Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 28981 |
| ensemblid | ENSG00000122970.16 |
| hgncid | 14313 |
| symbol | IFT81 |
| name | intraflagellar transport 81 |
| refseq_nuc | NM_014055.4 |
| refseq_prot | NP_054774.2 |
| ensembl_nuc | ENST00000242591.10 |
| ensembl_prot | ENSP00000242591.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 110124357 |
| end | 110218793 |
| strand | + |
| ver | v1.2 |
| region | chr12:110124357-110218793 |
| region5000 | chr12:110119357-110223793 |
| regionname0 | IFT81_chr12_110124357_110218793 |
| regionname5000 | IFT81_chr12_110119357_110223793 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 676 | 206 | 78 | 49 | 44 | 12 | 21 | 34 | IFT81_chr12_110119357_110223793 | IFT81 | MSDQI others(671): Show |
chr12 | 110119357 | 110223793 |
| a0002 | 0/0 | 676 | 9 | 6 | 3 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | MSDQI others(671): Show |
chr12 | 110119357 | 110223793 |
| a0003 | 0/0 | 676 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | MSDQI others(671): Show |
chr12 | 110119357 | 110223793 |
| a0004 | 0/0 | 676 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | MSDQI others(671): Show |
chr12 | 110119357 | 110223793 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2028 | 204 | 77 | 49 | 44 | 11 | 21 | IFT81_chr12_110119357_110223793 | IFT81 | ATGAG others(2023): Show |
chr12 | 110119357 | 110223793 | ||
| a0001c0004 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | ATGAG others(2023): Show |
chr12 | 110119357 | 110223793 | ||
| a0001c0005 | 0/0 | 2028 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | ATGAG others(2023): Show |
chr12 | 110119357 | 110223793 | ||
| a0002c0002 | 0/0 | 2028 | 9 | 6 | 3 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | ATGAG others(2023): Show |
chr12 | 110119357 | 110223793 | ||
| a0003c0003 | 0/0 | 2028 | 2 | 0 | 0 | 0 | 0 | 2 | IFT81_chr12_110119357_110223793 | IFT81 | ATGAG others(2023): Show |
chr12 | 110119357 | 110223793 | ||
| a0004c0006 | 0/0 | 2028 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | ATGAG others(2023): Show |
chr12 | 110119357 | 110223793 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3124 | 163 | 67 | 28 | 44 | 6 | 17 | IFT81_chr12_110119357_110223793 | IFT81 | GTTGC others(3119): Show |
chr12 | 110119357 | 110223793 |
| a0001c0001t0002 | 0/1 | 3124 | 34 | 9 | 16 | 0 | 4 | 4 | IFT81_chr12_110119357_110223793 | IFT81 | GTTGC others(3119): Show |
chr12 | 110119357 | 110223793 |
| a0001c0001t0003 | 0/0 | 3124 | 5 | 0 | 4 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | GTTGC others(3119): Show |
chr12 | 110119357 | 110223793 |
| a0001c0001t0005 | 0/0 | 3124 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | GTTGC others(3119): Show |
chr12 | 110119357 | 110223793 |
| a0001c0001t0006 | 0/0 | 3124 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | GTTGC others(3119): Show |
chr12 | 110119357 | 110223793 |
| a0001c0004t0001 | 0/0 | 3124 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | GTTGC others(3119): Show |
chr12 | 110119357 | 110223793 |
| a0001c0005t0001 | 0/0 | 3124 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | GTTGC others(3119): Show |
chr12 | 110119357 | 110223793 |
| a0002c0002t0001 | 0/0 | 3124 | 9 | 6 | 3 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | GTTGC others(3119): Show |
chr12 | 110119357 | 110223793 |
| a0003c0003t0004 | 0/0 | 3124 | 2 | 0 | 0 | 0 | 0 | 2 | IFT81_chr12_110119357_110223793 | IFT81 | GTTGC others(3119): Show |
chr12 | 110119357 | 110223793 |
| a0004c0006t0004 | 0/0 | 3124 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | GTTGC others(3119): Show |
chr12 | 110119357 | 110223793 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0084 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0210 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0006g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0004t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0005t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0002c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0002c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0003c0003t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0003c0003t0004g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0004c0006t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | GBR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | GBR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0190 | EUR | FIN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | FIN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0212 | EUR | FIN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | FIN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0174 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0209 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0045 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0044 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | CLM | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | CLM | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0200 | EUR | IBS | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01516 | hp2 | a0001 | c0005 | t0001 | g0089 | EUR | IBS | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PEL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0205 | AMR | PEL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0206 | AMR | PEL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0043 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0046 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0042 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03654 | hp2 | a0004 | c0006 | t0004 | g0076 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03688 | hp1 | a0003 | c0003 | t0004 | g0075 | SAS | STU | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | STU | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | STU | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG04115 | hp2 | a0003 | c0003 | t0004 | g0077 | SAS | STU | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | BEB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | STU | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | STU | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0194 | SAS | STU | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | YRI | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0039 | AFR | YRI | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0041 | AFR | ASW | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | ASW | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0215 | EUR | TSI | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | TSI | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | TSI | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0207 | EUR | TSI | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0040 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0021 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | USA | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | USA | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0210 | REF | REF | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0084 | REF | REF | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110129102 | A | G | 2 | a0003 a0004 |
3 | HG03654.hp2 HG03688.hp1 HG04115.hp2 |
missense_variant | MODERATE | c.401A>G | p.Asp134Gly | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/19 | 927/3124 | 401/2031 | 134/676 | chr12 | 110129102 | |||
| chr12:110135405 | C | G | 1 | a0002 | 9 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
missense_variant | MODERATE | c.664C>G | p.Leu222Val | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/19 | 1190/3124 | 664/2031 | 222/676 | chr12 | 110135405 | |||
| chr12:110136788 | G | T | 1 | a0004 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.709G>T | p.Val237Leu | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/19 | 1235/3124 | 709/2031 | 237/676 | chr12 | 110136788 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110180430 | A | G | 1 | a0001c0005 | 1 | HG01516.hp2 | synonymous_variant | LOW | c.1197A>G | p.Arg399Arg | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/19 | 1723/3124 | 1197/2031 | 399/676 | chr12 | 110180430 | |||
| chr12:110180484 | A | C | 1 | a0001c0004 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.1251A>C | p.Ile417Ile | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/19 | 1777/3124 | 1251/2031 | 417/676 | chr12 | 110180484 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110124404 | C | T | 1 | a0001c0001t0006 | 1 | HG00735.hp2 | 5_prime_UTR_variant | MODIFIER | c.-479C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/19 | 2977 | chr12 | 110124404 | ||||||
| chr12:110124692 | C | T | 1 | a0001c0001t0002 | 33 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(30): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-191C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/19 | chr12 | 110124692 | |||||||
| chr12:110124714 | G | A | 1 | a0001c0001t0003 | 5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-169G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/19 | 2667 | chr12 | 110124714 | ||||||
| chr12:110218646 | C | T | 1 | a0001c0001t0005 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*420C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 19/19 | 420 | chr12 | 110218646 | ||||||
| chr12:110218708 | T | G | 2 | a0003c0003t0004 a0004c0006t0004 |
3 | HG03654.hp2 HG03688.hp1 HG04115.hp2 |
3_prime_UTR_variant | MODIFIER | c.*482T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 19/19 | 482 | chr12 | 110218708 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110125105 | G | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(56): Show |
60 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.-22+244G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110125105 | |||||||
| chr12:110125247 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
3 | HG02630.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-22+386G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110125247 | |||||||
| chr12:110125805 | C | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(101): Show |
105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-22+944C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110125805 | |||||||
| chr12:110126132 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-21-1228G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110126132 | |||||||
| chr12:110126209 | C | A | 1 | a0001c0001t0001g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-21-1151C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110126209 | |||||||
| chr12:110126277 | C | CA | 9 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21-1064dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr12 | 110126277 | ||||||
| chr12:110126277 | CA | C | 49 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(46): Show |
49 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.-21-1064delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr12 | 110126277 | ||||||
| chr12:110126277 | CAA | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(55): Show |
59 | HG00323.hp2 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-21-1065_-21-1064d others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr12 | 110126277 | ||||||
| chr12:110126303 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(53): Show |
57 | HG00323.hp2 HG01099.hp1 HG01167.hp2 others(54): Show |
intron_variant | MODIFIER | c.-21-1057G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110126303 | |||||||
| chr12:110126854 | A | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
168 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.-21-506A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110126854 | |||||||
| chr12:110126929 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.-21-431C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110126929 | |||||||
| chr12:110126930 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-21-430A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110126930 | |||||||
| chr12:110127073 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-21-287G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110127073 | |||||||
| chr12:110127273 | C | T | 1 | a0001c0001t0001g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-21-87C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110127273 | |||||||
| chr12:110128786 | C | CA | 11 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0016 others(8): Show |
11 | HG00099.hp1 HG00738.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.249-140dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr12 | 110128786 | ||||||
| chr12:110128786 | CA | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(90): Show |
94 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.249-140delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr12 | 110128786 | ||||||
| chr12:110128786 | CAA | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG00323.hp1 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.249-141_249-140del others(2): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr12 | 110128786 | ||||||
| chr12:110129203 | C | G | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.429+73C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110129203 | |||||||
| chr12:110129490 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.429+360C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110129490 | |||||||
| chr12:110129617 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.429+487A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110129617 | |||||||
| chr12:110129650 | T | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0073 |
2 | NA18953.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.429+520T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110129650 | |||||||
| chr12:110129697 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0016 |
2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.429+567G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110129697 | |||||||
| chr12:110129835 | AT | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0074 a0001c0001t0001g0109 others(3): Show |
6 | HG01099.hp2 HG01168.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+720delT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr12 | 110129835 | ||||||
| chr12:110129850 | TA | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
10 | HG01167.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.429+725delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr12 | 110129850 | ||||||
| chr12:110129851 | A | T | 16 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0048 others(13): Show |
16 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.429+721A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110129851 | |||||||
| chr12:110130365 | C | CT | 50 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(47): Show |
50 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.429+1251dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr12 | 110130365 | ||||||
| chr12:110130416 | A | T | 1 | a0001c0001t0001g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.429+1286A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110130416 | |||||||
| chr12:110130818 | A | G | 43 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(40): Show |
44 | HG00323.hp2 HG01167.hp2 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.429+1688A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110130818 | |||||||
| chr12:110131118 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.430-1429C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110131118 | |||||||
| chr12:110131291 | C | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(101): Show |
105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.430-1256C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110131291 | |||||||
| chr12:110131317 | T | A | 1 | a0001c0001t0001g0167 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.430-1230T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110131317 | |||||||
| chr12:110131560 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(2): Show |
5 | HG01099.hp1 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-987C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110131560 | |||||||
| chr12:110131567 | C | T | 5 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-980C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110131567 | |||||||
| chr12:110131807 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.430-740A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110131807 | |||||||
| chr12:110131855 | T | C | 6 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 others(3): Show |
6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-692T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110131855 | |||||||
| chr12:110132143 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.430-404C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110132143 | |||||||
| chr12:110132255 | G | C | 2 | a0001c0001t0001g0169 a0001c0001t0006g0174 |
2 | HG00735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.430-292G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110132255 | |||||||
| chr12:110132315 | CCGGG | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0023 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-229_430-226del others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr12 | 110132315 | ||||||
| chr12:110132459 | C | CA | 20 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0018 others(17): Show |
20 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.430-72dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr12 | 110132459 | ||||||
| chr12:110132825 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.519+189G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110132825 | |||||||
| chr12:110132970 | C | CT | 18 | a0001c0001t0001g0006 a0001c0001t0001g0068 a0001c0001t0001g0069 others(15): Show |
18 | HG00423.hp2 HG00558.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.519+352dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr12 | 110132970 | ||||||
| chr12:110132970 | CT | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
103 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.519+352delT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr12 | 110132970 | ||||||
| chr12:110132970 | CTT | C | 5 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0211 others(2): Show |
5 | HG00323.hp2 HG01074.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+351_519+352del others(2): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr12 | 110132970 | ||||||
| chr12:110132997 | G | T | 1 | a0001c0001t0002g0204 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.519+361G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110132997 | |||||||
| chr12:110133097 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.519+461A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110133097 | |||||||
| chr12:110133180 | C | T | 39 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0112 others(36): Show |
39 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.519+544C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110133180 | |||||||
| chr12:110133459 | GA | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
173 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.519+838delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr12 | 110133459 | ||||||
| chr12:110133489 | ATGG | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0004t0001g0021 |
3 | HG02055.hp1 HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.519+859_519+861del others(3): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr12 | 110133489 | ||||||
| chr12:110133569 | A | G | 23 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0113 others(20): Show |
23 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.519+933A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110133569 | |||||||
| chr12:110133829 | A | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0037 |
2 | HG03491.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.520-1119A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110133829 | |||||||
| chr12:110134040 | A | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
129 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.520-908A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110134040 | |||||||
| chr12:110134158 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.520-790G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110134158 | |||||||
| chr12:110134307 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.520-641C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110134307 | |||||||
| chr12:110134308 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.520-640G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110134308 | |||||||
| chr12:110134335 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
108 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.520-613C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110134335 | |||||||
| chr12:110134388 | T | G | 7 | a0001c0001t0001g0051 a0001c0001t0001g0168 a0001c0001t0001g0170 others(4): Show |
7 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.520-560T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110134388 | |||||||
| chr12:110134424 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.520-524G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110134424 | |||||||
| chr12:110134491 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.520-457C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110134491 | |||||||
| chr12:110134580 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.520-368T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110134580 | |||||||
| chr12:110134732 | A | C | 2 | a0001c0001t0001g0169 a0001c0001t0006g0174 |
2 | HG00735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.520-216A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110134732 | |||||||
| chr12:110135064 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.585+51G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 6/18 | chr12 | 110135064 | |||||||
| chr12:110135108 | G | A | 19 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0018 others(16): Show |
19 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.585+95G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 6/18 | chr12 | 110135108 | |||||||
| chr12:110135141 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.585+128G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 6/18 | chr12 | 110135141 | |||||||
| chr12:110135535 | G | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(101): Show |
105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.696+98G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | chr12 | 110135535 | |||||||
| chr12:110135551 | T | C | 5 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.696+114T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | chr12 | 110135551 | |||||||
| chr12:110135629 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.696+192G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | chr12 | 110135629 | |||||||
| chr12:110135640 | G | A | 9 | a0002c0002t0001g0014 a0002c0002t0001g0038 a0002c0002t0001g0040 others(6): Show |
9 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.696+203G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | chr12 | 110135640 | |||||||
| chr12:110135721 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0023 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.696+284G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | chr12 | 110135721 | |||||||
| chr12:110135728 | A | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.696+291A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | chr12 | 110135728 | |||||||
| chr12:110135866 | GA | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(88): Show |
92 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.696+448delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr12 | 110135866 | ||||||
| chr12:110135866 | GAA | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 others(2): Show |
5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.696+447_696+448del others(2): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr12 | 110135866 | ||||||
| chr12:110135956 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG00558.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.696+519C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | chr12 | 110135956 | |||||||
| chr12:110136172 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.697-604C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | chr12 | 110136172 | |||||||
| chr12:110136480 | T | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0023 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.697-296T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | chr12 | 110136480 | |||||||
| chr12:110136583 | A | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.697-193A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | chr12 | 110136583 | |||||||
| chr12:110136870 | AATT | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0047 a0001c0001t0001g0048 others(19): Show |
23 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.781+16_781+18delTA others(1): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110136870 | ||||||
| chr12:110136942 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.781+82G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110136942 | |||||||
| chr12:110136947 | A | T | 1 | a0001c0001t0001g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.781+87A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110136947 | |||||||
| chr12:110137003 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01891.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.781+143G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110137003 | |||||||
| chr12:110137121 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0035 |
2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.781+261C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110137121 | |||||||
| chr12:110137148 | T | G | 1 | a0001c0001t0002g0179 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.781+288T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110137148 | |||||||
| chr12:110137300 | A | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0111 |
3 | HG02615.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.781+440A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110137300 | |||||||
| chr12:110137639 | G | A | 43 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(40): Show |
44 | HG00323.hp2 HG01167.hp2 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.781+779G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110137639 | |||||||
| chr12:110137691 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.781+831G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110137691 | |||||||
| chr12:110137740 | A | AAAAT | 4 | a0001c0001t0002g0175 a0001c0001t0002g0177 a0001c0001t0002g0203 others(1): Show |
4 | HG00642.hp2 HG02258.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.781+904_781+907dup others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110137740 | ||||||
| chr12:110137787 | T | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0022 |
3 | HG01099.hp1 HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.781+927T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110137787 | |||||||
| chr12:110137926 | T | TCTCTGGC others(354): Show |
1 | a0001c0001t0001g0037 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.781+1082_781+1083i others(363): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110137926 | ||||||
| chr12:110138057 | G | T | 1 | a0001c0001t0001g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.781+1197G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110138057 | |||||||
| chr12:110138130 | A | ATCTTTC | 2 | a0001c0001t0001g0169 a0001c0001t0006g0174 |
2 | HG00735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.781+1272_781+1277d others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110138130 | ||||||
| chr12:110138196 | C | T | 1 | a0001c0001t0002g0202 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.781+1336C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110138196 | |||||||
| chr12:110138200 | G | T | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.781+1340G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110138200 | |||||||
| chr12:110138290 | A | G | 19 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0018 others(16): Show |
19 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.781+1430A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110138290 | |||||||
| chr12:110138481 | G | A | 11 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0115 others(8): Show |
11 | HG00423.hp2 HG00558.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.781+1621G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110138481 | |||||||
| chr12:110138553 | C | G | 1 | a0001c0001t0001g0015 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.781+1693C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110138553 | |||||||
| chr12:110138668 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.781+1808G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110138668 | |||||||
| chr12:110139203 | G | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(39): Show |
43 | HG00323.hp2 HG01167.hp2 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.781+2343G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139203 | |||||||
| chr12:110139239 | A | C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(39): Show |
43 | HG00323.hp2 HG01167.hp2 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.781+2379A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139239 | |||||||
| chr12:110139336 | C | CA | 19 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0019 others(16): Show |
19 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.781+2495dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139336 | ||||||
| chr12:110139439 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.781+2579C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139439 | |||||||
| chr12:110139626 | T | A | 1 | a0001c0001t0002g0180 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.781+2766T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139626 | |||||||
| chr12:110139643 | G | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0016 others(4): Show |
7 | HG01099.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.781+2783G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139643 | |||||||
| chr12:110139664 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0006g0174 |
2 | HG00735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.781+2804C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139664 | |||||||
| chr12:110139707 | G | A | 1 | a0001c0001t0001g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.781+2847G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139707 | |||||||
| chr12:110139782 | CACAT | C | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.781+2938_781+2941d others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139782 | ||||||
| chr12:110139797 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.781+2937A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139797 | |||||||
| chr12:110139800 | C | A | 1 | a0001c0001t0002g0183 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.781+2940C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139800 | |||||||
| chr12:110139817 | A | T | 1 | a0001c0001t0002g0183 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.781+2957A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139817 | |||||||
| chr12:110139818 | T | A | 1 | a0001c0001t0002g0183 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.781+2958T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139818 | |||||||
| chr12:110139818 | T | TAAATA | 23 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(20): Show |
23 | HG00323.hp2 HG01099.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.781+2986_781+2990d others(7): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139818 | ||||||
| chr12:110139818 | T | TAAATAAA others(3): Show |
14 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(11): Show |
15 | HG00735.hp2 HG01167.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.781+2981_781+2990d others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139818 | ||||||
| chr12:110139818 | T | TAAATAAA others(8): Show |
10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0047 others(7): Show |
10 | HG01243.hp2 HG01891.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.781+2976_781+2990d others(17): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139818 | ||||||
| chr12:110139846 | A | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.781+2986A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139846 | |||||||
| chr12:110139847 | T | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.781+2987T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139847 | |||||||
| chr12:110139847 | T | TA | 6 | a0001c0001t0001g0010 a0002c0002t0001g0014 a0002c0002t0001g0040 others(3): Show |
6 | HG02109.hp2 HG02818.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.781+2990dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139847 | ||||||
| chr12:110139849 | A | AAATAAAA others(20): Show |
1 | a0001c0001t0001g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.781+2990_781+2991i others(29): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139849 | ||||||
| chr12:110139849 | A | AATAAAAT others(5): Show |
3 | a0001c0001t0002g0176 a0001c0001t0002g0187 a0001c0001t0002g0212 |
3 | HG00323.hp1 HG01928.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.781+2991_781+3002d others(14): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139849 | ||||||
| chr12:110139851 | T | A | 2 | a0001c0001t0002g0204 a0001c0004t0001g0021 |
2 | HG01109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.781+2991T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139851 | |||||||
| chr12:110139852 | A | T | 2 | a0001c0001t0002g0204 a0001c0004t0001g0021 |
2 | HG01109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.781+2992A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139852 | |||||||
| chr12:110139854 | A | AATAAAAT | 17 | a0001c0001t0002g0177 a0001c0001t0002g0188 a0001c0001t0002g0189 others(14): Show |
17 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.781+2996_781+3002d others(9): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139854 | ||||||
| chr12:110139859 | A | AAT | 6 | a0001c0001t0002g0175 a0001c0001t0002g0180 a0001c0001t0002g0184 others(3): Show |
6 | HG01123.hp1 HG01516.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.781+3001_781+3002d others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139859 | ||||||
| chr12:110139863 | A | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0002g0179 others(2): Show |
5 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+3003A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139863 | |||||||
| chr12:110139866 | T | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0002g0179 others(2): Show |
5 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+3006T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139866 | |||||||
| chr12:110139866 | T | TAAA | 27 | a0001c0001t0001g0055 a0001c0001t0002g0175 a0001c0001t0002g0176 others(24): Show |
27 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.781+3007_781+3008i others(5): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139866 | ||||||
| chr12:110139866 | T | TAAAATAA others(18): Show |
1 | a0002c0002t0001g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.781+3007_781+3008i others(27): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139866 | ||||||
| chr12:110139866 | T | TAAATAAA others(22): Show |
4 | a0002c0002t0001g0014 a0002c0002t0001g0040 a0002c0002t0001g0041 others(1): Show |
4 | HG02109.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.781+3007_781+3008i others(31): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139866 | ||||||
| chr12:110139866 | T | TATAAA | 45 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(42): Show |
45 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.781+3043_781+3047d others(7): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139866 | ||||||
| chr12:110139866 | T | TATAAAAT others(3): Show |
23 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(20): Show |
23 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.781+3038_781+3047d others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139866 | ||||||
| chr12:110139866 | T | TATAAAAT others(8): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0052 others(1): Show |
5 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+3033_781+3047d others(17): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139866 | ||||||
| chr12:110139866 | TATAAA | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0091 |
2 | HG03710.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.781+3043_781+3047d others(7): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139866 | ||||||
| chr12:110139868 | T | A | 2 | a0001c0001t0001g0010 a0001c0004t0001g0021 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.781+3008T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139868 | |||||||
| chr12:110139871 | A | T | 2 | a0001c0001t0001g0010 a0001c0004t0001g0021 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.781+3011A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139871 | |||||||
| chr12:110139873 | T | A | 1 | a0001c0001t0001g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.781+3013T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139873 | |||||||
| chr12:110139876 | A | T | 1 | a0001c0001t0001g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.781+3016A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139876 | |||||||
| chr12:110139903 | T | TAAAATAA others(18): Show |
2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.781+3047_781+3048i others(27): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139903 | ||||||
| chr12:110139955 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.781+3095G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139955 | |||||||
| chr12:110140035 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.781+3175C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110140035 | |||||||
| chr12:110140105 | T | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(55): Show |
59 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.781+3245T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110140105 | |||||||
| chr12:110140106 | T | A | 9 | a0002c0002t0001g0014 a0002c0002t0001g0038 a0002c0002t0001g0040 others(6): Show |
9 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.781+3246T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110140106 | |||||||
| chr12:110140288 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.782-3094G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110140288 | |||||||
| chr12:110140372 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.782-3010G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110140372 | |||||||
| chr12:110140387 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
108 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.782-2995C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110140387 | |||||||
| chr12:110140466 | T | G | 9 | a0002c0002t0001g0014 a0002c0002t0001g0038 a0002c0002t0001g0040 others(6): Show |
9 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.782-2916T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110140466 | |||||||
| chr12:110141018 | C | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(2): Show |
5 | HG01099.hp1 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.782-2364C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110141018 | |||||||
| chr12:110141198 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.782-2184G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110141198 | |||||||
| chr12:110141360 | TTTCTC | T | 4 | a0001c0001t0001g0061 a0003c0003t0004g0075 a0003c0003t0004g0077 others(1): Show |
4 | HG03654.hp2 HG03688.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.782-2013_782-2009d others(7): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110141360 | ||||||
| chr12:110141474 | G | A | 1 | a0001c0001t0002g0188 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.782-1908G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110141474 | |||||||
| chr12:110141612 | G | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
3 | HG02630.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.782-1770G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110141612 | |||||||
| chr12:110141823 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.782-1559G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110141823 | |||||||
| chr12:110142272 | A | G | 1 | a0001c0001t0005g0039 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.782-1110A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110142272 | |||||||
| chr12:110142329 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.782-1053G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110142329 | |||||||
| chr12:110142356 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.782-1026C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110142356 | |||||||
| chr12:110142418 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.782-964C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110142418 | |||||||
| chr12:110142533 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0060 |
2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.782-849A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110142533 | |||||||
| chr12:110142949 | C | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
10 | HG01167.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.782-433C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110142949 | |||||||
| chr12:110143081 | A | G | 1 | a0001c0001t0002g0175 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.782-301A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110143081 | |||||||
| chr12:110143099 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.782-283G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110143099 | |||||||
| chr12:110143215 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.782-167T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110143215 | |||||||
| chr12:110143926 | A | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0036 |
3 | HG00323.hp2 HG01175.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.945+381A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110143926 | |||||||
| chr12:110144007 | C | CT | 10 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0101 others(7): Show |
11 | HG01071.hp1 HG01081.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.945+483dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110144007 | ||||||
| chr12:110144007 | C | CTT | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0020 others(21): Show |
25 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.945+482_945+483dup others(2): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110144007 | ||||||
| chr12:110144007 | C | CTTT | 17 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(14): Show |
17 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.945+481_945+483dup others(3): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110144007 | ||||||
| chr12:110144007 | CT | C | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0109 others(6): Show |
9 | HG00735.hp2 HG00738.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.945+483delT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110144007 | ||||||
| chr12:110144302 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0004t0001g0021 |
3 | HG02055.hp1 HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.945+757C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110144302 | |||||||
| chr12:110144363 | C | T | 3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 |
3 | HG00621.hp2 NA18968.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.945+818C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110144363 | |||||||
| chr12:110144430 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0060 |
2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.945+885T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110144430 | |||||||
| chr12:110144533 | C | T | 5 | a0001c0001t0001g0067 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
5 | HG00423.hp1 NA18944.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.945+988C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110144533 | |||||||
| chr12:110144577 | C | G | 1 | a0001c0001t0002g0183 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.945+1032C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110144577 | |||||||
| chr12:110144711 | A | AT | 36 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0100 others(33): Show |
36 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.945+1169dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110144711 | ||||||
| chr12:110144756 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.945+1211C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110144756 | |||||||
| chr12:110144863 | C | CT | 6 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0133 others(3): Show |
6 | HG00735.hp1 HG01081.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.945+1341dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110144863 | ||||||
| chr12:110144863 | CT | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(79): Show |
83 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.945+1341delT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110144863 | ||||||
| chr12:110144898 | C | G | 1 | a0001c0001t0001g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.945+1353C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110144898 | |||||||
| chr12:110145028 | A | AT | 67 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(64): Show |
67 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.945+1506dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110145028 | ||||||
| chr12:110145028 | A | ATT | 26 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(23): Show |
27 | HG00738.hp1 HG01069.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.945+1505_945+1506d others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110145028 | ||||||
| chr12:110145140 | C | T | 9 | a0002c0002t0001g0014 a0002c0002t0001g0038 a0002c0002t0001g0040 others(6): Show |
9 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.945+1595C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110145140 | |||||||
| chr12:110145308 | G | T | 13 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 others(10): Show |
13 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.946-1645G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110145308 | |||||||
| chr12:110145443 | G | GT | 5 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0022 others(2): Show |
5 | HG01099.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.946-1497dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110145443 | ||||||
| chr12:110145478 | G | T | 1 | a0001c0001t0001g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.946-1475G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110145478 | |||||||
| chr12:110145781 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.946-1172A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110145781 | |||||||
| chr12:110145798 | ATTTTG | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
107 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.946-1130_946-1126d others(7): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110145798 | ||||||
| chr12:110145845 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01891.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.946-1108C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110145845 | |||||||
| chr12:110146107 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.946-846C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110146107 | |||||||
| chr12:110146446 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.946-507G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110146446 | |||||||
| chr12:110146584 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.946-369A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110146584 | |||||||
| chr12:110146707 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.946-246G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110146707 | |||||||
| chr12:110146721 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.946-232C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110146721 | |||||||
| chr12:110147179 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1041+131T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110147179 | |||||||
| chr12:110147275 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01891.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1041+227C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110147275 | |||||||
| chr12:110147311 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1041+263G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110147311 | |||||||
| chr12:110147502 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1041+454T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110147502 | |||||||
| chr12:110147632 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0004t0001g0021 |
3 | HG02055.hp1 HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1041+584A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110147632 | |||||||
| chr12:110147847 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1041+799A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110147847 | |||||||
| chr12:110147922 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+874A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110147922 | |||||||
| chr12:110148076 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1041+1028G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110148076 | |||||||
| chr12:110148367 | T | G | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1041+1319T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110148367 | |||||||
| chr12:110148473 | G | A | 33 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0001t0002g0177 others(30): Show |
33 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1041+1425G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110148473 | |||||||
| chr12:110148724 | T | A | 1 | a0001c0001t0001g0015 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1041+1676T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110148724 | |||||||
| chr12:110148748 | C | T | 1 | a0001c0001t0001g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1041+1700C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110148748 | |||||||
| chr12:110148837 | T | C | 10 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(7): Show |
10 | HG01099.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1041+1789T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110148837 | |||||||
| chr12:110148908 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1041+1860T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110148908 | |||||||
| chr12:110149780 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1041+2732T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110149780 | |||||||
| chr12:110149832 | G | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
129 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1041+2784G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110149832 | |||||||
| chr12:110149846 | C | T | 2 | a0001c0001t0002g0184 a0001c0001t0002g0204 |
2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1041+2798C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110149846 | |||||||
| chr12:110149857 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0016 |
2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1041+2809G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110149857 | |||||||
| chr12:110149912 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1041+2864C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110149912 | |||||||
| chr12:110149927 | T | A | 1 | a0001c0001t0002g0188 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1041+2879T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110149927 | |||||||
| chr12:110149987 | G | A | 2 | a0001c0001t0001g0169 a0001c0001t0006g0174 |
2 | HG00735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1041+2939G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110149987 | |||||||
| chr12:110150118 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1041+3070T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110150118 | |||||||
| chr12:110150129 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1041+3081C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110150129 | |||||||
| chr12:110150263 | C | A | 1 | a0001c0001t0002g0186 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1041+3215C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110150263 | |||||||
| chr12:110150263 | C | T | 1 | a0001c0001t0002g0183 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1041+3215C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110150263 | |||||||
| chr12:110150328 | A | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+3280A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110150328 | |||||||
| chr12:110150656 | AC | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+3609delC | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110150656 | |||||||
| chr12:110150776 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1041+3728C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110150776 | |||||||
| chr12:110150823 | G | C | 1 | a0001c0001t0001g0144 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1041+3775G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110150823 | |||||||
| chr12:110150994 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1041+3946T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110150994 | |||||||
| chr12:110151027 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1041+3979A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110151027 | |||||||
| chr12:110151187 | C | T | 1 | a0003c0003t0004g0077 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1041+4139C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110151187 | |||||||
| chr12:110151312 | G | A | 3 | a0001c0001t0001g0061 a0003c0003t0004g0075 a0004c0006t0004g0076 |
3 | HG03654.hp2 HG03688.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1041+4264G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110151312 | |||||||
| chr12:110151352 | C | G | 2 | a0001c0001t0003g0208 a0001c0001t0003g0209 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1041+4304C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110151352 | |||||||
| chr12:110151539 | T | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0022 |
3 | HG01099.hp1 HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1041+4491T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110151539 | |||||||
| chr12:110151685 | C | A | 5 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG02257.hp1 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1041+4637C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110151685 | |||||||
| chr12:110151764 | C | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+4716C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110151764 | |||||||
| chr12:110152057 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1041+5009A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110152057 | |||||||
| chr12:110152421 | A | C | 1 | a0001c0001t0001g0123 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1041+5373A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110152421 | |||||||
| chr12:110152517 | G | T | 1 | a0001c0001t0001g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1041+5469G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110152517 | |||||||
| chr12:110152539 | G | T | 1 | a0001c0004t0001g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1041+5491G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110152539 | |||||||
| chr12:110152629 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1041+5581G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110152629 | |||||||
| chr12:110152837 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0006g0174 |
2 | HG00735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1041+5789C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110152837 | |||||||
| chr12:110153077 | C | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0052 a0001c0001t0001g0053 others(5): Show |
9 | HG01167.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1041+6029C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110153077 | |||||||
| chr12:110153443 | T | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+6395T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110153443 | |||||||
| chr12:110153546 | G | A | 8 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 others(5): Show |
8 | HG01081.hp2 HG01943.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041+6498G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110153546 | |||||||
| chr12:110153671 | C | T | 2 | a0001c0001t0002g0184 a0001c0001t0002g0204 |
2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1041+6623C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110153671 | |||||||
| chr12:110153824 | G | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0047 others(20): Show |
24 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1041+6776G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110153824 | |||||||
| chr12:110154059 | C | T | 1 | a0001c0001t0002g0183 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1041+7011C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154059 | |||||||
| chr12:110154070 | G | A | 1 | a0001c0004t0001g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1041+7022G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154070 | |||||||
| chr12:110154163 | T | G | 1 | a0001c0001t0001g0142 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1041+7115T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154163 | |||||||
| chr12:110154276 | G | T | 1 | a0001c0001t0001g0158 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1041+7228G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154276 | |||||||
| chr12:110154284 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01891.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1041+7236G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154284 | |||||||
| chr12:110154353 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1041+7305G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154353 | |||||||
| chr12:110154551 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1041+7503C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154551 | |||||||
| chr12:110154666 | A | G | 1 | a0001c0001t0002g0182 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1041+7618A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154666 | |||||||
| chr12:110154758 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1041+7710T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154758 | |||||||
| chr12:110154954 | C | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+7906C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154954 | |||||||
| chr12:110154975 | A | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+7927A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154975 | |||||||
| chr12:110154977 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+7929G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154977 | |||||||
| chr12:110154978 | T | TGAGCCGA others(1): Show |
2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+7930_1041+793 others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154978 | |||||||
| chr12:110154979 | C | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+7931C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154979 | |||||||
| chr12:110154983 | A | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+7935A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154983 | |||||||
| chr12:110154986 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1042-7933T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154986 | |||||||
| chr12:110154987 | A | ATTGCACT others(67): Show |
2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1042-7930_1042-792 others(78): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr12 | 110154987 | ||||||
| chr12:110155018 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1042-7901A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110155018 | |||||||
| chr12:110155319 | G | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG00642.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1042-7600G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110155319 | |||||||
| chr12:110155373 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1042-7546C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110155373 | |||||||
| chr12:110155467 | T | TGCCCAAC others(312): Show |
2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1042-7436_1042-743 others(323): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr12 | 110155467 | ||||||
| chr12:110155500 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1042-7419C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110155500 | |||||||
| chr12:110155537 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1042-7382C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110155537 | |||||||
| chr12:110155604 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1042-7315G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110155604 | |||||||
| chr12:110155755 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1042-7164G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110155755 | |||||||
| chr12:110156387 | A | ACTTATTT others(327): Show |
1 | a0001c0001t0001g0007 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1042-6514_1042-651 others(338): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr12 | 110156387 | ||||||
| chr12:110156387 | A | ACTTATTT others(328): Show |
1 | a0001c0001t0001g0008 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1042-6514_1042-651 others(339): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr12 | 110156387 | ||||||
| chr12:110156415 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1042-6504G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110156415 | |||||||
| chr12:110156418 | T | A | 1 | a0001c0001t0001g0050 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1042-6501T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110156418 | |||||||
| chr12:110156465 | T | G | 33 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0001t0002g0177 others(30): Show |
33 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1042-6454T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110156465 | |||||||
| chr12:110156698 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(55): Show |
59 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.1042-6221C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110156698 | |||||||
| chr12:110156779 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1042-6140G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110156779 | |||||||
| chr12:110156806 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1042-6113C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110156806 | |||||||
| chr12:110156950 | T | A | 1 | a0001c0001t0001g0143 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1042-5969T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110156950 | |||||||
| chr12:110157014 | A | AT | 5 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
5 | HG00423.hp1 HG02258.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042-5890dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr12 | 110157014 | ||||||
| chr12:110157150 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1042-5769C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110157150 | |||||||
| chr12:110157206 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1042-5713G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110157206 | |||||||
| chr12:110157329 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1042-5590A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110157329 | |||||||
| chr12:110157566 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1042-5353T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110157566 | |||||||
| chr12:110157705 | A | T | 9 | a0002c0002t0001g0014 a0002c0002t0001g0038 a0002c0002t0001g0040 others(6): Show |
9 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1042-5214A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110157705 | |||||||
| chr12:110157831 | T | C | 16 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0115 others(13): Show |
16 | HG00423.hp2 HG00558.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1042-5088T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110157831 | |||||||
| chr12:110157909 | T | G | 4 | a0001c0001t0001g0061 a0003c0003t0004g0075 a0003c0003t0004g0077 others(1): Show |
4 | HG03654.hp2 HG03688.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042-5010T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110157909 | |||||||
| chr12:110158178 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1042-4741C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110158178 | |||||||
| chr12:110158390 | A | T | 1 | a0001c0001t0001g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1042-4529A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110158390 | |||||||
| chr12:110158598 | T | A | 3 | a0001c0001t0002g0180 a0001c0001t0002g0199 a0001c0001t0002g0202 |
3 | HG02717.hp1 HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1042-4321T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110158598 | |||||||
| chr12:110158763 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1042-4156G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110158763 | |||||||
| chr12:110158777 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0035 |
2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1042-4142G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110158777 | |||||||
| chr12:110158815 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1042-4104C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110158815 | |||||||
| chr12:110158842 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1042-4077C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110158842 | |||||||
| chr12:110158965 | G | A | 5 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1042-3954G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110158965 | |||||||
| chr12:110159266 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1042-3653C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110159266 | |||||||
| chr12:110159371 | G | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1042-3548G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110159371 | |||||||
| chr12:110159441 | T | C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(56): Show |
60 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.1042-3478T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110159441 | |||||||
| chr12:110159442 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1042-3477G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110159442 | |||||||
| chr12:110159499 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
75 | HG00323.hp2 HG00735.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.1042-3420C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110159499 | |||||||
| chr12:110159524 | T | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0059 others(1): Show |
4 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042-3395T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110159524 | |||||||
| chr12:110159628 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1042-3291C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110159628 | |||||||
| chr12:110159741 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1042-3178G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110159741 | |||||||
| chr12:110159790 | TCCAGCAA others(18): Show |
T | 1 | a0001c0001t0001g0178 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1042-3127_1042-310 others(29): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr12 | 110159790 | ||||||
| chr12:110159871 | G | T | 1 | a0001c0001t0001g0094 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1042-3048G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110159871 | |||||||
| chr12:110160015 | A | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(2): Show |
5 | HG01099.hp1 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042-2904A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110160015 | |||||||
| chr12:110160037 | C | T | 19 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0018 others(16): Show |
19 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1042-2882C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110160037 | |||||||
| chr12:110160076 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG00423.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.1042-2843G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110160076 | |||||||
| chr12:110160252 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1042-2667C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110160252 | |||||||
| chr12:110160514 | G | T | 19 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0018 others(16): Show |
19 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1042-2405G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110160514 | |||||||
| chr12:110160592 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1042-2327A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110160592 | |||||||
| chr12:110160906 | A | G | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG02258.hp2 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1042-2013A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110160906 | |||||||
| chr12:110161064 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1042-1855A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110161064 | |||||||
| chr12:110161134 | C | CT | 36 | a0001c0001t0001g0034 a0001c0001t0001g0050 a0001c0001t0001g0101 others(33): Show |
36 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1042-1767dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr12 | 110161134 | ||||||
| chr12:110161654 | A | G | 1 | a0001c0001t0002g0179 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1042-1265A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110161654 | |||||||
| chr12:110161734 | G | T | 10 | a0001c0001t0005g0039 a0002c0002t0001g0014 a0002c0002t0001g0038 others(7): Show |
10 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042-1185G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110161734 | |||||||
| chr12:110162148 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(55): Show |
59 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.1042-771C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110162148 | |||||||
| chr12:110162251 | GGTGTTAC others(43): Show |
G | 1 | a0001c0001t0006g0174 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1042-661_1042-612d others(52): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr12 | 110162251 | ||||||
| chr12:110162331 | CT | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
121 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1042-567delT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr12 | 110162331 | ||||||
| chr12:110162336 | T | C | 1 | a0001c0001t0006g0174 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1042-583T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110162336 | |||||||
| chr12:110162389 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(2): Show |
5 | HG01099.hp1 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042-530C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110162389 | |||||||
| chr12:110162440 | G | A | 33 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0001t0002g0177 others(30): Show |
33 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1042-479G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110162440 | |||||||
| chr12:110162587 | G | A | 1 | a0001c0001t0002g0201 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1042-332G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110162587 | |||||||
| chr12:110163312 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0060 |
2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1188+247C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110163312 | |||||||
| chr12:110163327 | G | A | 8 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 others(5): Show |
8 | HG01081.hp2 HG01943.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1188+262G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110163327 | |||||||
| chr12:110163614 | C | CT | 10 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0025 others(7): Show |
10 | HG01109.hp2 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.1188+568dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110163614 | ||||||
| chr12:110163614 | CT | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0057 others(4): Show |
7 | HG00738.hp1 HG01069.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1188+568delT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110163614 | ||||||
| chr12:110163646 | C | T | 8 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 others(5): Show |
8 | HG01081.hp2 HG01943.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1188+581C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110163646 | |||||||
| chr12:110163650 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1188+585C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110163650 | |||||||
| chr12:110163765 | G | A | 1 | a0001c0001t0002g0189 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1188+700G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110163765 | |||||||
| chr12:110163822 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1188+757G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110163822 | |||||||
| chr12:110163866 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1188+801G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110163866 | |||||||
| chr12:110164368 | C | T | 33 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0001t0002g0177 others(30): Show |
33 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1188+1303C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110164368 | |||||||
| chr12:110164404 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0037 |
2 | HG03491.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1188+1339G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110164404 | |||||||
| chr12:110164453 | G | A | 10 | a0001c0001t0005g0039 a0002c0002t0001g0014 a0002c0002t0001g0038 others(7): Show |
10 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1188+1388G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110164453 | |||||||
| chr12:110164470 | A | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
129 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1188+1405A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110164470 | |||||||
| chr12:110164571 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1188+1506G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110164571 | |||||||
| chr12:110164793 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1188+1728G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110164793 | |||||||
| chr12:110164795 | G | A | 4 | a0001c0001t0001g0080 a0001c0001t0001g0097 a0001c0001t0001g0100 others(1): Show |
4 | NA18944.hp2 NA18951.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1188+1730G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110164795 | |||||||
| chr12:110165006 | G | A | 16 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0115 others(13): Show |
16 | HG00423.hp2 HG00558.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1188+1941G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110165006 | |||||||
| chr12:110165038 | C | A | 1 | a0001c0001t0001g0025 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1188+1973C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110165038 | |||||||
| chr12:110165125 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1188+2060G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110165125 | |||||||
| chr12:110165401 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1188+2336A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110165401 | |||||||
| chr12:110165504 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1188+2439T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110165504 | |||||||
| chr12:110165956 | G | C | 1 | a0001c0001t0001g0122 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1188+2891G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110165956 | |||||||
| chr12:110166385 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1188+3320C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110166385 | |||||||
| chr12:110166413 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1188+3348C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110166413 | |||||||
| chr12:110166638 | A | G | 1 | a0001c0001t0006g0174 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1188+3573A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110166638 | |||||||
| chr12:110166650 | T | C | 10 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(7): Show |
10 | HG01099.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1188+3585T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110166650 | |||||||
| chr12:110166954 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1188+3889C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110166954 | |||||||
| chr12:110167010 | T | C | 1 | a0001c0001t0002g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1188+3945T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110167010 | |||||||
| chr12:110167179 | T | C | 4 | a0001c0001t0002g0186 a0001c0001t0002g0190 a0001c0001t0002g0191 others(1): Show |
4 | HG00280.hp1 HG01192.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1188+4114T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110167179 | |||||||
| chr12:110167495 | T | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0059 others(1): Show |
4 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1188+4430T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110167495 | |||||||
| chr12:110167583 | A | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0116 |
2 | HG01109.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1188+4518A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110167583 | |||||||
| chr12:110167754 | C | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(56): Show |
60 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.1188+4689C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110167754 | |||||||
| chr12:110167847 | C | CT | 45 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(42): Show |
46 | HG00323.hp2 HG01167.hp2 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.1188+4799dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110167847 | ||||||
| chr12:110168358 | T | C | 1 | a0001c0001t0001g0002 | 2 | HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1188+5293T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110168358 | |||||||
| chr12:110168506 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1188+5441C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110168506 | |||||||
| chr12:110168507 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1188+5442G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110168507 | |||||||
| chr12:110168863 | T | A | 9 | a0002c0002t0001g0014 a0002c0002t0001g0038 a0002c0002t0001g0040 others(6): Show |
9 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1188+5798T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110168863 | |||||||
| chr12:110168972 | C | T | 3 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 |
3 | HG02559.hp1 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1188+5907C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110168972 | |||||||
| chr12:110169023 | C | CCCTT | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
46 | HG00280.hp1 HG00323.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1188+6014_1188+601 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169023 | ||||||
| chr12:110169023 | C | CCCTTCCT others(1): Show |
11 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0055 others(8): Show |
11 | HG00323.hp1 HG01071.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.1188+6010_1188+601 others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169023 | ||||||
| chr12:110169023 | C | CCCTTCCT others(5): Show |
10 | a0001c0001t0001g0025 a0001c0001t0001g0211 a0001c0001t0002g0176 others(7): Show |
10 | HG00735.hp2 HG01081.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1188+6006_1188+601 others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169023 | ||||||
| chr12:110169023 | C | CCCTTCCT others(9): Show |
2 | a0001c0001t0001g0019 a0001c0001t0002g0183 |
2 | HG02886.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1188+6002_1188+601 others(20): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169023 | ||||||
| chr12:110169023 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0160 |
2 | HG02698.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1188+5958C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110169023 | |||||||
| chr12:110169023 | CCCTT | C | 42 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0035 others(39): Show |
42 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1188+6014_1188+601 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169023 | ||||||
| chr12:110169023 | CCCTTCCT others(1): Show |
C | 33 | a0001c0001t0001g0023 a0001c0001t0001g0059 a0001c0001t0001g0063 others(30): Show |
33 | HG00280.hp2 HG00423.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1188+6010_1188+601 others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169023 | ||||||
| chr12:110169023 | CCCTTCCT others(5): Show |
C | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(3): Show |
6 | HG00642.hp1 HG01074.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.1188+6006_1188+601 others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169023 | ||||||
| chr12:110169023 | CCCTTCCT others(9): Show |
C | 2 | a0001c0001t0001g0122 a0001c0001t0005g0039 |
2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1188+6002_1188+601 others(20): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169023 | ||||||
| chr12:110169023 | CCCTTCCT others(13): Show |
C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0136 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1188+5998_1188+601 others(24): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169023 | ||||||
| chr12:110169072 | CCTTCCTT others(3): Show |
C | 1 | a0001c0001t0001g0047 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1188+6010_1188+601 others(14): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169072 | ||||||
| chr12:110169080 | C | CCT | 3 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0046 |
3 | HG03453.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1188+6028_1188+602 others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169080 | ||||||
| chr12:110169080 | C | CCTTCCT | 6 | a0002c0002t0001g0014 a0002c0002t0001g0038 a0002c0002t0001g0040 others(3): Show |
6 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1188+6017_1188+601 others(10): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169080 | ||||||
| chr12:110169154 | C | G | 37 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0070 others(34): Show |
37 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.1188+6089C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110169154 | |||||||
| chr12:110169334 | C | G | 1 | a0001c0001t0001g0093 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1188+6269C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110169334 | |||||||
| chr12:110169398 | T | A | 1 | a0001c0001t0002g0212 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1188+6333T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110169398 | |||||||
| chr12:110169896 | C | G | 5 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1188+6831C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110169896 | |||||||
| chr12:110170046 | G | T | 1 | a0001c0001t0002g0194 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1188+6981G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110170046 | |||||||
| chr12:110170053 | C | T | 1 | a0001c0001t0002g0200 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1188+6988C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110170053 | |||||||
| chr12:110170113 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1188+7048C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110170113 | |||||||
| chr12:110170554 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1188+7489A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110170554 | |||||||
| chr12:110170571 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1188+7506C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110170571 | |||||||
| chr12:110170688 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1188+7623C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110170688 | |||||||
| chr12:110170732 | A | T | 1 | a0001c0001t0001g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1188+7667A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110170732 | |||||||
| chr12:110171264 | A | AT | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0016 others(9): Show |
12 | HG00738.hp1 HG01069.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1188+8213dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110171264 | ||||||
| chr12:110171587 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1188+8522T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110171587 | |||||||
| chr12:110171707 | TCTTGCCT others(12): Show |
T | 1 | a0001c0001t0001g0029 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1188+8644_1188+866 others(23): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110171707 | ||||||
| chr12:110171909 | C | T | 36 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0070 others(33): Show |
36 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.1189-8513C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110171909 | |||||||
| chr12:110172302 | GCCTCTGC others(2): Show |
G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0002c0002t0001g0042 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1189-8091_1189-808 others(13): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110172302 | ||||||
| chr12:110172358 | T | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1189-8064T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110172358 | |||||||
| chr12:110172358 | TGGTCTCC others(10): Show |
T | 20 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0018 others(17): Show |
20 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.1189-8032_1189-801 others(21): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110172358 | ||||||
| chr12:110172379 | C | A | 1 | a0001c0001t0001g0078 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1189-8043C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110172379 | |||||||
| chr12:110172418 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
3 | HG02630.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1189-8004G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110172418 | |||||||
| chr12:110172668 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1189-7754T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110172668 | |||||||
| chr12:110172807 | A | AC | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0124 others(5): Show |
8 | HG01109.hp2 HG01243.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.1189-7611dupC | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110172807 | ||||||
| chr12:110172858 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1189-7564A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110172858 | |||||||
| chr12:110173040 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0149 |
2 | NA18968.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1189-7382C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173040 | |||||||
| chr12:110173054 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1189-7368T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173054 | |||||||
| chr12:110173079 | C | T | 1 | a0001c0004t0001g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1189-7343C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173079 | |||||||
| chr12:110173154 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1189-7268A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173154 | |||||||
| chr12:110173245 | CCGTCCGG others(120): Show |
C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1189-7119_1189-699 others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110173245 | ||||||
| chr12:110173329 | G | A | 1 | a0001c0001t0002g0188 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1189-7093G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173329 | |||||||
| chr12:110173346 | G | A | 7 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0140 others(4): Show |
7 | HG00423.hp1 NA18944.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1189-7076G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173346 | |||||||
| chr12:110173357 | G | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0060 |
2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1189-7065G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173357 | |||||||
| chr12:110173439 | G | C | 11 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0024 others(8): Show |
11 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1189-6983G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173439 | |||||||
| chr12:110173524 | G | T | 1 | a0001c0001t0001g0050 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1189-6898G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173524 | |||||||
| chr12:110173756 | C | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1189-6666C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173756 | |||||||
| chr12:110173774 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1189-6648G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173774 | |||||||
| chr12:110173837 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1189-6585C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173837 | |||||||
| chr12:110173977 | G | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(5): Show |
8 | HG02055.hp1 HG02257.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1189-6445G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173977 | |||||||
| chr12:110174085 | G | A | 3 | a0001c0001t0002g0180 a0001c0001t0002g0199 a0001c0001t0002g0202 |
3 | HG02717.hp1 HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1189-6337G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174085 | |||||||
| chr12:110174147 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1189-6275G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174147 | |||||||
| chr12:110174258 | A | G | 1 | a0001c0001t0006g0174 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1189-6164A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174258 | |||||||
| chr12:110174272 | C | T | 9 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0134 others(6): Show |
9 | HG00423.hp1 HG00558.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.1189-6150C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174272 | |||||||
| chr12:110174277 | C | CA | 12 | a0001c0001t0001g0048 a0001c0001t0001g0080 a0001c0001t0001g0081 others(9): Show |
12 | HG00738.hp2 HG00741.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.1189-6115dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110174277 | ||||||
| chr12:110174277 | CA | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(84): Show |
89 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.1189-6115delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110174277 | ||||||
| chr12:110174277 | CAA | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(17): Show |
20 | HG00323.hp2 HG01175.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.1189-6116_1189-611 others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110174277 | ||||||
| chr12:110174277 | CAAA | C | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(4): Show |
7 | HG01081.hp2 HG01943.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1189-6117_1189-611 others(7): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110174277 | ||||||
| chr12:110174277 | CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0091 |
2 | HG02976.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1189-6129_1189-611 others(19): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110174277 | ||||||
| chr12:110174279 | AAAAAAAA others(171): Show |
A | 1 | a0001c0001t0001g0050 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1189-6122_1189-594 others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110174279 | ||||||
| chr12:110174292 | A | T | 1 | a0001c0001t0002g0175 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1189-6130A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174292 | |||||||
| chr12:110174293 | A | T | 1 | a0001c0001t0002g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1189-6129A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174293 | |||||||
| chr12:110174294 | A | T | 1 | a0001c0001t0002g0182 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1189-6128A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174294 | |||||||
| chr12:110174296 | A | T | 1 | a0001c0001t0002g0202 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1189-6126A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174296 | |||||||
| chr12:110174300 | A | T | 1 | a0001c0001t0002g0202 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1189-6122A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174300 | |||||||
| chr12:110174304 | A | AT | 2 | a0001c0001t0002g0195 a0001c0001t0002g0197 |
2 | HG01934.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1189-6118_1189-611 others(5): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174304 | |||||||
| chr12:110174304 | A | T | 31 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0001t0002g0177 others(28): Show |
31 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.1189-6118A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174304 | |||||||
| chr12:110174307 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0060 |
2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1189-6115A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174307 | |||||||
| chr12:110174372 | T | G | 1 | a0001c0001t0001g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1189-6050T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174372 | |||||||
| chr12:110174412 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1189-6010A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174412 | |||||||
| chr12:110174456 | A | AG | 6 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1189-5965dupG | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110174456 | ||||||
| chr12:110174457 | G | GA | 17 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(14): Show |
17 | HG00738.hp1 HG01069.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1189-5945dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110174457 | ||||||
| chr12:110174457 | G | GGA | 5 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(2): Show |
5 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-5965_1189-596 others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174457 | |||||||
| chr12:110174806 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1189-5616A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174806 | |||||||
| chr12:110174810 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1189-5612G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174810 | |||||||
| chr12:110174826 | A | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0051 a0001c0001t0001g0052 others(5): Show |
9 | HG01167.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1189-5596A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174826 | |||||||
| chr12:110174947 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1189-5475G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174947 | |||||||
| chr12:110175061 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1189-5361T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110175061 | |||||||
| chr12:110175063 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1189-5359G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110175063 | |||||||
| chr12:110175349 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1189-5073C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110175349 | |||||||
| chr12:110175578 | C | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1189-4844C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110175578 | |||||||
| chr12:110175580 | C | CT | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1189-4842_1189-484 others(5): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110175580 | |||||||
| chr12:110175581 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1189-4841G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110175581 | |||||||
| chr12:110175692 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1189-4730C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110175692 | |||||||
| chr12:110175708 | A | G | 3 | a0001c0001t0001g0093 a0001c0001t0001g0109 a0001c0001t0001g0149 |
3 | HG01928.hp1 NA18968.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1189-4714A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110175708 | |||||||
| chr12:110176409 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1189-4013A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110176409 | |||||||
| chr12:110176588 | C | T | 1 | a0001c0001t0002g0202 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1189-3834C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110176588 | |||||||
| chr12:110176604 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0022 |
3 | HG01099.hp1 HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1189-3818A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110176604 | |||||||
| chr12:110176622 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1189-3800A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110176622 | |||||||
| chr12:110176683 | C | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1189-3739C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110176683 | |||||||
| chr12:110176764 | T | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1189-3658T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110176764 | |||||||
| chr12:110176845 | A | G | 1 | a0001c0001t0002g0202 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1189-3577A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110176845 | |||||||
| chr12:110176864 | C | T | 1 | a0001c0001t0002g0175 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1189-3558C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110176864 | |||||||
| chr12:110177267 | T | TTTTTG | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0020 others(9): Show |
12 | HG00738.hp1 HG01069.hp2 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.1189-3126_1189-312 others(9): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110177267 | ||||||
| chr12:110177309 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1189-3113A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110177309 | |||||||
| chr12:110177338 | A | C | 2 | a0001c0001t0001g0169 a0001c0001t0006g0174 |
2 | HG00735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1189-3084A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110177338 | |||||||
| chr12:110177444 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
108 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1189-2978A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110177444 | |||||||
| chr12:110177574 | G | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0016 others(4): Show |
7 | HG01099.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1189-2848G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110177574 | |||||||
| chr12:110177690 | G | A | 2 | a0001c0001t0001g0169 a0001c0001t0006g0174 |
2 | HG00735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1189-2732G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110177690 | |||||||
| chr12:110177759 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1189-2663C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110177759 | |||||||
| chr12:110177869 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1189-2553C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110177869 | |||||||
| chr12:110178076 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1189-2346C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110178076 | |||||||
| chr12:110178088 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1189-2334C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110178088 | |||||||
| chr12:110178195 | C | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(41): Show |
45 | HG00323.hp2 HG01167.hp2 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.1189-2227C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110178195 | |||||||
| chr12:110178242 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1189-2180C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110178242 | |||||||
| chr12:110178414 | CA | C | 9 | a0001c0001t0001g0024 a0001c0001t0001g0055 a0001c0001t0001g0159 others(6): Show |
9 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.1189-1992delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178414 | ||||||
| chr12:110178777 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
3 | HG02630.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1189-1645G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110178777 | |||||||
| chr12:110178783 | T | TTTTTTGT others(1868): Show |
1 | a0001c0001t0001g0007 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | ||||||
| chr12:110178783 | T | TTTTTTGT others(1868): Show |
1 | a0001c0001t0001g0008 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | ||||||
| chr12:110178783 | T | TTTTTTGT others(1868): Show |
1 | a0001c0001t0001g0159 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | ||||||
| chr12:110178783 | T | TTTTTTGT others(1868): Show |
1 | a0001c0001t0001g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | ||||||
| chr12:110178783 | T | TTTTTTGT others(1868): Show |
1 | a0001c0001t0001g0118 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | ||||||
| chr12:110178783 | T | TTTTTTGT others(1868): Show |
1 | a0001c0001t0001g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | ||||||
| chr12:110178783 | T | TTTTTTGT others(1868): Show |
5 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | ||||||
| chr12:110178783 | T | TTTTTTGT others(1868): Show |
65 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0012 others(62): Show |
65 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | ||||||
| chr12:110178783 | T | TTTTTTGT others(1868): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | ||||||
| chr12:110178783 | T | TTTTTTGT others(1868): Show |
6 | a0001c0001t0001g0006 a0001c0001t0002g0186 a0001c0001t0002g0190 others(3): Show |
6 | HG00280.hp1 HG01192.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | ||||||
| chr12:110178783 | T | TTTTTTGT others(1868): Show |
42 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(39): Show |
43 | HG00323.hp2 HG01167.hp2 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | ||||||
| chr12:110178783 | T | TTTTTTGT others(1868): Show |
1 | a0001c0004t0001g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | ||||||
| chr12:110178783 | T | TTTTTTGT others(1868): Show |
7 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0140 others(4): Show |
7 | HG00423.hp1 NA18944.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | ||||||
| chr12:110178783 | T | TTTTTTGT others(1868): Show |
1 | a0001c0001t0001g0066 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | ||||||
| chr12:110178828 | G | T | 1 | a0001c0001t0001g0008 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1189-1594G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110178828 | |||||||
| chr12:110178897 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1189-1525G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110178897 | |||||||
| chr12:110179005 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1189-1417G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179005 | |||||||
| chr12:110179187 | A | G | 1 | a0001c0001t0006g0174 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1189-1235A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179187 | |||||||
| chr12:110179361 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1189-1061G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179361 | |||||||
| chr12:110179441 | G | T | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1189-981G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179441 | |||||||
| chr12:110179724 | T | TTA | 3 | a0001c0001t0002g0213 a0003c0003t0004g0077 a0004c0006t0004g0076 |
3 | HG01074.hp1 HG03654.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1189-649_1189-648d others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | ||||||
| chr12:110179724 | T | TTATATA | 2 | a0001c0001t0001g0063 a0001c0001t0001g0090 |
2 | HG01169.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1189-653_1189-648d others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | ||||||
| chr12:110179724 | TTA | T | 14 | a0001c0001t0001g0073 a0001c0001t0001g0079 a0001c0001t0001g0080 others(11): Show |
14 | HG01175.hp1 HG01361.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1189-649_1189-648d others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | ||||||
| chr12:110179724 | TTATA | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0106 a0001c0001t0001g0125 others(1): Show |
4 | HG01074.hp2 HG01891.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1189-651_1189-648d others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | ||||||
| chr12:110179724 | TTATATA | T | 3 | a0001c0001t0001g0095 a0001c0001t0001g0124 a0001c0001t0002g0181 |
3 | HG01243.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1189-653_1189-648d others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | ||||||
| chr12:110179724 | TTATATAT others(5): Show |
T | 1 | a0001c0001t0001g0127 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1189-659_1189-648d others(14): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | ||||||
| chr12:110179724 | TTATATAT others(7): Show |
T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0117 others(2): Show |
5 | HG01099.hp1 HG01099.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-661_1189-648d others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | ||||||
| chr12:110179724 | TTATATAT others(9): Show |
T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(3): Show |
6 | HG02630.hp1 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189-663_1189-648d others(18): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | ||||||
| chr12:110179724 | TTATATAT others(11): Show |
T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(6): Show |
9 | HG00735.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1189-665_1189-648d others(20): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | ||||||
| chr12:110179724 | TTATATAT others(13): Show |
T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0028 others(5): Show |
8 | HG00738.hp1 HG02559.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.1189-667_1189-648d others(22): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | ||||||
| chr12:110179724 | TTATATAT others(15): Show |
T | 16 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0026 others(13): Show |
16 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1189-669_1189-648d others(24): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | ||||||
| chr12:110179724 | TTATATAT others(17): Show |
T | 16 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(13): Show |
16 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.1189-671_1189-648d others(26): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | ||||||
| chr12:110179724 | TTATATAT others(19): Show |
T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0032 a0001c0001t0001g0119 others(1): Show |
4 | HG02257.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1189-673_1189-648d others(28): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | ||||||
| chr12:110179724 | TTATATAT others(21): Show |
T | 1 | a0001c0001t0001g0081 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1189-675_1189-648d others(30): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | ||||||
| chr12:110179739 | TATATATA others(29): Show |
T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0051 a0001c0001t0001g0052 others(5): Show |
9 | HG01167.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1189-681_1189-646d others(38): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179739 | ||||||
| chr12:110179744 | A | T | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1189-678A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179744 | |||||||
| chr12:110179745 | TATATATA others(23): Show |
T | 1 | a0001c0001t0001g0008 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1189-675_1189-646d others(32): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179745 | ||||||
| chr12:110179761 | T | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0023 others(2): Show |
5 | HG01099.hp1 HG02145.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-661T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179761 | |||||||
| chr12:110179763 | T | C | 9 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(6): Show |
9 | HG01099.hp1 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1189-659T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179763 | |||||||
| chr12:110179763 | TATATATA others(7): Show |
T | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1189-657_1189-644d others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179763 | ||||||
| chr12:110179765 | T | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(18): Show |
21 | HG01099.hp1 HG01099.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1189-657T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179765 | |||||||
| chr12:110179767 | T | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(24): Show |
27 | HG01099.hp1 HG01099.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1189-655T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179767 | |||||||
| chr12:110179767 | T | TACAC | 3 | a0001c0001t0003g0205 a0001c0001t0003g0208 a0001c0001t0003g0209 |
3 | HG01069.hp1 HG01071.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1189-654_1189-653i others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179767 | ||||||
| chr12:110179767 | TATATATA others(5): Show |
T | 1 | a0001c0001t0002g0182 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1189-653_1189-642d others(14): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179767 | ||||||
| chr12:110179769 | T | C | 67 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(64): Show |
67 | HG00323.hp2 HG00735.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.1189-653T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179769 | |||||||
| chr12:110179769 | T | TAC | 8 | a0001c0001t0001g0123 a0001c0001t0001g0154 a0001c0001t0001g0162 others(5): Show |
8 | HG00280.hp1 HG00642.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.1189-652_1189-651i others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179769 | ||||||
| chr12:110179769 | T | TACACAC | 2 | a0001c0001t0001g0152 a0001c0001t0001g0160 |
2 | HG00621.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1189-652_1189-651i others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179769 | ||||||
| chr12:110179769 | T | TACACACA others(3): Show |
2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG01943.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1189-652_1189-651i others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179769 | ||||||
| chr12:110179771 | T | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
97 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1189-651T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179771 | |||||||
| chr12:110179771 | T | TAC | 5 | a0001c0001t0001g0078 a0001c0001t0001g0105 a0001c0001t0001g0164 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-650_1189-649i others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179771 | ||||||
| chr12:110179771 | T | TACAC | 3 | a0001c0001t0002g0186 a0001c0001t0002g0192 a0001c0001t0003g0206 |
3 | HG01433.hp2 HG02293.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1189-650_1189-649i others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179771 | ||||||
| chr12:110179771 | T | TACACACA others(5): Show |
2 | a0001c0001t0001g0134 a0001c0001t0001g0165 |
2 | NA18948.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1189-650_1189-649i others(14): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179771 | ||||||
| chr12:110179771 | T | TACACACA others(7): Show |
1 | a0001c0001t0001g0211 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1189-650_1189-649i others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179771 | ||||||
| chr12:110179771 | T | TACACACA others(9): Show |
1 | a0001c0001t0001g0173 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1189-650_1189-649i others(18): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179771 | ||||||
| chr12:110179773 | T | C | 125 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
125 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.1189-649T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179773 | |||||||
| chr12:110179773 | T | TAC | 3 | a0001c0001t0001g0064 a0001c0001t0001g0082 a0001c0001t0001g0111 |
3 | HG02647.hp1 HG03209.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1189-617_1189-616d others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TACAC | 6 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0131 others(3): Show |
7 | HG01081.hp1 HG01109.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.1189-619_1189-616d others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TACACAC | 7 | a0001c0001t0001g0102 a0001c0001t0001g0115 a0001c0001t0001g0116 others(4): Show |
7 | HG00323.hp1 HG01168.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.1189-621_1189-616d others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TACACACA others(1): Show |
2 | a0001c0001t0001g0159 a0001c0001t0003g0207 |
2 | NA19001.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1189-623_1189-616d others(10): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TACACACA others(3): Show |
1 | a0001c0001t0001g0155 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1189-625_1189-616d others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TACACACA others(5): Show |
3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0150 |
3 | HG00621.hp2 HG01109.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.1189-627_1189-616d others(14): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TACACACA others(7): Show |
3 | a0001c0001t0001g0139 a0001c0001t0001g0167 a0001c0001t0001g0185 |
3 | HG01081.hp2 HG02523.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1189-629_1189-616d others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TACACACA others(9): Show |
1 | a0001c0001t0001g0178 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1189-631_1189-616d others(18): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TATAC | 3 | a0001c0001t0001g0085 a0001c0001t0001g0093 a0001c0001t0002g0216 |
3 | HG00741.hp2 HG01928.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1189-648_1189-647i others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TATACAC | 5 | a0001c0001t0001g0072 a0001c0001t0001g0107 a0001c0001t0001g0108 others(2): Show |
5 | HG00280.hp2 HG01123.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1189-648_1189-647i others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TATACACA others(1): Show |
2 | a0001c0001t0001g0112 a0001c0001t0002g0193 |
2 | HG00741.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1189-648_1189-647i others(10): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TATACACA others(3): Show |
3 | a0001c0001t0001g0143 a0001c0001t0001g0156 a0001c0001t0002g0194 |
3 | HG00423.hp2 HG04204.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1189-648_1189-647i others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TATACACA others(7): Show |
5 | a0001c0001t0001g0068 a0001c0001t0001g0135 a0001c0001t0001g0141 others(2): Show |
5 | HG00558.hp1 HG00558.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.1189-648_1189-647i others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TATACACA others(9): Show |
1 | a0001c0001t0001g0066 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1189-648_1189-647i others(18): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TATACACA others(15): Show |
1 | a0001c0001t0001g0168 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1189-648_1189-647i others(24): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TATATACA others(7): Show |
3 | a0001c0001t0001g0069 a0001c0001t0001g0147 a0001c0001t0001g0157 |
3 | HG04204.hp1 NA18952.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1189-648_1189-647i others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TATATACA others(9): Show |
1 | a0001c0001t0001g0161 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1189-648_1189-647i others(18): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TATATATA others(5): Show |
1 | a0001c0001t0002g0183 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1189-648_1189-647i others(14): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TATATATA others(7): Show |
2 | a0001c0001t0001g0067 a0001c0001t0001g0070 |
2 | NA19078.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1189-648_1189-647i others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TATATATA others(3): Show |
1 | a0001c0001t0001g0071 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1189-648_1189-647i others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TATATATA others(9): Show |
2 | a0001c0001t0001g0146 a0001c0001t0001g0148 |
2 | HG00423.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1189-648_1189-647i others(18): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TATATATA others(7): Show |
1 | a0001c0001t0002g0184 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1189-648_1189-647i others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TATATATA others(15): Show |
1 | a0001c0001t0001g0138 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1189-648_1189-647i others(24): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TATATATA others(15): Show |
1 | a0001c0001t0001g0140 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1189-648_1189-647i others(24): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TATATATA others(17): Show |
1 | a0001c0001t0001g0145 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1189-648_1189-647i others(26): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179773 | T | TATATATA others(23): Show |
1 | a0001c0001t0001g0142 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1189-648_1189-647i others(32): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | ||||||
| chr12:110179805 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1189-617C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179805 | |||||||
| chr12:110179806 | A | ACACACAC others(8): Show |
1 | a0001c0001t0001g0172 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1189-616_1189-615i others(17): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179806 | |||||||
| chr12:110179842 | A | AAT | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1189-568_1189-567d others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179842 | ||||||
| chr12:110179910 | G | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0008 |
2 | HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1189-512G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179910 | |||||||
| chr12:110180364 | A | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(2): Show |
5 | HG01099.hp1 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1189-58A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110180364 | |||||||
| chr12:110180707 | A | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(55): Show |
59 | HG00323.hp2 HG01069.hp2 HG01099.hp1 others(56): Show |
intron_variant | MODIFIER | c.1338+136A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110180707 | |||||||
| chr12:110180805 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1338+234A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110180805 | |||||||
| chr12:110180863 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1338+292G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110180863 | |||||||
| chr12:110181001 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG00423.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.1338+430G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110181001 | |||||||
| chr12:110181085 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(55): Show |
59 | HG00323.hp2 HG01069.hp2 HG01099.hp1 others(56): Show |
intron_variant | MODIFIER | c.1338+514C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110181085 | |||||||
| chr12:110181453 | G | C | 1 | a0001c0004t0001g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1338+882G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110181453 | |||||||
| chr12:110181544 | G | C | 8 | a0001c0001t0001g0112 a0001c0001t0001g0123 a0001c0001t0001g0128 others(5): Show |
8 | HG00099.hp2 HG00280.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1338+973G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110181544 | |||||||
| chr12:110181754 | C | T | 8 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 others(5): Show |
8 | HG01081.hp2 HG01943.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1338+1183C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110181754 | |||||||
| chr12:110181992 | T | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
61 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1338+1421T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110181992 | |||||||
| chr12:110182602 | A | T | 1 | a0001c0001t0002g0193 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1338+2031A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110182602 | |||||||
| chr12:110182631 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1338+2060G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110182631 | |||||||
| chr12:110182856 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
196 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1338+2285C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110182856 | |||||||
| chr12:110182871 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1338+2300C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110182871 | |||||||
| chr12:110182952 | G | A | 1 | a0001c0001t0002g0187 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1338+2381G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110182952 | |||||||
| chr12:110182960 | G | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(10): Show |
13 | HG01099.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1338+2389G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110182960 | |||||||
| chr12:110182976 | A | C | 1 | a0001c0001t0001g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1338+2405A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110182976 | |||||||
| chr12:110183010 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1338+2439C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110183010 | |||||||
| chr12:110183616 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1338+3045A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110183616 | |||||||
| chr12:110183638 | C | T | 12 | a0001c0001t0001g0050 a0001c0001t0001g0060 a0001c0001t0005g0039 others(9): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1338+3067C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110183638 | |||||||
| chr12:110183803 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1338+3232G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110183803 | |||||||
| chr12:110184089 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1338+3518G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184089 | |||||||
| chr12:110184139 | A | G | 1 | a0001c0001t0002g0175 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1338+3568A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184139 | |||||||
| chr12:110184153 | A | G | 1 | a0001c0001t0001g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1338+3582A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184153 | |||||||
| chr12:110184243 | G | C | 1 | a0001c0001t0001g0066 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1338+3672G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184243 | |||||||
| chr12:110184246 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1338+3675A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184246 | |||||||
| chr12:110184247 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1338+3676G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184247 | |||||||
| chr12:110184267 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1338+3696G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184267 | |||||||
| chr12:110184356 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1338+3785A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184356 | |||||||
| chr12:110184358 | T | A | 1 | a0001c0001t0001g0138 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1338+3787T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184358 | |||||||
| chr12:110184419 | T | G | 20 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0018 others(17): Show |
20 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.1338+3848T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184419 | |||||||
| chr12:110184505 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1338+3934C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184505 | |||||||
| chr12:110184738 | C | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(56): Show |
60 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.1338+4167C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184738 | |||||||
| chr12:110184908 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1338+4337A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184908 | |||||||
| chr12:110185185 | A | T | 1 | a0001c0001t0001g0056 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1338+4614A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110185185 | |||||||
| chr12:110185380 | C | T | 2 | a0001c0001t0002g0177 a0001c0001t0002g0203 |
2 | HG00642.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1338+4809C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110185380 | |||||||
| chr12:110185442 | G | A | 4 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0001c0001t0001g0087 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338+4871G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110185442 | |||||||
| chr12:110185852 | A | T | 1 | a0001c0001t0001g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1339-5068A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110185852 | |||||||
| chr12:110185907 | G | GA | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1339-5012dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr12 | 110185907 | ||||||
| chr12:110186132 | T | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0059 others(1): Show |
4 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1339-4788T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110186132 | |||||||
| chr12:110186169 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1339-4751G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110186169 | |||||||
| chr12:110186238 | C | CTTGT | 14 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(11): Show |
14 | HG00621.hp1 HG01099.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1339-4647_1339-464 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr12 | 110186238 | ||||||
| chr12:110186238 | CTTGT | C | 70 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0019 others(67): Show |
70 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.1339-4647_1339-464 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr12 | 110186238 | ||||||
| chr12:110186238 | CTTGTTTG others(1): Show |
C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(14): Show |
17 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.1339-4651_1339-464 others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr12 | 110186238 | ||||||
| chr12:110186288 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1339-4632G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110186288 | |||||||
| chr12:110186415 | G | A | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1339-4505G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110186415 | |||||||
| chr12:110186484 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1339-4436C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110186484 | |||||||
| chr12:110186496 | TC | T | 11 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0024 others(8): Show |
11 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1339-4423delC | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110186496 | |||||||
| chr12:110186717 | C | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1339-4203C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110186717 | |||||||
| chr12:110186746 | G | C | 1 | a0001c0001t0001g0094 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1339-4174G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110186746 | |||||||
| chr12:110186863 | G | A | 25 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0001t0002g0177 others(22): Show |
25 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.1339-4057G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110186863 | |||||||
| chr12:110186941 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1339-3979G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110186941 | |||||||
| chr12:110187254 | GTTGTTT | G | 25 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0001t0002g0177 others(22): Show |
25 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.1339-3645_1339-364 others(10): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr12 | 110187254 | ||||||
| chr12:110187344 | G | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
128 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.1339-3576G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110187344 | |||||||
| chr12:110187504 | A | G | 1 | a0001c0001t0002g0215 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1339-3416A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110187504 | |||||||
| chr12:110187517 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1339-3403G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110187517 | |||||||
| chr12:110187545 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1339-3375A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110187545 | |||||||
| chr12:110187704 | A | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1339-3216A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110187704 | |||||||
| chr12:110187772 | T | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0145 |
2 | NA18984.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1339-3148T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110187772 | |||||||
| chr12:110187847 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1339-3073G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110187847 | |||||||
| chr12:110188058 | C | T | 3 | a0001c0001t0003g0205 a0001c0001t0003g0208 a0001c0001t0003g0209 |
3 | HG01069.hp1 HG01071.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1339-2862C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110188058 | |||||||
| chr12:110188070 | C | T | 5 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1339-2850C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110188070 | |||||||
| chr12:110188186 | G | A | 1 | a0001c0001t0006g0174 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1339-2734G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110188186 | |||||||
| chr12:110188208 | G | A | 6 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 others(3): Show |
6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1339-2712G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110188208 | |||||||
| chr12:110188346 | A | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1339-2574A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110188346 | |||||||
| chr12:110188752 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1339-2168A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110188752 | |||||||
| chr12:110188768 | C | CA | 14 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(11): Show |
15 | HG01109.hp2 HG02145.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.1339-2137dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr12 | 110188768 | ||||||
| chr12:110188768 | CA | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(2): Show |
5 | HG00738.hp1 HG01069.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1339-2137delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr12 | 110188768 | ||||||
| chr12:110188853 | C | T | 9 | a0002c0002t0001g0014 a0002c0002t0001g0038 a0002c0002t0001g0040 others(6): Show |
9 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1339-2067C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110188853 | |||||||
| chr12:110188933 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1339-1987A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110188933 | |||||||
| chr12:110189272 | G | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1339-1648G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110189272 | |||||||
| chr12:110189282 | A | G | 5 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1339-1638A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110189282 | |||||||
| chr12:110189336 | TTTTA | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1339-1560_1339-155 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr12 | 110189336 | ||||||
| chr12:110189506 | A | G | 1 | a0001c0001t0002g0202 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1339-1414A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110189506 | |||||||
| chr12:110189624 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1339-1296C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110189624 | |||||||
| chr12:110189629 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
3 | HG02630.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1339-1291G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110189629 | |||||||
| chr12:110189876 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1339-1044A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110189876 | |||||||
| chr12:110190107 | C | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0036 |
3 | HG00323.hp2 HG01175.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1339-813C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110190107 | |||||||
| chr12:110190192 | A | AGAGTGCA others(4): Show |
1 | a0001c0001t0001g0066 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1339-727_1339-717d others(13): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr12 | 110190192 | ||||||
| chr12:110190475 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1339-445C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110190475 | |||||||
| chr12:110190504 | A | AT | 11 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(8): Show |
12 | HG00738.hp1 HG01069.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1339-406dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr12 | 110190504 | ||||||
| chr12:110191168 | CT | C | 9 | a0001c0001t0001g0066 a0001c0001t0001g0078 a0001c0001t0001g0143 others(6): Show |
9 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1467+134delT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr12 | 110191168 | ||||||
| chr12:110191441 | G | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1467+393G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110191441 | |||||||
| chr12:110191461 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
128 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.1467+413A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110191461 | |||||||
| chr12:110191687 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
107 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1467+639T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110191687 | |||||||
| chr12:110191766 | C | A | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1467+718C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110191766 | |||||||
| chr12:110191792 | C | T | 9 | a0002c0002t0001g0014 a0002c0002t0001g0038 a0002c0002t0001g0040 others(6): Show |
9 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1467+744C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110191792 | |||||||
| chr12:110191899 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0164 |
2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1468-718G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110191899 | |||||||
| chr12:110192011 | A | C | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1468-606A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110192011 | |||||||
| chr12:110192114 | T | C | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(1): Show |
4 | HG02257.hp1 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468-503T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110192114 | |||||||
| chr12:110192149 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1468-468C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110192149 | |||||||
| chr12:110192415 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1468-202C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110192415 | |||||||
| chr12:110192421 | G | A | 1 | a0001c0001t0003g0205 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1468-196G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110192421 | |||||||
| chr12:110192453 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1468-164T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110192453 | |||||||
| chr12:110192555 | A | C | 1 | a0001c0001t0001g0163 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1468-62A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110192555 | |||||||
| chr12:110192933 | A | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(2): Show |
5 | HG01099.hp1 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1557+227A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110192933 | |||||||
| chr12:110193263 | G | C | 2 | a0001c0001t0002g0184 a0001c0001t0002g0204 |
2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1557+557G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110193263 | |||||||
| chr12:110193316 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1557+610A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110193316 | |||||||
| chr12:110193323 | T | C | 1 | a0001c0001t0006g0174 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1557+617T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110193323 | |||||||
| chr12:110193486 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1557+780A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110193486 | |||||||
| chr12:110193581 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1557+875A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110193581 | |||||||
| chr12:110193647 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1557+941A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110193647 | |||||||
| chr12:110194076 | C | T | 5 | a0001c0001t0001g0140 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
5 | HG00423.hp1 NA18944.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1557+1370C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110194076 | |||||||
| chr12:110194137 | C | T | 7 | a0001c0001t0001g0061 a0001c0001t0001g0092 a0001c0001t0001g0093 others(4): Show |
7 | HG01516.hp2 HG01928.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.1557+1431C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110194137 | |||||||
| chr12:110194901 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1557+2195C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110194901 | |||||||
| chr12:110195986 | A | C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1557+3280A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110195986 | |||||||
| chr12:110195991 | T | C | 1 | a0001c0001t0002g0192 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1557+3285T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110195991 | |||||||
| chr12:110196005 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1557+3299C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110196005 | |||||||
| chr12:110196185 | T | A | 1 | a0001c0001t0001g0094 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1557+3479T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110196185 | |||||||
| chr12:110196300 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0059 |
2 | HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1557+3594C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110196300 | |||||||
| chr12:110196510 | A | C | 1 | a0001c0001t0001g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1557+3804A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110196510 | |||||||
| chr12:110196576 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1557+3870G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110196576 | |||||||
| chr12:110196713 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1557+4007C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110196713 | |||||||
| chr12:110196836 | A | C | 1 | a0001c0001t0001g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1557+4130A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110196836 | |||||||
| chr12:110197076 | A | G | 16 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0115 others(13): Show |
16 | HG00423.hp2 HG00558.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1557+4370A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197076 | |||||||
| chr12:110197172 | G | C | 8 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(5): Show |
8 | HG02055.hp1 HG02257.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1557+4466G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197172 | |||||||
| chr12:110197199 | G | T | 1 | a0001c0001t0001g0185 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1557+4493G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197199 | |||||||
| chr12:110197248 | G | GTAGA | 26 | a0001c0001t0001g0049 a0001c0001t0001g0059 a0001c0001t0001g0069 others(23): Show |
26 | HG00099.hp1 HG00423.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1557+4584_1557+458 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197248 | ||||||
| chr12:110197248 | G | GTAGATAG others(1): Show |
5 | a0001c0001t0001g0062 a0001c0001t0001g0102 a0001c0001t0001g0155 others(2): Show |
5 | HG01243.hp2 HG02071.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1557+4580_1557+458 others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197248 | ||||||
| chr12:110197248 | GTAGA | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.1557+4584_1557+458 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197248 | ||||||
| chr12:110197248 | GTAGATAG others(1): Show |
G | 19 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0018 others(16): Show |
19 | HG00323.hp2 HG01074.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1557+4580_1557+458 others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197248 | ||||||
| chr12:110197248 | GTAGATAG others(5): Show |
G | 3 | a0001c0001t0001g0006 a0001c0001t0003g0206 a0001c0001t0003g0207 |
3 | HG02293.hp1 HG03579.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1557+4576_1557+458 others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197248 | ||||||
| chr12:110197248 | GTAGATAG others(9): Show |
G | 3 | a0001c0001t0003g0205 a0001c0001t0003g0208 a0001c0001t0003g0209 |
3 | HG01069.hp1 HG01071.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1557+4572_1557+458 others(20): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197248 | ||||||
| chr12:110197252 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0002g0189 |
2 | HG02683.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1557+4546A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197252 | |||||||
| chr12:110197256 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1557+4550A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197256 | |||||||
| chr12:110197414 | A | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1557+4708A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197414 | |||||||
| chr12:110197438 | C | G | 1 | a0001c0001t0002g0194 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1557+4732C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197438 | |||||||
| chr12:110197445 | CT | C | 19 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0093 others(16): Show |
19 | HG00423.hp2 HG00558.hp2 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.1557+4750delT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197445 | ||||||
| chr12:110197555 | C | CAT | 24 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0063 others(21): Show |
24 | HG00423.hp2 HG00558.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1557+4877_1557+487 others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197555 | ||||||
| chr12:110197555 | C | CATAT | 14 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(11): Show |
14 | HG01069.hp1 HG01071.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1557+4875_1557+487 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197555 | ||||||
| chr12:110197555 | C | CATATAT | 3 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0002g0190 |
3 | HG00280.hp1 HG01243.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1557+4873_1557+487 others(10): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197555 | ||||||
| chr12:110197555 | C | CATATATA others(5): Show |
1 | a0001c0001t0001g0005 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1557+4867_1557+487 others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197555 | ||||||
| chr12:110197555 | C | CATATATA others(7): Show |
1 | a0001c0001t0001g0004 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1557+4865_1557+487 others(18): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197555 | ||||||
| chr12:110197555 | C | CATATATA others(9): Show |
1 | a0001c0001t0001g0007 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1557+4863_1557+487 others(20): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197555 | ||||||
| chr12:110197555 | C | CATATATA others(11): Show |
1 | a0001c0001t0001g0008 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1557+4861_1557+487 others(22): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197555 | ||||||
| chr12:110197555 | CAT | C | 13 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0049 others(10): Show |
13 | HG01081.hp2 HG01943.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1557+4877_1557+487 others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197555 | ||||||
| chr12:110197555 | CATAT | C | 32 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(29): Show |
33 | HG00323.hp2 HG01167.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1557+4875_1557+487 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197555 | ||||||
| chr12:110197555 | CATATATA others(5): Show |
C | 1 | a0001c0001t0001g0003 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1557+4867_1557+487 others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197555 | ||||||
| chr12:110197567 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1557+4861T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197567 | |||||||
| chr12:110197583 | T | C | 11 | a0001c0001t0001g0050 a0001c0001t0005g0039 a0002c0002t0001g0014 others(8): Show |
11 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1557+4877T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197583 | |||||||
| chr12:110197714 | T | A | 1 | a0001c0001t0001g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1557+5008T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197714 | |||||||
| chr12:110197799 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1557+5093G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197799 | |||||||
| chr12:110197932 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1557+5226G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197932 | |||||||
| chr12:110197958 | C | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(6): Show |
9 | HG01099.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1557+5252C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197958 | |||||||
| chr12:110198209 | T | C | 5 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1557+5503T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198209 | |||||||
| chr12:110198286 | T | G | 6 | a0001c0001t0002g0176 a0001c0001t0002g0188 a0001c0001t0002g0196 others(3): Show |
6 | HG01071.hp1 HG01081.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-5578T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198286 | |||||||
| chr12:110198287 | T | A | 1 | a0001c0001t0001g0165 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1558-5577T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198287 | |||||||
| chr12:110198505 | A | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(2): Show |
5 | HG01099.hp1 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1558-5359A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198505 | |||||||
| chr12:110198562 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1558-5302C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198562 | |||||||
| chr12:110198563 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1558-5301G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198563 | |||||||
| chr12:110198671 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1558-5193T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198671 | |||||||
| chr12:110198755 | A | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1558-5109A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198755 | |||||||
| chr12:110198816 | T | C | 2 | a0001c0001t0001g0074 a0001c0001t0002g0204 |
2 | HG01109.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1558-5048T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198816 | |||||||
| chr12:110198849 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1558-5015G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198849 | |||||||
| chr12:110198885 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0016 |
2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1558-4979C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198885 | |||||||
| chr12:110199361 | C | T | 3 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0001c0001t0001g0087 |
3 | HG01167.hp1 HG01169.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1558-4503C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110199361 | |||||||
| chr12:110199450 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0016 |
2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1558-4414T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110199450 | |||||||
| chr12:110199738 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1558-4126T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110199738 | |||||||
| chr12:110199883 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1558-3981C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110199883 | |||||||
| chr12:110200399 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1558-3465C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110200399 | |||||||
| chr12:110200508 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1558-3356C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110200508 | |||||||
| chr12:110200674 | GCACGGTG others(3): Show |
G | 9 | a0002c0002t0001g0014 a0002c0002t0001g0038 a0002c0002t0001g0040 others(6): Show |
9 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1558-3185_1558-317 others(14): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110200674 | ||||||
| chr12:110200720 | C | A | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1558-3144C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110200720 | |||||||
| chr12:110200729 | G | T | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1558-3135G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110200729 | |||||||
| chr12:110200824 | G | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1558-3040G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110200824 | |||||||
| chr12:110200906 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1558-2958C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110200906 | |||||||
| chr12:110200907 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1558-2957G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110200907 | |||||||
| chr12:110200960 | A | T | 1 | a0001c0001t0001g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1558-2904A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110200960 | |||||||
| chr12:110201187 | G | C | 3 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 |
3 | HG02559.hp1 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1558-2677G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110201187 | |||||||
| chr12:110201402 | CA | C | 7 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(4): Show |
7 | HG00735.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1558-2447delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110201402 | ||||||
| chr12:110201470 | C | T | 3 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0001c0001t0001g0087 |
3 | HG01167.hp1 HG01169.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1558-2394C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110201470 | |||||||
| chr12:110201520 | T | G | 5 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1558-2344T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110201520 | |||||||
| chr12:110201524 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1558-2340G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110201524 | |||||||
| chr12:110201599 | T | TTTTA | 8 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 others(5): Show |
8 | HG01081.hp2 HG01943.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1558-2241_1558-223 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110201599 | ||||||
| chr12:110201807 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1558-2057G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110201807 | |||||||
| chr12:110202248 | T | G | 5 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG02257.hp1 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1558-1616T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202248 | |||||||
| chr12:110202254 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1558-1610G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202254 | |||||||
| chr12:110202269 | T | G | 1 | a0001c0001t0001g0153 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1558-1595T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202269 | |||||||
| chr12:110202349 | A | C | 1 | a0001c0001t0001g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1558-1515A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202349 | |||||||
| chr12:110202393 | A | G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG00423.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.1558-1471A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202393 | |||||||
| chr12:110202453 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(53): Show |
57 | HG00323.hp2 HG01099.hp1 HG01167.hp2 others(54): Show |
intron_variant | MODIFIER | c.1558-1411C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202453 | |||||||
| chr12:110202457 | C | CT | 9 | a0001c0001t0001g0001 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
10 | HG01167.hp2 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1558-1393dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110202457 | ||||||
| chr12:110202512 | G | A | 1 | a0001c0001t0002g0196 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1558-1352G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202512 | |||||||
| chr12:110202522 | G | A | 8 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 others(5): Show |
8 | HG01081.hp2 HG01943.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1558-1342G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202522 | |||||||
| chr12:110202854 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1558-1010C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202854 | |||||||
| chr12:110202923 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1558-941A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202923 | |||||||
| chr12:110202923 | A | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01891.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1558-941A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202923 | |||||||
| chr12:110202994 | G | A | 5 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1558-870G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202994 | |||||||
| chr12:110203064 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1558-800A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110203064 | |||||||
| chr12:110203127 | A | T | 1 | a0001c0001t0001g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1558-737A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110203127 | |||||||
| chr12:110203470 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1558-394A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110203470 | |||||||
| chr12:110203498 | T | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1558-366T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110203498 | |||||||
| chr12:110204091 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1644+141C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 15/18 | chr12 | 110204091 | |||||||
| chr12:110204380 | T | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0051 a0001c0001t0001g0052 others(5): Show |
9 | HG01167.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1644+430T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 15/18 | chr12 | 110204380 | |||||||
| chr12:110204385 | A | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(70): Show |
74 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.1644+435A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 15/18 | chr12 | 110204385 | |||||||
| chr12:110204821 | C | G | 2 | a0001c0001t0002g0196 a0001c0001t0002g0197 |
2 | HG01071.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1645-622C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 15/18 | chr12 | 110204821 | |||||||
| chr12:110204965 | C | T | 8 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 others(5): Show |
8 | HG01081.hp2 HG01943.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1645-478C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 15/18 | chr12 | 110204965 | |||||||
| chr12:110205052 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1645-391G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 15/18 | chr12 | 110205052 | |||||||
| chr12:110205247 | G | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1645-196G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 15/18 | chr12 | 110205247 | |||||||
| chr12:110205409 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1645-34G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 15/18 | chr12 | 110205409 | |||||||
| chr12:110205955 | T | C | 4 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0142 others(1): Show |
4 | HG01934.hp1 HG02004.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.1802+275T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110205955 | |||||||
| chr12:110205974 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0060 |
2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1802+294C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110205974 | |||||||
| chr12:110206003 | G | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1802+323G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110206003 | |||||||
| chr12:110206240 | G | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(56): Show |
60 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.1802+560G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110206240 | |||||||
| chr12:110206490 | A | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1802+810A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110206490 | |||||||
| chr12:110206491 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1802+811G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110206491 | |||||||
| chr12:110206547 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1802+867C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110206547 | |||||||
| chr12:110206548 | G | A | 5 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1802+868G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110206548 | |||||||
| chr12:110206675 | T | TA | 12 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0030 others(9): Show |
12 | HG00741.hp1 HG00741.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1802+1015dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr12 | 110206675 | ||||||
| chr12:110206890 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1802+1210G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110206890 | |||||||
| chr12:110207034 | A | AT | 5 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1802+1367dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr12 | 110207034 | ||||||
| chr12:110207121 | C | A | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1802+1441C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110207121 | |||||||
| chr12:110207499 | C | T | 1 | a0002c0002t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1803-1672C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110207499 | |||||||
| chr12:110207545 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0164 |
2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1803-1626C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110207545 | |||||||
| chr12:110207556 | C | CT | 16 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0036 others(13): Show |
16 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1803-1591dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr12 | 110207556 | ||||||
| chr12:110207785 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1803-1386G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110207785 | |||||||
| chr12:110207808 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0037 |
2 | HG03491.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1803-1363C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110207808 | |||||||
| chr12:110207949 | A | T | 1 | a0002c0002t0001g0046 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1803-1222A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110207949 | |||||||
| chr12:110208024 | G | A | 19 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0018 others(16): Show |
19 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1803-1147G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110208024 | |||||||
| chr12:110208106 | C | T | 1 | a0001c0001t0002g0175 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1803-1065C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110208106 | |||||||
| chr12:110208403 | G | A | 2 | a0001c0001t0002g0184 a0001c0001t0002g0204 |
2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1803-768G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110208403 | |||||||
| chr12:110208475 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1803-696C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110208475 | |||||||
| chr12:110208656 | C | G | 1 | a0001c0001t0001g0073 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1803-515C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110208656 | |||||||
| chr12:110208665 | A | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1803-506A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110208665 | |||||||
| chr12:110208898 | G | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0051 a0001c0001t0001g0052 others(5): Show |
9 | HG01167.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1803-273G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110208898 | |||||||
| chr12:110209030 | T | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1803-141T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110209030 | |||||||
| chr12:110209035 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1803-136T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110209035 | |||||||
| chr12:110209069 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1803-102A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110209069 | |||||||
| chr12:110209394 | T | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1848+178T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110209394 | |||||||
| chr12:110209768 | C | CA | 9 | a0001c0001t0001g0006 a0001c0001t0001g0057 a0001c0001t0001g0168 others(6): Show |
9 | HG01081.hp2 HG01243.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1848+572dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110209768 | ||||||
| chr12:110209768 | CA | C | 7 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0033 others(4): Show |
7 | HG00738.hp2 HG02486.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1848+572delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110209768 | ||||||
| chr12:110209924 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1848+708G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110209924 | |||||||
| chr12:110210086 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1848+870A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210086 | |||||||
| chr12:110210257 | G | C | 1 | a0001c0001t0001g0136 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1848+1041G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210257 | |||||||
| chr12:110210564 | C | A | 1 | a0001c0001t0001g0067 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1848+1348C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210564 | |||||||
| chr12:110210687 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1848+1471C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210687 | |||||||
| chr12:110210793 | A | G | 10 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(7): Show |
10 | HG01099.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1848+1577A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210793 | |||||||
| chr12:110210849 | A | T | 1 | a0001c0001t0001g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1848+1633A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210849 | |||||||
| chr12:110210946 | C | G | 1 | a0001c0001t0001g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1848+1730C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210946 | |||||||
| chr12:110210951 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1848+1735G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210951 | |||||||
| chr12:110210954 | C | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1848+1738C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210954 | |||||||
| chr12:110210958 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1848+1742C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210958 | |||||||
| chr12:110210998 | G | A | 1 | a0001c0004t0001g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1848+1782G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210998 | |||||||
| chr12:110211030 | A | AT | 6 | a0001c0001t0001g0006 a0001c0001t0001g0068 a0001c0001t0001g0111 others(3): Show |
6 | HG00741.hp1 HG01243.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1848+1828dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110211030 | ||||||
| chr12:110211133 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1848+1917T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211133 | |||||||
| chr12:110211139 | C | T | 6 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 others(3): Show |
6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1848+1923C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211139 | |||||||
| chr12:110211175 | C | CT | 23 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(20): Show |
23 | HG01071.hp2 HG01099.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1848+1980dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110211175 | ||||||
| chr12:110211175 | CT | C | 10 | a0001c0001t0001g0160 a0001c0001t0001g0168 a0001c0001t0001g0170 others(7): Show |
10 | HG01943.hp1 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1848+1980delT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110211175 | ||||||
| chr12:110211175 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0029 |
2 | NA18952.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1848+1971_1848+198 others(14): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110211175 | ||||||
| chr12:110211175 | CTTTTTTT others(5): Show |
C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0051 a0001c0001t0001g0052 others(5): Show |
9 | HG01167.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1848+1969_1848+198 others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110211175 | ||||||
| chr12:110211179 | T | C | 14 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(11): Show |
14 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1848+1963T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211179 | |||||||
| chr12:110211188 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1848+1972T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211188 | |||||||
| chr12:110211190 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1848+1974T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211190 | |||||||
| chr12:110211191 | T | C | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01891.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1848+1975T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211191 | |||||||
| chr12:110211216 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1848+2000G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211216 | |||||||
| chr12:110211302 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1848+2086G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211302 | |||||||
| chr12:110211719 | C | T | 5 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG02257.hp1 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1848+2503C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211719 | |||||||
| chr12:110211806 | C | A | 1 | a0001c0001t0001g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1848+2590C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211806 | |||||||
| chr12:110211873 | A | G | 1 | a0001c0001t0001g0143 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1848+2657A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211873 | |||||||
| chr12:110211931 | A | G | 1 | a0001c0001t0002g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1848+2715A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211931 | |||||||
| chr12:110211985 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1848+2769G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211985 | |||||||
| chr12:110212226 | G | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0047 others(20): Show |
24 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1848+3010G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110212226 | |||||||
| chr12:110212242 | TA | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
125 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.1848+3044delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110212242 | ||||||
| chr12:110212537 | T | TAA | 5 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG02257.hp1 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1848+3334_1848+333 others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110212537 | ||||||
| chr12:110212635 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1848+3419A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110212635 | |||||||
| chr12:110212693 | C | T | 8 | a0001c0001t0001g0112 a0001c0001t0001g0123 a0001c0001t0001g0128 others(5): Show |
8 | HG00099.hp2 HG00280.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1848+3477C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110212693 | |||||||
| chr12:110212697 | C | A | 1 | a0001c0001t0001g0104 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1848+3481C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110212697 | |||||||
| chr12:110213062 | ACT | A | 5 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG02257.hp1 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1848+3849_1848+385 others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110213062 | ||||||
| chr12:110213105 | G | T | 1 | a0001c0001t0001g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1848+3889G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110213105 | |||||||
| chr12:110213122 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
3 | HG02630.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1848+3906G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110213122 | |||||||
| chr12:110213654 | C | G | 6 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0027 others(3): Show |
6 | NA18948.hp1 NA18952.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.1849-4390C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110213654 | |||||||
| chr12:110213729 | G | C | 1 | a0001c0001t0001g0110 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1849-4315G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110213729 | |||||||
| chr12:110213733 | C | A | 5 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1849-4311C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110213733 | |||||||
| chr12:110213783 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1849-4261G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110213783 | |||||||
| chr12:110214004 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0172 |
2 | HG01943.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1849-4040G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110214004 | |||||||
| chr12:110214055 | C | A | 1 | a0001c0001t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1849-3989C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110214055 | |||||||
| chr12:110214154 | G | T | 1 | a0001c0004t0001g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1849-3890G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110214154 | |||||||
| chr12:110214284 | G | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0047 others(21): Show |
25 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1849-3760G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110214284 | |||||||
| chr12:110214758 | A | G | 1 | a0001c0001t0002g0182 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1849-3286A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110214758 | |||||||
| chr12:110215080 | C | G | 5 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG02257.hp1 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1849-2964C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215080 | |||||||
| chr12:110215175 | C | T | 1 | a0002c0002t0001g0040 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1849-2869C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215175 | |||||||
| chr12:110215232 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1849-2812G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215232 | |||||||
| chr12:110215325 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1849-2719A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215325 | |||||||
| chr12:110215431 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1849-2613T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215431 | |||||||
| chr12:110215433 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1849-2611C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215433 | |||||||
| chr12:110215453 | C | CT | 42 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0019 others(39): Show |
42 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.1849-2562dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110215453 | ||||||
| chr12:110215453 | C | CTT | 19 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(16): Show |
19 | HG01099.hp1 HG01167.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.1849-2563_1849-256 others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110215453 | ||||||
| chr12:110215453 | C | CTTT | 6 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(3): Show |
6 | HG02486.hp1 HG02717.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1849-2564_1849-256 others(7): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110215453 | ||||||
| chr12:110215453 | C | CTTTT | 6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(3): Show |
6 | HG01168.hp1 HG01169.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1849-2565_1849-256 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110215453 | ||||||
| chr12:110215453 | C | CTTTTT | 5 | a0001c0001t0001g0015 a0002c0002t0001g0040 a0002c0002t0001g0041 others(2): Show |
5 | HG01243.hp2 HG02109.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1849-2566_1849-256 others(9): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110215453 | ||||||
| chr12:110215453 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1849-2591C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215453 | |||||||
| chr12:110215453 | CT | C | 15 | a0001c0001t0001g0069 a0001c0001t0001g0091 a0001c0001t0001g0094 others(12): Show |
15 | HG01074.hp1 HG01074.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.1849-2562delT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110215453 | ||||||
| chr12:110215453 | CTTT | C | 19 | a0001c0001t0001g0006 a0001c0001t0001g0096 a0001c0001t0002g0175 others(16): Show |
19 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.1849-2564_1849-256 others(7): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110215453 | ||||||
| chr12:110215524 | T | G | 10 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0001c0001t0001g0085 others(7): Show |
10 | HG00642.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1849-2520T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215524 | |||||||
| chr12:110215537 | C | T | 8 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 others(5): Show |
8 | HG01081.hp2 HG01943.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1849-2507C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215537 | |||||||
| chr12:110215584 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1849-2460C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215584 | |||||||
| chr12:110215628 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1849-2416A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215628 | |||||||
| chr12:110215677 | G | T | 1 | a0001c0001t0001g0115 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1849-2367G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215677 | |||||||
| chr12:110215701 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1849-2343T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215701 | |||||||
| chr12:110215736 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1849-2308G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215736 | |||||||
| chr12:110215789 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1849-2255A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215789 | |||||||
| chr12:110215839 | T | G | 1 | a0001c0001t0001g0066 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1849-2205T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215839 | |||||||
| chr12:110215892 | T | TAACAAAA others(335): Show |
1 | a0001c0001t0001g0005 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1849-2136_1849-213 others(346): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110215892 | ||||||
| chr12:110215894 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1849-2150A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215894 | |||||||
| chr12:110215895 | C | CAAAAACA others(337): Show |
1 | a0001c0001t0001g0003 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1849-2136_1849-213 others(348): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110215895 | ||||||
| chr12:110215895 | C | CAAAAACA others(338): Show |
1 | a0001c0001t0001g0004 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1849-2136_1849-213 others(349): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110215895 | ||||||
| chr12:110216052 | T | C | 19 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0018 others(16): Show |
19 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1849-1992T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110216052 | |||||||
| chr12:110216173 | G | GTTGTT | 2 | a0001c0001t0001g0122 a0001c0004t0001g0021 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1849-1843_1849-183 others(9): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110216173 | ||||||
| chr12:110216442 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1849-1602G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110216442 | |||||||
| chr12:110216516 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1849-1528T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110216516 | |||||||
| chr12:110216746 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1849-1298G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110216746 | |||||||
| chr12:110216899 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1849-1145G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110216899 | |||||||
| chr12:110217325 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1849-719G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110217325 | |||||||
| chr12:110217622 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1849-422C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110217622 | |||||||
| chr12:110217665 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0004t0001g0021 |
3 | HG02055.hp1 HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1849-379G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110217665 | |||||||
| chr12:110217786 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1849-258A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110217786 | |||||||
| chr12:110217814 | T | G | 1 | a0001c0001t0001g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1849-230T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110217814 | |||||||
| chr12:110217818 | G | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1849-226G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110217818 | |||||||
| chr12:110217877 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0059 |
2 | HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1849-167G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110217877 | |||||||
| chr12:110217900 | T | C | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01891.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1849-144T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110217900 | |||||||
| chr12:110217907 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1849-137G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110217907 | |||||||
| chr12:110217985 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1849-59C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110217985 |