Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51098 |
| ensemblid | ENSG00000101052.13 |
| hgncid | 15901 |
| symbol | IFT52 |
| name | intraflagellar transport 52 |
| refseq_nuc | NM_016004.5 |
| refseq_prot | NP_057088.2 |
| ensembl_nuc | ENST00000373030.8 |
| ensembl_prot | ENSP00000362121.3 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 43590937 |
| end | 43647299 |
| strand | + |
| ver | v1.2 |
| region | chr20:43590937-43647299 |
| region5000 | chr20:43585937-43652299 |
| regionname0 | IFT52_chr20_43590937_43647299 |
| regionname5000 | IFT52_chr20_43585937_43652299 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 437 | 295 | 77 | 64 | 106 | 10 | 36 | 80 | IFT52_chr20_43585937_43652299 | IFT52 | MEKEL others(432): Show |
chr20 | 43585937 | 43652299 |
| a0002 | 0/0 | 437 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | MEKEL others(432): Show |
chr20 | 43585937 | 43652299 |
| a0003 | 0/0 | 437 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | MEKEL others(432): Show |
chr20 | 43585937 | 43652299 |
| a0004 | 0/0 | 437 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | MEKEL others(432): Show |
chr20 | 43585937 | 43652299 |
| a0005 | 0/0 | 437 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | MEKEL others(432): Show |
chr20 | 43585937 | 43652299 |
| a0006 | 0/0 | 437 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | MEKEL others(432): Show |
chr20 | 43585937 | 43652299 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1311 | 179 | 44 | 45 | 56 | 10 | 24 | IFT52_chr20_43585937_43652299 | IFT52 | ATGGA others(1306): Show |
chr20 | 43585937 | 43652299 | ||
| a0001c0002 | 1/1 | 1311 | 109 | 27 | 18 | 50 | 0 | 12 | IFT52_chr20_43585937_43652299 | IFT52 | ATGGA others(1306): Show |
chr20 | 43585937 | 43652299 | ||
| a0001c0003 | 0/0 | 1311 | 6 | 5 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | ATGGA others(1306): Show |
chr20 | 43585937 | 43652299 | ||
| a0001c0006 | 0/0 | 1311 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | ATGGA others(1306): Show |
chr20 | 43585937 | 43652299 | ||
| a0002c0008 | 0/0 | 1311 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | ATGGA others(1306): Show |
chr20 | 43585937 | 43652299 | ||
| a0003c0007 | 0/0 | 1311 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | ATGGA others(1306): Show |
chr20 | 43585937 | 43652299 | ||
| a0004c0009 | 0/0 | 1311 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | ATGGA others(1306): Show |
chr20 | 43585937 | 43652299 | ||
| a0005c0004 | 0/0 | 1311 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | ATGGA others(1306): Show |
chr20 | 43585937 | 43652299 | ||
| a0006c0005 | 0/0 | 1311 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | ATGGA others(1306): Show |
chr20 | 43585937 | 43652299 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1754 | 178 | 44 | 45 | 55 | 10 | 24 | IFT52_chr20_43585937_43652299 | IFT52 | GCGTC others(1749): Show |
chr20 | 43585937 | 43652299 |
| a0001c0001t0002 | 0/0 | 1754 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | GCGTC others(1749): Show |
chr20 | 43585937 | 43652299 |
| a0001c0002t0001 | 1/1 | 1754 | 109 | 27 | 18 | 50 | 0 | 12 | IFT52_chr20_43585937_43652299 | IFT52 | GCGTC others(1749): Show |
chr20 | 43585937 | 43652299 |
| a0001c0003t0001 | 0/0 | 1754 | 6 | 5 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | GCGTC others(1749): Show |
chr20 | 43585937 | 43652299 |
| a0001c0006t0001 | 0/0 | 1754 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | GCGTC others(1749): Show |
chr20 | 43585937 | 43652299 |
| a0002c0008t0001 | 0/0 | 1754 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | GCGTC others(1749): Show |
chr20 | 43585937 | 43652299 |
| a0003c0007t0001 | 0/0 | 1754 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | GCGTC others(1749): Show |
chr20 | 43585937 | 43652299 |
| a0004c0009t0001 | 0/0 | 1754 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | GCGTC others(1749): Show |
chr20 | 43585937 | 43652299 |
| a0005c0004t0001 | 0/0 | 1754 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | GCGTC others(1749): Show |
chr20 | 43585937 | 43652299 |
| a0006c0005t0003 | 0/0 | 1754 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | GCGTC others(1749): Show |
chr20 | 43585937 | 43652299 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0001 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0003 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0003t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0003t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0003t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0001c0006t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0002c0008t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0003c0007t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0004c0009t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0005c0004t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| a0006c0005t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | GBR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | GBR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | FIN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | FIN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | FIN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | FIN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | CHS | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0129 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0080 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0020 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0079 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0059 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0056 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02056 | hp1 | a0002 | c0008 | t0001 | g0034 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02083 | hp2 | a0003 | c0007 | t0001 | g0093 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | KHV | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0052 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CDX | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | CDX | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0040 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0121 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0071 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0107 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0106 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0133 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0090 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0047 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0076 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0085 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0267 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0105 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0084 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0082 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | ESN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | ESN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0086 | AFR | MSL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0081 | AFR | MSL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | ESN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | GWD | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0089 | AFR | MSL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0050 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0078 | SAS | BEB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | BEB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | STU | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | STU | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | STU | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0103 | SAS | STU | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | STU | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18906 | hp1 | a0004 | c0009 | t0001 | g0021 | AFR | YRI | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | LWK | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | LWK | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | LWK | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0088 | AFR | LWK | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | YRI | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0022 | AFR | YRI | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA20129 | hp1 | a0005 | c0004 | t0001 | g0190 | AFR | ASW | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | TSI | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | TSI | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | TSI | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0092 | SAS | GIH | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0048 | SAS | GIH | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0087 | AFR | ACB | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | USA | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | USA | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | USA | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0023 | AFR | USA | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA21309 | hp1 | a0006 | c0005 | t0003 | g0157 | AFR | LWK | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| NA21309 | hp2 | a0001 | c0006 | t0001 | g0016 | AFR | LWK | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0049 | REF | REF | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0003 | REF | REF | IFT52_chr20_43585937_43652299 | IFT52 | chr20 | 43585937 | 43652299 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:43613966 | A | G | 1 | a0004 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.602A>G | p.Tyr201Cys | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/14 | 726/1754 | 602/1314 | 201/437 | chr20 | 43613966 | |||
| chr20:43623897 | G | C | 1 | a0005 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.775G>C | p.Asp259His | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/14 | 899/1754 | 775/1314 | 259/437 | chr20 | 43623897 | |||
| chr20:43623925 | C | T | 1 | a0002 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.803C>T | p.Thr268Ile | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/14 | 927/1754 | 803/1314 | 268/437 | chr20 | 43623925 | |||
| chr20:43635933 | G | A | 1 | a0003 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.931G>A | p.Glu311Lys | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 11/14 | 1055/1754 | 931/1314 | 311/437 | chr20 | 43635933 | |||
| chr20:43646955 | G | A | 1 | a0006 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1286G>A | p.Ser429Asn | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 14/14 | 1410/1754 | 1286/1314 | 429/437 | chr20 | 43646955 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:43596474 | G | A | 3 | a0001c0001 a0005c0004 a0006c0005 |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
synonymous_variant | LOW | c.159G>A | p.Val53Val | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/14 | 283/1754 | 159/1314 | 53/437 | chr20 | 43596474 | |||
| chr20:43613884 | T | C | 1 | a0001c0006 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.520T>C | p.Leu174Leu | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/14 | 644/1754 | 520/1314 | 174/437 | chr20 | 43613884 | |||
| chr20:43623947 | G | A | 1 | a0001c0003 | 6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
synonymous_variant | LOW | c.825G>A | p.Glu275Glu | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/14 | 949/1754 | 825/1314 | 275/437 | chr20 | 43623947 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:43647036 | A | G | 1 | a0006c0005t0003 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*53A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 14/14 | 53 | chr20 | 43647036 | ||||||
| chr20:43647063 | T | G | 1 | a0001c0001t0002 | 1 | NA19083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*80T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 14/14 | 80 | chr20 | 43647063 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:43591140 | G | T | 178 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(175): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-7+86G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43591140 | |||||||
| chr20:43591191 | G | A | 168 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(165): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-7+137G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43591191 | |||||||
| chr20:43591351 | A | G | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-7+297A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43591351 | |||||||
| chr20:43591642 | T | A | 1 | a0001c0001t0001g0108 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-7+588T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43591642 | |||||||
| chr20:43591713 | C | T | 25 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0082 others(22): Show |
27 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(24): Show |
intron_variant | MODIFIER | c.-7+659C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43591713 | |||||||
| chr20:43591718 | A | G | 1 | a0001c0002t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-7+664A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43591718 | |||||||
| chr20:43591728 | A | G | 178 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(175): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-7+674A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43591728 | |||||||
| chr20:43591792 | A | G | 1 | a0001c0002t0001g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-7+738A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43591792 | |||||||
| chr20:43591800 | G | A | 4 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+746G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43591800 | |||||||
| chr20:43592040 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0269 |
3 | HG01123.hp2 HG01346.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-7+986A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43592040 | |||||||
| chr20:43592125 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-7+1071C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43592125 | |||||||
| chr20:43592129 | T | A | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-7+1075T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43592129 | |||||||
| chr20:43592570 | C | CAA | 28 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0017 others(25): Show |
30 | HG01081.hp1 HG01884.hp1 HG02083.hp2 others(27): Show |
intron_variant | MODIFIER | c.-7+1530_-7+1531dup others(2): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43592570 | ||||||
| chr20:43592570 | CA | C | 158 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(155): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.-7+1531delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43592570 | ||||||
| chr20:43592660 | G | A | 217 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(214): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-7+1606G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43592660 | |||||||
| chr20:43592828 | C | T | 1 | a0001c0002t0001g0267 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-7+1774C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43592828 | |||||||
| chr20:43592922 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-6-1771G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43592922 | |||||||
| chr20:43592963 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-6-1730C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43592963 | |||||||
| chr20:43592966 | G | A | 168 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(165): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-6-1727G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43592966 | |||||||
| chr20:43592993 | T | G | 178 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(175): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-6-1700T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43592993 | |||||||
| chr20:43593098 | C | T | 14 | a0001c0002t0001g0011 a0001c0002t0001g0091 a0001c0002t0001g0092 others(11): Show |
15 | HG02083.hp2 HG03491.hp2 HG03492.hp1 others(12): Show |
intron_variant | MODIFIER | c.-6-1595C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593098 | |||||||
| chr20:43593113 | T | G | 22 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0086 others(19): Show |
24 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.-6-1580T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593113 | |||||||
| chr20:43593116 | G | T | 10 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(7): Show |
10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.-6-1577G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593116 | |||||||
| chr20:43593119 | G | T | 1 | a0001c0001t0001g0279 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-6-1574G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593119 | |||||||
| chr20:43593128 | A | T | 1 | a0001c0002t0001g0011 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-6-1565A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593128 | |||||||
| chr20:43593200 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-6-1493A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593200 | |||||||
| chr20:43593331 | G | A | 1 | a0001c0006t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-6-1362G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593331 | |||||||
| chr20:43593555 | G | A | 1 | a0001c0002t0001g0024 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-6-1138G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593555 | |||||||
| chr20:43593755 | G | T | 178 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(175): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-6-938G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593755 | |||||||
| chr20:43593801 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-6-892C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593801 | |||||||
| chr20:43593812 | C | T | 2 | a0001c0002t0001g0017 a0001c0002t0001g0018 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-6-881C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593812 | |||||||
| chr20:43593968 | G | A | 17 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0024 others(14): Show |
19 | HG01109.hp2 HG02056.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.-6-725G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43593968 | |||||||
| chr20:43594026 | C | T | 1 | a0001c0002t0001g0038 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-6-667C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43594026 | |||||||
| chr20:43594123 | C | G | 1 | a0001c0002t0001g0079 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-6-570C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43594123 | |||||||
| chr20:43594141 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-6-552C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43594141 | |||||||
| chr20:43594344 | T | C | 217 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(214): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-6-349T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43594344 | |||||||
| chr20:43594347 | G | A | 2 | a0001c0002t0001g0006 a0001c0002t0001g0019 |
3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-6-346G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43594347 | |||||||
| chr20:43594429 | A | T | 1 | a0001c0001t0001g0262 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-6-264A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 1/13 | chr20 | 43594429 | |||||||
| chr20:43594822 | C | T | 4 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.119+5C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43594822 | |||||||
| chr20:43595049 | C | G | 21 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0086 others(18): Show |
23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.119+232C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43595049 | |||||||
| chr20:43595087 | G | A | 4 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.119+270G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43595087 | |||||||
| chr20:43595174 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02055.hp1 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.119+357G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43595174 | |||||||
| chr20:43595316 | C | CAAAAA | 8 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(5): Show |
8 | HG01167.hp2 HG01243.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.119+517_119+521dup others(5): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43595316 | ||||||
| chr20:43595316 | CA | C | 152 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(149): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.119+521delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43595316 | ||||||
| chr20:43595316 | CAA | C | 14 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0250 others(11): Show |
14 | HG01243.hp2 HG02040.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.119+520_119+521del others(2): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43595316 | ||||||
| chr20:43595335 | A | G | 1 | a0001c0002t0001g0078 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.119+518A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43595335 | |||||||
| chr20:43595363 | A | G | 21 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0086 others(18): Show |
23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.119+546A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43595363 | |||||||
| chr20:43595370 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.119+553G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43595370 | |||||||
| chr20:43595415 | C | T | 7 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 others(4): Show |
7 | HG00738.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.119+598C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43595415 | |||||||
| chr20:43595463 | C | T | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.119+646C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43595463 | |||||||
| chr20:43595915 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.120-520C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43595915 | |||||||
| chr20:43596073 | T | C | 1 | a0001c0001t0001g0171 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.120-362T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43596073 | |||||||
| chr20:43596189 | T | C | 8 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0003t0001g0002 others(5): Show |
10 | HG01361.hp2 HG01884.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.120-246T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43596189 | |||||||
| chr20:43596255 | T | G | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.120-180T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 2/13 | chr20 | 43596255 | |||||||
| chr20:43596736 | C | CT | 10 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(7): Show |
11 | HG01243.hp2 HG01361.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.207+237dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43596736 | ||||||
| chr20:43596736 | CT | C | 164 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(161): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.207+237delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43596736 | ||||||
| chr20:43596765 | A | G | 3 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 |
3 | HG01167.hp1 HG01169.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.207+243A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43596765 | |||||||
| chr20:43596772 | C | T | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.207+250C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43596772 | |||||||
| chr20:43596783 | C | T | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.207+261C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43596783 | |||||||
| chr20:43596803 | G | A | 4 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+281G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43596803 | |||||||
| chr20:43596806 | A | G | 1 | a0001c0002t0001g0079 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.207+284A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43596806 | |||||||
| chr20:43596834 | C | G | 4 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+312C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43596834 | |||||||
| chr20:43596834 | C | T | 1 | a0001c0002t0001g0077 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.207+312C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43596834 | |||||||
| chr20:43597037 | A | G | 179 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.207+515A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597037 | |||||||
| chr20:43597042 | G | C | 219 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(216): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.207+520G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597042 | |||||||
| chr20:43597128 | T | C | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | NA18955.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.207+606T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597128 | |||||||
| chr20:43597198 | C | G | 26 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0082 others(23): Show |
28 | HG00735.hp2 HG01081.hp1 HG02083.hp2 others(25): Show |
intron_variant | MODIFIER | c.207+676C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597198 | |||||||
| chr20:43597283 | A | G | 167 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(164): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.207+761A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597283 | |||||||
| chr20:43597303 | G | A | 4 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+781G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597303 | |||||||
| chr20:43597381 | A | AAAAG | 259 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(256): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.207+867_207+870dup others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43597381 | ||||||
| chr20:43597460 | G | A | 1 | a0001c0002t0001g0132 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.207+938G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597460 | |||||||
| chr20:43597670 | G | T | 1 | a0001c0002t0001g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.207+1148G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597670 | |||||||
| chr20:43597767 | G | A | 6 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(3): Show |
6 | HG01243.hp2 HG02055.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+1245G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597767 | |||||||
| chr20:43597847 | C | T | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(170): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.207+1325C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597847 | |||||||
| chr20:43597866 | G | C | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(173): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.207+1344G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43597866 | |||||||
| chr20:43597890 | C | CA | 171 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(168): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.207+1389dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43597890 | ||||||
| chr20:43597890 | C | CAA | 31 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(28): Show |
33 | HG00735.hp1 HG00738.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.207+1388_207+1389d others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43597890 | ||||||
| chr20:43598145 | A | T | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.207+1623A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43598145 | |||||||
| chr20:43598150 | T | C | 26 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0086 others(23): Show |
28 | HG00735.hp2 HG01081.hp1 HG02083.hp2 others(25): Show |
intron_variant | MODIFIER | c.207+1628T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43598150 | |||||||
| chr20:43598365 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.207+1843G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43598365 | |||||||
| chr20:43598372 | G | A | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(151): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.207+1850G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43598372 | |||||||
| chr20:43598423 | G | A | 2 | a0001c0002t0001g0027 a0001c0002t0001g0081 |
2 | HG02135.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.207+1901G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43598423 | |||||||
| chr20:43598609 | C | T | 1 | a0004c0009t0001g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.207+2087C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43598609 | |||||||
| chr20:43598657 | C | T | 1 | a0001c0006t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.207+2135C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43598657 | |||||||
| chr20:43598706 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.207+2184A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43598706 | |||||||
| chr20:43598871 | A | G | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(170): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.207+2349A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43598871 | |||||||
| chr20:43599031 | G | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.207+2509G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43599031 | |||||||
| chr20:43599314 | C | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG02486.hp1 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.207+2792C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43599314 | |||||||
| chr20:43599545 | CT | C | 10 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(7): Show |
10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+3030delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43599545 | ||||||
| chr20:43599673 | G | A | 2 | a0001c0002t0001g0039 a0001c0002t0001g0040 |
2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.207+3151G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43599673 | |||||||
| chr20:43599898 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.207+3376A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43599898 | |||||||
| chr20:43600235 | A | G | 22 | a0001c0001t0001g0230 a0001c0002t0001g0010 a0001c0002t0001g0011 others(19): Show |
24 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.208-3525A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600235 | |||||||
| chr20:43600304 | A | AT | 18 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0265 others(15): Show |
19 | HG01433.hp2 HG02083.hp2 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.208-3441dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43600304 | ||||||
| chr20:43600344 | A | G | 179 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.208-3416A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600344 | |||||||
| chr20:43600397 | C | T | 2 | a0001c0002t0001g0101 a0001c0002t0001g0102 |
2 | NA18971.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.208-3363C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600397 | |||||||
| chr20:43600465 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.208-3295C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600465 | |||||||
| chr20:43600518 | G | A | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0002t0001g0028 |
3 | HG01069.hp1 HG01071.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.208-3242G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600518 | |||||||
| chr20:43600521 | A | G | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0002t0001g0028 |
3 | HG01069.hp1 HG01071.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.208-3239A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600521 | |||||||
| chr20:43600549 | CCGCCTTG others(9): Show |
C | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3210_208-3195d others(18): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600549 | |||||||
| chr20:43600551 | G | A | 16 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0119 others(13): Show |
16 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.208-3209G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600551 | |||||||
| chr20:43600569 | G | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3191G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600569 | |||||||
| chr20:43600570 | T | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3190T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600570 | |||||||
| chr20:43600571 | T | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3189T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600571 | |||||||
| chr20:43600572 | C | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3188C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600572 | |||||||
| chr20:43600573 | T | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3187T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600573 | |||||||
| chr20:43600575 | T | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3185T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600575 | |||||||
| chr20:43600576 | T | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3184T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600576 | |||||||
| chr20:43600579 | T | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3181T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600579 | |||||||
| chr20:43600585 | G | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3175G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600585 | |||||||
| chr20:43600587 | G | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3173G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600587 | |||||||
| chr20:43600588 | T | TAAAAAAA others(22): Show |
1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3171_208-3170i others(31): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43600588 | ||||||
| chr20:43600598 | C | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3162C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600598 | |||||||
| chr20:43600600 | C | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3160C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600600 | |||||||
| chr20:43600601 | T | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3159T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600601 | |||||||
| chr20:43600602 | C | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3158C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600602 | |||||||
| chr20:43600607 | T | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3153T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600607 | |||||||
| chr20:43600609 | C | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3151C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600609 | |||||||
| chr20:43600610 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.208-3150A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600610 | |||||||
| chr20:43600612 | G | C | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3148G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600612 | |||||||
| chr20:43600724 | A | T | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-3036A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600724 | |||||||
| chr20:43600762 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.208-2998G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600762 | |||||||
| chr20:43600830 | G | A | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(174): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.208-2930G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600830 | |||||||
| chr20:43600860 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.208-2900A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43600860 | |||||||
| chr20:43601206 | T | C | 9 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0081 others(6): Show |
11 | HG01361.hp2 HG01884.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.208-2554T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601206 | |||||||
| chr20:43601280 | A | C | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.208-2480A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601280 | |||||||
| chr20:43601419 | A | G | 1 | a0002c0008t0001g0034 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.208-2341A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601419 | |||||||
| chr20:43601524 | C | T | 1 | a0001c0002t0001g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.208-2236C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601524 | |||||||
| chr20:43601681 | C | A | 2 | a0001c0002t0001g0017 a0001c0002t0001g0018 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.208-2079C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601681 | |||||||
| chr20:43601754 | A | G | 21 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0086 others(18): Show |
23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.208-2006A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601754 | |||||||
| chr20:43601906 | A | G | 1 | a0001c0002t0001g0129 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.208-1854A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601906 | |||||||
| chr20:43601917 | A | G | 17 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0024 others(14): Show |
19 | HG01109.hp2 HG02056.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.208-1843A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601917 | |||||||
| chr20:43601932 | C | T | 1 | a0001c0002t0001g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.208-1828C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601932 | |||||||
| chr20:43601979 | C | T | 1 | a0001c0002t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.208-1781C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601979 | |||||||
| chr20:43601999 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0130 a0001c0001t0001g0135 others(8): Show |
13 | HG00642.hp2 HG00733.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.208-1761G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43601999 | |||||||
| chr20:43602004 | C | T | 217 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(214): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.208-1756C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602004 | |||||||
| chr20:43602055 | T | C | 158 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(155): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.208-1705T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602055 | |||||||
| chr20:43602113 | C | T | 2 | a0001c0002t0001g0006 a0001c0002t0001g0019 |
3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.208-1647C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602113 | |||||||
| chr20:43602136 | A | AT | 4 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0277 others(1): Show |
4 | HG00741.hp2 HG01243.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-1619dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602136 | ||||||
| chr20:43602136 | ATTTTTAT others(9): Show |
A | 1 | a0006c0005t0003g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.208-1621_208-1606d others(18): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602136 | ||||||
| chr20:43602137 | T | TTTTA | 19 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0087 others(16): Show |
21 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.208-1620_208-1619i others(6): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602137 | ||||||
| chr20:43602138 | T | TA | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0263 |
3 | HG02622.hp1 HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.208-1622_208-1621i others(3): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602138 | |||||||
| chr20:43602138 | T | TTA | 7 | a0001c0001t0001g0145 a0001c0001t0001g0161 a0001c0001t0001g0162 others(4): Show |
7 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-1621_208-1620i others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602138 | ||||||
| chr20:43602138 | T | TTATTTA | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG01106.hp2 HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.208-1621_208-1620i others(8): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602138 | ||||||
| chr20:43602138 | T | TTTTTA | 33 | a0001c0001t0001g0005 a0001c0001t0001g0108 a0001c0001t0001g0116 others(30): Show |
35 | HG00099.hp1 HG00597.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.208-1619_208-1618i others(7): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602138 | ||||||
| chr20:43602138 | T | TTTTTATT others(2): Show |
15 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0136 others(12): Show |
15 | HG01243.hp2 HG02055.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.208-1619_208-1618i others(11): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602138 | ||||||
| chr20:43602138 | T | TTTTTATT others(6): Show |
1 | a0001c0002t0001g0132 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.208-1619_208-1618i others(15): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602138 | ||||||
| chr20:43602139 | T | A | 9 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0244 others(6): Show |
9 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-1621T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602139 | |||||||
| chr20:43602142 | A | T | 110 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(107): Show |
116 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.208-1618A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602142 | |||||||
| chr20:43602143 | T | A | 18 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0187 others(15): Show |
18 | HG00099.hp2 HG00738.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.208-1617T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602143 | |||||||
| chr20:43602143 | T | TA | 10 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0131 others(7): Show |
10 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.208-1617_208-1616i others(3): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602143 | |||||||
| chr20:43602143 | T | TATTTA | 16 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0122 others(13): Show |
19 | HG00642.hp2 HG00741.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.208-1617_208-1616i others(7): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602143 | |||||||
| chr20:43602143 | T | TATTTATT others(2): Show |
55 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0113 others(52): Show |
57 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.208-1617_208-1616i others(11): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602143 | |||||||
| chr20:43602143 | T | TATTTATT others(6): Show |
11 | a0001c0001t0001g0015 a0001c0001t0001g0109 a0001c0001t0001g0110 others(8): Show |
12 | HG00733.hp1 HG00738.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.208-1617_208-1616i others(15): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602143 | |||||||
| chr20:43602143 | T | TTTA | 88 | a0001c0001t0001g0005 a0001c0001t0001g0108 a0001c0001t0001g0116 others(85): Show |
92 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.208-1615_208-1614i others(5): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602143 | ||||||
| chr20:43602143 | T | TTTTA | 32 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0024 others(29): Show |
36 | HG01099.hp1 HG01361.hp2 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.208-1581_208-1578d others(6): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602143 | ||||||
| chr20:43602143 | T | TTTTATTT others(1): Show |
7 | a0001c0002t0001g0019 a0001c0002t0001g0028 a0001c0002t0001g0029 others(4): Show |
7 | HG01109.hp2 HG02886.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.208-1585_208-1578d others(10): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602143 | ||||||
| chr20:43602143 | T | TTTTATTT others(5): Show |
2 | a0001c0002t0001g0018 a0001c0006t0001g0016 |
2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.208-1589_208-1578d others(14): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602143 | ||||||
| chr20:43602143 | T | TTTTATTT others(9): Show |
1 | a0001c0002t0001g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208-1593_208-1578d others(18): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43602143 | ||||||
| chr20:43602417 | C | T | 1 | a0001c0002t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.208-1343C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602417 | |||||||
| chr20:43602449 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.208-1311A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602449 | |||||||
| chr20:43602542 | T | C | 1 | a0001c0002t0001g0006 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.208-1218T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602542 | |||||||
| chr20:43602545 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.208-1215G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602545 | |||||||
| chr20:43602573 | A | G | 1 | a0001c0002t0001g0100 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.208-1187A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602573 | |||||||
| chr20:43602854 | T | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.208-906T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602854 | |||||||
| chr20:43602968 | C | A | 1 | a0006c0005t0003g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.208-792C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43602968 | |||||||
| chr20:43603074 | T | G | 1 | a0001c0001t0001g0262 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.208-686T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43603074 | |||||||
| chr20:43603082 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.208-678A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43603082 | |||||||
| chr20:43603151 | C | G | 4 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0033 others(1): Show |
6 | NA18946.hp1 NA18963.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-609C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43603151 | |||||||
| chr20:43603170 | C | T | 1 | a0001c0002t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.208-590C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43603170 | |||||||
| chr20:43603192 | G | T | 39 | a0001c0002t0001g0006 a0001c0002t0001g0010 a0001c0002t0001g0011 others(36): Show |
44 | HG01081.hp1 HG01361.hp2 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.208-568G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43603192 | |||||||
| chr20:43603218 | GC | G | 3 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG02486.hp1 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.208-541delC | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43603218 | |||||||
| chr20:43603230 | A | G | 1 | a0001c0003t0001g0020 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.208-530A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43603230 | |||||||
| chr20:43603548 | T | C | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.208-212T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43603548 | |||||||
| chr20:43603602 | A | T | 6 | a0001c0002t0001g0091 a0001c0002t0001g0095 a0001c0002t0001g0096 others(3): Show |
6 | NA18952.hp1 NA18972.hp1 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-158A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 3/13 | chr20 | 43603602 | |||||||
| chr20:43603943 | A | G | 1 | a0001c0002t0001g0006 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.337+54A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 4/13 | chr20 | 43603943 | |||||||
| chr20:43603947 | C | A | 10 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(7): Show |
10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.337+58C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 4/13 | chr20 | 43603947 | |||||||
| chr20:43603974 | T | C | 1 | a0001c0001t0001g0171 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.337+85T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 4/13 | chr20 | 43603974 | |||||||
| chr20:43604014 | C | G | 1 | a0001c0001t0001g0014 | 2 | HG03239.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.337+125C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 4/13 | chr20 | 43604014 | |||||||
| chr20:43604068 | C | T | 1 | a0004c0009t0001g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.338-115C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 4/13 | chr20 | 43604068 | |||||||
| chr20:43604099 | C | T | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.338-84C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 4/13 | chr20 | 43604099 | |||||||
| chr20:43604501 | G | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.413+243G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 5/13 | chr20 | 43604501 | |||||||
| chr20:43604555 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.413+297G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 5/13 | chr20 | 43604555 | |||||||
| chr20:43604642 | G | A | 1 | a0004c0009t0001g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.414-360G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 5/13 | chr20 | 43604642 | |||||||
| chr20:43605185 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.485+112G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605185 | |||||||
| chr20:43605439 | C | T | 1 | a0001c0002t0001g0121 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.485+366C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605439 | |||||||
| chr20:43605472 | C | T | 2 | a0001c0002t0001g0006 a0001c0002t0001g0019 |
3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.485+399C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605472 | |||||||
| chr20:43605473 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.485+400G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605473 | |||||||
| chr20:43605503 | C | T | 10 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(7): Show |
10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+430C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605503 | |||||||
| chr20:43605582 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.485+509T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605582 | |||||||
| chr20:43605618 | C | T | 3 | a0001c0001t0001g0221 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG01123.hp1 HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.485+545C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605618 | |||||||
| chr20:43605806 | T | G | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+733T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605806 | |||||||
| chr20:43605810 | A | G | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+737A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605810 | |||||||
| chr20:43605811 | T | A | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+738T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605811 | |||||||
| chr20:43605813 | C | A | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+740C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605813 | |||||||
| chr20:43605819 | T | G | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+746T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605819 | |||||||
| chr20:43605820 | G | A | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+747G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605820 | |||||||
| chr20:43605821 | T | G | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+748T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605821 | |||||||
| chr20:43605825 | T | C | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+752T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605825 | |||||||
| chr20:43605826 | G | T | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+753G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605826 | |||||||
| chr20:43605828 | C | T | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+755C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605828 | |||||||
| chr20:43605830 | A | T | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+757A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605830 | |||||||
| chr20:43605831 | A | C | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+758A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605831 | |||||||
| chr20:43605832 | A | T | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+759A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605832 | |||||||
| chr20:43605834 | G | T | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+761G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605834 | |||||||
| chr20:43605835 | C | T | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+762C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605835 | |||||||
| chr20:43605836 | A | C | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+763A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605836 | |||||||
| chr20:43605840 | G | T | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+767G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605840 | |||||||
| chr20:43605841 | A | C | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+768A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605841 | |||||||
| chr20:43605844 | A | C | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+771A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605844 | |||||||
| chr20:43605848 | T | C | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+775T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605848 | |||||||
| chr20:43605849 | G | GTTGTTGT others(3): Show |
1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+777_485+778ins others(10): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43605849 | ||||||
| chr20:43605852 | T | A | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+779T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605852 | |||||||
| chr20:43605853 | C | G | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+780C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605853 | |||||||
| chr20:43605857 | A | G | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+784A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605857 | |||||||
| chr20:43605858 | C | A | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+785C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605858 | |||||||
| chr20:43605863 | A | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0216 |
2 | HG03654.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.485+790A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43605863 | |||||||
| chr20:43606012 | C | T | 4 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+939C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43606012 | |||||||
| chr20:43606215 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.485+1142C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43606215 | |||||||
| chr20:43606216 | G | C | 1 | a0001c0006t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.485+1143G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43606216 | |||||||
| chr20:43606273 | C | CT | 34 | a0001c0001t0001g0134 a0001c0001t0001g0214 a0001c0001t0001g0215 others(31): Show |
36 | HG01109.hp2 HG01175.hp1 HG01433.hp1 others(33): Show |
intron_variant | MODIFIER | c.485+1218dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43606273 | ||||||
| chr20:43606296 | T | C | 217 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(214): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.485+1223T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43606296 | |||||||
| chr20:43606507 | C | T | 2 | a0001c0002t0001g0105 a0001c0002t0001g0107 |
2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.485+1434C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43606507 | |||||||
| chr20:43606591 | A | AT | 11 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(8): Show |
11 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.485+1531dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43606591 | ||||||
| chr20:43606956 | AAAATGAA others(33): Show |
A | 1 | a0001c0001t0001g0269 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.485+1885_485+1924d others(42): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43606956 | ||||||
| chr20:43607059 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.485+1986C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607059 | |||||||
| chr20:43607078 | C | T | 27 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0017 others(24): Show |
29 | HG01081.hp1 HG01884.hp1 HG02083.hp2 others(26): Show |
intron_variant | MODIFIER | c.485+2005C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607078 | |||||||
| chr20:43607159 | G | T | 1 | a0004c0009t0001g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.485+2086G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607159 | |||||||
| chr20:43607171 | C | T | 1 | a0001c0002t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.485+2098C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607171 | |||||||
| chr20:43607185 | T | TGGACGGG others(42): Show |
1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+2115_485+2116i others(51): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43607185 | ||||||
| chr20:43607185 | TGGATGGG others(42): Show |
T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02055.hp1 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.485+2116_485+2164d others(51): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43607185 | ||||||
| chr20:43607189 | T | C | 175 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(172): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.485+2116T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607189 | |||||||
| chr20:43607189 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.485+2116T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607189 | |||||||
| chr20:43607189 | TGGGGCGG others(42): Show |
T | 24 | a0001c0002t0001g0006 a0001c0002t0001g0010 a0001c0002t0001g0011 others(21): Show |
27 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(24): Show |
intron_variant | MODIFIER | c.485+2179_485+2227d others(51): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43607189 | ||||||
| chr20:43607255 | C | T | 4 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+2182C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607255 | |||||||
| chr20:43607260 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.485+2187G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607260 | |||||||
| chr20:43607378 | TGGCTGCC others(33): Show |
T | 1 | a0001c0001t0001g0263 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.485+2341_485+2380d others(42): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43607378 | ||||||
| chr20:43607419 | G | A | 27 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0017 others(24): Show |
29 | HG01081.hp1 HG01884.hp1 HG02083.hp2 others(26): Show |
intron_variant | MODIFIER | c.485+2346G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607419 | |||||||
| chr20:43607429 | C | T | 8 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(5): Show |
8 | HG01891.hp2 HG02055.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.485+2356C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607429 | |||||||
| chr20:43607491 | G | A | 1 | a0001c0002t0001g0267 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.485+2418G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607491 | |||||||
| chr20:43607695 | C | G | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.485+2622C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607695 | |||||||
| chr20:43607739 | C | CG | 4 | a0001c0002t0001g0030 a0001c0002t0001g0051 a0001c0002t0001g0063 others(1): Show |
4 | HG01175.hp1 HG02056.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+2670dupG | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43607739 | ||||||
| chr20:43607814 | G | A | 179 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.485+2741G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607814 | |||||||
| chr20:43607928 | C | T | 21 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0086 others(18): Show |
23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.485+2855C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607928 | |||||||
| chr20:43607938 | A | T | 1 | a0001c0002t0001g0099 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.485+2865A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43607938 | |||||||
| chr20:43608021 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02683.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.485+2948G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43608021 | |||||||
| chr20:43608031 | A | G | 179 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.485+2958A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43608031 | |||||||
| chr20:43608039 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.485+2966T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43608039 | |||||||
| chr20:43608057 | A | AG | 179 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.485+2984_485+2985i others(3): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43608057 | |||||||
| chr20:43608161 | GGGGAGAG others(5): Show |
G | 1 | a0001c0001t0001g0226 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.485+3106_485+3117d others(14): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43608161 | ||||||
| chr20:43608403 | T | A | 5 | a0001c0001t0001g0158 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+3330T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43608403 | |||||||
| chr20:43608404 | A | T | 1 | a0001c0001t0001g0257 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.485+3331A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43608404 | |||||||
| chr20:43608427 | C | A | 179 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.485+3354C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43608427 | |||||||
| chr20:43608765 | G | A | 10 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(7): Show |
10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+3692G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43608765 | |||||||
| chr20:43608862 | T | C | 234 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(231): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.485+3789T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43608862 | |||||||
| chr20:43608863 | G | A | 21 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0086 others(18): Show |
23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.485+3790G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43608863 | |||||||
| chr20:43609208 | C | T | 1 | a0001c0002t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.485+4135C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43609208 | |||||||
| chr20:43609284 | A | G | 1 | a0001c0002t0001g0050 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.485+4211A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43609284 | |||||||
| chr20:43609547 | G | A | 6 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0082 others(3): Show |
6 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.486-4303G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43609547 | |||||||
| chr20:43609610 | A | T | 169 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(166): Show |
177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.486-4240A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43609610 | |||||||
| chr20:43609775 | C | CA | 8 | a0001c0001t0001g0145 a0001c0001t0001g0223 a0001c0002t0001g0028 others(5): Show |
8 | HG01074.hp1 HG01109.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.486-4051dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43609775 | ||||||
| chr20:43609775 | CA | C | 181 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(178): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.486-4051delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43609775 | ||||||
| chr20:43609775 | CAA | C | 6 | a0001c0001t0001g0124 a0001c0001t0001g0136 a0001c0001t0001g0213 others(3): Show |
6 | HG01169.hp1 HG02071.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.486-4052_486-4051d others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43609775 | ||||||
| chr20:43609957 | A | T | 2 | a0001c0002t0001g0006 a0001c0002t0001g0019 |
3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.486-3893A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43609957 | |||||||
| chr20:43609962 | A | AAAATT | 5 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(2): Show |
5 | HG02055.hp2 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.486-3867_486-3863d others(7): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43609962 | ||||||
| chr20:43609962 | A | T | 17 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0008 others(14): Show |
20 | HG01109.hp2 HG02056.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.486-3888A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43609962 | |||||||
| chr20:43609967 | T | A | 34 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0119 others(31): Show |
36 | HG01081.hp1 HG02040.hp1 HG02083.hp2 others(33): Show |
intron_variant | MODIFIER | c.486-3883T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43609967 | |||||||
| chr20:43610111 | C | A | 1 | a0001c0001t0001g0164 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.486-3739C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43610111 | |||||||
| chr20:43610182 | C | T | 179 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.486-3668C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43610182 | |||||||
| chr20:43610184 | C | T | 1 | a0001c0002t0001g0078 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.486-3666C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43610184 | |||||||
| chr20:43610217 | G | A | 179 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.486-3633G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43610217 | |||||||
| chr20:43610271 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.486-3579G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43610271 | |||||||
| chr20:43610291 | C | CA | 7 | a0001c0002t0001g0031 a0001c0002t0001g0044 a0001c0002t0001g0056 others(4): Show |
7 | HG00544.hp2 HG01981.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-3542dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43610291 | ||||||
| chr20:43610291 | CA | C | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(170): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.486-3542delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43610291 | ||||||
| chr20:43610312 | TA | T | 169 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(166): Show |
177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.486-3530delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43610312 | ||||||
| chr20:43610447 | A | T | 10 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(7): Show |
10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.486-3403A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43610447 | |||||||
| chr20:43610460 | G | A | 234 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(231): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.486-3390G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43610460 | |||||||
| chr20:43610505 | A | G | 179 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.486-3345A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43610505 | |||||||
| chr20:43610828 | T | C | 30 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0017 others(27): Show |
32 | HG01081.hp1 HG01884.hp1 HG02083.hp2 others(29): Show |
intron_variant | MODIFIER | c.486-3022T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43610828 | |||||||
| chr20:43610917 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.486-2933T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43610917 | |||||||
| chr20:43611441 | C | CT | 9 | a0001c0002t0001g0040 a0001c0002t0001g0042 a0001c0002t0001g0051 others(6): Show |
9 | HG00544.hp2 HG01175.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.486-2382dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43611441 | ||||||
| chr20:43611441 | CT | C | 34 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0010 others(31): Show |
38 | HG01109.hp2 HG02056.hp1 HG02083.hp2 others(35): Show |
intron_variant | MODIFIER | c.486-2382delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43611441 | ||||||
| chr20:43611441 | CTT | C | 25 | a0001c0001t0001g0110 a0001c0001t0001g0125 a0001c0001t0001g0126 others(22): Show |
25 | HG00438.hp1 HG00741.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.486-2383_486-2382d others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43611441 | ||||||
| chr20:43611441 | CTTT | C | 158 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(155): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.486-2384_486-2382d others(5): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43611441 | ||||||
| chr20:43611441 | CTTTTTTT others(7): Show |
C | 1 | a0001c0006t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486-2395_486-2382d others(16): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43611441 | ||||||
| chr20:43611598 | C | T | 1 | a0005c0004t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.486-2252C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43611598 | |||||||
| chr20:43611599 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.486-2251G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43611599 | |||||||
| chr20:43611729 | G | A | 4 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-2121G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43611729 | |||||||
| chr20:43611757 | C | A | 179 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.486-2093C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43611757 | |||||||
| chr20:43611859 | A | G | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.486-1991A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43611859 | |||||||
| chr20:43611964 | A | T | 1 | a0001c0002t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.486-1886A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43611964 | |||||||
| chr20:43612010 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.486-1840A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43612010 | |||||||
| chr20:43612090 | G | A | 164 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(161): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.486-1760G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43612090 | |||||||
| chr20:43612248 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.486-1602A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43612248 | |||||||
| chr20:43612707 | A | ACAAT | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(173): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.486-1140_486-1139i others(6): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43612707 | ||||||
| chr20:43612707 | A | T | 1 | a0001c0001t0001g0278 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.486-1143A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43612707 | |||||||
| chr20:43612750 | A | G | 1 | a0001c0003t0001g0023 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.486-1100A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43612750 | |||||||
| chr20:43612754 | G | T | 36 | a0001c0001t0001g0005 a0001c0001t0001g0108 a0001c0001t0001g0120 others(33): Show |
38 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.486-1096G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43612754 | |||||||
| chr20:43612764 | T | G | 1 | a0001c0001t0001g0269 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.486-1086T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43612764 | |||||||
| chr20:43613171 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG00741.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.486-679G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43613171 | |||||||
| chr20:43613179 | C | A | 4 | a0001c0003t0001g0002 a0001c0003t0001g0020 a0001c0003t0001g0022 others(1): Show |
6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.486-671C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43613179 | |||||||
| chr20:43613226 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0130 a0001c0001t0001g0135 others(8): Show |
13 | HG00642.hp2 HG00733.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.486-624C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43613226 | |||||||
| chr20:43613311 | C | T | 1 | a0001c0002t0001g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.486-539C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43613311 | |||||||
| chr20:43613321 | C | G | 1 | a0001c0006t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486-529C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43613321 | |||||||
| chr20:43613359 | T | G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0214 |
2 | NA18973.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.486-491T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43613359 | |||||||
| chr20:43613492 | T | A | 1 | a0001c0001t0001g0168 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.486-358T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43613492 | |||||||
| chr20:43613519 | C | T | 1 | a0001c0002t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.486-331C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43613519 | |||||||
| chr20:43613716 | C | A | 10 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(7): Show |
10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.486-134C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43613716 | |||||||
| chr20:43613812 | T | A | 21 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0086 others(18): Show |
23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.486-38T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 6/13 | chr20 | 43613812 | |||||||
| chr20:43614060 | C | T | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(174): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.612+84C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43614060 | |||||||
| chr20:43614303 | C | T | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(174): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.612+327C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43614303 | |||||||
| chr20:43614342 | C | T | 2 | a0001c0002t0001g0006 a0001c0002t0001g0019 |
3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.612+366C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43614342 | |||||||
| chr20:43614477 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.612+501C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43614477 | |||||||
| chr20:43614481 | G | A | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(174): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.612+505G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43614481 | |||||||
| chr20:43614546 | G | T | 157 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(154): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.612+570G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43614546 | |||||||
| chr20:43614744 | C | T | 4 | a0001c0001t0001g0126 a0001c0001t0001g0166 a0001c0001t0001g0175 others(1): Show |
4 | HG00280.hp1 HG01175.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.612+768C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43614744 | |||||||
| chr20:43614809 | C | CT | 14 | a0001c0001t0001g0196 a0001c0001t0001g0199 a0001c0002t0001g0047 others(11): Show |
16 | HG01361.hp2 HG02027.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.612+850dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr20 | 43614809 | ||||||
| chr20:43614810 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.612+834T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43614810 | |||||||
| chr20:43614923 | C | T | 16 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0024 others(13): Show |
18 | HG01109.hp2 HG02056.hp1 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.612+947C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43614923 | |||||||
| chr20:43615165 | T | C | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(174): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.612+1189T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615165 | |||||||
| chr20:43615177 | G | A | 1 | a0001c0002t0001g0267 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.612+1201G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615177 | |||||||
| chr20:43615205 | G | A | 12 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(9): Show |
12 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.612+1229G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615205 | |||||||
| chr20:43615213 | T | C | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.612+1237T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615213 | |||||||
| chr20:43615223 | A | G | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(174): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.612+1247A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615223 | |||||||
| chr20:43615287 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.612+1311C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615287 | |||||||
| chr20:43615295 | A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.612+1319A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615295 | |||||||
| chr20:43615363 | A | G | 167 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(164): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.612+1387A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615363 | |||||||
| chr20:43615383 | A | G | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.612+1407A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615383 | |||||||
| chr20:43615619 | C | T | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(174): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.612+1643C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615619 | |||||||
| chr20:43615657 | G | T | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(174): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.612+1681G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615657 | |||||||
| chr20:43615761 | A | C | 1 | a0001c0001t0001g0269 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.612+1785A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615761 | |||||||
| chr20:43615762 | C | A | 1 | a0001c0001t0001g0269 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.612+1786C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43615762 | |||||||
| chr20:43615938 | GA | G | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(174): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.612+1972delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr20 | 43615938 | ||||||
| chr20:43616008 | C | T | 1 | a0001c0006t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.612+2032C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43616008 | |||||||
| chr20:43616043 | A | T | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.612+2067A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43616043 | |||||||
| chr20:43616509 | C | CA | 10 | a0001c0001t0001g0136 a0001c0001t0001g0142 a0001c0001t0001g0223 others(7): Show |
10 | HG01934.hp2 HG01981.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.613-2414dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr20 | 43616509 | ||||||
| chr20:43616509 | CA | C | 8 | a0001c0001t0001g0113 a0001c0002t0001g0081 a0001c0002t0001g0091 others(5): Show |
8 | HG01109.hp1 HG03486.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.613-2414delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr20 | 43616509 | ||||||
| chr20:43616660 | T | C | 3 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0268 |
3 | HG01891.hp2 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.613-2280T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43616660 | |||||||
| chr20:43616667 | T | C | 4 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-2273T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43616667 | |||||||
| chr20:43616796 | G | A | 21 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0086 others(18): Show |
23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.613-2144G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43616796 | |||||||
| chr20:43617343 | A | G | 3 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG02486.hp1 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.613-1597A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617343 | |||||||
| chr20:43617449 | GT | G | 175 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(172): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.613-1479delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr20 | 43617449 | ||||||
| chr20:43617450 | T | G | 1 | a0001c0001t0001g0269 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.613-1490T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617450 | |||||||
| chr20:43617479 | T | G | 10 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(7): Show |
10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.613-1461T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617479 | |||||||
| chr20:43617494 | G | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.613-1446G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617494 | |||||||
| chr20:43617558 | C | G | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(174): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.613-1382C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617558 | |||||||
| chr20:43617591 | G | A | 2 | a0001c0001t0001g0251 a0001c0001t0001g0255 |
2 | HG02055.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.613-1349G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617591 | |||||||
| chr20:43617628 | G | T | 1 | a0001c0002t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.613-1312G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617628 | |||||||
| chr20:43617632 | C | T | 4 | a0001c0003t0001g0002 a0001c0003t0001g0020 a0001c0003t0001g0022 others(1): Show |
6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.613-1308C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617632 | |||||||
| chr20:43617644 | A | G | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(174): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.613-1296A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617644 | |||||||
| chr20:43617664 | G | A | 1 | a0001c0002t0001g0067 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.613-1276G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617664 | |||||||
| chr20:43617886 | G | T | 4 | a0001c0003t0001g0002 a0001c0003t0001g0020 a0001c0003t0001g0022 others(1): Show |
6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.613-1054G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43617886 | |||||||
| chr20:43618214 | A | AT | 9 | a0001c0001t0001g0154 a0001c0001t0001g0269 a0001c0001t0001g0270 others(6): Show |
9 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.613-709dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr20 | 43618214 | ||||||
| chr20:43618214 | AT | A | 42 | a0001c0001t0001g0114 a0001c0001t0001g0116 a0001c0001t0001g0118 others(39): Show |
44 | HG00323.hp1 HG00544.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.613-709delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr20 | 43618214 | ||||||
| chr20:43618214 | ATT | A | 5 | a0001c0002t0001g0060 a0001c0003t0001g0002 a0001c0003t0001g0020 others(2): Show |
7 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.613-710_613-709del others(2): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr20 | 43618214 | ||||||
| chr20:43618508 | G | T | 2 | a0001c0002t0001g0006 a0001c0002t0001g0019 |
3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.613-432G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43618508 | |||||||
| chr20:43618516 | C | T | 167 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(164): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.613-424C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43618516 | |||||||
| chr20:43618571 | T | G | 1 | a0001c0002t0001g0033 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.613-369T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43618571 | |||||||
| chr20:43618584 | C | T | 7 | a0001c0001t0001g0270 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
7 | HG00741.hp2 HG01167.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.613-356C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43618584 | |||||||
| chr20:43618648 | A | ATT | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(174): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.613-284_613-283dup others(2): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr20 | 43618648 | ||||||
| chr20:43618714 | C | G | 1 | a0001c0001t0001g0243 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.613-226C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43618714 | |||||||
| chr20:43618736 | G | A | 4 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-204G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43618736 | |||||||
| chr20:43618775 | G | A | 6 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(3): Show |
6 | HG01243.hp2 HG02055.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.613-165G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 7/13 | chr20 | 43618775 | |||||||
| chr20:43619166 | C | T | 4 | a0001c0001t0001g0140 a0001c0001t0001g0188 a0001c0001t0001g0208 others(1): Show |
4 | HG00735.hp1 HG01074.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.699+140C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43619166 | |||||||
| chr20:43619167 | GAGTCAGG others(3): Show |
G | 1 | a0001c0001t0001g0216 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.699+146_699+155del others(10): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr20 | 43619167 | ||||||
| chr20:43619517 | A | G | 1 | a0001c0002t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.699+491A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43619517 | |||||||
| chr20:43619576 | G | C | 4 | a0001c0003t0001g0002 a0001c0003t0001g0020 a0001c0003t0001g0022 others(1): Show |
6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.699+550G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43619576 | |||||||
| chr20:43619631 | G | A | 19 | a0001c0002t0001g0009 a0001c0002t0001g0053 a0001c0002t0001g0055 others(16): Show |
20 | HG00544.hp2 HG01496.hp1 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.699+605G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43619631 | |||||||
| chr20:43619727 | A | G | 1 | a0001c0002t0001g0267 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.699+701A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43619727 | |||||||
| chr20:43619910 | C | CT | 158 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(155): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.699+908dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr20 | 43619910 | ||||||
| chr20:43619910 | C | CTT | 31 | a0001c0001t0001g0117 a0001c0001t0001g0119 a0001c0001t0001g0125 others(28): Show |
33 | HG00597.hp2 HG01109.hp2 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.699+907_699+908dup others(2): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr20 | 43619910 | ||||||
| chr20:43619910 | CT | C | 27 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0017 others(24): Show |
29 | HG01884.hp1 HG02027.hp1 HG02083.hp2 others(26): Show |
intron_variant | MODIFIER | c.699+908delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr20 | 43619910 | ||||||
| chr20:43619982 | C | T | 215 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(212): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.700-875C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43619982 | |||||||
| chr20:43620020 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.700-837G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43620020 | |||||||
| chr20:43620026 | C | T | 166 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.700-831C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43620026 | |||||||
| chr20:43620117 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.700-740A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43620117 | |||||||
| chr20:43620208 | T | A | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(173): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.700-649T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43620208 | |||||||
| chr20:43620421 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.700-436G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43620421 | |||||||
| chr20:43620545 | C | A | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(173): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.700-312C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43620545 | |||||||
| chr20:43620571 | G | A | 1 | a0001c0002t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.700-286G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43620571 | |||||||
| chr20:43620571 | G | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.700-286G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43620571 | |||||||
| chr20:43620758 | C | T | 215 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(212): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.700-99C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | chr20 | 43620758 | |||||||
| chr20:43620839 | C | CT | 185 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(182): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
splice_region_variant&intron_variant | LOW | c.700-8dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr20 | 43620839 | ||||||
| chr20:43620849 | T | TA | 4 | a0001c0001t0001g0113 a0001c0001t0001g0177 a0001c0001t0001g0256 others(1): Show |
4 | HG00597.hp1 HG01109.hp1 NA18951.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.700-6dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr20 | 43620849 | ||||||
| chr20:43621202 | T | C | 1 | a0001c0002t0001g0072 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.768+277T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43621202 | |||||||
| chr20:43621765 | C | T | 1 | a0001c0006t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.768+840C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43621765 | |||||||
| chr20:43621802 | C | T | 214 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(211): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.768+877C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43621802 | |||||||
| chr20:43622442 | CA | C | 166 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.769-1438delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43622442 | ||||||
| chr20:43622538 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.769-1353G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43622538 | |||||||
| chr20:43622660 | A | ATATGTAA others(20): Show |
1 | a0001c0002t0001g0064 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.769-1202_769-1176d others(29): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43622660 | ||||||
| chr20:43622684 | A | ATTTTATG others(21): Show |
1 | a0002c0008t0001g0034 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.769-1153_769-1126d others(30): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43622684 | ||||||
| chr20:43622711 | AT | A | 10 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(7): Show |
10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.769-1175delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43622711 | ||||||
| chr20:43622715 | TTATGTAA others(78): Show |
T | 1 | a0004c0009t0001g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.769-1142_769-1058d others(87): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43622715 | ||||||
| chr20:43622739 | AT | A | 10 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(7): Show |
10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.769-1147delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43622739 | ||||||
| chr20:43622745 | ATGTAAAT others(20): Show |
A | 5 | a0001c0001t0001g0110 a0001c0001t0001g0112 a0001c0001t0001g0169 others(2): Show |
5 | HG00738.hp1 HG02280.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.769-1125_769-1099d others(29): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43622745 | ||||||
| chr20:43622765 | A | AT | 160 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(157): Show |
168 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.769-1126_769-1125i others(3): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43622765 | |||||||
| chr20:43622765 | A | ATATTTTT others(22): Show |
11 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0131 others(8): Show |
11 | HG00099.hp1 HG01106.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.769-1126_769-1125i others(31): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43622765 | |||||||
| chr20:43622766 | A | T | 4 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.769-1125A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43622766 | |||||||
| chr20:43622767 | A | ATT | 34 | a0001c0002t0001g0006 a0001c0002t0001g0010 a0001c0002t0001g0011 others(31): Show |
39 | HG01081.hp1 HG01361.hp2 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.769-1123_769-1122d others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43622767 | ||||||
| chr20:43622767 | A | ATTTTTAT others(23): Show |
4 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.769-1122_769-1121i others(32): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43622767 | ||||||
| chr20:43622767 | A | T | 171 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(168): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.769-1124A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43622767 | |||||||
| chr20:43622770 | G | A | 38 | a0001c0002t0001g0006 a0001c0002t0001g0010 a0001c0002t0001g0011 others(35): Show |
43 | HG01081.hp1 HG01361.hp2 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.769-1121G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43622770 | |||||||
| chr20:43622770 | G | T | 230 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(227): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.769-1121G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43622770 | |||||||
| chr20:43622772 | G | A | 171 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(168): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.769-1119G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43622772 | |||||||
| chr20:43622802 | A | ATGTAAAT others(23): Show |
1 | a0001c0002t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.769-1065_769-1036d others(32): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43622802 | ||||||
| chr20:43622802 | A | G | 42 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0109 others(39): Show |
44 | HG00323.hp2 HG00544.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.769-1089A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43622802 | |||||||
| chr20:43623190 | A | G | 6 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(3): Show |
6 | HG01243.hp2 HG02055.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.769-701A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43623190 | |||||||
| chr20:43623507 | G | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0112 |
2 | HG00738.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.769-384G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43623507 | |||||||
| chr20:43623555 | G | A | 2 | a0001c0006t0001g0016 a0004c0009t0001g0021 |
2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.769-336G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43623555 | |||||||
| chr20:43623685 | G | T | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(173): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.769-206G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 9/13 | chr20 | 43623685 | |||||||
| chr20:43624215 | T | G | 4 | a0001c0003t0001g0002 a0001c0003t0001g0020 a0001c0003t0001g0022 others(1): Show |
6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.923+170T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43624215 | |||||||
| chr20:43624548 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0220 |
2 | HG03669.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.923+503G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43624548 | |||||||
| chr20:43624560 | G | A | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.923+515G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43624560 | |||||||
| chr20:43624681 | A | G | 2 | a0001c0006t0001g0016 a0004c0009t0001g0021 |
2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.923+636A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43624681 | |||||||
| chr20:43624707 | G | A | 1 | a0003c0007t0001g0093 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.923+662G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43624707 | |||||||
| chr20:43624902 | A | G | 178 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(175): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.923+857A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43624902 | |||||||
| chr20:43624975 | G | A | 1 | a0001c0002t0001g0006 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.923+930G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43624975 | |||||||
| chr20:43625215 | A | T | 215 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(212): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.923+1170A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43625215 | |||||||
| chr20:43625255 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.923+1210A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43625255 | |||||||
| chr20:43625258 | C | A | 170 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(167): Show |
178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.923+1213C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43625258 | |||||||
| chr20:43625315 | C | A | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.923+1270C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43625315 | |||||||
| chr20:43625564 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.923+1519A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43625564 | |||||||
| chr20:43625635 | C | T | 4 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+1590C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43625635 | |||||||
| chr20:43625684 | A | G | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02055.hp1 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.923+1639A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43625684 | |||||||
| chr20:43625798 | A | G | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.923+1753A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43625798 | |||||||
| chr20:43625801 | A | AGAG | 11 | a0001c0001t0001g0012 a0001c0001t0001g0134 a0001c0001t0001g0139 others(8): Show |
12 | HG02027.hp2 HG02132.hp1 HG04184.hp2 others(9): Show |
intron_variant | MODIFIER | c.923+1760_923+1762d others(5): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43625801 | ||||||
| chr20:43626022 | G | GA | 182 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(179): Show |
192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.923+1998dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43626022 | ||||||
| chr20:43626022 | G | GAA | 21 | a0001c0001t0001g0110 a0001c0001t0001g0119 a0001c0001t0001g0148 others(18): Show |
21 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.923+1997_923+1998d others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43626022 | ||||||
| chr20:43626077 | A | G | 4 | a0001c0001t0001g0135 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG00642.hp2 HG01074.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.923+2032A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43626077 | |||||||
| chr20:43626187 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.923+2142A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43626187 | |||||||
| chr20:43626243 | A | C | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.923+2198A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43626243 | |||||||
| chr20:43626466 | G | A | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.923+2421G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43626466 | |||||||
| chr20:43626622 | C | T | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.923+2577C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43626622 | |||||||
| chr20:43626797 | AAGTGTTG others(2): Show |
A | 157 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(154): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.923+2755_923+2763d others(11): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43626797 | ||||||
| chr20:43626862 | T | G | 17 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0024 others(14): Show |
19 | HG01109.hp2 HG02056.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.923+2817T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43626862 | |||||||
| chr20:43627039 | C | T | 1 | a0001c0002t0001g0027 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.923+2994C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627039 | |||||||
| chr20:43627091 | C | T | 3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0257 |
3 | HG01433.hp2 HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.923+3046C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627091 | |||||||
| chr20:43627162 | A | G | 2 | a0001c0006t0001g0016 a0004c0009t0001g0021 |
2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.923+3117A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627162 | |||||||
| chr20:43627170 | A | G | 164 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(161): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.923+3125A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627170 | |||||||
| chr20:43627171 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.923+3126A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627171 | |||||||
| chr20:43627224 | G | A | 166 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.923+3179G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627224 | |||||||
| chr20:43627274 | A | G | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.923+3229A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627274 | |||||||
| chr20:43627281 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.923+3236G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627281 | |||||||
| chr20:43627402 | C | G | 1 | a0001c0001t0001g0216 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.923+3357C>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627402 | |||||||
| chr20:43627489 | T | G | 1 | a0001c0002t0001g0090 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.923+3444T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627489 | |||||||
| chr20:43627596 | A | C | 4 | a0001c0001t0001g0192 a0001c0001t0001g0207 a0001c0001t0001g0211 others(1): Show |
4 | NA18973.hp1 NA18975.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+3551A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627596 | |||||||
| chr20:43627805 | C | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02683.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.923+3760C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627805 | |||||||
| chr20:43627904 | T | G | 1 | a0004c0009t0001g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.923+3859T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627904 | |||||||
| chr20:43627904 | TAG | T | 71 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0210 others(68): Show |
82 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.923+3876_923+3877d others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43627904 | ||||||
| chr20:43627906 | G | T | 81 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0108 others(78): Show |
84 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.923+3861G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627906 | |||||||
| chr20:43627908 | G | T | 30 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0002t0001g0001 others(27): Show |
33 | HG00544.hp2 HG00642.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.923+3863G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627908 | |||||||
| chr20:43627914 | G | A | 8 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0082 others(5): Show |
8 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.923+3869G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627914 | |||||||
| chr20:43627916 | G | A | 19 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0086 others(16): Show |
21 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.923+3871G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627916 | |||||||
| chr20:43627920 | G | GT | 6 | a0001c0001t0001g0186 a0001c0001t0001g0250 a0001c0001t0001g0251 others(3): Show |
6 | HG01243.hp1 HG01243.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+3875_923+3876i others(3): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627920 | |||||||
| chr20:43627920 | GA | G | 153 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(150): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.923+3876delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627920 | |||||||
| chr20:43627920 | GAGT | G | 9 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0029 others(6): Show |
9 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.923+3876_923+3878d others(5): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627920 | |||||||
| chr20:43627921 | A | T | 36 | a0001c0001t0001g0115 a0001c0001t0001g0126 a0001c0001t0001g0148 others(33): Show |
36 | HG00597.hp1 HG00642.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.923+3876A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627921 | |||||||
| chr20:43627922 | G | T | 186 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(183): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.923+3877G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627922 | |||||||
| chr20:43627990 | G | A | 166 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.923+3945G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43627990 | |||||||
| chr20:43628219 | AC | A | 10 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(7): Show |
10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.923+4175delC | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43628219 | |||||||
| chr20:43628225 | A | G | 232 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(229): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.923+4180A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43628225 | |||||||
| chr20:43628363 | G | A | 1 | a0001c0002t0001g0077 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.923+4318G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43628363 | |||||||
| chr20:43628428 | G | A | 9 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0131 others(6): Show |
9 | HG01168.hp1 HG01169.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.923+4383G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43628428 | |||||||
| chr20:43628854 | C | CA | 165 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(162): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.923+4821dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43628854 | ||||||
| chr20:43628990 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.923+4945T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43628990 | |||||||
| chr20:43629348 | CT | C | 157 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(154): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.923+5304delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43629348 | |||||||
| chr20:43629351 | C | T | 157 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(154): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.923+5306C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43629351 | |||||||
| chr20:43629352 | A | G | 157 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(154): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.923+5307A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43629352 | |||||||
| chr20:43629354 | GCTCC | G | 157 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(154): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.923+5310_923+5313d others(6): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43629354 | |||||||
| chr20:43629359 | G | A | 6 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0082 others(3): Show |
6 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+5314G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43629359 | |||||||
| chr20:43629417 | C | T | 1 | a0001c0002t0001g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.923+5372C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43629417 | |||||||
| chr20:43629500 | C | A | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(173): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.923+5455C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43629500 | |||||||
| chr20:43629510 | T | G | 232 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(229): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.923+5465T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43629510 | |||||||
| chr20:43629523 | C | T | 4 | a0001c0003t0001g0002 a0001c0003t0001g0020 a0001c0003t0001g0022 others(1): Show |
6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.923+5478C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43629523 | |||||||
| chr20:43629916 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.923+5871C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43629916 | |||||||
| chr20:43630012 | G | A | 1 | a0001c0002t0001g0027 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.924-5914G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630012 | |||||||
| chr20:43630022 | T | A | 50 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(47): Show |
54 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.924-5904T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630022 | |||||||
| chr20:43630095 | ACAG | A | 21 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0086 others(18): Show |
23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.924-5829_924-5827d others(5): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43630095 | ||||||
| chr20:43630232 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.924-5694C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630232 | |||||||
| chr20:43630320 | C | T | 175 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(172): Show |
183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.924-5606C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630320 | |||||||
| chr20:43630476 | T | G | 1 | a0001c0002t0001g0006 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.924-5450T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630476 | |||||||
| chr20:43630558 | G | GTCAACTA others(6): Show |
1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-5367_924-5355d others(15): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43630558 | ||||||
| chr20:43630614 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.924-5312A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630614 | |||||||
| chr20:43630645 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.924-5281G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630645 | |||||||
| chr20:43630662 | T | A | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-5264T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630662 | |||||||
| chr20:43630680 | T | A | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-5246T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630680 | |||||||
| chr20:43630780 | G | A | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-5146G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630780 | |||||||
| chr20:43630837 | G | A | 6 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(3): Show |
6 | HG01243.hp2 HG02055.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.924-5089G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630837 | |||||||
| chr20:43630996 | T | C | 215 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(212): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.924-4930T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43630996 | |||||||
| chr20:43631074 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.924-4852T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631074 | |||||||
| chr20:43631141 | T | A | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-4785T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631141 | |||||||
| chr20:43631292 | A | G | 2 | a0001c0006t0001g0016 a0004c0009t0001g0021 |
2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.924-4634A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631292 | |||||||
| chr20:43631380 | AC | A | 2 | a0001c0002t0001g0006 a0001c0002t0001g0019 |
3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.924-4544delC | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43631380 | ||||||
| chr20:43631446 | T | C | 1 | a0001c0002t0001g0267 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.924-4480T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631446 | |||||||
| chr20:43631478 | T | A | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-4448T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631478 | |||||||
| chr20:43631519 | G | A | 6 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0082 others(3): Show |
6 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.924-4407G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631519 | |||||||
| chr20:43631607 | T | C | 157 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(154): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.924-4319T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631607 | |||||||
| chr20:43631635 | T | A | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-4291T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631635 | |||||||
| chr20:43631693 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.924-4233G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631693 | |||||||
| chr20:43631801 | G | C | 17 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0024 others(14): Show |
19 | HG01109.hp2 HG02056.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.924-4125G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631801 | |||||||
| chr20:43631828 | A | T | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-4098A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631828 | |||||||
| chr20:43631924 | C | CT | 15 | a0001c0001t0001g0265 a0001c0001t0001g0275 a0001c0002t0001g0006 others(12): Show |
18 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.924-3984dupT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43631924 | ||||||
| chr20:43631924 | CT | C | 6 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0167 others(3): Show |
6 | HG01168.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.924-3984delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43631924 | ||||||
| chr20:43631931 | T | A | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-3995T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43631931 | |||||||
| chr20:43632050 | C | T | 232 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(229): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.924-3876C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632050 | |||||||
| chr20:43632095 | T | A | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-3831T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632095 | |||||||
| chr20:43632113 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.924-3813C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632113 | |||||||
| chr20:43632122 | T | A | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-3804T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632122 | |||||||
| chr20:43632167 | C | T | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.924-3759C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632167 | |||||||
| chr20:43632205 | G | A | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.924-3721G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632205 | |||||||
| chr20:43632294 | T | A | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-3632T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632294 | |||||||
| chr20:43632313 | T | C | 2 | a0001c0001t0001g0217 a0001c0001t0001g0265 |
2 | HG02040.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.924-3613T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632313 | |||||||
| chr20:43632410 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.924-3516G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632410 | |||||||
| chr20:43632505 | C | T | 19 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0024 others(16): Show |
21 | HG01109.hp2 HG02056.hp1 HG02135.hp1 others(18): Show |
intron_variant | MODIFIER | c.924-3421C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632505 | |||||||
| chr20:43632657 | C | A | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-3269C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632657 | |||||||
| chr20:43632835 | G | T | 10 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(7): Show |
10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.924-3091G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632835 | |||||||
| chr20:43632909 | T | A | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-3017T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632909 | |||||||
| chr20:43632936 | T | C | 1 | a0001c0002t0001g0025 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.924-2990T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43632936 | |||||||
| chr20:43632995 | C | CATTT | 27 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0017 others(24): Show |
29 | HG01081.hp1 HG01884.hp1 HG02083.hp2 others(26): Show |
intron_variant | MODIFIER | c.924-2930_924-2927d others(6): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43632995 | ||||||
| chr20:43633053 | T | A | 2 | a0001c0006t0001g0016 a0004c0009t0001g0021 |
2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.924-2873T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633053 | |||||||
| chr20:43633089 | A | G | 1 | a0004c0009t0001g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.924-2837A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633089 | |||||||
| chr20:43633179 | A | T | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-2747A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633179 | |||||||
| chr20:43633189 | C | A | 17 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0024 others(14): Show |
19 | HG01109.hp2 HG02056.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.924-2737C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633189 | |||||||
| chr20:43633267 | C | T | 4 | a0001c0003t0001g0002 a0001c0003t0001g0020 a0001c0003t0001g0022 others(1): Show |
6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.924-2659C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633267 | |||||||
| chr20:43633291 | C | T | 4 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0206 others(1): Show |
4 | HG00544.hp1 HG01981.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-2635C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633291 | |||||||
| chr20:43633304 | T | A | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-2622T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633304 | |||||||
| chr20:43633359 | A | C | 10 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(7): Show |
10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.924-2567A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633359 | |||||||
| chr20:43633553 | C | A | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-2373C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633553 | |||||||
| chr20:43633581 | G | A | 4 | a0001c0003t0001g0002 a0001c0003t0001g0020 a0001c0003t0001g0022 others(1): Show |
6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.924-2345G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633581 | |||||||
| chr20:43633626 | T | A | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-2300T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633626 | |||||||
| chr20:43633697 | G | T | 1 | a0001c0001t0001g0219 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.924-2229G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633697 | |||||||
| chr20:43633831 | A | T | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-2095A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633831 | |||||||
| chr20:43633832 | T | A | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-2094T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633832 | |||||||
| chr20:43633927 | G | A | 1 | a0001c0002t0001g0006 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.924-1999G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633927 | |||||||
| chr20:43633954 | A | G | 2 | a0001c0006t0001g0016 a0004c0009t0001g0021 |
2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.924-1972A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633954 | |||||||
| chr20:43633980 | A | T | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-1946A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43633980 | |||||||
| chr20:43634024 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.924-1902C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634024 | |||||||
| chr20:43634055 | C | A | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-1871C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634055 | |||||||
| chr20:43634175 | T | A | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-1751T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634175 | |||||||
| chr20:43634214 | GA | G | 256 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(253): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.924-1701delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43634214 | ||||||
| chr20:43634228 | G | A | 170 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(167): Show |
178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.924-1698G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634228 | |||||||
| chr20:43634367 | T | A | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-1559T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634367 | |||||||
| chr20:43634372 | TAAATCAA others(3): Show |
T | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.924-1550_924-1541d others(12): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43634372 | ||||||
| chr20:43634401 | A | G | 4 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-1525A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634401 | |||||||
| chr20:43634424 | C | T | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.924-1502C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634424 | |||||||
| chr20:43634473 | T | G | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(173): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.924-1453T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634473 | |||||||
| chr20:43634475 | C | A | 1 | a0001c0001t0001g0204 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.924-1451C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634475 | |||||||
| chr20:43634476 | A | T | 1 | a0001c0001t0001g0111 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.924-1450A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634476 | |||||||
| chr20:43634525 | G | A | 2 | a0001c0006t0001g0016 a0004c0009t0001g0021 |
2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.924-1401G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634525 | |||||||
| chr20:43634528 | A | G | 2 | a0001c0002t0001g0017 a0001c0002t0001g0018 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.924-1398A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634528 | |||||||
| chr20:43634698 | A | G | 1 | a0001c0002t0001g0006 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.924-1228A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634698 | |||||||
| chr20:43634811 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.924-1115A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634811 | |||||||
| chr20:43634857 | C | T | 2 | a0001c0002t0001g0017 a0001c0002t0001g0018 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.924-1069C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634857 | |||||||
| chr20:43634941 | C | T | 1 | a0001c0002t0001g0078 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.924-985C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634941 | |||||||
| chr20:43634947 | G | A | 1 | a0001c0002t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.924-979G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634947 | |||||||
| chr20:43634959 | A | G | 2 | a0001c0006t0001g0016 a0004c0009t0001g0021 |
2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.924-967A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43634959 | |||||||
| chr20:43635026 | G | A | 5 | a0001c0002t0001g0054 a0001c0002t0001g0062 a0001c0002t0001g0063 others(2): Show |
5 | HG02056.hp2 NA18973.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.924-900G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635026 | |||||||
| chr20:43635170 | A | C | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(173): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.924-756A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635170 | |||||||
| chr20:43635187 | GA | G | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(174): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.924-726delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43635187 | ||||||
| chr20:43635232 | A | G | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(173): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.924-694A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635232 | |||||||
| chr20:43635287 | A | G | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(173): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.924-639A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635287 | |||||||
| chr20:43635353 | C | T | 2 | a0001c0002t0001g0006 a0001c0002t0001g0019 |
3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.924-573C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635353 | |||||||
| chr20:43635364 | C | T | 1 | a0001c0002t0001g0085 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.924-562C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635364 | |||||||
| chr20:43635377 | G | A | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(173): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.924-549G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635377 | |||||||
| chr20:43635389 | C | T | 3 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 |
3 | HG02886.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.924-537C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635389 | |||||||
| chr20:43635548 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0178 |
2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.924-378C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635548 | |||||||
| chr20:43635558 | A | C | 10 | a0001c0001t0001g0004 a0001c0001t0001g0135 a0001c0001t0001g0145 others(7): Show |
12 | HG00642.hp2 HG00741.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.924-368A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635558 | |||||||
| chr20:43635674 | C | A | 21 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0086 others(18): Show |
23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.924-252C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635674 | |||||||
| chr20:43635728 | T | C | 4 | a0001c0003t0001g0002 a0001c0003t0001g0020 a0001c0003t0001g0022 others(1): Show |
6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.924-198T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635728 | |||||||
| chr20:43635862 | G | A | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(173): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.924-64G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635862 | |||||||
| chr20:43635873 | G | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0226 |
2 | NA18966.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.924-53G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 10/13 | chr20 | 43635873 | |||||||
| chr20:43636086 | T | C | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(173): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1011+73T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 11/13 | chr20 | 43636086 | |||||||
| chr20:43636367 | C | T | 6 | a0001c0001t0001g0126 a0001c0001t0001g0166 a0001c0001t0001g0170 others(3): Show |
6 | HG00280.hp1 HG01069.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1011+354C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 11/13 | chr20 | 43636367 | |||||||
| chr20:43636401 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1011+388T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 11/13 | chr20 | 43636401 | |||||||
| chr20:43636597 | G | C | 10 | a0001c0001t0001g0004 a0001c0001t0001g0135 a0001c0001t0001g0145 others(7): Show |
12 | HG00642.hp2 HG00741.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.1012-548G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 11/13 | chr20 | 43636597 | |||||||
| chr20:43636802 | G | A | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1012-343G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 11/13 | chr20 | 43636802 | |||||||
| chr20:43636867 | T | C | 11 | a0001c0002t0001g0009 a0001c0002t0001g0053 a0001c0002t0001g0058 others(8): Show |
12 | HG00544.hp2 HG02027.hp1 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.1012-278T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 11/13 | chr20 | 43636867 | |||||||
| chr20:43637010 | A | G | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(173): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1012-135A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 11/13 | chr20 | 43637010 | |||||||
| chr20:43637012 | G | A | 6 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0082 others(3): Show |
6 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1012-133G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 11/13 | chr20 | 43637012 | |||||||
| chr20:43637060 | T | C | 215 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(212): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1012-85T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 11/13 | chr20 | 43637060 | |||||||
| chr20:43637326 | G | A | 166 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1120+73G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43637326 | |||||||
| chr20:43637416 | C | T | 10 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(7): Show |
10 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1120+163C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43637416 | |||||||
| chr20:43637501 | G | A | 3 | a0001c0001t0001g0221 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG01123.hp1 HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1120+248G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43637501 | |||||||
| chr20:43637510 | G | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG02486.hp1 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1120+257G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43637510 | |||||||
| chr20:43637545 | G | A | 1 | a0001c0002t0001g0086 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1120+292G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43637545 | |||||||
| chr20:43637706 | T | C | 3 | a0001c0003t0001g0002 a0001c0003t0001g0022 a0001c0003t0001g0023 |
5 | HG02615.hp2 HG02922.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1120+453T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43637706 | |||||||
| chr20:43637734 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1120+481T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43637734 | |||||||
| chr20:43637738 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1120+485C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43637738 | |||||||
| chr20:43637938 | T | C | 5 | a0001c0002t0001g0081 a0001c0003t0001g0002 a0001c0003t0001g0020 others(2): Show |
7 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1120+685T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43637938 | |||||||
| chr20:43638193 | AT | A | 209 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(206): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1120+954delT | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43638193 | ||||||
| chr20:43638193 | ATT | A | 6 | a0001c0001t0001g0126 a0001c0001t0001g0166 a0001c0001t0001g0170 others(3): Show |
6 | HG00280.hp1 HG01069.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120+953_1120+954d others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43638193 | ||||||
| chr20:43638230 | G | A | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1120+977G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43638230 | |||||||
| chr20:43638268 | G | A | 3 | a0001c0002t0001g0032 a0001c0002t0001g0036 a0001c0002t0001g0038 |
3 | HG02135.hp1 NA18939.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1120+1015G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43638268 | |||||||
| chr20:43638352 | G | C | 1 | a0001c0001t0001g0203 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1120+1099G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43638352 | |||||||
| chr20:43638399 | C | T | 2 | a0001c0002t0001g0017 a0001c0002t0001g0018 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1120+1146C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43638399 | |||||||
| chr20:43638694 | T | C | 3 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0249 |
3 | HG02258.hp2 HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1120+1441T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43638694 | |||||||
| chr20:43638832 | A | G | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02055.hp1 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1120+1579A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43638832 | |||||||
| chr20:43638934 | A | T | 2 | a0001c0002t0001g0006 a0001c0002t0001g0019 |
3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1120+1681A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43638934 | |||||||
| chr20:43639168 | A | G | 1 | a0001c0002t0001g0068 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1120+1915A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639168 | |||||||
| chr20:43639236 | C | CA | 166 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(163): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1120+2000dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43639236 | ||||||
| chr20:43639236 | C | CAA | 15 | a0001c0001t0001g0159 a0001c0001t0001g0191 a0001c0001t0001g0192 others(12): Show |
15 | HG00438.hp1 HG00438.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1120+1999_1120+200 others(6): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43639236 | ||||||
| chr20:43639265 | C | A | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1120+2012C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639265 | |||||||
| chr20:43639266 | G | A | 1 | a0001c0002t0001g0026 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1120+2013G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639266 | |||||||
| chr20:43639297 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1120+2044A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639297 | |||||||
| chr20:43639379 | C | CA | 23 | a0001c0001t0001g0271 a0001c0002t0001g0010 a0001c0002t0001g0011 others(20): Show |
25 | HG01081.hp1 HG01243.hp1 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.1120+2135dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43639379 | ||||||
| chr20:43639390 | G | C | 166 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1120+2137G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639390 | |||||||
| chr20:43639408 | C | A | 1 | a0004c0009t0001g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1120+2155C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639408 | |||||||
| chr20:43639421 | G | A | 6 | a0001c0002t0001g0091 a0001c0002t0001g0095 a0001c0002t0001g0096 others(3): Show |
6 | NA18952.hp1 NA18972.hp1 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120+2168G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639421 | |||||||
| chr20:43639539 | G | A | 17 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0024 others(14): Show |
19 | HG01109.hp2 HG02056.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.1120+2286G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639539 | |||||||
| chr20:43639584 | C | T | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1120+2331C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639584 | |||||||
| chr20:43639618 | C | T | 1 | a0001c0002t0001g0063 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1120+2365C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639618 | |||||||
| chr20:43639680 | A | T | 1 | a0001c0002t0001g0075 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1120+2427A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639680 | |||||||
| chr20:43639681 | T | A | 1 | a0001c0001t0001g0184 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1120+2428T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639681 | |||||||
| chr20:43639701 | C | T | 179 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1120+2448C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639701 | |||||||
| chr20:43639763 | C | T | 1 | a0001c0002t0001g0086 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1120+2510C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639763 | |||||||
| chr20:43639796 | C | T | 1 | a0001c0002t0001g0011 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1120+2543C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639796 | |||||||
| chr20:43639968 | C | T | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(173): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1121-2511C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43639968 | |||||||
| chr20:43640181 | G | A | 4 | a0001c0003t0001g0002 a0001c0003t0001g0020 a0001c0003t0001g0022 others(1): Show |
6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121-2298G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43640181 | |||||||
| chr20:43640222 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1121-2257C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43640222 | |||||||
| chr20:43640232 | G | A | 5 | a0001c0002t0001g0009 a0001c0002t0001g0053 a0001c0002t0001g0058 others(2): Show |
6 | NA18941.hp1 NA18945.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121-2247G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43640232 | |||||||
| chr20:43640423 | G | C | 1 | a0001c0002t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1121-2056G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43640423 | |||||||
| chr20:43641030 | C | CA | 6 | a0001c0002t0001g0041 a0001c0002t0001g0051 a0001c0002t0001g0070 others(3): Show |
6 | HG01175.hp1 HG02257.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121-1425dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43641030 | ||||||
| chr20:43641030 | CA | C | 31 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0017 others(28): Show |
35 | HG01109.hp2 HG01361.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.1121-1425delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43641030 | ||||||
| chr20:43641030 | CAA | C | 21 | a0001c0002t0001g0006 a0001c0002t0001g0010 a0001c0002t0001g0011 others(18): Show |
24 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.1121-1426_1121-142 others(6): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43641030 | ||||||
| chr20:43641030 | CAAAA | C | 7 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0118 others(4): Show |
7 | HG02071.hp1 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1121-1428_1121-142 others(8): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43641030 | ||||||
| chr20:43641030 | CAAAAA | C | 164 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(161): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.1121-1429_1121-142 others(9): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43641030 | ||||||
| chr20:43641104 | A | G | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(173): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1121-1375A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43641104 | |||||||
| chr20:43641112 | T | A | 1 | a0004c0009t0001g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1121-1367T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43641112 | |||||||
| chr20:43641183 | T | C | 1 | a0001c0002t0001g0054 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1121-1296T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43641183 | |||||||
| chr20:43641218 | T | G | 215 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(212): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1121-1261T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43641218 | |||||||
| chr20:43641640 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1121-839C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43641640 | |||||||
| chr20:43641694 | C | T | 36 | a0001c0002t0001g0006 a0001c0002t0001g0010 a0001c0002t0001g0011 others(33): Show |
41 | HG01081.hp1 HG01361.hp2 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.1121-785C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43641694 | |||||||
| chr20:43641722 | C | T | 4 | a0001c0003t0001g0002 a0001c0003t0001g0020 a0001c0003t0001g0022 others(1): Show |
6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121-757C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43641722 | |||||||
| chr20:43641773 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1121-706C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43641773 | |||||||
| chr20:43642023 | A | T | 21 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0086 others(18): Show |
23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.1121-456A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43642023 | |||||||
| chr20:43642197 | C | T | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(173): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1121-282C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43642197 | |||||||
| chr20:43642281 | T | C | 166 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1121-198T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 12/13 | chr20 | 43642281 | |||||||
| chr20:43642680 | C | T | 2 | a0001c0002t0001g0064 a0001c0002t0001g0069 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1266+56C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642680 | |||||||
| chr20:43642708 | C | T | 1 | a0001c0002t0001g0077 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1266+84C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642708 | |||||||
| chr20:43642734 | T | G | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(174): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1266+110T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642734 | |||||||
| chr20:43642800 | G | T | 2 | a0001c0002t0001g0039 a0001c0002t0001g0040 |
2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1266+176G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642800 | |||||||
| chr20:43642918 | A | G | 12 | a0001c0001t0001g0115 a0001c0001t0001g0232 a0001c0002t0001g0091 others(9): Show |
12 | NA18952.hp1 NA18959.hp2 NA18963.hp2 others(9): Show |
intron_variant | MODIFIER | c.1266+294A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642918 | |||||||
| chr20:43642930 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0232 |
2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1266+306G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642930 | |||||||
| chr20:43642932 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0232 |
2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1266+308T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642932 | |||||||
| chr20:43642936 | G | A | 14 | a0001c0002t0001g0011 a0001c0002t0001g0091 a0001c0002t0001g0092 others(11): Show |
15 | HG02083.hp2 HG03491.hp2 HG03492.hp1 others(12): Show |
intron_variant | MODIFIER | c.1266+312G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642936 | |||||||
| chr20:43642936 | G | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0232 |
2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1266+312G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642936 | |||||||
| chr20:43642938 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0232 |
2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1266+314A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642938 | |||||||
| chr20:43642941 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0232 |
2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1266+317C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642941 | |||||||
| chr20:43642942 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0232 |
2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1266+318A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642942 | |||||||
| chr20:43642955 | T | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0232 |
2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1266+331T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642955 | |||||||
| chr20:43642962 | T | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0232 |
2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1266+338T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642962 | |||||||
| chr20:43642972 | G | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0232 |
2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1266+348G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43642972 | |||||||
| chr20:43643037 | C | T | 1 | a0001c0002t0001g0086 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1266+413C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43643037 | |||||||
| chr20:43643119 | A | G | 1 | a0001c0002t0001g0077 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1266+495A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43643119 | |||||||
| chr20:43643164 | C | CA | 159 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(156): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.1266+549dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr20 | 43643164 | ||||||
| chr20:43643164 | C | CAA | 7 | a0001c0001t0001g0152 a0001c0001t0001g0184 a0001c0001t0001g0213 others(4): Show |
7 | HG01192.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1266+548_1266+549d others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr20 | 43643164 | ||||||
| chr20:43643174 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1266+550C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43643174 | |||||||
| chr20:43643177 | AAAAAC | A | 3 | a0001c0002t0001g0043 a0001c0002t0001g0051 a0001c0002t0001g0106 |
3 | HG01099.hp1 HG01175.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1266+568_1266+572d others(7): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr20 | 43643177 | ||||||
| chr20:43643192 | C | CA | 6 | a0001c0001t0001g0113 a0001c0001t0001g0213 a0001c0002t0001g0035 others(3): Show |
6 | HG01109.hp1 HG02056.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1266+578dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr20 | 43643192 | ||||||
| chr20:43643197 | A | C | 1 | a0001c0002t0001g0027 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1266+573A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43643197 | |||||||
| chr20:43643224 | ACCTGTAA others(2717): Show |
A | 175 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(172): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1266+636_1267-953d others(2): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr20 | 43643224 | ||||||
| chr20:43643243 | TGGGAGGC others(2718): Show |
T | 1 | a0001c0001t0002g0174 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1266+622_1267-966d others(2): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr20 | 43643243 | ||||||
| chr20:43643509 | C | T | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1266+885C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43643509 | |||||||
| chr20:43644101 | T | C | 56 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0008 others(53): Show |
63 | HG01081.hp1 HG01109.hp2 HG01361.hp2 others(60): Show |
intron_variant | MODIFIER | c.1266+1477T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644101 | |||||||
| chr20:43644102 | G | A | 27 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0017 others(24): Show |
29 | HG01081.hp1 HG01884.hp1 HG02083.hp2 others(26): Show |
intron_variant | MODIFIER | c.1266+1478G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644102 | |||||||
| chr20:43644186 | A | ATTCCTTG others(2): Show |
39 | a0001c0002t0001g0006 a0001c0002t0001g0010 a0001c0002t0001g0011 others(36): Show |
44 | HG01081.hp1 HG01361.hp2 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.1266+1562_1266+156 others(13): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644186 | |||||||
| chr20:43644202 | G | A | 1 | a0001c0002t0001g0069 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1266+1578G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644202 | |||||||
| chr20:43644294 | G | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1670G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644294 | |||||||
| chr20:43644306 | T | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1682T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644306 | |||||||
| chr20:43644309 | A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1685A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644309 | |||||||
| chr20:43644311 | T | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1687T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644311 | |||||||
| chr20:43644312 | G | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1688G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644312 | |||||||
| chr20:43644313 | T | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1689T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644313 | |||||||
| chr20:43644321 | G | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1697G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644321 | |||||||
| chr20:43644325 | A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1701A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644325 | |||||||
| chr20:43644327 | C | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1703C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644327 | |||||||
| chr20:43644328 | C | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1704C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644328 | |||||||
| chr20:43644330 | T | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1706T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644330 | |||||||
| chr20:43644333 | T | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1709T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644333 | |||||||
| chr20:43644334 | A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1710A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644334 | |||||||
| chr20:43644335 | A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1711A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644335 | |||||||
| chr20:43644337 | C | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1713C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644337 | |||||||
| chr20:43644342 | G | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1718G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644342 | |||||||
| chr20:43644343 | A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1719A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644343 | |||||||
| chr20:43644348 | G | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1724G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644348 | |||||||
| chr20:43644350 | T | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1726T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644350 | |||||||
| chr20:43644355 | T | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1731T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644355 | |||||||
| chr20:43644357 | A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1733A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644357 | |||||||
| chr20:43644359 | A | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1735A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644359 | |||||||
| chr20:43644362 | A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1738A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644362 | |||||||
| chr20:43644363 | T | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1739T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644363 | |||||||
| chr20:43644366 | G | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1742G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644366 | |||||||
| chr20:43644371 | A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1747A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644371 | |||||||
| chr20:43644372 | C | T | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1266+1748C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644372 | |||||||
| chr20:43644375 | A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1751A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644375 | |||||||
| chr20:43644377 | A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1753A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644377 | |||||||
| chr20:43644378 | G | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1754G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644378 | |||||||
| chr20:43644383 | A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1759A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644383 | |||||||
| chr20:43644386 | A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1762A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644386 | |||||||
| chr20:43644388 | C | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1764C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644388 | |||||||
| chr20:43644390 | A | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1766A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644390 | |||||||
| chr20:43644391 | G | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1767G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644391 | |||||||
| chr20:43644392 | G | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1768G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644392 | |||||||
| chr20:43644393 | A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1769A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644393 | |||||||
| chr20:43644395 | T | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1771T>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644395 | |||||||
| chr20:43644400 | G | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1776G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644400 | |||||||
| chr20:43644402 | G | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1778G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644402 | |||||||
| chr20:43644408 | T | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1784T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644408 | |||||||
| chr20:43644412 | T | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1788T>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644412 | |||||||
| chr20:43644419 | A | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1795A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644419 | |||||||
| chr20:43644421 | G | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1797G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644421 | |||||||
| chr20:43644423 | A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1799A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644423 | |||||||
| chr20:43644436 | A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1812A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644436 | |||||||
| chr20:43644440 | G | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1816G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644440 | |||||||
| chr20:43644442 | A | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1818A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644442 | |||||||
| chr20:43644451 | A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1827A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644451 | |||||||
| chr20:43644452 | G | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1828G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644452 | |||||||
| chr20:43644454 | A | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1830A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644454 | |||||||
| chr20:43644459 | A | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1835A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644459 | |||||||
| chr20:43644460 | G | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1836G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644460 | |||||||
| chr20:43644462 | G | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1838G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644462 | |||||||
| chr20:43644464 | A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1840A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644464 | |||||||
| chr20:43644465 | C | A | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1841C>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644465 | |||||||
| chr20:43644466 | A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1842A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644466 | |||||||
| chr20:43644470 | A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1846A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644470 | |||||||
| chr20:43644472 | A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1848A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644472 | |||||||
| chr20:43644473 | A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1849A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644473 | |||||||
| chr20:43644474 | G | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1850G>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644474 | |||||||
| chr20:43644477 | A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1853A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644477 | |||||||
| chr20:43644478 | A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1854A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644478 | |||||||
| chr20:43644479 | A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1855A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644479 | |||||||
| chr20:43644480 | A | C | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1856A>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644480 | |||||||
| chr20:43644482 | A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1858A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644482 | |||||||
| chr20:43644491 | A | G | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1867A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644491 | |||||||
| chr20:43644492 | A | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266+1868A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644492 | |||||||
| chr20:43644649 | G | A | 1 | a0001c0002t0001g0024 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1266+2025G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644649 | |||||||
| chr20:43644705 | G | A | 3 | a0001c0002t0001g0088 a0001c0002t0001g0090 a0001c0002t0001g0104 |
3 | HG01081.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1266+2081G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644705 | |||||||
| chr20:43644730 | A | G | 39 | a0001c0002t0001g0006 a0001c0002t0001g0010 a0001c0002t0001g0011 others(36): Show |
44 | HG01081.hp1 HG01361.hp2 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.1266+2106A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43644730 | |||||||
| chr20:43645137 | G | A | 2 | a0001c0002t0001g0017 a0001c0002t0001g0018 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1267-1799G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43645137 | |||||||
| chr20:43645385 | G | A | 1 | a0001c0002t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1267-1551G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43645385 | |||||||
| chr20:43645401 | C | T | 21 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0086 others(18): Show |
23 | HG01081.hp1 HG02083.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.1267-1535C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43645401 | |||||||
| chr20:43645733 | G | A | 4 | a0001c0003t0001g0002 a0001c0003t0001g0020 a0001c0003t0001g0022 others(1): Show |
6 | HG01361.hp2 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1267-1203G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43645733 | |||||||
| chr20:43645820 | A | G | 39 | a0001c0002t0001g0006 a0001c0002t0001g0010 a0001c0002t0001g0011 others(36): Show |
44 | HG01081.hp1 HG01361.hp2 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.1267-1116A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43645820 | |||||||
| chr20:43645864 | A | T | 37 | a0001c0002t0001g0006 a0001c0002t0001g0010 a0001c0002t0001g0017 others(34): Show |
41 | HG01081.hp1 HG01361.hp2 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.1267-1072A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43645864 | |||||||
| chr20:43645865 | A | T | 2 | a0001c0002t0001g0011 a0001c0002t0001g0092 |
3 | HG03491.hp2 HG03492.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1267-1071A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43645865 | |||||||
| chr20:43645975 | C | T | 2 | a0001c0002t0001g0017 a0001c0002t0001g0018 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1267-961C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43645975 | |||||||
| chr20:43646067 | C | T | 1 | a0001c0002t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1267-869C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43646067 | |||||||
| chr20:43646068 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1267-868G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43646068 | |||||||
| chr20:43646069 | C | T | 29 | a0001c0001t0001g0012 a0001c0001t0001g0110 a0001c0001t0001g0111 others(26): Show |
30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1267-867C>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43646069 | |||||||
| chr20:43646168 | G | A | 1 | a0001c0002t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1267-768G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43646168 | |||||||
| chr20:43646209 | C | CA | 16 | a0001c0002t0001g0011 a0001c0002t0001g0033 a0001c0002t0001g0040 others(13): Show |
17 | HG02056.hp1 HG02083.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1267-711dupA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr20 | 43646209 | ||||||
| chr20:43646209 | C | CAA | 8 | a0001c0002t0001g0010 a0001c0002t0001g0086 a0001c0002t0001g0087 others(5): Show |
9 | HG01081.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1267-712_1267-711d others(4): Show |
IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr20 | 43646209 | ||||||
| chr20:43646209 | CA | C | 172 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(169): Show |
180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.1267-711delA | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr20 | 43646209 | ||||||
| chr20:43646336 | A | T | 1 | a0001c0001t0001g0166 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1267-600A>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43646336 | |||||||
| chr20:43646508 | T | C | 4 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1267-428T>C | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43646508 | |||||||
| chr20:43646528 | G | A | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 |
3 | HG02602.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1267-408G>A | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43646528 | |||||||
| chr20:43646772 | A | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0183 |
2 | HG02300.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1267-164A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43646772 | |||||||
| chr20:43646812 | A | G | 1 | a0001c0002t0001g0048 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1267-124A>G | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43646812 | |||||||
| chr20:43646859 | G | T | 232 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(229): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1267-77G>T | IFT52 | ENSG00000101052.13 | transcript | ENST00000373030.8 | protein_coding | 13/13 | chr20 | 43646859 |