Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8100 |
| ensemblid | ENSG00000032742.18 |
| hgncid | 20606 |
| symbol | IFT88 |
| name | intraflagellar transport 88 |
| refseq_nuc | NM_006531.5 |
| refseq_prot | NP_006522.2 |
| ensembl_nuc | ENST00000351808.10 |
| ensembl_prot | ENSP00000261632.5 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 20567157 |
| end | 20691444 |
| strand | + |
| ver | v1.2 |
| region | chr13:20567157-20691444 |
| region5000 | chr13:20562157-20696444 |
| regionname0 | IFT88_chr13_20567157_20691444 |
| regionname5000 | IFT88_chr13_20562157_20696444 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 824 | 223 | 38 | 31 | 114 | 10 | 29 | 94 | IFT88_chr13_20562157_20696444 | IFT88 | MMQNV others(819): Show |
chr13 | 20562157 | 20696444 |
| a0002 | 1/0 | 824 | 35 | 21 | 9 | 0 | 4 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | MMQNV others(819): Show |
chr13 | 20562157 | 20696444 |
| a0003 | 0/0 | 824 | 28 | 18 | 6 | 0 | 2 | 2 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | MMQNV others(819): Show |
chr13 | 20562157 | 20696444 |
| a0004 | 0/0 | 824 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | MMQNV others(819): Show |
chr13 | 20562157 | 20696444 |
| a0005 | 0/0 | 824 | 5 | 0 | 0 | 1 | 0 | 4 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | MMQNV others(819): Show |
chr13 | 20562157 | 20696444 |
| a0006 | 0/0 | 824 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | MMQNV others(819): Show |
chr13 | 20562157 | 20696444 |
| a0007 | 0/0 | 824 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | MMQNV others(819): Show |
chr13 | 20562157 | 20696444 |
| a0008 | 0/0 | 824 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | MMQNV others(819): Show |
chr13 | 20562157 | 20696444 |
| a0009 | 0/0 | 824 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | MMQNV others(819): Show |
chr13 | 20562157 | 20696444 |
| a0010 | 0/0 | 824 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | MMQNV others(819): Show |
chr13 | 20562157 | 20696444 |
| a0011 | 0/0 | 824 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | MMQNV others(819): Show |
chr13 | 20562157 | 20696444 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2472 | 215 | 30 | 31 | 114 | 10 | 29 | IFT88_chr13_20562157_20696444 | IFT88 | ATGAT others(2467): Show |
chr13 | 20562157 | 20696444 | ||
| a0001c0004 | 0/0 | 2472 | 8 | 8 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | ATGAT others(2467): Show |
chr13 | 20562157 | 20696444 | ||
| a0002c0002 | 1/0 | 2472 | 33 | 19 | 9 | 0 | 4 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | ATGAT others(2467): Show |
chr13 | 20562157 | 20696444 | ||
| a0002c0010 | 0/0 | 2472 | 2 | 2 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | ATGAT others(2467): Show |
chr13 | 20562157 | 20696444 | ||
| a0003c0003 | 0/0 | 2472 | 26 | 16 | 6 | 0 | 2 | 2 | IFT88_chr13_20562157_20696444 | IFT88 | ATGAT others(2467): Show |
chr13 | 20562157 | 20696444 | ||
| a0003c0009 | 0/0 | 2472 | 2 | 2 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | ATGAT others(2467): Show |
chr13 | 20562157 | 20696444 | ||
| a0004c0005 | 0/0 | 2472 | 7 | 6 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | ATGAT others(2467): Show |
chr13 | 20562157 | 20696444 | ||
| a0005c0006 | 0/0 | 2472 | 5 | 0 | 0 | 1 | 0 | 4 | IFT88_chr13_20562157_20696444 | IFT88 | ATGAT others(2467): Show |
chr13 | 20562157 | 20696444 | ||
| a0006c0007 | 0/0 | 2472 | 3 | 1 | 2 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | ATGAT others(2467): Show |
chr13 | 20562157 | 20696444 | ||
| a0007c0008 | 0/0 | 2472 | 3 | 3 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | ATGAT others(2467): Show |
chr13 | 20562157 | 20696444 | ||
| a0008c0011 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | ATGAT others(2467): Show |
chr13 | 20562157 | 20696444 | ||
| a0009c0014 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | ATGAT others(2467): Show |
chr13 | 20562157 | 20696444 | ||
| a0010c0012 | 0/0 | 2472 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | ATGAT others(2467): Show |
chr13 | 20562157 | 20696444 | ||
| a0011c0013 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | ATGAT others(2467): Show |
chr13 | 20562157 | 20696444 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2850 | 212 | 29 | 31 | 113 | 9 | 29 | IFT88_chr13_20562157_20696444 | IFT88 | CTTGG others(2845): Show |
chr13 | 20562157 | 20696444 |
| a0001c0001t0002 | 0/0 | 2850 | 1 | 0 | 0 | 0 | 1 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | CTTGG others(2845): Show |
chr13 | 20562157 | 20696444 |
| a0001c0001t0003 | 0/0 | 2850 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | CTTGG others(2845): Show |
chr13 | 20562157 | 20696444 |
| a0001c0001t0004 | 0/0 | 2850 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | CTTGG others(2845): Show |
chr13 | 20562157 | 20696444 |
| a0001c0004t0001 | 0/0 | 2850 | 8 | 8 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | CTTGG others(2845): Show |
chr13 | 20562157 | 20696444 |
| a0002c0002t0001 | 1/0 | 2850 | 33 | 19 | 9 | 0 | 4 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | CTTGG others(2845): Show |
chr13 | 20562157 | 20696444 |
| a0002c0010t0001 | 0/0 | 2850 | 2 | 2 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | CTTGG others(2845): Show |
chr13 | 20562157 | 20696444 |
| a0003c0003t0001 | 0/0 | 2850 | 26 | 16 | 6 | 0 | 2 | 2 | IFT88_chr13_20562157_20696444 | IFT88 | CTTGG others(2845): Show |
chr13 | 20562157 | 20696444 |
| a0003c0009t0001 | 0/0 | 2850 | 2 | 2 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | CTTGG others(2845): Show |
chr13 | 20562157 | 20696444 |
| a0004c0005t0001 | 0/0 | 2850 | 7 | 6 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | CTTGG others(2845): Show |
chr13 | 20562157 | 20696444 |
| a0005c0006t0001 | 0/0 | 2850 | 5 | 0 | 0 | 1 | 0 | 4 | IFT88_chr13_20562157_20696444 | IFT88 | CTTGG others(2845): Show |
chr13 | 20562157 | 20696444 |
| a0006c0007t0001 | 0/0 | 2850 | 3 | 1 | 2 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | CTTGG others(2845): Show |
chr13 | 20562157 | 20696444 |
| a0007c0008t0001 | 0/0 | 2850 | 3 | 3 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | CTTGG others(2845): Show |
chr13 | 20562157 | 20696444 |
| a0008c0011t0001 | 0/0 | 2850 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | CTTGG others(2845): Show |
chr13 | 20562157 | 20696444 |
| a0009c0014t0001 | 0/0 | 2850 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | CTTGG others(2845): Show |
chr13 | 20562157 | 20696444 |
| a0010c0012t0001 | 0/0 | 2850 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | CTTGG others(2845): Show |
chr13 | 20562157 | 20696444 |
| a0011c0013t0001 | 0/0 | 2850 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | CTTGG others(2845): Show |
chr13 | 20562157 | 20696444 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0279 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0004t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0004t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0004t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0004t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0004t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0004t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0004t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0001c0004t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0010t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0002c0010t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0009t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0003c0009t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0004c0005t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0004c0005t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0004c0005t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0004c0005t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0004c0005t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0004c0005t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0004c0005t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0005c0006t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0005c0006t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0005c0006t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0005c0006t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0005c0006t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0006c0007t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0006c0007t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0006c0007t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0007c0008t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0007c0008t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0007c0008t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0008c0011t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0009c0014t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0010c0012t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| a0011c0013t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0289 | EUR | GBR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | GBR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | GBR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0283 | EUR | FIN | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0230 | EUR | FIN | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | FIN | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | FIN | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00639 | hp1 | a0006 | c0007 | t0001 | g0232 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0287 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00735 | hp1 | a0003 | c0003 | t0001 | g0120 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00735 | hp2 | a0004 | c0005 | t0001 | g0169 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0148 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0155 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01069 | hp2 | a0003 | c0003 | t0001 | g0128 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01071 | hp1 | a0003 | c0003 | t0001 | g0129 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0150 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0151 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01106 | hp1 | a0003 | c0003 | t0001 | g0147 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0286 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01109 | hp2 | a0003 | c0003 | t0001 | g0142 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0157 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01243 | hp1 | a0006 | c0007 | t0001 | g0233 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01256 | hp1 | a0003 | c0003 | t0001 | g0126 | AMR | CLM | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01361 | hp1 | a0008 | c0011 | t0001 | g0125 | AMR | CLM | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0006 | EUR | IBS | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0006 | EUR | IBS | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | IBS | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0153 | AMR | PEL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02055 | hp1 | a0001 | c0004 | t0001 | g0110 | AFR | ACB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02055 | hp2 | a0003 | c0009 | t0001 | g0132 | AFR | ACB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02145 | hp1 | a0003 | c0003 | t0001 | g0138 | AFR | ACB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02145 | hp2 | a0001 | c0004 | t0001 | g0008 | AFR | ACB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02257 | hp1 | a0004 | c0005 | t0001 | g0163 | AFR | ACB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02257 | hp2 | a0003 | c0003 | t0001 | g0140 | AFR | ACB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02258 | hp2 | a0006 | c0007 | t0001 | g0234 | AFR | ACB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0285 | AFR | ACB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0061 | AFR | ACB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02572 | hp2 | a0007 | c0008 | t0001 | g0159 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02602 | hp1 | a0005 | c0006 | t0001 | g0175 | SAS | PJL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02615 | hp2 | a0003 | c0003 | t0001 | g0127 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02622 | hp1 | a0003 | c0009 | t0001 | g0133 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02647 | hp1 | a0009 | c0014 | t0001 | g0094 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02647 | hp2 | a0007 | c0008 | t0001 | g0160 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0113 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02723 | hp1 | a0003 | c0003 | t0001 | g0136 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0293 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02735 | hp1 | a0003 | c0003 | t0001 | g0122 | SAS | PJL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0112 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02886 | hp1 | a0004 | c0005 | t0001 | g0167 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02896 | hp1 | a0004 | c0005 | t0001 | g0166 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0139 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0137 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0290 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02922 | hp2 | a0004 | c0005 | t0001 | g0168 | AFR | ESN | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02965 | hp1 | a0001 | c0004 | t0001 | g0111 | AFR | ESN | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0292 | AFR | ESN | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03017 | hp1 | a0010 | c0012 | t0001 | g0192 | SAS | PJL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03017 | hp2 | a0005 | c0006 | t0001 | g0172 | SAS | PJL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03041 | hp1 | a0004 | c0005 | t0001 | g0164 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0156 | AFR | MSL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | MSL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0284 | AFR | ESN | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03130 | hp2 | a0001 | c0004 | t0001 | g0009 | AFR | ESN | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03139 | hp1 | a0003 | c0003 | t0001 | g0146 | AFR | ESN | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0154 | AFR | ESN | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0288 | AFR | ESN | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0161 | AFR | ESN | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03225 | hp1 | a0002 | c0010 | t0001 | g0116 | AFR | MSL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03453 | hp1 | a0002 | c0010 | t0001 | g0115 | AFR | MSL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | MSL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03486 | hp1 | a0003 | c0003 | t0001 | g0123 | AFR | MSL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | MSL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03516 | hp1 | a0003 | c0003 | t0001 | g0124 | AFR | ESN | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0152 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03540 | hp2 | a0003 | c0003 | t0001 | g0131 | AFR | GWD | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | MSL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03579 | hp2 | a0001 | c0004 | t0001 | g0011 | AFR | MSL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | STU | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | STU | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03927 | hp2 | a0005 | c0006 | t0001 | g0173 | SAS | BEB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG04184 | hp1 | a0005 | c0006 | t0001 | g0174 | SAS | BEB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG04199 | hp1 | a0003 | c0003 | t0001 | g0141 | SAS | STU | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | STU | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | STU | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | STU | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18522 | hp1 | a0003 | c0003 | t0001 | g0134 | AFR | YRI | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18522 | hp2 | a0001 | c0004 | t0001 | g0095 | AFR | YRI | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18906 | hp1 | a0004 | c0005 | t0001 | g0165 | AFR | YRI | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18906 | hp2 | a0003 | c0003 | t0001 | g0145 | AFR | YRI | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18957 | hp1 | a0005 | c0006 | t0001 | g0176 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18993 | hp1 | a0011 | c0013 | t0001 | g0281 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19030 | hp2 | a0003 | c0003 | t0001 | g0143 | AFR | LWK | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19043 | hp1 | a0003 | c0003 | t0001 | g0144 | AFR | LWK | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19240 | hp1 | a0001 | c0004 | t0001 | g0012 | AFR | YRI | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA19240 | hp2 | a0003 | c0003 | t0001 | g0135 | AFR | YRI | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA20129 | hp1 | a0003 | c0003 | t0001 | g0121 | AFR | ASW | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ASW | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | TSI | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA20752 | hp2 | a0003 | c0003 | t0001 | g0171 | EUR | TSI | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | TSI | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA20805 | hp2 | a0003 | c0003 | t0001 | g0130 | EUR | TSI | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | GIH | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | GIH | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0149 | AFR | ACB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | ACB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0114 | AFR | MSL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0291 | AFR | USA | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | USA | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA21309 | hp1 | a0007 | c0008 | t0001 | g0158 | AFR | LWK | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0279 | REF | REF | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0119 | REF | REF | IFT88_chr13_20562157_20696444 | IFT88 | chr13 | 20562157 | 20696444 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:20591006 | A | G | 1 | a0007 | 3 | HG02572.hp2 HG02647.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.250A>G | p.Thr84Ala | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 5/26 | 356/2850 | 250/2475 | 84/824 | chr13 | 20591006 | |||
| chr13:20592352 | C | T | 1 | a0009 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.346C>T | p.Leu116Phe | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/26 | 452/2850 | 346/2475 | 116/824 | chr13 | 20592352 | |||
| chr13:20598669 | A | G | 1 | a0004 | 7 | HG00735.hp2 HG02257.hp1 HG02886.hp1 others(4): Show |
missense_variant | MODERATE | c.613A>G | p.Ser205Gly | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 10/26 | 719/2850 | 613/2475 | 205/824 | chr13 | 20598669 | |||
| chr13:20601932 | G | A | 1 | a0005 | 5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.1040G>A | p.Ser347Asn | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/26 | 1146/2850 | 1040/2475 | 347/824 | chr13 | 20601932 | |||
| chr13:20605099 | G | A | 1 | a0008 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.1106G>A | p.Arg369His | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/26 | 1212/2850 | 1106/2475 | 369/824 | chr13 | 20605099 | |||
| chr13:20615801 | T | A | 1 | a0010 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.1121T>A | p.Met374Lys | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/26 | 1227/2850 | 1121/2475 | 374/824 | chr13 | 20615801 | |||
| chr13:20615802 | G | A | 2 | a0003 a0008 |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
missense_variant | MODERATE | c.1122G>A | p.Met374Ile | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/26 | 1228/2850 | 1122/2475 | 374/824 | chr13 | 20615802 | |||
| chr13:20631053 | G | A | 6 | a0001 a0004 a0006 others(3): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
missense_variant | MODERATE | c.1337G>A | p.Ser446Asn | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/26 | 1443/2850 | 1337/2475 | 446/824 | chr13 | 20631053 | |||
| chr13:20643565 | G | A | 1 | a0005 | 5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
missense_variant | MODERATE | c.1793G>A | p.Arg598His | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 19/26 | 1899/2850 | 1793/2475 | 598/824 | chr13 | 20643565 | |||
| chr13:20653910 | A | G | 1 | a0011 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.1984A>G | p.Ser662Gly | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/26 | 2090/2850 | 1984/2475 | 662/824 | chr13 | 20653910 | |||
| chr13:20653914 | G | C | 1 | a0006 | 3 | HG00639.hp1 HG01243.hp1 HG02258.hp2 |
missense_variant | MODERATE | c.1988G>C | p.Cys663Ser | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/26 | 2094/2850 | 1988/2475 | 663/824 | chr13 | 20653914 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:20591668 | A | G | 1 | a0001c0004 | 8 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
synonymous_variant | LOW | c.315A>G | p.Lys105Lys | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 6/26 | 421/2850 | 315/2475 | 105/824 | chr13 | 20591668 | |||
| chr13:20656426 | C | T | 1 | a0002c0010 | 2 | HG03225.hp1 HG03453.hp1 |
synonymous_variant | LOW | c.2064C>T | p.Val688Val | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/26 | 2170/2850 | 2064/2475 | 688/824 | chr13 | 20656426 | |||
| chr13:20691154 | A | G | 1 | a0003c0009 | 2 | HG02055.hp2 HG02622.hp1 |
synonymous_variant | LOW | c.2454A>G | p.Gly818Gly | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 26/26 | 2560/2850 | 2454/2475 | 818/824 | chr13 | 20691154 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:20567165 | C | G | 1 | a0001c0001t0004 | 1 | NA18988.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-98C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/26 | chr13 | 20567165 | |||||||
| chr13:20567185 | G | C | 1 | a0001c0001t0002 | 1 | HG00323.hp2 | 5_prime_UTR_variant | MODIFIER | c.-78G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/26 | 7201 | chr13 | 20567185 | ||||||
| chr13:20691294 | G | A | 1 | a0001c0001t0003 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*119G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 26/26 | 119 | chr13 | 20691294 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:20567278 | C | G | 7 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7+22C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20567278 | |||||||
| chr13:20567343 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(107): Show |
111 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.-7+87G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20567343 | |||||||
| chr13:20567344 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-7+88C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20567344 | |||||||
| chr13:20567359 | C | T | 19 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0007 others(16): Show |
22 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.-7+103C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20567359 | |||||||
| chr13:20567408 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-7+152G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20567408 | |||||||
| chr13:20567413 | C | T | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.-7+157C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20567413 | |||||||
| chr13:20567676 | CA | C | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+421delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20567676 | |||||||
| chr13:20567683 | A | G | 46 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 others(43): Show |
46 | HG00597.hp2 HG00621.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.-7+427A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20567683 | |||||||
| chr13:20567707 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7+451G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20567707 | |||||||
| chr13:20567742 | C | T | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-7+486C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20567742 | |||||||
| chr13:20567864 | G | T | 6 | a0001c0001t0001g0237 a0001c0001t0001g0239 a0001c0001t0001g0243 others(3): Show |
6 | HG00621.hp1 NA18952.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+608G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20567864 | |||||||
| chr13:20567868 | G | GT | 7 | a0001c0001t0001g0109 a0001c0001t0001g0117 a0001c0001t0001g0235 others(4): Show |
7 | HG01192.hp1 HG01978.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7+624dupT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 20567868 | ||||||
| chr13:20567910 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-7+654A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20567910 | |||||||
| chr13:20568049 | C | T | 1 | a0011c0013t0001g0281 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-7+793C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20568049 | |||||||
| chr13:20568107 | G | T | 11 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(8): Show |
11 | NA18747.hp1 NA18946.hp1 NA18948.hp2 others(8): Show |
intron_variant | MODIFIER | c.-7+851G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20568107 | |||||||
| chr13:20568229 | G | T | 1 | a0001c0001t0001g0097 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-7+973G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20568229 | |||||||
| chr13:20568302 | A | G | 3 | a0006c0007t0001g0232 a0006c0007t0001g0233 a0006c0007t0001g0234 |
3 | HG00639.hp1 HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-7+1046A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20568302 | |||||||
| chr13:20568491 | G | A | 14 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0007 others(11): Show |
17 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.-7+1235G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20568491 | |||||||
| chr13:20568534 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-7+1278C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20568534 | |||||||
| chr13:20568566 | A | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-7+1310A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20568566 | |||||||
| chr13:20568629 | T | G | 1 | a0001c0001t0003g0236 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-7+1373T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20568629 | |||||||
| chr13:20568693 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-7+1437A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20568693 | |||||||
| chr13:20568739 | A | T | 2 | a0001c0004t0001g0095 a0001c0004t0001g0110 |
2 | HG02055.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-7+1483A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20568739 | |||||||
| chr13:20568780 | C | T | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+1524C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20568780 | |||||||
| chr13:20568865 | C | T | 1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-7+1609C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20568865 | |||||||
| chr13:20568962 | C | T | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | HG01243.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-7+1706C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20568962 | |||||||
| chr13:20568982 | A | G | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
82 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.-7+1726A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20568982 | |||||||
| chr13:20569009 | G | A | 14 | a0002c0002t0001g0148 a0002c0002t0001g0149 a0002c0002t0001g0150 others(11): Show |
14 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7+1753G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20569009 | |||||||
| chr13:20569078 | C | A | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7+1822C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20569078 | |||||||
| chr13:20569144 | T | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
82 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.-7+1888T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20569144 | |||||||
| chr13:20569256 | AAAAT | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(94): Show |
98 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.-7+2005_-7+2008del others(4): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 20569256 | ||||||
| chr13:20569268 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-7+2012A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20569268 | |||||||
| chr13:20569344 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-7+2088C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20569344 | |||||||
| chr13:20569391 | G | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(161): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-7+2135G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20569391 | |||||||
| chr13:20569432 | G | C | 1 | a0001c0001t0001g0237 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-7+2176G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20569432 | |||||||
| chr13:20569456 | C | T | 19 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(16): Show |
19 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.-7+2200C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20569456 | |||||||
| chr13:20569462 | G | A | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+2206G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20569462 | |||||||
| chr13:20569465 | G | C | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+2209G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20569465 | |||||||
| chr13:20569467 | A | G | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+2211A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20569467 | |||||||
| chr13:20569496 | T | C | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+2240T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20569496 | |||||||
| chr13:20569568 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
82 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.-7+2312G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20569568 | |||||||
| chr13:20569571 | C | T | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(294): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.-7+2315C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20569571 | |||||||
| chr13:20569586 | A | AT | 152 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(149): Show |
153 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.-7+2337dupT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 20569586 | ||||||
| chr13:20569586 | A | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-7+2330A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20569586 | |||||||
| chr13:20569674 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-7+2418A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20569674 | |||||||
| chr13:20569797 | G | A | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7+2541G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20569797 | |||||||
| chr13:20569852 | C | A | 1 | a0003c0003t0001g0122 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-7+2596C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20569852 | |||||||
| chr13:20569976 | C | T | 19 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(16): Show |
19 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.-7+2720C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20569976 | |||||||
| chr13:20569994 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-7+2738G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20569994 | |||||||
| chr13:20570038 | CA | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.-7+2797delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 20570038 | ||||||
| chr13:20570358 | A | G | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
82 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.-7+3102A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20570358 | |||||||
| chr13:20570366 | A | G | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-7+3110A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20570366 | |||||||
| chr13:20570547 | A | T | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-7+3291A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20570547 | |||||||
| chr13:20570619 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-7+3363T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20570619 | |||||||
| chr13:20570664 | C | T | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-7+3408C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20570664 | |||||||
| chr13:20570676 | A | AAATAGAT others(1): Show |
259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.-7+3423_-7+3424ins others(8): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 20570676 | ||||||
| chr13:20570684 | G | T | 8 | a0001c0004t0001g0008 a0001c0004t0001g0009 a0001c0004t0001g0010 others(5): Show |
8 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+3428G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20570684 | |||||||
| chr13:20570819 | C | CTGAATTA | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.-6-3559_-6-3558ins others(7): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 20570819 | ||||||
| chr13:20570901 | A | T | 1 | a0001c0001t0001g0109 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-6-3479A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20570901 | |||||||
| chr13:20570924 | G | A | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-6-3456G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20570924 | |||||||
| chr13:20570984 | A | G | 19 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(16): Show |
19 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.-6-3396A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20570984 | |||||||
| chr13:20571079 | C | T | 4 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(1): Show |
4 | NA18954.hp1 NA18974.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-3301C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20571079 | |||||||
| chr13:20571140 | C | G | 2 | a0002c0010t0001g0115 a0002c0010t0001g0116 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-6-3240C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20571140 | |||||||
| chr13:20571154 | C | T | 8 | a0001c0004t0001g0008 a0001c0004t0001g0009 a0001c0004t0001g0010 others(5): Show |
8 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6-3226C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20571154 | |||||||
| chr13:20571162 | T | A | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6-3218T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20571162 | |||||||
| chr13:20571216 | G | A | 1 | a0005c0006t0001g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-6-3164G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20571216 | |||||||
| chr13:20571286 | G | A | 1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-6-3094G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20571286 | |||||||
| chr13:20571463 | C | CTT | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
82 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.-6-2916_-6-2915dup others(2): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 20571463 | ||||||
| chr13:20571505 | T | C | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6-2875T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20571505 | |||||||
| chr13:20571744 | G | C | 3 | a0006c0007t0001g0232 a0006c0007t0001g0233 a0006c0007t0001g0234 |
3 | HG00639.hp1 HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-6-2636G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20571744 | |||||||
| chr13:20571776 | G | T | 4 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
4 | HG02630.hp1 HG02818.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-2604G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20571776 | |||||||
| chr13:20571949 | T | A | 4 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(1): Show |
4 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-2431T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20571949 | |||||||
| chr13:20572037 | C | CT | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.-6-2336dupT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 20572037 | ||||||
| chr13:20572093 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(161): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-6-2287A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20572093 | |||||||
| chr13:20572359 | C | G | 1 | a0001c0001t0001g0274 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-6-2021C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20572359 | |||||||
| chr13:20572369 | C | A | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(1): Show |
4 | HG02523.hp2 NA18955.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-2011C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20572369 | |||||||
| chr13:20572572 | C | T | 3 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 |
3 | HG02717.hp2 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-6-1808C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20572572 | |||||||
| chr13:20572589 | G | A | 7 | a0004c0005t0001g0163 a0004c0005t0001g0164 a0004c0005t0001g0165 others(4): Show |
7 | HG00735.hp2 HG02257.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6-1791G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20572589 | |||||||
| chr13:20572753 | T | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 |
3 | HG01099.hp1 HG01261.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-6-1627T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20572753 | |||||||
| chr13:20572777 | TC | T | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6-1600delC | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 20572777 | ||||||
| chr13:20572905 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(95): Show |
99 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.-6-1475C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20572905 | |||||||
| chr13:20573169 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-6-1211C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20573169 | |||||||
| chr13:20573264 | G | C | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6-1116G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20573264 | |||||||
| chr13:20573277 | ACCAGTGA others(13): Show |
A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(153): Show |
157 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.-6-1102_-6-1083del others(20): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20573277 | |||||||
| chr13:20573945 | T | G | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-435T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20573945 | |||||||
| chr13:20574269 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(90): Show |
94 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.-6-111G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20574269 | |||||||
| chr13:20574340 | C | T | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-40C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 1/25 | chr13 | 20574340 | |||||||
| chr13:20574912 | G | A | 1 | a0002c0010t0001g0115 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.90+437G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20574912 | |||||||
| chr13:20575065 | GT | G | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.90+601delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20575065 | ||||||
| chr13:20575249 | A | G | 1 | a0001c0004t0001g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.90+774A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20575249 | |||||||
| chr13:20575489 | T | C | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.90+1014T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20575489 | |||||||
| chr13:20575869 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 |
3 | HG01099.hp1 HG01261.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.90+1394G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20575869 | |||||||
| chr13:20575883 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.90+1408C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20575883 | |||||||
| chr13:20576221 | G | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.90+1746G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20576221 | |||||||
| chr13:20576222 | AT | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.90+1753delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20576222 | ||||||
| chr13:20576306 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.90+1831C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20576306 | |||||||
| chr13:20576908 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.90+2433T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20576908 | |||||||
| chr13:20577150 | T | G | 1 | a0001c0001t0001g0240 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.90+2675T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20577150 | |||||||
| chr13:20577178 | A | G | 8 | a0001c0004t0001g0008 a0001c0004t0001g0009 a0001c0004t0001g0010 others(5): Show |
8 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.90+2703A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20577178 | |||||||
| chr13:20577190 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.90+2715T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20577190 | |||||||
| chr13:20577297 | A | G | 1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.90+2822A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20577297 | |||||||
| chr13:20577483 | A | C | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.90+3008A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20577483 | |||||||
| chr13:20577672 | G | C | 14 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0007 others(11): Show |
17 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.90+3197G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20577672 | |||||||
| chr13:20577784 | A | G | 1 | a0001c0001t0001g0229 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.90+3309A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20577784 | |||||||
| chr13:20577857 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.90+3382C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20577857 | |||||||
| chr13:20577983 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.90+3508G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20577983 | |||||||
| chr13:20578034 | C | CTTTTTTT others(3): Show |
1 | a0001c0004t0001g0095 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.90+3578_90+3587dup others(10): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20578034 | ||||||
| chr13:20578034 | C | CTTTTTTT others(4): Show |
2 | a0001c0004t0001g0009 a0001c0004t0001g0110 |
2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.90+3577_90+3587dup others(11): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20578034 | ||||||
| chr13:20578034 | C | CTTTTTTT others(5): Show |
2 | a0001c0004t0001g0010 a0001c0004t0001g0011 |
2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.90+3576_90+3587dup others(12): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20578034 | ||||||
| chr13:20578034 | C | CTTTTTTT others(9): Show |
1 | a0005c0006t0001g0173 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.90+3572_90+3587dup others(16): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20578034 | ||||||
| chr13:20578034 | C | CTTTTTTT others(10): Show |
1 | a0005c0006t0001g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.90+3571_90+3587dup others(17): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20578034 | ||||||
| chr13:20578034 | C | CTTTTTTT others(11): Show |
1 | a0005c0006t0001g0175 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.90+3570_90+3587dup others(18): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20578034 | ||||||
| chr13:20578034 | C | CTTTTTTT others(17): Show |
1 | a0005c0006t0001g0174 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.90+3564_90+3587dup others(24): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20578034 | ||||||
| chr13:20578034 | C | CTTTTTTT others(23): Show |
1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.90+3587_90+3588ins others(30): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20578034 | ||||||
| chr13:20578034 | CT | C | 10 | a0001c0001t0001g0004 a0001c0001t0001g0077 a0001c0001t0001g0190 others(7): Show |
10 | HG00140.hp2 HG01978.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.90+3587delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20578034 | ||||||
| chr13:20578034 | CTT | C | 29 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0085 others(26): Show |
29 | HG00323.hp1 HG00621.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.90+3586_90+3587del others(2): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20578034 | ||||||
| chr13:20578034 | CTTT | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.90+3585_90+3587del others(3): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20578034 | ||||||
| chr13:20578034 | CTTTTTTT | C | 14 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0007 others(11): Show |
17 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.90+3581_90+3587del others(7): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20578034 | ||||||
| chr13:20578034 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0053 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.90+3578_90+3587del others(10): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20578034 | ||||||
| chr13:20578034 | CTTTTTTT others(6): Show |
C | 21 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(18): Show |
21 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.90+3575_90+3587del others(13): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20578034 | ||||||
| chr13:20578094 | G | A | 19 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0007 others(16): Show |
22 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.90+3619G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20578094 | |||||||
| chr13:20578284 | T | C | 14 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0007 others(11): Show |
17 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.90+3809T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20578284 | |||||||
| chr13:20578293 | C | T | 1 | a0004c0005t0001g0169 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.90+3818C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20578293 | |||||||
| chr13:20578329 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.90+3854G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20578329 | |||||||
| chr13:20578358 | C | CT | 13 | a0001c0001t0001g0014 a0001c0001t0001g0077 a0001c0001t0001g0078 others(10): Show |
14 | HG02723.hp2 HG02738.hp2 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.90+3906dupT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20578358 | ||||||
| chr13:20578358 | CT | C | 37 | a0001c0001t0001g0118 a0001c0001t0001g0184 a0001c0001t0001g0241 others(34): Show |
39 | HG00280.hp1 HG00733.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.90+3906delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20578358 | ||||||
| chr13:20578468 | T | C | 5 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.90+3993T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20578468 | |||||||
| chr13:20578642 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.90+4167T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20578642 | |||||||
| chr13:20578643 | G | C | 1 | a0001c0001t0001g0077 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.90+4168G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20578643 | |||||||
| chr13:20578644 | G | A | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.90+4169G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20578644 | |||||||
| chr13:20578838 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.91-4119C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20578838 | |||||||
| chr13:20578848 | C | T | 1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.91-4109C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20578848 | |||||||
| chr13:20579198 | G | A | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.91-3759G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20579198 | |||||||
| chr13:20579293 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.91-3664A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20579293 | |||||||
| chr13:20579331 | T | G | 2 | a0002c0002t0001g0112 a0002c0002t0001g0113 |
2 | HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.91-3626T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20579331 | |||||||
| chr13:20579400 | G | A | 8 | a0001c0004t0001g0008 a0001c0004t0001g0009 a0001c0004t0001g0010 others(5): Show |
8 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.91-3557G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20579400 | |||||||
| chr13:20579526 | G | T | 8 | a0001c0001t0001g0162 a0004c0005t0001g0163 a0004c0005t0001g0164 others(5): Show |
8 | HG00735.hp2 HG02257.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.91-3431G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20579526 | |||||||
| chr13:20579762 | C | T | 2 | a0001c0001t0001g0080 a0003c0003t0001g0147 |
2 | HG00741.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.91-3195C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20579762 | |||||||
| chr13:20580073 | A | G | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.91-2884A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20580073 | |||||||
| chr13:20580177 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.91-2780A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20580177 | |||||||
| chr13:20580249 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.91-2708G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20580249 | |||||||
| chr13:20580459 | GTGAGCCA others(19): Show |
G | 1 | a0001c0001t0004g0242 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.91-2471_91-2446del others(26): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20580459 | ||||||
| chr13:20580485 | A | G | 2 | a0001c0001t0001g0297 a0001c0001t0001g0299 |
2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.91-2472A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20580485 | |||||||
| chr13:20580724 | C | CT | 17 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0227 others(14): Show |
20 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.91-2214dupT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20580724 | ||||||
| chr13:20580724 | CTTTTTTT others(3): Show |
C | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.91-2223_91-2214del others(10): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20580724 | ||||||
| chr13:20580726 | T | TTC | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.91-2230_91-2229ins others(2): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20580726 | ||||||
| chr13:20580727 | T | TC | 18 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(15): Show |
18 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.91-2230_91-2229ins others(1): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20580727 | |||||||
| chr13:20580728 | T | C | 1 | a0002c0002t0001g0157 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.91-2229T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20580728 | |||||||
| chr13:20580772 | G | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.91-2185G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20580772 | |||||||
| chr13:20580811 | C | T | 1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.91-2146C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20580811 | |||||||
| chr13:20580812 | G | A | 5 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.91-2145G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20580812 | |||||||
| chr13:20580870 | C | T | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.91-2087C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20580870 | |||||||
| chr13:20581019 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 |
3 | HG01099.hp1 HG01261.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.91-1938C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20581019 | |||||||
| chr13:20581105 | A | G | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-1852A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20581105 | |||||||
| chr13:20581164 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.91-1793T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20581164 | |||||||
| chr13:20581524 | G | T | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.91-1433G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20581524 | |||||||
| chr13:20581537 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.91-1420G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20581537 | |||||||
| chr13:20581558 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.91-1399A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20581558 | |||||||
| chr13:20581559 | T | C | 1 | a0005c0006t0001g0173 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.91-1398T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20581559 | |||||||
| chr13:20581688 | TA | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(103): Show |
107 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.91-1262delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20581688 | ||||||
| chr13:20581694 | A | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(103): Show |
107 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.91-1263A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20581694 | |||||||
| chr13:20581761 | G | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(103): Show |
107 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.91-1196G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20581761 | |||||||
| chr13:20581807 | C | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.91-1150C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20581807 | |||||||
| chr13:20581823 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.91-1134A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20581823 | |||||||
| chr13:20581846 | C | G | 14 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0007 others(11): Show |
17 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.91-1111C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20581846 | |||||||
| chr13:20581852 | CA | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(131): Show |
135 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.91-1087delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20581852 | ||||||
| chr13:20581852 | CAA | C | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.91-1088_91-1087del others(2): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20581852 | ||||||
| chr13:20581896 | G | C | 5 | a0002c0002t0001g0007 a0002c0002t0001g0290 a0002c0002t0001g0291 others(2): Show |
6 | HG02723.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-1061G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20581896 | |||||||
| chr13:20582000 | A | G | 19 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0007 others(16): Show |
22 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.91-957A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20582000 | |||||||
| chr13:20582077 | A | G | 21 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(18): Show |
21 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.91-880A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20582077 | |||||||
| chr13:20582083 | CAG | C | 7 | a0004c0005t0001g0163 a0004c0005t0001g0164 a0004c0005t0001g0165 others(4): Show |
7 | HG00735.hp2 HG02257.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.91-871_91-870delAG | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 20582083 | ||||||
| chr13:20582364 | T | C | 14 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0007 others(11): Show |
17 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.91-593T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20582364 | |||||||
| chr13:20582433 | C | T | 2 | a0002c0002t0001g0112 a0002c0002t0001g0113 |
2 | HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.91-524C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20582433 | |||||||
| chr13:20582434 | G | A | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 |
3 | HG00673.hp2 HG02080.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.91-523G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20582434 | |||||||
| chr13:20582579 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.91-378G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20582579 | |||||||
| chr13:20582607 | G | C | 19 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0007 others(16): Show |
22 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.91-350G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20582607 | |||||||
| chr13:20582860 | G | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.91-97G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 2/25 | chr13 | 20582860 | |||||||
| chr13:20583118 | GA | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.153+100delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20583118 | |||||||
| chr13:20583185 | A | G | 7 | a0001c0001t0001g0237 a0001c0001t0001g0243 a0001c0001t0001g0270 others(4): Show |
7 | HG00621.hp1 NA18952.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.153+166A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20583185 | |||||||
| chr13:20583240 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.153+221T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20583240 | |||||||
| chr13:20583294 | C | T | 8 | a0001c0004t0001g0008 a0001c0004t0001g0009 a0001c0004t0001g0010 others(5): Show |
8 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.153+275C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20583294 | |||||||
| chr13:20583305 | G | C | 1 | a0001c0001t0001g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.153+286G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20583305 | |||||||
| chr13:20583347 | T | A | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.153+328T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20583347 | |||||||
| chr13:20583632 | G | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.153+613G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20583632 | |||||||
| chr13:20583730 | T | C | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.153+711T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20583730 | |||||||
| chr13:20583776 | G | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.153+757G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20583776 | |||||||
| chr13:20583884 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.153+865C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20583884 | |||||||
| chr13:20584156 | T | TAA | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(230): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.153+1148_153+1149d others(4): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 20584156 | ||||||
| chr13:20584156 | TA | T | 14 | a0002c0002t0001g0148 a0002c0002t0001g0149 a0002c0002t0001g0150 others(11): Show |
14 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.153+1149delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 20584156 | ||||||
| chr13:20584169 | T | A | 3 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 |
3 | HG02559.hp1 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.153+1150T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20584169 | |||||||
| chr13:20584676 | A | G | 1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.153+1657A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20584676 | |||||||
| chr13:20584698 | A | G | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.153+1679A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20584698 | |||||||
| chr13:20584793 | A | C | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.153+1774A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20584793 | |||||||
| chr13:20584800 | A | G | 4 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(1): Show |
4 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+1781A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20584800 | |||||||
| chr13:20584811 | G | A | 1 | a0001c0001t0001g0021 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.153+1792G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20584811 | |||||||
| chr13:20584814 | G | A | 8 | a0001c0001t0001g0162 a0004c0005t0001g0163 a0004c0005t0001g0164 others(5): Show |
8 | HG00735.hp2 HG02257.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.153+1795G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20584814 | |||||||
| chr13:20584861 | A | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.153+1842A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20584861 | |||||||
| chr13:20584897 | G | A | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.153+1878G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20584897 | |||||||
| chr13:20584971 | C | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(236): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.153+1952C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20584971 | |||||||
| chr13:20585036 | T | C | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.153+2017T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20585036 | |||||||
| chr13:20585061 | G | A | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
125 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.153+2042G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20585061 | |||||||
| chr13:20585114 | T | C | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+2095T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20585114 | |||||||
| chr13:20585247 | T | C | 1 | a0004c0005t0001g0168 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.153+2228T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20585247 | |||||||
| chr13:20585304 | C | G | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG01081.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.153+2285C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20585304 | |||||||
| chr13:20585316 | A | G | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG00140.hp1 HG00639.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.153+2297A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20585316 | |||||||
| chr13:20585419 | G | A | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.153+2400G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20585419 | |||||||
| chr13:20585579 | C | T | 2 | a0001c0004t0001g0010 a0001c0004t0001g0011 |
2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.153+2560C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20585579 | |||||||
| chr13:20585988 | A | G | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.153+2969A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20585988 | |||||||
| chr13:20586056 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.153+3037C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20586056 | |||||||
| chr13:20586090 | A | G | 3 | a0006c0007t0001g0232 a0006c0007t0001g0233 a0006c0007t0001g0234 |
3 | HG00639.hp1 HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.153+3071A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20586090 | |||||||
| chr13:20586353 | C | A | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.153+3334C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20586353 | |||||||
| chr13:20586510 | C | T | 1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.154-3301C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20586510 | |||||||
| chr13:20586542 | T | TA | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.154-3269_154-3268i others(3): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20586542 | |||||||
| chr13:20586564 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.154-3247A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20586564 | |||||||
| chr13:20586907 | A | AT | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.154-2896dupT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 20586907 | ||||||
| chr13:20586907 | A | T | 1 | a0001c0001t0001g0096 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.154-2904A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20586907 | |||||||
| chr13:20587160 | C | T | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-2651C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20587160 | |||||||
| chr13:20587254 | C | CT | 27 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(24): Show |
30 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.154-2546dupT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 20587254 | ||||||
| chr13:20587340 | G | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.154-2471G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20587340 | |||||||
| chr13:20587353 | G | T | 1 | a0001c0001t0001g0269 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.154-2458G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20587353 | |||||||
| chr13:20587362 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.154-2449A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20587362 | |||||||
| chr13:20587367 | C | A | 1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.154-2444C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20587367 | |||||||
| chr13:20587454 | C | T | 14 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0007 others(11): Show |
17 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.154-2357C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20587454 | |||||||
| chr13:20587585 | G | A | 2 | a0002c0002t0001g0287 a0002c0002t0001g0289 |
2 | HG00099.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.154-2226G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20587585 | |||||||
| chr13:20587605 | C | G | 1 | a0001c0001t0001g0223 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.154-2206C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20587605 | |||||||
| chr13:20587751 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.154-2060A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20587751 | |||||||
| chr13:20587863 | T | G | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.154-1948T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20587863 | |||||||
| chr13:20587877 | G | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.154-1934G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20587877 | |||||||
| chr13:20587933 | A | G | 1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.154-1878A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20587933 | |||||||
| chr13:20587996 | CT | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.154-1801delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 20587996 | ||||||
| chr13:20587996 | CTT | C | 7 | a0001c0001t0001g0170 a0004c0005t0001g0163 a0004c0005t0001g0164 others(4): Show |
7 | HG00735.hp2 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-1802_154-1801d others(4): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 20587996 | ||||||
| chr13:20588011 | CCTGGCTC others(18): Show |
C | 1 | a0003c0003t0001g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.154-1797_154-1773d others(27): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 20588011 | ||||||
| chr13:20588063 | G | T | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.154-1748G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20588063 | |||||||
| chr13:20588319 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.154-1492A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20588319 | |||||||
| chr13:20588370 | G | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.154-1441G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20588370 | |||||||
| chr13:20588477 | A | C | 1 | a0001c0001t0001g0067 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.154-1334A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20588477 | |||||||
| chr13:20588504 | T | G | 1 | a0002c0010t0001g0116 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.154-1307T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20588504 | |||||||
| chr13:20588801 | C | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(103): Show |
107 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.154-1010C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20588801 | |||||||
| chr13:20588934 | G | A | 7 | a0001c0004t0001g0008 a0001c0004t0001g0009 a0001c0004t0001g0010 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-877G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20588934 | |||||||
| chr13:20588995 | G | A | 1 | a0001c0001t0001g0249 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.154-816G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20588995 | |||||||
| chr13:20589375 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.154-436T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20589375 | |||||||
| chr13:20589589 | A | G | 3 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 |
3 | HG02717.hp2 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.154-222A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20589589 | |||||||
| chr13:20589662 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.154-149C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20589662 | |||||||
| chr13:20589719 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.154-92A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 3/25 | chr13 | 20589719 | |||||||
| chr13:20590111 | G | T | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.210+244G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 4/25 | chr13 | 20590111 | |||||||
| chr13:20590136 | A | G | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.210+269A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 4/25 | chr13 | 20590136 | |||||||
| chr13:20590315 | T | G | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.210+448T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 4/25 | chr13 | 20590315 | |||||||
| chr13:20590341 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.210+474C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 4/25 | chr13 | 20590341 | |||||||
| chr13:20590374 | G | T | 1 | a0001c0001t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.210+507G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 4/25 | chr13 | 20590374 | |||||||
| chr13:20590448 | T | C | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.211-519T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 4/25 | chr13 | 20590448 | |||||||
| chr13:20590551 | C | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.211-416C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 4/25 | chr13 | 20590551 | |||||||
| chr13:20590593 | T | G | 8 | a0001c0004t0001g0008 a0001c0004t0001g0009 a0001c0004t0001g0010 others(5): Show |
8 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.211-374T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 4/25 | chr13 | 20590593 | |||||||
| chr13:20590675 | G | A | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-292G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 4/25 | chr13 | 20590675 | |||||||
| chr13:20590834 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.211-133G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 4/25 | chr13 | 20590834 | |||||||
| chr13:20591150 | CT | C | 14 | a0002c0002t0001g0148 a0002c0002t0001g0149 a0002c0002t0001g0150 others(11): Show |
14 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.264+133delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr13 | 20591150 | ||||||
| chr13:20591153 | T | A | 14 | a0002c0002t0001g0148 a0002c0002t0001g0149 a0002c0002t0001g0150 others(11): Show |
14 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.264+133T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 5/25 | chr13 | 20591153 | |||||||
| chr13:20591882 | T | C | 1 | a0001c0001t0001g0250 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.328+201T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 6/25 | chr13 | 20591882 | |||||||
| chr13:20591898 | A | T | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.328+217A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 6/25 | chr13 | 20591898 | |||||||
| chr13:20591969 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.328+288G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 6/25 | chr13 | 20591969 | |||||||
| chr13:20591978 | A | G | 1 | a0002c0002t0001g0156 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.328+297A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 6/25 | chr13 | 20591978 | |||||||
| chr13:20592126 | A | G | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | HG01243.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.329-209A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 6/25 | chr13 | 20592126 | |||||||
| chr13:20592443 | G | A | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.398+39G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20592443 | |||||||
| chr13:20592748 | G | A | 55 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(52): Show |
55 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.398+344G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20592748 | |||||||
| chr13:20592768 | T | G | 1 | a0001c0001t0001g0100 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.398+364T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20592768 | |||||||
| chr13:20592773 | T | TAATTACA others(21): Show |
19 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(16): Show |
19 | HG00408.hp2 HG02071.hp1 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.398+388_398+415dup others(28): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr13 | 20592773 | ||||||
| chr13:20592922 | T | TTA | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.398+518_398+519ins others(2): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20592922 | |||||||
| chr13:20592925 | C | A | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.398+521C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20592925 | |||||||
| chr13:20592926 | C | A | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.398+522C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20592926 | |||||||
| chr13:20592927 | A | T | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.398+523A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20592927 | |||||||
| chr13:20592928 | T | A | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.398+524T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20592928 | |||||||
| chr13:20593191 | A | G | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.398+787A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20593191 | |||||||
| chr13:20593471 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.398+1067G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20593471 | |||||||
| chr13:20593600 | T | G | 3 | a0006c0007t0001g0232 a0006c0007t0001g0233 a0006c0007t0001g0234 |
3 | HG00639.hp1 HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.398+1196T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20593600 | |||||||
| chr13:20593604 | T | C | 14 | a0002c0002t0001g0148 a0002c0002t0001g0149 a0002c0002t0001g0150 others(11): Show |
14 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.398+1200T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20593604 | |||||||
| chr13:20593669 | A | G | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.398+1265A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20593669 | |||||||
| chr13:20593683 | G | A | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.398+1279G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20593683 | |||||||
| chr13:20593703 | A | G | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.398+1299A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20593703 | |||||||
| chr13:20593896 | A | T | 4 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(1): Show |
4 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.398+1492A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20593896 | |||||||
| chr13:20593986 | A | G | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(291): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.398+1582A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20593986 | |||||||
| chr13:20594062 | T | TA | 29 | a0001c0001t0001g0074 a0001c0001t0001g0080 a0001c0001t0001g0118 others(26): Show |
29 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.398+1672dupA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr13 | 20594062 | ||||||
| chr13:20594062 | TA | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0065 a0001c0001t0001g0109 others(6): Show |
9 | HG01169.hp2 HG02647.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.398+1672delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr13 | 20594062 | ||||||
| chr13:20594273 | A | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.398+1869A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20594273 | |||||||
| chr13:20594283 | T | C | 1 | a0002c0002t0001g0288 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.399-1867T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20594283 | |||||||
| chr13:20594354 | G | C | 55 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(52): Show |
55 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.399-1796G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20594354 | |||||||
| chr13:20594553 | A | T | 1 | a0002c0002t0001g0293 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.399-1597A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20594553 | |||||||
| chr13:20594964 | G | A | 1 | a0002c0002t0001g0148 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.399-1186G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20594964 | |||||||
| chr13:20595034 | GT | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(96): Show |
100 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.399-1115delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20595034 | |||||||
| chr13:20595035 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.399-1115T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20595035 | |||||||
| chr13:20595067 | A | G | 1 | a0001c0001t0001g0272 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.399-1083A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20595067 | |||||||
| chr13:20595209 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(96): Show |
100 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.399-941A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20595209 | |||||||
| chr13:20595222 | C | T | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.399-928C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20595222 | |||||||
| chr13:20595469 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.399-681T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20595469 | |||||||
| chr13:20595556 | C | T | 55 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(52): Show |
55 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.399-594C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20595556 | |||||||
| chr13:20595581 | C | T | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.399-569C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20595581 | |||||||
| chr13:20595647 | A | G | 1 | a0003c0003t0001g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.399-503A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20595647 | |||||||
| chr13:20595667 | C | T | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.399-483C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20595667 | |||||||
| chr13:20595739 | C | G | 7 | a0002c0002t0001g0148 a0002c0002t0001g0152 a0002c0002t0001g0153 others(4): Show |
7 | HG00741.hp1 HG01069.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.399-411C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20595739 | |||||||
| chr13:20595742 | T | C | 2 | a0001c0004t0001g0010 a0001c0004t0001g0011 |
2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.399-408T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20595742 | |||||||
| chr13:20595779 | C | T | 7 | a0002c0002t0001g0148 a0002c0002t0001g0152 a0002c0002t0001g0153 others(4): Show |
7 | HG00741.hp1 HG01069.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.399-371C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | chr13 | 20595779 | |||||||
| chr13:20596054 | G | GTAAAA | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.399-66_399-62dupAT others(3): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr13 | 20596054 | ||||||
| chr13:20596054 | G | GTAAAATA others(3): Show |
11 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0118 others(8): Show |
11 | HG01081.hp1 HG01358.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.399-71_399-62dupAT others(8): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr13 | 20596054 | ||||||
| chr13:20596304 | T | C | 1 | a0002c0002t0001g0283 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.489+64T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 8/25 | chr13 | 20596304 | |||||||
| chr13:20596309 | C | T | 5 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0298 others(2): Show |
5 | HG02615.hp1 HG02809.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+69C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 8/25 | chr13 | 20596309 | |||||||
| chr13:20596420 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.489+180A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 8/25 | chr13 | 20596420 | |||||||
| chr13:20596451 | C | T | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(291): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.489+211C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 8/25 | chr13 | 20596451 | |||||||
| chr13:20596461 | A | AG | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+224dupG | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr13 | 20596461 | ||||||
| chr13:20596530 | A | G | 59 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(56): Show |
62 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.489+290A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 8/25 | chr13 | 20596530 | |||||||
| chr13:20596577 | G | A | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.489+337G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 8/25 | chr13 | 20596577 | |||||||
| chr13:20596890 | CAG | C | 3 | a0003c0003t0001g0124 a0007c0008t0001g0159 a0007c0008t0001g0160 |
3 | HG02572.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.490-124_490-123del others(2): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 8/25 | chr13 | 20596890 | |||||||
| chr13:20596979 | C | T | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-36C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 8/25 | chr13 | 20596979 | |||||||
| chr13:20597186 | T | G | 1 | a0001c0001t0001g0076 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.594+67T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597186 | |||||||
| chr13:20597299 | C | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(127): Show |
131 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.594+180C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597299 | |||||||
| chr13:20597360 | A | G | 1 | a0003c0003t0001g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.594+241A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597360 | |||||||
| chr13:20597427 | T | C | 7 | a0001c0001t0001g0275 a0001c0001t0001g0277 a0001c0004t0001g0009 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.594+308T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597427 | |||||||
| chr13:20597473 | C | A | 1 | a0001c0001t0001g0189 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.594+354C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597473 | |||||||
| chr13:20597473 | C | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(93): Show |
100 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.594+354C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597473 | |||||||
| chr13:20597473 | C | T | 1 | a0003c0003t0001g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.594+354C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597473 | |||||||
| chr13:20597482 | C | T | 76 | a0001c0001t0001g0118 a0001c0001t0001g0162 a0001c0001t0001g0170 others(73): Show |
76 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.594+363C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597482 | |||||||
| chr13:20597510 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | NA18970.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.594+391C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597510 | |||||||
| chr13:20597515 | C | T | 1 | a0006c0007t0001g0234 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.594+396C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597515 | |||||||
| chr13:20597560 | T | C | 3 | a0001c0001t0001g0170 a0001c0004t0001g0008 a0001c0004t0001g0012 |
3 | HG02109.hp2 HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.594+441T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597560 | |||||||
| chr13:20597601 | G | A | 10 | a0001c0001t0001g0241 a0001c0001t0001g0252 a0001c0001t0001g0253 others(7): Show |
10 | HG01884.hp2 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.594+482G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597601 | |||||||
| chr13:20597603 | G | T | 1 | a0001c0001t0001g0266 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.594+484G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597603 | |||||||
| chr13:20597604 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.594+485T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597604 | |||||||
| chr13:20597612 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 |
3 | HG01099.hp1 HG01261.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.594+493C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597612 | |||||||
| chr13:20597629 | A | G | 8 | a0001c0001t0001g0070 a0002c0002t0001g0005 a0002c0002t0001g0006 others(5): Show |
10 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.594+510A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597629 | |||||||
| chr13:20597636 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.594+517T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597636 | |||||||
| chr13:20597646 | G | A | 148 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(145): Show |
148 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.594+527G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597646 | |||||||
| chr13:20597647 | A | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0170 |
2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.594+528A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597647 | |||||||
| chr13:20597669 | G | A | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(275): Show |
282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.594+550G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597669 | |||||||
| chr13:20597684 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.594+565C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597684 | |||||||
| chr13:20597685 | G | A | 8 | a0003c0003t0001g0126 a0003c0003t0001g0127 a0003c0003t0001g0128 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.594+566G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597685 | |||||||
| chr13:20597693 | A | G | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(291): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.594+574A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597693 | |||||||
| chr13:20597733 | G | A | 22 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0124 others(19): Show |
22 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.594+614G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597733 | |||||||
| chr13:20597745 | C | CAA | 22 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(19): Show |
22 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.594+635_594+636dup others(2): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr13 | 20597745 | ||||||
| chr13:20597754 | A | AAAATAT | 21 | a0003c0003t0001g0120 a0003c0003t0001g0122 a0003c0003t0001g0124 others(18): Show |
21 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.594+636_594+637ins others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr13 | 20597754 | ||||||
| chr13:20597754 | A | AAT | 5 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(2): Show |
5 | HG01169.hp2 HG02683.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+650_594+651dup others(2): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr13 | 20597754 | ||||||
| chr13:20597754 | A | AATATATA others(15): Show |
4 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(1): Show |
4 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+651_594+652ins others(22): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr13 | 20597754 | ||||||
| chr13:20597754 | A | AT | 4 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0001g0227 others(1): Show |
4 | HG01978.hp2 HG02071.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.594+635_594+636ins others(1): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597754 | |||||||
| chr13:20597754 | A | ATAT | 4 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
4 | HG00408.hp2 NA18951.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+635_594+636ins others(3): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597754 | |||||||
| chr13:20597754 | A | T | 13 | a0001c0001t0001g0212 a0001c0001t0001g0241 a0001c0001t0001g0252 others(10): Show |
13 | HG01884.hp2 HG02630.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.594+635A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597754 | |||||||
| chr13:20597756 | T | A | 11 | a0001c0001t0001g0025 a0001c0001t0001g0091 a0001c0001t0001g0092 others(8): Show |
11 | HG01243.hp2 HG02559.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.594+637T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597756 | |||||||
| chr13:20597762 | T | C | 2 | a0001c0004t0001g0095 a0001c0004t0001g0110 |
2 | HG02055.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.594+643T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597762 | |||||||
| chr13:20597769 | A | T | 1 | a0001c0001t0001g0052 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.594+650A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597769 | |||||||
| chr13:20597771 | T | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.594+652T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597771 | |||||||
| chr13:20597773 | T | A | 37 | a0001c0001t0001g0118 a0001c0001t0001g0213 a0001c0001t0001g0214 others(34): Show |
37 | HG00408.hp2 HG00741.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.594+654T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597773 | |||||||
| chr13:20597788 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.594+669G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20597788 | |||||||
| chr13:20598195 | C | T | 9 | a0001c0001t0001g0241 a0001c0001t0001g0252 a0001c0001t0001g0254 others(6): Show |
9 | HG01884.hp2 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.595-456C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20598195 | |||||||
| chr13:20598215 | ATAAAT | A | 3 | a0002c0002t0001g0006 a0002c0002t0001g0287 a0002c0002t0001g0289 |
4 | HG00099.hp1 HG00733.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.595-432_595-428del others(5): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr13 | 20598215 | ||||||
| chr13:20598259 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.595-392A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20598259 | |||||||
| chr13:20598273 | G | T | 49 | a0001c0004t0001g0111 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.595-378G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20598273 | |||||||
| chr13:20598303 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.595-348G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 9/25 | chr13 | 20598303 | |||||||
| chr13:20598768 | T | C | 1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.697+15T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 10/25 | chr13 | 20598768 | |||||||
| chr13:20599686 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.812+121C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20599686 | |||||||
| chr13:20599687 | G | A | 48 | a0002c0002t0001g0148 a0002c0002t0001g0149 a0002c0002t0001g0150 others(45): Show |
48 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.812+122G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20599687 | |||||||
| chr13:20599787 | A | G | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.812+222A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20599787 | |||||||
| chr13:20599835 | T | C | 2 | a0001c0001t0001g0270 a0001c0001t0001g0274 |
2 | HG00621.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.812+270T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20599835 | |||||||
| chr13:20599908 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.812+343C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20599908 | |||||||
| chr13:20599914 | C | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
109 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.812+349C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20599914 | |||||||
| chr13:20599973 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.812+408A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20599973 | |||||||
| chr13:20600072 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.812+507A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20600072 | |||||||
| chr13:20600105 | A | G | 1 | a0001c0001t0001g0060 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.812+540A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20600105 | |||||||
| chr13:20600344 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.812+779A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20600344 | |||||||
| chr13:20600388 | C | A | 1 | a0004c0005t0001g0168 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.812+823C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20600388 | |||||||
| chr13:20600506 | T | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(111): Show |
115 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.812+941T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20600506 | |||||||
| chr13:20600681 | G | T | 1 | a0001c0004t0001g0009 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.813-1024G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20600681 | |||||||
| chr13:20600716 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.813-989A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20600716 | |||||||
| chr13:20600719 | TA | T | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.813-982delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr13 | 20600719 | ||||||
| chr13:20600792 | C | A | 5 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.813-913C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20600792 | |||||||
| chr13:20600824 | C | T | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.813-881C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20600824 | |||||||
| chr13:20600826 | A | C | 14 | a0002c0002t0001g0148 a0002c0002t0001g0149 a0002c0002t0001g0150 others(11): Show |
14 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.813-879A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20600826 | |||||||
| chr13:20600859 | C | T | 1 | a0001c0004t0001g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.813-846C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20600859 | |||||||
| chr13:20601071 | A | T | 4 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(1): Show |
4 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.813-634A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20601071 | |||||||
| chr13:20601078 | C | G | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
121 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.813-627C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20601078 | |||||||
| chr13:20601194 | C | T | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.813-511C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20601194 | |||||||
| chr13:20601202 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.813-503C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20601202 | |||||||
| chr13:20601223 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.813-482C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20601223 | |||||||
| chr13:20601298 | A | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.813-407A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20601298 | |||||||
| chr13:20601300 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.813-405A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20601300 | |||||||
| chr13:20601365 | GAA | G | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.813-326_813-325del others(2): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr13 | 20601365 | ||||||
| chr13:20601607 | A | T | 4 | a0002c0002t0001g0149 a0002c0002t0001g0150 a0002c0002t0001g0151 others(1): Show |
4 | HG01074.hp2 HG01099.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.813-98A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20601607 | |||||||
| chr13:20601618 | C | T | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.813-87C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 11/25 | chr13 | 20601618 | |||||||
| chr13:20601975 | T | C | 4 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(1): Show |
4 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1041+42T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20601975 | |||||||
| chr13:20602128 | A | G | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1041+195A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20602128 | |||||||
| chr13:20602194 | TA | T | 5 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 others(2): Show |
5 | HG00597.hp2 HG00673.hp2 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.1041+263delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | INFO_REALIGN_3_PRIME | chr13 | 20602194 | ||||||
| chr13:20602206 | C | CT | 16 | a0001c0001t0001g0062 a0001c0001t0001g0191 a0001c0004t0001g0009 others(13): Show |
18 | HG00280.hp1 HG00733.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1041+293dupT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | INFO_REALIGN_3_PRIME | chr13 | 20602206 | ||||||
| chr13:20602206 | C | CTT | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.1041+292_1041+293d others(4): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | INFO_REALIGN_3_PRIME | chr13 | 20602206 | ||||||
| chr13:20602206 | C | CTTT | 21 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0081 others(18): Show |
21 | HG00673.hp2 HG02258.hp1 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.1041+291_1041+293d others(5): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | INFO_REALIGN_3_PRIME | chr13 | 20602206 | ||||||
| chr13:20602230 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(94): Show |
98 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1041+297A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20602230 | |||||||
| chr13:20602354 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1041+421G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20602354 | |||||||
| chr13:20602485 | A | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.1041+552A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20602485 | |||||||
| chr13:20602513 | C | T | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1041+580C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20602513 | |||||||
| chr13:20602745 | T | C | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1041+812T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20602745 | |||||||
| chr13:20602755 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1041+822C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20602755 | |||||||
| chr13:20602808 | G | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1041+875G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20602808 | |||||||
| chr13:20602836 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.1041+903T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20602836 | |||||||
| chr13:20603009 | A | G | 1 | a0003c0003t0001g0124 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1041+1076A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20603009 | |||||||
| chr13:20603012 | C | T | 1 | a0001c0001t0004g0242 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1041+1079C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20603012 | |||||||
| chr13:20603230 | C | T | 53 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(50): Show |
53 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.1041+1297C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20603230 | |||||||
| chr13:20603386 | C | CA | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1041+1470dupA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | INFO_REALIGN_3_PRIME | chr13 | 20603386 | ||||||
| chr13:20603386 | CA | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0024 others(68): Show |
72 | HG00673.hp1 HG00741.hp1 HG01069.hp1 others(69): Show |
intron_variant | MODIFIER | c.1041+1470delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | INFO_REALIGN_3_PRIME | chr13 | 20603386 | ||||||
| chr13:20603454 | C | T | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1041+1521C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20603454 | |||||||
| chr13:20603621 | C | T | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1042-1414C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20603621 | |||||||
| chr13:20603650 | C | T | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1042-1385C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20603650 | |||||||
| chr13:20603835 | C | T | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1042-1200C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20603835 | |||||||
| chr13:20603883 | G | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0282 |
2 | HG01192.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1042-1152G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20603883 | |||||||
| chr13:20604116 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1042-919T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20604116 | |||||||
| chr13:20604414 | G | A | 1 | a0001c0001t0004g0242 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1042-621G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20604414 | |||||||
| chr13:20604536 | T | G | 1 | a0001c0001t0003g0236 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1042-499T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20604536 | |||||||
| chr13:20604630 | T | A | 1 | a0001c0001t0001g0067 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1042-405T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20604630 | |||||||
| chr13:20604807 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1042-228T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20604807 | |||||||
| chr13:20604809 | G | A | 2 | a0003c0009t0001g0132 a0003c0009t0001g0133 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1042-226G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20604809 | |||||||
| chr13:20604834 | A | C | 1 | a0001c0001t0001g0052 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1042-201A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20604834 | |||||||
| chr13:20604835 | G | C | 1 | a0001c0001t0001g0052 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1042-200G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 12/25 | chr13 | 20604835 | |||||||
| chr13:20605166 | AG | A | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1112+62delG | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20605166 | |||||||
| chr13:20605256 | T | G | 1 | a0001c0001t0001g0294 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1112+151T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20605256 | |||||||
| chr13:20605552 | A | G | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1112+447A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20605552 | |||||||
| chr13:20605580 | G | A | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1112+475G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20605580 | |||||||
| chr13:20605610 | A | G | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1112+505A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20605610 | |||||||
| chr13:20605638 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1112+533C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20605638 | |||||||
| chr13:20605868 | G | A | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1112+763G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20605868 | |||||||
| chr13:20606025 | A | ATGAT | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1112+922_1112+925d others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr13 | 20606025 | ||||||
| chr13:20606108 | G | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
110 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1112+1003G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20606108 | |||||||
| chr13:20606201 | C | G | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1112+1096C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20606201 | |||||||
| chr13:20606430 | C | T | 2 | a0002c0010t0001g0115 a0002c0010t0001g0116 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1112+1325C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20606430 | |||||||
| chr13:20606437 | C | A | 1 | a0001c0001t0001g0052 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1112+1332C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20606437 | |||||||
| chr13:20606650 | G | A | 5 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1112+1545G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20606650 | |||||||
| chr13:20606681 | C | T | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1112+1576C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20606681 | |||||||
| chr13:20606729 | A | T | 1 | a0002c0002t0001g0114 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1112+1624A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20606729 | |||||||
| chr13:20607055 | G | T | 7 | a0004c0005t0001g0163 a0004c0005t0001g0164 a0004c0005t0001g0165 others(4): Show |
7 | HG00735.hp2 HG02257.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112+1950G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20607055 | |||||||
| chr13:20607068 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1112+1963C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20607068 | |||||||
| chr13:20607206 | C | CG | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 |
3 | HG00673.hp2 HG02080.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.1112+2102dupG | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr13 | 20607206 | ||||||
| chr13:20607275 | C | T | 3 | a0006c0007t0001g0232 a0006c0007t0001g0233 a0006c0007t0001g0234 |
3 | HG00639.hp1 HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1112+2170C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20607275 | |||||||
| chr13:20607471 | C | T | 1 | a0003c0003t0001g0141 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1112+2366C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20607471 | |||||||
| chr13:20607509 | TG | T | 11 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(8): Show |
11 | NA18747.hp1 NA18946.hp1 NA18948.hp2 others(8): Show |
intron_variant | MODIFIER | c.1112+2405delG | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20607509 | |||||||
| chr13:20607520 | C | A | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1112+2415C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20607520 | |||||||
| chr13:20607538 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1112+2433G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20607538 | |||||||
| chr13:20607542 | C | A | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1112+2437C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20607542 | |||||||
| chr13:20607561 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1112+2456A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20607561 | |||||||
| chr13:20608058 | C | A | 2 | a0001c0004t0001g0095 a0001c0004t0001g0110 |
2 | HG02055.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1112+2953C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20608058 | |||||||
| chr13:20608189 | G | A | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1112+3084G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20608189 | |||||||
| chr13:20608252 | C | T | 1 | a0002c0002t0001g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1112+3147C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20608252 | |||||||
| chr13:20608287 | C | T | 7 | a0004c0005t0001g0163 a0004c0005t0001g0164 a0004c0005t0001g0165 others(4): Show |
7 | HG00735.hp2 HG02257.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112+3182C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20608287 | |||||||
| chr13:20608316 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1112+3211G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20608316 | |||||||
| chr13:20608327 | G | A | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1112+3222G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20608327 | |||||||
| chr13:20608430 | C | G | 7 | a0004c0005t0001g0163 a0004c0005t0001g0164 a0004c0005t0001g0165 others(4): Show |
7 | HG00735.hp2 HG02257.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112+3325C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20608430 | |||||||
| chr13:20608471 | C | G | 1 | a0002c0002t0001g0148 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1112+3366C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20608471 | |||||||
| chr13:20608654 | A | G | 1 | a0001c0004t0001g0008 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1112+3549A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20608654 | |||||||
| chr13:20608655 | G | A | 1 | a0003c0003t0001g0147 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1112+3550G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20608655 | |||||||
| chr13:20608677 | C | T | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1112+3572C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20608677 | |||||||
| chr13:20608723 | C | G | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1112+3618C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20608723 | |||||||
| chr13:20608739 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1112+3634C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20608739 | |||||||
| chr13:20608794 | A | G | 1 | a0003c0003t0001g0124 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1112+3689A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20608794 | |||||||
| chr13:20608802 | A | G | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1112+3697A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20608802 | |||||||
| chr13:20608855 | C | T | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1112+3750C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20608855 | |||||||
| chr13:20608936 | G | A | 1 | a0002c0010t0001g0115 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1112+3831G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20608936 | |||||||
| chr13:20608965 | A | G | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1112+3860A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20608965 | |||||||
| chr13:20609051 | C | A | 1 | a0010c0012t0001g0192 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1112+3946C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20609051 | |||||||
| chr13:20609126 | C | T | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1112+4021C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20609126 | |||||||
| chr13:20609193 | G | A | 7 | a0004c0005t0001g0163 a0004c0005t0001g0164 a0004c0005t0001g0165 others(4): Show |
7 | HG00735.hp2 HG02257.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112+4088G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20609193 | |||||||
| chr13:20609266 | A | C | 1 | a0001c0001t0001g0300 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1112+4161A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20609266 | |||||||
| chr13:20609315 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1112+4210A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20609315 | |||||||
| chr13:20609459 | T | A | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1112+4354T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20609459 | |||||||
| chr13:20609642 | G | T | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1112+4537G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20609642 | |||||||
| chr13:20609704 | A | G | 11 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(8): Show |
11 | NA18747.hp1 NA18946.hp1 NA18948.hp2 others(8): Show |
intron_variant | MODIFIER | c.1112+4599A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20609704 | |||||||
| chr13:20609724 | A | G | 1 | a0001c0004t0001g0011 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1112+4619A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20609724 | |||||||
| chr13:20609765 | AAAAAAAC | A | 55 | a0001c0004t0001g0009 a0002c0002t0001g0061 a0002c0002t0001g0112 others(52): Show |
55 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.1112+4678_1112+468 others(11): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr13 | 20609765 | ||||||
| chr13:20610004 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1112+4899C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20610004 | |||||||
| chr13:20610092 | T | C | 1 | a0001c0001t0001g0027 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1112+4987T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20610092 | |||||||
| chr13:20610104 | G | GT | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.1112+5011dupT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr13 | 20610104 | ||||||
| chr13:20610104 | G | GTT | 29 | a0001c0001t0001g0118 a0001c0001t0001g0209 a0001c0001t0001g0210 others(26): Show |
29 | HG00735.hp2 HG02055.hp1 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.1112+5010_1112+501 others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr13 | 20610104 | ||||||
| chr13:20610327 | T | C | 9 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0283 others(6): Show |
11 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.1112+5222T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20610327 | |||||||
| chr13:20610336 | C | T | 9 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0283 others(6): Show |
11 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.1112+5231C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20610336 | |||||||
| chr13:20610383 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1112+5278G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20610383 | |||||||
| chr13:20610493 | C | T | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1113-5300C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20610493 | |||||||
| chr13:20610679 | CA | C | 42 | a0001c0001t0001g0004 a0001c0001t0001g0177 a0001c0001t0001g0188 others(39): Show |
43 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1113-5103delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr13 | 20610679 | ||||||
| chr13:20610795 | G | A | 6 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113-4998G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20610795 | |||||||
| chr13:20610804 | C | T | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113-4989C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20610804 | |||||||
| chr13:20610885 | T | G | 1 | a0001c0001t0001g0022 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1113-4908T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20610885 | |||||||
| chr13:20610889 | A | G | 10 | a0003c0003t0001g0134 a0003c0003t0001g0135 a0003c0003t0001g0136 others(7): Show |
10 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1113-4904A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20610889 | |||||||
| chr13:20611139 | A | G | 4 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0221 others(1): Show |
4 | NA18948.hp1 NA18950.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113-4654A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20611139 | |||||||
| chr13:20611157 | A | G | 5 | a0001c0001t0001g0187 a0001c0001t0001g0239 a0001c0001t0001g0249 others(2): Show |
5 | NA18942.hp1 NA18946.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113-4636A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20611157 | |||||||
| chr13:20611162 | C | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1113-4631C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20611162 | |||||||
| chr13:20611361 | C | T | 1 | a0005c0006t0001g0173 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1113-4432C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20611361 | |||||||
| chr13:20611371 | A | C | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113-4422A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20611371 | |||||||
| chr13:20611514 | CA | C | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
131 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.1113-4252delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr13 | 20611514 | ||||||
| chr13:20611514 | CAA | C | 6 | a0001c0001t0001g0177 a0001c0001t0001g0188 a0001c0001t0001g0202 others(3): Show |
6 | HG00323.hp1 HG00642.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113-4253_1113-425 others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr13 | 20611514 | ||||||
| chr13:20611514 | CAAAA | C | 20 | a0001c0001t0001g0025 a0001c0001t0001g0051 a0001c0001t0001g0062 others(17): Show |
20 | HG00408.hp1 HG01169.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1113-4255_1113-425 others(8): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr13 | 20611514 | ||||||
| chr13:20611514 | CAAAAA | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(82): Show |
86 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.1113-4256_1113-425 others(9): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr13 | 20611514 | ||||||
| chr13:20611514 | CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0263 a0002c0002t0001g0112 a0002c0002t0001g0113 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113-4259_1113-425 others(12): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr13 | 20611514 | ||||||
| chr13:20611587 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1113-4206C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20611587 | |||||||
| chr13:20611770 | A | C | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113-4023A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20611770 | |||||||
| chr13:20611869 | T | G | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(291): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1113-3924T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20611869 | |||||||
| chr13:20611970 | ATAAACT | A | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1113-3818_1113-381 others(10): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr13 | 20611970 | ||||||
| chr13:20612051 | T | C | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1113-3742T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20612051 | |||||||
| chr13:20612110 | T | TA | 34 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(31): Show |
34 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1113-3674dupA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr13 | 20612110 | ||||||
| chr13:20612114 | A | AAAAAAAT others(8): Show |
15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1113-3674_1113-367 others(19): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr13 | 20612114 | ||||||
| chr13:20612119 | A | G | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1113-3674A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20612119 | |||||||
| chr13:20612149 | A | T | 1 | a0002c0002t0001g0157 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1113-3644A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20612149 | |||||||
| chr13:20612219 | G | A | 6 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113-3574G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20612219 | |||||||
| chr13:20612287 | G | A | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113-3506G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20612287 | |||||||
| chr13:20612310 | G | T | 1 | a0002c0002t0001g0288 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1113-3483G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20612310 | |||||||
| chr13:20612811 | C | A | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1113-2982C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20612811 | |||||||
| chr13:20612866 | T | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1113-2927T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20612866 | |||||||
| chr13:20612996 | AAAG | A | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113-2792_1113-279 others(7): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr13 | 20612996 | ||||||
| chr13:20613169 | A | G | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1113-2624A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20613169 | |||||||
| chr13:20613252 | A | G | 1 | a0002c0002t0001g0154 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1113-2541A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20613252 | |||||||
| chr13:20613307 | A | G | 1 | a0001c0001t0001g0297 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1113-2486A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20613307 | |||||||
| chr13:20613405 | T | C | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1113-2388T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20613405 | |||||||
| chr13:20613413 | TATA | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
111 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1113-2375_1113-237 others(7): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr13 | 20613413 | ||||||
| chr13:20613543 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1113-2250A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20613543 | |||||||
| chr13:20613675 | CA | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(94): Show |
98 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1113-2115delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr13 | 20613675 | ||||||
| chr13:20613770 | G | A | 2 | a0001c0004t0001g0095 a0001c0004t0001g0110 |
2 | HG02055.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1113-2023G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20613770 | |||||||
| chr13:20613951 | A | ACAGAAAG others(10): Show |
294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(291): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1113-1842_1113-184 others(21): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20613951 | |||||||
| chr13:20613952 | T | G | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(291): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1113-1841T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20613952 | |||||||
| chr13:20614167 | A | G | 12 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(9): Show |
12 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1113-1626A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20614167 | |||||||
| chr13:20614200 | G | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(108): Show |
112 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1113-1593G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20614200 | |||||||
| chr13:20614314 | A | G | 3 | a0006c0007t0001g0232 a0006c0007t0001g0233 a0006c0007t0001g0234 |
3 | HG00639.hp1 HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1113-1479A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20614314 | |||||||
| chr13:20614514 | G | T | 1 | a0001c0001t0001g0191 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1113-1279G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20614514 | |||||||
| chr13:20614537 | C | G | 7 | a0004c0005t0001g0163 a0004c0005t0001g0164 a0004c0005t0001g0165 others(4): Show |
7 | HG00735.hp2 HG02257.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113-1256C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20614537 | |||||||
| chr13:20614651 | G | A | 6 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113-1142G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20614651 | |||||||
| chr13:20614658 | A | G | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1113-1135A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20614658 | |||||||
| chr13:20614716 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1113-1077T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20614716 | |||||||
| chr13:20614817 | C | CT | 42 | a0001c0001t0001g0118 a0001c0001t0001g0237 a0001c0001t0001g0238 others(39): Show |
42 | HG00597.hp2 HG00621.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.1113-960dupT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr13 | 20614817 | ||||||
| chr13:20614817 | C | CTTTTTTT | 83 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(80): Show |
84 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1113-966_1113-960d others(9): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr13 | 20614817 | ||||||
| chr13:20614817 | C | CTTTTTTT others(1): Show |
8 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(5): Show |
8 | HG01099.hp1 HG01261.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113-967_1113-960d others(10): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr13 | 20614817 | ||||||
| chr13:20614817 | C | CTTTTTTT others(4): Show |
1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1113-970_1113-960d others(13): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr13 | 20614817 | ||||||
| chr13:20614832 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1113-961T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20614832 | |||||||
| chr13:20614834 | G | T | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1113-959G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20614834 | |||||||
| chr13:20614836 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1113-957G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20614836 | |||||||
| chr13:20614839 | G | A | 1 | a0003c0009t0001g0132 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1113-954G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20614839 | |||||||
| chr13:20615001 | G | A | 6 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113-792G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20615001 | |||||||
| chr13:20615081 | C | T | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1113-712C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20615081 | |||||||
| chr13:20615111 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1113-682G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20615111 | |||||||
| chr13:20615187 | T | C | 8 | a0001c0001t0001g0162 a0004c0005t0001g0163 a0004c0005t0001g0164 others(5): Show |
8 | HG00735.hp2 HG02257.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113-606T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20615187 | |||||||
| chr13:20615247 | A | G | 2 | a0001c0004t0001g0095 a0001c0004t0001g0110 |
2 | HG02055.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1113-546A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20615247 | |||||||
| chr13:20615339 | G | A | 1 | a0006c0007t0001g0232 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1113-454G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20615339 | |||||||
| chr13:20615348 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(59): Show |
65 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1113-445T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20615348 | |||||||
| chr13:20615554 | A | G | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113-239A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20615554 | |||||||
| chr13:20615612 | C | T | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113-181C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20615612 | |||||||
| chr13:20615702 | T | C | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113-91T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20615702 | |||||||
| chr13:20615739 | C | T | 1 | a0002c0002t0001g0288 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1113-54C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20615739 | |||||||
| chr13:20615749 | T | C | 1 | a0004c0005t0001g0166 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1113-44T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 13/25 | chr13 | 20615749 | |||||||
| chr13:20615891 | A | G | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1199+12A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20615891 | |||||||
| chr13:20616006 | ATAT | A | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1199+129_1199+131d others(5): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr13 | 20616006 | ||||||
| chr13:20616084 | C | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1199+205C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20616084 | |||||||
| chr13:20616095 | A | T | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1199+216A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20616095 | |||||||
| chr13:20616405 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1199+526A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20616405 | |||||||
| chr13:20616704 | C | T | 2 | a0003c0003t0001g0141 a0003c0003t0001g0147 |
2 | HG01106.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1199+825C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20616704 | |||||||
| chr13:20616926 | T | A | 1 | a0002c0002t0001g0293 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1199+1047T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20616926 | |||||||
| chr13:20616935 | G | T | 1 | a0001c0001t0001g0052 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1199+1056G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20616935 | |||||||
| chr13:20616942 | T | G | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1199+1063T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20616942 | |||||||
| chr13:20617165 | A | G | 1 | a0004c0005t0001g0166 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1199+1286A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20617165 | |||||||
| chr13:20617238 | G | A | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG01081.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1199+1359G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20617238 | |||||||
| chr13:20617739 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(83): Show |
87 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.1199+1860G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20617739 | |||||||
| chr13:20617838 | G | A | 1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1199+1959G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20617838 | |||||||
| chr13:20617839 | G | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1199+1960G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20617839 | |||||||
| chr13:20617846 | C | T | 1 | a0002c0002t0001g0286 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1199+1967C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20617846 | |||||||
| chr13:20617847 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1199+1968G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20617847 | |||||||
| chr13:20617862 | C | T | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1199+1983C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20617862 | |||||||
| chr13:20617874 | A | G | 7 | a0002c0002t0001g0005 a0002c0002t0001g0112 a0002c0002t0001g0113 others(4): Show |
8 | HG00280.hp1 HG01358.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1199+1995A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20617874 | |||||||
| chr13:20618094 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1199+2215G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20618094 | |||||||
| chr13:20618111 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1199+2232G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20618111 | |||||||
| chr13:20618122 | ATGTTAGC others(929): Show |
A | 1 | a0001c0001t0001g0210 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1199+2263_1199+319 others(4): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr13 | 20618122 | ||||||
| chr13:20618163 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1199+2284G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20618163 | |||||||
| chr13:20618184 | C | T | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1199+2305C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20618184 | |||||||
| chr13:20618189 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(92): Show |
96 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.1199+2310G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20618189 | |||||||
| chr13:20618207 | A | C | 1 | a0001c0001t0001g0081 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1199+2328A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20618207 | |||||||
| chr13:20618207 | A | G | 1 | a0003c0003t0001g0122 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1199+2328A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20618207 | |||||||
| chr13:20618479 | G | C | 1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1199+2600G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20618479 | |||||||
| chr13:20618510 | T | A | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1199+2631T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20618510 | |||||||
| chr13:20618687 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1199+2808C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20618687 | |||||||
| chr13:20618766 | C | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
111 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1199+2887C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20618766 | |||||||
| chr13:20618859 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1199+2980C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20618859 | |||||||
| chr13:20618861 | CT | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.1199+2994delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr13 | 20618861 | ||||||
| chr13:20618862 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1199+2983T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20618862 | |||||||
| chr13:20618868 | T | C | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1199+2989T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20618868 | |||||||
| chr13:20618949 | T | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.1199+3070T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20618949 | |||||||
| chr13:20618996 | A | G | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1199+3117A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20618996 | |||||||
| chr13:20619008 | T | A | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1199+3129T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20619008 | |||||||
| chr13:20619013 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1199+3134C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20619013 | |||||||
| chr13:20619315 | A | G | 1 | a0002c0010t0001g0116 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1199+3436A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20619315 | |||||||
| chr13:20619607 | T | C | 1 | a0002c0002t0001g0148 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1199+3728T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20619607 | |||||||
| chr13:20619740 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1199+3861A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20619740 | |||||||
| chr13:20619822 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(108): Show |
112 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1199+3943C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20619822 | |||||||
| chr13:20620006 | C | G | 1 | a0001c0001t0001g0084 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1199+4127C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20620006 | |||||||
| chr13:20620180 | T | C | 8 | a0001c0001t0001g0162 a0004c0005t0001g0163 a0004c0005t0001g0164 others(5): Show |
8 | HG00735.hp2 HG02257.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1199+4301T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20620180 | |||||||
| chr13:20620291 | G | A | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1199+4412G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20620291 | |||||||
| chr13:20620336 | G | T | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1199+4457G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20620336 | |||||||
| chr13:20620683 | AGC | A | 6 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0283 others(3): Show |
8 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.1199+4805_1199+480 others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20620683 | |||||||
| chr13:20620707 | A | T | 1 | a0002c0002t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1199+4828A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20620707 | |||||||
| chr13:20620714 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1199+4835T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20620714 | |||||||
| chr13:20620780 | C | T | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1199+4901C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20620780 | |||||||
| chr13:20620809 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1199+4930G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20620809 | |||||||
| chr13:20620847 | T | C | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1200-4903T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20620847 | |||||||
| chr13:20620865 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1200-4885A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20620865 | |||||||
| chr13:20620934 | A | G | 4 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(1): Show |
4 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200-4816A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20620934 | |||||||
| chr13:20621043 | A | G | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1200-4707A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20621043 | |||||||
| chr13:20621126 | C | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG00140.hp1 HG00639.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.1200-4624C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20621126 | |||||||
| chr13:20621493 | C | T | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1200-4257C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20621493 | |||||||
| chr13:20621525 | A | AT | 7 | a0003c0003t0001g0120 a0003c0003t0001g0123 a0003c0003t0001g0142 others(4): Show |
7 | HG00735.hp1 HG01109.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200-4224dupT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr13 | 20621525 | ||||||
| chr13:20621526 | T | TA | 6 | a0002c0002t0001g0006 a0002c0002t0001g0283 a0002c0002t0001g0284 others(3): Show |
7 | HG00099.hp1 HG00280.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200-4193dupA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr13 | 20621526 | ||||||
| chr13:20621526 | T | TAAAAAAA | 7 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(4): Show |
7 | HG00741.hp1 HG01169.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200-4199_1200-419 others(11): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr13 | 20621526 | ||||||
| chr13:20621526 | TAAAAAAA others(11): Show |
T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0053 others(14): Show |
18 | HG00639.hp1 HG00673.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1200-4210_1200-419 others(22): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr13 | 20621526 | ||||||
| chr13:20621526 | TAAAAAAA others(12): Show |
T | 214 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1200-4211_1200-419 others(23): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr13 | 20621526 | ||||||
| chr13:20621527 | A | T | 18 | a0003c0003t0001g0121 a0003c0003t0001g0122 a0003c0003t0001g0124 others(15): Show |
18 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1200-4223A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20621527 | |||||||
| chr13:20621528 | A | T | 1 | a0003c0003t0001g0134 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1200-4222A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20621528 | |||||||
| chr13:20621529 | A | T | 1 | a0003c0003t0001g0130 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1200-4221A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20621529 | |||||||
| chr13:20621586 | A | G | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1200-4164A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20621586 | |||||||
| chr13:20621589 | CT | C | 6 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1200-4152delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr13 | 20621589 | ||||||
| chr13:20621646 | T | C | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1200-4104T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20621646 | |||||||
| chr13:20621987 | T | A | 54 | a0002c0002t0001g0061 a0002c0002t0001g0112 a0002c0002t0001g0113 others(51): Show |
54 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.1200-3763T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20621987 | |||||||
| chr13:20622268 | G | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(273): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.1200-3482G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20622268 | |||||||
| chr13:20622337 | A | G | 1 | a0003c0003t0001g0171 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1200-3413A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20622337 | |||||||
| chr13:20622540 | G | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1200-3210G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20622540 | |||||||
| chr13:20622587 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02056.hp2 HG02293.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1200-3163G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20622587 | |||||||
| chr13:20622594 | T | A | 1 | a0001c0001t0001g0162 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1200-3156T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20622594 | |||||||
| chr13:20622644 | T | C | 15 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(12): Show |
15 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1200-3106T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20622644 | |||||||
| chr13:20622750 | G | T | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1200-3000G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20622750 | |||||||
| chr13:20622992 | A | T | 27 | a0001c0001t0001g0117 a0001c0001t0001g0178 a0001c0001t0001g0179 others(24): Show |
27 | HG00408.hp2 HG01261.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1200-2758A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20622992 | |||||||
| chr13:20623082 | C | T | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1200-2668C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20623082 | |||||||
| chr13:20623156 | T | C | 8 | a0001c0001t0001g0162 a0004c0005t0001g0163 a0004c0005t0001g0164 others(5): Show |
8 | HG00735.hp2 HG02257.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1200-2594T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20623156 | |||||||
| chr13:20623280 | G | T | 2 | a0001c0001t0001g0187 a0001c0001t0001g0262 |
2 | NA18942.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1200-2470G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20623280 | |||||||
| chr13:20623424 | A | G | 1 | a0003c0003t0001g0130 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1200-2326A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20623424 | |||||||
| chr13:20623535 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1200-2215C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20623535 | |||||||
| chr13:20623586 | T | G | 1 | a0004c0005t0001g0163 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1200-2164T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20623586 | |||||||
| chr13:20623807 | G | A | 1 | a0002c0002t0001g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1200-1943G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20623807 | |||||||
| chr13:20623891 | G | A | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 |
3 | HG00408.hp2 NA19057.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1200-1859G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20623891 | |||||||
| chr13:20624010 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1200-1740C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20624010 | |||||||
| chr13:20624124 | C | T | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1200-1626C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20624124 | |||||||
| chr13:20624231 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1200-1519T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20624231 | |||||||
| chr13:20624326 | G | T | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.1200-1424G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20624326 | |||||||
| chr13:20624408 | G | A | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200-1342G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20624408 | |||||||
| chr13:20624458 | G | A | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1200-1292G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20624458 | |||||||
| chr13:20624533 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0201 |
2 | NA18944.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1200-1217A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20624533 | |||||||
| chr13:20624549 | C | T | 1 | a0003c0003t0001g0147 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1200-1201C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20624549 | |||||||
| chr13:20624802 | T | C | 1 | a0001c0001t0003g0236 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1200-948T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20624802 | |||||||
| chr13:20624868 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1200-882C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20624868 | |||||||
| chr13:20624964 | C | G | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1200-786C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20624964 | |||||||
| chr13:20624988 | A | G | 15 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(12): Show |
15 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1200-762A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20624988 | |||||||
| chr13:20624999 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1200-751C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20624999 | |||||||
| chr13:20625054 | CT | C | 6 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0001c0001t0001g0068 others(3): Show |
6 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1200-695delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20625054 | |||||||
| chr13:20625058 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02258.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1200-692C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20625058 | |||||||
| chr13:20625086 | A | G | 3 | a0006c0007t0001g0232 a0006c0007t0001g0233 a0006c0007t0001g0234 |
3 | HG00639.hp1 HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1200-664A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20625086 | |||||||
| chr13:20625126 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(162): Show |
166 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1200-624C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20625126 | |||||||
| chr13:20625155 | C | G | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1200-595C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20625155 | |||||||
| chr13:20625454 | C | T | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200-296C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20625454 | |||||||
| chr13:20625455 | G | A | 34 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(31): Show |
34 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1200-295G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20625455 | |||||||
| chr13:20625625 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1200-125G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20625625 | |||||||
| chr13:20625680 | T | G | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1200-70T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | chr13 | 20625680 | |||||||
| chr13:20625709 | AAAAC | A | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1200-37_1200-34del others(4): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr13 | 20625709 | ||||||
| chr13:20625897 | C | G | 1 | a0001c0001t0001g0059 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1299+48C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20625897 | |||||||
| chr13:20625941 | C | T | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1299+92C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20625941 | |||||||
| chr13:20626039 | G | GTTTC | 6 | a0002c0002t0001g0148 a0002c0002t0001g0152 a0002c0002t0001g0161 others(3): Show |
6 | HG00741.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1299+194_1299+197d others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 20626039 | ||||||
| chr13:20626043 | C | CTTTTTTT others(8): Show |
1 | a0005c0006t0001g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1299+215_1299+229d others(17): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 20626043 | ||||||
| chr13:20626043 | C | CTTTTTTT others(11): Show |
1 | a0005c0006t0001g0174 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1299+212_1299+229d others(20): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 20626043 | ||||||
| chr13:20626043 | C | CTTTTTTT others(12): Show |
1 | a0005c0006t0001g0175 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1299+211_1299+229d others(21): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 20626043 | ||||||
| chr13:20626043 | CT | C | 7 | a0002c0002t0001g0286 a0002c0002t0001g0288 a0002c0002t0001g0293 others(4): Show |
7 | HG00735.hp2 HG01109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1299+229delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 20626043 | ||||||
| chr13:20626043 | CTT | C | 10 | a0001c0004t0001g0009 a0002c0002t0001g0005 a0002c0002t0001g0006 others(7): Show |
12 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.1299+228_1299+229d others(4): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 20626043 | ||||||
| chr13:20626043 | CTTT | C | 7 | a0001c0001t0001g0200 a0001c0001t0001g0216 a0001c0001t0001g0219 others(4): Show |
7 | HG00408.hp2 HG01261.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1299+227_1299+229d others(5): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 20626043 | ||||||
| chr13:20626043 | CTTTT | C | 17 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0213 others(14): Show |
17 | HG01358.hp2 HG02071.hp1 HG02886.hp2 others(14): Show |
intron_variant | MODIFIER | c.1299+226_1299+229d others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 20626043 | ||||||
| chr13:20626043 | CTTTTT | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(54): Show |
60 | HG00140.hp2 HG00280.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1299+225_1299+229d others(7): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 20626043 | ||||||
| chr13:20626043 | CTTTTTT | C | 44 | a0001c0001t0001g0118 a0001c0001t0001g0177 a0001c0001t0001g0179 others(41): Show |
44 | HG00323.hp1 HG00597.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1299+224_1299+229d others(8): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 20626043 | ||||||
| chr13:20626043 | CTTTTTTT others(1): Show |
C | 26 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(23): Show |
26 | HG00735.hp1 HG01071.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1299+222_1299+229d others(10): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 20626043 | ||||||
| chr13:20626043 | CTTTTTTT others(2): Show |
C | 14 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0023 others(11): Show |
14 | HG01069.hp2 HG01081.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1299+221_1299+229d others(11): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 20626043 | ||||||
| chr13:20626043 | CTTTTTTT others(3): Show |
C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0016 others(80): Show |
84 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.1299+220_1299+229d others(12): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 20626043 | ||||||
| chr13:20626043 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0086 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1299+219_1299+229d others(13): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 20626043 | ||||||
| chr13:20626043 | CTTTTTTT others(11): Show |
C | 3 | a0006c0007t0001g0232 a0006c0007t0001g0233 a0006c0007t0001g0234 |
3 | HG00639.hp1 HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1299+212_1299+229d others(20): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 20626043 | ||||||
| chr13:20626044 | T | TTTC | 6 | a0002c0002t0001g0149 a0002c0002t0001g0153 a0002c0002t0001g0154 others(3): Show |
6 | HG01069.hp1 HG01169.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1299+197_1299+198i others(5): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 20626044 | ||||||
| chr13:20626121 | C | T | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1299+272C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20626121 | |||||||
| chr13:20626132 | C | G | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1299+283C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20626132 | |||||||
| chr13:20626153 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0201 |
2 | NA18944.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1299+304C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20626153 | |||||||
| chr13:20626210 | A | G | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
177 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.1299+361A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20626210 | |||||||
| chr13:20626262 | G | A | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1299+413G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20626262 | |||||||
| chr13:20626268 | G | A | 6 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(3): Show |
6 | HG02735.hp2 HG02738.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1299+419G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20626268 | |||||||
| chr13:20626302 | C | T | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1299+453C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20626302 | |||||||
| chr13:20626312 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1299+463G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20626312 | |||||||
| chr13:20626350 | G | A | 1 | a0004c0005t0001g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1299+501G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20626350 | |||||||
| chr13:20626496 | A | G | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1299+647A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20626496 | |||||||
| chr13:20627027 | T | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1299+1178T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20627027 | |||||||
| chr13:20627068 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1299+1219G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20627068 | |||||||
| chr13:20627131 | A | G | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1299+1282A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20627131 | |||||||
| chr13:20627163 | A | T | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1299+1314A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20627163 | |||||||
| chr13:20627337 | T | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(162): Show |
166 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1299+1488T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20627337 | |||||||
| chr13:20627451 | C | T | 8 | a0001c0001t0001g0162 a0004c0005t0001g0163 a0004c0005t0001g0164 others(5): Show |
8 | HG00735.hp2 HG02257.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+1602C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20627451 | |||||||
| chr13:20627455 | C | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
4 | HG01169.hp2 HG02683.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1299+1606C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20627455 | |||||||
| chr13:20627488 | G | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02056.hp2 HG02293.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1299+1639G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20627488 | |||||||
| chr13:20627569 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1299+1720G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20627569 | |||||||
| chr13:20627587 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1299+1738C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20627587 | |||||||
| chr13:20627729 | TCA | T | 5 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1299+1881_1299+188 others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20627729 | |||||||
| chr13:20627730 | C | CA | 7 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0283 others(4): Show |
9 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.1299+1904dupA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 20627730 | ||||||
| chr13:20627730 | CA | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(110): Show |
116 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1299+1904delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 20627730 | ||||||
| chr13:20627730 | CAA | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(117): Show |
121 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1299+1903_1299+190 others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 20627730 | ||||||
| chr13:20627730 | CAAA | C | 30 | a0001c0001t0001g0052 a0001c0001t0001g0070 a0003c0003t0001g0122 others(27): Show |
30 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.1299+1902_1299+190 others(7): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 20627730 | ||||||
| chr13:20627732 | A | G | 5 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1299+1883A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20627732 | |||||||
| chr13:20627733 | A | G | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1299+1884A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20627733 | |||||||
| chr13:20627752 | AAGG | A | 9 | a0001c0001t0001g0241 a0001c0001t0001g0252 a0001c0001t0001g0254 others(6): Show |
9 | HG01884.hp2 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1299+1904_1299+190 others(7): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20627752 | |||||||
| chr13:20627948 | T | A | 1 | a0001c0001t0001g0239 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1299+2099T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20627948 | |||||||
| chr13:20628175 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1299+2326A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20628175 | |||||||
| chr13:20628211 | T | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(106): Show |
112 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.1299+2362T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20628211 | |||||||
| chr13:20628258 | T | G | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1299+2409T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20628258 | |||||||
| chr13:20628300 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1299+2451C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20628300 | |||||||
| chr13:20628383 | C | T | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299+2534C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20628383 | |||||||
| chr13:20628620 | C | T | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1300-2396C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20628620 | |||||||
| chr13:20628711 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1300-2305G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20628711 | |||||||
| chr13:20628777 | C | T | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1300-2239C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20628777 | |||||||
| chr13:20629005 | A | T | 8 | a0001c0004t0001g0008 a0001c0004t0001g0009 a0001c0004t0001g0010 others(5): Show |
8 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1300-2011A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20629005 | |||||||
| chr13:20629255 | A | C | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1300-1761A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20629255 | |||||||
| chr13:20629387 | G | A | 3 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 |
3 | HG02559.hp1 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1300-1629G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20629387 | |||||||
| chr13:20629472 | C | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
114 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.1300-1544C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20629472 | |||||||
| chr13:20629566 | A | G | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1300-1450A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20629566 | |||||||
| chr13:20629824 | G | A | 1 | a0001c0001t0001g0239 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1300-1192G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20629824 | |||||||
| chr13:20629922 | A | G | 1 | a0001c0001t0001g0195 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1300-1094A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20629922 | |||||||
| chr13:20629968 | C | T | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1300-1048C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20629968 | |||||||
| chr13:20629969 | G | A | 1 | a0001c0001t0001g0257 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1300-1047G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20629969 | |||||||
| chr13:20630155 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1300-861C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20630155 | |||||||
| chr13:20630169 | A | G | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1300-847A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20630169 | |||||||
| chr13:20630203 | C | T | 1 | a0002c0002t0001g0283 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1300-813C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20630203 | |||||||
| chr13:20630213 | T | C | 1 | a0001c0001t0001g0300 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1300-803T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20630213 | |||||||
| chr13:20630234 | T | C | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1300-782T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20630234 | |||||||
| chr13:20630289 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1300-727T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20630289 | |||||||
| chr13:20630602 | A | C | 1 | a0003c0003t0001g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1300-414A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20630602 | |||||||
| chr13:20630836 | A | G | 3 | a0003c0003t0001g0136 a0003c0003t0001g0137 a0003c0003t0001g0139 |
3 | HG02723.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1300-180A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20630836 | |||||||
| chr13:20630907 | T | C | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1300-109T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20630907 | |||||||
| chr13:20630983 | A | G | 2 | a0002c0002t0001g0112 a0002c0002t0001g0113 |
2 | HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1300-33A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20630983 | |||||||
| chr13:20630985 | TG | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1300-29delG | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 20630985 | ||||||
| chr13:20631001 | A | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1300-15A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 15/25 | chr13 | 20631001 | |||||||
| chr13:20631480 | T | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1386+378T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20631480 | |||||||
| chr13:20631600 | C | T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0053 others(4): Show |
8 | HG00673.hp1 HG03831.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.1386+498C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20631600 | |||||||
| chr13:20631694 | TG | T | 5 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1386+594delG | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr13 | 20631694 | ||||||
| chr13:20631746 | G | A | 1 | a0002c0002t0001g0288 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1386+644G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20631746 | |||||||
| chr13:20631907 | G | A | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1386+805G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20631907 | |||||||
| chr13:20631925 | T | C | 2 | a0002c0002t0001g0112 a0002c0002t0001g0113 |
2 | HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1386+823T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20631925 | |||||||
| chr13:20631995 | T | TA | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
115 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1386+893_1386+894i others(3): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20631995 | |||||||
| chr13:20632139 | C | CA | 23 | a0001c0001t0001g0296 a0003c0003t0001g0120 a0003c0003t0001g0121 others(20): Show |
23 | HG00735.hp1 HG00735.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1386+1056dupA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr13 | 20632139 | ||||||
| chr13:20632139 | CA | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1386+1056delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr13 | 20632139 | ||||||
| chr13:20632222 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1386+1120A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20632222 | |||||||
| chr13:20632531 | G | A | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1386+1429G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20632531 | |||||||
| chr13:20632772 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1386+1670G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20632772 | |||||||
| chr13:20633009 | T | G | 8 | a0001c0001t0001g0162 a0004c0005t0001g0163 a0004c0005t0001g0164 others(5): Show |
8 | HG00735.hp2 HG02257.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1386+1907T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20633009 | |||||||
| chr13:20633022 | T | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1386+1920T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20633022 | |||||||
| chr13:20633133 | T | C | 54 | a0002c0002t0001g0061 a0002c0002t0001g0112 a0002c0002t0001g0113 others(51): Show |
54 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.1386+2031T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20633133 | |||||||
| chr13:20633506 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1386+2404A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20633506 | |||||||
| chr13:20633875 | C | T | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1386+2773C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20633875 | |||||||
| chr13:20634050 | G | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
115 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1386+2948G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20634050 | |||||||
| chr13:20634169 | A | C | 1 | a0001c0001t0001g0246 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1386+3067A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20634169 | |||||||
| chr13:20634203 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1386+3101G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20634203 | |||||||
| chr13:20634247 | G | A | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1386+3145G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20634247 | |||||||
| chr13:20634255 | A | T | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1386+3153A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20634255 | |||||||
| chr13:20634339 | C | T | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1386+3237C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20634339 | |||||||
| chr13:20634583 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1386+3481C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20634583 | |||||||
| chr13:20634616 | A | G | 9 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0283 others(6): Show |
11 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.1386+3514A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20634616 | |||||||
| chr13:20634643 | C | T | 6 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1386+3541C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20634643 | |||||||
| chr13:20634735 | C | CA | 34 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(31): Show |
34 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1387-3584dupA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr13 | 20634735 | ||||||
| chr13:20634735 | C | CAA | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1387-3585_1387-358 others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr13 | 20634735 | ||||||
| chr13:20634739 | A | C | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1387-3593A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20634739 | |||||||
| chr13:20634746 | A | G | 5 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(2): Show |
5 | HG00408.hp2 NA18951.hp2 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.1387-3586A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20634746 | |||||||
| chr13:20634770 | G | A | 3 | a0003c0003t0001g0126 a0003c0003t0001g0171 a0008c0011t0001g0125 |
3 | HG01256.hp1 HG01361.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1387-3562G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20634770 | |||||||
| chr13:20634802 | AT | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(162): Show |
166 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1387-3518delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr13 | 20634802 | ||||||
| chr13:20634803 | T | A | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1387-3529T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20634803 | |||||||
| chr13:20634836 | A | G | 6 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1387-3496A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20634836 | |||||||
| chr13:20634847 | G | A | 1 | a0002c0002t0001g0155 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1387-3485G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20634847 | |||||||
| chr13:20634872 | A | C | 10 | a0003c0003t0001g0134 a0003c0003t0001g0135 a0003c0003t0001g0136 others(7): Show |
10 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1387-3460A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20634872 | |||||||
| chr13:20634947 | C | G | 6 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(3): Show |
6 | HG02735.hp2 HG02738.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1387-3385C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20634947 | |||||||
| chr13:20634988 | G | T | 1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1387-3344G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20634988 | |||||||
| chr13:20635055 | T | C | 3 | a0006c0007t0001g0232 a0006c0007t0001g0233 a0006c0007t0001g0234 |
3 | HG00639.hp1 HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1387-3277T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20635055 | |||||||
| chr13:20635234 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1387-3098G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20635234 | |||||||
| chr13:20635254 | A | T | 1 | a0001c0001t0001g0049 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1387-3078A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20635254 | |||||||
| chr13:20635373 | G | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
111 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1387-2959G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20635373 | |||||||
| chr13:20635446 | A | G | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1387-2886A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20635446 | |||||||
| chr13:20635498 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(92): Show |
96 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.1387-2834A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20635498 | |||||||
| chr13:20635554 | C | A | 1 | a0001c0001t0001g0053 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1387-2778C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20635554 | |||||||
| chr13:20635572 | G | T | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1387-2760G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20635572 | |||||||
| chr13:20635747 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1387-2585A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20635747 | |||||||
| chr13:20635830 | G | A | 3 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 |
3 | HG02559.hp1 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1387-2502G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20635830 | |||||||
| chr13:20635892 | A | C | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1387-2440A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20635892 | |||||||
| chr13:20635902 | A | C | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1387-2430A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20635902 | |||||||
| chr13:20636559 | T | A | 1 | a0007c0008t0001g0158 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1387-1773T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20636559 | |||||||
| chr13:20636570 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1387-1762A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20636570 | |||||||
| chr13:20636660 | T | G | 1 | a0001c0001t0001g0297 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1387-1672T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20636660 | |||||||
| chr13:20636765 | T | A | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1387-1567T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20636765 | |||||||
| chr13:20636776 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1387-1556G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20636776 | |||||||
| chr13:20636795 | C | T | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1387-1537C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20636795 | |||||||
| chr13:20637319 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1387-1013C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20637319 | |||||||
| chr13:20637437 | C | G | 6 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0283 others(3): Show |
8 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.1387-895C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20637437 | |||||||
| chr13:20637644 | C | G | 1 | a0001c0001t0001g0271 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1387-688C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20637644 | |||||||
| chr13:20637647 | C | G | 1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1387-685C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20637647 | |||||||
| chr13:20637727 | T | A | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1387-605T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20637727 | |||||||
| chr13:20637759 | C | A | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1387-573C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20637759 | |||||||
| chr13:20637772 | G | C | 6 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0283 others(3): Show |
8 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.1387-560G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20637772 | |||||||
| chr13:20637860 | T | C | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1387-472T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20637860 | |||||||
| chr13:20637861 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02258.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1387-471G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20637861 | |||||||
| chr13:20637893 | C | T | 3 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0131 |
3 | HG00735.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1387-439C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20637893 | |||||||
| chr13:20638120 | CTG | C | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1387-209_1387-208d others(4): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr13 | 20638120 | ||||||
| chr13:20638229 | C | T | 4 | a0003c0003t0001g0127 a0003c0003t0001g0128 a0003c0003t0001g0129 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1387-103C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 16/25 | chr13 | 20638229 | |||||||
| chr13:20638600 | C | CT | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1573+83dupT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr13 | 20638600 | ||||||
| chr13:20638711 | T | G | 1 | a0001c0001t0001g0301 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1573+193T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20638711 | |||||||
| chr13:20638889 | A | T | 3 | a0006c0007t0001g0232 a0006c0007t0001g0233 a0006c0007t0001g0234 |
3 | HG00639.hp1 HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1573+371A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20638889 | |||||||
| chr13:20638896 | C | T | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1573+378C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20638896 | |||||||
| chr13:20638987 | T | C | 4 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(1): Show |
4 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1573+469T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20638987 | |||||||
| chr13:20639132 | G | A | 3 | a0001c0001t0001g0241 a0001c0001t0001g0254 a0001c0001t0001g0255 |
3 | HG02886.hp2 HG02895.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1573+614G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20639132 | |||||||
| chr13:20639342 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1573+824T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20639342 | |||||||
| chr13:20639481 | A | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 |
3 | HG01099.hp1 HG01261.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1573+963A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20639481 | |||||||
| chr13:20639614 | A | T | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1573+1096A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20639614 | |||||||
| chr13:20639786 | C | CT | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
119 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1573+1288dupT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr13 | 20639786 | ||||||
| chr13:20639786 | CT | C | 8 | a0001c0001t0001g0065 a0001c0001t0001g0084 a0001c0001t0001g0092 others(5): Show |
8 | HG01099.hp2 HG01169.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1573+1288delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr13 | 20639786 | ||||||
| chr13:20639786 | CTT | C | 7 | a0001c0001t0002g0015 a0001c0004t0001g0008 a0001c0004t0001g0009 others(4): Show |
7 | HG00323.hp2 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1573+1287_1573+128 others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr13 | 20639786 | ||||||
| chr13:20639786 | CTTT | C | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1573+1286_1573+128 others(7): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr13 | 20639786 | ||||||
| chr13:20639934 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1574-1356G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20639934 | |||||||
| chr13:20639935 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0034 others(2): Show |
5 | HG02738.hp2 HG03490.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.1574-1355C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20639935 | |||||||
| chr13:20639946 | G | A | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1574-1344G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20639946 | |||||||
| chr13:20640116 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1574-1174T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20640116 | |||||||
| chr13:20640292 | G | A | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1574-998G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20640292 | |||||||
| chr13:20640293 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1574-997C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20640293 | |||||||
| chr13:20640297 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0196 a0001c0001t0001g0268 |
4 | NA18942.hp2 NA18964.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1574-993G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20640297 | |||||||
| chr13:20640330 | T | C | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1574-960T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20640330 | |||||||
| chr13:20640382 | G | A | 15 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(12): Show |
15 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1574-908G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20640382 | |||||||
| chr13:20640442 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1574-848G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20640442 | |||||||
| chr13:20640446 | G | A | 16 | a0001c0001t0001g0118 a0001c0001t0001g0253 a0001c0001t0001g0295 others(13): Show |
16 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1574-844G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20640446 | |||||||
| chr13:20640462 | A | G | 4 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0123 others(1): Show |
4 | HG00735.hp1 HG03486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1574-828A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20640462 | |||||||
| chr13:20640463 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1574-827C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20640463 | |||||||
| chr13:20640571 | A | AAAAT | 97 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(94): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.1574-681_1574-678d others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr13 | 20640571 | ||||||
| chr13:20640571 | A | AAAATAAA others(1): Show |
34 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0048 others(31): Show |
34 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1574-685_1574-678d others(10): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr13 | 20640571 | ||||||
| chr13:20640571 | A | AAAATAAA others(5): Show |
3 | a0003c0003t0001g0122 a0003c0003t0001g0146 a0005c0006t0001g0176 |
3 | HG02735.hp1 HG03139.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1574-689_1574-678d others(14): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr13 | 20640571 | ||||||
| chr13:20640571 | AAAAT | A | 23 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(20): Show |
23 | HG01074.hp2 HG01099.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.1574-681_1574-678d others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr13 | 20640571 | ||||||
| chr13:20640571 | AAAATAAA others(5): Show |
A | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
122 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1574-689_1574-678d others(14): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr13 | 20640571 | ||||||
| chr13:20640581 | A | C | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1574-709A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20640581 | |||||||
| chr13:20640804 | T | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
111 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1574-486T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20640804 | |||||||
| chr13:20640857 | C | A | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1574-433C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20640857 | |||||||
| chr13:20640975 | G | A | 2 | a0002c0010t0001g0115 a0002c0010t0001g0116 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1574-315G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20640975 | |||||||
| chr13:20640976 | T | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG02809.hp1 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1574-314T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20640976 | |||||||
| chr13:20641007 | C | T | 1 | a0004c0005t0001g0167 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1574-283C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20641007 | |||||||
| chr13:20641046 | C | T | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1574-244C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20641046 | |||||||
| chr13:20641079 | C | A | 2 | a0002c0002t0001g0284 a0002c0002t0001g0285 |
2 | HG02280.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1574-211C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20641079 | |||||||
| chr13:20641126 | A | G | 2 | a0002c0010t0001g0115 a0002c0010t0001g0116 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1574-164A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20641126 | |||||||
| chr13:20641240 | A | G | 1 | a0001c0001t0003g0236 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1574-50A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 17/25 | chr13 | 20641240 | |||||||
| chr13:20641605 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1682+207A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | chr13 | 20641605 | |||||||
| chr13:20641615 | C | T | 1 | a0002c0002t0001g0287 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1682+217C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | chr13 | 20641615 | |||||||
| chr13:20641665 | G | T | 10 | a0003c0003t0001g0122 a0003c0003t0001g0126 a0003c0003t0001g0127 others(7): Show |
10 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.1682+267G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | chr13 | 20641665 | |||||||
| chr13:20641707 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1682+309A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | chr13 | 20641707 | |||||||
| chr13:20641713 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1682+315G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | chr13 | 20641713 | |||||||
| chr13:20642397 | A | G | 1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1682+999A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | chr13 | 20642397 | |||||||
| chr13:20642398 | G | T | 1 | a0001c0001t0001g0227 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1682+1000G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | chr13 | 20642398 | |||||||
| chr13:20642475 | G | A | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1683-980G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | chr13 | 20642475 | |||||||
| chr13:20642479 | C | G | 39 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(36): Show |
39 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1683-976C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | chr13 | 20642479 | |||||||
| chr13:20642634 | T | C | 1 | a0001c0001t0001g0265 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1683-821T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | chr13 | 20642634 | |||||||
| chr13:20642711 | C | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
122 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1683-744C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | chr13 | 20642711 | |||||||
| chr13:20642783 | T | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(161): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1683-672T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | chr13 | 20642783 | |||||||
| chr13:20642867 | G | C | 1 | a0002c0002t0001g0288 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1683-588G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | chr13 | 20642867 | |||||||
| chr13:20642936 | A | C | 1 | a0003c0003t0001g0135 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1683-519A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | chr13 | 20642936 | |||||||
| chr13:20642978 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1683-477G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | chr13 | 20642978 | |||||||
| chr13:20643019 | C | CA | 10 | a0001c0001t0001g0075 a0001c0001t0001g0194 a0001c0001t0001g0260 others(7): Show |
12 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.1683-421dupA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr13 | 20643019 | ||||||
| chr13:20643019 | CA | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0016 others(98): Show |
102 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1683-421delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr13 | 20643019 | ||||||
| chr13:20643019 | CAA | C | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1683-422_1683-421d others(4): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr13 | 20643019 | ||||||
| chr13:20643121 | T | G | 1 | a0003c0003t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1683-334T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | chr13 | 20643121 | |||||||
| chr13:20643326 | T | C | 2 | a0001c0001t0001g0187 a0001c0001t0001g0262 |
2 | NA18942.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1683-129T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | chr13 | 20643326 | |||||||
| chr13:20643392 | T | C | 1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1683-63T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | chr13 | 20643392 | |||||||
| chr13:20643409 | T | C | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1683-46T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 18/25 | chr13 | 20643409 | |||||||
| chr13:20643875 | T | A | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1833+270T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 19/25 | chr13 | 20643875 | |||||||
| chr13:20643948 | T | C | 3 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0131 |
3 | HG00735.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1833+343T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 19/25 | chr13 | 20643948 | |||||||
| chr13:20644104 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1833+499C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 19/25 | chr13 | 20644104 | |||||||
| chr13:20644167 | G | C | 1 | a0001c0001t0001g0206 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1833+562G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 19/25 | chr13 | 20644167 | |||||||
| chr13:20644185 | A | G | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1833+580A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 19/25 | chr13 | 20644185 | |||||||
| chr13:20644456 | G | A | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1834-387G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 19/25 | chr13 | 20644456 | |||||||
| chr13:20644489 | G | A | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1834-354G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 19/25 | chr13 | 20644489 | |||||||
| chr13:20644497 | C | A | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1834-346C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 19/25 | chr13 | 20644497 | |||||||
| chr13:20645214 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1949+256C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20645214 | |||||||
| chr13:20645230 | C | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
123 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1949+272C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20645230 | |||||||
| chr13:20645240 | C | T | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1949+282C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20645240 | |||||||
| chr13:20645379 | C | T | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1949+421C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20645379 | |||||||
| chr13:20645592 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1949+634C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20645592 | |||||||
| chr13:20645672 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1949+714G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20645672 | |||||||
| chr13:20645707 | C | G | 1 | a0001c0001t0001g0098 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1949+749C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20645707 | |||||||
| chr13:20645841 | C | T | 1 | a0003c0003t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1949+883C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20645841 | |||||||
| chr13:20645959 | T | G | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1949+1001T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20645959 | |||||||
| chr13:20646011 | A | C | 8 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0152 others(5): Show |
8 | HG00741.hp1 HG01069.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1949+1053A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20646011 | |||||||
| chr13:20646113 | GTTGA | G | 3 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 |
3 | HG02559.hp1 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1949+1158_1949+116 others(8): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr13 | 20646113 | ||||||
| chr13:20646136 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | NA18993.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1949+1178C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20646136 | |||||||
| chr13:20646296 | C | CT | 15 | a0001c0001t0001g0071 a0001c0001t0001g0077 a0001c0001t0001g0118 others(12): Show |
15 | HG02071.hp2 HG02257.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1949+1355dupT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr13 | 20646296 | ||||||
| chr13:20646296 | CT | C | 9 | a0001c0001t0001g0056 a0002c0002t0001g0290 a0003c0003t0001g0135 others(6): Show |
9 | HG00639.hp1 HG01256.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1949+1355delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr13 | 20646296 | ||||||
| chr13:20646342 | G | A | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1949+1384G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20646342 | |||||||
| chr13:20646469 | ATTTTTG | A | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.1949+1534_1949+153 others(10): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr13 | 20646469 | ||||||
| chr13:20646480 | T | C | 1 | a0002c0010t0001g0115 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1949+1522T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20646480 | |||||||
| chr13:20646538 | G | A | 4 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(1): Show |
4 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1949+1580G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20646538 | |||||||
| chr13:20646609 | C | T | 5 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1949+1651C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20646609 | |||||||
| chr13:20646726 | G | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02258.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1949+1768G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20646726 | |||||||
| chr13:20646743 | C | T | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1949+1785C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20646743 | |||||||
| chr13:20646875 | C | T | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.1949+1917C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20646875 | |||||||
| chr13:20647181 | G | C | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1949+2223G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20647181 | |||||||
| chr13:20647430 | A | C | 1 | a0001c0001t0001g0033 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1949+2472A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20647430 | |||||||
| chr13:20647571 | T | G | 1 | a0001c0001t0001g0038 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1949+2613T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20647571 | |||||||
| chr13:20647611 | C | T | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.1949+2653C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20647611 | |||||||
| chr13:20647833 | C | T | 6 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1949+2875C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20647833 | |||||||
| chr13:20647989 | A | AT | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1949+3033dupT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr13 | 20647989 | ||||||
| chr13:20648122 | C | T | 3 | a0002c0002t0001g0148 a0002c0002t0001g0153 a0002c0002t0001g0157 |
3 | HG00741.hp1 HG01169.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1949+3164C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20648122 | |||||||
| chr13:20648280 | C | T | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1949+3322C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20648280 | |||||||
| chr13:20648382 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1949+3424C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20648382 | |||||||
| chr13:20648517 | C | A | 1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1949+3559C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20648517 | |||||||
| chr13:20648632 | C | T | 3 | a0006c0007t0001g0232 a0006c0007t0001g0233 a0006c0007t0001g0234 |
3 | HG00639.hp1 HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1949+3674C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20648632 | |||||||
| chr13:20648738 | T | G | 5 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1949+3780T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20648738 | |||||||
| chr13:20649048 | A | G | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1949+4090A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20649048 | |||||||
| chr13:20649201 | A | G | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1949+4243A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20649201 | |||||||
| chr13:20649209 | T | C | 3 | a0004c0005t0001g0164 a0004c0005t0001g0167 a0004c0005t0001g0168 |
3 | HG02886.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1949+4251T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20649209 | |||||||
| chr13:20649236 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1949+4278G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20649236 | |||||||
| chr13:20649483 | C | A | 1 | a0002c0002t0001g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1950-4393C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20649483 | |||||||
| chr13:20649688 | G | GA | 5 | a0001c0001t0001g0241 a0001c0001t0001g0252 a0001c0001t0001g0254 others(2): Show |
5 | HG01884.hp2 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1950-4184dupA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr13 | 20649688 | ||||||
| chr13:20649871 | A | G | 1 | a0002c0002t0001g0285 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1950-4005A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20649871 | |||||||
| chr13:20650139 | A | G | 2 | a0003c0003t0001g0120 a0003c0003t0001g0121 |
2 | HG00735.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1950-3737A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20650139 | |||||||
| chr13:20650233 | C | A | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1950-3643C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20650233 | |||||||
| chr13:20650271 | A | T | 21 | a0003c0003t0001g0122 a0003c0003t0001g0124 a0003c0003t0001g0126 others(18): Show |
21 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1950-3605A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20650271 | |||||||
| chr13:20650362 | G | A | 11 | a0003c0003t0001g0122 a0003c0003t0001g0124 a0003c0003t0001g0126 others(8): Show |
11 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1950-3514G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20650362 | |||||||
| chr13:20650364 | A | G | 6 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950-3512A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20650364 | |||||||
| chr13:20650445 | A | G | 3 | a0006c0007t0001g0232 a0006c0007t0001g0233 a0006c0007t0001g0234 |
3 | HG00639.hp1 HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1950-3431A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20650445 | |||||||
| chr13:20650466 | C | T | 1 | a0001c0001t0001g0003 | 2 | HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1950-3410C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20650466 | |||||||
| chr13:20650471 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1950-3405C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20650471 | |||||||
| chr13:20651138 | G | A | 4 | a0001c0001t0001g0212 a0001c0001t0001g0221 a0001c0001t0001g0243 others(1): Show |
4 | NA18948.hp1 NA18950.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1950-2738G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20651138 | |||||||
| chr13:20651241 | G | A | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1950-2635G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20651241 | |||||||
| chr13:20651422 | T | A | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1950-2454T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20651422 | |||||||
| chr13:20651423 | T | C | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1950-2453T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20651423 | |||||||
| chr13:20651425 | C | A | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1950-2451C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20651425 | |||||||
| chr13:20651428 | ATGTT | A | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1950-2444_1950-244 others(8): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr13 | 20651428 | ||||||
| chr13:20651429 | T | A | 44 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(41): Show |
44 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.1950-2447T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20651429 | |||||||
| chr13:20651430 | G | A | 44 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(41): Show |
44 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.1950-2446G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20651430 | |||||||
| chr13:20651431 | T | C | 44 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(41): Show |
44 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.1950-2445T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20651431 | |||||||
| chr13:20651432 | T | A | 44 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(41): Show |
44 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.1950-2444T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20651432 | |||||||
| chr13:20651564 | G | T | 1 | a0001c0001t0001g0045 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1950-2312G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20651564 | |||||||
| chr13:20651602 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1950-2274A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20651602 | |||||||
| chr13:20651657 | G | A | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1950-2219G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20651657 | |||||||
| chr13:20651700 | GTTA | G | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1950-2166_1950-216 others(7): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr13 | 20651700 | ||||||
| chr13:20651766 | T | C | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1950-2110T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20651766 | |||||||
| chr13:20651786 | A | G | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1950-2090A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20651786 | |||||||
| chr13:20651890 | A | T | 1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1950-1986A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20651890 | |||||||
| chr13:20652052 | T | C | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1950-1824T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20652052 | |||||||
| chr13:20652388 | G | C | 15 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(12): Show |
15 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1950-1488G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20652388 | |||||||
| chr13:20652469 | T | TA | 5 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1950-1398dupA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr13 | 20652469 | ||||||
| chr13:20652470 | A | T | 1 | a0001c0001t0001g0184 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1950-1406A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20652470 | |||||||
| chr13:20652491 | T | C | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1950-1385T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20652491 | |||||||
| chr13:20652540 | C | T | 11 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(8): Show |
11 | NA18747.hp1 NA18946.hp1 NA18948.hp2 others(8): Show |
intron_variant | MODIFIER | c.1950-1336C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20652540 | |||||||
| chr13:20652706 | C | T | 189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
192 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.1950-1170C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20652706 | |||||||
| chr13:20652786 | A | T | 3 | a0005c0006t0001g0172 a0005c0006t0001g0174 a0005c0006t0001g0175 |
3 | HG02602.hp1 HG03017.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1950-1090A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20652786 | |||||||
| chr13:20652927 | G | A | 1 | a0003c0003t0001g0124 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1950-949G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20652927 | |||||||
| chr13:20652974 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1950-902G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20652974 | |||||||
| chr13:20653043 | A | C | 3 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0131 |
3 | HG00735.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1950-833A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20653043 | |||||||
| chr13:20653301 | G | A | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.1950-575G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20653301 | |||||||
| chr13:20653518 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(94): Show |
98 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1950-358G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | chr13 | 20653518 | |||||||
| chr13:20653603 | TG | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
111 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1950-270delG | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr13 | 20653603 | ||||||
| chr13:20653949 | C | A | 1 | a0001c0001t0001g0261 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2002+21C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | chr13 | 20653949 | |||||||
| chr13:20653962 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2002+34T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | chr13 | 20653962 | |||||||
| chr13:20654092 | A | C | 1 | a0001c0001t0001g0178 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2002+164A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | chr13 | 20654092 | |||||||
| chr13:20654139 | A | G | 1 | a0004c0005t0001g0166 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2002+211A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | chr13 | 20654139 | |||||||
| chr13:20654531 | T | C | 1 | a0003c0003t0001g0171 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2002+603T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | chr13 | 20654531 | |||||||
| chr13:20654768 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2002+840G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | chr13 | 20654768 | |||||||
| chr13:20654928 | C | A | 1 | a0001c0001t0001g0238 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2002+1000C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | chr13 | 20654928 | |||||||
| chr13:20655156 | G | A | 1 | a0001c0004t0001g0008 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2003-1209G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | chr13 | 20655156 | |||||||
| chr13:20655333 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2003-1032G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | chr13 | 20655333 | |||||||
| chr13:20655349 | T | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.2003-1016T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | chr13 | 20655349 | |||||||
| chr13:20655372 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2003-993G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | chr13 | 20655372 | |||||||
| chr13:20655441 | C | CA | 16 | a0001c0001t0001g0118 a0001c0001t0001g0229 a0001c0001t0001g0259 others(13): Show |
16 | HG00639.hp1 HG01243.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2003-911dupA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr13 | 20655441 | ||||||
| chr13:20655441 | CA | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(91): Show |
95 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.2003-911delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr13 | 20655441 | ||||||
| chr13:20655455 | C | A | 2 | a0003c0003t0001g0135 a0003c0009t0001g0132 |
2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2003-910C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | chr13 | 20655455 | |||||||
| chr13:20655455 | CA | C | 47 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(44): Show |
47 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.2003-902delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr13 | 20655455 | ||||||
| chr13:20655456 | A | C | 2 | a0003c0003t0001g0135 a0003c0009t0001g0132 |
2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2003-909A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | chr13 | 20655456 | |||||||
| chr13:20655464 | C | A | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2003-901C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | chr13 | 20655464 | |||||||
| chr13:20655485 | T | C | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2003-880T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | chr13 | 20655485 | |||||||
| chr13:20655488 | C | T | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.2003-877C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | chr13 | 20655488 | |||||||
| chr13:20655489 | C | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(62): Show |
68 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.2003-876C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | chr13 | 20655489 | |||||||
| chr13:20656030 | C | T | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.2003-335C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | chr13 | 20656030 | |||||||
| chr13:20656121 | T | TAAAAAAA others(3): Show |
1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2003-244_2003-243i others(12): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | chr13 | 20656121 | |||||||
| chr13:20656122 | T | A | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2003-243T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | chr13 | 20656122 | |||||||
| chr13:20656122 | T | TAAAAAAA others(2): Show |
37 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0035 others(34): Show |
37 | HG00408.hp2 HG00639.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.2003-237_2003-229d others(11): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr13 | 20656122 | ||||||
| chr13:20656122 | T | TAAAAAAA others(3): Show |
206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.2003-238_2003-229d others(12): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr13 | 20656122 | ||||||
| chr13:20656122 | T | TAAAAAAA others(4): Show |
33 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0162 others(30): Show |
33 | HG00673.hp2 HG00735.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.2003-239_2003-229d others(13): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr13 | 20656122 | ||||||
| chr13:20656122 | T | TAAAAAAA others(5): Show |
3 | a0003c0003t0001g0123 a0003c0003t0001g0142 a0005c0006t0001g0175 |
3 | HG01109.hp2 HG02602.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2003-240_2003-229d others(14): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr13 | 20656122 | ||||||
| chr13:20656122 | T | TAAAAAAA others(9): Show |
1 | a0002c0002t0001g0114 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2003-229_2003-228i others(18): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr13 | 20656122 | ||||||
| chr13:20656122 | T | TAAAAAAA others(10): Show |
4 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0010t0001g0115 others(1): Show |
4 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2003-229_2003-228i others(19): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr13 | 20656122 | ||||||
| chr13:20656269 | C | T | 1 | a0003c0003t0001g0138 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2003-96C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 21/25 | chr13 | 20656269 | |||||||
| chr13:20656522 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2068+92C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20656522 | |||||||
| chr13:20656589 | A | G | 3 | a0006c0007t0001g0232 a0006c0007t0001g0233 a0006c0007t0001g0234 |
3 | HG00639.hp1 HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2068+159A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20656589 | |||||||
| chr13:20656615 | A | G | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2068+185A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20656615 | |||||||
| chr13:20656787 | A | C | 6 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2068+357A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20656787 | |||||||
| chr13:20656831 | C | T | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.2068+401C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20656831 | |||||||
| chr13:20656868 | A | C | 1 | a0003c0003t0001g0147 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2068+438A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20656868 | |||||||
| chr13:20656971 | G | T | 2 | a0002c0002t0001g0112 a0002c0002t0001g0113 |
2 | HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2068+541G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20656971 | |||||||
| chr13:20657005 | C | T | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2068+575C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20657005 | |||||||
| chr13:20657191 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2068+761A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20657191 | |||||||
| chr13:20657488 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2068+1058A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20657488 | |||||||
| chr13:20657762 | A | AAAAT | 17 | a0001c0001t0001g0060 a0001c0001t0001g0170 a0001c0004t0001g0008 others(14): Show |
17 | HG00280.hp1 HG00733.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.2068+1365_2068+136 others(8): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr13 | 20657762 | ||||||
| chr13:20657762 | A | AAAATAAA others(1): Show |
8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0095 others(5): Show |
8 | HG00639.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2068+1361_2068+136 others(12): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr13 | 20657762 | ||||||
| chr13:20657762 | A | AAAATAAA others(5): Show |
1 | a0002c0002t0001g0285 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2068+1357_2068+136 others(16): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr13 | 20657762 | ||||||
| chr13:20657762 | AAAATAAA others(5): Show |
A | 1 | a0001c0001t0001g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2068+1357_2068+136 others(16): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr13 | 20657762 | ||||||
| chr13:20657954 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2068+1524G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20657954 | |||||||
| chr13:20658107 | T | G | 1 | a0001c0001t0001g0212 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2068+1677T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20658107 | |||||||
| chr13:20658245 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(92): Show |
96 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.2068+1815C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20658245 | |||||||
| chr13:20658251 | C | CA | 95 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(92): Show |
96 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.2068+1822dupA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr13 | 20658251 | ||||||
| chr13:20658253 | T | C | 54 | a0002c0002t0001g0061 a0002c0002t0001g0112 a0002c0002t0001g0113 others(51): Show |
54 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.2068+1823T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20658253 | |||||||
| chr13:20658259 | A | G | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.2068+1829A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20658259 | |||||||
| chr13:20658370 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2068+1940C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20658370 | |||||||
| chr13:20658401 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2068+1971A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20658401 | |||||||
| chr13:20658455 | G | A | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | HG01243.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2068+2025G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20658455 | |||||||
| chr13:20658488 | T | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02056.hp2 HG02293.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.2068+2058T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20658488 | |||||||
| chr13:20658544 | G | A | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.2068+2114G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20658544 | |||||||
| chr13:20658611 | C | T | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.2068+2181C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20658611 | |||||||
| chr13:20658844 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(162): Show |
166 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.2068+2414C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20658844 | |||||||
| chr13:20658922 | A | G | 1 | a0001c0001t0004g0242 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2068+2492A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20658922 | |||||||
| chr13:20659399 | T | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.2068+2969T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20659399 | |||||||
| chr13:20659426 | C | A | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.2068+2996C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20659426 | |||||||
| chr13:20659648 | CT | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.2068+3231delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr13 | 20659648 | ||||||
| chr13:20659648 | CTT | C | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2068+3230_2068+323 others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr13 | 20659648 | ||||||
| chr13:20659686 | C | T | 1 | a0003c0003t0001g0142 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2068+3256C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20659686 | |||||||
| chr13:20659882 | T | G | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.2068+3452T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20659882 | |||||||
| chr13:20660198 | T | C | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2069-3300T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20660198 | |||||||
| chr13:20660378 | A | G | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.2069-3120A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20660378 | |||||||
| chr13:20660465 | A | C | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2069-3033A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20660465 | |||||||
| chr13:20660480 | A | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 |
3 | HG01099.hp1 HG01261.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2069-3018A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20660480 | |||||||
| chr13:20660614 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.2069-2884G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20660614 | |||||||
| chr13:20660706 | G | C | 1 | a0003c0003t0001g0124 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2069-2792G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20660706 | |||||||
| chr13:20660828 | C | A | 10 | a0003c0003t0001g0134 a0003c0003t0001g0135 a0003c0003t0001g0136 others(7): Show |
10 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2069-2670C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20660828 | |||||||
| chr13:20660945 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2069-2553T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20660945 | |||||||
| chr13:20660998 | C | G | 1 | a0001c0001t0001g0097 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2069-2500C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20660998 | |||||||
| chr13:20661194 | C | T | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2069-2304C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20661194 | |||||||
| chr13:20661454 | G | A | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.2069-2044G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20661454 | |||||||
| chr13:20661488 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2069-2010C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20661488 | |||||||
| chr13:20661525 | G | C | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2069-1973G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20661525 | |||||||
| chr13:20661549 | A | G | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.2069-1949A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20661549 | |||||||
| chr13:20661553 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2069-1945G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20661553 | |||||||
| chr13:20661602 | G | T | 1 | a0003c0003t0001g0142 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2069-1896G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20661602 | |||||||
| chr13:20661734 | T | TA | 10 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(7): Show |
10 | HG02055.hp1 HG02559.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.2069-1749dupA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr13 | 20661734 | ||||||
| chr13:20661734 | TA | T | 45 | a0001c0001t0001g0101 a0001c0001t0001g0118 a0001c0001t0001g0181 others(42): Show |
45 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.2069-1749delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr13 | 20661734 | ||||||
| chr13:20661734 | TAA | T | 16 | a0001c0004t0001g0111 a0002c0002t0001g0061 a0002c0002t0001g0148 others(13): Show |
16 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2069-1750_2069-174 others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr13 | 20661734 | ||||||
| chr13:20661845 | C | A | 54 | a0002c0002t0001g0061 a0002c0002t0001g0112 a0002c0002t0001g0113 others(51): Show |
54 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.2069-1653C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20661845 | |||||||
| chr13:20662053 | T | G | 1 | a0001c0001t0001g0085 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2069-1445T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20662053 | |||||||
| chr13:20662335 | C | G | 5 | a0001c0001t0001g0198 a0001c0001t0001g0244 a0001c0001t0001g0246 others(2): Show |
5 | HG00597.hp2 HG00673.hp2 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.2069-1163C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20662335 | |||||||
| chr13:20662393 | A | G | 6 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0283 others(3): Show |
8 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.2069-1105A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20662393 | |||||||
| chr13:20662492 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2069-1006C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20662492 | |||||||
| chr13:20662739 | TTG | T | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2069-755_2069-754d others(4): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr13 | 20662739 | ||||||
| chr13:20663070 | A | C | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(291): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2069-428A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20663070 | |||||||
| chr13:20663206 | G | A | 2 | a0001c0001t0001g0259 a0001c0001t0001g0260 |
2 | HG02602.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2069-292G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20663206 | |||||||
| chr13:20663274 | G | A | 54 | a0002c0002t0001g0061 a0002c0002t0001g0112 a0002c0002t0001g0113 others(51): Show |
54 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.2069-224G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20663274 | |||||||
| chr13:20663277 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2069-221A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20663277 | |||||||
| chr13:20663349 | G | T | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2069-149G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 22/25 | chr13 | 20663349 | |||||||
| chr13:20663937 | C | A | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2175+333C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20663937 | |||||||
| chr13:20664053 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0079 |
2 | HG02698.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2175+449T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20664053 | |||||||
| chr13:20664116 | A | C | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2175+512A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20664116 | |||||||
| chr13:20664322 | A | G | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2175+718A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20664322 | |||||||
| chr13:20664649 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2175+1045G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20664649 | |||||||
| chr13:20664751 | A | G | 1 | a0001c0001t0004g0242 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2175+1147A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20664751 | |||||||
| chr13:20664764 | A | C | 5 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2175+1160A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20664764 | |||||||
| chr13:20664817 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2175+1213C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20664817 | |||||||
| chr13:20664819 | C | T | 2 | a0003c0003t0001g0141 a0003c0003t0001g0147 |
2 | HG01106.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2175+1215C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20664819 | |||||||
| chr13:20664855 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0253 |
2 | HG02698.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2175+1251A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20664855 | |||||||
| chr13:20664895 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0230 |
2 | HG00280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2175+1291C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20664895 | |||||||
| chr13:20664896 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0230 |
2 | HG00280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2175+1292A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20664896 | |||||||
| chr13:20664897 | C | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0230 |
2 | HG00280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2175+1293C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20664897 | |||||||
| chr13:20664904 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2175+1300T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20664904 | |||||||
| chr13:20664906 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2175+1302T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20664906 | |||||||
| chr13:20664907 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2175+1303G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20664907 | |||||||
| chr13:20664935 | C | G | 1 | a0001c0001t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2175+1331C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20664935 | |||||||
| chr13:20664936 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2175+1332A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20664936 | |||||||
| chr13:20664939 | C | T | 1 | a0001c0001t0001g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2175+1335C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20664939 | |||||||
| chr13:20664947 | A | C | 1 | a0001c0001t0001g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2175+1343A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20664947 | |||||||
| chr13:20664952 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2175+1348A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20664952 | |||||||
| chr13:20665014 | G | A | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2175+1410G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20665014 | |||||||
| chr13:20665035 | T | C | 33 | a0001c0001t0001g0187 a0001c0001t0001g0198 a0001c0001t0001g0202 others(30): Show |
33 | HG00597.hp2 HG00621.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.2175+1431T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20665035 | |||||||
| chr13:20665058 | A | G | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(1): Show |
4 | HG02523.hp2 NA18955.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.2175+1454A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20665058 | |||||||
| chr13:20665078 | CA | C | 69 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(66): Show |
69 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.2175+1487delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr13 | 20665078 | ||||||
| chr13:20665108 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2175+1504A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20665108 | |||||||
| chr13:20665118 | C | T | 1 | a0001c0004t0001g0110 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2175+1514C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20665118 | |||||||
| chr13:20665139 | A | T | 15 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(12): Show |
15 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2175+1535A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20665139 | |||||||
| chr13:20665144 | A | G | 1 | a0003c0003t0001g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2175+1540A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20665144 | |||||||
| chr13:20665238 | A | G | 4 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(1): Show |
4 | HG02717.hp2 HG02818.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2175+1634A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20665238 | |||||||
| chr13:20665261 | G | T | 1 | a0001c0001t0001g0060 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2175+1657G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20665261 | |||||||
| chr13:20665464 | T | C | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2175+1860T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20665464 | |||||||
| chr13:20665802 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(162): Show |
166 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.2175+2198C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20665802 | |||||||
| chr13:20665960 | G | T | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.2175+2356G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20665960 | |||||||
| chr13:20666020 | G | T | 1 | a0001c0001t0001g0205 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2175+2416G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20666020 | |||||||
| chr13:20666052 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2175+2448C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20666052 | |||||||
| chr13:20666101 | G | C | 1 | a0001c0001t0001g0244 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2175+2497G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20666101 | |||||||
| chr13:20666197 | T | C | 1 | a0002c0002t0001g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2175+2593T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20666197 | |||||||
| chr13:20666392 | G | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.2175+2788G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20666392 | |||||||
| chr13:20666658 | C | G | 1 | a0001c0001t0001g0253 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2175+3054C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20666658 | |||||||
| chr13:20666808 | C | T | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(291): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2175+3204C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20666808 | |||||||
| chr13:20666845 | C | A | 1 | a0001c0001t0001g0269 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2175+3241C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20666845 | |||||||
| chr13:20666845 | C | T | 2 | a0003c0009t0001g0132 a0003c0009t0001g0133 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.2175+3241C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20666845 | |||||||
| chr13:20666850 | A | G | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2175+3246A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20666850 | |||||||
| chr13:20667008 | G | A | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(291): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2175+3404G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20667008 | |||||||
| chr13:20667051 | G | A | 2 | a0001c0004t0001g0095 a0001c0004t0001g0110 |
2 | HG02055.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2175+3447G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20667051 | |||||||
| chr13:20667093 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2175+3489A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20667093 | |||||||
| chr13:20667130 | A | G | 15 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(12): Show |
15 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2175+3526A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20667130 | |||||||
| chr13:20667368 | G | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | NA19057.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2176-3605G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20667368 | |||||||
| chr13:20667609 | AT | A | 291 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(288): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.2176-3350delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr13 | 20667609 | ||||||
| chr13:20667626 | T | G | 2 | a0002c0002t0001g0284 a0002c0002t0001g0285 |
2 | HG02280.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2176-3347T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20667626 | |||||||
| chr13:20667684 | C | T | 36 | a0001c0001t0001g0187 a0001c0001t0001g0198 a0001c0001t0001g0202 others(33): Show |
36 | HG00597.hp2 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.2176-3289C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20667684 | |||||||
| chr13:20667694 | G | A | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2176-3279G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20667694 | |||||||
| chr13:20667694 | G | GGCCTC | 10 | a0003c0003t0001g0134 a0003c0003t0001g0135 a0003c0003t0001g0136 others(7): Show |
10 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2176-3278_2176-327 others(9): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr13 | 20667694 | ||||||
| chr13:20667732 | G | A | 1 | a0002c0002t0001g0114 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2176-3241G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20667732 | |||||||
| chr13:20667734 | G | A | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2176-3239G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20667734 | |||||||
| chr13:20667868 | G | A | 69 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(66): Show |
69 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.2176-3105G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20667868 | |||||||
| chr13:20667876 | T | C | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2176-3097T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20667876 | |||||||
| chr13:20667962 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2176-3011C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20667962 | |||||||
| chr13:20667998 | T | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.2176-2975T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20667998 | |||||||
| chr13:20668006 | A | G | 1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2176-2967A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20668006 | |||||||
| chr13:20668009 | CT | C | 69 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(66): Show |
69 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.2176-2962delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr13 | 20668009 | ||||||
| chr13:20668032 | T | C | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.2176-2941T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20668032 | |||||||
| chr13:20668136 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2176-2837G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20668136 | |||||||
| chr13:20668136 | G | C | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2176-2837G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20668136 | |||||||
| chr13:20668173 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0177 a0001c0001t0001g0188 others(8): Show |
12 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.2176-2800G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20668173 | |||||||
| chr13:20668201 | G | A | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.2176-2772G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20668201 | |||||||
| chr13:20668256 | C | T | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.2176-2717C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20668256 | |||||||
| chr13:20668364 | CT | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.2176-2598delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr13 | 20668364 | ||||||
| chr13:20668504 | A | G | 9 | a0001c0001t0001g0179 a0001c0001t0001g0213 a0001c0001t0001g0214 others(6): Show |
9 | HG00408.hp2 HG02071.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.2176-2469A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20668504 | |||||||
| chr13:20668620 | C | G | 1 | a0002c0002t0001g0287 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2176-2353C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20668620 | |||||||
| chr13:20668667 | G | A | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.2176-2306G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20668667 | |||||||
| chr13:20668703 | C | T | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.2176-2270C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20668703 | |||||||
| chr13:20669251 | T | C | 1 | a0002c0002t0001g0155 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2176-1722T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20669251 | |||||||
| chr13:20669291 | A | G | 4 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
4 | NA18969.hp1 NA18995.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.2176-1682A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20669291 | |||||||
| chr13:20669303 | A | G | 1 | a0004c0005t0001g0167 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2176-1670A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20669303 | |||||||
| chr13:20669312 | C | T | 50 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(47): Show |
50 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.2176-1661C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20669312 | |||||||
| chr13:20669314 | C | G | 1 | a0002c0002t0001g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2176-1659C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20669314 | |||||||
| chr13:20669424 | A | AT | 42 | a0001c0001t0001g0182 a0001c0001t0001g0231 a0001c0001t0001g0277 others(39): Show |
42 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.2176-1534dupT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr13 | 20669424 | ||||||
| chr13:20669424 | A | ATT | 11 | a0003c0003t0001g0122 a0003c0003t0001g0126 a0003c0003t0001g0127 others(8): Show |
11 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.2176-1535_2176-153 others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr13 | 20669424 | ||||||
| chr13:20669424 | AT | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(92): Show |
96 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.2176-1534delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr13 | 20669424 | ||||||
| chr13:20669584 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2176-1389C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20669584 | |||||||
| chr13:20669712 | C | A | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2176-1261C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20669712 | |||||||
| chr13:20670523 | C | CT | 99 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(96): Show |
100 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.2176-427dupT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr13 | 20670523 | ||||||
| chr13:20670523 | CT | C | 22 | a0001c0001t0001g0185 a0001c0004t0001g0008 a0001c0004t0001g0012 others(19): Show |
22 | HG01069.hp1 HG01074.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.2176-427delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr13 | 20670523 | ||||||
| chr13:20670523 | CTT | C | 33 | a0002c0002t0001g0113 a0002c0010t0001g0116 a0003c0003t0001g0120 others(30): Show |
33 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.2176-428_2176-427d others(4): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr13 | 20670523 | ||||||
| chr13:20670546 | T | A | 15 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(12): Show |
15 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2176-427T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20670546 | |||||||
| chr13:20670552 | C | T | 1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2176-421C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20670552 | |||||||
| chr13:20670553 | A | G | 1 | a0009c0014t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2176-420A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20670553 | |||||||
| chr13:20670889 | T | G | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2176-84T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 23/25 | chr13 | 20670889 | |||||||
| chr13:20671114 | A | G | 4 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(1): Show |
4 | HG02717.hp2 HG02818.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2242+75A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20671114 | |||||||
| chr13:20671156 | C | T | 1 | a0002c0002t0001g0289 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2242+117C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20671156 | |||||||
| chr13:20671249 | AT | A | 26 | a0002c0010t0001g0116 a0003c0003t0001g0122 a0003c0003t0001g0124 others(23): Show |
26 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.2242+211delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20671249 | |||||||
| chr13:20671257 | T | C | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2242+218T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20671257 | |||||||
| chr13:20671329 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(92): Show |
96 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.2242+290C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20671329 | |||||||
| chr13:20671548 | A | G | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2242+509A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20671548 | |||||||
| chr13:20671592 | C | A | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.2242+553C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20671592 | |||||||
| chr13:20671706 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(92): Show |
96 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.2242+667A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20671706 | |||||||
| chr13:20671739 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2242+700A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20671739 | |||||||
| chr13:20671758 | G | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
111 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.2242+719G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20671758 | |||||||
| chr13:20671822 | T | C | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2242+783T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20671822 | |||||||
| chr13:20671832 | C | G | 1 | a0001c0001t0001g0224 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2242+793C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20671832 | |||||||
| chr13:20671935 | A | C | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2242+896A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20671935 | |||||||
| chr13:20671978 | A | G | 1 | a0003c0003t0001g0126 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2242+939A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20671978 | |||||||
| chr13:20672030 | G | A | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2242+991G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20672030 | |||||||
| chr13:20672134 | T | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.2242+1095T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20672134 | |||||||
| chr13:20672158 | A | G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0058 others(3): Show |
6 | HG00621.hp2 NA18944.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.2242+1119A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20672158 | |||||||
| chr13:20672396 | T | C | 2 | a0002c0010t0001g0115 a0002c0010t0001g0116 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2242+1357T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20672396 | |||||||
| chr13:20672450 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2242+1411C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20672450 | |||||||
| chr13:20672618 | A | C | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2242+1579A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20672618 | |||||||
| chr13:20672876 | TG | T | 69 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(66): Show |
69 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.2242+1839delG | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20672876 | ||||||
| chr13:20673026 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.2242+1987C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20673026 | |||||||
| chr13:20673036 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2242+1997G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20673036 | |||||||
| chr13:20673071 | T | C | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.2242+2032T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20673071 | |||||||
| chr13:20673077 | T | G | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2242+2038T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20673077 | |||||||
| chr13:20673245 | G | GT | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2242+2207dupT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20673245 | ||||||
| chr13:20673264 | C | T | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2242+2225C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20673264 | |||||||
| chr13:20673357 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2242+2318C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20673357 | |||||||
| chr13:20673404 | A | C | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2242+2365A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20673404 | |||||||
| chr13:20673762 | T | C | 32 | a0001c0004t0001g0008 a0001c0004t0001g0012 a0001c0004t0001g0111 others(29): Show |
32 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.2242+2723T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20673762 | |||||||
| chr13:20673858 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2242+2819A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20673858 | |||||||
| chr13:20673889 | A | C | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2242+2850A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20673889 | |||||||
| chr13:20673995 | C | G | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2242+2956C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20673995 | |||||||
| chr13:20674004 | C | T | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.2242+2965C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674004 | |||||||
| chr13:20674086 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0042 |
2 | HG00099.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2242+3047C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674086 | |||||||
| chr13:20674121 | G | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.2242+3082G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674121 | |||||||
| chr13:20674143 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2242+3104G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674143 | |||||||
| chr13:20674179 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2242+3140G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674179 | |||||||
| chr13:20674292 | A | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
123 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.2242+3253A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674292 | |||||||
| chr13:20674339 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2242+3300T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674339 | |||||||
| chr13:20674342 | C | T | 44 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(41): Show |
44 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.2242+3303C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674342 | |||||||
| chr13:20674495 | C | T | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2242+3456C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674495 | |||||||
| chr13:20674496 | C | G | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2242+3457C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674496 | |||||||
| chr13:20674580 | A | T | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2242+3541A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674580 | |||||||
| chr13:20674589 | T | A | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2242+3550T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674589 | |||||||
| chr13:20674702 | T | TTA | 9 | a0001c0001t0001g0062 a0001c0001t0001g0178 a0001c0001t0001g0199 others(6): Show |
9 | HG01261.hp1 HG02080.hp2 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.2242+3685_2242+368 others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20674702 | ||||||
| chr13:20674702 | TTA | T | 19 | a0001c0001t0001g0118 a0002c0002t0001g0005 a0002c0002t0001g0006 others(16): Show |
21 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.2242+3685_2242+368 others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20674702 | ||||||
| chr13:20674702 | TTATA | T | 10 | a0001c0004t0001g0008 a0001c0004t0001g0010 a0001c0004t0001g0011 others(7): Show |
10 | HG02145.hp2 HG02559.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.2242+3683_2242+368 others(8): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20674702 | ||||||
| chr13:20674716 | A | G | 56 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 others(53): Show |
56 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.2242+3677A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674716 | |||||||
| chr13:20674717 | TATA | T | 6 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 others(3): Show |
6 | HG02572.hp1 HG02615.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2242+3679_2242+368 others(7): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674717 | |||||||
| chr13:20674717 | TATATA | T | 50 | a0001c0004t0001g0009 a0001c0004t0001g0012 a0001c0004t0001g0095 others(47): Show |
50 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.2242+3679_2242+368 others(9): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674717 | |||||||
| chr13:20674718 | A | G | 2 | a0001c0001t0001g0118 a0002c0002t0001g0114 |
2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2242+3679A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674718 | |||||||
| chr13:20674720 | A | G | 10 | a0001c0004t0001g0008 a0001c0004t0001g0010 a0001c0004t0001g0011 others(7): Show |
10 | HG02145.hp2 HG02559.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.2242+3681A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674720 | |||||||
| chr13:20674720 | A | T | 2 | a0001c0001t0001g0118 a0002c0002t0001g0114 |
2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2242+3681A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674720 | |||||||
| chr13:20674722 | A | AT | 34 | a0001c0001t0001g0187 a0001c0001t0001g0190 a0001c0001t0001g0198 others(31): Show |
34 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.2242+3684dupT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20674722 | ||||||
| chr13:20674722 | A | G | 1 | a0003c0003t0001g0124 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2242+3683A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674722 | |||||||
| chr13:20674722 | A | T | 21 | a0001c0001t0001g0118 a0001c0001t0001g0255 a0001c0001t0001g0269 others(18): Show |
21 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.2242+3683A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674722 | |||||||
| chr13:20674723 | TA | T | 3 | a0001c0001t0001g0179 a0002c0002t0001g0284 a0002c0002t0001g0290 |
3 | HG02897.hp2 HG03130.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2242+3685delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674723 | |||||||
| chr13:20674724 | A | AT | 38 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0036 others(35): Show |
39 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.2242+3706dupT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20674724 | ||||||
| chr13:20674724 | A | ATATTTTT others(15): Show |
1 | a0001c0001t0001g0261 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2242+3686_2242+368 others(26): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20674724 | ||||||
| chr13:20674724 | A | ATT | 6 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0186 others(3): Show |
6 | HG02071.hp1 HG04204.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.2242+3705_2242+370 others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20674724 | ||||||
| chr13:20674724 | A | T | 123 | a0001c0001t0001g0118 a0001c0001t0001g0187 a0001c0001t0001g0190 others(120): Show |
124 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(121): Show |
intron_variant | MODIFIER | c.2242+3685A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674724 | |||||||
| chr13:20674724 | AT | A | 72 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(69): Show |
72 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.2242+3706delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20674724 | ||||||
| chr13:20674725 | T | TA | 12 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(9): Show |
14 | HG00673.hp1 HG02258.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.2242+3686_2242+368 others(5): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674725 | |||||||
| chr13:20674726 | T | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0052 a0001c0001t0001g0058 others(2): Show |
5 | HG02738.hp2 HG03831.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.2242+3687T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674726 | |||||||
| chr13:20674727 | T | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0016 others(70): Show |
74 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.2242+3688T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674727 | |||||||
| chr13:20674727 | T | G | 2 | a0003c0003t0001g0143 a0005c0006t0001g0176 |
2 | NA18957.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2242+3688T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674727 | |||||||
| chr13:20674728 | T | A | 3 | a0001c0001t0001g0088 a0001c0001t0001g0099 a0001c0001t0001g0109 |
3 | NA18747.hp1 NA18954.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.2242+3689T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674728 | |||||||
| chr13:20674728 | T | G | 46 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(43): Show |
46 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.2242+3689T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674728 | |||||||
| chr13:20674729 | T | A | 5 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0047 others(2): Show |
5 | HG02523.hp1 HG02630.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.2242+3690T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674729 | |||||||
| chr13:20674729 | T | G | 1 | a0003c0003t0001g0124 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2242+3690T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674729 | |||||||
| chr13:20674731 | T | A | 1 | a0001c0001t0001g0053 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2242+3692T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674731 | |||||||
| chr13:20674735 | T | G | 1 | a0005c0006t0001g0173 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2242+3696T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674735 | |||||||
| chr13:20674736 | T | G | 4 | a0002c0002t0001g0149 a0002c0002t0001g0150 a0002c0002t0001g0151 others(1): Show |
4 | HG01074.hp2 HG01099.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.2242+3697T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674736 | |||||||
| chr13:20674747 | A | T | 1 | a0001c0001t0001g0261 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2242+3708A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674747 | |||||||
| chr13:20674748 | G | T | 1 | a0001c0001t0001g0261 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2242+3709G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674748 | |||||||
| chr13:20674807 | G | A | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2242+3768G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674807 | |||||||
| chr13:20674872 | C | T | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2242+3833C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674872 | |||||||
| chr13:20674916 | T | C | 4 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(1): Show |
4 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.2242+3877T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20674916 | |||||||
| chr13:20675132 | A | C | 69 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(66): Show |
69 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.2242+4093A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20675132 | |||||||
| chr13:20675141 | C | T | 15 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(12): Show |
15 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2242+4102C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20675141 | |||||||
| chr13:20675314 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2242+4275G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20675314 | |||||||
| chr13:20675387 | C | G | 14 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(11): Show |
14 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.2242+4348C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20675387 | |||||||
| chr13:20675424 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2242+4385A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20675424 | |||||||
| chr13:20675532 | T | C | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2242+4493T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20675532 | |||||||
| chr13:20675533 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2242+4494G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20675533 | |||||||
| chr13:20675534 | C | G | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2242+4495C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20675534 | |||||||
| chr13:20675566 | T | A | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2242+4527T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20675566 | |||||||
| chr13:20675598 | G | T | 3 | a0006c0007t0001g0232 a0006c0007t0001g0233 a0006c0007t0001g0234 |
3 | HG00639.hp1 HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2242+4559G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20675598 | |||||||
| chr13:20675696 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2242+4657A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20675696 | |||||||
| chr13:20675698 | C | T | 1 | a0010c0012t0001g0192 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2242+4659C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20675698 | |||||||
| chr13:20675720 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2242+4681A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20675720 | |||||||
| chr13:20675934 | C | T | 69 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(66): Show |
69 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.2242+4895C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20675934 | |||||||
| chr13:20675979 | A | G | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2242+4940A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20675979 | |||||||
| chr13:20676039 | G | A | 3 | a0006c0007t0001g0232 a0006c0007t0001g0233 a0006c0007t0001g0234 |
3 | HG00639.hp1 HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2242+5000G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20676039 | |||||||
| chr13:20676086 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.2242+5047T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20676086 | |||||||
| chr13:20676316 | T | C | 1 | a0001c0004t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2242+5277T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20676316 | |||||||
| chr13:20676442 | A | T | 1 | a0001c0001t0001g0188 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2242+5403A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20676442 | |||||||
| chr13:20676599 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0177 a0001c0001t0001g0188 others(8): Show |
12 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.2242+5560G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20676599 | |||||||
| chr13:20676768 | T | C | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2242+5729T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20676768 | |||||||
| chr13:20676806 | G | T | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.2242+5767G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20676806 | |||||||
| chr13:20676944 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0042 |
2 | HG00099.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2242+5905C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20676944 | |||||||
| chr13:20677032 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2242+5993A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20677032 | |||||||
| chr13:20677073 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.2242+6034C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20677073 | |||||||
| chr13:20677096 | T | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
123 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.2242+6057T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20677096 | |||||||
| chr13:20677222 | G | A | 1 | a0002c0002t0001g0114 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2242+6183G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20677222 | |||||||
| chr13:20677388 | TC | T | 9 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0283 others(6): Show |
11 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.2242+6351delC | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20677388 | ||||||
| chr13:20677476 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2242+6437C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20677476 | |||||||
| chr13:20677518 | G | A | 8 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0152 others(5): Show |
8 | HG00741.hp1 HG01069.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.2242+6479G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20677518 | |||||||
| chr13:20677619 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2242+6580G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20677619 | |||||||
| chr13:20677710 | T | C | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2242+6671T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20677710 | |||||||
| chr13:20677943 | A | G | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2242+6904A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20677943 | |||||||
| chr13:20678119 | T | C | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(291): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2242+7080T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20678119 | |||||||
| chr13:20678243 | T | A | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2242+7204T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20678243 | |||||||
| chr13:20678322 | G | A | 54 | a0002c0002t0001g0061 a0002c0002t0001g0112 a0002c0002t0001g0113 others(51): Show |
54 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.2242+7283G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20678322 | |||||||
| chr13:20678353 | G | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.2242+7314G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20678353 | |||||||
| chr13:20678387 | A | C | 1 | a0001c0001t0001g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2242+7348A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20678387 | |||||||
| chr13:20678481 | A | G | 54 | a0002c0002t0001g0061 a0002c0002t0001g0112 a0002c0002t0001g0113 others(51): Show |
54 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.2242+7442A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20678481 | |||||||
| chr13:20678550 | G | C | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(291): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2242+7511G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20678550 | |||||||
| chr13:20678579 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2242+7540C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20678579 | |||||||
| chr13:20678742 | A | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 |
3 | HG01099.hp1 HG01261.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2242+7703A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20678742 | |||||||
| chr13:20678796 | A | G | 3 | a0007c0008t0001g0158 a0007c0008t0001g0159 a0007c0008t0001g0160 |
3 | HG02572.hp2 HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2242+7757A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20678796 | |||||||
| chr13:20678833 | C | T | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.2242+7794C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20678833 | |||||||
| chr13:20678946 | GTTAATAG others(3027): Show |
G | 1 | a0001c0001t0001g0186 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2242+7908_2243-872 others(4): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20678946 | |||||||
| chr13:20679004 | G | A | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2242+7965G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20679004 | |||||||
| chr13:20679146 | A | G | 7 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0053 others(4): Show |
8 | HG00673.hp1 HG03831.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.2242+8107A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20679146 | |||||||
| chr13:20679157 | G | A | 3 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 |
3 | HG02559.hp1 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2242+8118G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20679157 | |||||||
| chr13:20679255 | T | A | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2242+8216T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20679255 | |||||||
| chr13:20679350 | G | A | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
191 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.2242+8311G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20679350 | |||||||
| chr13:20679427 | C | T | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2242+8388C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20679427 | |||||||
| chr13:20679525 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2242+8486G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20679525 | |||||||
| chr13:20679619 | T | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2242+8580T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20679619 | |||||||
| chr13:20679684 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2242+8645A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20679684 | |||||||
| chr13:20679688 | A | G | 1 | a0001c0001t0001g0249 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2242+8649A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20679688 | |||||||
| chr13:20679854 | G | A | 69 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(66): Show |
69 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.2242+8815G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20679854 | |||||||
| chr13:20679861 | T | C | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.2242+8822T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20679861 | |||||||
| chr13:20679943 | G | C | 1 | a0001c0001t0001g0280 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2242+8904G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20679943 | |||||||
| chr13:20679980 | T | C | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2242+8941T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20679980 | |||||||
| chr13:20680053 | G | A | 54 | a0002c0002t0001g0061 a0002c0002t0001g0112 a0002c0002t0001g0113 others(51): Show |
54 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.2242+9014G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20680053 | |||||||
| chr13:20680219 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02056.hp2 HG02293.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.2242+9180G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20680219 | |||||||
| chr13:20680227 | C | T | 9 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
9 | HG00099.hp2 HG00642.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.2242+9188C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20680227 | |||||||
| chr13:20680244 | G | A | 3 | a0006c0007t0001g0232 a0006c0007t0001g0233 a0006c0007t0001g0234 |
3 | HG00639.hp1 HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2242+9205G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20680244 | |||||||
| chr13:20680379 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(91): Show |
95 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.2242+9340A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20680379 | |||||||
| chr13:20680499 | G | A | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2242+9460G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20680499 | |||||||
| chr13:20680569 | T | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2242+9530T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20680569 | |||||||
| chr13:20680700 | C | A | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2242+9661C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20680700 | |||||||
| chr13:20680702 | G | C | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2242+9663G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20680702 | |||||||
| chr13:20680707 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2242+9668G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20680707 | |||||||
| chr13:20680713 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2242+9674G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20680713 | |||||||
| chr13:20680808 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2242+9769G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20680808 | |||||||
| chr13:20680808 | G | GA | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
175 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.2242+9771dupA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20680808 | ||||||
| chr13:20680810 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2242+9771A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20680810 | |||||||
| chr13:20680870 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 |
3 | HG01099.hp1 HG01261.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2242+9831G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20680870 | |||||||
| chr13:20680903 | A | G | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2243-9802A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20680903 | |||||||
| chr13:20681026 | C | T | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2243-9679C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20681026 | |||||||
| chr13:20681346 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2243-9359C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20681346 | |||||||
| chr13:20681410 | T | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2243-9295T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20681410 | |||||||
| chr13:20681464 | A | G | 1 | a0005c0006t0001g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2243-9241A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20681464 | |||||||
| chr13:20681550 | G | A | 54 | a0002c0002t0001g0061 a0002c0002t0001g0112 a0002c0002t0001g0113 others(51): Show |
54 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.2243-9155G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20681550 | |||||||
| chr13:20681783 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2243-8922C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20681783 | |||||||
| chr13:20681835 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0042 |
2 | HG00099.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2243-8870C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20681835 | |||||||
| chr13:20681859 | C | G | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2243-8846C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20681859 | |||||||
| chr13:20681906 | A | T | 2 | a0002c0002t0001g0007 a0002c0002t0001g0290 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2243-8799A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20681906 | |||||||
| chr13:20681925 | T | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | HG01256.hp2 HG01258.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.2243-8780T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20681925 | |||||||
| chr13:20681983 | T | A | 1 | a0001c0001t0001g0186 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2243-8722T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20681983 | |||||||
| chr13:20681985 | T | A | 1 | a0001c0001t0001g0186 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2243-8720T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20681985 | |||||||
| chr13:20681987 | A | C | 1 | a0001c0001t0001g0186 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2243-8718A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20681987 | |||||||
| chr13:20681990 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2243-8715G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20681990 | |||||||
| chr13:20681996 | A | T | 1 | a0001c0001t0001g0186 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2243-8709A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20681996 | |||||||
| chr13:20682002 | TTGTTTTC others(1871): Show |
T | 1 | a0001c0001t0001g0186 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2243-8702_2243-682 others(4): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20682002 | |||||||
| chr13:20682012 | A | C | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.2243-8693A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20682012 | |||||||
| chr13:20682029 | C | A | 1 | a0001c0001t0001g0264 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2243-8676C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20682029 | |||||||
| chr13:20682034 | A | G | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2243-8671A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20682034 | |||||||
| chr13:20682141 | A | G | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.2243-8564A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20682141 | |||||||
| chr13:20682197 | T | TA | 4 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(1): Show |
4 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.2243-8507dupA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20682197 | ||||||
| chr13:20682368 | A | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2243-8337A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20682368 | |||||||
| chr13:20682477 | T | A | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
122 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.2243-8228T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20682477 | |||||||
| chr13:20682529 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2243-8176A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20682529 | |||||||
| chr13:20682564 | A | G | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.2243-8141A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20682564 | |||||||
| chr13:20682657 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2243-8048G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20682657 | |||||||
| chr13:20682848 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.2243-7857G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20682848 | |||||||
| chr13:20683011 | C | T | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2243-7694C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20683011 | |||||||
| chr13:20683191 | C | T | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2243-7514C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20683191 | |||||||
| chr13:20683192 | G | A | 31 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0003c0003t0001g0120 others(28): Show |
31 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.2243-7513G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20683192 | |||||||
| chr13:20683528 | C | A | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2243-7177C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20683528 | |||||||
| chr13:20683640 | G | A | 2 | a0001c0004t0001g0008 a0001c0004t0001g0012 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2243-7065G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20683640 | |||||||
| chr13:20683652 | C | T | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2243-7053C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20683652 | |||||||
| chr13:20683656 | C | T | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.2243-7049C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20683656 | |||||||
| chr13:20683742 | A | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
122 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.2243-6963A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20683742 | |||||||
| chr13:20683790 | A | T | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2243-6915A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20683790 | |||||||
| chr13:20683881 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2243-6824G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20683881 | |||||||
| chr13:20683906 | TG | T | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2243-6798delG | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20683906 | |||||||
| chr13:20684086 | C | A | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2243-6619C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20684086 | |||||||
| chr13:20684189 | T | C | 189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
192 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.2243-6516T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20684189 | |||||||
| chr13:20684419 | T | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
177 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.2243-6286T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20684419 | |||||||
| chr13:20684463 | T | C | 2 | a0003c0003t0001g0137 a0003c0003t0001g0139 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2243-6242T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20684463 | |||||||
| chr13:20684559 | G | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.2243-6146G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20684559 | |||||||
| chr13:20684617 | C | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
111 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.2243-6088C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20684617 | |||||||
| chr13:20684621 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.2243-6084G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20684621 | |||||||
| chr13:20684652 | C | A | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2243-6053C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20684652 | |||||||
| chr13:20684719 | A | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(90): Show |
94 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.2243-5986A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20684719 | |||||||
| chr13:20684741 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2243-5964C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20684741 | |||||||
| chr13:20684822 | G | T | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.2243-5883G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20684822 | |||||||
| chr13:20684831 | C | T | 4 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(1): Show |
4 | NA18954.hp1 NA18974.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.2243-5874C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20684831 | |||||||
| chr13:20684923 | G | A | 15 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(12): Show |
15 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2243-5782G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20684923 | |||||||
| chr13:20684940 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2243-5765C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20684940 | |||||||
| chr13:20685188 | C | T | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2243-5517C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20685188 | |||||||
| chr13:20685198 | A | G | 54 | a0002c0002t0001g0061 a0002c0002t0001g0112 a0002c0002t0001g0113 others(51): Show |
54 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.2243-5507A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20685198 | |||||||
| chr13:20685229 | A | T | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.2243-5476A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20685229 | |||||||
| chr13:20685230 | G | C | 2 | a0003c0003t0001g0137 a0003c0003t0001g0139 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2243-5475G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20685230 | |||||||
| chr13:20685254 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2243-5451G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20685254 | |||||||
| chr13:20685325 | C | T | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.2243-5380C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20685325 | |||||||
| chr13:20685417 | T | G | 1 | a0003c0003t0001g0171 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2243-5288T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20685417 | |||||||
| chr13:20685518 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2243-5187G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20685518 | |||||||
| chr13:20685518 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2243-5187G>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20685518 | |||||||
| chr13:20685573 | T | C | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.2243-5132T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20685573 | |||||||
| chr13:20685583 | G | A | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.2243-5122G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20685583 | |||||||
| chr13:20685593 | G | A | 28 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0030 others(25): Show |
28 | HG00621.hp2 HG02056.hp2 HG02293.hp2 others(25): Show |
intron_variant | MODIFIER | c.2243-5112G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20685593 | |||||||
| chr13:20685649 | T | G | 1 | a0006c0007t0001g0233 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2243-5056T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20685649 | |||||||
| chr13:20685710 | A | G | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.2243-4995A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20685710 | |||||||
| chr13:20685711 | C | T | 2 | a0001c0004t0001g0095 a0001c0004t0001g0110 |
2 | HG02055.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2243-4994C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20685711 | |||||||
| chr13:20685864 | A | G | 1 | a0005c0006t0001g0173 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2243-4841A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20685864 | |||||||
| chr13:20685951 | C | T | 5 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2243-4754C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20685951 | |||||||
| chr13:20685960 | T | A | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2243-4745T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20685960 | |||||||
| chr13:20686009 | C | T | 3 | a0006c0007t0001g0232 a0006c0007t0001g0233 a0006c0007t0001g0234 |
3 | HG00639.hp1 HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2243-4696C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20686009 | |||||||
| chr13:20686040 | T | TC | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2243-4664dupC | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20686040 | ||||||
| chr13:20686297 | C | G | 1 | a0001c0001t0001g0239 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2243-4408C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20686297 | |||||||
| chr13:20686333 | C | A | 5 | a0005c0006t0001g0172 a0005c0006t0001g0173 a0005c0006t0001g0174 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.2243-4372C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20686333 | |||||||
| chr13:20686547 | TTAAAGA | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
109 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.2243-4151_2243-414 others(10): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20686547 | ||||||
| chr13:20686560 | A | T | 1 | a0001c0001t0001g0216 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2243-4145A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20686560 | |||||||
| chr13:20686569 | AT | A | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
191 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.2243-4130delT | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20686569 | ||||||
| chr13:20686639 | TATG | T | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2243-4063_2243-406 others(7): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20686639 | ||||||
| chr13:20686658 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2243-4047G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20686658 | |||||||
| chr13:20686790 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2243-3915A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20686790 | |||||||
| chr13:20687022 | C | CA | 37 | a0001c0001t0001g0026 a0001c0001t0001g0031 a0001c0001t0001g0032 others(34): Show |
37 | HG00738.hp2 HG01192.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.2243-3656dupA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20687022 | ||||||
| chr13:20687022 | C | CAA | 8 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0276 others(5): Show |
8 | HG01516.hp1 HG02257.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2243-3657_2243-365 others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20687022 | ||||||
| chr13:20687022 | CA | C | 23 | a0001c0001t0001g0042 a0001c0001t0001g0098 a0001c0001t0001g0118 others(20): Show |
24 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.2243-3656delA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20687022 | ||||||
| chr13:20687022 | CAA | C | 10 | a0001c0004t0001g0111 a0002c0002t0001g0112 a0002c0002t0001g0113 others(7): Show |
10 | HG02055.hp2 HG02572.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.2243-3657_2243-365 others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20687022 | ||||||
| chr13:20687022 | CAAA | C | 45 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(42): Show |
45 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.2243-3658_2243-365 others(7): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20687022 | ||||||
| chr13:20687022 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0092 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2243-3669_2243-365 others(18): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20687022 | ||||||
| chr13:20687036 | A | C | 1 | a0003c0009t0001g0132 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2243-3669A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20687036 | |||||||
| chr13:20687037 | A | C | 28 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(25): Show |
28 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.2243-3668A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20687037 | |||||||
| chr13:20687048 | A | AC | 10 | a0001c0001t0001g0237 a0001c0001t0001g0239 a0001c0001t0001g0240 others(7): Show |
10 | HG01192.hp1 HG02056.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.2243-3657_2243-365 others(5): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20687048 | |||||||
| chr13:20687048 | A | C | 27 | a0001c0001t0001g0187 a0001c0001t0001g0198 a0001c0001t0001g0202 others(24): Show |
27 | HG00597.hp2 HG00621.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.2243-3657A>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20687048 | |||||||
| chr13:20687128 | T | C | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.2243-3577T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20687128 | |||||||
| chr13:20687278 | G | C | 3 | a0006c0007t0001g0232 a0006c0007t0001g0233 a0006c0007t0001g0234 |
3 | HG00639.hp1 HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2243-3427G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20687278 | |||||||
| chr13:20687407 | TAC | T | 72 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(69): Show |
72 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.2243-3292_2243-329 others(6): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20687407 | ||||||
| chr13:20687589 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2243-3116C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20687589 | |||||||
| chr13:20687721 | T | TA | 49 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(46): Show |
49 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.2243-2977dupA | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20687721 | ||||||
| chr13:20687855 | A | AAAAGAGT others(4): Show |
69 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(66): Show |
69 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.2243-2849_2243-284 others(15): Show |
IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr13 | 20687855 | ||||||
| chr13:20687857 | T | A | 69 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(66): Show |
69 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.2243-2848T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20687857 | |||||||
| chr13:20687976 | T | G | 1 | a0001c0001t0001g0162 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2243-2729T>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20687976 | |||||||
| chr13:20688084 | C | T | 7 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2243-2621C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20688084 | |||||||
| chr13:20688309 | C | G | 1 | a0001c0001t0001g0080 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2243-2396C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20688309 | |||||||
| chr13:20688451 | A | G | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.2243-2254A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20688451 | |||||||
| chr13:20688729 | A | G | 15 | a0002c0002t0001g0061 a0002c0002t0001g0148 a0002c0002t0001g0149 others(12): Show |
15 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.2243-1976A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20688729 | |||||||
| chr13:20688810 | T | C | 2 | a0003c0003t0001g0128 a0003c0003t0001g0129 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2243-1895T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20688810 | |||||||
| chr13:20688895 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2243-1810T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20688895 | |||||||
| chr13:20688937 | A | T | 1 | a0001c0001t0001g0265 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2243-1768A>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20688937 | |||||||
| chr13:20688941 | T | A | 5 | a0001c0004t0001g0009 a0001c0004t0001g0010 a0001c0004t0001g0011 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2243-1764T>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20688941 | |||||||
| chr13:20689300 | T | C | 29 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0003c0003t0001g0122 others(26): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2243-1405T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20689300 | |||||||
| chr13:20689390 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2243-1315G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20689390 | |||||||
| chr13:20689485 | C | A | 15 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(12): Show |
15 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2243-1220C>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20689485 | |||||||
| chr13:20689557 | C | T | 1 | a0005c0006t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2243-1148C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20689557 | |||||||
| chr13:20689650 | C | T | 2 | a0006c0007t0001g0233 a0006c0007t0001g0234 |
2 | HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2243-1055C>T | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20689650 | |||||||
| chr13:20689842 | G | A | 54 | a0002c0002t0001g0061 a0002c0002t0001g0112 a0002c0002t0001g0113 others(51): Show |
54 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.2243-863G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20689842 | |||||||
| chr13:20689913 | T | C | 9 | a0001c0001t0001g0118 a0001c0001t0001g0295 a0001c0001t0001g0296 others(6): Show |
9 | HG02145.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2243-792T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20689913 | |||||||
| chr13:20689962 | G | A | 1 | a0004c0005t0001g0168 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2243-743G>A | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20689962 | |||||||
| chr13:20690269 | T | C | 4 | a0002c0002t0001g0061 a0002c0002t0001g0154 a0002c0002t0001g0155 others(1): Show |
4 | HG01069.hp1 HG02280.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2243-436T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20690269 | |||||||
| chr13:20690426 | C | G | 6 | a0001c0001t0001g0187 a0001c0001t0001g0239 a0001c0001t0001g0249 others(3): Show |
6 | HG01978.hp1 NA18942.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.2243-279C>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20690426 | |||||||
| chr13:20690514 | T | C | 2 | a0002c0010t0001g0115 a0002c0010t0001g0116 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2243-191T>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20690514 | |||||||
| chr13:20690522 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2243-183A>G | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20690522 | |||||||
| chr13:20690618 | G | C | 2 | a0001c0004t0001g0095 a0001c0004t0001g0110 |
2 | HG02055.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2243-87G>C | IFT88 | ENSG00000032742.18 | transcript | ENST00000351808.10 | protein_coding | 24/25 | chr13 | 20690618 |