3 | HG01081.hp1 HG02738.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.369+2719_369+2720i others(100): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599650 | ||||||
| chr16:1599650
|
G | GGGGGTGT others(91): Show |
1 | a0001c0002t0001g0118 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.369+2719_369+2720i others(100): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599650 | ||||||
| chr16:1599650
|
G | GGGGGTGT others(90): Show |
129 | a0001c0001t0003g0123a0001c0002t0001g0005a0001c0002t0001g0013others(126): Show | 129 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.369+2719_369+2720i others(99): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599650 | ||||||
| chr16:1599650
|
G | GGGGGTGT others(91): Show |
1 | a0001c0002t0001g0085 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.369+2719_369+2720i others(100): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599650 | ||||||
| chr16:1599656
|
G | T | 10 | a0001c0002t0001g0074a0001c0002t0001g0100a0001c0002t0001g0207others(7): Show | 10 | HG00741.hp1 HG02056.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.369+2714C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599656 | ||||||
| chr16:1599659
|
CA | C | 134 | a0001c0001t0003g0123a0001c0002t0001g0005a0001c0002t0001g0013others(131): Show | 134 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.369+2710delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599659 | ||||||
| chr16:1599660
|
A | G | 12 | a0001c0002t0001g0074a0001c0002t0001g0100a0001c0002t0001g0207others(9): Show | 12 | HG00741.hp1 HG01175.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.369+2710T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599660 | ||||||
| chr16:1599662
|
C | CCCCCCGC others(90): Show |
1 | a0001c0002t0003g0208 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.369+2707_369+2708i others(99): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599662 | ||||||
| chr16:1599662
|
C | G | 134 | a0001c0001t0003g0123a0001c0002t0001g0005a0001c0002t0001g0013others(131): Show | 134 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.369+2708G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599662 | ||||||
| chr16:1599666
|
C | T | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2704G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599666 | ||||||
| chr16:1599668
|
C | G | 34 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0005t0001g0141others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.369+2702G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599668 | ||||||
| chr16:1599668
|
C | T | 3 | a0001c0010t0001g0125a0001c0010t0001g0126a0027c0036t0003g0132 | 3 | HG03098.hp1 NA18971.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.369+2702G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599668 | ||||||
| chr16:1599670
|
C | T | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2700G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599670 | ||||||
| chr16:1599685
|
C | T | 2 | a0001c0002t0001g0129a0003c0005t0001g0147 | 2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.369+2685G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599685 | ||||||
| chr16:1599686
|
G | A | 137 | a0001c0001t0003g0123a0001c0002t0001g0005a0001c0002t0001g0013others(134): Show | 137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.369+2684C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599686 | ||||||
| chr16:1599689
|
C | T | 1 | a0001c0001t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.369+2681G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599689 | ||||||
| chr16:1599690
|
G | A | 137 | a0001c0001t0003g0123a0001c0002t0001g0005a0001c0002t0001g0013others(134): Show | 137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.369+2680C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599690 | ||||||
| chr16:1599690
|
G | GGGAGGGA others(269): Show |
1 | a0001c0002t0001g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.369+2679_369+2680i others(278): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599690 | ||||||
| chr16:1599690
|
G | GGGAGGGA others(268): Show |
1 | a0003c0005t0001g0147 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.369+2679_369+2680i others(277): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599690 | ||||||
| chr16:1599690
|
G | GGGAGGGA others(92): Show |
1 | a0001c0002t0001g0217 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.369+2679_369+2680i others(101): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599690 | ||||||
| chr16:1599690
|
G | GGGAGGGA others(91): Show |
6 | a0001c0002t0001g0074a0001c0002t0001g0100a0001c0002t0001g0207others(3): Show | 6 | HG02056.hp1 HG02080.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+2679_369+2680i others(100): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599690 | ||||||
| chr16:1599690
|
G | GGGAGGGA others(91): Show |
2 | a0003c0005t0001g0145a0003c0005t0001g0148 | 2 | HG03017.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.369+2679_369+2680i others(100): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599690 | ||||||
| chr16:1599713
|
C | T | 2 | a0001c0001t0002g0324a0001c0001t0002g0325 | 2 | NA18945.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.369+2657G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599713 | ||||||
| chr16:1599759
|
G | T | 188 | a0001c0001t0002g0174a0001c0001t0003g0038a0001c0001t0003g0123others(185): Show | 188 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.369+2611C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599759 | ||||||
| chr16:1599795
|
C | G | 1 | a0002c0003t0003g0019 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.369+2575G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599795 | ||||||
| chr16:1599796
|
G | A | 107 | a0001c0001t0003g0123a0001c0002t0001g0005a0001c0002t0001g0013others(104): Show | 107 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.369+2574C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599796 | ||||||
| chr16:1599799
|
C | T | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+2571G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599799 | ||||||
| chr16:1599800
|
G | A | 12 | a0001c0002t0001g0224a0006c0007t0003g0159a0006c0007t0003g0160others(9): Show | 12 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.369+2570C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599800 | ||||||
| chr16:1599817
|
A | G | 200 | a0001c0001t0002g0174a0001c0001t0003g0038a0001c0001t0003g0123others(197): Show | 200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.369+2553T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599817 | ||||||
| chr16:1599827
|
T | TG | 200 | a0001c0001t0002g0174a0001c0001t0002g0310a0001c0001t0003g0038others(197): Show | 200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.369+2542dupC | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599827 | ||||||
| chr16:1599867
|
G | A | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+2503C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599867 | ||||||
| chr16:1599910
|
T | C | 9 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(6): Show | 9 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.369+2460A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599910 | ||||||
| chr16:1599966
|
T | C | 1 | a0001c0004t0003g0115 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.369+2404A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1599966 | ||||||
| chr16:1600316
|
G | A | 1 | a0001c0002t0001g0070 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.369+2054C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600316 | ||||||
| chr16:1600460
|
AT | A | 12 | a0001c0001t0002g0200a0001c0002t0001g0072a0001c0002t0001g0073others(9): Show | 12 | HG01081.hp1 HG02015.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.369+1909delA | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600460 | ||||||
| chr16:1600462
|
T | TA | 7 | a0001c0001t0002g0174a0001c0001t0002g0236a0001c0001t0002g0241others(4): Show | 7 | HG01109.hp1 HG01255.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.369+1907_369+1908i others(3): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600462 | ||||||
| chr16:1600462
|
TTA | T | 43 | a0001c0001t0003g0038a0002c0003t0003g0006a0002c0003t0003g0011others(40): Show | 43 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.369+1906_369+1907d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600462 | ||||||
| chr16:1600463
|
T | A | 17 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0184others(14): Show | 17 | HG01070.hp1 HG01109.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.369+1907A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600463 | ||||||
| chr16:1600463
|
T | TA | 47 | a0001c0001t0002g0178a0001c0001t0002g0180a0001c0001t0002g0181others(44): Show | 47 | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.369+1906dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600463 | ||||||
| chr16:1600463
|
TA | T | 136 | a0001c0001t0002g0318a0001c0001t0003g0123a0001c0002t0001g0005others(133): Show | 136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.369+1906delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600463 | ||||||
| chr16:1600463
|
TAA | T | 6 | a0001c0002t0001g0067a0001c0002t0001g0196a0001c0004t0001g0117others(3): Show | 6 | HG01884.hp2 HG02080.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+1905_369+1906d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600463 | ||||||
| chr16:1600465
|
A | T | 1 | a0001c0002t0001g0118 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.369+1905T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600465 | ||||||
| chr16:1600617
|
G | A | 1 | a0001c0001t0002g0272 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.369+1753C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600617 | ||||||
| chr16:1600685
|
G | A | 3 | a0001c0002t0001g0081a0001c0004t0003g0082a0025c0041t0001g0062 | 3 | NA18961.hp2 NA19005.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.369+1685C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600685 | ||||||
| chr16:1600730
|
T | G | 2 | a0001c0001t0002g0273a0001c0001t0002g0274 | 2 | HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.369+1640A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600730 | ||||||
| chr16:1600905
|
A | G | 1 | a0002c0003t0003g0033 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.369+1465T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600905 | ||||||
| chr16:1600906
|
G | A | 1 | a0012c0023t0001g0060 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.369+1464C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600906 | ||||||
| chr16:1600936
|
T | A | 1 | a0012c0023t0001g0060 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.369+1434A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600936 | ||||||
| chr16:1600945
|
A | G | 268 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0178others(265): Show | 268 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.369+1425T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600945 | ||||||
| chr16:1600978
|
A | T | 1 | a0002c0003t0003g0022 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.369+1392T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1600978 | ||||||
| chr16:1601079
|
A | G | 1 | a0001c0004t0001g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.369+1291T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1601079 | ||||||
| chr16:1601167
|
G | T | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.369+1203C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1601167 | ||||||
| chr16:1601257
|
C | T | 37 | a0001c0001t0003g0038a0002c0003t0003g0006a0002c0003t0003g0007others(34): Show | 37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.369+1113G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1601257 | ||||||
| chr16:1601263
|
CA | C | 6 | a0001c0001t0002g0174a0001c0001t0002g0236a0001c0001t0002g0242others(3): Show | 6 | HG02735.hp1 HG03041.hp2 NA19057.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+1106delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1601263 | ||||||
| chr16:1601290
|
A | G | 1 | a0001c0004t0003g0101 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.369+1080T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1601290 | ||||||
| chr16:1601593
|
G | A | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+777C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1601593 | ||||||
| chr16:1601880
|
G | A | 11 | a0001c0002t0001g0047a0001c0002t0001g0049a0001c0002t0001g0069others(8): Show | 11 | HG02258.hp2 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.369+490C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1601880 | ||||||
| chr16:1602192
|
C | T | 1 | a0016c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.369+178G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1602192 | ||||||
| chr16:1602226
|
T | C | 2 | a0001c0002t0001g0333a0001c0002t0001g0334 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.369+144A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | 1602226 | ||||||
| chr16:1602613
|
T | A | 197 | a0001c0001t0003g0038a0001c0001t0003g0123a0001c0002t0001g0005others(194): Show | 197 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.148-22A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1602613 | ||||||
| chr16:1602620
|
A | G | 37 | a0001c0001t0003g0038a0002c0003t0003g0006a0002c0003t0003g0007others(34): Show | 37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.148-29T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1602620 | ||||||
| chr16:1602664
|
G | A | 13 | a0001c0002t0001g0311a0002c0003t0003g0032a0006c0007t0003g0159others(10): Show | 13 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(10): Show |
intron_variant | MODIFIER | c.148-73C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1602664 | ||||||
| chr16:1602812
|
C | T | 11 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(8): Show | 11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.148-221G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1602812 | ||||||
| chr16:1602828
|
T | C | 1 | a0001c0001t0002g0206 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.148-237A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1602828 | ||||||
| chr16:1602921
|
C | A | 1 | a0001c0004t0003g0101 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.148-330G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1602921 | ||||||
| chr16:1602998
|
G | A | 6 | a0003c0005t0003g0063a0007c0013t0001g0191a0007c0013t0001g0192others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-407C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1602998 | ||||||
| chr16:1603067
|
C | T | 1 | a0003c0005t0003g0151 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.148-476G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603067 | ||||||
| chr16:1603205
|
C | T | 197 | a0001c0001t0003g0038a0001c0001t0003g0123a0001c0002t0001g0005others(194): Show | 197 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.148-614G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603205 | ||||||
| chr16:1603222
|
C | G | 4 | a0009c0011t0003g0042a0009c0011t0003g0043a0009c0011t0003g0044others(1): Show | 4 | HG01257.hp2 HG01261.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-631G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603222 | ||||||
| chr16:1603259
|
C | T | 3 | a0001c0001t0002g0256a0001c0001t0002g0258a0001c0001t0002g0261 | 3 | NA18953.hp2 NA18957.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.148-668G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603259 | ||||||
| chr16:1603577
|
A | G | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.148-986T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603577 | ||||||
| chr16:1603630
|
G | A | 1 | a0001c0001t0002g0181 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.148-1039C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603630 | ||||||
| chr16:1603641
|
C | T | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.148-1050G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603641 | ||||||
| chr16:1603708
|
C | A | 1 | a0001c0002t0001g0102 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.148-1117G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603708 | ||||||
| chr16:1603733
|
G | A | 11 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(8): Show | 11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.148-1142C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603733 | ||||||
| chr16:1603770
|
C | T | 1 | a0004c0006t0002g0204 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.148-1179G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603770 | ||||||
| chr16:1603777
|
G | A | 1 | a0001c0002t0001g0084 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.148-1186C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603777 | ||||||
| chr16:1603863
|
C | T | 9 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(6): Show | 9 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-1272G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1603863 | ||||||
| chr16:1604193
|
C | G | 1 | a0001c0001t0002g0253 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.148-1602G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604193 | ||||||
| chr16:1604264
|
G | A | 39 | a0001c0001t0002g0296a0001c0001t0002g0297a0001c0001t0003g0038others(36): Show | 39 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.148-1673C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604264 | ||||||
| chr16:1604274
|
C | CGT | 42 | a0001c0001t0002g0290a0001c0001t0002g0291a0001c0002t0001g0104others(39): Show | 42 | HG00408.hp2 HG00673.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.148-1685_148-1684d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | ||||||
| chr16:1604274
|
C | CGTGT | 54 | a0001c0001t0002g0004a0001c0001t0002g0246a0001c0001t0002g0247others(51): Show | 54 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.148-1687_148-1684d others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | ||||||
| chr16:1604274
|
C | CGTGTGT | 43 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0276others(40): Show | 43 | HG00323.hp1 HG00544.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.148-1689_148-1684d others(8): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | ||||||
| chr16:1604274
|
C | CGTGTGTG others(1): Show |
46 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0182others(43): Show | 46 | HG00280.hp2 HG00408.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.148-1691_148-1684d others(10): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | ||||||
| chr16:1604274
|
C | CGTGTGTG others(3): Show |
29 | a0001c0001t0002g0174a0001c0001t0002g0241a0001c0001t0002g0261others(26): Show | 29 | HG00099.hp1 HG00609.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.148-1693_148-1684d others(12): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | ||||||
| chr16:1604274
|
C | CGTGTGTG others(5): Show |
20 | a0001c0001t0002g0200a0001c0001t0002g0303a0001c0001t0002g0304others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.148-1695_148-1684d others(14): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | ||||||
| chr16:1604274
|
C | CGTGTGTG others(7): Show |
10 | a0001c0001t0002g0206a0001c0001t0002g0236a0001c0001t0002g0239others(7): Show | 10 | HG01070.hp1 HG01081.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.148-1697_148-1684d others(16): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | ||||||
| chr16:1604274
|
C | CGTGTGTG others(9): Show |
13 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0004g0170others(10): Show | 13 | HG01109.hp2 HG01496.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.148-1699_148-1684d others(18): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | ||||||
| chr16:1604274
|
C | CGTGTGTG others(11): Show |
12 | a0001c0001t0002g0169a0001c0001t0002g0228a0001c0001t0002g0229others(9): Show | 12 | HG01099.hp2 HG01361.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.148-1701_148-1684d others(20): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | ||||||
| chr16:1604274
|
C | CGTGTGTG others(13): Show |
7 | a0001c0001t0002g0226a0001c0001t0002g0253a0001c0001t0002g0255others(4): Show | 7 | HG00642.hp1 HG02148.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.148-1703_148-1684d others(22): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | ||||||
| chr16:1604274
|
C | CGTGTGTG others(15): Show |
3 | a0001c0001t0002g0205a0004c0006t0002g0204a0011c0012t0003g0051 | 3 | HG01256.hp1 HG03209.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.148-1705_148-1684d others(24): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | ||||||
| chr16:1604274
|
C | CGTGTGTG others(17): Show |
2 | a0001c0001t0002g0252a0001c0001t0002g0301 | 2 | HG02257.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.148-1707_148-1684d others(26): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | ||||||
| chr16:1604274
|
CGT | C | 13 | a0001c0001t0002g0293a0001c0002t0001g0120a0001c0002t0001g0121others(10): Show | 13 | HG02083.hp2 HG02109.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.148-1685_148-1684d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | ||||||
| chr16:1604274
|
CGTGT | C | 14 | a0001c0001t0002g0184a0001c0020t0003g0138a0001c0020t0003g0139others(11): Show | 14 | HG00280.hp1 HG00609.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.148-1687_148-1684d others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | ||||||
| chr16:1604274
|
CGTGTGTG others(5): Show |
C | 2 | a0003c0005t0001g0156a0003c0005t0001g0157 | 2 | NA19057.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.148-1695_148-1684d others(14): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | ||||||
| chr16:1604274
|
CGTGTGTG others(7): Show |
C | 2 | a0001c0001t0002g0046a0001c0001t0002g0294 | 2 | HG03490.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.148-1697_148-1684d others(16): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604274 | ||||||
| chr16:1604298
|
TGTGTGTG others(13): Show |
T | 1 | a0001c0001t0004g0251 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.148-1727_148-1708d others(22): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604298 | ||||||
| chr16:1604304
|
TGTGTGTG others(7): Show |
T | 1 | a0001c0001t0002g0250 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.148-1727_148-1714d others(16): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604304 | ||||||
| chr16:1604306
|
TGTGTGTG others(5): Show |
T | 1 | a0023c0051t0004g0249 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.148-1727_148-1716d others(14): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604306 | ||||||
| chr16:1604318
|
G | T | 39 | a0001c0001t0002g0205a0001c0001t0002g0226a0001c0001t0002g0228others(36): Show | 39 | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.148-1727C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604318 | ||||||
| chr16:1604335
|
T | TGAGG | 196 | a0001c0001t0003g0038a0001c0001t0003g0123a0001c0002t0001g0005others(193): Show | 196 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.148-1745_148-1744i others(6): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604335 | ||||||
| chr16:1604336
|
A | G | 1 | a0017c0029t0003g0188 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.148-1745T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604336 | ||||||
| chr16:1604386
|
A | G | 1 | a0001c0004t0003g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.148-1795T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604386 | ||||||
| chr16:1604436
|
T | G | 1 | a0001c0001t0002g0295 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.148-1845A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604436 | ||||||
| chr16:1604444
|
C | T | 2 | a0011c0012t0003g0201a0011c0012t0003g0202 | 2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.148-1853G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604444 | ||||||
| chr16:1604524
|
C | G | 1 | a0001c0004t0001g0066 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.148-1933G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604524 | ||||||
| chr16:1604524
|
C | T | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.148-1933G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604524 | ||||||
| chr16:1604752
|
C | A | 197 | a0001c0001t0003g0038a0001c0001t0003g0123a0001c0002t0001g0005others(194): Show | 197 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.148-2161G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604752 | ||||||
| chr16:1604780
|
G | A | 2 | a0001c0001t0002g0296a0001c0001t0002g0297 | 2 | NA18991.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.148-2189C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604780 | ||||||
| chr16:1604945
|
G | A | 159 | a0001c0001t0003g0123a0001c0002t0001g0005a0001c0002t0001g0013others(156): Show | 159 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.147+2175C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604945 | ||||||
| chr16:1604947
|
G | A | 148 | a0001c0001t0003g0123a0001c0002t0001g0005a0001c0002t0001g0013others(145): Show | 148 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.147+2173C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1604947 | ||||||
| chr16:1605031
|
C | T | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.147+2089G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605031 | ||||||
| chr16:1605072
|
T | C | 4 | a0009c0011t0003g0042a0009c0011t0003g0043a0009c0011t0003g0044others(1): Show | 4 | HG01257.hp2 HG01261.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+2048A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605072 | ||||||
| chr16:1605198
|
G | A | 1 | a0001c0001t0002g0182 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.147+1922C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605198 | ||||||
| chr16:1605278
|
A | T | 2 | a0010c0021t0002g0315a0010c0021t0002g0316 | 2 | HG02056.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.147+1842T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605278 | ||||||
| chr16:1605353
|
T | C | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.147+1767A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605353 | ||||||
| chr16:1605356
|
G | A | 1 | a0001c0002t0001g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.147+1764C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605356 | ||||||
| chr16:1605396
|
C | T | 1 | a0001c0002t0001g0065 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.147+1724G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605396 | ||||||
| chr16:1605438
|
C | T | 37 | a0001c0001t0003g0038a0002c0003t0003g0006a0002c0003t0003g0007others(34): Show | 37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.147+1682G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605438 | ||||||
| chr16:1605443
|
T | C | 1 | a0003c0005t0001g0157 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.147+1677A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605443 | ||||||
| chr16:1605605
|
C | T | 4 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0019t0003g0136others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.147+1515G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605605 | ||||||
| chr16:1605758
|
G | A | 1 | a0001c0001t0003g0123 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.147+1362C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605758 | ||||||
| chr16:1605896
|
G | A | 1 | a0001c0001t0002g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.147+1224C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1605896 | ||||||
| chr16:1606015
|
G | A | 1 | a0001c0004t0003g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.147+1105C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606015 | ||||||
| chr16:1606216
|
G | A | 1 | a0005c0039t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.147+904C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606216 | ||||||
| chr16:1606229
|
C | A | 2 | a0001c0001t0002g0299a0001c0001t0002g0300 | 2 | HG01081.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.147+891G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606229 | ||||||
| chr16:1606255
|
G | A | 1 | a0017c0029t0003g0188 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.147+865C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606255 | ||||||
| chr16:1606320
|
G | A | 32 | a0003c0005t0001g0141a0003c0005t0001g0142a0003c0005t0001g0143others(29): Show | 32 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.147+800C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606320 | ||||||
| chr16:1606395
|
C | A | 1 | a0001c0001t0002g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.147+725G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606395 | ||||||
| chr16:1606438
|
A | C | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.147+682T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606438 | ||||||
| chr16:1606506
|
G | T | 1 | a0001c0001t0002g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.147+614C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606506 | ||||||
| chr16:1606531
|
G | A | 1 | a0016c0027t0003g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.147+589C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606531 | ||||||
| chr16:1606563
|
C | T | 1 | a0001c0002t0010g0186 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.147+557G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606563 | ||||||
| chr16:1606564
|
G | A | 2 | a0007c0013t0001g0194a0007c0060t0001g0195 | 2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.147+556C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606564 | ||||||
| chr16:1606622
|
G | A | 1 | a0001c0001t0002g0302 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.147+498C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606622 | ||||||
| chr16:1606632
|
G | T | 1 | a0001c0001t0002g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.147+488C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606632 | ||||||
| chr16:1606764
|
A | G | 201 | a0001c0001t0003g0038a0001c0001t0003g0123a0001c0002t0001g0005others(198): Show | 201 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.147+356T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606764 | ||||||
| chr16:1606866
|
C | T | 1 | a0003c0005t0003g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.147+254G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606866 | ||||||
| chr16:1606928
|
A | G | 6 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+192T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606928 | ||||||
| chr16:1606935
|
C | T | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.147+185G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1606935 | ||||||
| chr16:1607011
|
C | T | 109 | a0001c0001t0003g0123a0001c0002t0001g0005a0001c0002t0001g0013others(106): Show | 109 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.147+109G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1607011 | ||||||
| chr16:1607033
|
CAT | C | 37 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0005t0001g0141others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.147+85_147+86delAT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 3/30 | chr16 | 1607033 | ||||||
| chr16:1607349
|
A | T | 158 | a0001c0001t0003g0123a0001c0002t0001g0005a0001c0002t0001g0013others(155): Show | 158 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.-31-52T>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1607349 | ||||||
| chr16:1607426
|
C | T | 1 | a0006c0007t0003g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-31-129G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1607426 | ||||||
| chr16:1607510
|
C | A | 1 | a0027c0036t0003g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-31-213G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1607510 | ||||||
| chr16:1607753
|
C | T | 109 | a0001c0001t0003g0123a0001c0002t0001g0005a0001c0002t0001g0013others(106): Show | 109 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.-31-456G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1607753 | ||||||
| chr16:1607834
|
C | A | 1 | a0005c0009t0004g0167 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-31-537G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1607834 | ||||||
| chr16:1607852
|
C | T | 37 | a0001c0001t0003g0038a0002c0003t0003g0006a0002c0003t0003g0007others(34): Show | 37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.-31-555G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1607852 | ||||||
| chr16:1607976
|
C | T | 11 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(8): Show | 11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.-31-679G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1607976 | ||||||
| chr16:1608032
|
A | C | 1 | a0001c0010t0004g0225 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-31-735T>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608032 | ||||||
| chr16:1608055
|
T | C | 201 | a0001c0001t0003g0038a0001c0001t0003g0123a0001c0002t0001g0005others(198): Show | 201 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.-31-758A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608055 | ||||||
| chr16:1608085
|
G | C | 37 | a0001c0001t0003g0038a0002c0003t0003g0006a0002c0003t0003g0007others(34): Show | 37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.-31-788C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608085 | ||||||
| chr16:1608100
|
TAG | T | 146 | a0001c0001t0003g0123a0001c0002t0001g0005a0001c0002t0001g0013others(143): Show | 146 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.-31-805_-31-804del others(2): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608100 | ||||||
| chr16:1608153
|
C | G | 201 | a0001c0001t0003g0038a0001c0001t0003g0123a0001c0002t0001g0005others(198): Show | 201 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.-31-856G>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608153 | ||||||
| chr16:1608333
|
G | T | 1 | a0001c0002t0003g0064 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-31-1036C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608333 | ||||||
| chr16:1608391
|
G | A | 6 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31-1094C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608391 | ||||||
| chr16:1608418
|
T | C | 6 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31-1121A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608418 | ||||||
| chr16:1608453
|
C | T | 37 | a0001c0001t0003g0038a0002c0003t0003g0006a0002c0003t0003g0007others(34): Show | 37 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.-31-1156G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608453 | ||||||
| chr16:1608526
|
C | T | 5 | a0007c0013t0001g0191a0007c0013t0001g0192a0007c0013t0001g0193others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31-1229G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608526 | ||||||
| chr16:1608631
|
C | CA | 110 | a0001c0001t0002g0184a0001c0001t0002g0303a0001c0001t0002g0304others(107): Show | 110 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.-31-1335dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608631 | ||||||
| chr16:1608631
|
C | CAA | 44 | a0001c0002t0001g0128a0001c0002t0001g0129a0001c0002t0001g0131others(41): Show | 44 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.-31-1336_-31-1335d others(4): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608631 | ||||||
| chr16:1608631
|
CA | C | 6 | a0005c0009t0004g0166a0005c0009t0004g0167a0011c0012t0003g0051others(3): Show | 6 | HG01070.hp1 HG02258.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31-1335delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608631 | ||||||
| chr16:1608926
|
C | T | 1 | a0003c0018t0001g0133 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-31-1629G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1608926 | ||||||
| chr16:1609127
|
T | C | 201 | a0001c0001t0003g0038a0001c0001t0003g0123a0001c0002t0001g0005others(198): Show | 201 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.-32+1537A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1609127 | ||||||
| chr16:1609722
|
T | G | 37 | a0001c0020t0003g0138a0001c0020t0003g0139a0003c0005t0001g0141others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.-32+942A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1609722 | ||||||
| chr16:1609856
|
C | A | 11 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(8): Show | 11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32+808G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1609856 | ||||||
| chr16:1609857
|
T | G | 11 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(8): Show | 11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32+807A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1609857 | ||||||
| chr16:1609960
|
C | T | 7 | a0003c0017t0001g0058a0003c0017t0001g0059a0008c0015t0003g0053others(4): Show | 7 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32+704G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1609960 | ||||||
| chr16:1610075
|
T | A | 2 | a0001c0001t0002g0324a0001c0001t0002g0325 | 2 | NA18945.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-32+589A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1610075 | ||||||
| chr16:1610088
|
T | C | 2 | a0004c0006t0002g0313a0004c0026t0004g0312 | 2 | HG00733.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-32+576A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1610088 | ||||||
| chr16:1610121
|
GC | G | 3 | a0002c0003t0003g0007a0002c0003t0003g0008a0002c0003t0003g0009 | 3 | NA18941.hp1 NA18953.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-32+542delG | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1610121 | ||||||
| chr16:1610127
|
C | T | 1 | a0001c0001t0002g0314 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-32+537G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1610127 | ||||||
| chr16:1610152
|
CG | C | 12 | a0001c0001t0002g0314a0001c0001t0002g0317a0001c0001t0002g0318others(9): Show | 12 | HG02056.hp2 HG02074.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.-32+511delC | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1610152 | ||||||
| chr16:1610206
|
T | C | 11 | a0006c0007t0003g0159a0006c0007t0003g0160a0006c0007t0003g0161others(8): Show | 11 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32+458A>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1610206 | ||||||
| chr16:1610263
|
T | A | 1 | a0001c0001t0002g0326 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-32+401A>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1610263 | ||||||
| chr16:1610273
|
A | G | 200 | a0001c0001t0003g0038a0001c0001t0003g0123a0001c0002t0001g0005others(197): Show | 200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.-32+391T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1610273 | ||||||
| chr16:1610285
|
G | T | 2 | a0011c0012t0003g0051a0011c0012t0003g0052 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-32+379C>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1610285 | ||||||
| chr16:1610612
|
G | C | 1 | a0001c0004t0003g0185 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-32+52C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 2/30 | chr16 | 1610612 | ||||||
| chr16:1610923
|
T | G | 1 | a0001c0001t0003g0038 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-221-70A>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1610923 | ||||||
| chr16:1610938
|
C | T | 1 | a0003c0059t0001g0050 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-221-85G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1610938 | ||||||
| chr16:1610993
|
C | A | 1 | a0010c0040t0003g0187 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-221-140G>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1610993 | ||||||
| chr16:1611167
|
G | A | 3 | a0002c0003t0003g0006a0002c0003t0003g0039a0002c0003t0003g0040 | 3 | NA18950.hp2 NA18990.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.-221-314C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611167 | ||||||
| chr16:1611169
|
G | A | 1 | a0017c0029t0003g0188 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-221-316C>T | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611169 | ||||||
| chr16:1611280
|
G | C | 1 | a0001c0004t0003g0189 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-221-427C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611280 | ||||||
| chr16:1611293
|
C | T | 1 | a0001c0002t0001g0049 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-221-440G>A | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611293 | ||||||
| chr16:1611490
|
C | CA | 24 | a0001c0001t0002g0200a0001c0001t0002g0329a0001c0001t0002g0330others(21): Show | 24 | HG01074.hp2 HG01109.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.-222+477dupT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611490 | ||||||
| chr16:1611490
|
CA | C | 8 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0002t0001g0005others(5): Show | 8 | HG01256.hp1 HG02895.hp1 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.-222+477delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611490 | ||||||
| chr16:1611620
|
G | C | 2 | a0011c0012t0003g0201a0011c0012t0003g0202 | 2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-222+348C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611620 | ||||||
| chr16:1611700
|
A | G | 202 | a0001c0001t0002g0169a0001c0001t0002g0174a0001c0001t0002g0178others(199): Show | 202 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.-222+268T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611700 | ||||||
| chr16:1611741
|
G | C | 2 | a0001c0002t0001g0333a0001c0002t0001g0334 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-222+227C>G | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611741 | ||||||
| chr16:1611813
|
CA | C | 42 | a0001c0001t0002g0046a0001c0001t0003g0038a0001c0002t0001g0005others(39): Show | 42 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-222+154delT | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611813 | ||||||
| chr16:1611825
|
A | G | 1 | a0001c0001t0002g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-222+143T>C | IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 1/30 | chr16 | 1611825 |