Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55081 |
| ensemblid | ENSG00000114446.5 |
| hgncid | 17367 |
| symbol | IFT57 |
| name | intraflagellar transport 57 |
| refseq_nuc | NM_018010.4 |
| refseq_prot | NP_060480.1 |
| ensembl_nuc | ENST00000264538.4 |
| ensembl_prot | ENSP00000264538.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 108160812 |
| end | 108222424 |
| strand | - |
| ver | v1.2 |
| region | chr3:108160812-108222424 |
| region5000 | chr3:108155812-108227424 |
| regionname0 | IFT57_chr3_108160812_108222424 |
| regionname5000 | IFT57_chr3_108155812_108227424 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 429 | 350 | 81 | 65 | 157 | 8 | 37 | 123 | IFT57_chr3_108155812_108227424 | IFT57 | MTAAL others(424): Show |
chr3 | 108155812 | 108227424 |
| a0002 | 0/0 | 429 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | MTAAL others(424): Show |
chr3 | 108155812 | 108227424 |
| a0003 | 0/0 | 429 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | MTAAL others(424): Show |
chr3 | 108155812 | 108227424 |
| a0004 | 0/0 | 429 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | MTAAL others(424): Show |
chr3 | 108155812 | 108227424 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1287 | 296 | 62 | 54 | 134 | 8 | 36 | IFT57_chr3_108155812_108227424 | IFT57 | ATGAC others(1282): Show |
chr3 | 108155812 | 108227424 | ||
| a0001c0002 | 0/0 | 1287 | 36 | 6 | 10 | 19 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | ATGAC others(1282): Show |
chr3 | 108155812 | 108227424 | ||
| a0001c0003 | 0/0 | 1287 | 7 | 7 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | ATGAC others(1282): Show |
chr3 | 108155812 | 108227424 | ||
| a0001c0004 | 0/0 | 1287 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | ATGAC others(1282): Show |
chr3 | 108155812 | 108227424 | ||
| a0001c0005 | 0/0 | 1287 | 3 | 3 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | ATGAC others(1282): Show |
chr3 | 108155812 | 108227424 | ||
| a0001c0007 | 0/0 | 1287 | 2 | 1 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | ATGAC others(1282): Show |
chr3 | 108155812 | 108227424 | ||
| a0001c0008 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | ATGAC others(1282): Show |
chr3 | 108155812 | 108227424 | ||
| a0001c0009 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | ATGAC others(1282): Show |
chr3 | 108155812 | 108227424 | ||
| a0001c0012 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | ATGAC others(1282): Show |
chr3 | 108155812 | 108227424 | ||
| a0002c0006 | 0/0 | 1287 | 2 | 0 | 1 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | ATGAC others(1282): Show |
chr3 | 108155812 | 108227424 | ||
| a0003c0011 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | ATGAC others(1282): Show |
chr3 | 108155812 | 108227424 | ||
| a0004c0010 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | ATGAC others(1282): Show |
chr3 | 108155812 | 108227424 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3055 | 90 | 25 | 29 | 19 | 6 | 11 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3050): Show |
chr3 | 108155812 | 108227424 |
| a0001c0001t0002 | 0/0 | 3057 | 87 | 10 | 9 | 61 | 0 | 7 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3052): Show |
chr3 | 108155812 | 108227424 |
| a0001c0001t0003 | 0/0 | 3056 | 79 | 16 | 4 | 51 | 1 | 7 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3051): Show |
chr3 | 108155812 | 108227424 |
| a0001c0001t0005 | 0/1 | 3056 | 24 | 3 | 9 | 1 | 1 | 9 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3051): Show |
chr3 | 108155812 | 108227424 |
| a0001c0001t0006 | 1/0 | 3057 | 6 | 5 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3052): Show |
chr3 | 108155812 | 108227424 |
| a0001c0001t0008 | 0/0 | 3055 | 2 | 0 | 2 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3050): Show |
chr3 | 108155812 | 108227424 |
| a0001c0001t0009 | 0/0 | 3055 | 2 | 0 | 0 | 0 | 0 | 2 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3050): Show |
chr3 | 108155812 | 108227424 |
| a0001c0001t0010 | 0/0 | 3062 | 2 | 2 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3057): Show |
chr3 | 108155812 | 108227424 |
| a0001c0001t0011 | 0/0 | 3055 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3050): Show |
chr3 | 108155812 | 108227424 |
| a0001c0001t0012 | 0/0 | 3057 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3052): Show |
chr3 | 108155812 | 108227424 |
| a0001c0001t0013 | 0/0 | 3056 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3051): Show |
chr3 | 108155812 | 108227424 |
| a0001c0001t0014 | 0/0 | 3056 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3051): Show |
chr3 | 108155812 | 108227424 |
| a0001c0002t0004 | 0/0 | 3062 | 31 | 2 | 9 | 19 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3057): Show |
chr3 | 108155812 | 108227424 |
| a0001c0002t0007 | 0/0 | 3062 | 4 | 4 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3057): Show |
chr3 | 108155812 | 108227424 |
| a0001c0002t0016 | 0/0 | 3061 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3056): Show |
chr3 | 108155812 | 108227424 |
| a0001c0003t0001 | 0/0 | 3055 | 7 | 7 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3050): Show |
chr3 | 108155812 | 108227424 |
| a0001c0004t0003 | 0/0 | 3056 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3051): Show |
chr3 | 108155812 | 108227424 |
| a0001c0005t0006 | 0/0 | 3057 | 3 | 3 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3052): Show |
chr3 | 108155812 | 108227424 |
| a0001c0007t0002 | 0/0 | 3057 | 2 | 1 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3052): Show |
chr3 | 108155812 | 108227424 |
| a0001c0008t0002 | 0/0 | 3057 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3052): Show |
chr3 | 108155812 | 108227424 |
| a0001c0009t0006 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3052): Show |
chr3 | 108155812 | 108227424 |
| a0001c0012t0015 | 0/0 | 3062 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3057): Show |
chr3 | 108155812 | 108227424 |
| a0002c0006t0005 | 0/0 | 3056 | 2 | 0 | 1 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3051): Show |
chr3 | 108155812 | 108227424 |
| a0003c0011t0003 | 0/0 | 3056 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3051): Show |
chr3 | 108155812 | 108227424 |
| a0004c0010t0003 | 0/0 | 3056 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | GCCTG others(3051): Show |
chr3 | 108155812 | 108227424 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0002 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0009 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0010 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0239 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0005g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0006g0020 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0008g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0009g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0009g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0010g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0010g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0011g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0012g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0013g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0001t0014g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0007g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0007g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0007g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0007g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0002t0016g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0003t0001g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0003t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0004t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0004t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0004t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0005t0006g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0005t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0007t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0007t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0008t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0009t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0001c0012t0015g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0002c0006t0005g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0002c0006t0005g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0003c0011t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| a0004c0010t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | GBR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0214 | EUR | GBR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | FIN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | FIN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00408 | hp2 | a0001 | c0002 | t0004 | g0058 | EAS | CHS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | CHS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | CHS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00558 | hp1 | a0001 | c0002 | t0004 | g0048 | EAS | CHS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00673 | hp1 | a0001 | c0002 | t0004 | g0049 | EAS | CHS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0233 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00738 | hp2 | a0001 | c0002 | t0004 | g0064 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0252 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG00741 | hp2 | a0001 | c0001 | t0008 | g0024 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0235 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0248 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01070 | hp2 | a0001 | c0002 | t0004 | g0044 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0247 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01106 | hp1 | a0001 | c0002 | t0004 | g0062 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0245 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0029 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01175 | hp1 | a0001 | c0002 | t0004 | g0040 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01175 | hp2 | a0001 | c0001 | t0014 | g0240 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01192 | hp1 | a0001 | c0007 | t0002 | g0131 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01255 | hp2 | a0001 | c0002 | t0004 | g0063 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0285 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01257 | hp1 | a0001 | c0002 | t0016 | g0042 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01257 | hp2 | a0002 | c0006 | t0005 | g0232 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01258 | hp1 | a0001 | c0002 | t0004 | g0043 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0286 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0030 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01346 | hp2 | a0001 | c0002 | t0004 | g0056 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0231 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0278 | EUR | IBS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0028 | EUR | IBS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0234 | EUR | IBS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | IBS | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01891 | hp2 | a0001 | c0012 | t0015 | g0297 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01981 | hp1 | a0001 | c0002 | t0004 | g0055 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02004 | hp2 | a0001 | c0001 | t0008 | g0024 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02040 | hp2 | a0001 | c0002 | t0004 | g0051 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02055 | hp1 | a0001 | c0002 | t0007 | g0298 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02080 | hp2 | a0001 | c0002 | t0004 | g0039 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02129 | hp2 | a0001 | c0002 | t0004 | g0038 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02132 | hp2 | a0001 | c0002 | t0004 | g0013 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02135 | hp1 | a0001 | c0002 | t0004 | g0053 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0238 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0228 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | CDX | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | CDX | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | CDX | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | CDX | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0226 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02300 | hp2 | a0001 | c0002 | t0004 | g0041 | AMR | PEL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02451 | hp1 | a0001 | c0002 | t0004 | g0066 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0236 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02615 | hp1 | a0001 | c0009 | t0006 | g0155 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0037 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0292 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0152 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02698 | hp1 | a0001 | c0001 | t0005 | g0250 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02717 | hp2 | a0001 | c0005 | t0006 | g0156 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0157 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0030 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0265 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0036 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0149 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0225 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0253 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02922 | hp2 | a0001 | c0002 | t0007 | g0301 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0153 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0154 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03017 | hp2 | a0001 | c0001 | t0009 | g0223 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03130 | hp1 | a0001 | c0001 | t0010 | g0148 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03139 | hp1 | a0001 | c0002 | t0007 | g0299 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03139 | hp2 | a0001 | c0007 | t0002 | g0130 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | ESN | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03209 | hp2 | a0001 | c0005 | t0006 | g0021 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0028 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0246 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03579 | hp2 | a0001 | c0005 | t0006 | g0021 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0237 | SAS | STU | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03704 | hp1 | a0001 | c0002 | t0004 | g0059 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03710 | hp1 | a0002 | c0006 | t0005 | g0249 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0283 | SAS | PJL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0029 | SAS | BEB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0274 | SAS | BEB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0230 | SAS | BEB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0287 | SAS | STU | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | BEB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG04199 | hp1 | a0001 | c0001 | t0009 | g0216 | SAS | STU | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0282 | SAS | STU | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0254 | SAS | STU | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | STU | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | YRI | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | YRI | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18612 | hp1 | a0001 | c0002 | t0004 | g0045 | EAS | CHB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | CHB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | CHB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | CHB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | YRI | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0151 | AFR | YRI | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18939 | hp2 | a0001 | c0004 | t0003 | g0147 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18944 | hp1 | a0001 | c0002 | t0004 | g0046 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18957 | hp2 | a0001 | c0004 | t0003 | g0146 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18966 | hp1 | a0001 | c0002 | t0004 | g0060 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18974 | hp2 | a0001 | c0001 | t0012 | g0081 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18983 | hp1 | a0003 | c0011 | t0003 | g0260 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18989 | hp2 | a0001 | c0002 | t0004 | g0054 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18994 | hp2 | a0001 | c0004 | t0003 | g0145 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19002 | hp2 | a0001 | c0002 | t0004 | g0052 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19005 | hp1 | a0001 | c0002 | t0004 | g0061 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19007 | hp1 | a0001 | c0008 | t0002 | g0035 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0272 | AFR | LWK | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19057 | hp1 | a0001 | c0002 | t0004 | g0050 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19058 | hp1 | a0001 | c0002 | t0004 | g0057 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19084 | hp1 | a0001 | c0002 | t0004 | g0067 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19085 | hp2 | a0001 | c0002 | t0004 | g0013 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19091 | hp2 | a0001 | c0002 | t0004 | g0047 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19240 | hp1 | a0004 | c0010 | t0003 | g0242 | AFR | YRI | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA19240 | hp2 | a0001 | c0002 | t0004 | g0065 | AFR | YRI | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | ASW | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ASW | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | GIH | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0229 | SAS | GIH | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02109 | hp1 | a0001 | c0002 | t0007 | g0300 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0266 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | ACB | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0221 | AFR | MSL | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA18955 | hp2 | a0001 | c0001 | t0011 | g0276 | EAS | JPT | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA20300 | hp1 | a0001 | c0001 | t0013 | g0243 | AFR | USA | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0264 | AFR | USA | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0244 | AFR | LWK | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0239 | REF | REF | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0020 | REF | REF | IFT57_chr3_108155812_108227424 | IFT57 | chr3 | 108155812 | 108227424 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:108162535 | T | C | 1 | a0002 | 2 | HG01257.hp2 HG03710.hp1 |
missense_variant | MODERATE | c.1232A>G | p.Asn411Ser | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1334/3057 | 1232/1290 | 411/429 | chr3 | 108162535 | |||
| chr3:108165477 | T | C | 1 | a0004 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.998A>G | p.Gln333Arg | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/11 | 1100/3057 | 998/1290 | 333/429 | chr3 | 108165477 | |||
| chr3:108167814 | T | G | 1 | a0003 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.828A>C | p.Glu276Asp | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 7/11 | 930/3057 | 828/1290 | 276/429 | chr3 | 108167814 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:108165455 | C | T | 1 | a0001c0003 | 7 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(4): Show |
synonymous_variant | LOW | c.1020G>A | p.Thr340Thr | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/11 | 1122/3057 | 1020/1290 | 340/429 | chr3 | 108165455 | |||
| chr3:108167832 | C | T | 1 | a0001c0009 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.810G>A | p.Gln270Gln | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 7/11 | 912/3057 | 810/1290 | 270/429 | chr3 | 108167832 | |||
| chr3:108206655 | G | A | 1 | a0001c0007 | 2 | HG01192.hp1 HG03139.hp2 |
synonymous_variant | LOW | c.627C>T | p.Asn209Asn | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/11 | 729/3057 | 627/1290 | 209/429 | chr3 | 108206655 | |||
| chr3:108218561 | C | T | 1 | a0001c0002 | 36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
synonymous_variant | LOW | c.468G>A | p.Leu156Leu | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/11 | 570/3057 | 468/1290 | 156/429 | chr3 | 108218561 | |||
| chr3:108219425 | G | A | 1 | a0001c0005 | 3 | HG02717.hp2 HG03209.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.360C>T | p.Ser120Ser | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/11 | 462/3057 | 360/1290 | 120/429 | chr3 | 108219425 | |||
| chr3:108219425 | G | C | 1 | a0001c0004 | 3 | NA18939.hp2 NA18957.hp2 NA18994.hp2 |
synonymous_variant | LOW | c.360C>G | p.Ser120Ser | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/11 | 462/3057 | 360/1290 | 120/429 | chr3 | 108219425 | |||
| chr3:108222161 | G | C | 1 | a0001c0012 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.162C>G | p.Leu54Leu | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/11 | 264/3057 | 162/1290 | 54/429 | chr3 | 108222161 | |||
| chr3:108222227 | C | G | 1 | a0001c0008 | 1 | NA19007.hp1 | synonymous_variant | LOW | c.96G>C | p.Arg32Arg | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/11 | 198/3057 | 96/1290 | 32/429 | chr3 | 108222227 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:108160883 | G | C | 5 | a0001c0001t0010 a0001c0002t0004 a0001c0002t0007 others(2): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1594C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1594 | chr3 | 108160883 | ||||||
| chr3:108161139 | T | C | 12 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(9): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*1338A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1338 | chr3 | 108161139 | ||||||
| chr3:108161222 | C | CT | 9 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0012 others(6): Show |
130 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*1254dupA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1254 | chr3 | 108161222 | ||||||
| chr3:108161222 | CT | C | 5 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(2): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1254delA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1254 | chr3 | 108161222 | ||||||
| chr3:108161257 | A | C | 1 | a0001c0012t0015 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1220T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1220 | chr3 | 108161257 | ||||||
| chr3:108161265 | T | C | 1 | a0001c0001t0012 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1212A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1212 | chr3 | 108161265 | ||||||
| chr3:108161295 | T | C | 1 | a0001c0001t0008 | 2 | HG00741.hp2 HG02004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1182A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1182 | chr3 | 108161295 | ||||||
| chr3:108161301 | C | CACTA | 5 | a0001c0001t0010 a0001c0002t0004 a0001c0002t0007 others(2): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1175_*1176insTAGT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1175 | chr3 | 108161301 | ||||||
| chr3:108161306 | T | C | 4 | a0001c0001t0010 a0001c0002t0004 a0001c0002t0007 others(1): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1171A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1171 | chr3 | 108161306 | ||||||
| chr3:108161325 | T | C | 1 | a0001c0001t0013 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1152A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 1152 | chr3 | 108161325 | ||||||
| chr3:108161536 | T | TA | 4 | a0001c0001t0010 a0001c0002t0004 a0001c0002t0007 others(1): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*940dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 940 | chr3 | 108161536 | ||||||
| chr3:108161536 | TA | T | 17 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(14): Show |
304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
3_prime_UTR_variant | MODIFIER | c.*940delT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 940 | chr3 | 108161536 | ||||||
| chr3:108161607 | C | T | 1 | a0001c0001t0010 | 2 | HG02818.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*870G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 870 | chr3 | 108161607 | ||||||
| chr3:108161626 | T | G | 5 | a0001c0001t0010 a0001c0002t0004 a0001c0002t0007 others(2): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*851A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 851 | chr3 | 108161626 | ||||||
| chr3:108161639 | T | C | 1 | a0001c0001t0014 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*838A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 838 | chr3 | 108161639 | ||||||
| chr3:108161673 | T | C | 1 | a0001c0002t0007 | 4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*804A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 804 | chr3 | 108161673 | ||||||
| chr3:108161818 | T | G | 1 | a0001c0001t0009 | 2 | HG03017.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*659A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 659 | chr3 | 108161818 | ||||||
| chr3:108161973 | GT | G | 5 | a0001c0001t0010 a0001c0002t0004 a0001c0002t0007 others(2): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*503delA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 503 | chr3 | 108161973 | ||||||
| chr3:108162072 | T | C | 5 | a0001c0001t0010 a0001c0002t0004 a0001c0002t0007 others(2): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*405A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 405 | chr3 | 108162072 | ||||||
| chr3:108162130 | G | A | 5 | a0001c0001t0010 a0001c0002t0004 a0001c0002t0007 others(2): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*347C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 347 | chr3 | 108162130 | ||||||
| chr3:108162291 | T | A | 5 | a0001c0001t0010 a0001c0002t0004 a0001c0002t0007 others(2): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*186A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 186 | chr3 | 108162291 | ||||||
| chr3:108162305 | T | C | 4 | a0001c0001t0010 a0001c0002t0004 a0001c0002t0007 others(1): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*172A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 11/11 | 172 | chr3 | 108162305 | ||||||
| chr3:108222354 | G | A | 1 | a0001c0002t0007 | 4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-32C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/11 | chr3 | 108222354 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:108162759 | G | T | 1 | a0001c0001t0001g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1112-104C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108162759 | |||||||
| chr3:108162854 | G | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1112-199C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108162854 | |||||||
| chr3:108162864 | T | C | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.1112-209A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108162864 | |||||||
| chr3:108162949 | G | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1112-294C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108162949 | |||||||
| chr3:108162983 | G | A | 2 | a0001c0001t0005g0036 a0001c0001t0005g0037 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1112-328C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108162983 | |||||||
| chr3:108163230 | C | A | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1111+433G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108163230 | |||||||
| chr3:108163329 | A | C | 1 | a0001c0001t0003g0284 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1111+334T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108163329 | |||||||
| chr3:108163444 | G | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1111+219C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108163444 | |||||||
| chr3:108163452 | C | G | 1 | a0001c0001t0002g0077 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1111+211G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108163452 | |||||||
| chr3:108163510 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1111+153G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108163510 | |||||||
| chr3:108163651 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1111+12C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 10/10 | chr3 | 108163651 | |||||||
| chr3:108163796 | G | A | 198 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(195): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.1045-67C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108163796 | |||||||
| chr3:108164105 | T | C | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.1045-376A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108164105 | |||||||
| chr3:108164385 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1045-656A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108164385 | |||||||
| chr3:108164404 | A | T | 1 | a0001c0002t0004g0051 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1045-675T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108164404 | |||||||
| chr3:108164442 | G | A | 1 | a0001c0001t0003g0292 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1045-713C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108164442 | |||||||
| chr3:108164561 | ACTAT | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1045-836_1045-833d others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108164561 | |||||||
| chr3:108164683 | C | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1044+748G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108164683 | |||||||
| chr3:108164820 | G | A | 4 | a0001c0001t0005g0247 a0001c0001t0005g0248 a0002c0006t0005g0232 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1044+611C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108164820 | |||||||
| chr3:108164921 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1044+510T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108164921 | |||||||
| chr3:108165122 | G | A | 1 | a0001c0001t0005g0231 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1044+309C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108165122 | |||||||
| chr3:108165161 | TG | T | 35 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(32): Show |
36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1044+269delC | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108165161 | |||||||
| chr3:108165162 | GT | G | 3 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0012t0015g0297 |
3 | HG01891.hp2 HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1044+268delA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108165162 | |||||||
| chr3:108165180 | A | C | 1 | a0001c0001t0003g0277 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1044+251T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108165180 | |||||||
| chr3:108165285 | T | C | 31 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(28): Show |
32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.1044+146A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108165285 | |||||||
| chr3:108165346 | T | G | 1 | a0001c0001t0003g0274 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1044+85A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108165346 | |||||||
| chr3:108165364 | T | C | 298 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(295): Show |
350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.1044+67A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108165364 | |||||||
| chr3:108165373 | C | T | 1 | a0001c0001t0005g0028 | 2 | HG01515.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1044+58G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108165373 | |||||||
| chr3:108165422 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1044+9T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 9/10 | chr3 | 108165422 | |||||||
| chr3:108165646 | A | G | 1 | a0001c0001t0002g0120 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.982-153T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 8/10 | chr3 | 108165646 | |||||||
| chr3:108165978 | A | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.982-485T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 8/10 | chr3 | 108165978 | |||||||
| chr3:108166081 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.982-588T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 8/10 | chr3 | 108166081 | |||||||
| chr3:108166229 | C | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.981+625G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 8/10 | chr3 | 108166229 | |||||||
| chr3:108166258 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.981+596G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 8/10 | chr3 | 108166258 | |||||||
| chr3:108166284 | C | T | 10 | a0001c0001t0002g0014 a0001c0001t0002g0016 a0001c0001t0002g0080 others(7): Show |
12 | HG01358.hp1 HG01993.hp1 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.981+570G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 8/10 | chr3 | 108166284 | |||||||
| chr3:108166469 | CTT | C | 84 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(81): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.981+383_981+384del others(2): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 8/10 | chr3 | 108166469 | |||||||
| chr3:108166636 | G | C | 35 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(32): Show |
36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.981+218C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 8/10 | chr3 | 108166636 | |||||||
| chr3:108166812 | T | C | 2 | a0002c0006t0005g0232 a0002c0006t0005g0249 |
2 | HG01257.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.981+42A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 8/10 | chr3 | 108166812 | |||||||
| chr3:108167028 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.850-43T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 7/10 | chr3 | 108167028 | |||||||
| chr3:108167331 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.850-346A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 7/10 | chr3 | 108167331 | |||||||
| chr3:108167461 | G | C | 1 | a0001c0001t0001g0195 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.849+332C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 7/10 | chr3 | 108167461 | |||||||
| chr3:108167774 | C | T | 1 | a0001c0001t0003g0259 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.849+19G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 7/10 | chr3 | 108167774 | |||||||
| chr3:108167892 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.778-28A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108167892 | |||||||
| chr3:108167919 | C | A | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-55G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108167919 | |||||||
| chr3:108168078 | C | T | 35 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(32): Show |
36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.778-214G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108168078 | |||||||
| chr3:108168245 | T | G | 1 | a0001c0001t0001g0199 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.778-381A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108168245 | |||||||
| chr3:108168259 | G | A | 2 | a0001c0005t0006g0021 a0001c0005t0006g0156 |
3 | HG02717.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.778-395C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108168259 | |||||||
| chr3:108168521 | A | C | 1 | a0001c0001t0001g0205 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.778-657T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108168521 | |||||||
| chr3:108168558 | C | T | 31 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(28): Show |
32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.778-694G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108168558 | |||||||
| chr3:108168741 | G | A | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-877C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108168741 | |||||||
| chr3:108168863 | A | G | 3 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0244 |
3 | HG02615.hp2 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.778-999T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108168863 | |||||||
| chr3:108168866 | T | C | 3 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0244 |
3 | HG02615.hp2 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.778-1002A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108168866 | |||||||
| chr3:108168909 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-1045T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108168909 | |||||||
| chr3:108168974 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-1110G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108168974 | |||||||
| chr3:108169059 | A | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-1195T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169059 | |||||||
| chr3:108169087 | T | G | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.778-1223A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169087 | |||||||
| chr3:108169230 | T | C | 291 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(288): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.778-1366A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169230 | |||||||
| chr3:108169237 | T | G | 291 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(288): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.778-1373A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169237 | |||||||
| chr3:108169283 | A | G | 2 | a0001c0002t0004g0063 a0001c0002t0004g0064 |
2 | HG00738.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.778-1419T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169283 | |||||||
| chr3:108169401 | A | G | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.778-1537T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169401 | |||||||
| chr3:108169466 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.778-1602G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169466 | |||||||
| chr3:108169513 | A | G | 148 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(145): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.778-1649T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169513 | |||||||
| chr3:108169596 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-1732G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169596 | |||||||
| chr3:108169676 | A | T | 35 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(32): Show |
36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.778-1812T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169676 | |||||||
| chr3:108169821 | C | G | 1 | a0001c0001t0003g0277 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.778-1957G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169821 | |||||||
| chr3:108169887 | G | A | 299 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(296): Show |
351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.778-2023C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169887 | |||||||
| chr3:108169910 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-2046G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169910 | |||||||
| chr3:108169994 | T | G | 15 | a0001c0001t0001g0234 a0001c0001t0005g0028 a0001c0001t0005g0029 others(12): Show |
18 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.778-2130A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108169994 | |||||||
| chr3:108170020 | T | C | 93 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0014 others(90): Show |
104 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.778-2156A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108170020 | |||||||
| chr3:108170085 | G | A | 4 | a0001c0001t0001g0174 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG01255.hp1 HG01261.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-2221C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108170085 | |||||||
| chr3:108170295 | G | A | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.778-2431C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108170295 | |||||||
| chr3:108170402 | G | T | 1 | a0001c0001t0002g0104 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.778-2538C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108170402 | |||||||
| chr3:108170668 | C | CA | 81 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
96 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.778-2805dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108170668 | |||||||
| chr3:108170900 | G | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-3036C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108170900 | |||||||
| chr3:108170913 | A | G | 1 | a0001c0001t0003g0157 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.778-3049T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108170913 | |||||||
| chr3:108170956 | C | A | 1 | a0001c0001t0001g0290 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.778-3092G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108170956 | |||||||
| chr3:108171116 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-3252A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171116 | |||||||
| chr3:108171132 | C | G | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-3268G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171132 | |||||||
| chr3:108171214 | G | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-3350C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171214 | |||||||
| chr3:108171371 | C | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.778-3507G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171371 | |||||||
| chr3:108171401 | T | C | 2 | a0001c0003t0001g0225 a0001c0003t0001g0226 |
2 | HG02280.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.778-3537A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171401 | |||||||
| chr3:108171421 | A | C | 1 | a0001c0001t0002g0105 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.778-3557T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171421 | |||||||
| chr3:108171457 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-3593A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171457 | |||||||
| chr3:108171469 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.778-3605C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171469 | |||||||
| chr3:108171483 | G | A | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-3619C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171483 | |||||||
| chr3:108171548 | G | A | 1 | a0001c0001t0006g0152 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.778-3684C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171548 | |||||||
| chr3:108171573 | G | A | 1 | a0001c0001t0003g0261 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.778-3709C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171573 | |||||||
| chr3:108171613 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-3749T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171613 | |||||||
| chr3:108171654 | G | A | 4 | a0001c0001t0005g0247 a0001c0001t0005g0248 a0002c0006t0005g0232 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-3790C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171654 | |||||||
| chr3:108171657 | T | C | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-3793A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171657 | |||||||
| chr3:108171685 | C | G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0205 |
2 | HG01243.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.778-3821G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171685 | |||||||
| chr3:108171716 | A | G | 2 | a0001c0001t0010g0148 a0001c0001t0010g0149 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.778-3852T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171716 | |||||||
| chr3:108171951 | G | GCATA | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.778-4091_778-4088d others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108171951 | |||||||
| chr3:108172080 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-4216A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108172080 | |||||||
| chr3:108172151 | T | C | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-4287A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108172151 | |||||||
| chr3:108172218 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-4354G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108172218 | |||||||
| chr3:108172298 | C | A | 3 | a0001c0002t0004g0038 a0001c0002t0004g0057 a0001c0002t0004g0067 |
3 | HG02129.hp2 NA19058.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.778-4434G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108172298 | |||||||
| chr3:108172335 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.778-4471C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108172335 | |||||||
| chr3:108172349 | A | G | 40 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0010g0148 others(37): Show |
41 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.778-4485T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108172349 | |||||||
| chr3:108172366 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-4502T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108172366 | |||||||
| chr3:108172604 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-4740T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108172604 | |||||||
| chr3:108172726 | G | A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0222 a0001c0001t0001g0224 |
3 | HG00280.hp2 HG02451.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.778-4862C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108172726 | |||||||
| chr3:108172923 | A | G | 2 | a0001c0001t0002g0093 a0001c0001t0002g0111 |
2 | NA19084.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.778-5059T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108172923 | |||||||
| chr3:108173186 | C | A | 1 | a0001c0001t0003g0241 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.778-5322G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173186 | |||||||
| chr3:108173230 | T | C | 89 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0014 others(86): Show |
100 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.778-5366A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173230 | |||||||
| chr3:108173250 | T | C | 1 | a0001c0002t0004g0044 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.778-5386A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173250 | |||||||
| chr3:108173254 | A | AAC | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00673.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.778-5392_778-5391d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173254 | |||||||
| chr3:108173728 | G | A | 1 | a0001c0001t0003g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.778-5864C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173728 | |||||||
| chr3:108173766 | C | CTG | 38 | a0001c0001t0001g0165 a0001c0001t0001g0185 a0001c0001t0001g0186 others(35): Show |
43 | HG00408.hp1 HG00621.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.778-5904_778-5903d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | |||||||
| chr3:108173766 | C | CTGTG | 22 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0073 others(19): Show |
25 | HG00558.hp2 HG01192.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.778-5906_778-5903d others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | |||||||
| chr3:108173766 | C | CTGTGTG | 7 | a0001c0001t0002g0014 a0001c0001t0002g0085 a0001c0001t0002g0105 others(4): Show |
8 | HG02683.hp1 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.778-5908_778-5903d others(8): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | |||||||
| chr3:108173766 | C | CTGTGTGT others(1): Show |
5 | a0001c0001t0002g0078 a0001c0001t0002g0084 a0001c0001t0002g0095 others(2): Show |
5 | HG00673.hp2 HG01934.hp2 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-5910_778-5903d others(10): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | |||||||
| chr3:108173766 | C | CTGTGTGT others(3): Show |
4 | a0001c0001t0002g0090 a0001c0001t0002g0125 a0001c0001t0002g0135 others(1): Show |
4 | HG00642.hp2 HG01167.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-5912_778-5903d others(12): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | |||||||
| chr3:108173766 | C | CTGTGTGT others(5): Show |
3 | a0001c0001t0002g0129 a0001c0001t0002g0136 a0001c0001t0006g0153 |
3 | HG02257.hp1 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.778-5914_778-5903d others(14): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | |||||||
| chr3:108173766 | C | CTGTGTGT others(13): Show |
2 | a0001c0001t0003g0285 a0001c0001t0003g0286 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.778-5922_778-5903d others(22): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | |||||||
| chr3:108173766 | CTG | C | 29 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0192 others(26): Show |
31 | HG00423.hp2 HG00741.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.778-5904_778-5903d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | |||||||
| chr3:108173766 | CTGTG | C | 77 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
92 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.778-5906_778-5903d others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | |||||||
| chr3:108173766 | CTGTGTG | C | 38 | a0001c0001t0001g0202 a0001c0001t0003g0292 a0001c0001t0005g0233 others(35): Show |
43 | HG00408.hp2 HG00558.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.778-5908_778-5903d others(8): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | |||||||
| chr3:108173766 | CTGTGTGT others(1): Show |
C | 5 | a0001c0001t0001g0166 a0001c0001t0001g0205 a0001c0001t0002g0115 others(2): Show |
5 | HG01070.hp2 NA18951.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-5910_778-5903d others(10): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173766 | |||||||
| chr3:108173798 | GTGTGTGT others(7): Show |
G | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-5948_778-5935d others(16): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173798 | |||||||
| chr3:108173806 | G | A | 33 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(30): Show |
34 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.778-5942C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173806 | |||||||
| chr3:108173808 | G | A | 64 | a0001c0001t0001g0234 a0001c0001t0001g0251 a0001c0001t0003g0241 others(61): Show |
69 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.778-5944C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173808 | |||||||
| chr3:108173808 | G | GTA | 13 | a0001c0001t0003g0011 a0001c0001t0003g0031 a0001c0001t0003g0227 others(10): Show |
14 | HG00423.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.778-5946_778-5945d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173808 | |||||||
| chr3:108173808 | G | GTGTA | 5 | a0001c0001t0003g0001 a0001c0001t0003g0253 a0001c0001t0003g0271 others(2): Show |
5 | HG02080.hp1 HG02922.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-5945_778-5944i others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173808 | |||||||
| chr3:108173808 | G | GTGTGTA | 15 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(12): Show |
18 | HG02155.hp2 HG02165.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.778-5945_778-5944i others(8): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173808 | |||||||
| chr3:108173808 | G | GTGTGTGT others(1): Show |
22 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0009 others(19): Show |
30 | HG00642.hp1 HG01515.hp1 HG02071.hp1 others(27): Show |
intron_variant | MODIFIER | c.778-5945_778-5944i others(10): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173808 | |||||||
| chr3:108173808 | G | GTGTGTGT others(3): Show |
5 | a0001c0001t0003g0010 a0001c0001t0003g0068 a0001c0001t0003g0272 others(2): Show |
5 | HG03041.hp1 HG04199.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-5945_778-5944i others(12): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173808 | |||||||
| chr3:108173808 | G | GTGTGTGT others(11): Show |
1 | a0001c0001t0003g0071 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.778-5945_778-5944i others(20): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173808 | |||||||
| chr3:108173810 | A | G | 5 | a0001c0001t0002g0016 a0001c0001t0002g0093 a0001c0001t0002g0095 others(2): Show |
5 | HG02074.hp2 NA18991.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-5946T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173810 | |||||||
| chr3:108173870 | C | CA | 6 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(3): Show |
7 | HG00408.hp2 HG02080.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.778-6007dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173870 | |||||||
| chr3:108173871 | A | G | 1 | a0001c0001t0003g0282 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.778-6007T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173871 | |||||||
| chr3:108173934 | T | C | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.778-6070A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173934 | |||||||
| chr3:108173997 | A | AAT | 75 | a0001c0001t0001g0160 a0001c0001t0001g0163 a0001c0001t0001g0167 others(72): Show |
82 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.778-6134_778-6133i others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173997 | |||||||
| chr3:108173997 | A | AATGT | 77 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0002g0004 others(74): Show |
98 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.778-6134_778-6133i others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173997 | |||||||
| chr3:108173997 | A | AATGTGT | 20 | a0001c0001t0001g0219 a0001c0001t0002g0073 a0001c0001t0002g0085 others(17): Show |
22 | HG01891.hp1 HG02135.hp1 HG02155.hp2 others(19): Show |
intron_variant | MODIFIER | c.778-6134_778-6133i others(8): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173997 | |||||||
| chr3:108173997 | A | AATGTGTG others(1): Show |
6 | a0001c0001t0003g0033 a0001c0001t0003g0264 a0001c0001t0003g0265 others(3): Show |
7 | HG02165.hp1 HG02165.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.778-6134_778-6133i others(10): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173997 | |||||||
| chr3:108173997 | AGT | A | 20 | a0001c0001t0001g0026 a0001c0001t0001g0170 a0001c0001t0001g0172 others(17): Show |
21 | HG00738.hp2 HG01099.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.778-6135_778-6134d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173997 | |||||||
| chr3:108173997 | AGTGT | A | 3 | a0001c0001t0001g0173 a0001c0001t0003g0068 a0001c0003t0001g0225 |
3 | HG01192.hp2 HG02896.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.778-6137_778-6134d others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173997 | |||||||
| chr3:108173997 | AGTGTGT | A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0289 |
3 | HG01069.hp2 HG01071.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.778-6139_778-6134d others(8): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173997 | |||||||
| chr3:108173997 | AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0001g0290 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.778-6145_778-6134d others(14): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173997 | |||||||
| chr3:108173997 | AGTGTGTG others(13): Show |
A | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-6153_778-6134d others(22): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173997 | |||||||
| chr3:108173998 | G | A | 91 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(88): Show |
111 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.778-6134C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108173998 | |||||||
| chr3:108174000 | G | A | 20 | a0001c0001t0001g0026 a0001c0001t0001g0170 a0001c0001t0001g0172 others(17): Show |
21 | HG00738.hp2 HG01099.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.778-6136C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174000 | |||||||
| chr3:108174002 | G | A | 3 | a0001c0001t0001g0173 a0001c0001t0003g0068 a0001c0003t0001g0225 |
3 | HG01192.hp2 HG02896.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.778-6138C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174002 | |||||||
| chr3:108174004 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0289 |
3 | HG01069.hp2 HG01071.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.778-6140C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174004 | |||||||
| chr3:108174006 | G | A | 2 | a0001c0001t0001g0288 a0001c0001t0003g0157 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.778-6142C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174006 | |||||||
| chr3:108174010 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.778-6146C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174010 | |||||||
| chr3:108174018 | G | A | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-6154C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174018 | |||||||
| chr3:108174019 | T | C | 2 | a0001c0001t0003g0227 a0001c0001t0003g0228 |
2 | HG02145.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.778-6155A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174019 | |||||||
| chr3:108174045 | T | TGTG | 4 | a0001c0001t0003g0010 a0001c0001t0005g0030 a0001c0001t0005g0287 others(1): Show |
4 | HG02602.hp1 HG02738.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.778-6182_778-6181i others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174045 | |||||||
| chr3:108174045 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0220 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.778-6182_778-6181i others(13): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174045 | |||||||
| chr3:108174046 | T | G | 1 | a0001c0003t0001g0221 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.778-6182A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174046 | |||||||
| chr3:108174155 | G | T | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-6291C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174155 | |||||||
| chr3:108174194 | G | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0009 others(42): Show |
66 | HG00423.hp1 HG00642.hp1 HG01256.hp1 others(63): Show |
intron_variant | MODIFIER | c.778-6330C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174194 | |||||||
| chr3:108174211 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-6347T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174211 | |||||||
| chr3:108174302 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-6438A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174302 | |||||||
| chr3:108174314 | T | C | 1 | a0001c0001t0002g0114 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.778-6450A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174314 | |||||||
| chr3:108174344 | TGAA | T | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.778-6483_778-6481d others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174344 | |||||||
| chr3:108174393 | C | T | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-6529G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174393 | |||||||
| chr3:108174414 | C | T | 1 | a0001c0002t0004g0055 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.778-6550G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174414 | |||||||
| chr3:108174457 | G | A | 1 | a0001c0001t0002g0098 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.778-6593C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174457 | |||||||
| chr3:108174474 | T | TTACAATG others(313): Show |
2 | a0001c0002t0007g0299 a0001c0002t0007g0301 |
2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.778-6611_778-6610i others(322): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174474 | |||||||
| chr3:108174474 | T | TTACAATG others(314): Show |
2 | a0001c0002t0007g0298 a0001c0002t0007g0300 |
2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.778-6611_778-6610i others(323): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174474 | |||||||
| chr3:108174474 | T | TTACAATG others(319): Show |
9 | a0001c0002t0004g0038 a0001c0002t0004g0039 a0001c0002t0004g0046 others(6): Show |
9 | HG00408.hp2 HG00558.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.778-6611_778-6610i others(328): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174474 | |||||||
| chr3:108174474 | T | TTACAATG others(320): Show |
8 | a0001c0002t0004g0013 a0001c0002t0004g0045 a0001c0002t0004g0047 others(5): Show |
9 | HG00673.hp1 HG01346.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.778-6611_778-6610i others(329): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174474 | |||||||
| chr3:108174474 | T | TTACAATG others(321): Show |
8 | a0001c0002t0004g0043 a0001c0002t0004g0050 a0001c0002t0004g0051 others(5): Show |
8 | HG00738.hp2 HG01255.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.778-6611_778-6610i others(330): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174474 | |||||||
| chr3:108174474 | T | TTACAATG others(322): Show |
2 | a0001c0002t0004g0054 a0001c0002t0004g0060 |
2 | NA18966.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.778-6611_778-6610i others(331): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174474 | |||||||
| chr3:108174474 | T | TTACAATG others(323): Show |
2 | a0001c0002t0004g0040 a0001c0002t0004g0062 |
2 | HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.778-6611_778-6610i others(332): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174474 | |||||||
| chr3:108174474 | T | TTACAATG others(324): Show |
1 | a0001c0002t0004g0041 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.778-6611_778-6610i others(333): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174474 | |||||||
| chr3:108174474 | T | TTACAATG others(325): Show |
1 | a0001c0002t0004g0044 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.778-6611_778-6610i others(334): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174474 | |||||||
| chr3:108174581 | T | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-6717A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174581 | |||||||
| chr3:108174620 | T | A | 1 | a0001c0001t0013g0243 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.778-6756A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174620 | |||||||
| chr3:108174630 | A | T | 1 | a0001c0001t0013g0243 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.778-6766T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174630 | |||||||
| chr3:108174669 | T | C | 1 | a0001c0001t0013g0243 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.778-6805A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174669 | |||||||
| chr3:108174732 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-6868A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174732 | |||||||
| chr3:108174790 | C | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-6926G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174790 | |||||||
| chr3:108174893 | A | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.778-7029T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174893 | |||||||
| chr3:108174924 | G | A | 1 | a0001c0001t0005g0238 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.778-7060C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174924 | |||||||
| chr3:108174927 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.778-7063A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174927 | |||||||
| chr3:108174944 | A | G | 1 | a0001c0001t0002g0092 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.778-7080T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174944 | |||||||
| chr3:108174979 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.778-7115T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108174979 | |||||||
| chr3:108175003 | A | G | 51 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0009 others(48): Show |
72 | HG00423.hp1 HG00642.hp1 HG01256.hp1 others(69): Show |
intron_variant | MODIFIER | c.778-7139T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175003 | |||||||
| chr3:108175054 | T | C | 1 | a0001c0001t0002g0124 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.778-7190A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175054 | |||||||
| chr3:108175125 | G | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-7261C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175125 | |||||||
| chr3:108175160 | G | T | 1 | a0001c0001t0001g0173 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.778-7296C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175160 | |||||||
| chr3:108175195 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.778-7331C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175195 | |||||||
| chr3:108175257 | T | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-7393A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175257 | |||||||
| chr3:108175270 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-7406A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175270 | |||||||
| chr3:108175386 | G | A | 4 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(1): Show |
4 | HG02622.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-7522C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175386 | |||||||
| chr3:108175504 | A | T | 1 | a0001c0001t0001g0169 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.778-7640T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175504 | |||||||
| chr3:108175539 | T | C | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.778-7675A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175539 | |||||||
| chr3:108175558 | G | A | 2 | a0001c0001t0003g0150 a0001c0001t0006g0153 |
2 | HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.778-7694C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175558 | |||||||
| chr3:108175645 | C | A | 35 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(32): Show |
36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.778-7781G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175645 | |||||||
| chr3:108175722 | A | G | 2 | a0001c0001t0003g0150 a0001c0001t0006g0153 |
2 | HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.778-7858T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175722 | |||||||
| chr3:108175745 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-7881A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175745 | |||||||
| chr3:108175802 | TA | T | 23 | a0001c0001t0001g0234 a0001c0001t0001g0251 a0001c0001t0002g0137 others(20): Show |
26 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.778-7939delT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175802 | |||||||
| chr3:108175832 | G | A | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.778-7968C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175832 | |||||||
| chr3:108175972 | C | A | 3 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0246 |
3 | HG02145.hp2 HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.778-8108G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175972 | |||||||
| chr3:108175993 | C | A | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.778-8129G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108175993 | |||||||
| chr3:108176063 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.778-8199G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176063 | |||||||
| chr3:108176142 | G | A | 31 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(28): Show |
32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.778-8278C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176142 | |||||||
| chr3:108176191 | T | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-8327A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176191 | |||||||
| chr3:108176211 | G | A | 1 | a0001c0001t0014g0240 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.778-8347C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176211 | |||||||
| chr3:108176212 | C | A | 1 | a0001c0001t0014g0240 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.778-8348G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176212 | |||||||
| chr3:108176280 | T | C | 1 | a0001c0001t0006g0151 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.778-8416A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176280 | |||||||
| chr3:108176360 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-8496G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176360 | |||||||
| chr3:108176361 | A | G | 198 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(195): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.778-8497T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176361 | |||||||
| chr3:108176479 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-8615T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176479 | |||||||
| chr3:108176550 | A | T | 15 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0174 others(12): Show |
18 | HG00099.hp2 HG00738.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.778-8686T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176550 | |||||||
| chr3:108176649 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-8785A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176649 | |||||||
| chr3:108176670 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.778-8806C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176670 | |||||||
| chr3:108176695 | C | T | 1 | a0001c0001t0003g0241 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.778-8831G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176695 | |||||||
| chr3:108176697 | C | T | 1 | a0001c0001t0002g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.778-8833G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176697 | |||||||
| chr3:108176732 | T | C | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.778-8868A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176732 | |||||||
| chr3:108176736 | C | T | 198 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(195): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.778-8872G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176736 | |||||||
| chr3:108176746 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-8882G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176746 | |||||||
| chr3:108176887 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-9023A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176887 | |||||||
| chr3:108176914 | A | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-9050T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108176914 | |||||||
| chr3:108177027 | T | C | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-9163A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177027 | |||||||
| chr3:108177044 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-9180A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177044 | |||||||
| chr3:108177054 | T | C | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-9190A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177054 | |||||||
| chr3:108177228 | T | C | 31 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(28): Show |
32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.778-9364A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177228 | |||||||
| chr3:108177261 | C | T | 22 | a0001c0001t0001g0234 a0001c0001t0001g0251 a0001c0001t0005g0028 others(19): Show |
25 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.778-9397G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177261 | |||||||
| chr3:108177275 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0178 |
3 | HG01099.hp1 HG01109.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.778-9411G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177275 | |||||||
| chr3:108177319 | T | C | 1 | a0001c0001t0005g0235 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.778-9455A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177319 | |||||||
| chr3:108177324 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-9460A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177324 | |||||||
| chr3:108177334 | C | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.778-9470G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177334 | |||||||
| chr3:108177421 | C | A | 89 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0014 others(86): Show |
100 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.778-9557G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177421 | |||||||
| chr3:108177617 | T | C | 1 | a0001c0001t0002g0132 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.778-9753A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177617 | |||||||
| chr3:108177639 | A | AT | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-9776_778-9775i others(3): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177639 | |||||||
| chr3:108177715 | T | C | 31 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(28): Show |
32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.778-9851A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177715 | |||||||
| chr3:108177722 | G | A | 5 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(2): Show |
6 | HG00741.hp2 HG01099.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-9858C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177722 | |||||||
| chr3:108177770 | T | G | 1 | a0001c0001t0001g0176 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.778-9906A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177770 | |||||||
| chr3:108177864 | C | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-10000G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177864 | |||||||
| chr3:108177937 | T | C | 2 | a0001c0001t0005g0036 a0001c0001t0005g0037 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.778-10073A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177937 | |||||||
| chr3:108177955 | T | C | 1 | a0001c0001t0009g0223 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.778-10091A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108177955 | |||||||
| chr3:108178030 | T | C | 5 | a0001c0001t0003g0150 a0001c0001t0006g0151 a0001c0001t0006g0152 others(2): Show |
5 | HG02647.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-10166A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178030 | |||||||
| chr3:108178125 | A | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-10261T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178125 | |||||||
| chr3:108178137 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-10273A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178137 | |||||||
| chr3:108178365 | T | G | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-10501A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178365 | |||||||
| chr3:108178392 | A | G | 39 | a0001c0001t0003g0274 a0001c0001t0010g0148 a0001c0001t0010g0149 others(36): Show |
40 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.778-10528T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178392 | |||||||
| chr3:108178447 | G | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-10583C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178447 | |||||||
| chr3:108178660 | C | T | 1 | a0001c0001t0003g0273 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.778-10796G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178660 | |||||||
| chr3:108178698 | C | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-10834G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178698 | |||||||
| chr3:108178807 | T | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-10943A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178807 | |||||||
| chr3:108178841 | C | T | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-10977G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178841 | |||||||
| chr3:108178859 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-10995G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178859 | |||||||
| chr3:108178891 | AATTCCAG others(13): Show |
A | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.778-11047_778-1102 others(24): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178891 | |||||||
| chr3:108178906 | G | A | 1 | a0001c0001t0005g0030 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.778-11042C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108178906 | |||||||
| chr3:108179073 | C | T | 2 | a0001c0001t0001g0251 a0001c0001t0005g0252 |
2 | HG00280.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.778-11209G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179073 | |||||||
| chr3:108179089 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.778-11225C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179089 | |||||||
| chr3:108179289 | G | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.778-11425C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179289 | |||||||
| chr3:108179424 | C | T | 2 | a0001c0001t0002g0093 a0001c0012t0015g0297 |
2 | HG01891.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.778-11560G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179424 | |||||||
| chr3:108179425 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.778-11561C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179425 | |||||||
| chr3:108179584 | C | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0179 a0001c0001t0001g0180 others(1): Show |
6 | HG02040.hp1 HG02074.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-11720G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179584 | |||||||
| chr3:108179682 | G | A | 84 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(81): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.778-11818C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179682 | |||||||
| chr3:108179701 | T | C | 1 | a0001c0001t0005g0244 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.777+11820A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179701 | |||||||
| chr3:108179716 | T | C | 1 | a0001c0001t0002g0078 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.777+11805A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179716 | |||||||
| chr3:108179746 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+11775G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179746 | |||||||
| chr3:108179771 | G | A | 1 | a0001c0001t0003g0278 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.777+11750C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179771 | |||||||
| chr3:108179786 | T | G | 4 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0106 others(1): Show |
4 | HG02523.hp1 NA18943.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+11735A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179786 | |||||||
| chr3:108179880 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+11641G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179880 | |||||||
| chr3:108179881 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.777+11640C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179881 | |||||||
| chr3:108179905 | T | TA | 298 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(295): Show |
350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.777+11615dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108179905 | |||||||
| chr3:108180156 | G | C | 1 | a0001c0001t0002g0085 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.777+11365C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108180156 | |||||||
| chr3:108180242 | A | G | 1 | a0001c0001t0002g0111 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.777+11279T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108180242 | |||||||
| chr3:108180475 | C | A | 1 | a0001c0002t0004g0044 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.777+11046G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108180475 | |||||||
| chr3:108180491 | C | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+11030G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108180491 | |||||||
| chr3:108180666 | T | C | 22 | a0001c0001t0001g0234 a0001c0001t0001g0251 a0001c0001t0005g0028 others(19): Show |
25 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.777+10855A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108180666 | |||||||
| chr3:108180670 | C | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+10851G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108180670 | |||||||
| chr3:108180733 | T | C | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+10788A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108180733 | |||||||
| chr3:108180801 | C | T | 1 | a0001c0001t0003g0256 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.777+10720G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108180801 | |||||||
| chr3:108180811 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+10710G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108180811 | |||||||
| chr3:108180985 | A | G | 5 | a0001c0001t0003g0150 a0001c0001t0006g0151 a0001c0001t0006g0152 others(2): Show |
5 | HG02647.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.777+10536T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108180985 | |||||||
| chr3:108181009 | T | C | 4 | a0001c0002t0007g0298 a0001c0002t0007g0299 a0001c0002t0007g0300 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+10512A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181009 | |||||||
| chr3:108181064 | C | T | 50 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0009 others(47): Show |
71 | HG00423.hp1 HG00642.hp1 HG01256.hp1 others(68): Show |
intron_variant | MODIFIER | c.777+10457G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181064 | |||||||
| chr3:108181114 | A | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+10407T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181114 | |||||||
| chr3:108181117 | G | A | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.777+10404C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181117 | |||||||
| chr3:108181173 | C | A | 291 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(288): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.777+10348G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181173 | |||||||
| chr3:108181255 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+10266T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181255 | |||||||
| chr3:108181260 | C | CT | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+10260dupA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181260 | |||||||
| chr3:108181471 | A | C | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+10050T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181471 | |||||||
| chr3:108181515 | G | A | 1 | a0001c0002t0004g0062 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.777+10006C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181515 | |||||||
| chr3:108181577 | C | T | 79 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0014 others(76): Show |
90 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.777+9944G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181577 | |||||||
| chr3:108181604 | T | C | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+9917A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181604 | |||||||
| chr3:108181655 | G | A | 1 | a0001c0001t0005g0236 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.777+9866C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181655 | |||||||
| chr3:108181795 | G | A | 198 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(195): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.777+9726C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181795 | |||||||
| chr3:108181892 | G | A | 39 | a0001c0001t0003g0241 a0001c0001t0010g0148 a0001c0001t0010g0149 others(36): Show |
40 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.777+9629C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108181892 | |||||||
| chr3:108182032 | T | A | 291 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(288): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.777+9489A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182032 | |||||||
| chr3:108182218 | G | A | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+9303C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182218 | |||||||
| chr3:108182313 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.777+9208G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182313 | |||||||
| chr3:108182337 | G | A | 25 | a0001c0001t0001g0234 a0001c0001t0001g0251 a0001c0001t0005g0028 others(22): Show |
28 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.777+9184C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182337 | |||||||
| chr3:108182375 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+9146A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182375 | |||||||
| chr3:108182397 | G | C | 1 | a0001c0001t0005g0244 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.777+9124C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182397 | |||||||
| chr3:108182409 | T | G | 1 | a0001c0002t0004g0052 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.777+9112A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182409 | |||||||
| chr3:108182410 | G | A | 1 | a0001c0001t0002g0133 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.777+9111C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182410 | |||||||
| chr3:108182758 | C | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+8763G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182758 | |||||||
| chr3:108182796 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+8725A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182796 | |||||||
| chr3:108182834 | A | T | 79 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0014 others(76): Show |
90 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.777+8687T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182834 | |||||||
| chr3:108182901 | T | C | 1 | a0001c0001t0013g0243 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.777+8620A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182901 | |||||||
| chr3:108182975 | G | C | 31 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(28): Show |
32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.777+8546C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108182975 | |||||||
| chr3:108183021 | A | G | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.777+8500T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183021 | |||||||
| chr3:108183212 | C | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+8309G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183212 | |||||||
| chr3:108183236 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+8285G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183236 | |||||||
| chr3:108183253 | C | G | 1 | a0001c0001t0012g0081 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.777+8268G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183253 | |||||||
| chr3:108183312 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.777+8209G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183312 | |||||||
| chr3:108183381 | C | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+8140G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183381 | |||||||
| chr3:108183542 | C | A | 1 | a0001c0001t0002g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.777+7979G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183542 | |||||||
| chr3:108183609 | T | C | 2 | a0001c0001t0005g0036 a0001c0001t0005g0037 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.777+7912A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183609 | |||||||
| chr3:108183617 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+7904A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183617 | |||||||
| chr3:108183631 | G | C | 1 | a0001c0002t0004g0053 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.777+7890C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183631 | |||||||
| chr3:108183646 | A | C | 89 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0014 others(86): Show |
100 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.777+7875T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183646 | |||||||
| chr3:108183655 | G | A | 3 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 |
3 | HG02257.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.777+7866C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183655 | |||||||
| chr3:108183665 | A | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+7856T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183665 | |||||||
| chr3:108183746 | T | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+7775A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183746 | |||||||
| chr3:108183877 | C | G | 1 | a0001c0001t0002g0124 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.777+7644G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108183877 | |||||||
| chr3:108184036 | A | G | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+7485T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184036 | |||||||
| chr3:108184052 | A | T | 4 | a0001c0002t0007g0298 a0001c0002t0007g0299 a0001c0002t0007g0300 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+7469T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184052 | |||||||
| chr3:108184100 | G | A | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.777+7421C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184100 | |||||||
| chr3:108184101 | T | G | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.777+7420A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184101 | |||||||
| chr3:108184119 | C | T | 9 | a0001c0001t0002g0015 a0001c0001t0002g0086 a0001c0001t0002g0094 others(6): Show |
10 | HG01361.hp1 HG02132.hp1 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.777+7402G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184119 | |||||||
| chr3:108184154 | G | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+7367C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184154 | |||||||
| chr3:108184228 | A | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+7293T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184228 | |||||||
| chr3:108184306 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.777+7215G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184306 | |||||||
| chr3:108184335 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.777+7186A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184335 | |||||||
| chr3:108184369 | T | A | 25 | a0001c0001t0001g0234 a0001c0001t0001g0251 a0001c0001t0005g0028 others(22): Show |
28 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.777+7152A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184369 | |||||||
| chr3:108184515 | T | C | 84 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(81): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.777+7006A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184515 | |||||||
| chr3:108184517 | C | CA | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+7003dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184517 | |||||||
| chr3:108184582 | T | C | 4 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(1): Show |
4 | HG02622.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+6939A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184582 | |||||||
| chr3:108184639 | A | G | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+6882T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184639 | |||||||
| chr3:108184668 | T | C | 1 | a0001c0001t0002g0115 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.777+6853A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184668 | |||||||
| chr3:108184734 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+6787A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184734 | |||||||
| chr3:108184941 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+6580A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108184941 | |||||||
| chr3:108185137 | T | C | 4 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(1): Show |
4 | HG02622.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+6384A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185137 | |||||||
| chr3:108185200 | A | G | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+6321T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185200 | |||||||
| chr3:108185223 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+6298T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185223 | |||||||
| chr3:108185255 | C | T | 7 | a0001c0001t0002g0005 a0001c0001t0002g0103 a0001c0001t0002g0104 others(4): Show |
9 | HG00558.hp2 HG01496.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.777+6266G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185255 | |||||||
| chr3:108185258 | C | G | 4 | a0001c0002t0007g0298 a0001c0002t0007g0299 a0001c0002t0007g0300 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+6263G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185258 | |||||||
| chr3:108185374 | G | A | 1 | a0001c0002t0004g0044 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.777+6147C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185374 | |||||||
| chr3:108185474 | C | T | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG03130.hp2 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.777+6047G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185474 | |||||||
| chr3:108185551 | A | AT | 84 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0027 others(81): Show |
107 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.777+5969dupA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185551 | |||||||
| chr3:108185551 | A | ATT | 26 | a0001c0001t0001g0025 a0001c0001t0001g0161 a0001c0001t0001g0180 others(23): Show |
32 | HG00423.hp1 HG01071.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.777+5968_777+5969d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185551 | |||||||
| chr3:108185551 | AT | A | 73 | a0001c0001t0001g0172 a0001c0001t0002g0004 a0001c0001t0002g0005 others(70): Show |
84 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.777+5969delA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185551 | |||||||
| chr3:108185591 | G | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+5930C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185591 | |||||||
| chr3:108185595 | G | T | 51 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0009 others(48): Show |
72 | HG00423.hp1 HG00642.hp1 HG01256.hp1 others(69): Show |
intron_variant | MODIFIER | c.777+5926C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185595 | |||||||
| chr3:108185619 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.777+5902G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185619 | |||||||
| chr3:108185636 | G | A | 1 | a0001c0001t0003g0150 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.777+5885C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185636 | |||||||
| chr3:108185780 | G | C | 1 | a0001c0001t0001g0206 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.777+5741C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185780 | |||||||
| chr3:108185821 | T | C | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.777+5700A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185821 | |||||||
| chr3:108185834 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.777+5687T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185834 | |||||||
| chr3:108185925 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.777+5596C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108185925 | |||||||
| chr3:108186000 | G | A | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.777+5521C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186000 | |||||||
| chr3:108186182 | T | G | 84 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(81): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.777+5339A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186182 | |||||||
| chr3:108186257 | C | T | 1 | a0001c0001t0013g0243 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.777+5264G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186257 | |||||||
| chr3:108186321 | C | CA | 86 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0014 others(83): Show |
98 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.777+5199dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186321 | |||||||
| chr3:108186321 | C | CAA | 37 | a0001c0001t0001g0022 a0001c0001t0001g0161 a0001c0001t0001g0162 others(34): Show |
41 | HG00280.hp1 HG00735.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.777+5198_777+5199d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186321 | |||||||
| chr3:108186321 | C | CAAA | 128 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(125): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.777+5197_777+5199d others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186321 | |||||||
| chr3:108186321 | C | CAAAA | 4 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0003g0011 others(1): Show |
6 | HG02145.hp2 HG02738.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+5196_777+5199d others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186321 | |||||||
| chr3:108186321 | CAAA | C | 35 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(32): Show |
36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.777+5197_777+5199d others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186321 | |||||||
| chr3:108186469 | G | A | 2 | a0001c0001t0006g0151 a0001c0001t0006g0152 |
2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.777+5052C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186469 | |||||||
| chr3:108186492 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+5029T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186492 | |||||||
| chr3:108186534 | G | A | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+4987C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186534 | |||||||
| chr3:108186581 | A | G | 1 | a0001c0001t0001g0195 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.777+4940T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186581 | |||||||
| chr3:108186913 | A | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+4608T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108186913 | |||||||
| chr3:108187190 | T | A | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.777+4331A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187190 | |||||||
| chr3:108187335 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.777+4186C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187335 | |||||||
| chr3:108187395 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+4126G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187395 | |||||||
| chr3:108187519 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.777+4002G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187519 | |||||||
| chr3:108187587 | T | TA | 6 | a0001c0001t0001g0006 a0001c0001t0001g0179 a0001c0001t0001g0180 others(3): Show |
8 | HG02040.hp1 HG02074.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.777+3933dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187587 | |||||||
| chr3:108187590 | A | G | 2 | a0001c0001t0003g0257 a0001c0001t0003g0263 |
2 | NA18969.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.777+3931T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187590 | |||||||
| chr3:108187597 | A | AG | 35 | a0001c0001t0005g0287 a0001c0001t0010g0148 a0001c0001t0010g0149 others(32): Show |
36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.777+3923dupC | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187597 | |||||||
| chr3:108187643 | T | TA | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+3877dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187643 | |||||||
| chr3:108187791 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+3730T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187791 | |||||||
| chr3:108187829 | ATTTCT | A | 5 | a0001c0001t0002g0132 a0001c0001t0003g0068 a0001c0001t0003g0069 others(2): Show |
5 | HG02622.hp2 HG03041.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.777+3687_777+3691d others(7): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187829 | |||||||
| chr3:108187886 | T | C | 1 | a0001c0001t0001g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.777+3635A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187886 | |||||||
| chr3:108187941 | TG | T | 5 | a0001c0002t0004g0040 a0001c0002t0007g0298 a0001c0002t0007g0299 others(2): Show |
5 | HG01175.hp1 HG02055.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.777+3579delC | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187941 | |||||||
| chr3:108187942 | G | T | 33 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(30): Show |
34 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.777+3579C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187942 | |||||||
| chr3:108187952 | T | A | 35 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(32): Show |
36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.777+3569A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108187952 | |||||||
| chr3:108188008 | A | AT | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+3512_777+3513i others(3): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108188008 | |||||||
| chr3:108188038 | C | T | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.777+3483G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108188038 | |||||||
| chr3:108188099 | C | A | 2 | a0001c0001t0003g0285 a0001c0001t0003g0286 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.777+3422G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108188099 | |||||||
| chr3:108188328 | T | C | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.777+3193A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108188328 | |||||||
| chr3:108188576 | T | G | 1 | a0001c0001t0001g0180 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.777+2945A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108188576 | |||||||
| chr3:108188679 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+2842A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108188679 | |||||||
| chr3:108188753 | G | C | 2 | a0001c0001t0002g0074 a0001c0001t0002g0143 |
2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.777+2768C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108188753 | |||||||
| chr3:108188761 | G | C | 1 | a0001c0001t0003g0279 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.777+2760C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108188761 | |||||||
| chr3:108188971 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+2550A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108188971 | |||||||
| chr3:108189016 | A | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+2505T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189016 | |||||||
| chr3:108189077 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+2444G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189077 | |||||||
| chr3:108189078 | C | A | 1 | a0001c0002t0004g0047 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.777+2443G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189078 | |||||||
| chr3:108189127 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+2394A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189127 | |||||||
| chr3:108189153 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+2368A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189153 | |||||||
| chr3:108189334 | C | T | 31 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(28): Show |
32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.777+2187G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189334 | |||||||
| chr3:108189468 | G | T | 1 | a0001c0001t0001g0194 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.777+2053C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189468 | |||||||
| chr3:108189544 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+1977T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189544 | |||||||
| chr3:108189556 | T | C | 3 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0244 |
3 | HG02615.hp2 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.777+1965A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189556 | |||||||
| chr3:108189573 | G | C | 2 | a0001c0001t0010g0148 a0001c0001t0010g0149 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.777+1948C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189573 | |||||||
| chr3:108189736 | C | A | 1 | a0001c0001t0006g0151 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.777+1785G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189736 | |||||||
| chr3:108189753 | T | TAGAAAAT others(9): Show |
38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+1767_777+1768i others(18): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189753 | |||||||
| chr3:108189887 | A | ATGT | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+1633_777+1634i others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189887 | |||||||
| chr3:108189941 | G | A | 3 | a0001c0001t0001g0171 a0001c0001t0001g0201 a0001c0001t0008g0024 |
4 | HG00741.hp2 HG01099.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+1580C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189941 | |||||||
| chr3:108189958 | T | C | 1 | a0001c0001t0010g0149 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.777+1563A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108189958 | |||||||
| chr3:108190067 | A | C | 1 | a0001c0001t0001g0182 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.777+1454T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190067 | |||||||
| chr3:108190187 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+1334A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190187 | |||||||
| chr3:108190264 | T | G | 1 | a0001c0001t0002g0089 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.777+1257A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190264 | |||||||
| chr3:108190321 | C | T | 1 | a0004c0010t0003g0242 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.777+1200G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190321 | |||||||
| chr3:108190402 | A | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+1119T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190402 | |||||||
| chr3:108190452 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+1069T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190452 | |||||||
| chr3:108190489 | T | C | 1 | a0001c0001t0003g0266 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.777+1032A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190489 | |||||||
| chr3:108190507 | C | T | 1 | a0001c0001t0006g0152 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.777+1014G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190507 | |||||||
| chr3:108190615 | T | C | 5 | a0001c0001t0003g0150 a0001c0001t0006g0151 a0001c0001t0006g0152 others(2): Show |
5 | HG02647.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.777+906A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190615 | |||||||
| chr3:108190913 | C | T | 4 | a0001c0001t0002g0073 a0001c0001t0002g0129 a0001c0007t0002g0130 others(1): Show |
4 | HG01192.hp1 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.777+608G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190913 | |||||||
| chr3:108190941 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.777+580A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108190941 | |||||||
| chr3:108191093 | C | T | 22 | a0001c0001t0001g0234 a0001c0001t0001g0251 a0001c0001t0005g0028 others(19): Show |
25 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.777+428G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108191093 | |||||||
| chr3:108191228 | A | G | 4 | a0001c0003t0001g0003 a0001c0003t0001g0221 a0001c0003t0001g0225 others(1): Show |
7 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.777+293T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108191228 | |||||||
| chr3:108191457 | CT | C | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0009g0216 |
3 | HG02683.hp2 HG04199.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.777+63delA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108191457 | |||||||
| chr3:108191480 | C | CTT | 35 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(32): Show |
36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.777+39_777+40dupAA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 6/10 | chr3 | 108191480 | |||||||
| chr3:108191844 | A | T | 1 | a0001c0001t0005g0250 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.655-201T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108191844 | |||||||
| chr3:108191910 | A | T | 1 | a0001c0001t0005g0237 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.655-267T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108191910 | |||||||
| chr3:108192045 | G | A | 1 | a0001c0001t0003g0262 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.655-402C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192045 | |||||||
| chr3:108192125 | T | C | 2 | a0001c0001t0010g0148 a0001c0001t0010g0149 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.655-482A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192125 | |||||||
| chr3:108192137 | A | G | 1 | a0001c0001t0001g0007 | 3 | NA18947.hp1 NA18988.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.655-494T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192137 | |||||||
| chr3:108192174 | CA | C | 238 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(235): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.655-532delT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192174 | |||||||
| chr3:108192174 | CAA | C | 9 | a0001c0001t0001g0171 a0001c0001t0001g0201 a0001c0001t0002g0079 others(6): Show |
9 | HG01099.hp2 HG01167.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.655-533_655-532del others(2): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192174 | |||||||
| chr3:108192196 | A | G | 2 | a0001c0001t0010g0148 a0001c0001t0010g0149 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.655-553T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192196 | |||||||
| chr3:108192197 | G | A | 2 | a0001c0001t0010g0148 a0001c0001t0010g0149 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.655-554C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192197 | |||||||
| chr3:108192197 | G | GA | 36 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(33): Show |
37 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.655-555_655-554ins others(1): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192197 | |||||||
| chr3:108192199 | G | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-556C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192199 | |||||||
| chr3:108192255 | T | C | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.655-612A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192255 | |||||||
| chr3:108192317 | AATTT | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-678_655-675del others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192317 | |||||||
| chr3:108192336 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-693G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192336 | |||||||
| chr3:108192351 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-708G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192351 | |||||||
| chr3:108192352 | G | A | 2 | a0001c0005t0006g0021 a0001c0005t0006g0156 |
3 | HG02717.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.655-709C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192352 | |||||||
| chr3:108192382 | T | A | 299 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(296): Show |
351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.655-739A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192382 | |||||||
| chr3:108192503 | T | C | 1 | a0001c0002t0004g0048 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.655-860A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192503 | |||||||
| chr3:108192537 | G | A | 198 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(195): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.655-894C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192537 | |||||||
| chr3:108192571 | T | G | 93 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0014 others(90): Show |
104 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.655-928A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192571 | |||||||
| chr3:108192676 | T | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-1033A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192676 | |||||||
| chr3:108192698 | T | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-1055A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192698 | |||||||
| chr3:108192761 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-1118G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192761 | |||||||
| chr3:108192812 | T | G | 1 | a0001c0001t0001g0208 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.655-1169A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192812 | |||||||
| chr3:108192823 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-1180T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192823 | |||||||
| chr3:108192847 | A | T | 1 | a0001c0001t0002g0105 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.655-1204T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192847 | |||||||
| chr3:108192892 | T | A | 1 | a0001c0001t0002g0018 | 2 | NA18971.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.655-1249A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192892 | |||||||
| chr3:108192908 | CT | C | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.655-1266delA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108192908 | |||||||
| chr3:108193042 | A | G | 2 | a0001c0001t0010g0148 a0001c0001t0010g0149 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.655-1399T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193042 | |||||||
| chr3:108193100 | C | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0179 a0001c0001t0001g0180 others(1): Show |
6 | HG02040.hp1 HG02074.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-1457G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193100 | |||||||
| chr3:108193118 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-1475A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193118 | |||||||
| chr3:108193361 | C | G | 39 | a0001c0001t0002g0126 a0001c0001t0010g0148 a0001c0001t0010g0149 others(36): Show |
40 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.655-1718G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193361 | |||||||
| chr3:108193504 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-1861G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193504 | |||||||
| chr3:108193518 | A | C | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.655-1875T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193518 | |||||||
| chr3:108193551 | C | T | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.655-1908G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193551 | |||||||
| chr3:108193588 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-1945A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193588 | |||||||
| chr3:108193641 | G | A | 1 | a0001c0001t0005g0238 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.655-1998C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193641 | |||||||
| chr3:108193827 | T | A | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.655-2184A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193827 | |||||||
| chr3:108193968 | G | T | 93 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0014 others(90): Show |
104 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.655-2325C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108193968 | |||||||
| chr3:108194212 | C | A | 22 | a0001c0001t0001g0234 a0001c0001t0001g0251 a0001c0001t0005g0028 others(19): Show |
25 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.655-2569G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108194212 | |||||||
| chr3:108194260 | A | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-2617T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108194260 | |||||||
| chr3:108194286 | C | T | 3 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0244 |
3 | HG02615.hp2 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.655-2643G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108194286 | |||||||
| chr3:108194438 | C | T | 2 | a0001c0003t0001g0225 a0001c0003t0001g0226 |
2 | HG02280.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.655-2795G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108194438 | |||||||
| chr3:108194477 | T | TA | 25 | a0001c0001t0001g0234 a0001c0001t0001g0251 a0001c0001t0005g0028 others(22): Show |
28 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.655-2835dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108194477 | |||||||
| chr3:108194477 | TAA | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-2836_655-2835d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108194477 | |||||||
| chr3:108194565 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.655-2922G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108194565 | |||||||
| chr3:108194620 | T | C | 1 | a0001c0001t0002g0117 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.655-2977A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108194620 | |||||||
| chr3:108195002 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-3359T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195002 | |||||||
| chr3:108195024 | G | A | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | HG00673.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.655-3381C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195024 | |||||||
| chr3:108195149 | A | G | 6 | a0001c0001t0001g0022 a0001c0001t0001g0158 a0001c0001t0001g0161 others(3): Show |
7 | HG01934.hp1 HG01978.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-3506T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195149 | |||||||
| chr3:108195196 | C | T | 2 | a0001c0001t0010g0148 a0001c0001t0010g0149 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.655-3553G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195196 | |||||||
| chr3:108195215 | C | T | 7 | a0001c0001t0001g0160 a0001c0001t0002g0134 a0001c0001t0002g0135 others(4): Show |
7 | HG00099.hp1 HG02257.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-3572G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195215 | |||||||
| chr3:108195278 | C | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.655-3635G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195278 | |||||||
| chr3:108195298 | G | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-3655C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195298 | |||||||
| chr3:108195358 | CT | C | 89 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0014 others(86): Show |
100 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.655-3716delA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195358 | |||||||
| chr3:108195394 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-3751A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195394 | |||||||
| chr3:108195466 | G | A | 22 | a0001c0001t0001g0234 a0001c0001t0001g0251 a0001c0001t0005g0028 others(19): Show |
25 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.655-3823C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195466 | |||||||
| chr3:108195547 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.655-3904A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195547 | |||||||
| chr3:108195827 | C | T | 2 | a0001c0001t0010g0148 a0001c0001t0010g0149 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.655-4184G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195827 | |||||||
| chr3:108195920 | T | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-4277A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195920 | |||||||
| chr3:108195947 | T | A | 1 | a0001c0002t0004g0049 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.655-4304A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195947 | |||||||
| chr3:108195994 | G | A | 4 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(1): Show |
4 | HG02622.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.655-4351C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108195994 | |||||||
| chr3:108196078 | T | C | 4 | a0001c0002t0007g0298 a0001c0002t0007g0299 a0001c0002t0007g0300 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.655-4435A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108196078 | |||||||
| chr3:108196164 | A | T | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-4521T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108196164 | |||||||
| chr3:108196258 | C | CACCCTCA others(6): Show |
38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-4628_655-4616d others(15): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108196258 | |||||||
| chr3:108196341 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.655-4698C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108196341 | |||||||
| chr3:108196350 | A | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-4707T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108196350 | |||||||
| chr3:108196374 | A | T | 1 | a0001c0001t0001g0159 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.655-4731T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108196374 | |||||||
| chr3:108196667 | T | G | 1 | a0001c0002t0004g0058 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.655-5024A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108196667 | |||||||
| chr3:108196709 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0194 others(2): Show |
9 | HG00621.hp2 NA18943.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.655-5066C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108196709 | |||||||
| chr3:108196848 | C | T | 1 | a0001c0001t0003g0268 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.655-5205G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108196848 | |||||||
| chr3:108196909 | T | C | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG02896.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.655-5266A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108196909 | |||||||
| chr3:108197108 | G | A | 1 | a0001c0001t0005g0250 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.655-5465C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197108 | |||||||
| chr3:108197211 | A | G | 41 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0121 others(38): Show |
42 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.655-5568T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197211 | |||||||
| chr3:108197279 | C | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.655-5636G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197279 | |||||||
| chr3:108197314 | G | A | 2 | a0001c0002t0004g0050 a0001c0002t0004g0061 |
2 | NA19005.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.655-5671C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197314 | |||||||
| chr3:108197341 | T | A | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.655-5698A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197341 | |||||||
| chr3:108197407 | C | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-5764G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197407 | |||||||
| chr3:108197415 | A | C | 1 | a0001c0001t0002g0087 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.655-5772T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197415 | |||||||
| chr3:108197419 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-5776G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197419 | |||||||
| chr3:108197483 | C | G | 3 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0244 |
3 | HG02615.hp2 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.655-5840G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197483 | |||||||
| chr3:108197570 | G | A | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.655-5927C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197570 | |||||||
| chr3:108197572 | T | C | 31 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(28): Show |
32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.655-5929A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197572 | |||||||
| chr3:108197778 | G | A | 4 | a0001c0001t0002g0073 a0001c0001t0002g0129 a0001c0007t0002g0130 others(1): Show |
4 | HG01192.hp1 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.655-6135C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197778 | |||||||
| chr3:108197900 | A | G | 2 | a0001c0001t0010g0148 a0001c0001t0010g0149 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.655-6257T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108197900 | |||||||
| chr3:108198072 | T | C | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.655-6429A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108198072 | |||||||
| chr3:108198078 | A | G | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.655-6435T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108198078 | |||||||
| chr3:108198156 | T | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-6513A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108198156 | |||||||
| chr3:108198385 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-6742G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108198385 | |||||||
| chr3:108198397 | T | C | 1 | a0001c0001t0002g0142 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.655-6754A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108198397 | |||||||
| chr3:108198471 | T | C | 1 | a0004c0010t0003g0242 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.655-6828A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108198471 | |||||||
| chr3:108198484 | C | G | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.655-6841G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108198484 | |||||||
| chr3:108198556 | C | T | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.655-6913G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108198556 | |||||||
| chr3:108198958 | A | AT | 31 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(28): Show |
32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.655-7316dupA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108198958 | |||||||
| chr3:108198977 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-7334A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108198977 | |||||||
| chr3:108199003 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.655-7360T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199003 | |||||||
| chr3:108199113 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.655-7470C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199113 | |||||||
| chr3:108199372 | T | C | 89 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0014 others(86): Show |
100 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.654+7256A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199372 | |||||||
| chr3:108199453 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.654+7175C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199453 | |||||||
| chr3:108199632 | T | C | 2 | a0001c0001t0002g0119 a0001c0001t0002g0120 |
2 | HG04184.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.654+6996A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199632 | |||||||
| chr3:108199683 | T | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0191 others(7): Show |
14 | HG00621.hp2 HG01516.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.654+6945A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199683 | |||||||
| chr3:108199787 | TTGGGTTT others(4): Show |
T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.654+6830_654+6840d others(13): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199787 | |||||||
| chr3:108199794 | T | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+6834A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199794 | |||||||
| chr3:108199799 | TGGG | T | 3 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0293 |
3 | NA19010.hp2 NA19056.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.654+6826_654+6828d others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199799 | |||||||
| chr3:108199830 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.654+6798C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199830 | |||||||
| chr3:108199901 | T | G | 1 | a0001c0001t0005g0252 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.654+6727A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199901 | |||||||
| chr3:108199931 | G | A | 1 | a0001c0001t0002g0121 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.654+6697C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108199931 | |||||||
| chr3:108200277 | A | T | 7 | a0001c0001t0002g0086 a0001c0001t0002g0094 a0001c0001t0002g0099 others(4): Show |
7 | HG01361.hp1 NA18957.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.654+6351T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200277 | |||||||
| chr3:108200293 | T | C | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.654+6335A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200293 | |||||||
| chr3:108200382 | C | T | 1 | a0001c0001t0005g0229 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.654+6246G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200382 | |||||||
| chr3:108200414 | A | G | 1 | a0001c0001t0002g0099 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.654+6214T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200414 | |||||||
| chr3:108200444 | G | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+6184C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200444 | |||||||
| chr3:108200501 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+6127A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200501 | |||||||
| chr3:108200556 | T | C | 1 | a0001c0001t0003g0070 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.654+6072A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200556 | |||||||
| chr3:108200633 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+5995G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200633 | |||||||
| chr3:108200693 | A | T | 4 | a0001c0002t0007g0298 a0001c0002t0007g0299 a0001c0002t0007g0300 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.654+5935T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200693 | |||||||
| chr3:108200731 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+5897T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200731 | |||||||
| chr3:108200738 | T | C | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.654+5890A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200738 | |||||||
| chr3:108200768 | T | C | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.654+5860A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200768 | |||||||
| chr3:108200921 | G | C | 1 | a0001c0001t0002g0122 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.654+5707C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200921 | |||||||
| chr3:108200925 | G | A | 7 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(4): Show |
7 | HG01069.hp2 HG01071.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+5703C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108200925 | |||||||
| chr3:108201014 | C | T | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.654+5614G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108201014 | |||||||
| chr3:108201083 | C | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+5545G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108201083 | |||||||
| chr3:108201156 | G | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.654+5472C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108201156 | |||||||
| chr3:108201274 | C | T | 2 | a0001c0001t0005g0036 a0001c0001t0005g0037 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.654+5354G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108201274 | |||||||
| chr3:108201292 | C | T | 2 | a0001c0001t0003g0032 a0001c0001t0003g0267 |
3 | NA18951.hp1 NA18968.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.654+5336G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108201292 | |||||||
| chr3:108201772 | T | C | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+4856A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108201772 | |||||||
| chr3:108201973 | T | C | 1 | a0001c0007t0002g0131 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.654+4655A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108201973 | |||||||
| chr3:108202076 | G | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+4552C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202076 | |||||||
| chr3:108202091 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+4537A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202091 | |||||||
| chr3:108202096 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+4532A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202096 | |||||||
| chr3:108202132 | T | C | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.654+4496A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202132 | |||||||
| chr3:108202158 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.654+4470G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202158 | |||||||
| chr3:108202233 | G | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+4395C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202233 | |||||||
| chr3:108202241 | G | A | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.654+4387C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202241 | |||||||
| chr3:108202404 | C | T | 4 | a0001c0001t0001g0197 a0001c0001t0001g0222 a0001c0001t0001g0224 others(1): Show |
4 | HG00280.hp2 HG02451.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+4224G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202404 | |||||||
| chr3:108202454 | C | G | 3 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 |
3 | HG02257.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.654+4174G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202454 | |||||||
| chr3:108202590 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+4038A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202590 | |||||||
| chr3:108202869 | G | A | 2 | a0001c0001t0010g0148 a0001c0001t0010g0149 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.654+3759C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202869 | |||||||
| chr3:108202944 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.654+3684G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108202944 | |||||||
| chr3:108203008 | G | A | 33 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(30): Show |
34 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.654+3620C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203008 | |||||||
| chr3:108203015 | T | C | 34 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(31): Show |
35 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.654+3613A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203015 | |||||||
| chr3:108203269 | C | T | 22 | a0001c0001t0001g0234 a0001c0001t0001g0251 a0001c0001t0005g0028 others(19): Show |
25 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.654+3359G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203269 | |||||||
| chr3:108203320 | T | C | 1 | a0001c0001t0003g0281 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.654+3308A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203320 | |||||||
| chr3:108203425 | A | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+3203T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203425 | |||||||
| chr3:108203563 | TGTCA | T | 31 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(28): Show |
32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.654+3061_654+3064d others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203563 | |||||||
| chr3:108203613 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.654+3015T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203613 | |||||||
| chr3:108203660 | T | C | 2 | a0001c0005t0006g0021 a0001c0005t0006g0156 |
3 | HG02717.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.654+2968A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203660 | |||||||
| chr3:108203716 | T | G | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.654+2912A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203716 | |||||||
| chr3:108203724 | A | G | 35 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(32): Show |
36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.654+2904T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203724 | |||||||
| chr3:108203852 | T | A | 4 | a0001c0002t0007g0298 a0001c0002t0007g0299 a0001c0002t0007g0300 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.654+2776A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203852 | |||||||
| chr3:108203887 | G | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+2741C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203887 | |||||||
| chr3:108203960 | T | C | 1 | a0001c0001t0002g0123 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.654+2668A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108203960 | |||||||
| chr3:108204008 | A | G | 1 | a0001c0002t0007g0298 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.654+2620T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108204008 | |||||||
| chr3:108204313 | AGTTAT | A | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.654+2310_654+2314d others(7): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108204313 | |||||||
| chr3:108204404 | G | A | 31 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(28): Show |
32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.654+2224C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108204404 | |||||||
| chr3:108204440 | T | C | 2 | a0001c0001t0010g0148 a0001c0001t0010g0149 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.654+2188A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108204440 | |||||||
| chr3:108204444 | C | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+2184G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108204444 | |||||||
| chr3:108204486 | C | A | 1 | a0001c0001t0001g0027 | 2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.654+2142G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108204486 | |||||||
| chr3:108204685 | T | G | 1 | a0004c0010t0003g0242 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.654+1943A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108204685 | |||||||
| chr3:108204749 | T | C | 2 | a0001c0001t0003g0282 a0001c0001t0003g0283 |
2 | HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.654+1879A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108204749 | |||||||
| chr3:108204853 | A | G | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.654+1775T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108204853 | |||||||
| chr3:108204893 | C | G | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.654+1735G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108204893 | |||||||
| chr3:108205254 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+1374T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205254 | |||||||
| chr3:108205303 | T | C | 1 | a0001c0002t0004g0059 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.654+1325A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205303 | |||||||
| chr3:108205372 | G | GT | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+1255dupA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205372 | |||||||
| chr3:108205386 | A | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+1242T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205386 | |||||||
| chr3:108205415 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+1213T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205415 | |||||||
| chr3:108205417 | C | T | 1 | a0001c0001t0002g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.654+1211G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205417 | |||||||
| chr3:108205493 | T | C | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.654+1135A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205493 | |||||||
| chr3:108205495 | T | A | 291 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(288): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.654+1133A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205495 | |||||||
| chr3:108205650 | GAGGATTC others(5): Show |
G | 4 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0144 others(1): Show |
4 | NA18972.hp1 NA18995.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+966_654+977del others(12): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205650 | |||||||
| chr3:108205677 | A | T | 1 | a0001c0001t0001g0211 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.654+951T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205677 | |||||||
| chr3:108205678 | AGGACTAA others(378): Show |
A | 1 | a0001c0001t0001g0211 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.654+565_654+949del | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205678 | |||||||
| chr3:108205802 | ATAT | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+823_654+825del others(3): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205802 | |||||||
| chr3:108205808 | T | C | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.654+820A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205808 | |||||||
| chr3:108205811 | CAT | C | 6 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0241 others(3): Show |
6 | HG02145.hp2 HG02895.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+815_654+816del others(2): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205811 | |||||||
| chr3:108205814 | ATTATATA others(4): Show |
A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+803_654+813del others(11): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205814 | |||||||
| chr3:108205836 | TTTAA | T | 25 | a0001c0001t0001g0234 a0001c0001t0001g0251 a0001c0001t0005g0028 others(22): Show |
28 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.654+788_654+791del others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205836 | |||||||
| chr3:108205910 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.654+718A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205910 | |||||||
| chr3:108205942 | TA | T | 79 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0014 others(76): Show |
90 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.654+685delT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205942 | |||||||
| chr3:108205946 | T | TTATAATA others(23): Show |
6 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(3): Show |
6 | HG00642.hp1 HG01515.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.654+652_654+681dup others(30): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205946 | |||||||
| chr3:108205946 | T | TTATAATA others(53): Show |
1 | a0001c0001t0003g0009 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.654+681_654+682ins others(60): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205946 | |||||||
| chr3:108205954 | TATAA | T | 25 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0158 others(22): Show |
28 | HG00099.hp1 HG00741.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.654+670_654+673del others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205954 | |||||||
| chr3:108205956 | TA | T | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+671delT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205956 | |||||||
| chr3:108205957 | A | AAATATAT others(22): Show |
1 | a0001c0001t0003g0264 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.654+642_654+670dup others(29): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205957 | |||||||
| chr3:108205963 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+665T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205963 | |||||||
| chr3:108205966 | ATATAT | A | 34 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(31): Show |
35 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.654+657_654+661del others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205966 | |||||||
| chr3:108205966 | ATATATTT others(25): Show |
A | 1 | a0001c0002t0004g0051 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.654+630_654+661del others(32): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205966 | |||||||
| chr3:108205972 | T | A | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.654+656A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205972 | |||||||
| chr3:108205976 | A | T | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.654+652T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205976 | |||||||
| chr3:108205977 | T | A | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.654+651A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205977 | |||||||
| chr3:108205978 | A | T | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.654+650T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205978 | |||||||
| chr3:108205980 | A | T | 35 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(32): Show |
36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.654+648T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205980 | |||||||
| chr3:108205983 | A | T | 34 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(31): Show |
35 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.654+645T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205983 | |||||||
| chr3:108205986 | TA | T | 34 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(31): Show |
35 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.654+641delT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205986 | |||||||
| chr3:108205994 | T | TAA | 35 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(32): Show |
36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.654+633_654+634ins others(2): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205994 | |||||||
| chr3:108205994 | T | TTA | 108 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.654+632_654+633dup others(2): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205994 | |||||||
| chr3:108205998 | G | A | 35 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(32): Show |
36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.654+630C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108205998 | |||||||
| chr3:108206004 | T | A | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.654+624A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206004 | |||||||
| chr3:108206009 | C | T | 1 | a0001c0002t0004g0051 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.654+619G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206009 | |||||||
| chr3:108206013 | TATATA | T | 34 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(31): Show |
35 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.654+610_654+614del others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206013 | |||||||
| chr3:108206026 | G | A | 35 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(32): Show |
36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.654+602C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206026 | |||||||
| chr3:108206028 | ATAT | A | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+597_654+599del others(3): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206028 | |||||||
| chr3:108206029 | T | A | 1 | a0001c0002t0004g0051 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.654+599A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206029 | |||||||
| chr3:108206034 | T | C | 1 | a0001c0002t0004g0051 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.654+594A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206034 | |||||||
| chr3:108206035 | TTATAA | T | 34 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(31): Show |
35 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.654+588_654+592del others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206035 | |||||||
| chr3:108206046 | ATT | A | 8 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(5): Show |
10 | NA18939.hp1 NA18945.hp2 NA18971.hp2 others(7): Show |
intron_variant | MODIFIER | c.654+580_654+581del others(2): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206046 | |||||||
| chr3:108206048 | T | A | 34 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(31): Show |
35 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.654+580A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206048 | |||||||
| chr3:108206057 | TTTATATA others(3): Show |
T | 34 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(31): Show |
35 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.654+561_654+570del others(10): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206057 | |||||||
| chr3:108206067 | A | T | 1 | a0001c0002t0004g0051 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.654+561T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206067 | |||||||
| chr3:108206068 | T | A | 35 | a0001c0001t0001g0211 a0001c0002t0004g0013 a0001c0002t0004g0038 others(32): Show |
36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.654+560A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206068 | |||||||
| chr3:108206068 | TA | T | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0185 others(11): Show |
18 | HG00621.hp2 HG00735.hp1 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.654+559delT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206068 | |||||||
| chr3:108206069 | A | T | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.654+559T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206069 | |||||||
| chr3:108206069 | AATATATT | A | 4 | a0001c0001t0002g0018 a0001c0001t0002g0140 a0001c0001t0002g0141 others(1): Show |
5 | NA18971.hp1 NA18979.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.654+552_654+558del others(7): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206069 | |||||||
| chr3:108206072 | A | T | 1 | a0001c0001t0001g0211 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.654+556T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206072 | |||||||
| chr3:108206075 | T | A | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.654+553A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206075 | |||||||
| chr3:108206076 | T | A | 1 | a0001c0001t0001g0211 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.654+552A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206076 | |||||||
| chr3:108206111 | A | T | 1 | a0001c0001t0003g0292 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.654+517T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206111 | |||||||
| chr3:108206125 | A | AAT | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+501_654+502dup others(2): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206125 | |||||||
| chr3:108206147 | T | A | 6 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0241 others(3): Show |
6 | HG02145.hp2 HG02895.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+481A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206147 | |||||||
| chr3:108206316 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.654+312C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206316 | |||||||
| chr3:108206361 | T | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+267A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206361 | |||||||
| chr3:108206419 | A | G | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.654+209T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206419 | |||||||
| chr3:108206476 | A | G | 1 | a0001c0001t0003g0253 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.654+152T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206476 | |||||||
| chr3:108206507 | A | G | 1 | a0001c0001t0003g0246 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.654+121T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206507 | |||||||
| chr3:108206545 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.654+83G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206545 | |||||||
| chr3:108206549 | G | A | 89 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0014 others(86): Show |
100 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.654+79C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206549 | |||||||
| chr3:108206601 | G | A | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.654+27C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 5/10 | chr3 | 108206601 | |||||||
| chr3:108206839 | G | A | 159 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(156): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.586-143C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108206839 | |||||||
| chr3:108206962 | G | C | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.586-266C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108206962 | |||||||
| chr3:108207147 | A | G | 6 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0241 others(3): Show |
6 | HG02145.hp2 HG02895.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.586-451T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207147 | |||||||
| chr3:108207250 | A | G | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.586-554T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207250 | |||||||
| chr3:108207253 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.586-557C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207253 | |||||||
| chr3:108207279 | T | A | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.586-583A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207279 | |||||||
| chr3:108207298 | T | A | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.586-602A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207298 | |||||||
| chr3:108207379 | TC | T | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG03130.hp2 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.586-684delG | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207379 | |||||||
| chr3:108207411 | C | T | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.586-715G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207411 | |||||||
| chr3:108207415 | T | C | 2 | a0001c0001t0010g0148 a0001c0001t0010g0149 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.586-719A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207415 | |||||||
| chr3:108207493 | C | T | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.586-797G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207493 | |||||||
| chr3:108207570 | T | C | 3 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG00099.hp2 HG00738.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.586-874A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207570 | |||||||
| chr3:108207671 | C | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.586-975G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207671 | |||||||
| chr3:108207781 | C | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.586-1085G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207781 | |||||||
| chr3:108207912 | G | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.586-1216C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207912 | |||||||
| chr3:108207936 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.586-1240C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207936 | |||||||
| chr3:108207974 | C | T | 4 | a0001c0001t0003g0157 a0001c0001t0003g0264 a0001c0001t0003g0265 others(1): Show |
4 | HG02486.hp1 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-1278G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108207974 | |||||||
| chr3:108208038 | G | A | 1 | a0001c0003t0001g0226 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.586-1342C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208038 | |||||||
| chr3:108208047 | G | GA | 47 | a0001c0001t0001g0168 a0001c0001t0003g0001 a0001c0001t0003g0002 others(44): Show |
68 | HG00642.hp1 HG01256.hp1 HG01258.hp2 others(65): Show |
intron_variant | MODIFIER | c.586-1352dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208047 | |||||||
| chr3:108208047 | GA | G | 39 | a0001c0001t0002g0094 a0001c0001t0010g0148 a0001c0001t0010g0149 others(36): Show |
40 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.586-1352delT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208047 | |||||||
| chr3:108208163 | G | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0178 |
3 | HG01099.hp1 HG01109.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.586-1467C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208163 | |||||||
| chr3:108208170 | T | C | 4 | a0001c0002t0007g0298 a0001c0002t0007g0299 a0001c0002t0007g0300 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.586-1474A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208170 | |||||||
| chr3:108208277 | T | A | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.586-1581A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208277 | |||||||
| chr3:108208307 | C | T | 1 | a0001c0001t0003g0256 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.586-1611G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208307 | |||||||
| chr3:108208397 | T | C | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.586-1701A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208397 | |||||||
| chr3:108208421 | T | C | 38 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.586-1725A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208421 | |||||||
| chr3:108208442 | C | T | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.586-1746G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208442 | |||||||
| chr3:108208573 | T | C | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.586-1877A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208573 | |||||||
| chr3:108208653 | G | A | 4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-1957C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208653 | |||||||
| chr3:108208747 | C | G | 1 | a0001c0001t0002g0092 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.586-2051G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208747 | |||||||
| chr3:108208793 | A | G | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.586-2097T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208793 | |||||||
| chr3:108208794 | A | C | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.586-2098T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208794 | |||||||
| chr3:108208913 | C | G | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.586-2217G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108208913 | |||||||
| chr3:108209178 | G | A | 1 | a0001c0001t0002g0124 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.586-2482C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209178 | |||||||
| chr3:108209183 | T | C | 1 | a0001c0001t0003g0012 | 3 | NA18941.hp2 NA19007.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.586-2487A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209183 | |||||||
| chr3:108209193 | T | C | 39 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0001t0013g0243 others(36): Show |
40 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.586-2497A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209193 | |||||||
| chr3:108209288 | T | G | 1 | a0001c0001t0014g0240 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.586-2592A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209288 | |||||||
| chr3:108209477 | G | A | 2 | a0001c0001t0002g0090 a0001c0001t0002g0125 |
2 | HG00642.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.586-2781C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209477 | |||||||
| chr3:108209566 | T | C | 4 | a0001c0001t0002g0005 a0001c0001t0002g0126 a0001c0001t0002g0127 others(1): Show |
6 | HG00558.hp2 HG01496.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.586-2870A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209566 | |||||||
| chr3:108209585 | G | A | 1 | a0001c0001t0003g0284 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.586-2889C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209585 | |||||||
| chr3:108209593 | A | G | 1 | a0001c0002t0004g0040 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.586-2897T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209593 | |||||||
| chr3:108209649 | T | C | 1 | a0001c0001t0003g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.586-2953A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209649 | |||||||
| chr3:108209710 | C | T | 25 | a0001c0001t0001g0234 a0001c0001t0001g0251 a0001c0001t0005g0028 others(22): Show |
28 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.586-3014G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209710 | |||||||
| chr3:108209715 | T | C | 1 | a0001c0002t0004g0044 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.586-3019A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209715 | |||||||
| chr3:108209725 | A | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG01192.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.586-3029T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209725 | |||||||
| chr3:108209823 | T | C | 4 | a0001c0002t0007g0298 a0001c0002t0007g0299 a0001c0002t0007g0300 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.586-3127A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209823 | |||||||
| chr3:108209916 | A | ATG | 81 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
96 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.586-3222_586-3221d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209916 | |||||||
| chr3:108209916 | A | ATGTG | 32 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(29): Show |
33 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.586-3224_586-3221d others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209916 | |||||||
| chr3:108209916 | A | ATGTGTG | 4 | a0001c0002t0004g0040 a0001c0002t0004g0062 a0001c0002t0004g0063 others(1): Show |
4 | HG00738.hp2 HG01106.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-3226_586-3221d others(8): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209916 | |||||||
| chr3:108209916 | ATG | A | 7 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0007g0298 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.586-3222_586-3221d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108209916 | |||||||
| chr3:108210061 | T | C | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.586-3365A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210061 | |||||||
| chr3:108210073 | G | T | 1 | a0001c0003t0001g0225 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.586-3377C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210073 | |||||||
| chr3:108210187 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.586-3491G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210187 | |||||||
| chr3:108210194 | C | T | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.586-3498G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210194 | |||||||
| chr3:108210246 | G | A | 6 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0241 others(3): Show |
6 | HG02145.hp2 HG02895.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.586-3550C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210246 | |||||||
| chr3:108210255 | C | G | 79 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0014 others(76): Show |
90 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.586-3559G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210255 | |||||||
| chr3:108210293 | C | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.586-3597G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210293 | |||||||
| chr3:108210299 | G | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.586-3603C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210299 | |||||||
| chr3:108210304 | T | C | 1 | a0001c0001t0002g0132 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.586-3608A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210304 | |||||||
| chr3:108210332 | C | CT | 11 | a0001c0001t0002g0083 a0001c0001t0002g0087 a0001c0001t0002g0088 others(8): Show |
11 | HG00408.hp1 HG00642.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.585+3598dupA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210332 | |||||||
| chr3:108210332 | C | CTT | 22 | a0001c0001t0001g0234 a0001c0001t0001g0251 a0001c0001t0005g0028 others(19): Show |
25 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.585+3597_585+3598d others(4): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210332 | |||||||
| chr3:108210332 | C | CTTTTTTT | 22 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(19): Show |
23 | HG00408.hp2 HG00738.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.585+3592_585+3598d others(9): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210332 | |||||||
| chr3:108210332 | C | CTTTTTTT others(1): Show |
7 | a0001c0002t0004g0041 a0001c0002t0004g0045 a0001c0002t0004g0046 others(4): Show |
7 | HG00558.hp1 HG00673.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.585+3591_585+3598d others(10): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210332 | |||||||
| chr3:108210332 | C | CTTTTTTT others(3): Show |
4 | a0001c0002t0007g0298 a0001c0002t0007g0299 a0001c0002t0007g0300 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.585+3589_585+3598d others(12): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210332 | |||||||
| chr3:108210332 | CT | C | 81 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
96 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.585+3598delA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210332 | |||||||
| chr3:108210381 | C | T | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.585+3550G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210381 | |||||||
| chr3:108210418 | C | T | 6 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0241 others(3): Show |
6 | HG02145.hp2 HG02895.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+3513G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210418 | |||||||
| chr3:108210438 | G | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+3493C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210438 | |||||||
| chr3:108210492 | CCTGT | C | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+3435_585+3438d others(6): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210492 | |||||||
| chr3:108210671 | A | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0179 a0001c0001t0001g0180 others(1): Show |
6 | HG02040.hp1 HG02074.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+3260T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210671 | |||||||
| chr3:108210741 | A | T | 2 | a0001c0001t0010g0148 a0001c0001t0010g0149 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.585+3190T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210741 | |||||||
| chr3:108210852 | G | A | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+3079C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210852 | |||||||
| chr3:108210960 | C | A | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.585+2971G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210960 | |||||||
| chr3:108210974 | C | A | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.585+2957G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108210974 | |||||||
| chr3:108211158 | C | T | 197 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(194): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.585+2773G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108211158 | |||||||
| chr3:108211295 | G | A | 2 | a0001c0001t0010g0148 a0001c0001t0010g0149 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.585+2636C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108211295 | |||||||
| chr3:108211362 | C | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+2569G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108211362 | |||||||
| chr3:108211363 | G | T | 22 | a0001c0001t0001g0234 a0001c0001t0001g0251 a0001c0001t0005g0028 others(19): Show |
25 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.585+2568C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108211363 | |||||||
| chr3:108211514 | T | C | 1 | a0001c0003t0001g0221 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.585+2417A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108211514 | |||||||
| chr3:108211631 | T | A | 1 | a0001c0001t0003g0071 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.585+2300A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108211631 | |||||||
| chr3:108211666 | C | T | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.585+2265G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108211666 | |||||||
| chr3:108211731 | T | A | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.585+2200A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108211731 | |||||||
| chr3:108212050 | A | G | 1 | a0001c0001t0002g0086 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.585+1881T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212050 | |||||||
| chr3:108212177 | T | G | 1 | a0001c0001t0006g0154 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.585+1754A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212177 | |||||||
| chr3:108212239 | T | A | 3 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0246 |
3 | HG02145.hp2 HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.585+1692A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212239 | |||||||
| chr3:108212243 | T | C | 2 | a0001c0001t0006g0151 a0001c0001t0006g0152 |
2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.585+1688A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212243 | |||||||
| chr3:108212331 | C | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+1600G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212331 | |||||||
| chr3:108212385 | A | G | 4 | a0001c0001t0002g0075 a0001c0001t0002g0083 a0001c0001t0002g0084 others(1): Show |
4 | HG00673.hp2 NA18995.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.585+1546T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212385 | |||||||
| chr3:108212524 | A | G | 1 | a0001c0001t0002g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.585+1407T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212524 | |||||||
| chr3:108212592 | TA | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+1338delT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212592 | |||||||
| chr3:108212727 | T | C | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+1204A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212727 | |||||||
| chr3:108212774 | C | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0179 a0001c0001t0001g0180 others(1): Show |
6 | HG02040.hp1 HG02074.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+1157G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212774 | |||||||
| chr3:108212832 | A | T | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.585+1099T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212832 | |||||||
| chr3:108212886 | T | C | 4 | a0001c0001t0002g0018 a0001c0001t0002g0140 a0001c0001t0002g0141 others(1): Show |
5 | NA18971.hp1 NA18979.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.585+1045A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108212886 | |||||||
| chr3:108213036 | T | C | 10 | a0001c0002t0004g0040 a0001c0002t0004g0041 a0001c0002t0004g0043 others(7): Show |
10 | HG00738.hp2 HG01070.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.585+895A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213036 | |||||||
| chr3:108213063 | G | T | 1 | a0001c0001t0003g0254 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.585+868C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213063 | |||||||
| chr3:108213066 | T | G | 5 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(2): Show |
6 | HG00741.hp2 HG01099.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+865A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213066 | |||||||
| chr3:108213130 | G | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+801C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213130 | |||||||
| chr3:108213153 | A | G | 1 | a0001c0001t0003g0253 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.585+778T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213153 | |||||||
| chr3:108213185 | G | A | 1 | a0001c0001t0005g0245 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.585+746C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213185 | |||||||
| chr3:108213294 | G | GT | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+636dupA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213294 | |||||||
| chr3:108213298 | G | T | 196 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(193): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.585+633C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213298 | |||||||
| chr3:108213310 | A | G | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+621T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213310 | |||||||
| chr3:108213333 | A | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+598T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213333 | |||||||
| chr3:108213458 | T | G | 197 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(194): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.585+473A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213458 | |||||||
| chr3:108213571 | C | T | 4 | a0001c0002t0007g0298 a0001c0002t0007g0299 a0001c0002t0007g0300 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.585+360G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213571 | |||||||
| chr3:108213573 | T | C | 2 | a0001c0001t0002g0074 a0001c0001t0002g0143 |
2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.585+358A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213573 | |||||||
| chr3:108213774 | G | A | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.585+157C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213774 | |||||||
| chr3:108213890 | C | A | 4 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(1): Show |
4 | HG01109.hp2 HG01433.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.585+41G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 4/10 | chr3 | 108213890 | |||||||
| chr3:108214292 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.495-271A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214292 | |||||||
| chr3:108214323 | C | T | 1 | a0001c0001t0005g0036 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.495-302G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214323 | |||||||
| chr3:108214483 | G | T | 2 | a0001c0001t0005g0036 a0001c0001t0005g0037 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.495-462C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214483 | |||||||
| chr3:108214503 | C | T | 1 | a0001c0001t0006g0151 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.495-482G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214503 | |||||||
| chr3:108214586 | A | G | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-565T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214586 | |||||||
| chr3:108214606 | A | G | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.495-585T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214606 | |||||||
| chr3:108214620 | T | C | 2 | a0001c0001t0010g0148 a0001c0001t0010g0149 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.495-599A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214620 | |||||||
| chr3:108214630 | T | C | 1 | a0001c0009t0006g0155 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.495-609A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214630 | |||||||
| chr3:108214751 | A | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-730T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214751 | |||||||
| chr3:108214756 | A | AC | 5 | a0001c0001t0002g0014 a0001c0001t0002g0079 a0001c0001t0002g0080 others(2): Show |
6 | HG02523.hp2 NA18953.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.495-736_495-735ins others(1): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214756 | |||||||
| chr3:108214757 | A | C | 5 | a0001c0001t0002g0014 a0001c0001t0002g0079 a0001c0001t0002g0080 others(2): Show |
6 | HG02523.hp2 NA18953.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.495-736T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214757 | |||||||
| chr3:108214765 | T | A | 1 | a0001c0001t0001g0222 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.495-744A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214765 | |||||||
| chr3:108214946 | A | G | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-925T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108214946 | |||||||
| chr3:108215199 | A | G | 4 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(1): Show |
4 | HG02622.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.495-1178T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215199 | |||||||
| chr3:108215213 | AT | A | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-1193delA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215213 | |||||||
| chr3:108215267 | A | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-1246T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215267 | |||||||
| chr3:108215356 | G | A | 1 | a0001c0012t0015g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.495-1335C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215356 | |||||||
| chr3:108215455 | C | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-1434G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215455 | |||||||
| chr3:108215514 | G | A | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-1493C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215514 | |||||||
| chr3:108215543 | C | T | 2 | a0001c0001t0006g0151 a0001c0001t0006g0152 |
2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.495-1522G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215543 | |||||||
| chr3:108215565 | G | A | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-1544C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215565 | |||||||
| chr3:108215567 | T | TA | 5 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0246 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.495-1547dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215567 | |||||||
| chr3:108215610 | A | G | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-1589T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215610 | |||||||
| chr3:108215622 | AATC | A | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-1604_495-1602d others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215622 | |||||||
| chr3:108215627 | T | C | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-1606A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215627 | |||||||
| chr3:108215663 | G | T | 4 | a0001c0002t0004g0041 a0001c0002t0004g0043 a0001c0002t0004g0044 others(1): Show |
4 | HG01070.hp2 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.495-1642C>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215663 | |||||||
| chr3:108215702 | T | A | 2 | a0001c0002t0004g0038 a0001c0002t0004g0067 |
2 | HG02129.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.495-1681A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215702 | |||||||
| chr3:108215739 | A | C | 2 | a0001c0001t0005g0247 a0001c0001t0005g0248 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.495-1718T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215739 | |||||||
| chr3:108215910 | C | T | 3 | a0001c0001t0002g0076 a0001c0001t0002g0077 a0001c0001t0002g0078 |
3 | HG01243.hp2 HG01934.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.495-1889G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215910 | |||||||
| chr3:108215915 | G | A | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.495-1894C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108215915 | |||||||
| chr3:108216039 | T | C | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-2018A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108216039 | |||||||
| chr3:108216131 | T | C | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.495-2110A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108216131 | |||||||
| chr3:108216253 | C | T | 1 | a0001c0002t0004g0040 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.495-2232G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108216253 | |||||||
| chr3:108216307 | A | G | 197 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(194): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.494+2228T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108216307 | |||||||
| chr3:108216351 | G | A | 196 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(193): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.494+2184C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108216351 | |||||||
| chr3:108216438 | G | A | 2 | a0001c0001t0005g0247 a0001c0001t0005g0248 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.494+2097C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108216438 | |||||||
| chr3:108216696 | T | C | 31 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(28): Show |
32 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.494+1839A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108216696 | |||||||
| chr3:108216704 | A | G | 1 | a0001c0001t0002g0019 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.494+1831T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108216704 | |||||||
| chr3:108216852 | A | G | 1 | a0001c0001t0002g0075 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.494+1683T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108216852 | |||||||
| chr3:108217288 | T | C | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.494+1247A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217288 | |||||||
| chr3:108217403 | C | T | 1 | a0001c0001t0003g0150 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.494+1132G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217403 | |||||||
| chr3:108217426 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.494+1109G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217426 | |||||||
| chr3:108217478 | T | G | 1 | a0001c0001t0002g0144 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.494+1057A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217478 | |||||||
| chr3:108217521 | A | G | 1 | a0001c0001t0002g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.494+1014T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217521 | |||||||
| chr3:108217648 | T | C | 1 | a0002c0006t0005g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.494+887A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217648 | |||||||
| chr3:108217671 | AAT | A | 3 | a0001c0001t0001g0224 a0001c0001t0005g0250 a0001c0001t0009g0223 |
3 | HG02698.hp1 HG03017.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.494+862_494+863del others(2): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217671 | |||||||
| chr3:108217711 | C | A | 197 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(194): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.494+824G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217711 | |||||||
| chr3:108217727 | T | TA | 34 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0040 others(31): Show |
35 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.494+807dupT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217727 | |||||||
| chr3:108217728 | A | T | 83 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(80): Show |
97 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.494+807T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217728 | |||||||
| chr3:108217769 | G | C | 1 | a0001c0001t0002g0019 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.494+766C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217769 | |||||||
| chr3:108217794 | G | A | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.494+741C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217794 | |||||||
| chr3:108217851 | T | C | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.494+684A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108217851 | |||||||
| chr3:108218003 | A | AAATAT | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.494+527_494+531dup others(5): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218003 | |||||||
| chr3:108218147 | T | G | 2 | a0001c0001t0001g0251 a0001c0001t0005g0252 |
2 | HG00280.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.494+388A>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218147 | |||||||
| chr3:108218233 | A | G | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.494+302T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218233 | |||||||
| chr3:108218241 | TA | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.494+293delT | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218241 | |||||||
| chr3:108218243 | A | T | 4 | a0001c0002t0007g0298 a0001c0002t0007g0299 a0001c0002t0007g0300 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+292T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218243 | |||||||
| chr3:108218318 | C | G | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.494+217G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218318 | |||||||
| chr3:108218318 | C | T | 1 | a0001c0001t0003g0150 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.494+217G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218318 | |||||||
| chr3:108218384 | T | C | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.494+151A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218384 | |||||||
| chr3:108218439 | A | G | 197 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(194): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.494+96T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218439 | |||||||
| chr3:108218455 | GTTCAATT others(42): Show |
G | 1 | a0001c0002t0004g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.494+31_494+79delTT others(47): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218455 | |||||||
| chr3:108218513 | C | T | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.494+22G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 3/10 | chr3 | 108218513 | |||||||
| chr3:108218697 | C | T | 25 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0158 others(22): Show |
28 | HG00099.hp1 HG00741.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.376-44G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108218697 | |||||||
| chr3:108218724 | G | A | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.376-71C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108218724 | |||||||
| chr3:108218755 | C | T | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.376-102G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108218755 | |||||||
| chr3:108219095 | G | A | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.375+315C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108219095 | |||||||
| chr3:108219106 | G | C | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.375+304C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108219106 | |||||||
| chr3:108219116 | A | AT | 158 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.375+293dupA | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108219116 | |||||||
| chr3:108219194 | T | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0009 others(42): Show |
66 | HG00423.hp1 HG00642.hp1 HG01256.hp1 others(63): Show |
intron_variant | MODIFIER | c.375+216A>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108219194 | |||||||
| chr3:108219195 | A | T | 2 | a0001c0001t0003g0227 a0001c0001t0003g0228 |
2 | HG02145.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.375+215T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108219195 | |||||||
| chr3:108219213 | A | G | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.375+197T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108219213 | |||||||
| chr3:108219364 | A | C | 4 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(1): Show |
4 | HG02622.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.375+46T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108219364 | |||||||
| chr3:108219393 | G | C | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.375+17C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 2/10 | chr3 | 108219393 | |||||||
| chr3:108219594 | T | C | 2 | a0001c0003t0001g0225 a0001c0003t0001g0226 |
2 | HG02280.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.213-22A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108219594 | |||||||
| chr3:108219696 | A | G | 1 | a0001c0001t0002g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.213-124T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108219696 | |||||||
| chr3:108219737 | C | A | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.213-165G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108219737 | |||||||
| chr3:108219737 | C | T | 84 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(81): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.213-165G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108219737 | |||||||
| chr3:108219965 | C | T | 4 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(1): Show |
4 | HG02622.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.213-393G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108219965 | |||||||
| chr3:108220025 | G | A | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.213-453C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108220025 | |||||||
| chr3:108220218 | A | T | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.213-646T>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108220218 | |||||||
| chr3:108220239 | A | C | 1 | a0001c0001t0003g0157 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.213-667T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108220239 | |||||||
| chr3:108220378 | C | G | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.213-806G>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108220378 | |||||||
| chr3:108220714 | A | AC | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.213-1143_213-1142i others(3): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108220714 | |||||||
| chr3:108220828 | T | C | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.213-1256A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108220828 | |||||||
| chr3:108220937 | A | C | 37 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0002t0004g0013 others(34): Show |
38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.212+1174T>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108220937 | |||||||
| chr3:108221184 | G | A | 1 | a0001c0001t0005g0287 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.212+927C>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221184 | |||||||
| chr3:108221245 | T | C | 2 | a0001c0001t0010g0148 a0001c0001t0010g0149 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.212+866A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221245 | |||||||
| chr3:108221287 | A | G | 35 | a0001c0002t0004g0013 a0001c0002t0004g0038 a0001c0002t0004g0039 others(32): Show |
36 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.212+824T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221287 | |||||||
| chr3:108221611 | A | G | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.212+500T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221611 | |||||||
| chr3:108221722 | A | AG | 291 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(288): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.212+388_212+389ins others(1): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221722 | |||||||
| chr3:108221759 | T | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG01106.hp2 HG02895.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.212+352A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221759 | |||||||
| chr3:108221768 | T | C | 1 | a0001c0001t0003g0292 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.212+343A>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221768 | |||||||
| chr3:108221789 | ATT | A | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.212+320_212+321del others(2): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221789 | |||||||
| chr3:108221926 | A | G | 1 | a0001c0001t0002g0293 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.212+185T>C | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221926 | |||||||
| chr3:108221927 | G | C | 1 | a0001c0001t0002g0293 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.212+184C>G | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221927 | |||||||
| chr3:108221934 | C | A | 1 | a0001c0001t0001g0294 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.212+177G>T | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108221934 | |||||||
| chr3:108222076 | C | T | 2 | a0001c0001t0005g0036 a0001c0001t0005g0037 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.212+35G>A | IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108222076 | |||||||
| chr3:108222077 | AGGCACCC others(17): Show |
A | 3 | a0001c0001t0003g0034 a0001c0001t0003g0295 a0001c0001t0003g0296 |
4 | HG02165.hp2 NA18747.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.212+10_212+33delGG others(22): Show |
IFT57 | ENSG00000114446.5 | transcript | ENST00000264538.4 | protein_coding | 1/10 | chr3 | 108222077 |