Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26160 |
| ensemblid | ENSG00000138002.16 |
| hgncid | 30391 |
| symbol | IFT172 |
| name | intraflagellar transport 172 |
| refseq_nuc | NM_015662.3 |
| refseq_prot | NP_056477.1 |
| ensembl_nuc | ENST00000260570.8 |
| ensembl_prot | ENSP00000260570.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 27444377 |
| end | 27489743 |
| strand | - |
| ver | v1.2 |
| region | chr2:27444377-27489743 |
| region5000 | chr2:27439377-27494743 |
| regionname0 | IFT172_chr2_27444377_27489743 |
| regionname5000 | IFT172_chr2_27439377_27494743 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1749 | 209 | 73 | 51 | 50 | 10 | 23 | 35 | IFT172_chr2_27439377_27494743 | IFT172 | MHLKH others(1744): Show |
chr2 | 27439377 | 27494743 |
| a0002 | 0/0 | 1749 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | MHLKH others(1744): Show |
chr2 | 27439377 | 27494743 |
| a0003 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | MHLKH others(1744): Show |
chr2 | 27439377 | 27494743 |
| a0004 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | MHLKH others(1744): Show |
chr2 | 27439377 | 27494743 |
| a0005 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | MHLKH others(1744): Show |
chr2 | 27439377 | 27494743 |
| a0006 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | MHLKH others(1744): Show |
chr2 | 27439377 | 27494743 |
| a0007 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | MHLKH others(1744): Show |
chr2 | 27439377 | 27494743 |
| a0008 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | MHLKH others(1744): Show |
chr2 | 27439377 | 27494743 |
| a0009 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | MHLKH others(1744): Show |
chr2 | 27439377 | 27494743 |
| a0010 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | MHLKH others(1744): Show |
chr2 | 27439377 | 27494743 |
| a0011 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | MHLKH others(1744): Show |
chr2 | 27439377 | 27494743 |
| a0012 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | MHLKH others(1744): Show |
chr2 | 27439377 | 27494743 |
| a0013 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | MHLKH others(1744): Show |
chr2 | 27439377 | 27494743 |
| a0014 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | MHLKH others(1744): Show |
chr2 | 27439377 | 27494743 |
| a0015 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | MHLKH others(1744): Show |
chr2 | 27439377 | 27494743 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 5247 | 124 | 50 | 26 | 29 | 5 | 13 | IFT172_chr2_27439377_27494743 | IFT172 | ATGCA others(5242): Show |
chr2 | 27439377 | 27494743 | ||
| a0001c0002 | 0/1 | 5247 | 81 | 19 | 25 | 21 | 5 | 10 | IFT172_chr2_27439377_27494743 | IFT172 | ATGCA others(5242): Show |
chr2 | 27439377 | 27494743 | ||
| a0001c0003 | 0/0 | 5247 | 2 | 2 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | ATGCA others(5242): Show |
chr2 | 27439377 | 27494743 | ||
| a0001c0013 | 0/0 | 5247 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | ATGCA others(5242): Show |
chr2 | 27439377 | 27494743 | ||
| a0001c0019 | 0/0 | 5247 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | ATGCA others(5242): Show |
chr2 | 27439377 | 27494743 | ||
| a0002c0004 | 0/0 | 5247 | 2 | 2 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | ATGCA others(5242): Show |
chr2 | 27439377 | 27494743 | ||
| a0003c0012 | 0/0 | 5247 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | ATGCA others(5242): Show |
chr2 | 27439377 | 27494743 | ||
| a0004c0010 | 0/0 | 5247 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | ATGCA others(5242): Show |
chr2 | 27439377 | 27494743 | ||
| a0005c0007 | 0/0 | 5247 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | ATGCA others(5242): Show |
chr2 | 27439377 | 27494743 | ||
| a0006c0014 | 0/0 | 5247 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | ATGCA others(5242): Show |
chr2 | 27439377 | 27494743 | ||
| a0007c0018 | 0/0 | 5247 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | ATGCA others(5242): Show |
chr2 | 27439377 | 27494743 | ||
| a0008c0015 | 0/0 | 5247 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | ATGCA others(5242): Show |
chr2 | 27439377 | 27494743 | ||
| a0009c0009 | 0/0 | 5247 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | ATGCA others(5242): Show |
chr2 | 27439377 | 27494743 | ||
| a0010c0011 | 0/0 | 5247 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | ATGCA others(5242): Show |
chr2 | 27439377 | 27494743 | ||
| a0011c0006 | 0/0 | 5247 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | ATGCA others(5242): Show |
chr2 | 27439377 | 27494743 | ||
| a0012c0008 | 0/0 | 5247 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | ATGCA others(5242): Show |
chr2 | 27439377 | 27494743 | ||
| a0013c0017 | 0/0 | 5247 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | ATGCA others(5242): Show |
chr2 | 27439377 | 27494743 | ||
| a0014c0016 | 0/0 | 5247 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | ATGCA others(5242): Show |
chr2 | 27439377 | 27494743 | ||
| a0015c0005 | 0/0 | 5247 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | ATGCA others(5242): Show |
chr2 | 27439377 | 27494743 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5395 | 34 | 30 | 4 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | AGTGC others(5390): Show |
chr2 | 27439377 | 27494743 |
| a0001c0001t0002 | 1/0 | 5395 | 90 | 20 | 22 | 29 | 5 | 13 | IFT172_chr2_27439377_27494743 | IFT172 | AGTGC others(5390): Show |
chr2 | 27439377 | 27494743 |
| a0001c0002t0001 | 0/1 | 5395 | 81 | 19 | 25 | 21 | 5 | 10 | IFT172_chr2_27439377_27494743 | IFT172 | AGTGC others(5390): Show |
chr2 | 27439377 | 27494743 |
| a0001c0003t0001 | 0/0 | 5395 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | AGTGC others(5390): Show |
chr2 | 27439377 | 27494743 |
| a0001c0003t0002 | 0/0 | 5395 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | AGTGC others(5390): Show |
chr2 | 27439377 | 27494743 |
| a0001c0013t0002 | 0/0 | 5395 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | AGTGC others(5390): Show |
chr2 | 27439377 | 27494743 |
| a0001c0019t0001 | 0/0 | 5395 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | AGTGC others(5390): Show |
chr2 | 27439377 | 27494743 |
| a0002c0004t0001 | 0/0 | 5395 | 2 | 2 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | AGTGC others(5390): Show |
chr2 | 27439377 | 27494743 |
| a0003c0012t0002 | 0/0 | 5395 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | AGTGC others(5390): Show |
chr2 | 27439377 | 27494743 |
| a0004c0010t0002 | 0/0 | 5395 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | AGTGC others(5390): Show |
chr2 | 27439377 | 27494743 |
| a0005c0007t0002 | 0/0 | 5395 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | AGTGC others(5390): Show |
chr2 | 27439377 | 27494743 |
| a0006c0014t0001 | 0/0 | 5395 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | AGTGC others(5390): Show |
chr2 | 27439377 | 27494743 |
| a0007c0018t0002 | 0/0 | 5395 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | AGTGC others(5390): Show |
chr2 | 27439377 | 27494743 |
| a0008c0015t0002 | 0/0 | 5395 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | AGTGC others(5390): Show |
chr2 | 27439377 | 27494743 |
| a0009c0009t0001 | 0/0 | 5395 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | AGTGC others(5390): Show |
chr2 | 27439377 | 27494743 |
| a0010c0011t0002 | 0/0 | 5395 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | AGTGC others(5390): Show |
chr2 | 27439377 | 27494743 |
| a0011c0006t0002 | 0/0 | 5395 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | AGTGC others(5390): Show |
chr2 | 27439377 | 27494743 |
| a0012c0008t0002 | 0/0 | 5395 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | AGTGC others(5390): Show |
chr2 | 27439377 | 27494743 |
| a0013c0017t0001 | 0/0 | 5395 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | AGTGC others(5390): Show |
chr2 | 27439377 | 27494743 |
| a0014c0016t0002 | 0/0 | 5395 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | AGTGC others(5390): Show |
chr2 | 27439377 | 27494743 |
| a0015c0005t0001 | 0/0 | 5395 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | AGTGC others(5390): Show |
chr2 | 27439377 | 27494743 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0002 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0020 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0001 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0011 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0060 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0003t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0003t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0013t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0001c0019t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0002c0004t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0002c0004t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0003c0012t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0004c0010t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0005c0007t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0006c0014t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0007c0018t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0008c0015t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0009c0009t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0010c0011t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0011c0006t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0012c0008t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0013c0017t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0014c0016t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| a0015c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0017 | EUR | GBR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0077 | EUR | GBR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0133 | EUR | FIN | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | FIN | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0096 | EUR | FIN | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0187 | EUR | FIN | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | CHS | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | CHS | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | CHS | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0089 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0082 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0068 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0070 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0081 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0091 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0098 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0049 | AMR | PUR | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | CLM | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01256 | hp2 | a0003 | c0012 | t0002 | g0156 | AMR | CLM | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | CLM | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | CLM | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | CLM | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | CLM | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0076 | AMR | CLM | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0088 | AMR | CLM | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0047 | AMR | CLM | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | CLM | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | CLM | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0056 | AMR | CLM | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0161 | EUR | IBS | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0145 | EUR | IBS | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0012 | EUR | IBS | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01884 | hp1 | a0004 | c0010 | t0002 | g0029 | AFR | ACB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | ACB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PEL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0046 | AMR | PEL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02040 | hp1 | a0005 | c0007 | t0002 | g0140 | EAS | KHV | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | KHV | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | KHV | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | KHV | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | KHV | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0053 | AFR | ACB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | ACB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | CDX | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | CDX | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0084 | AFR | ACB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | ACB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0065 | AFR | GWD | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02572 | hp2 | a0001 | c0013 | t0002 | g0034 | AFR | GWD | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | GWD | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | GWD | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0014 | SAS | PJL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0094 | SAS | PJL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02818 | hp1 | a0006 | c0014 | t0001 | g0079 | AFR | GWD | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | GWD | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | ESN | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0063 | AFR | ESN | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | ESN | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0097 | AFR | GWD | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03041 | hp2 | a0002 | c0004 | t0001 | g0128 | AFR | GWD | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0055 | AFR | ESN | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ESN | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ESN | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | MSL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | MSL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0061 | AFR | MSL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0066 | SAS | PJL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03490 | hp2 | a0007 | c0018 | t0002 | g0167 | SAS | PJL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0073 | SAS | PJL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03491 | hp2 | a0008 | c0015 | t0002 | g0166 | SAS | PJL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03540 | hp1 | a0001 | c0019 | t0001 | g0118 | AFR | GWD | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0071 | SAS | PJL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03688 | hp1 | a0009 | c0009 | t0001 | g0054 | SAS | STU | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03688 | hp2 | a0010 | c0011 | t0002 | g0178 | SAS | STU | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03704 | hp1 | a0011 | c0006 | t0002 | g0144 | SAS | PJL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03710 | hp2 | a0012 | c0008 | t0002 | g0157 | SAS | PJL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | BEB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0100 | SAS | BEB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | BEB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0171 | SAS | BEB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0092 | SAS | STU | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0078 | SAS | STU | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | STU | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | CHB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | CHB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18963 | hp2 | a0013 | c0017 | t0001 | g0080 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA19030 | hp1 | a0002 | c0004 | t0001 | g0129 | AFR | LWK | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA19030 | hp2 | a0014 | c0016 | t0002 | g0153 | AFR | LWK | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | YRI | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | YRI | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ASW | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | ASW | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0069 | SAS | GIH | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA20905 | hp2 | a0015 | c0005 | t0001 | g0051 | SAS | GIH | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0058 | AFR | ACB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0062 | AFR | ACB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ACB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | MSL | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | USA | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | USA | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA20300 | hp1 | a0001 | c0003 | t0002 | g0025 | AFR | USA | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | USA | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | LWK | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0060 | REF | REF | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0020 | REF | REF | IFT172_chr2_27439377_27494743 | IFT172 | chr2 | 27439377 | 27494743 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:27447546 | G | A | 1 | a0009 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.4628C>T | p.Thr1543Met | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/48 | 4718/5395 | 4628/5250 | 1543/1749 | chr2 | 27447546 | |||
| chr2:27447581 | G | C | 1 | a0010 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.4593C>G | p.Phe1531Leu | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/48 | 4683/5395 | 4593/5250 | 1531/1749 | chr2 | 27447581 | |||
| chr2:27448980 | G | A | 1 | a0003 | 1 | HG01256.hp2 | missense_variant | MODERATE | c.4363C>T | p.Arg1455Trp | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 40/48 | 4453/5395 | 4363/5250 | 1455/1749 | chr2 | 27448980 | |||
| chr2:27449331 | C | T | 1 | a0004 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.4274G>A | p.Gly1425Asp | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 39/48 | 4364/5395 | 4274/5250 | 1425/1749 | chr2 | 27449331 | |||
| chr2:27450061 | T | A | 1 | a0009 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.3987A>T | p.Gln1329His | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 36/48 | 4077/5395 | 3987/5250 | 1329/1749 | chr2 | 27450061 | |||
| chr2:27454083 | C | G | 1 | a0014 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.3610G>C | p.Val1204Leu | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 33/48 | 3700/5395 | 3610/5250 | 1204/1749 | chr2 | 27454083 | |||
| chr2:27457879 | G | C | 1 | a0006 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.3073C>G | p.Pro1025Ala | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 28/48 | 3163/5395 | 3073/5250 | 1025/1749 | chr2 | 27457879 | |||
| chr2:27458798 | C | T | 1 | a0002 | 2 | HG03041.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.2858G>A | p.Arg953His | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 26/48 | 2948/5395 | 2858/5250 | 953/1749 | chr2 | 27458798 | |||
| chr2:27459442 | C | T | 1 | a0012 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.2723G>A | p.Arg908Gln | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 25/48 | 2813/5395 | 2723/5250 | 908/1749 | chr2 | 27459442 | |||
| chr2:27459764 | G | C | 1 | a0008 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.2587C>G | p.His863Asp | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 24/48 | 2677/5395 | 2587/5250 | 863/1749 | chr2 | 27459764 | |||
| chr2:27459800 | C | A | 1 | a0014 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.2551G>T | p.Val851Leu | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 24/48 | 2641/5395 | 2551/5250 | 851/1749 | chr2 | 27459800 | |||
| chr2:27461447 | C | T | 1 | a0005 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.2264G>A | p.Arg755Gln | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 22/48 | 2354/5395 | 2264/5250 | 755/1749 | chr2 | 27461447 | |||
| chr2:27461797 | G | A | 1 | a0013 | 1 | NA18963.hp2 | missense_variant | MODERATE | c.2155C>T | p.His719Tyr | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 21/48 | 2245/5395 | 2155/5250 | 719/1749 | chr2 | 27461797 | |||
| chr2:27472341 | T | A | 1 | a0007 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.1433A>T | p.Asn478Ile | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 15/48 | 1523/5395 | 1433/5250 | 478/1749 | chr2 | 27472341 | |||
| chr2:27481215 | C | T | 1 | a0011 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.616G>A | p.Ala206Thr | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 8/48 | 706/5395 | 616/5250 | 206/1749 | chr2 | 27481215 | |||
| chr2:27485430 | C | T | 1 | a0015 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.113G>A | p.Arg38Gln | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 2/48 | 203/5395 | 113/5250 | 38/1749 | chr2 | 27485430 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:27453420 | A | T | 5 | a0001c0002 a0006c0014 a0009c0009 others(2): Show |
84 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(81): Show |
synonymous_variant | LOW | c.3915T>A | p.Ser1305Ser | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/48 | 4005/5395 | 3915/5250 | 1305/1749 | chr2 | 27453420 | |||
| chr2:27456525 | G | A | 1 | a0001c0013 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.3357C>T | p.His1119His | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 30/48 | 3447/5395 | 3357/5250 | 1119/1749 | chr2 | 27456525 | |||
| chr2:27476714 | A | G | 1 | a0001c0003 | 2 | HG02145.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.1338T>C | p.Asn446Asn | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/48 | 1428/5395 | 1338/5250 | 446/1749 | chr2 | 27476714 | |||
| chr2:27478070 | T | C | 1 | a0001c0019 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.1092A>G | p.Gly364Gly | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 11/48 | 1182/5395 | 1092/5250 | 364/1749 | chr2 | 27478070 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:27444430 | A | G | 9 | a0001c0001t0001 a0001c0002t0001 a0001c0003t0001 others(6): Show |
122 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*2T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 48/48 | 2 | chr2 | 27444430 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:27444653 | T | TTTTG | 130 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(127): Show |
148 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.5161-136_5161-133d others(6): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 47/47 | chr2 | 27444653 | |||||||
| chr2:27444768 | C | A | 4 | a0001c0001t0002g0139 a0001c0001t0002g0160 a0010c0011t0002g0178 others(1): Show |
4 | HG03017.hp2 HG03688.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.5160+246G>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 47/47 | chr2 | 27444768 | |||||||
| chr2:27444951 | G | GT | 12 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0188 others(9): Show |
14 | HG00733.hp2 HG01167.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.5160+62dupA | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 47/47 | chr2 | 27444951 | |||||||
| chr2:27446029 | G | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4756-41C>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 43/47 | chr2 | 27446029 | |||||||
| chr2:27446132 | TAGG | T | 10 | a0001c0002t0001g0050 a0001c0002t0001g0059 a0001c0002t0001g0061 others(7): Show |
10 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.4755+125_4755+127d others(5): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 43/47 | chr2 | 27446132 | |||||||
| chr2:27446150 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4755+110G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 43/47 | chr2 | 27446150 | |||||||
| chr2:27446251 | C | G | 1 | a0004c0010t0002g0029 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4755+9G>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 43/47 | chr2 | 27446251 | |||||||
| chr2:27446408 | C | T | 1 | a0002c0004t0001g0128 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4660-53G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446408 | |||||||
| chr2:27446474 | AT | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(103): Show |
122 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.4660-120delA | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446474 | |||||||
| chr2:27446498 | G | GT | 103 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0052 others(100): Show |
119 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.4660-144dupA | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446498 | |||||||
| chr2:27446511 | T | C | 2 | a0001c0001t0002g0173 a0001c0001t0002g0175 |
2 | HG01175.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.4660-156A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446511 | |||||||
| chr2:27446680 | A | AT | 19 | a0001c0001t0001g0110 a0001c0001t0001g0127 a0001c0001t0002g0033 others(16): Show |
19 | HG00597.hp2 HG00639.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.4660-326dupA | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446680 | |||||||
| chr2:27446680 | A | ATT | 10 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0126 others(7): Show |
12 | HG00738.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.4660-327_4660-326d others(4): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446680 | |||||||
| chr2:27446680 | A | ATTT | 30 | a0001c0001t0001g0113 a0001c0002t0001g0001 a0001c0002t0001g0008 others(27): Show |
39 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.4660-328_4660-326d others(5): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446680 | |||||||
| chr2:27446680 | A | ATTTT | 20 | a0001c0002t0001g0010 a0001c0002t0001g0013 a0001c0002t0001g0015 others(17): Show |
23 | HG00735.hp1 HG01243.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.4660-329_4660-326d others(6): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446680 | |||||||
| chr2:27446680 | A | ATTTTT | 11 | a0001c0001t0001g0052 a0001c0002t0001g0042 a0001c0002t0001g0057 others(8): Show |
11 | HG00735.hp2 HG00738.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.4660-330_4660-326d others(7): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446680 | |||||||
| chr2:27446680 | A | ATTTTTT | 5 | a0001c0001t0001g0039 a0001c0001t0001g0196 a0001c0002t0001g0065 others(2): Show |
5 | HG01346.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.4660-331_4660-326d others(8): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446680 | |||||||
| chr2:27446680 | AT | A | 10 | a0001c0001t0001g0125 a0001c0001t0001g0192 a0001c0001t0002g0006 others(7): Show |
11 | HG01167.hp2 HG01361.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.4660-326delA | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446680 | |||||||
| chr2:27446680 | ATTTTTT | A | 8 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0119 others(5): Show |
8 | HG02486.hp1 HG02622.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.4660-331_4660-326d others(8): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446680 | |||||||
| chr2:27446680 | ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4660-335_4660-326d others(12): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446680 | |||||||
| chr2:27446748 | G | A | 3 | a0001c0002t0001g0063 a0001c0002t0001g0098 a0001c0002t0001g0099 |
3 | HG01243.hp1 HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.4660-393C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446748 | |||||||
| chr2:27446768 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4660-413G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446768 | |||||||
| chr2:27446856 | T | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(103): Show |
122 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.4660-501A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446856 | |||||||
| chr2:27446857 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4660-502C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446857 | |||||||
| chr2:27446865 | AATTTTTT others(2): Show |
A | 3 | a0001c0001t0002g0017 a0007c0018t0002g0167 a0008c0015t0002g0166 |
4 | HG00099.hp1 HG01109.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.4660-519_4660-511d others(11): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446865 | |||||||
| chr2:27446889 | C | T | 2 | a0001c0001t0002g0035 a0001c0001t0002g0037 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.4660-534G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446889 | |||||||
| chr2:27446927 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4660-572G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446927 | |||||||
| chr2:27446943 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4659+572G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446943 | |||||||
| chr2:27446978 | CGTGAGCC others(137): Show |
C | 1 | a0001c0001t0002g0026 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4659+393_4659+536d others(2): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27446978 | |||||||
| chr2:27447051 | C | T | 1 | a0001c0002t0001g0058 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4659+464G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27447051 | |||||||
| chr2:27447087 | C | T | 1 | a0001c0001t0002g0185 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.4659+428G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27447087 | |||||||
| chr2:27447440 | G | A | 71 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0009 others(68): Show |
83 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.4659+75C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27447440 | |||||||
| chr2:27447489 | T | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0113 a0001c0001t0001g0114 |
5 | HG00738.hp2 HG02717.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.4659+26A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 42/47 | chr2 | 27447489 | |||||||
| chr2:27447747 | G | C | 1 | a0009c0009t0001g0054 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4539+65C>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 41/47 | chr2 | 27447747 | |||||||
| chr2:27447963 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4429-41G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 40/47 | chr2 | 27447963 | |||||||
| chr2:27448096 | T | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4429-174A>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 40/47 | chr2 | 27448096 | |||||||
| chr2:27448116 | T | G | 1 | a0001c0002t0001g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4429-194A>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 40/47 | chr2 | 27448116 | |||||||
| chr2:27448149 | G | C | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02257.hp2 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.4429-227C>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 40/47 | chr2 | 27448149 | |||||||
| chr2:27448168 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0113 a0001c0001t0001g0114 |
5 | HG00738.hp2 HG02717.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.4429-246G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 40/47 | chr2 | 27448168 | |||||||
| chr2:27448224 | C | T | 2 | a0001c0002t0001g0090 a0001c0002t0001g0091 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.4429-302G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 40/47 | chr2 | 27448224 | |||||||
| chr2:27448388 | T | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(102): Show |
121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.4429-466A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 40/47 | chr2 | 27448388 | |||||||
| chr2:27448389 | G | A | 2 | a0002c0004t0001g0128 a0002c0004t0001g0129 |
2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4429-467C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 40/47 | chr2 | 27448389 | |||||||
| chr2:27448390 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(102): Show |
121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.4429-468G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 40/47 | chr2 | 27448390 | |||||||
| chr2:27448433 | A | G | 1 | a0008c0015t0002g0166 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.4428+482T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 40/47 | chr2 | 27448433 | |||||||
| chr2:27448910 | G | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0113 a0001c0001t0001g0114 |
5 | HG00738.hp2 HG02717.hp1 HG02922.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.4428+5C>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 40/47 | chr2 | 27448910 | |||||||
| chr2:27449417 | G | A | 1 | a0001c0001t0002g0022 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4225-37C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 38/47 | chr2 | 27449417 | |||||||
| chr2:27449438 | G | A | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.4225-58C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 38/47 | chr2 | 27449438 | |||||||
| chr2:27449444 | G | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4224+55C>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 38/47 | chr2 | 27449444 | |||||||
| chr2:27450329 | T | C | 1 | a0001c0002t0001g0077 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3952-233A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27450329 | |||||||
| chr2:27450362 | C | T | 1 | a0001c0002t0001g0061 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3952-266G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27450362 | |||||||
| chr2:27450931 | T | C | 109 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(106): Show |
125 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.3952-835A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27450931 | |||||||
| chr2:27450949 | C | CT | 81 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0052 others(78): Show |
97 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.3952-854dupA | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27450949 | |||||||
| chr2:27450949 | C | CTT | 22 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(19): Show |
22 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.3952-854_3952-853i others(4): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27450949 | |||||||
| chr2:27450951 | G | T | 109 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(106): Show |
125 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.3952-855C>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27450951 | |||||||
| chr2:27450951 | GT | G | 9 | a0001c0001t0002g0006 a0001c0001t0002g0022 a0001c0001t0002g0023 others(6): Show |
10 | HG01981.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.3952-856delA | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27450951 | |||||||
| chr2:27450986 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3952-890T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27450986 | |||||||
| chr2:27451072 | G | A | 3 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 |
3 | HG01109.hp1 HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3952-976C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27451072 | |||||||
| chr2:27451153 | G | T | 1 | a0001c0002t0001g0161 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3952-1057C>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27451153 | |||||||
| chr2:27451258 | C | T | 2 | a0001c0001t0002g0154 a0003c0012t0002g0156 |
2 | HG01256.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.3952-1162G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27451258 | |||||||
| chr2:27451492 | G | A | 2 | a0001c0002t0001g0069 a0001c0002t0001g0070 |
2 | HG00738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.3952-1396C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27451492 | |||||||
| chr2:27451565 | C | T | 1 | a0001c0002t0001g0047 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3952-1469G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27451565 | |||||||
| chr2:27451706 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3952-1610G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27451706 | |||||||
| chr2:27451989 | GTA | G | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG01109.hp1 HG02559.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.3951+1393_3951+139 others(6): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27451989 | |||||||
| chr2:27451989 | GTATA | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(101): Show |
120 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.3951+1391_3951+139 others(8): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27451989 | |||||||
| chr2:27452027 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3951+1357A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27452027 | |||||||
| chr2:27452044 | G | A | 1 | a0001c0003t0001g0053 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3951+1340C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27452044 | |||||||
| chr2:27452063 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3951+1321G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27452063 | |||||||
| chr2:27452064 | AAAC | A | 27 | a0001c0001t0002g0004 a0001c0001t0002g0017 a0001c0001t0002g0038 others(24): Show |
30 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(27): Show |
intron_variant | MODIFIER | c.3951+1317_3951+131 others(7): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27452064 | |||||||
| chr2:27452124 | G | A | 5 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(2): Show |
5 | HG00733.hp2 HG01167.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.3951+1260C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27452124 | |||||||
| chr2:27452450 | A | G | 2 | a0002c0004t0001g0128 a0002c0004t0001g0129 |
2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3951+934T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27452450 | |||||||
| chr2:27452477 | G | A | 1 | a0005c0007t0002g0140 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3951+907C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27452477 | |||||||
| chr2:27452688 | T | C | 2 | a0002c0004t0001g0128 a0002c0004t0001g0129 |
2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3951+696A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27452688 | |||||||
| chr2:27452718 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3951+666G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 35/47 | chr2 | 27452718 | |||||||
| chr2:27453575 | A | G | 1 | a0001c0001t0002g0159 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3821+55T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 34/47 | chr2 | 27453575 | |||||||
| chr2:27454474 | A | G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0188 a0001c0001t0001g0189 others(6): Show |
11 | HG00733.hp2 HG01167.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.3466-56T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 31/47 | chr2 | 27454474 | |||||||
| chr2:27454824 | G | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(103): Show |
122 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.3372-164C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 30/47 | chr2 | 27454824 | |||||||
| chr2:27454896 | C | T | 4 | a0001c0002t0001g0068 a0001c0002t0001g0077 a0001c0002t0001g0096 others(1): Show |
4 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(1): Show |
intron_variant | MODIFIER | c.3372-236G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 30/47 | chr2 | 27454896 | |||||||
| chr2:27454911 | C | T | 19 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0021 others(16): Show |
21 | HG01074.hp1 HG01884.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.3372-251G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 30/47 | chr2 | 27454911 | |||||||
| chr2:27454961 | C | T | 1 | a0001c0001t0002g0170 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3372-301G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 30/47 | chr2 | 27454961 | |||||||
| chr2:27455088 | A | G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0188 a0001c0001t0001g0189 others(6): Show |
11 | HG00733.hp2 HG01167.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.3372-428T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 30/47 | chr2 | 27455088 | |||||||
| chr2:27455218 | C | T | 3 | a0001c0001t0002g0018 a0001c0001t0002g0149 a0001c0001t0002g0169 |
4 | NA18950.hp1 NA18983.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.3372-558G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 30/47 | chr2 | 27455218 | |||||||
| chr2:27455222 | C | T | 6 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0150 others(3): Show |
6 | HG00408.hp1 HG02132.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.3372-562G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 30/47 | chr2 | 27455222 | |||||||
| chr2:27455272 | T | G | 1 | a0012c0008t0002g0157 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3372-612A>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 30/47 | chr2 | 27455272 | |||||||
| chr2:27455430 | C | T | 1 | a0001c0002t0001g0056 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3372-770G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 30/47 | chr2 | 27455430 | |||||||
| chr2:27455604 | A | G | 130 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(127): Show |
148 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.3371+907T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 30/47 | chr2 | 27455604 | |||||||
| chr2:27455861 | A | G | 3 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 |
3 | HG01109.hp1 HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3371+650T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 30/47 | chr2 | 27455861 | |||||||
| chr2:27455871 | T | C | 1 | a0001c0001t0002g0179 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3371+640A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 30/47 | chr2 | 27455871 | |||||||
| chr2:27455939 | C | T | 1 | a0001c0002t0001g0083 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3371+572G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 30/47 | chr2 | 27455939 | |||||||
| chr2:27455952 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0188 a0001c0001t0001g0189 others(6): Show |
11 | HG00733.hp2 HG01167.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.3371+559C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 30/47 | chr2 | 27455952 | |||||||
| chr2:27456002 | A | G | 1 | a0014c0016t0002g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3371+509T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 30/47 | chr2 | 27456002 | |||||||
| chr2:27456175 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3371+336G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 30/47 | chr2 | 27456175 | |||||||
| chr2:27456289 | C | T | 1 | a0001c0001t0002g0179 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3371+222G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 30/47 | chr2 | 27456289 | |||||||
| chr2:27456693 | C | T | 1 | a0001c0003t0002g0025 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3229-40G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 29/47 | chr2 | 27456693 | |||||||
| chr2:27456838 | A | G | 1 | a0001c0002t0001g0074 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3229-185T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 29/47 | chr2 | 27456838 | |||||||
| chr2:27456895 | A | G | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.3229-242T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 29/47 | chr2 | 27456895 | |||||||
| chr2:27456908 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0127 |
2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3229-255C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 29/47 | chr2 | 27456908 | |||||||
| chr2:27457045 | A | C | 1 | a0001c0002t0001g0055 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3229-392T>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 29/47 | chr2 | 27457045 | |||||||
| chr2:27457052 | A | G | 74 | a0001c0001t0001g0126 a0001c0001t0002g0155 a0001c0002t0001g0001 others(71): Show |
86 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.3229-399T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 29/47 | chr2 | 27457052 | |||||||
| chr2:27457091 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0127 |
2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3229-438G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 29/47 | chr2 | 27457091 | |||||||
| chr2:27457224 | C | T | 1 | a0001c0002t0001g0067 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.3228+415G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 29/47 | chr2 | 27457224 | |||||||
| chr2:27457283 | A | G | 3 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | HG02622.hp1 HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3228+356T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 29/47 | chr2 | 27457283 | |||||||
| chr2:27457316 | T | A | 1 | a0001c0001t0001g0039 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3228+323A>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 29/47 | chr2 | 27457316 | |||||||
| chr2:27458462 | C | T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.2878-239G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 26/47 | chr2 | 27458462 | |||||||
| chr2:27458530 | G | A | 15 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(12): Show |
15 | HG01891.hp2 HG02109.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.2877+249C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 26/47 | chr2 | 27458530 | |||||||
| chr2:27458578 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2877+201A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 26/47 | chr2 | 27458578 | |||||||
| chr2:27458631 | G | A | 1 | a0001c0001t0002g0093 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2877+148C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 26/47 | chr2 | 27458631 | |||||||
| chr2:27458667 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2877+112G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 26/47 | chr2 | 27458667 | |||||||
| chr2:27458731 | A | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(103): Show |
122 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.2877+48T>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 26/47 | chr2 | 27458731 | |||||||
| chr2:27458991 | A | T | 1 | a0001c0002t0001g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2788-123T>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 25/47 | chr2 | 27458991 | |||||||
| chr2:27459372 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02622.hp2 | splice_region_variant&intron_variant | LOW | c.2787+6G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 25/47 | chr2 | 27459372 | |||||||
| chr2:27459870 | G | A | 11 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(8): Show |
11 | HG01891.hp2 HG02109.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2522-41C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 23/47 | chr2 | 27459870 | |||||||
| chr2:27459983 | G | T | 73 | a0001c0001t0001g0126 a0001c0002t0001g0001 a0001c0002t0001g0008 others(70): Show |
85 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.2522-154C>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 23/47 | chr2 | 27459983 | |||||||
| chr2:27460286 | T | G | 23 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0021 others(20): Show |
25 | HG01074.hp1 HG01109.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.2522-457A>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 23/47 | chr2 | 27460286 | |||||||
| chr2:27460406 | T | A | 1 | a0001c0001t0002g0171 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2522-577A>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 23/47 | chr2 | 27460406 | |||||||
| chr2:27460554 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2521+461G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 23/47 | chr2 | 27460554 | |||||||
| chr2:27460601 | A | G | 1 | a0001c0001t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2521+414T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 23/47 | chr2 | 27460601 | |||||||
| chr2:27460659 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2521+356T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 23/47 | chr2 | 27460659 | |||||||
| chr2:27460832 | C | G | 1 | a0012c0008t0002g0157 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2521+183G>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 23/47 | chr2 | 27460832 | |||||||
| chr2:27461112 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2443-19A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 22/47 | chr2 | 27461112 | |||||||
| chr2:27461198 | C | T | 1 | a0001c0001t0002g0186 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2442+71G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 22/47 | chr2 | 27461198 | |||||||
| chr2:27461253 | A | T | 1 | a0001c0001t0002g0016 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2442+16T>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 22/47 | chr2 | 27461253 | |||||||
| chr2:27461597 | T | C | 1 | a0001c0003t0002g0025 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2194-80A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 21/47 | chr2 | 27461597 | |||||||
| chr2:27461638 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2193+121A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 21/47 | chr2 | 27461638 | |||||||
| chr2:27461867 | A | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(103): Show |
122 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.2116-31T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 20/47 | chr2 | 27461867 | |||||||
| chr2:27462090 | T | C | 130 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(127): Show |
148 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.2116-254A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 20/47 | chr2 | 27462090 | |||||||
| chr2:27462147 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(101): Show |
120 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.2116-311G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 20/47 | chr2 | 27462147 | |||||||
| chr2:27462248 | G | A | 1 | a0001c0002t0001g0055 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2116-412C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 20/47 | chr2 | 27462248 | |||||||
| chr2:27462402 | C | T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.2115+299G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 20/47 | chr2 | 27462402 | |||||||
| chr2:27462521 | G | A | 126 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(123): Show |
143 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.2115+180C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 20/47 | chr2 | 27462521 | |||||||
| chr2:27462547 | G | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2115+154C>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 20/47 | chr2 | 27462547 | |||||||
| chr2:27462839 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2023-46A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 19/47 | chr2 | 27462839 | |||||||
| chr2:27463529 | CT | C | 90 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(87): Show |
105 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.1938-349delA | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 18/47 | chr2 | 27463529 | |||||||
| chr2:27463529 | CTT | C | 13 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0001t0001g0191 others(10): Show |
14 | HG00733.hp2 HG01106.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1938-350_1938-349d others(4): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 18/47 | chr2 | 27463529 | |||||||
| chr2:27463613 | A | G | 14 | a0001c0001t0002g0019 a0001c0001t0002g0026 a0001c0001t0002g0028 others(11): Show |
15 | HG01071.hp1 HG01071.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1938-432T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 18/47 | chr2 | 27463613 | |||||||
| chr2:27463728 | G | A | 1 | a0014c0016t0002g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1938-547C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 18/47 | chr2 | 27463728 | |||||||
| chr2:27463912 | A | C | 1 | a0001c0001t0001g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1938-731T>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 18/47 | chr2 | 27463912 | |||||||
| chr2:27463957 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1938-776C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 18/47 | chr2 | 27463957 | |||||||
| chr2:27464044 | T | C | 1 | a0001c0002t0001g0068 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1938-863A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 18/47 | chr2 | 27464044 | |||||||
| chr2:27464077 | C | T | 1 | a0001c0002t0001g0108 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1938-896G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 18/47 | chr2 | 27464077 | |||||||
| chr2:27464132 | A | C | 16 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(13): Show |
16 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1938-951T>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 18/47 | chr2 | 27464132 | |||||||
| chr2:27464169 | T | A | 1 | a0001c0001t0002g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1938-988A>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 18/47 | chr2 | 27464169 | |||||||
| chr2:27464691 | T | A | 1 | a0001c0001t0001g0039 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1937+720A>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 18/47 | chr2 | 27464691 | |||||||
| chr2:27464695 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1937+716G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 18/47 | chr2 | 27464695 | |||||||
| chr2:27464764 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1937+647G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 18/47 | chr2 | 27464764 | |||||||
| chr2:27464854 | G | C | 2 | a0001c0002t0001g0069 a0001c0002t0001g0070 |
2 | HG00738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1937+557C>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 18/47 | chr2 | 27464854 | |||||||
| chr2:27464925 | A | AT | 106 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0110 others(103): Show |
122 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1937+485dupA | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 18/47 | chr2 | 27464925 | |||||||
| chr2:27465323 | C | T | 1 | a0001c0001t0002g0028 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1937+88G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 18/47 | chr2 | 27465323 | |||||||
| chr2:27465326 | C | T | 1 | a0001c0002t0001g0009 | 2 | NA18966.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1937+85G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 18/47 | chr2 | 27465326 | |||||||
| chr2:27465571 | ACAG | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1830-56_1830-54del others(3): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 17/47 | chr2 | 27465571 | |||||||
| chr2:27465604 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1830-86C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 17/47 | chr2 | 27465604 | |||||||
| chr2:27465608 | A | G | 1 | a0001c0001t0002g0138 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1830-90T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 17/47 | chr2 | 27465608 | |||||||
| chr2:27465616 | C | A | 3 | a0001c0002t0001g0013 a0001c0002t0001g0073 a0001c0002t0001g0076 |
4 | HG01257.hp1 HG01258.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1830-98G>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 17/47 | chr2 | 27465616 | |||||||
| chr2:27465676 | C | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0113 a0001c0001t0001g0114 |
5 | HG00738.hp2 HG02717.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1829+70G>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 17/47 | chr2 | 27465676 | |||||||
| chr2:27465709 | C | G | 16 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(13): Show |
16 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1829+37G>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 17/47 | chr2 | 27465709 | |||||||
| chr2:27465734 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(102): Show |
121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1829+12G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 17/47 | chr2 | 27465734 | |||||||
| chr2:27465977 | G | A | 1 | a0001c0002t0001g0070 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1693-95C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27465977 | |||||||
| chr2:27466120 | T | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02257.hp2 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1693-238A>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27466120 | |||||||
| chr2:27466306 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1693-424C>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27466306 | |||||||
| chr2:27466358 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1693-476T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27466358 | |||||||
| chr2:27466659 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1693-777T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27466659 | |||||||
| chr2:27466697 | CA | C | 2 | a0001c0001t0002g0134 a0001c0001t0002g0187 |
2 | HG00323.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.1693-816delT | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27466697 | |||||||
| chr2:27466833 | A | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(102): Show |
121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1693-951T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27466833 | |||||||
| chr2:27467032 | T | C | 83 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0188 others(80): Show |
97 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1693-1150A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27467032 | |||||||
| chr2:27467299 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0188 a0001c0001t0001g0193 others(1): Show |
6 | HG02559.hp2 HG03453.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1693-1417C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27467299 | |||||||
| chr2:27467396 | G | A | 1 | a0001c0003t0002g0025 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1693-1514C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27467396 | |||||||
| chr2:27467418 | G | GA | 16 | a0001c0001t0002g0019 a0001c0001t0002g0087 a0001c0001t0002g0135 others(13): Show |
17 | HG00408.hp1 HG00408.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1693-1537dupT | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27467418 | |||||||
| chr2:27467418 | GA | G | 14 | a0001c0001t0001g0123 a0001c0001t0002g0006 a0001c0001t0002g0021 others(11): Show |
15 | HG01074.hp1 HG01257.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.1693-1537delT | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27467418 | |||||||
| chr2:27467418 | GAA | G | 6 | a0001c0001t0001g0039 a0001c0001t0001g0193 a0001c0001t0002g0130 others(3): Show |
6 | HG01109.hp1 HG01346.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1693-1538_1693-153 others(6): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27467418 | |||||||
| chr2:27467418 | GAAA | G | 27 | a0001c0001t0001g0005 a0001c0001t0001g0122 a0001c0001t0001g0125 others(24): Show |
32 | HG01106.hp1 HG01106.hp2 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1693-1539_1693-153 others(7): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27467418 | |||||||
| chr2:27467418 | GAAAA | G | 60 | a0001c0001t0001g0052 a0001c0001t0001g0112 a0001c0001t0001g0115 others(57): Show |
69 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1693-1540_1693-153 others(8): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27467418 | |||||||
| chr2:27467418 | GAAAAA | G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0110 a0001c0001t0001g0111 others(7): Show |
12 | HG00280.hp1 HG00738.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1693-1541_1693-153 others(9): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27467418 | |||||||
| chr2:27467418 | GAAAAAAA others(9): Show |
G | 1 | a0001c0001t0002g0028 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1693-1552_1693-153 others(20): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27467418 | |||||||
| chr2:27467419 | A | G | 1 | a0012c0008t0002g0157 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1693-1537T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27467419 | |||||||
| chr2:27467613 | C | CA | 10 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0002g0109 others(7): Show |
10 | HG01175.hp1 HG01175.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1693-1732dupT | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27467613 | |||||||
| chr2:27467613 | C | CAA | 4 | a0001c0001t0001g0003 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
6 | HG00738.hp2 HG02717.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1693-1733_1693-173 others(6): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27467613 | |||||||
| chr2:27467613 | CA | C | 79 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0110 others(76): Show |
92 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1693-1732delT | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27467613 | |||||||
| chr2:27467724 | C | CCTAA | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02257.hp2 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1693-1846_1693-184 others(8): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27467724 | |||||||
| chr2:27467770 | C | T | 1 | a0009c0009t0001g0054 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1693-1888G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27467770 | |||||||
| chr2:27468113 | T | C | 3 | a0001c0001t0002g0006 a0001c0001t0002g0031 a0001c0001t0002g0032 |
4 | HG02258.hp2 HG02647.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1693-2231A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27468113 | |||||||
| chr2:27468124 | C | T | 71 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0009 others(68): Show |
83 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1693-2242G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27468124 | |||||||
| chr2:27468159 | C | CA | 22 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0022 others(19): Show |
23 | HG01074.hp1 HG01109.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1693-2278dupT | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27468159 | |||||||
| chr2:27468159 | CA | C | 109 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(106): Show |
125 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1693-2278delT | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27468159 | |||||||
| chr2:27468271 | C | G | 1 | a0007c0018t0002g0167 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1693-2389G>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27468271 | |||||||
| chr2:27468327 | G | C | 1 | a0001c0002t0001g0106 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1693-2445C>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27468327 | |||||||
| chr2:27468378 | G | A | 3 | a0001c0001t0002g0086 a0001c0001t0002g0087 a0001c0001t0002g0093 |
3 | HG02004.hp2 HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1693-2496C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27468378 | |||||||
| chr2:27468426 | G | T | 3 | a0001c0001t0002g0017 a0007c0018t0002g0167 a0008c0015t0002g0166 |
4 | HG00099.hp1 HG01109.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1692+2502C>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27468426 | |||||||
| chr2:27468484 | T | A | 1 | a0001c0003t0002g0025 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1692+2444A>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27468484 | |||||||
| chr2:27468485 | C | A | 1 | a0001c0003t0002g0025 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1692+2443G>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27468485 | |||||||
| chr2:27468721 | C | A | 55 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0009 others(52): Show |
67 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1692+2207G>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27468721 | |||||||
| chr2:27468836 | G | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02257.hp2 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1692+2092C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27468836 | |||||||
| chr2:27469170 | G | A | 1 | a0001c0001t0002g0165 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1692+1758C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27469170 | |||||||
| chr2:27469347 | T | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(102): Show |
121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1692+1581A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27469347 | |||||||
| chr2:27469374 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1692+1554G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27469374 | |||||||
| chr2:27469394 | A | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(102): Show |
121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1692+1534T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27469394 | |||||||
| chr2:27469561 | G | C | 1 | a0001c0001t0002g0172 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1692+1367C>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27469561 | |||||||
| chr2:27469738 | A | C | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1692+1190T>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27469738 | |||||||
| chr2:27469764 | A | G | 193 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(190): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1692+1164T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27469764 | |||||||
| chr2:27470026 | C | T | 11 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(8): Show |
11 | HG01891.hp2 HG02109.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1692+902G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27470026 | |||||||
| chr2:27470106 | A | G | 71 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0009 others(68): Show |
83 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1692+822T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27470106 | |||||||
| chr2:27470169 | C | T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1692+759G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27470169 | |||||||
| chr2:27470216 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0188 |
4 | HG06807.hp1 NA18906.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1692+712G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27470216 | |||||||
| chr2:27470230 | G | A | 11 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(8): Show |
11 | HG01891.hp2 HG02109.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1692+698C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27470230 | |||||||
| chr2:27470270 | GAAAA | G | 71 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0009 others(68): Show |
83 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1692+654_1692+657d others(6): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27470270 | |||||||
| chr2:27470618 | T | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(102): Show |
121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1692+310A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27470618 | |||||||
| chr2:27470703 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1692+225G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27470703 | |||||||
| chr2:27470863 | G | A | 2 | a0002c0004t0001g0128 a0002c0004t0001g0129 |
2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1692+65C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 16/47 | chr2 | 27470863 | |||||||
| chr2:27471310 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1525-215C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 15/47 | chr2 | 27471310 | |||||||
| chr2:27471518 | A | G | 1 | a0001c0001t0002g0022 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1525-423T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 15/47 | chr2 | 27471518 | |||||||
| chr2:27471663 | C | T | 2 | a0001c0001t0002g0150 a0001c0001t0002g0151 |
2 | NA18990.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1525-568G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 15/47 | chr2 | 27471663 | |||||||
| chr2:27471708 | T | C | 2 | a0001c0002t0001g0056 a0001c0002t0001g0057 |
2 | HG01496.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1524+542A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 15/47 | chr2 | 27471708 | |||||||
| chr2:27471756 | G | A | 1 | a0001c0003t0001g0053 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1524+494C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 15/47 | chr2 | 27471756 | |||||||
| chr2:27471963 | G | A | 1 | a0008c0015t0002g0166 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1524+287C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 15/47 | chr2 | 27471963 | |||||||
| chr2:27472038 | CA | C | 101 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(98): Show |
117 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1524+211delT | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 15/47 | chr2 | 27472038 | |||||||
| chr2:27472208 | T | C | 1 | a0001c0002t0001g0076 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1524+42A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 15/47 | chr2 | 27472208 | |||||||
| chr2:27472523 | C | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0196 a0001c0003t0001g0053 |
3 | HG02145.hp1 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1412-161G>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27472523 | |||||||
| chr2:27473030 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1412-668T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27473030 | |||||||
| chr2:27473195 | T | C | 1 | a0001c0002t0001g0094 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1412-833A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27473195 | |||||||
| chr2:27473240 | G | A | 1 | a0001c0002t0001g0108 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1412-878C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27473240 | |||||||
| chr2:27473295 | G | A | 1 | a0001c0001t0002g0168 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1412-933C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27473295 | |||||||
| chr2:27473332 | T | C | 3 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 |
3 | HG01109.hp1 HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1412-970A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27473332 | |||||||
| chr2:27473333 | T | G | 2 | a0001c0001t0002g0007 a0001c0001t0002g0040 |
3 | HG02723.hp2 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1412-971A>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27473333 | |||||||
| chr2:27473340 | A | C | 104 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0052 others(101): Show |
120 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1412-978T>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27473340 | |||||||
| chr2:27473369 | C | CA | 22 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0002g0033 others(19): Show |
22 | HG00099.hp2 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.1412-1008dupT | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27473369 | |||||||
| chr2:27473422 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0113 a0001c0001t0001g0114 |
5 | HG00738.hp2 HG02717.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1412-1060G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27473422 | |||||||
| chr2:27473638 | A | G | 1 | a0001c0002t0001g0094 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1412-1276T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27473638 | |||||||
| chr2:27473669 | G | A | 1 | a0006c0014t0001g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1412-1307C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27473669 | |||||||
| chr2:27473740 | A | C | 1 | a0001c0003t0001g0053 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1412-1378T>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27473740 | |||||||
| chr2:27473870 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0052 others(99): Show |
118 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1412-1508G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27473870 | |||||||
| chr2:27474027 | C | T | 1 | a0001c0003t0001g0053 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1412-1665G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27474027 | |||||||
| chr2:27474044 | G | T | 1 | a0001c0001t0002g0184 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1412-1682C>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27474044 | |||||||
| chr2:27474051 | G | A | 1 | a0001c0001t0002g0172 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1412-1689C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27474051 | |||||||
| chr2:27474054 | C | T | 3 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0195 |
3 | HG02257.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1412-1692G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27474054 | |||||||
| chr2:27474081 | T | A | 10 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(7): Show |
10 | HG01891.hp2 HG02109.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1412-1719A>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27474081 | |||||||
| chr2:27474234 | A | T | 11 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(8): Show |
11 | HG01891.hp2 HG02109.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1412-1872T>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27474234 | |||||||
| chr2:27475017 | T | G | 1 | a0001c0002t0001g0097 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1411+1624A>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27475017 | |||||||
| chr2:27475086 | C | CAGA | 105 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(102): Show |
121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1411+1552_1411+155 others(7): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27475086 | |||||||
| chr2:27475260 | T | C | 1 | a0001c0002t0001g0097 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1411+1381A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27475260 | |||||||
| chr2:27475476 | C | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(101): Show |
120 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1411+1165G>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27475476 | |||||||
| chr2:27475667 | T | C | 2 | a0002c0004t0001g0128 a0002c0004t0001g0129 |
2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1411+974A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27475667 | |||||||
| chr2:27475762 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0188 |
4 | HG06807.hp1 NA18906.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411+879G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27475762 | |||||||
| chr2:27475777 | CT | C | 104 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(101): Show |
120 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1411+863delA | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27475777 | |||||||
| chr2:27475875 | G | A | 3 | a0001c0001t0002g0173 a0001c0001t0002g0174 a0001c0001t0002g0175 |
3 | HG01071.hp1 HG01175.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1411+766C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27475875 | |||||||
| chr2:27476158 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1411+483C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27476158 | |||||||
| chr2:27476416 | A | C | 1 | a0001c0003t0002g0025 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1411+225T>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27476416 | |||||||
| chr2:27476449 | T | C | 1 | a0001c0002t0001g0100 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1411+192A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27476449 | |||||||
| chr2:27476514 | A | G | 1 | a0001c0001t0002g0149 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1411+127T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27476514 | |||||||
| chr2:27476602 | T | C | 1 | a0001c0002t0001g0092 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1411+39A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 14/47 | chr2 | 27476602 | |||||||
| chr2:27476882 | G | A | 1 | a0013c0017t0001g0080 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1326-156C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 13/47 | chr2 | 27476882 | |||||||
| chr2:27476921 | C | G | 2 | a0001c0002t0001g0101 a0001c0002t0001g0102 |
2 | NA18990.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1326-195G>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 13/47 | chr2 | 27476921 | |||||||
| chr2:27476922 | C | T | 11 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0026 others(8): Show |
12 | HG01074.hp1 HG01884.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1326-196G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 13/47 | chr2 | 27476922 | |||||||
| chr2:27476994 | T | C | 4 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0083 others(1): Show |
4 | HG00735.hp1 HG00741.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1325+223A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 13/47 | chr2 | 27476994 | |||||||
| chr2:27477159 | A | T | 1 | a0001c0001t0002g0137 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1325+58T>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 13/47 | chr2 | 27477159 | |||||||
| chr2:27477355 | C | T | 1 | a0001c0001t0002g0148 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1222-35G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 12/47 | chr2 | 27477355 | |||||||
| chr2:27477446 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0188 |
4 | HG06807.hp1 NA18906.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1221+113G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 12/47 | chr2 | 27477446 | |||||||
| chr2:27477511 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1221+48A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 12/47 | chr2 | 27477511 | |||||||
| chr2:27477684 | C | T | 5 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG01891.hp2 HG02109.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1168-72G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 11/47 | chr2 | 27477684 | |||||||
| chr2:27478342 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1006-186G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 10/47 | chr2 | 27478342 | |||||||
| chr2:27478462 | A | G | 2 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
2 | HG00408.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1006-306T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 10/47 | chr2 | 27478462 | |||||||
| chr2:27478529 | G | A | 6 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG01891.hp2 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006-373C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 10/47 | chr2 | 27478529 | |||||||
| chr2:27478575 | C | G | 1 | a0001c0002t0001g0059 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1006-419G>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 10/47 | chr2 | 27478575 | |||||||
| chr2:27478856 | T | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0188 a0001c0001t0001g0189 others(6): Show |
11 | HG00733.hp2 HG01167.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1005+653A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 10/47 | chr2 | 27478856 | |||||||
| chr2:27479151 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1005+358G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 10/47 | chr2 | 27479151 | |||||||
| chr2:27479159 | A | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(105): Show |
124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.1005+350T>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 10/47 | chr2 | 27479159 | |||||||
| chr2:27479343 | G | T | 1 | a0001c0001t0002g0145 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1005+166C>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 10/47 | chr2 | 27479343 | |||||||
| chr2:27479472 | G | A | 2 | a0002c0004t0001g0128 a0002c0004t0001g0129 |
2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1005+37C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 10/47 | chr2 | 27479472 | |||||||
| chr2:27479747 | A | G | 1 | a0001c0002t0001g0059 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.910-143T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 9/47 | chr2 | 27479747 | |||||||
| chr2:27480604 | C | T | 1 | a0001c0003t0001g0053 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.785+442G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 8/47 | chr2 | 27480604 | |||||||
| chr2:27480628 | A | G | 108 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(105): Show |
124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.785+418T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 8/47 | chr2 | 27480628 | |||||||
| chr2:27480787 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.785+259C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 8/47 | chr2 | 27480787 | |||||||
| chr2:27480840 | G | C | 3 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 |
3 | HG01109.hp1 HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.785+206C>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 8/47 | chr2 | 27480840 | |||||||
| chr2:27481294 | C | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0002t0001g0085 |
3 | HG02451.hp1 HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.571-34G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27481294 | |||||||
| chr2:27481425 | T | TCA | 21 | a0001c0001t0001g0124 a0001c0001t0001g0191 a0001c0001t0001g0192 others(18): Show |
22 | HG00323.hp2 HG00639.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.571-167_571-166dup others(2): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27481425 | |||||||
| chr2:27481425 | TCA | T | 14 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0112 others(11): Show |
16 | HG00597.hp2 HG00738.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.571-167_571-166del others(2): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27481425 | |||||||
| chr2:27481425 | TCACACAC others(1): Show |
T | 3 | a0001c0001t0002g0131 a0002c0004t0001g0128 a0002c0004t0001g0129 |
3 | HG03041.hp2 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.571-173_571-166del others(8): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27481425 | |||||||
| chr2:27481436 | CACACACA others(11): Show |
C | 2 | a0001c0002t0001g0090 a0001c0002t0001g0091 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.571-194_571-177del others(18): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27481436 | |||||||
| chr2:27481442 | CACACACA others(5): Show |
C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.571-194_571-183del others(12): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27481442 | |||||||
| chr2:27481454 | T | C | 7 | a0001c0002t0001g0050 a0001c0002t0001g0059 a0001c0002t0001g0061 others(4): Show |
7 | HG00639.hp1 HG01346.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-194A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27481454 | |||||||
| chr2:27481545 | C | CT | 9 | a0001c0001t0001g0193 a0001c0002t0001g0008 a0001c0002t0001g0043 others(6): Show |
10 | HG01106.hp2 HG01361.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.571-286dupA | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27481545 | |||||||
| chr2:27481709 | T | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0196 a0001c0003t0001g0053 |
3 | HG02145.hp1 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571-449A>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27481709 | |||||||
| chr2:27481888 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.571-628C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27481888 | |||||||
| chr2:27482029 | G | A | 5 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 others(2): Show |
5 | HG01255.hp1 HG01261.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-769C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27482029 | |||||||
| chr2:27482278 | C | T | 1 | a0009c0009t0001g0054 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.570+1011G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27482278 | |||||||
| chr2:27482295 | T | C | 1 | a0001c0001t0002g0093 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.570+994A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27482295 | |||||||
| chr2:27482394 | G | A | 1 | a0001c0002t0001g0048 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.570+895C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27482394 | |||||||
| chr2:27482396 | G | C | 1 | a0001c0002t0001g0094 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.570+893C>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27482396 | |||||||
| chr2:27482502 | T | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(105): Show |
124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.570+787A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27482502 | |||||||
| chr2:27482570 | T | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(105): Show |
124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.570+719A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27482570 | |||||||
| chr2:27482733 | A | G | 1 | a0001c0001t0002g0130 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.570+556T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27482733 | |||||||
| chr2:27482781 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.570+508G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27482781 | |||||||
| chr2:27483001 | C | CT | 23 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0052 others(20): Show |
27 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.570+287dupA | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27483001 | |||||||
| chr2:27483001 | C | CTT | 67 | a0001c0001t0002g0086 a0001c0001t0002g0087 a0001c0001t0002g0093 others(64): Show |
79 | HG00099.hp2 HG00280.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.570+286_570+287dup others(2): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27483001 | |||||||
| chr2:27483062 | G | T | 1 | a0001c0003t0002g0025 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.570+227C>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 7/47 | chr2 | 27483062 | |||||||
| chr2:27483427 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0113 a0001c0001t0001g0114 |
5 | HG00738.hp2 HG02717.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.483-51G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 6/47 | chr2 | 27483427 | |||||||
| chr2:27483773 | T | C | 74 | a0001c0001t0002g0086 a0001c0001t0002g0087 a0001c0001t0002g0093 others(71): Show |
86 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.402+99A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 5/47 | chr2 | 27483773 | |||||||
| chr2:27483786 | C | T | 1 | a0001c0001t0002g0136 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.402+86G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 5/47 | chr2 | 27483786 | |||||||
| chr2:27483949 | G | A | 11 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(8): Show |
11 | HG01891.hp2 HG02109.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.337-12C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 4/47 | chr2 | 27483949 | |||||||
| chr2:27484499 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.297-233C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 3/47 | chr2 | 27484499 | |||||||
| chr2:27485297 | G | A | 2 | a0002c0004t0001g0128 a0002c0004t0001g0129 |
2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.183+63C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 2/47 | chr2 | 27485297 | |||||||
| chr2:27485871 | G | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.40-368C>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27485871 | |||||||
| chr2:27485894 | TGAGA | T | 2 | a0001c0002t0001g0101 a0001c0002t0001g0102 |
2 | NA18990.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.40-395_40-392delTC others(2): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27485894 | |||||||
| chr2:27485929 | C | T | 3 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 |
3 | HG01109.hp1 HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.40-426G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27485929 | |||||||
| chr2:27485948 | G | T | 1 | a0001c0001t0001g0039 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.40-445C>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27485948 | |||||||
| chr2:27486034 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.40-531G>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27486034 | |||||||
| chr2:27486643 | A | G | 1 | a0001c0001t0002g0135 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.40-1140T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27486643 | |||||||
| chr2:27486766 | T | G | 5 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(2): Show |
5 | HG02257.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-1263A>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27486766 | |||||||
| chr2:27487098 | A | G | 108 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(105): Show |
124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.40-1595T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27487098 | |||||||
| chr2:27487109 | A | C | 1 | a0001c0002t0001g0050 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.40-1606T>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27487109 | |||||||
| chr2:27487142 | A | T | 1 | a0001c0003t0002g0025 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.40-1639T>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27487142 | |||||||
| chr2:27487224 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.40-1721G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27487224 | |||||||
| chr2:27487508 | T | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.40-2005A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27487508 | |||||||
| chr2:27487554 | C | T | 4 | a0001c0001t0002g0016 a0001c0001t0002g0109 a0001c0001t0002g0134 others(1): Show |
5 | HG00323.hp2 HG00733.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-2051G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27487554 | |||||||
| chr2:27487711 | G | C | 8 | a0001c0002t0001g0015 a0001c0002t0001g0101 a0001c0002t0001g0102 others(5): Show |
9 | NA18950.hp2 NA18955.hp1 NA18981.hp1 others(6): Show |
intron_variant | MODIFIER | c.39+1904C>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27487711 | |||||||
| chr2:27487949 | G | A | 1 | a0001c0002t0001g0108 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.39+1666C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27487949 | |||||||
| chr2:27487958 | G | C | 1 | a0001c0002t0001g0108 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.39+1657C>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27487958 | |||||||
| chr2:27488141 | C | T | 8 | a0001c0002t0001g0001 a0001c0002t0001g0043 a0001c0002t0001g0044 others(5): Show |
12 | HG00597.hp1 HG01074.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.39+1474G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27488141 | |||||||
| chr2:27488160 | T | A | 4 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(1): Show |
4 | HG00280.hp1 HG01109.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+1455A>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27488160 | |||||||
| chr2:27488222 | C | T | 3 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 |
3 | HG01109.hp1 HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.39+1393G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27488222 | |||||||
| chr2:27488235 | C | T | 1 | a0001c0002t0001g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.39+1380G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27488235 | |||||||
| chr2:27488287 | G | C | 1 | a0001c0001t0002g0186 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.39+1328C>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27488287 | |||||||
| chr2:27488290 | A | C | 19 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0021 others(16): Show |
21 | HG01074.hp1 HG01884.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.39+1325T>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27488290 | |||||||
| chr2:27488389 | G | A | 86 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0188 others(83): Show |
100 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.39+1226C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27488389 | |||||||
| chr2:27488390 | G | GGACT | 86 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0188 others(83): Show |
100 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.39+1224_39+1225ins others(4): Show |
IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27488390 | |||||||
| chr2:27488396 | C | T | 1 | a0001c0003t0002g0025 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.39+1219G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27488396 | |||||||
| chr2:27488397 | G | A | 1 | a0001c0001t0002g0187 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.39+1218C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27488397 | |||||||
| chr2:27488763 | A | G | 3 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | HG02622.hp1 HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.39+852T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27488763 | |||||||
| chr2:27488764 | T | C | 109 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(106): Show |
125 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.39+851A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27488764 | |||||||
| chr2:27488838 | G | A | 21 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0022 others(18): Show |
22 | HG01074.hp1 HG01109.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.39+777C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27488838 | |||||||
| chr2:27488847 | C | G | 1 | a0001c0001t0001g0039 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.39+768G>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27488847 | |||||||
| chr2:27488915 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.39+700C>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27488915 | |||||||
| chr2:27488936 | G | C | 1 | a0001c0002t0001g0133 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.39+679C>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27488936 | |||||||
| chr2:27488945 | G | T | 1 | a0001c0001t0001g0039 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.39+670C>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27488945 | |||||||
| chr2:27489026 | A | G | 133 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0039 others(130): Show |
151 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.39+589T>C | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27489026 | |||||||
| chr2:27489116 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.39+499A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27489116 | |||||||
| chr2:27489153 | A | T | 1 | a0001c0001t0002g0021 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.39+462T>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27489153 | |||||||
| chr2:27489255 | T | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0188 a0001c0001t0001g0189 others(6): Show |
11 | HG00733.hp2 HG01167.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.39+360A>G | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27489255 | |||||||
| chr2:27489257 | C | T | 1 | a0001c0001t0002g0038 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.39+358G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27489257 | |||||||
| chr2:27489503 | T | A | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.39+112A>T | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27489503 | |||||||
| chr2:27489541 | C | T | 18 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0022 others(15): Show |
19 | HG01074.hp1 HG01884.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.39+74G>A | IFT172 | ENSG00000138002.16 | transcript | ENST00000260570.8 | protein_coding | 1/47 | chr2 | 27489541 |