Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7289 |
| ensemblid | ENSG00000078246.17 |
| hgncid | 12425 |
| symbol | TULP3 |
| name | TUB like protein 3 |
| refseq_nuc | NM_003324.5 |
| refseq_prot | NP_003315.2 |
| ensembl_nuc | ENST00000448120.7 |
| ensembl_prot | ENSP00000410051.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 2890891 |
| end | 2941138 |
| strand | + |
| ver | v1.2 |
| region | chr12:2890891-2941138 |
| region5000 | chr12:2885891-2946138 |
| regionname0 | TULP3_chr12_2890891_2941138 |
| regionname5000 | TULP3_chr12_2885891_2946138 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 442 | 354 | 88 | 66 | 152 | 12 | 34 | 122 | TULP3_chr12_2885891_2946138 | TULP3 | MEASR others(437): Show |
chr12 | 2885891 | 2946138 |
| a0002 | 0/0 | 442 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | MEASR others(437): Show |
chr12 | 2885891 | 2946138 |
| a0003 | 0/0 | 442 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TULP3_chr12_2885891_2946138 | TULP3 | MEASR others(437): Show |
chr12 | 2885891 | 2946138 |
| a0004 | 0/0 | 442 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | MEASR others(437): Show |
chr12 | 2885891 | 2946138 |
| a0005 | 0/0 | 442 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | MEASR others(437): Show |
chr12 | 2885891 | 2946138 |
| a0006 | 0/0 | 442 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | MEASR others(437): Show |
chr12 | 2885891 | 2946138 |
| a0007 | 0/0 | 442 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | MEASR others(437): Show |
chr12 | 2885891 | 2946138 |
| a0008 | 0/0 | 442 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | MEASR others(437): Show |
chr12 | 2885891 | 2946138 |
| a0009 | 0/0 | 442 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | MEASR others(437): Show |
chr12 | 2885891 | 2946138 |
| a0010 | 0/0 | 442 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | MEASR others(437): Show |
chr12 | 2885891 | 2946138 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1326 | 265 | 71 | 49 | 112 | 7 | 24 | TULP3_chr12_2885891_2946138 | TULP3 | ATGGA others(1321): Show |
chr12 | 2885891 | 2946138 | ||
| a0001c0002 | 0/0 | 1326 | 85 | 15 | 16 | 39 | 5 | 10 | TULP3_chr12_2885891_2946138 | TULP3 | ATGGA others(1321): Show |
chr12 | 2885891 | 2946138 | ||
| a0001c0006 | 0/0 | 1326 | 2 | 2 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ATGGA others(1321): Show |
chr12 | 2885891 | 2946138 | ||
| a0001c0013 | 0/0 | 1326 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ATGGA others(1321): Show |
chr12 | 2885891 | 2946138 | ||
| a0001c0014 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ATGGA others(1321): Show |
chr12 | 2885891 | 2946138 | ||
| a0002c0003 | 0/0 | 1326 | 7 | 6 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ATGGA others(1321): Show |
chr12 | 2885891 | 2946138 | ||
| a0003c0004 | 0/0 | 1326 | 3 | 0 | 0 | 3 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ATGGA others(1321): Show |
chr12 | 2885891 | 2946138 | ||
| a0004c0005 | 0/0 | 1326 | 2 | 2 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ATGGA others(1321): Show |
chr12 | 2885891 | 2946138 | ||
| a0005c0010 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ATGGA others(1321): Show |
chr12 | 2885891 | 2946138 | ||
| a0006c0007 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ATGGA others(1321): Show |
chr12 | 2885891 | 2946138 | ||
| a0007c0008 | 0/0 | 1326 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ATGGA others(1321): Show |
chr12 | 2885891 | 2946138 | ||
| a0008c0012 | 0/0 | 1326 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ATGGA others(1321): Show |
chr12 | 2885891 | 2946138 | ||
| a0009c0011 | 0/0 | 1326 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ATGGA others(1321): Show |
chr12 | 2885891 | 2946138 | ||
| a0010c0009 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ATGGA others(1321): Show |
chr12 | 2885891 | 2946138 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3192 | 133 | 27 | 28 | 58 | 6 | 14 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3187): Show |
chr12 | 2885891 | 2946138 |
| a0001c0001t0002 | 0/1 | 3192 | 95 | 18 | 18 | 47 | 1 | 10 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3187): Show |
chr12 | 2885891 | 2946138 |
| a0001c0001t0004 | 0/0 | 3078 | 24 | 19 | 2 | 3 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3073): Show |
chr12 | 2885891 | 2946138 |
| a0001c0001t0007 | 1/0 | 3080 | 5 | 3 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3075): Show |
chr12 | 2885891 | 2946138 |
| a0001c0001t0011 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3187): Show |
chr12 | 2885891 | 2946138 |
| a0001c0001t0013 | 0/0 | 3078 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3073): Show |
chr12 | 2885891 | 2946138 |
| a0001c0001t0014 | 0/0 | 3080 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3075): Show |
chr12 | 2885891 | 2946138 |
| a0001c0001t0015 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3187): Show |
chr12 | 2885891 | 2946138 |
| a0001c0001t0016 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3187): Show |
chr12 | 2885891 | 2946138 |
| a0001c0001t0017 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3187): Show |
chr12 | 2885891 | 2946138 |
| a0001c0001t0018 | 0/0 | 3191 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3186): Show |
chr12 | 2885891 | 2946138 |
| a0001c0001t0021 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3187): Show |
chr12 | 2885891 | 2946138 |
| a0001c0002t0003 | 0/0 | 3077 | 64 | 4 | 11 | 36 | 4 | 9 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3072): Show |
chr12 | 2885891 | 2946138 |
| a0001c0002t0005 | 0/0 | 3076 | 9 | 5 | 1 | 2 | 1 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3071): Show |
chr12 | 2885891 | 2946138 |
| a0001c0002t0008 | 0/0 | 3077 | 5 | 0 | 4 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3072): Show |
chr12 | 2885891 | 2946138 |
| a0001c0002t0009 | 0/0 | 3078 | 3 | 3 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3073): Show |
chr12 | 2885891 | 2946138 |
| a0001c0002t0010 | 0/0 | 3078 | 3 | 3 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3073): Show |
chr12 | 2885891 | 2946138 |
| a0001c0002t0019 | 0/0 | 3036 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3031): Show |
chr12 | 2885891 | 2946138 |
| a0001c0006t0011 | 0/0 | 3192 | 2 | 2 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3187): Show |
chr12 | 2885891 | 2946138 |
| a0001c0013t0001 | 0/0 | 3192 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3187): Show |
chr12 | 2885891 | 2946138 |
| a0001c0014t0001 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3187): Show |
chr12 | 2885891 | 2946138 |
| a0002c0003t0006 | 0/0 | 3190 | 7 | 6 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3185): Show |
chr12 | 2885891 | 2946138 |
| a0003c0004t0003 | 0/0 | 3077 | 3 | 0 | 0 | 3 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3072): Show |
chr12 | 2885891 | 2946138 |
| a0004c0005t0012 | 0/0 | 3078 | 2 | 2 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3073): Show |
chr12 | 2885891 | 2946138 |
| a0005c0010t0002 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3187): Show |
chr12 | 2885891 | 2946138 |
| a0006c0007t0001 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3187): Show |
chr12 | 2885891 | 2946138 |
| a0007c0008t0002 | 0/0 | 3192 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3187): Show |
chr12 | 2885891 | 2946138 |
| a0008c0012t0003 | 0/0 | 3077 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3072): Show |
chr12 | 2885891 | 2946138 |
| a0009c0011t0020 | 0/0 | 3078 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3073): Show |
chr12 | 2885891 | 2946138 |
| a0010c0009t0001 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | ACTCT others(3187): Show |
chr12 | 2885891 | 2946138 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0010 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0007g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0007g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0007g0320 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0007g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0011g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0013g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0014g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0015g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0016g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0017g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0018g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0001t0021g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0002 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0005g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0008g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0008g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0008g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0008g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0009g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0009g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0009g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0010g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0010g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0010g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0002t0019g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0006t0011g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0006t0011g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0013t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0001c0014t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0002c0003t0006g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0002c0003t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0002c0003t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0002c0003t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0002c0003t0006g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0002c0003t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0002c0003t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0003c0004t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0003c0004t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0003c0004t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0004c0005t0012g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0004c0005t0012g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0005c0010t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0006c0007t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0007c0008t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0008c0012t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0009c0011t0020g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| a0010c0009t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0003 | g0002 | EUR | GBR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00099 | hp2 | a0001 | c0002 | t0003 | g0188 | EUR | GBR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0271 | EUR | GBR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0260 | EUR | GBR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00280 | hp1 | a0001 | c0002 | t0003 | g0192 | EUR | FIN | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0289 | EUR | FIN | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | CHS | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00423 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | CHS | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | CHS | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00438 | hp1 | a0001 | c0002 | t0003 | g0151 | EAS | CHS | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | CHS | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00558 | hp2 | a0005 | c0010 | t0002 | g0102 | EAS | CHS | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | CHS | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00597 | hp2 | a0006 | c0007 | t0001 | g0236 | EAS | CHS | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0357 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01069 | hp2 | a0001 | c0002 | t0008 | g0181 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01070 | hp1 | a0007 | c0008 | t0002 | g0091 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01071 | hp1 | a0001 | c0002 | t0008 | g0005 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0246 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0164 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01109 | hp1 | a0002 | c0003 | t0006 | g0136 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01168 | hp2 | a0001 | c0002 | t0003 | g0214 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01175 | hp1 | a0001 | c0002 | t0008 | g0161 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01175 | hp2 | a0001 | c0013 | t0001 | g0344 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01243 | hp2 | a0001 | c0002 | t0008 | g0205 | AMR | PUR | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | CLM | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | CLM | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0195 | AMR | CLM | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01257 | hp1 | a0001 | c0002 | t0003 | g0217 | AMR | CLM | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0356 | AMR | CLM | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0184 | AMR | CLM | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0131 | AMR | CLM | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | CLM | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0155 | AMR | CLM | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0178 | AMR | CLM | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01496 | hp1 | a0001 | c0002 | t0005 | g0143 | AMR | CLM | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | CLM | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01515 | hp1 | a0001 | c0002 | t0003 | g0216 | EUR | IBS | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | IBS | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01516 | hp1 | a0001 | c0002 | t0005 | g0187 | EUR | IBS | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0265 | EUR | IBS | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01891 | hp1 | a0002 | c0003 | t0006 | g0137 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PEL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01952 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0186 | AMR | PEL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG01993 | hp2 | a0001 | c0002 | t0003 | g0193 | AMR | PEL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | KHV | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02055 | hp1 | a0001 | c0001 | t0013 | g0097 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02071 | hp1 | a0001 | c0001 | t0016 | g0340 | EAS | KHV | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02071 | hp2 | a0001 | c0002 | t0003 | g0183 | EAS | KHV | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | KHV | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | KHV | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02132 | hp2 | a0001 | c0002 | t0003 | g0179 | EAS | KHV | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | KHV | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02135 | hp2 | a0001 | c0002 | t0003 | g0209 | EAS | KHV | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0133 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02148 | hp2 | a0001 | c0002 | t0003 | g0182 | AMR | PEL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | CDX | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0125 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0355 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0129 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PEL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02451 | hp1 | a0001 | c0002 | t0003 | g0148 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02523 | hp1 | a0001 | c0002 | t0003 | g0175 | EAS | KHV | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | KHV | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02615 | hp1 | a0001 | c0002 | t0005 | g0113 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02615 | hp2 | a0001 | c0001 | t0014 | g0315 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02622 | hp2 | a0002 | c0003 | t0006 | g0140 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02630 | hp1 | a0001 | c0002 | t0009 | g0006 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0349 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0111 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02683 | hp1 | a0001 | c0002 | t0003 | g0189 | SAS | PJL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | PJL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0245 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02717 | hp2 | a0004 | c0005 | t0012 | g0144 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02723 | hp1 | a0004 | c0005 | t0012 | g0145 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02735 | hp2 | a0001 | c0002 | t0003 | g0185 | SAS | PJL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02809 | hp2 | a0001 | c0002 | t0003 | g0095 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0134 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02886 | hp1 | a0001 | c0002 | t0005 | g0114 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0094 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0122 | AFR | ESN | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ESN | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ESN | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02970 | hp1 | a0001 | c0002 | t0003 | g0147 | AFR | ESN | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | ESN | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0127 | AFR | ESN | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | ESN | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03017 | hp2 | a0001 | c0002 | t0003 | g0180 | SAS | PJL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0082 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03041 | hp2 | a0002 | c0003 | t0006 | g0138 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03098 | hp1 | a0001 | c0002 | t0010 | g0363 | AFR | MSL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | MSL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0130 | AFR | ESN | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ESN | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03195 | hp1 | a0001 | c0002 | t0005 | g0112 | AFR | ESN | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | ESN | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | MSL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03209 | hp2 | a0002 | c0003 | t0006 | g0142 | AFR | MSL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03225 | hp1 | a0001 | c0001 | t0017 | g0117 | AFR | MSL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0096 | AFR | MSL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03453 | hp2 | a0001 | c0006 | t0011 | g0362 | AFR | MSL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03486 | hp1 | a0002 | c0003 | t0006 | g0141 | AFR | MSL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03486 | hp2 | a0001 | c0002 | t0005 | g0115 | AFR | MSL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03516 | hp1 | a0001 | c0006 | t0011 | g0359 | AFR | ESN | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0132 | AFR | ESN | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03540 | hp1 | a0001 | c0002 | t0005 | g0116 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0124 | AFR | GWD | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | MSL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03669 | hp2 | a0001 | c0002 | t0008 | g0005 | SAS | PJL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | STU | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | STU | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03831 | hp2 | a0001 | c0002 | t0003 | g0176 | SAS | BEB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03927 | hp1 | a0001 | c0002 | t0003 | g0006 | SAS | BEB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | BEB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG04115 | hp1 | a0001 | c0002 | t0003 | g0198 | SAS | STU | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | BEB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0353 | SAS | BEB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | STU | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG04199 | hp2 | a0001 | c0002 | t0003 | g0158 | SAS | STU | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG04204 | hp1 | a0001 | c0002 | t0003 | g0204 | SAS | STU | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | STU | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | STU | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | STU | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0247 | AFR | YRI | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | YRI | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0190 | EAS | CHB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18906 | hp1 | a0002 | c0003 | t0006 | g0139 | AFR | YRI | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | YRI | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18941 | hp1 | a0001 | c0002 | t0003 | g0196 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18944 | hp2 | a0003 | c0004 | t0003 | g0160 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18945 | hp2 | a0001 | c0002 | t0003 | g0171 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18952 | hp1 | a0001 | c0002 | t0003 | g0213 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18952 | hp2 | a0001 | c0001 | t0021 | g0059 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18961 | hp2 | a0001 | c0002 | t0003 | g0156 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18963 | hp1 | a0001 | c0002 | t0003 | g0191 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18964 | hp1 | a0001 | c0002 | t0003 | g0172 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18967 | hp1 | a0001 | c0002 | t0003 | g0152 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18969 | hp2 | a0001 | c0002 | t0003 | g0154 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18971 | hp1 | a0001 | c0002 | t0003 | g0210 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18973 | hp1 | a0001 | c0002 | t0003 | g0202 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18979 | hp1 | a0001 | c0002 | t0003 | g0203 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18982 | hp2 | a0001 | c0002 | t0003 | g0170 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18983 | hp1 | a0001 | c0002 | t0003 | g0199 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18986 | hp2 | a0001 | c0002 | t0005 | g0150 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18988 | hp2 | a0001 | c0002 | t0003 | g0194 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18989 | hp1 | a0001 | c0002 | t0003 | g0165 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18991 | hp2 | a0001 | c0002 | t0003 | g0211 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18992 | hp2 | a0001 | c0002 | t0003 | g0197 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18994 | hp2 | a0001 | c0002 | t0019 | g0174 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18995 | hp1 | a0001 | c0002 | t0003 | g0173 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18999 | hp2 | a0001 | c0002 | t0003 | g0159 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19002 | hp1 | a0010 | c0009 | t0001 | g0301 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19002 | hp2 | a0003 | c0004 | t0003 | g0149 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19004 | hp1 | a0001 | c0002 | t0003 | g0206 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19010 | hp1 | a0001 | c0002 | t0003 | g0207 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19030 | hp2 | a0001 | c0002 | t0010 | g0358 | AFR | LWK | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | LWK | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19043 | hp2 | a0001 | c0001 | t0011 | g0360 | AFR | LWK | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19054 | hp2 | a0001 | c0002 | t0003 | g0208 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19056 | hp2 | a0001 | c0002 | t0003 | g0163 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19058 | hp1 | a0001 | c0002 | t0003 | g0212 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19063 | hp1 | a0001 | c0001 | t0018 | g0072 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19064 | hp2 | a0003 | c0004 | t0003 | g0166 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19065 | hp1 | a0001 | c0001 | t0015 | g0087 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19065 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19066 | hp1 | a0001 | c0002 | t0003 | g0153 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19068 | hp1 | a0001 | c0002 | t0005 | g0167 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19074 | hp1 | a0001 | c0002 | t0003 | g0200 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19090 | hp1 | a0001 | c0002 | t0003 | g0162 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19090 | hp2 | a0001 | c0014 | t0001 | g0352 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | YRI | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | YRI | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0123 | AFR | ASW | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ASW | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | TSI | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0068 | EUR | TSI | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | GIH | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA20905 | hp2 | a0001 | c0002 | t0003 | g0177 | SAS | GIH | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0331 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02486 | hp1 | a0001 | c0002 | t0003 | g0168 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02486 | hp2 | a0008 | c0012 | t0003 | g0169 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02559 | hp1 | a0001 | c0002 | t0009 | g0157 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03471 | hp1 | a0009 | c0011 | t0020 | g0146 | AFR | MSL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG03471 | hp2 | a0001 | c0002 | t0009 | g0004 | AFR | MSL | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | USA | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| HG06807 | hp2 | a0001 | c0002 | t0010 | g0361 | AFR | USA | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0128 | AFR | USA | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | USA | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | LWK | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0010 | REF | REF | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0320 | REF | REF | TULP3_chr12_2885891_2946138 | TULP3 | chr12 | 2885891 | 2946138 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:2930271 | G | A | 1 | a0006 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.418G>A | p.Asp140Asn | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 5/11 | 475/3080 | 418/1329 | 140/442 | chr12 | 2930271 | |||
| chr12:2931050 | C | A | 1 | a0007 | 1 | HG01070.hp1 | missense_variant | MODERATE | c.506C>A | p.Ser169Tyr | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/11 | 563/3080 | 506/1329 | 169/442 | chr12 | 2931050 | |||
| chr12:2931067 | G | A | 1 | a0010 | 1 | NA19002.hp1 | missense_variant | MODERATE | c.523G>A | p.Ala175Thr | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/11 | 580/3080 | 523/1329 | 175/442 | chr12 | 2931067 | |||
| chr12:2931157 | C | T | 1 | a0003 | 3 | NA18944.hp2 NA19002.hp2 NA19064.hp2 |
missense_variant | MODERATE | c.613C>T | p.Arg205Trp | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/11 | 670/3080 | 613/1329 | 205/442 | chr12 | 2931157 | |||
| chr12:2933500 | G | A | 1 | a0005 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.779G>A | p.Arg260His | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 7/11 | 836/3080 | 779/1329 | 260/442 | chr12 | 2933500 | |||
| chr12:2934520 | G | A | 1 | a0009 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.883G>A | p.Gly295Arg | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/11 | 940/3080 | 883/1329 | 295/442 | chr12 | 2934520 | |||
| chr12:2934524 | C | A | 1 | a0002 | 7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
missense_variant | MODERATE | c.887C>A | p.Ala296Glu | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/11 | 944/3080 | 887/1329 | 296/442 | chr12 | 2934524 | |||
| chr12:2938199 | G | C | 1 | a0008 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.1109G>C | p.Ser370Thr | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 10/11 | 1166/3080 | 1109/1329 | 370/442 | chr12 | 2938199 | |||
| chr12:2938229 | G | A | 1 | a0004 | 2 | HG02717.hp2 HG02723.hp1 |
missense_variant | MODERATE | c.1139G>A | p.Arg380His | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 10/11 | 1196/3080 | 1139/1329 | 380/442 | chr12 | 2938229 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:2931180 | A | G | 1 | a0001c0014 | 1 | NA19090.hp2 | synonymous_variant | LOW | c.636A>G | p.Gly212Gly | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/11 | 693/3080 | 636/1329 | 212/442 | chr12 | 2931180 | |||
| chr12:2931198 | C | T | 1 | a0001c0013 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.654C>T | p.Phe218Phe | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/11 | 711/3080 | 654/1329 | 218/442 | chr12 | 2931198 | |||
| chr12:2933447 | A | G | 1 | a0001c0006 | 2 | HG03453.hp2 HG03516.hp1 |
synonymous_variant | LOW | c.726A>G | p.Lys242Lys | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 7/11 | 783/3080 | 726/1329 | 242/442 | chr12 | 2933447 | |||
| chr12:2937636 | A | G | 6 | a0001c0002 a0002c0003 a0003c0004 others(3): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
synonymous_variant | LOW | c.930A>G | p.Thr310Thr | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 9/11 | 987/3080 | 930/1329 | 310/442 | chr12 | 2937636 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:2890910 | A | G | 3 | a0001c0001t0011 a0001c0002t0010 a0001c0006t0011 |
6 | HG03098.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-38A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/11 | 38 | chr12 | 2890910 | ||||||
| chr12:2890939 | G | T | 1 | a0001c0001t0021 | 1 | NA18952.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-9G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/11 | chr12 | 2890939 | |||||||
| chr12:2939560 | T | C | 4 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0014 others(1): Show |
29 | HG01346.hp1 HG01943.hp1 HG02055.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*116T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 116 | chr12 | 2939560 | ||||||
| chr12:2939577 | A | ACACACAC others(105): Show |
1 | a0002c0003t0006 | 7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*133_*134insCACACA others(106): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 134 | chr12 | 2939577 | ||||||
| chr12:2939580 | C | A | 1 | a0002c0003t0006 | 7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*136C>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 136 | chr12 | 2939580 | ||||||
| chr12:2939580 | C | CACACACA others(105): Show |
3 | a0001c0002t0005 a0004c0005t0012 a0009c0011t0020 |
9 | HG01496.hp1 HG02615.hp1 HG02717.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*144_*145insGAAGAG others(106): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 145 | INFO_REALIGN_3_PRIME | chr12 | 2939580 | |||||
| chr12:2939580 | C | CACACACA others(105): Show |
3 | a0001c0001t0004 a0001c0001t0013 a0001c0002t0010 |
28 | HG01346.hp1 HG01943.hp1 HG02055.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*144_*145insGAAGAG others(106): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 145 | INFO_REALIGN_3_PRIME | chr12 | 2939580 | |||||
| chr12:2939589 | A | AAAGAGCA others(105): Show |
15 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0011 others(12): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
3_prime_UTR_variant | MODIFIER | c.*257_*368dupGAAGAG others(106): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 369 | INFO_REALIGN_3_PRIME | chr12 | 2939589 | |||||
| chr12:2939589 | A | G | 14 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0014 others(11): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*145A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 145 | chr12 | 2939589 | ||||||
| chr12:2939613 | G | A | 1 | a0001c0002t0008 | 5 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*169G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 169 | chr12 | 2939613 | ||||||
| chr12:2939617 | C | T | 1 | a0001c0001t0014 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*173C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 173 | chr12 | 2939617 | ||||||
| chr12:2939821 | C | T | 1 | a0001c0001t0013 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*377C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 377 | chr12 | 2939821 | ||||||
| chr12:2939907 | G | A | 1 | a0001c0001t0015 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*463G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 463 | chr12 | 2939907 | ||||||
| chr12:2940031 | C | T | 1 | a0009c0011t0020 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*587C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 587 | chr12 | 2940031 | ||||||
| chr12:2940321 | TA | T | 7 | a0001c0001t0018 a0001c0002t0003 a0001c0002t0008 others(4): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*894delA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 894 | INFO_REALIGN_3_PRIME | chr12 | 2940321 | |||||
| chr12:2940321 | TAA | T | 5 | a0001c0001t0004 a0001c0001t0013 a0001c0002t0005 others(2): Show |
39 | HG01346.hp1 HG01496.hp1 HG01516.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*893_*894delAA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 893 | INFO_REALIGN_3_PRIME | chr12 | 2940321 | |||||
| chr12:2940465 | C | T | 6 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0018 others(3): Show |
99 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1021C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 1021 | chr12 | 2940465 | ||||||
| chr12:2940472 | T | C | 1 | a0001c0001t0016 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1028T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 1028 | chr12 | 2940472 | ||||||
| chr12:2940508 | T | TA | 1 | a0002c0003t0006 | 7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1065dupA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 1066 | INFO_REALIGN_3_PRIME | chr12 | 2940508 | |||||
| chr12:2940532 | T | C | 13 | a0001c0001t0004 a0001c0001t0013 a0001c0002t0003 others(10): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*1088T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 1088 | chr12 | 2940532 | ||||||
| chr12:2940631 | G | T | 1 | a0002c0003t0006 | 7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1187G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 1187 | chr12 | 2940631 | ||||||
| chr12:2940701 | C | T | 3 | a0001c0001t0004 a0001c0001t0013 a0001c0002t0010 |
28 | HG01346.hp1 HG01943.hp1 HG02055.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1257C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 1257 | chr12 | 2940701 | ||||||
| chr12:2940725 | G | A | 1 | a0001c0001t0017 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1281G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 1281 | chr12 | 2940725 | ||||||
| chr12:2940772 | C | T | 9 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0008 others(6): Show |
94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*1328C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 1328 | chr12 | 2940772 | ||||||
| chr12:2940773 | G | A | 1 | a0001c0001t0013 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1329G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 1329 | chr12 | 2940773 | ||||||
| chr12:2940950 | TACACGAC others(34): Show |
T | 1 | a0001c0002t0019 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1507_*1547delACAC others(37): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 1507 | chr12 | 2940950 | ||||||
| chr12:2941054 | TTG | T | 9 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0008 others(6): Show |
94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*1617_*1618delTG | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 11/11 | 1617 | INFO_REALIGN_3_PRIME | chr12 | 2941054 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:2891146 | C | T | 6 | a0001c0001t0011g0360 a0001c0002t0010g0358 a0001c0002t0010g0361 others(3): Show |
6 | HG03098.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+158C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2891146 | |||||||
| chr12:2891152 | T | C | 1 | a0001c0001t0002g0001 | 3 | HG02165.hp1 NA18971.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.41+164T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2891152 | |||||||
| chr12:2891237 | T | C | 229 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0135 others(226): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.41+249T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2891237 | |||||||
| chr12:2891294 | C | T | 2 | a0001c0001t0001g0356 a0001c0001t0001g0357 |
2 | HG00642.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.41+306C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2891294 | |||||||
| chr12:2891356 | G | A | 214 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0135 others(211): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.41+368G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2891356 | |||||||
| chr12:2891457 | G | A | 216 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0135 others(213): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.41+469G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2891457 | |||||||
| chr12:2891544 | G | C | 5 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(2): Show |
5 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.41+556G>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2891544 | |||||||
| chr12:2891714 | C | T | 221 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(218): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.41+726C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2891714 | |||||||
| chr12:2891806 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.41+818C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2891806 | |||||||
| chr12:2891843 | C | G | 77 | a0001c0001t0001g0201 a0001c0002t0003g0002 a0001c0002t0003g0003 others(74): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.41+855C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2891843 | |||||||
| chr12:2891915 | C | A | 215 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(212): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.41+927C>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2891915 | |||||||
| chr12:2892036 | C | A | 131 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(128): Show |
133 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.41+1048C>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2892036 | |||||||
| chr12:2892064 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.41+1076A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2892064 | |||||||
| chr12:2892082 | T | TA | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.41+1104dupA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2892082 | ||||||
| chr12:2892102 | G | A | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+1114G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2892102 | |||||||
| chr12:2892109 | T | G | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+1121T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2892109 | |||||||
| chr12:2892178 | G | A | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+1190G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2892178 | |||||||
| chr12:2892203 | T | C | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+1215T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2892203 | |||||||
| chr12:2892327 | A | G | 225 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(222): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.41+1339A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2892327 | |||||||
| chr12:2892357 | C | A | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+1369C>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2892357 | |||||||
| chr12:2892450 | AT | A | 225 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(222): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.41+1468delT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2892450 | ||||||
| chr12:2892461 | A | G | 225 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(222): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.41+1473A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2892461 | |||||||
| chr12:2892535 | C | T | 6 | a0001c0001t0011g0360 a0001c0002t0010g0358 a0001c0002t0010g0361 others(3): Show |
6 | HG03098.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+1547C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2892535 | |||||||
| chr12:2892550 | T | G | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+1562T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2892550 | |||||||
| chr12:2892585 | A | C | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+1597A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2892585 | |||||||
| chr12:2892651 | A | G | 1 | a0001c0002t0003g0213 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.41+1663A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2892651 | |||||||
| chr12:2892745 | G | C | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+1757G>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2892745 | |||||||
| chr12:2892746 | G | A | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+1758G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2892746 | |||||||
| chr12:2892753 | G | C | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.41+1765G>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2892753 | |||||||
| chr12:2892873 | A | AT | 177 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0135 others(174): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.41+1900dupT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2892873 | ||||||
| chr12:2892873 | A | ATT | 31 | a0001c0001t0002g0118 a0001c0001t0002g0119 a0001c0001t0002g0120 others(28): Show |
31 | HG01346.hp1 HG02129.hp1 HG02135.hp2 others(28): Show |
intron_variant | MODIFIER | c.41+1899_41+1900dup others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2892873 | ||||||
| chr12:2892873 | AT | A | 10 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0011g0360 others(7): Show |
10 | HG01361.hp1 HG02451.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.41+1900delT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2892873 | ||||||
| chr12:2892937 | T | C | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+1949T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2892937 | |||||||
| chr12:2893013 | C | T | 1 | a0002c0003t0006g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.41+2025C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893013 | |||||||
| chr12:2893060 | T | A | 5 | a0001c0002t0005g0112 a0001c0002t0005g0113 a0001c0002t0005g0114 others(2): Show |
5 | HG02615.hp1 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.41+2072T>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893060 | |||||||
| chr12:2893115 | A | G | 225 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(222): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.41+2127A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893115 | |||||||
| chr12:2893246 | A | G | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+2258A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893246 | |||||||
| chr12:2893286 | G | A | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+2298G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893286 | |||||||
| chr12:2893327 | G | GGTTT | 70 | a0001c0001t0001g0201 a0001c0002t0003g0002 a0001c0002t0003g0003 others(67): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.41+2339_41+2340ins others(4): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893327 | |||||||
| chr12:2893327 | G | GGTTTT | 6 | a0001c0002t0003g0151 a0001c0002t0003g0202 a0001c0002t0003g0203 others(3): Show |
6 | HG00438.hp1 HG01243.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+2339_41+2340ins others(5): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893327 | |||||||
| chr12:2893327 | G | GT | 20 | a0001c0001t0001g0009 a0001c0001t0001g0224 a0001c0001t0001g0228 others(17): Show |
20 | HG00642.hp2 HG01109.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.41+2356dupT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2893327 | ||||||
| chr12:2893327 | G | GTTT | 8 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0017g0117 others(5): Show |
8 | HG01891.hp1 HG02622.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.41+2354_41+2356dup others(3): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2893327 | ||||||
| chr12:2893327 | G | GTTTT | 84 | a0001c0001t0001g0024 a0001c0001t0002g0001 a0001c0001t0002g0011 others(81): Show |
86 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.41+2353_41+2356dup others(4): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2893327 | ||||||
| chr12:2893327 | G | GTTTTT | 36 | a0001c0001t0001g0135 a0001c0001t0002g0083 a0001c0001t0002g0084 others(33): Show |
36 | HG00558.hp2 HG00741.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.41+2352_41+2356dup others(5): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2893327 | ||||||
| chr12:2893327 | G | GTTTTTT | 11 | a0001c0001t0002g0106 a0001c0001t0004g0107 a0001c0001t0004g0108 others(8): Show |
11 | HG00735.hp1 HG01346.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.41+2351_41+2356dup others(6): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2893327 | ||||||
| chr12:2893344 | T | C | 5 | a0001c0001t0011g0360 a0001c0002t0010g0358 a0001c0002t0010g0361 others(2): Show |
5 | HG03453.hp2 HG03516.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.41+2356T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893344 | |||||||
| chr12:2893368 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.41+2380G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893368 | |||||||
| chr12:2893372 | A | G | 212 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(209): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.41+2384A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893372 | |||||||
| chr12:2893406 | T | G | 1 | a0001c0001t0001g0233 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.41+2418T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893406 | |||||||
| chr12:2893410 | T | G | 3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0006c0007t0001g0236 |
3 | HG00597.hp2 HG02040.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.41+2422T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893410 | |||||||
| chr12:2893476 | G | A | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+2488G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893476 | |||||||
| chr12:2893518 | T | A | 77 | a0001c0001t0001g0201 a0001c0002t0003g0002 a0001c0002t0003g0003 others(74): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.41+2530T>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893518 | |||||||
| chr12:2893568 | G | A | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.41+2580G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893568 | |||||||
| chr12:2893601 | G | T | 1 | a0001c0001t0002g0081 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.41+2613G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893601 | |||||||
| chr12:2893716 | GT | G | 204 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(201): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.41+2740delT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2893716 | ||||||
| chr12:2893716 | GTT | G | 20 | a0001c0001t0002g0014 a0001c0001t0002g0018 a0001c0001t0002g0019 others(17): Show |
20 | HG00735.hp1 HG01070.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.41+2739_41+2740del others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2893716 | ||||||
| chr12:2893762 | T | C | 6 | a0001c0001t0011g0360 a0001c0002t0010g0358 a0001c0002t0010g0361 others(3): Show |
6 | HG03098.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+2774T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893762 | |||||||
| chr12:2893769 | T | C | 1 | a0001c0001t0001g0009 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.41+2781T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893769 | |||||||
| chr12:2893811 | A | AT | 80 | a0001c0001t0001g0201 a0001c0001t0002g0001 a0001c0001t0002g0012 others(77): Show |
82 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.41+2828dupT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2893811 | ||||||
| chr12:2893817 | A | T | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.41+2829A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893817 | |||||||
| chr12:2893856 | A | C | 225 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(222): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.41+2868A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893856 | |||||||
| chr12:2893923 | T | C | 4 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(1): Show |
4 | NA18951.hp1 NA18992.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+2935T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893923 | |||||||
| chr12:2893983 | T | C | 3 | a0001c0002t0005g0112 a0001c0002t0005g0113 a0001c0002t0005g0114 |
3 | HG02615.hp1 HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.41+2995T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2893983 | |||||||
| chr12:2894124 | A | C | 1 | a0001c0001t0017g0117 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.41+3136A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894124 | |||||||
| chr12:2894187 | G | A | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+3199G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894187 | |||||||
| chr12:2894224 | A | G | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+3236A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894224 | |||||||
| chr12:2894287 | C | CG | 27 | a0001c0001t0001g0224 a0001c0001t0001g0332 a0001c0001t0001g0333 others(24): Show |
27 | HG00597.hp1 HG00639.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.41+3306dupG | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2894287 | ||||||
| chr12:2894295 | C | T | 217 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(214): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.41+3307C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894295 | |||||||
| chr12:2894298 | G | T | 2 | a0002c0003t0006g0139 a0004c0005t0012g0144 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.41+3310G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894298 | |||||||
| chr12:2894300 | C | G | 2 | a0002c0003t0006g0139 a0004c0005t0012g0144 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.41+3312C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894300 | |||||||
| chr12:2894300 | CG | C | 108 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(105): Show |
110 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.41+3322delG | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2894300 | ||||||
| chr12:2894302 | G | C | 6 | a0001c0001t0011g0360 a0001c0002t0010g0358 a0001c0002t0010g0361 others(3): Show |
6 | HG03098.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+3314G>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894302 | |||||||
| chr12:2894303 | G | C | 2 | a0002c0003t0006g0139 a0004c0005t0012g0144 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.41+3315G>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894303 | |||||||
| chr12:2894308 | G | C | 1 | a0001c0001t0001g0243 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.41+3320G>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894308 | |||||||
| chr12:2894308 | GGGA | G | 213 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(210): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.41+3321_41+3323del others(3): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894308 | |||||||
| chr12:2894311 | A | G | 2 | a0002c0003t0006g0139 a0004c0005t0012g0144 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.41+3323A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894311 | |||||||
| chr12:2894329 | A | C | 6 | a0001c0001t0011g0360 a0001c0002t0010g0358 a0001c0002t0010g0361 others(3): Show |
6 | HG03098.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+3341A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894329 | |||||||
| chr12:2894440 | C | T | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+3452C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894440 | |||||||
| chr12:2894499 | C | T | 1 | a0001c0002t0005g0143 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.41+3511C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894499 | |||||||
| chr12:2894538 | A | AACACACA others(3): Show |
1 | a0001c0001t0011g0360 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.41+3569_41+3578dup others(10): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2894538 | ||||||
| chr12:2894538 | A | AACACACA others(7): Show |
3 | a0001c0002t0010g0361 a0001c0002t0010g0363 a0001c0006t0011g0362 |
3 | HG03098.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.41+3565_41+3578dup others(14): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2894538 | ||||||
| chr12:2894538 | A | AACACACA others(15): Show |
1 | a0001c0006t0011g0359 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.41+3557_41+3578dup others(22): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2894538 | ||||||
| chr12:2894538 | A | ACACACAC others(12): Show |
1 | a0001c0002t0010g0358 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.41+3550_41+3551ins others(19): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894538 | |||||||
| chr12:2894538 | AAC | A | 234 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(231): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.41+3577_41+3578del others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2894538 | ||||||
| chr12:2894538 | AACAC | A | 94 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(91): Show |
96 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.41+3575_41+3578del others(4): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2894538 | ||||||
| chr12:2894643 | C | G | 2 | a0004c0005t0012g0144 a0004c0005t0012g0145 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.41+3655C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894643 | |||||||
| chr12:2894648 | C | T | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+3660C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894648 | |||||||
| chr12:2894677 | C | T | 2 | a0001c0001t0001g0347 a0001c0001t0001g0348 |
2 | NA18942.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.41+3689C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894677 | |||||||
| chr12:2894692 | A | G | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+3704A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894692 | |||||||
| chr12:2894735 | A | G | 77 | a0001c0001t0001g0201 a0001c0002t0003g0002 a0001c0002t0003g0003 others(74): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.41+3747A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894735 | |||||||
| chr12:2894787 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.41+3799C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894787 | |||||||
| chr12:2894790 | G | A | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+3802G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894790 | |||||||
| chr12:2894815 | ACCTGGGA others(13): Show |
A | 108 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0222 others(105): Show |
109 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.41+3828_41+3847del others(20): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894815 | |||||||
| chr12:2894845 | G | T | 99 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(96): Show |
101 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.41+3857G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894845 | |||||||
| chr12:2894850 | C | T | 2 | a0001c0001t0002g0075 a0001c0001t0002g0076 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.41+3862C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894850 | |||||||
| chr12:2894964 | A | G | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+3976A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2894964 | |||||||
| chr12:2895035 | C | T | 2 | a0001c0001t0002g0075 a0001c0001t0002g0076 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.41+4047C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2895035 | |||||||
| chr12:2895094 | T | A | 4 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0349 others(1): Show |
4 | HG01884.hp1 HG02145.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+4106T>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2895094 | |||||||
| chr12:2895155 | A | G | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.41+4167A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2895155 | |||||||
| chr12:2895223 | C | T | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+4235C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2895223 | |||||||
| chr12:2895334 | A | G | 97 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(94): Show |
99 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.41+4346A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2895334 | |||||||
| chr12:2895340 | G | T | 1 | a0001c0001t0002g0074 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.41+4352G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2895340 | |||||||
| chr12:2895360 | G | A | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+4372G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2895360 | |||||||
| chr12:2895633 | A | G | 1 | a0001c0001t0013g0097 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.41+4645A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2895633 | |||||||
| chr12:2895677 | C | A | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+4689C>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2895677 | |||||||
| chr12:2895678 | CTCTT | C | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+4693_41+4696del others(4): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2895678 | ||||||
| chr12:2895788 | G | A | 15 | a0001c0001t0004g0013 a0001c0001t0004g0094 a0001c0001t0004g0122 others(12): Show |
15 | HG01346.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.41+4800G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2895788 | |||||||
| chr12:2895842 | A | G | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+4854A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2895842 | |||||||
| chr12:2895854 | A | G | 224 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(221): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.41+4866A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2895854 | |||||||
| chr12:2895865 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.41+4877G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2895865 | |||||||
| chr12:2895909 | C | CGTATCTA others(1): Show |
219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+4921_41+4922ins others(8): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2895909 | |||||||
| chr12:2895911 | T | C | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+4923T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2895911 | |||||||
| chr12:2895943 | C | CT | 16 | a0001c0001t0001g0330 a0001c0001t0002g0018 a0001c0001t0002g0083 others(13): Show |
16 | HG01346.hp1 HG02257.hp1 HG02717.hp2 others(13): Show |
intron_variant | MODIFIER | c.41+4969dupT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2895943 | ||||||
| chr12:2895943 | C | CTT | 194 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(191): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.41+4968_41+4969dup others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2895943 | ||||||
| chr12:2895992 | G | T | 3 | a0001c0001t0011g0360 a0001c0006t0011g0359 a0001c0006t0011g0362 |
3 | HG03453.hp2 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.41+5004G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2895992 | |||||||
| chr12:2896090 | A | C | 15 | a0001c0001t0004g0013 a0001c0001t0004g0094 a0001c0001t0004g0122 others(12): Show |
15 | HG01346.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.41+5102A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2896090 | |||||||
| chr12:2896128 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.41+5140C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2896128 | |||||||
| chr12:2896159 | T | C | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+5171T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2896159 | |||||||
| chr12:2896186 | C | G | 1 | a0001c0001t0004g0127 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.41+5198C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2896186 | |||||||
| chr12:2896215 | C | T | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+5227C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2896215 | |||||||
| chr12:2896219 | C | T | 2 | a0001c0001t0002g0021 a0001c0001t0002g0022 |
2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.41+5231C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2896219 | |||||||
| chr12:2896422 | AT | A | 6 | a0001c0001t0011g0360 a0001c0002t0010g0358 a0001c0002t0010g0361 others(3): Show |
6 | HG03098.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+5435delT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2896422 | |||||||
| chr12:2896519 | T | C | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+5531T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2896519 | |||||||
| chr12:2896562 | C | T | 1 | a0001c0002t0005g0143 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.41+5574C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2896562 | |||||||
| chr12:2896680 | G | T | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+5692G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2896680 | |||||||
| chr12:2896791 | G | A | 6 | a0001c0001t0011g0360 a0001c0002t0010g0358 a0001c0002t0010g0361 others(3): Show |
6 | HG03098.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+5803G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2896791 | |||||||
| chr12:2897018 | T | A | 1 | a0001c0002t0010g0358 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.41+6030T>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2897018 | |||||||
| chr12:2897036 | T | C | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+6048T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2897036 | |||||||
| chr12:2897121 | T | C | 6 | a0001c0001t0011g0360 a0001c0002t0010g0358 a0001c0002t0010g0361 others(3): Show |
6 | HG03098.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+6133T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2897121 | |||||||
| chr12:2897201 | G | C | 1 | a0001c0002t0003g0153 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.41+6213G>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2897201 | |||||||
| chr12:2897202 | A | G | 225 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(222): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.41+6214A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2897202 | |||||||
| chr12:2897234 | C | T | 225 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(222): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.41+6246C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2897234 | |||||||
| chr12:2897265 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.41+6277C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2897265 | |||||||
| chr12:2897322 | TAATAC | T | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+6336_41+6340del others(5): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2897322 | ||||||
| chr12:2897463 | G | A | 6 | a0001c0001t0002g0027 a0001c0001t0002g0081 a0001c0001t0002g0218 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+6475G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2897463 | |||||||
| chr12:2897512 | C | G | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+6524C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2897512 | |||||||
| chr12:2897527 | G | A | 1 | a0001c0002t0003g0154 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.41+6539G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2897527 | |||||||
| chr12:2897647 | C | G | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+6659C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2897647 | |||||||
| chr12:2897706 | C | T | 15 | a0001c0001t0004g0013 a0001c0001t0004g0094 a0001c0001t0004g0122 others(12): Show |
15 | HG01346.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.41+6718C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2897706 | |||||||
| chr12:2897771 | T | TAAA | 6 | a0001c0001t0002g0073 a0001c0001t0002g0220 a0001c0001t0002g0221 others(3): Show |
6 | HG01167.hp2 HG01168.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+6801_41+6803dup others(3): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2897771 | ||||||
| chr12:2897771 | T | TAAAA | 177 | a0001c0001t0001g0024 a0001c0001t0001g0201 a0001c0001t0002g0001 others(174): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.41+6800_41+6803dup others(4): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2897771 | ||||||
| chr12:2897771 | T | TAAAAA | 34 | a0001c0001t0002g0011 a0001c0001t0002g0021 a0001c0001t0002g0022 others(31): Show |
34 | HG01257.hp1 HG01346.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.41+6799_41+6803dup others(5): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2897771 | ||||||
| chr12:2897771 | TA | T | 11 | a0001c0001t0001g0242 a0001c0001t0001g0253 a0001c0001t0001g0323 others(8): Show |
11 | HG01255.hp2 HG02896.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.41+6803delA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2897771 | ||||||
| chr12:2897946 | C | T | 108 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0222 others(105): Show |
109 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.41+6958C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2897946 | |||||||
| chr12:2898079 | C | CAA | 9 | a0001c0001t0004g0096 a0001c0001t0004g0110 a0001c0001t0004g0111 others(6): Show |
9 | HG01168.hp2 HG02647.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.41+7109_41+7110dup others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2898079 | ||||||
| chr12:2898079 | C | CAAA | 136 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(133): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.41+7108_41+7110dup others(3): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2898079 | ||||||
| chr12:2898079 | C | CAAAA | 68 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0016 others(65): Show |
70 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.41+7107_41+7110dup others(4): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2898079 | ||||||
| chr12:2898079 | C | CAAAAA | 6 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(3): Show |
6 | HG00544.hp2 HG01993.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+7106_41+7110dup others(5): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2898079 | ||||||
| chr12:2898079 | CA | C | 6 | a0001c0001t0001g0241 a0001c0001t0001g0309 a0001c0001t0001g0310 others(3): Show |
6 | HG00558.hp1 HG02683.hp2 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+7110delA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2898079 | ||||||
| chr12:2898432 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.41+7444G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2898432 | |||||||
| chr12:2898445 | A | T | 3 | a0001c0001t0011g0360 a0001c0006t0011g0359 a0001c0006t0011g0362 |
3 | HG03453.hp2 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.41+7457A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2898445 | |||||||
| chr12:2898643 | G | T | 4 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0324 others(1): Show |
4 | HG01952.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+7655G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2898643 | |||||||
| chr12:2898868 | C | CAG | 224 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(221): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.41+7880_41+7881ins others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2898868 | |||||||
| chr12:2898928 | A | G | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+7940A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2898928 | |||||||
| chr12:2898934 | A | C | 225 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(222): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.41+7946A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2898934 | |||||||
| chr12:2898977 | T | C | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+7989T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2898977 | |||||||
| chr12:2899064 | G | C | 1 | a0001c0001t0002g0033 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.41+8076G>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2899064 | |||||||
| chr12:2899116 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.41+8128C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2899116 | |||||||
| chr12:2899202 | G | A | 5 | a0001c0002t0005g0112 a0001c0002t0005g0113 a0001c0002t0005g0114 others(2): Show |
5 | HG02615.hp1 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.41+8214G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2899202 | |||||||
| chr12:2899337 | C | A | 1 | a0001c0001t0002g0034 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.41+8349C>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2899337 | |||||||
| chr12:2899345 | C | CA | 9 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0330 others(6): Show |
9 | HG03098.hp1 HG03453.hp2 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.41+8376dupA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2899345 | ||||||
| chr12:2899345 | C | CAA | 12 | a0001c0001t0002g0068 a0001c0001t0002g0073 a0001c0001t0002g0120 others(9): Show |
12 | HG01109.hp1 HG01891.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.41+8375_41+8376dup others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2899345 | ||||||
| chr12:2899345 | C | CAAA | 115 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(112): Show |
117 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.41+8374_41+8376dup others(3): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2899345 | ||||||
| chr12:2899345 | C | CAAAA | 83 | a0001c0001t0002g0014 a0001c0001t0002g0016 a0001c0001t0002g0027 others(80): Show |
86 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.41+8373_41+8376dup others(4): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2899345 | ||||||
| chr12:2899345 | C | CAAAAA | 9 | a0001c0002t0003g0155 a0001c0002t0003g0156 a0001c0002t0003g0162 others(6): Show |
9 | HG01175.hp1 HG01361.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.41+8372_41+8376dup others(5): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2899345 | ||||||
| chr12:2899365 | C | A | 1 | a0001c0002t0003g0193 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.41+8377C>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2899365 | |||||||
| chr12:2899368 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.41+8380C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2899368 | |||||||
| chr12:2899397 | C | T | 216 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(213): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.41+8409C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2899397 | |||||||
| chr12:2899631 | C | G | 1 | a0001c0001t0002g0067 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.41+8643C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2899631 | |||||||
| chr12:2899720 | T | C | 1 | a0001c0001t0002g0025 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.41+8732T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2899720 | |||||||
| chr12:2899750 | G | A | 13 | a0001c0001t0001g0244 a0001c0001t0001g0252 a0001c0001t0007g0245 others(10): Show |
13 | HG01106.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.41+8762G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2899750 | |||||||
| chr12:2899776 | T | C | 1 | a0002c0003t0006g0139 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.41+8788T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2899776 | |||||||
| chr12:2899790 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.41+8802G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2899790 | |||||||
| chr12:2899818 | A | G | 1 | a0001c0001t0002g0030 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.41+8830A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2899818 | |||||||
| chr12:2899871 | C | T | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+8883C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2899871 | |||||||
| chr12:2899879 | C | T | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+8891C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2899879 | |||||||
| chr12:2899893 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0002g0016 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.41+8915_41+8928del others(14): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2899893 | ||||||
| chr12:2899894 | AAAAAAAA others(6): Show |
A | 113 | a0001c0001t0001g0135 a0001c0001t0002g0001 a0001c0001t0002g0011 others(110): Show |
115 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.41+8915_41+8927del others(13): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2899894 | ||||||
| chr12:2899895 | AAAAAAAA others(5): Show |
A | 83 | a0001c0001t0001g0024 a0001c0001t0001g0201 a0001c0001t0002g0021 others(80): Show |
85 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.41+8915_41+8926del others(12): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2899895 | ||||||
| chr12:2899896 | AAAAAAAC others(4): Show |
A | 16 | a0001c0001t0002g0106 a0001c0002t0003g0151 a0001c0002t0003g0152 others(13): Show |
16 | HG00438.hp1 HG00735.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.41+8915_41+8925del others(11): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2899896 | ||||||
| chr12:2899897 | AAAAAACA others(3): Show |
A | 1 | a0001c0002t0003g0203 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.41+8915_41+8924del others(10): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2899897 | ||||||
| chr12:2899902 | ACAAAC | A | 5 | a0002c0003t0006g0137 a0002c0003t0006g0138 a0002c0003t0006g0139 others(2): Show |
5 | HG01891.hp1 HG02622.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.41+8915_41+8919del others(5): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2899902 | |||||||
| chr12:2899902 | ACAAACAA others(10): Show |
A | 1 | a0001c0001t0013g0097 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.41+8915_41+8931del others(17): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2899902 | |||||||
| chr12:2899907 | C | A | 6 | a0001c0001t0011g0360 a0001c0002t0010g0358 a0001c0006t0011g0359 others(3): Show |
6 | HG01109.hp1 HG03209.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+8919C>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2899907 | |||||||
| chr12:2899919 | C | A | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.41+8931C>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2899919 | |||||||
| chr12:2899924 | A | C | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+8936A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2899924 | |||||||
| chr12:2899954 | T | TCTGTAAT others(2): Show |
7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+8968_41+8976dup others(9): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2899954 | ||||||
| chr12:2899992 | G | A | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+9004G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2899992 | |||||||
| chr12:2900060 | C | CA | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+9080dupA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2900060 | ||||||
| chr12:2900181 | C | G | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0201 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.41+9193C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2900181 | |||||||
| chr12:2900257 | A | G | 2 | a0004c0005t0012g0144 a0004c0005t0012g0145 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.41+9269A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2900257 | |||||||
| chr12:2900373 | G | A | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-9156G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2900373 | |||||||
| chr12:2900491 | A | G | 36 | a0001c0001t0002g0012 a0001c0001t0002g0017 a0001c0001t0002g0027 others(33): Show |
36 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.42-9038A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2900491 | |||||||
| chr12:2900602 | C | CT | 14 | a0001c0001t0001g0330 a0001c0001t0011g0360 a0001c0002t0010g0358 others(11): Show |
14 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.42-8917dupT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2900602 | ||||||
| chr12:2900602 | C | CTT | 211 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(208): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.42-8918_42-8917dup others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2900602 | ||||||
| chr12:2900694 | A | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
8 | HG01192.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.42-8835A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2900694 | |||||||
| chr12:2900697 | CT | C | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-8821delT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2900697 | ||||||
| chr12:2900739 | T | G | 4 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(1): Show |
4 | HG00408.hp1 NA18944.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-8790T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2900739 | |||||||
| chr12:2900778 | C | T | 1 | a0001c0002t0003g0206 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.42-8751C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2900778 | |||||||
| chr12:2900824 | C | T | 15 | a0001c0001t0004g0013 a0001c0001t0004g0094 a0001c0001t0004g0122 others(12): Show |
15 | HG01346.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.42-8705C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2900824 | |||||||
| chr12:2900858 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.42-8671C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2900858 | |||||||
| chr12:2900876 | C | CT | 8 | a0001c0001t0001g0228 a0001c0001t0001g0233 a0001c0001t0001g0252 others(5): Show |
8 | HG00438.hp2 HG01891.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.42-8634dupT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2900876 | ||||||
| chr12:2900876 | CTTT | C | 213 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(210): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.42-8636_42-8634del others(3): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2900876 | ||||||
| chr12:2901044 | T | C | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-8485T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2901044 | |||||||
| chr12:2901148 | T | C | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-8381T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2901148 | |||||||
| chr12:2901294 | TTC | T | 119 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(116): Show |
121 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.42-8233_42-8232del others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2901294 | ||||||
| chr12:2901295 | TC | T | 86 | a0001c0001t0017g0117 a0001c0002t0003g0002 a0001c0002t0003g0003 others(83): Show |
89 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.42-8233delC | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2901295 | |||||||
| chr12:2901296 | C | T | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-8233C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2901296 | |||||||
| chr12:2901310 | TTC | T | 11 | a0001c0001t0002g0054 a0001c0001t0002g0081 a0001c0001t0002g0103 others(8): Show |
11 | HG01109.hp1 HG01346.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.42-8217_42-8216del others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2901310 | ||||||
| chr12:2901312 | C | CT | 196 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0260 others(193): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.42-8201dupT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2901312 | ||||||
| chr12:2901312 | C | CTT | 15 | a0001c0001t0001g0304 a0001c0001t0017g0117 a0001c0002t0003g0003 others(12): Show |
15 | HG01106.hp2 HG01952.hp1 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.42-8202_42-8201dup others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2901312 | ||||||
| chr12:2901312 | CTTT | C | 6 | a0001c0001t0011g0360 a0001c0002t0010g0358 a0001c0002t0010g0361 others(3): Show |
6 | HG03098.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-8203_42-8201del others(3): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2901312 | ||||||
| chr12:2901315 | T | TC | 5 | a0001c0002t0005g0112 a0001c0002t0005g0113 a0001c0002t0005g0114 others(2): Show |
5 | HG02615.hp1 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-8214_42-8213ins others(1): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2901315 | |||||||
| chr12:2901467 | T | C | 224 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(221): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.42-8062T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2901467 | |||||||
| chr12:2901474 | C | G | 2 | a0001c0006t0011g0359 a0001c0006t0011g0362 |
2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.42-8055C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2901474 | |||||||
| chr12:2901621 | C | T | 224 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(221): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.42-7908C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2901621 | |||||||
| chr12:2901643 | G | A | 6 | a0001c0001t0011g0360 a0001c0002t0010g0358 a0001c0002t0010g0361 others(3): Show |
6 | HG03098.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-7886G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2901643 | |||||||
| chr12:2901662 | T | C | 224 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(221): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.42-7867T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2901662 | |||||||
| chr12:2901686 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.42-7843A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2901686 | |||||||
| chr12:2901733 | T | A | 2 | a0001c0002t0010g0361 a0001c0002t0010g0363 |
2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.42-7796T>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2901733 | |||||||
| chr12:2901733 | T | C | 358 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(355): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.42-7796T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2901733 | |||||||
| chr12:2901807 | A | G | 1 | a0001c0001t0001g0351 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.42-7722A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2901807 | |||||||
| chr12:2901832 | G | A | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-7697G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2901832 | |||||||
| chr12:2901887 | A | G | 1 | a0001c0002t0003g0159 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.42-7642A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2901887 | |||||||
| chr12:2901978 | T | G | 1 | a0001c0001t0002g0035 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.42-7551T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2901978 | |||||||
| chr12:2901979 | G | T | 1 | a0001c0001t0002g0035 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.42-7550G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2901979 | |||||||
| chr12:2902105 | T | A | 1 | a0001c0001t0002g0035 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.42-7424T>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2902105 | |||||||
| chr12:2902196 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.42-7333C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2902196 | |||||||
| chr12:2902507 | C | T | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-7022C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2902507 | |||||||
| chr12:2902562 | G | A | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-6967G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2902562 | |||||||
| chr12:2902575 | C | T | 1 | a0001c0002t0003g0192 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.42-6954C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2902575 | |||||||
| chr12:2902576 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.42-6953G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2902576 | |||||||
| chr12:2902600 | A | C | 2 | a0001c0001t0001g0231 a0001c0001t0001g0305 |
2 | HG03491.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.42-6929A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2902600 | |||||||
| chr12:2902737 | G | A | 6 | a0001c0001t0011g0360 a0001c0002t0010g0358 a0001c0002t0010g0361 others(3): Show |
6 | HG03098.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-6792G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2902737 | |||||||
| chr12:2902782 | A | G | 2 | a0001c0001t0002g0040 a0001c0001t0002g0066 |
2 | NA19068.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.42-6747A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2902782 | |||||||
| chr12:2902852 | A | G | 1 | a0001c0001t0002g0011 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.42-6677A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2902852 | |||||||
| chr12:2902864 | A | AT | 13 | a0001c0001t0001g0224 a0001c0001t0001g0330 a0001c0001t0002g0055 others(10): Show |
13 | HG01109.hp1 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.42-6650dupT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2902864 | ||||||
| chr12:2902864 | A | ATT | 200 | a0001c0001t0001g0024 a0001c0001t0002g0001 a0001c0001t0002g0011 others(197): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.42-6651_42-6650dup others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2902864 | ||||||
| chr12:2902864 | A | ATTT | 7 | a0001c0001t0001g0135 a0001c0001t0002g0069 a0001c0001t0002g0093 others(4): Show |
7 | HG00741.hp1 HG02055.hp1 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-6652_42-6650dup others(3): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2902864 | ||||||
| chr12:2902894 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.42-6635C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2902894 | |||||||
| chr12:2902907 | G | C | 6 | a0001c0001t0011g0360 a0001c0002t0010g0358 a0001c0002t0010g0361 others(3): Show |
6 | HG03098.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-6622G>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2902907 | |||||||
| chr12:2903002 | C | T | 6 | a0001c0001t0011g0360 a0001c0002t0010g0358 a0001c0002t0010g0361 others(3): Show |
6 | HG03098.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-6527C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2903002 | |||||||
| chr12:2903018 | T | C | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-6511T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2903018 | |||||||
| chr12:2903081 | C | T | 1 | a0001c0002t0010g0358 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.42-6448C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2903081 | |||||||
| chr12:2903099 | T | C | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-6430T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2903099 | |||||||
| chr12:2903214 | A | G | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-6315A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2903214 | |||||||
| chr12:2903285 | G | A | 6 | a0001c0001t0011g0360 a0001c0002t0010g0358 a0001c0002t0010g0361 others(3): Show |
6 | HG03098.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-6244G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2903285 | |||||||
| chr12:2903368 | G | A | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-6161G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2903368 | |||||||
| chr12:2903389 | C | T | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-6140C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2903389 | |||||||
| chr12:2903486 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.42-6043C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2903486 | |||||||
| chr12:2903511 | A | G | 224 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(221): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.42-6018A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2903511 | |||||||
| chr12:2903519 | G | A | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG01358.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.42-6010G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2903519 | |||||||
| chr12:2903522 | A | G | 1 | a0001c0002t0010g0358 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.42-6007A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2903522 | |||||||
| chr12:2903562 | CAA | C | 215 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(212): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.42-5954_42-5953del others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2903562 | ||||||
| chr12:2903578 | A | G | 2 | a0004c0005t0012g0144 a0004c0005t0012g0145 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.42-5951A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2903578 | |||||||
| chr12:2903579 | A | C | 2 | a0004c0005t0012g0144 a0004c0005t0012g0145 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.42-5950A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2903579 | |||||||
| chr12:2903757 | C | T | 1 | a0001c0002t0003g0197 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.42-5772C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2903757 | |||||||
| chr12:2903769 | G | A | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-5760G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2903769 | |||||||
| chr12:2903793 | G | T | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-5736G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2903793 | |||||||
| chr12:2903819 | G | A | 5 | a0001c0002t0005g0112 a0001c0002t0005g0113 a0001c0002t0005g0114 others(2): Show |
5 | HG02615.hp1 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-5710G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2903819 | |||||||
| chr12:2903852 | C | T | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-5677C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2903852 | |||||||
| chr12:2903869 | C | T | 97 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(94): Show |
99 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.42-5660C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2903869 | |||||||
| chr12:2903972 | C | T | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-5557C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2903972 | |||||||
| chr12:2904028 | C | T | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-5501C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2904028 | |||||||
| chr12:2904163 | C | T | 2 | a0001c0001t0001g0303 a0001c0001t0001g0345 |
2 | NA18959.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.42-5366C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2904163 | |||||||
| chr12:2904166 | G | T | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-5363G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2904166 | |||||||
| chr12:2904227 | G | T | 1 | a0001c0001t0014g0315 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.42-5302G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2904227 | |||||||
| chr12:2904352 | A | G | 2 | a0004c0005t0012g0144 a0004c0005t0012g0145 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.42-5177A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2904352 | |||||||
| chr12:2904586 | C | T | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.42-4943C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2904586 | |||||||
| chr12:2904590 | T | G | 2 | a0001c0001t0002g0075 a0001c0001t0002g0076 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.42-4939T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2904590 | |||||||
| chr12:2904657 | A | G | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.42-4872A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2904657 | |||||||
| chr12:2904762 | GT | G | 15 | a0001c0001t0004g0013 a0001c0001t0004g0094 a0001c0001t0004g0122 others(12): Show |
15 | HG01346.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.42-4765delT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2904762 | ||||||
| chr12:2904933 | C | T | 1 | a0001c0001t0017g0117 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.42-4596C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2904933 | |||||||
| chr12:2905084 | C | CAA | 143 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(140): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.42-4436_42-4435dup others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2905084 | ||||||
| chr12:2905084 | C | CAAAA | 17 | a0001c0001t0004g0013 a0001c0001t0004g0094 a0001c0001t0004g0122 others(14): Show |
17 | HG01346.hp1 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.42-4438_42-4435dup others(4): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2905084 | ||||||
| chr12:2905187 | C | CTT | 213 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(210): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.42-4331_42-4330dup others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2905187 | ||||||
| chr12:2905343 | G | A | 7 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(4): Show |
7 | HG00558.hp1 NA18942.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-4186G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2905343 | |||||||
| chr12:2905374 | C | T | 1 | a0001c0001t0002g0033 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.42-4155C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2905374 | |||||||
| chr12:2905406 | G | T | 1 | a0001c0001t0001g0302 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.42-4123G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2905406 | |||||||
| chr12:2905464 | A | G | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-4065A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2905464 | |||||||
| chr12:2905642 | G | A | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-3887G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2905642 | |||||||
| chr12:2905665 | C | G | 1 | a0001c0001t0001g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.42-3864C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2905665 | |||||||
| chr12:2905711 | G | A | 1 | a0001c0002t0010g0358 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.42-3818G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2905711 | |||||||
| chr12:2905715 | T | TC | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-3814_42-3813ins others(1): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2905715 | |||||||
| chr12:2905729 | A | C | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.42-3800A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2905729 | |||||||
| chr12:2905842 | G | A | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-3687G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2905842 | |||||||
| chr12:2905856 | G | T | 4 | a0001c0001t0007g0245 a0001c0001t0007g0246 a0001c0001t0007g0247 others(1): Show |
4 | HG01106.hp1 HG02109.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-3673G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2905856 | |||||||
| chr12:2905995 | C | T | 77 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0016 others(74): Show |
79 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.42-3534C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2905995 | |||||||
| chr12:2906015 | CTGTGTAA others(23): Show |
C | 2 | a0001c0001t0007g0247 a0001c0001t0007g0331 |
2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.42-3512_42-3483del others(30): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2906015 | ||||||
| chr12:2906020 | T | TA | 98 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(95): Show |
100 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.42-3497dupA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2906020 | ||||||
| chr12:2906032 | A | AAT | 10 | a0001c0001t0002g0014 a0001c0001t0002g0035 a0001c0001t0002g0083 others(7): Show |
10 | HG00735.hp1 HG01070.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.42-3497_42-3496ins others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2906032 | |||||||
| chr12:2906033 | T | A | 115 | a0001c0001t0002g0071 a0001c0001t0002g0218 a0001c0001t0004g0013 others(112): Show |
118 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.42-3496T>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2906033 | |||||||
| chr12:2906034 | T | A | 1 | a0001c0002t0003g0212 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.42-3495T>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2906034 | |||||||
| chr12:2906045 | T | G | 1 | a0001c0002t0003g0002 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.42-3484T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2906045 | |||||||
| chr12:2906122 | C | T | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-3407C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2906122 | |||||||
| chr12:2906156 | A | G | 2 | a0001c0002t0010g0361 a0001c0002t0010g0363 |
2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.42-3373A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2906156 | |||||||
| chr12:2906216 | C | G | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-3313C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2906216 | |||||||
| chr12:2906261 | ACCTCGTG others(9): Show |
A | 4 | a0001c0001t0004g0096 a0001c0001t0004g0110 a0001c0001t0004g0111 others(1): Show |
4 | HG02055.hp1 HG02647.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-3262_42-3247del others(16): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2906261 | ||||||
| chr12:2906348 | C | T | 1 | a0001c0002t0003g0190 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.42-3181C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2906348 | |||||||
| chr12:2906476 | A | C | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.42-3053A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2906476 | |||||||
| chr12:2906533 | T | C | 1 | a0001c0001t0001g0357 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.42-2996T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2906533 | |||||||
| chr12:2906548 | C | T | 1 | a0001c0001t0004g0129 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.42-2981C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2906548 | |||||||
| chr12:2906556 | T | C | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-2973T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2906556 | |||||||
| chr12:2906625 | G | A | 1 | a0001c0002t0003g0154 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.42-2904G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2906625 | |||||||
| chr12:2906759 | T | C | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.42-2770T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2906759 | |||||||
| chr12:2906773 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.42-2756G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2906773 | |||||||
| chr12:2906797 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.42-2732T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2906797 | |||||||
| chr12:2907104 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.42-2425G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2907104 | |||||||
| chr12:2907255 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
8 | HG01192.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.42-2274G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2907255 | |||||||
| chr12:2907304 | C | T | 3 | a0001c0001t0002g0019 a0001c0001t0002g0086 a0001c0001t0002g0121 |
3 | HG02970.hp2 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.42-2225C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2907304 | |||||||
| chr12:2907429 | C | T | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-2100C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2907429 | |||||||
| chr12:2907462 | G | A | 2 | a0001c0001t0004g0122 a0001c0001t0004g0130 |
2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.42-2067G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2907462 | |||||||
| chr12:2907475 | C | CAAAAAAA others(1): Show |
10 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0077 others(7): Show |
10 | HG00408.hp2 HG00558.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.42-2046_42-2039dup others(8): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2907475 | ||||||
| chr12:2907475 | C | CAAAAAAA others(2): Show |
158 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(155): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.42-2047_42-2039dup others(9): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2907475 | ||||||
| chr12:2907475 | C | CAAAAAAA others(3): Show |
40 | a0001c0001t0001g0135 a0001c0001t0002g0021 a0001c0001t0002g0027 others(37): Show |
40 | HG00438.hp1 HG01175.hp1 HG01496.hp1 others(37): Show |
intron_variant | MODIFIER | c.42-2048_42-2039dup others(10): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2907475 | ||||||
| chr12:2907475 | C | CAAAAAAA others(4): Show |
5 | a0001c0001t0001g0024 a0001c0002t0003g0155 a0001c0002t0003g0164 others(2): Show |
5 | HG01106.hp2 HG01361.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-2049_42-2039dup others(11): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2907475 | ||||||
| chr12:2907489 | AATAC | A | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-2038_42-2035del others(4): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2907489 | ||||||
| chr12:2907659 | A | AT | 208 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(205): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.42-1870_42-1869ins others(1): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2907659 | |||||||
| chr12:2907660 | A | AT | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-1869_42-1868ins others(1): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2907660 | |||||||
| chr12:2907660 | A | T | 209 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(206): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.42-1869A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2907660 | |||||||
| chr12:2907661 | A | T | 221 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(218): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.42-1868A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2907661 | |||||||
| chr12:2907689 | C | T | 1 | a0009c0011t0020g0146 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.42-1840C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2907689 | |||||||
| chr12:2907728 | C | CT | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-1794dupT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2907728 | ||||||
| chr12:2907755 | G | C | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-1774G>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2907755 | |||||||
| chr12:2907767 | T | G | 2 | a0004c0005t0012g0144 a0004c0005t0012g0145 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.42-1762T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2907767 | |||||||
| chr12:2907877 | A | G | 2 | a0004c0005t0012g0144 a0004c0005t0012g0145 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.42-1652A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2907877 | |||||||
| chr12:2907936 | G | A | 125 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(122): Show |
127 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.42-1593G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2907936 | |||||||
| chr12:2907998 | A | G | 1 | a0001c0002t0005g0143 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.42-1531A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2907998 | |||||||
| chr12:2908053 | A | G | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-1476A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2908053 | |||||||
| chr12:2908191 | C | A | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.42-1338C>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2908191 | |||||||
| chr12:2908346 | A | G | 2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | HG00558.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.42-1183A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2908346 | |||||||
| chr12:2908414 | T | C | 1 | a0001c0001t0001g0262 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.42-1115T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2908414 | |||||||
| chr12:2908425 | G | GTTTT | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-1102_42-1101ins others(4): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2908425 | ||||||
| chr12:2908491 | C | G | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-1038C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2908491 | |||||||
| chr12:2908501 | T | C | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-1028T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2908501 | |||||||
| chr12:2908612 | C | CAG | 221 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(218): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.42-917_42-916insAG | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2908612 | |||||||
| chr12:2908630 | C | G | 1 | a0001c0002t0003g0210 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.42-899C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2908630 | |||||||
| chr12:2908708 | C | G | 2 | a0001c0002t0003g0189 a0001c0002t0003g0204 |
2 | HG02683.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.42-821C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2908708 | |||||||
| chr12:2908710 | G | A | 77 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(74): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.42-819G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2908710 | |||||||
| chr12:2908857 | T | TA | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-671dupA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2908857 | ||||||
| chr12:2908939 | C | T | 2 | a0001c0006t0011g0359 a0001c0006t0011g0362 |
2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.42-590C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2908939 | |||||||
| chr12:2908992 | C | T | 4 | a0001c0002t0003g0155 a0001c0002t0003g0188 a0001c0002t0003g0216 others(1): Show |
4 | HG00099.hp2 HG01361.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-537C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2908992 | |||||||
| chr12:2909150 | T | C | 1 | a0001c0002t0003g0095 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.42-379T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2909150 | |||||||
| chr12:2909278 | G | A | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.42-251G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2909278 | |||||||
| chr12:2909304 | T | G | 1 | a0001c0002t0005g0143 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.42-225T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2909304 | |||||||
| chr12:2909359 | G | A | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.42-170G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2909359 | |||||||
| chr12:2909484 | C | T | 1 | a0001c0001t0017g0117 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.42-45C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | chr12 | 2909484 | |||||||
| chr12:2909509 | AT | A | 214 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0225 others(211): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
splice_region_variant&intron_variant | LOW | c.42-6delT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2909509 | ||||||
| chr12:2909509 | ATT | A | 6 | a0001c0001t0002g0073 a0001c0002t0003g0170 a0001c0002t0003g0202 others(3): Show |
6 | HG03098.hp1 HG06807.hp2 NA18973.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.42-7_42-6delTT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 2909509 | ||||||
| chr12:2909636 | G | C | 74 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(71): Show |
77 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.93+56G>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2909636 | |||||||
| chr12:2909701 | G | T | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+121G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2909701 | |||||||
| chr12:2909711 | G | T | 1 | a0010c0009t0001g0301 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.93+131G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2909711 | |||||||
| chr12:2909859 | G | T | 70 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0222 others(67): Show |
71 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.93+279G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2909859 | |||||||
| chr12:2909956 | T | G | 209 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(206): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.93+376T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2909956 | |||||||
| chr12:2909985 | G | A | 125 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(122): Show |
127 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.93+405G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2909985 | |||||||
| chr12:2910019 | A | G | 221 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(218): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.93+439A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2910019 | |||||||
| chr12:2910030 | C | T | 1 | a0001c0002t0009g0157 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.93+450C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2910030 | |||||||
| chr12:2910031 | G | A | 15 | a0001c0001t0004g0013 a0001c0001t0004g0094 a0001c0001t0004g0122 others(12): Show |
15 | HG01346.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.93+451G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2910031 | |||||||
| chr12:2910086 | A | C | 1 | a0001c0001t0002g0035 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.93+506A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2910086 | |||||||
| chr12:2910089 | G | A | 1 | a0001c0001t0011g0360 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.93+509G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2910089 | |||||||
| chr12:2910093 | C | G | 25 | a0001c0001t0004g0013 a0001c0001t0004g0015 a0001c0001t0004g0023 others(22): Show |
25 | HG01346.hp1 HG01943.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.93+513C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2910093 | |||||||
| chr12:2910101 | A | G | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.93+521A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2910101 | |||||||
| chr12:2910142 | A | C | 2 | a0001c0001t0002g0018 a0001c0001t0002g0020 |
2 | HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.93+562A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2910142 | |||||||
| chr12:2910183 | C | T | 1 | a0001c0001t0004g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.93+603C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2910183 | |||||||
| chr12:2910201 | G | A | 1 | a0001c0001t0002g0011 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.93+621G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2910201 | |||||||
| chr12:2910243 | G | C | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.93+663G>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2910243 | |||||||
| chr12:2910279 | GA | G | 216 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(213): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.93+710delA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2910279 | ||||||
| chr12:2910293 | C | T | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.93+713C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2910293 | |||||||
| chr12:2910321 | C | T | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.93+741C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2910321 | |||||||
| chr12:2910359 | A | G | 7 | a0001c0001t0001g0243 a0001c0002t0005g0112 a0001c0002t0005g0113 others(4): Show |
7 | HG02615.hp1 HG02886.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.93+779A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2910359 | |||||||
| chr12:2910550 | A | G | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+970A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2910550 | |||||||
| chr12:2910838 | G | A | 1 | a0001c0002t0003g0216 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.93+1258G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2910838 | |||||||
| chr12:2910906 | G | A | 2 | a0001c0002t0003g0163 a0001c0002t0003g0171 |
2 | NA18945.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.93+1326G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2910906 | |||||||
| chr12:2911091 | GT | G | 8 | a0001c0001t0004g0013 a0001c0001t0004g0128 a0001c0001t0004g0129 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.93+1522delT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911091 | ||||||
| chr12:2911259 | G | A | 1 | a0001c0001t0002g0011 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.93+1679G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2911259 | |||||||
| chr12:2911478 | A | G | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0254 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.93+1898A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2911478 | |||||||
| chr12:2911500 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.93+1920C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2911500 | |||||||
| chr12:2911501 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.93+1921T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2911501 | |||||||
| chr12:2911519 | A | ATTTT | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.93+1942_93+1943ins others(4): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911519 | ||||||
| chr12:2911540 | A | T | 216 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(213): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.93+1960A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2911540 | |||||||
| chr12:2911611 | C | T | 1 | a0001c0001t0004g0015 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.93+2031C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2911611 | |||||||
| chr12:2911639 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.93+2059A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2911639 | |||||||
| chr12:2911645 | G | A | 4 | a0001c0001t0007g0245 a0001c0001t0007g0246 a0001c0001t0007g0247 others(1): Show |
4 | HG01106.hp1 HG02109.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.93+2065G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2911645 | |||||||
| chr12:2911650 | C | G | 1 | a0001c0001t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.93+2070C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2911650 | |||||||
| chr12:2911664 | C | CTT | 8 | a0001c0001t0001g0238 a0001c0001t0001g0248 a0001c0001t0001g0249 others(5): Show |
8 | HG00140.hp2 HG00639.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.93+2126_93+2127dup others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | C | CTTT | 11 | a0001c0001t0001g0007 a0001c0001t0001g0250 a0001c0001t0001g0257 others(8): Show |
12 | HG00642.hp2 HG01099.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.93+2125_93+2127dup others(3): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | C | CTTTT | 23 | a0001c0001t0001g0225 a0001c0001t0001g0227 a0001c0001t0001g0234 others(20): Show |
23 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.93+2124_93+2127dup others(4): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | C | CTTTTT | 24 | a0001c0001t0001g0008 a0001c0001t0001g0228 a0001c0001t0001g0231 others(21): Show |
25 | HG00597.hp1 HG00735.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.93+2123_93+2127dup others(5): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | C | CTTTTTT | 10 | a0001c0001t0001g0222 a0001c0001t0001g0243 a0001c0001t0001g0262 others(7): Show |
10 | HG00544.hp1 HG01169.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.93+2122_93+2127dup others(6): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | C | CTTTTTTT | 6 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0244 others(3): Show |
6 | HG01167.hp1 HG01358.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.93+2121_93+2127dup others(7): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | C | CTTTTTTT others(3): Show |
7 | a0001c0001t0001g0239 a0001c0001t0001g0241 a0001c0001t0001g0251 others(4): Show |
7 | HG02273.hp2 HG04204.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+2118_93+2127dup others(10): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | C | CTTTTTTT others(4): Show |
3 | a0001c0001t0001g0240 a0001c0001t0001g0254 a0001c0001t0001g0304 |
3 | HG02602.hp2 NA18951.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.93+2117_93+2127dup others(11): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001g0279 a0001c0001t0001g0308 |
2 | HG04228.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.93+2116_93+2127dup others(12): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0263 a0001c0001t0001g0339 |
2 | NA18967.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.93+2115_93+2127dup others(13): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0242 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.93+2112_93+2127dup others(16): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0014g0315 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.93+2102_93+2127dup others(26): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0266 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.93+2117_93+2127del others(11): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.93+2116_93+2127del others(12): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0201 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.93+2113_93+2127del others(15): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0302 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.93+2112_93+2127del others(16): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0001g0348 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.93+2111_93+2127del others(17): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | CTTTTTTT others(11): Show |
C | 3 | a0001c0001t0001g0316 a0001c0001t0001g0332 a0001c0001t0001g0347 |
3 | HG02135.hp1 HG02965.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.93+2110_93+2127del others(18): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | CTTTTTTT others(12): Show |
C | 25 | a0001c0001t0002g0021 a0001c0001t0002g0028 a0001c0001t0002g0029 others(22): Show |
25 | HG00438.hp1 HG00741.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.93+2109_93+2127del others(19): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | CTTTTTTT others(13): Show |
C | 165 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0135 others(162): Show |
169 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.93+2108_93+2127del others(20): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | CTTTTTTT others(14): Show |
C | 27 | a0001c0001t0002g0073 a0001c0001t0002g0120 a0001c0002t0003g0002 others(24): Show |
28 | HG00099.hp1 HG00099.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.93+2107_93+2127del others(21): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | CTTTTTTT others(15): Show |
C | 10 | a0001c0001t0001g0255 a0001c0001t0001g0280 a0001c0001t0001g0281 others(7): Show |
10 | HG01891.hp1 HG02165.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.93+2106_93+2127del others(22): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | CTTTTTTT others(16): Show |
C | 1 | a0002c0003t0006g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.93+2105_93+2127del others(23): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | CTTTTTTT others(17): Show |
C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0229 |
2 | HG01109.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.93+2104_93+2127del others(24): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | CTTTTTTT others(18): Show |
C | 1 | a0001c0001t0007g0245 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93+2103_93+2127del others(25): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911664 | CTTTTTTT others(22): Show |
C | 1 | a0001c0001t0001g0317 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.93+2099_93+2127del others(29): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2911664 | ||||||
| chr12:2911834 | C | T | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.93+2254C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2911834 | |||||||
| chr12:2911921 | T | A | 3 | a0001c0001t0001g0287 a0001c0001t0001g0297 a0010c0009t0001g0301 |
3 | HG00544.hp1 NA19002.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.93+2341T>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2911921 | |||||||
| chr12:2912016 | A | T | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.93+2436A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2912016 | |||||||
| chr12:2912114 | A | G | 2 | a0001c0001t0001g0223 a0001c0001t0001g0318 |
2 | HG01167.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.93+2534A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2912114 | |||||||
| chr12:2912403 | G | A | 19 | a0001c0001t0002g0014 a0001c0001t0002g0018 a0001c0001t0002g0019 others(16): Show |
19 | HG00735.hp1 HG01070.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.93+2823G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2912403 | |||||||
| chr12:2912729 | A | G | 1 | a0007c0008t0002g0091 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.93+3149A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2912729 | |||||||
| chr12:2912774 | A | G | 2 | a0001c0002t0003g0203 a0001c0002t0005g0150 |
2 | NA18979.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.93+3194A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2912774 | |||||||
| chr12:2912843 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.93+3263G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2912843 | |||||||
| chr12:2912855 | C | T | 8 | a0001c0001t0001g0287 a0001c0001t0001g0292 a0001c0001t0001g0293 others(5): Show |
8 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(5): Show |
intron_variant | MODIFIER | c.93+3275C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2912855 | |||||||
| chr12:2912894 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.93+3314G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2912894 | |||||||
| chr12:2912966 | G | A | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+3386G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2912966 | |||||||
| chr12:2912979 | T | TTC | 77 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(74): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.93+3400_93+3401ins others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2912979 | ||||||
| chr12:2912982 | T | C | 86 | a0001c0001t0001g0244 a0001c0002t0003g0002 a0001c0002t0003g0003 others(83): Show |
89 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.93+3402T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2912982 | |||||||
| chr12:2912982 | T | TC | 133 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(130): Show |
135 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.93+3402_93+3403ins others(1): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2912982 | |||||||
| chr12:2913099 | T | G | 1 | a0008c0012t0003g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93+3519T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2913099 | |||||||
| chr12:2913148 | G | A | 3 | a0001c0001t0001g0267 a0001c0001t0001g0270 a0001c0001t0001g0271 |
3 | HG00140.hp1 HG00639.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.93+3568G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2913148 | |||||||
| chr12:2913148 | G | T | 3 | a0001c0001t0001g0325 a0001c0001t0001g0341 a0001c0001t0001g0354 |
3 | NA18941.hp2 NA18956.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.93+3568G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2913148 | |||||||
| chr12:2913198 | A | AGT | 7 | a0001c0001t0004g0082 a0001c0001t0004g0096 a0001c0001t0004g0110 others(4): Show |
7 | HG01346.hp1 HG02055.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.93+3619_93+3620dup others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2913198 | ||||||
| chr12:2913201 | T | G | 24 | a0001c0001t0004g0013 a0001c0001t0004g0015 a0001c0001t0004g0023 others(21): Show |
24 | HG01346.hp1 HG01943.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.93+3621T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2913201 | |||||||
| chr12:2913201 | T | TTG | 132 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(129): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.93+3641_93+3642dup others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2913201 | ||||||
| chr12:2913201 | T | TTGTG | 23 | a0001c0001t0001g0024 a0001c0001t0002g0019 a0001c0001t0002g0021 others(20): Show |
23 | HG01109.hp1 HG02129.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.93+3639_93+3642dup others(4): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2913201 | ||||||
| chr12:2913201 | T | TTGTGTG | 15 | a0001c0001t0002g0014 a0001c0001t0002g0062 a0001c0001t0002g0065 others(12): Show |
15 | HG01099.hp2 HG01106.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.93+3637_93+3642dup others(6): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2913201 | ||||||
| chr12:2913201 | T | TTGTGTGT others(1): Show |
21 | a0001c0001t0002g0011 a0001c0001t0002g0026 a0001c0001t0002g0078 others(18): Show |
22 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.93+3635_93+3642dup others(8): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2913201 | ||||||
| chr12:2913201 | T | TTGTGTGT others(3): Show |
1 | a0001c0001t0001g0135 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.93+3633_93+3642dup others(10): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2913201 | ||||||
| chr12:2913221 | GTA | G | 3 | a0001c0001t0002g0105 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG00741.hp1 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.93+3643_93+3644del others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2913221 | ||||||
| chr12:2913223 | A | G | 217 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(214): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.93+3643A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2913223 | |||||||
| chr12:2913243 | C | G | 1 | a0001c0001t0001g0279 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.93+3663C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2913243 | |||||||
| chr12:2913248 | AT | A | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.93+3677delT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2913248 | ||||||
| chr12:2913274 | T | G | 221 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(218): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.93+3694T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2913274 | |||||||
| chr12:2913366 | G | T | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.93+3786G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2913366 | |||||||
| chr12:2913401 | C | G | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+3821C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2913401 | |||||||
| chr12:2913594 | C | T | 1 | a0001c0001t0002g0090 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.93+4014C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2913594 | |||||||
| chr12:2913670 | A | G | 221 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(218): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.93+4090A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2913670 | |||||||
| chr12:2913703 | C | T | 97 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(94): Show |
99 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.93+4123C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2913703 | |||||||
| chr12:2913760 | G | A | 2 | a0001c0002t0003g0156 a0001c0002t0003g0207 |
2 | NA18961.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.93+4180G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2913760 | |||||||
| chr12:2913892 | A | G | 5 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(2): Show |
5 | HG00408.hp1 NA18944.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.93+4312A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2913892 | |||||||
| chr12:2913997 | C | T | 2 | a0004c0005t0012g0144 a0004c0005t0012g0145 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.93+4417C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2913997 | |||||||
| chr12:2914125 | C | CTT | 14 | a0001c0001t0001g0310 a0001c0001t0002g0030 a0001c0001t0002g0073 others(11): Show |
14 | HG00544.hp2 HG01168.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.93+4560_93+4561dup others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2914125 | ||||||
| chr12:2914125 | C | CTTT | 175 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(172): Show |
180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.93+4559_93+4561dup others(3): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2914125 | ||||||
| chr12:2914125 | C | CTTTT | 28 | a0001c0001t0002g0055 a0001c0001t0002g0065 a0001c0001t0002g0077 others(25): Show |
28 | HG00735.hp1 HG01346.hp1 HG01943.hp1 others(25): Show |
intron_variant | MODIFIER | c.93+4558_93+4561dup others(4): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2914125 | ||||||
| chr12:2914188 | A | C | 1 | a0001c0002t0005g0114 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.93+4608A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2914188 | |||||||
| chr12:2914197 | T | C | 99 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(96): Show |
101 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.93+4617T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2914197 | |||||||
| chr12:2914206 | C | A | 125 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(122): Show |
127 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.93+4626C>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2914206 | |||||||
| chr12:2914224 | A | G | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG02040.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.93+4644A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2914224 | |||||||
| chr12:2914312 | C | T | 1 | a0001c0001t0002g0090 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.93+4732C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2914312 | |||||||
| chr12:2914344 | G | C | 2 | a0004c0005t0012g0144 a0004c0005t0012g0145 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.93+4764G>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2914344 | |||||||
| chr12:2914376 | A | T | 125 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(122): Show |
127 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.93+4796A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2914376 | |||||||
| chr12:2914451 | C | T | 1 | a0001c0001t0017g0117 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.93+4871C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2914451 | |||||||
| chr12:2914555 | T | C | 221 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(218): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.93+4975T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2914555 | |||||||
| chr12:2914583 | T | C | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.93+5003T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2914583 | |||||||
| chr12:2914724 | C | A | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.93+5144C>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2914724 | |||||||
| chr12:2914821 | T | G | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.93+5241T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2914821 | |||||||
| chr12:2915088 | A | G | 1 | a0001c0001t0001g0302 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.93+5508A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2915088 | |||||||
| chr12:2915233 | A | G | 1 | a0009c0011t0020g0146 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.94-5530A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2915233 | |||||||
| chr12:2915452 | T | C | 1 | a0001c0002t0019g0174 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.94-5311T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2915452 | |||||||
| chr12:2915545 | G | GT | 357 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(354): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.94-5206dupT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2915545 | ||||||
| chr12:2915579 | G | T | 97 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(94): Show |
99 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.94-5184G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2915579 | |||||||
| chr12:2915603 | A | T | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.94-5160A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2915603 | |||||||
| chr12:2915773 | T | C | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-4990T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2915773 | |||||||
| chr12:2915912 | A | G | 1 | a0001c0002t0003g0202 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.94-4851A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2915912 | |||||||
| chr12:2916114 | A | G | 6 | a0001c0002t0005g0112 a0001c0002t0005g0113 a0001c0002t0005g0114 others(3): Show |
6 | HG02615.hp1 HG02886.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.94-4649A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2916114 | |||||||
| chr12:2916207 | C | A | 1 | a0001c0001t0001g0321 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.94-4556C>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2916207 | |||||||
| chr12:2916266 | T | C | 2 | a0004c0005t0012g0144 a0004c0005t0012g0145 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.94-4497T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2916266 | |||||||
| chr12:2916282 | A | G | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.94-4481A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2916282 | |||||||
| chr12:2916293 | C | T | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.94-4470C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2916293 | |||||||
| chr12:2916406 | A | AGCCCCAG | 224 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(221): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.94-4355_94-4354ins others(7): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2916406 | ||||||
| chr12:2916411 | G | T | 224 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(221): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.94-4352G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2916411 | |||||||
| chr12:2916423 | T | G | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.94-4340T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2916423 | |||||||
| chr12:2916500 | G | A | 221 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(218): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.94-4263G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2916500 | |||||||
| chr12:2916532 | G | A | 25 | a0001c0001t0004g0013 a0001c0001t0004g0015 a0001c0001t0004g0023 others(22): Show |
25 | HG01346.hp1 HG01943.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.94-4231G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2916532 | |||||||
| chr12:2916532 | G | C | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-4231G>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2916532 | |||||||
| chr12:2916600 | T | C | 1 | a0001c0001t0001g0276 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.94-4163T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2916600 | |||||||
| chr12:2916607 | A | G | 5 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(2): Show |
5 | HG02129.hp1 NA18951.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-4156A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2916607 | |||||||
| chr12:2916729 | C | G | 2 | a0001c0001t0002g0028 a0001c0001t0002g0063 |
2 | NA18998.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.94-4034C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2916729 | |||||||
| chr12:2916842 | A | T | 2 | a0001c0006t0011g0359 a0001c0006t0011g0362 |
2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.94-3921A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2916842 | |||||||
| chr12:2917067 | C | T | 1 | a0001c0001t0001g0328 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.94-3696C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2917067 | |||||||
| chr12:2917615 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.94-3148T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2917615 | |||||||
| chr12:2917659 | T | C | 100 | a0001c0001t0001g0272 a0001c0001t0002g0001 a0001c0001t0002g0011 others(97): Show |
102 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.94-3104T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2917659 | |||||||
| chr12:2917688 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.94-3075C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2917688 | |||||||
| chr12:2917709 | T | C | 1 | a0001c0001t0002g0058 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.94-3054T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2917709 | |||||||
| chr12:2917737 | C | T | 1 | a0001c0002t0003g0200 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.94-3026C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2917737 | |||||||
| chr12:2917739 | C | T | 2 | a0001c0001t0001g0356 a0001c0001t0001g0357 |
2 | HG00642.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.94-3024C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2917739 | |||||||
| chr12:2917751 | C | G | 2 | a0001c0001t0002g0086 a0001c0001t0002g0121 |
2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.94-3012C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2917751 | |||||||
| chr12:2917753 | T | G | 4 | a0001c0002t0010g0361 a0001c0002t0010g0363 a0004c0005t0012g0144 others(1): Show |
4 | HG02717.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-3010T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2917753 | |||||||
| chr12:2917809 | G | A | 1 | a0001c0002t0003g0190 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.94-2954G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2917809 | |||||||
| chr12:2917853 | T | G | 5 | a0001c0002t0005g0112 a0001c0002t0005g0113 a0001c0002t0005g0114 others(2): Show |
5 | HG02615.hp1 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-2910T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2917853 | |||||||
| chr12:2917876 | C | CA | 216 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(213): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.94-2877dupA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2917876 | ||||||
| chr12:2918246 | C | G | 1 | a0001c0002t0010g0358 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.94-2517C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2918246 | |||||||
| chr12:2918246 | C | T | 223 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0248 others(220): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.94-2517C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2918246 | |||||||
| chr12:2918274 | T | A | 2 | a0001c0006t0011g0359 a0001c0006t0011g0362 |
2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.94-2489T>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2918274 | |||||||
| chr12:2918304 | G | A | 1 | a0001c0001t0002g0014 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.94-2459G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2918304 | |||||||
| chr12:2918413 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.94-2350A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2918413 | |||||||
| chr12:2918570 | T | A | 3 | a0001c0001t0004g0096 a0001c0001t0004g0110 a0001c0001t0004g0111 |
3 | HG02647.hp1 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.94-2193T>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2918570 | |||||||
| chr12:2918570 | T | C | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.94-2193T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2918570 | |||||||
| chr12:2918603 | T | C | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.94-2160T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2918603 | |||||||
| chr12:2918643 | C | T | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.94-2120C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2918643 | |||||||
| chr12:2918700 | C | T | 4 | a0001c0001t0004g0015 a0001c0001t0004g0107 a0001c0001t0004g0108 others(1): Show |
4 | HG01943.hp1 NA18949.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-2063C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2918700 | |||||||
| chr12:2918775 | G | C | 1 | a0001c0001t0002g0093 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.94-1988G>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2918775 | |||||||
| chr12:2918793 | G | C | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-1970G>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2918793 | |||||||
| chr12:2918912 | G | A | 5 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(2): Show |
5 | HG00408.hp1 NA18944.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-1851G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2918912 | |||||||
| chr12:2919067 | T | C | 5 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(2): Show |
5 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-1696T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2919067 | |||||||
| chr12:2919171 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.94-1592C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2919171 | |||||||
| chr12:2919225 | T | C | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.94-1538T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2919225 | |||||||
| chr12:2919316 | A | C | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.94-1447A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2919316 | |||||||
| chr12:2919343 | A | G | 1 | a0001c0001t0002g0014 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.94-1420A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2919343 | |||||||
| chr12:2919562 | T | C | 2 | a0001c0001t0002g0118 a0001c0001t0002g0119 |
2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.94-1201T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2919562 | |||||||
| chr12:2919671 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.94-1092T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2919671 | |||||||
| chr12:2919776 | T | C | 1 | a0001c0002t0003g0198 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.94-987T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2919776 | |||||||
| chr12:2920033 | TA | T | 7 | a0001c0001t0001g0253 a0001c0001t0001g0271 a0001c0001t0002g0056 others(4): Show |
7 | HG00140.hp1 HG01975.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.94-717delA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 2920033 | ||||||
| chr12:2920180 | A | T | 1 | a0001c0001t0001g0309 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.94-583A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2920180 | |||||||
| chr12:2920247 | C | T | 1 | a0001c0001t0007g0247 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.94-516C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2920247 | |||||||
| chr12:2920278 | GGCAAGCA others(3): Show |
G | 1 | a0002c0003t0006g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.94-484_94-475delGC others(8): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2920278 | |||||||
| chr12:2920346 | C | G | 1 | a0001c0002t0003g0175 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.94-417C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2920346 | |||||||
| chr12:2920361 | T | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0229 |
2 | HG01109.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.94-402T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2920361 | |||||||
| chr12:2920370 | A | G | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.94-393A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2920370 | |||||||
| chr12:2920414 | C | T | 2 | a0001c0002t0003g0147 a0001c0002t0003g0148 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.94-349C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2920414 | |||||||
| chr12:2920503 | G | A | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.94-260G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2920503 | |||||||
| chr12:2920551 | T | G | 1 | a0001c0001t0001g0353 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.94-212T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2920551 | |||||||
| chr12:2920697 | C | T | 10 | a0001c0001t0004g0015 a0001c0001t0004g0023 a0001c0001t0004g0082 others(7): Show |
10 | HG01943.hp1 HG02055.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.94-66C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 2/10 | chr12 | 2920697 | |||||||
| chr12:2921362 | G | A | 11 | a0001c0001t0007g0245 a0001c0001t0007g0246 a0001c0001t0007g0247 others(8): Show |
11 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.253+440G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 3/10 | chr12 | 2921362 | |||||||
| chr12:2921372 | C | T | 1 | a0001c0001t0001g0353 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.253+450C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 3/10 | chr12 | 2921372 | |||||||
| chr12:2921412 | A | AT | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.253+492dupT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 2921412 | ||||||
| chr12:2921423 | G | A | 1 | a0006c0007t0001g0236 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.253+501G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 3/10 | chr12 | 2921423 | |||||||
| chr12:2921560 | A | G | 220 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(217): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.253+638A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 3/10 | chr12 | 2921560 | |||||||
| chr12:2921607 | G | A | 1 | a0001c0002t0003g0095 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.254-655G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 3/10 | chr12 | 2921607 | |||||||
| chr12:2921679 | A | G | 1 | a0001c0002t0003g0185 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.254-583A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 3/10 | chr12 | 2921679 | |||||||
| chr12:2921690 | A | G | 1 | a0001c0001t0017g0117 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.254-572A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 3/10 | chr12 | 2921690 | |||||||
| chr12:2921744 | A | C | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.254-518A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 3/10 | chr12 | 2921744 | |||||||
| chr12:2921995 | A | C | 4 | a0001c0001t0002g0026 a0001c0001t0002g0078 a0001c0001t0002g0079 others(1): Show |
4 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.254-267A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 3/10 | chr12 | 2921995 | |||||||
| chr12:2922192 | T | C | 222 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0288 others(219): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.254-70T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 3/10 | chr12 | 2922192 | |||||||
| chr12:2922193 | G | A | 1 | a0001c0002t0003g0151 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.254-69G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 3/10 | chr12 | 2922193 | |||||||
| chr12:2922443 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.394+41C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2922443 | |||||||
| chr12:2922666 | T | C | 221 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(218): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.394+264T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2922666 | |||||||
| chr12:2922759 | T | C | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.394+357T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2922759 | |||||||
| chr12:2922855 | A | AT | 10 | a0001c0001t0001g0259 a0001c0001t0001g0267 a0001c0001t0001g0269 others(7): Show |
10 | HG00741.hp2 HG03098.hp1 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.394+469dupT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 2922855 | ||||||
| chr12:2922855 | A | ATTT | 16 | a0001c0001t0001g0024 a0001c0001t0002g0018 a0001c0001t0002g0022 others(13): Show |
16 | HG01109.hp1 HG01256.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.394+467_394+469dup others(3): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 2922855 | ||||||
| chr12:2922855 | A | ATTTT | 178 | a0001c0001t0001g0135 a0001c0001t0002g0001 a0001c0001t0002g0011 others(175): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.394+466_394+469dup others(4): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 2922855 | ||||||
| chr12:2922855 | A | ATTTTT | 21 | a0001c0001t0002g0029 a0001c0001t0002g0032 a0001c0001t0002g0040 others(18): Show |
21 | HG01175.hp1 HG01261.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.394+465_394+469dup others(5): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 2922855 | ||||||
| chr12:2922947 | G | A | 2 | a0001c0001t0002g0077 a0001c0002t0003g0211 |
2 | NA18991.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.394+545G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2922947 | |||||||
| chr12:2922955 | G | A | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.394+553G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2922955 | |||||||
| chr12:2922995 | A | G | 1 | a0001c0002t0003g0185 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.394+593A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2922995 | |||||||
| chr12:2923056 | G | A | 1 | a0001c0001t0011g0360 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.394+654G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2923056 | |||||||
| chr12:2923098 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.394+696G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2923098 | |||||||
| chr12:2923147 | C | A | 15 | a0001c0001t0004g0013 a0001c0001t0004g0094 a0001c0001t0004g0122 others(12): Show |
15 | HG01346.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.394+745C>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2923147 | |||||||
| chr12:2923648 | C | CA | 10 | a0001c0001t0002g0054 a0001c0001t0021g0059 a0001c0002t0005g0112 others(7): Show |
10 | HG02615.hp1 HG02886.hp1 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.394+1261dupA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 2923648 | ||||||
| chr12:2923648 | CA | C | 10 | a0001c0001t0001g0249 a0001c0001t0001g0283 a0001c0001t0001g0354 others(7): Show |
10 | HG01070.hp1 HG01099.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.394+1261delA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 2923648 | ||||||
| chr12:2923784 | C | T | 1 | a0001c0002t0005g0143 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.394+1382C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2923784 | |||||||
| chr12:2923817 | C | CA | 9 | a0001c0001t0001g0250 a0001c0001t0001g0271 a0001c0001t0001g0304 others(6): Show |
9 | HG00140.hp1 HG01175.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.394+1428dupA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 2923817 | ||||||
| chr12:2923817 | CA | C | 16 | a0001c0001t0002g0011 a0001c0001t0004g0013 a0001c0001t0004g0094 others(13): Show |
16 | HG01346.hp1 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.394+1428delA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 2923817 | ||||||
| chr12:2923849 | G | A | 1 | a0001c0001t0004g0023 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.394+1447G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2923849 | |||||||
| chr12:2923932 | G | A | 79 | a0001c0001t0001g0347 a0001c0001t0001g0348 a0001c0002t0003g0002 others(76): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.394+1530G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2923932 | |||||||
| chr12:2923932 | G | T | 2 | a0004c0005t0012g0144 a0004c0005t0012g0145 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.394+1530G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2923932 | |||||||
| chr12:2924278 | G | A | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.394+1876G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924278 | |||||||
| chr12:2924675 | T | C | 1 | a0001c0001t0002g0074 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.394+2273T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924675 | |||||||
| chr12:2924688 | T | TA | 8 | a0001c0001t0001g0330 a0001c0001t0001g0335 a0002c0003t0006g0136 others(5): Show |
8 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.394+2301dupA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 2924688 | ||||||
| chr12:2924688 | TA | T | 8 | a0001c0001t0001g0242 a0001c0001t0001g0260 a0001c0001t0001g0271 others(5): Show |
8 | HG00140.hp1 HG00140.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.394+2301delA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 2924688 | ||||||
| chr12:2924689 | A | T | 208 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(205): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.394+2287A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924689 | |||||||
| chr12:2924690 | A | T | 4 | a0001c0001t0001g0135 a0001c0001t0002g0031 a0001c0001t0002g0052 others(1): Show |
4 | HG02273.hp1 NA18966.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.394+2288A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924690 | |||||||
| chr12:2924771 | T | TAAGCAAT others(9): Show |
1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2369_394+2370i others(18): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924771 | |||||||
| chr12:2924773 | G | C | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2371G>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924773 | |||||||
| chr12:2924781 | G | A | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2379G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924781 | |||||||
| chr12:2924785 | T | G | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2383T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924785 | |||||||
| chr12:2924788 | A | G | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2386A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924788 | |||||||
| chr12:2924793 | G | T | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2391G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924793 | |||||||
| chr12:2924798 | G | A | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2396G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924798 | |||||||
| chr12:2924799 | A | G | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2397A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924799 | |||||||
| chr12:2924804 | A | T | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2402A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924804 | |||||||
| chr12:2924820 | T | C | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2418T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924820 | |||||||
| chr12:2924825 | G | C | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2423G>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924825 | |||||||
| chr12:2924827 | CTGTGTGT others(6): Show |
C | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2426_394+2438d others(15): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924827 | |||||||
| chr12:2924842 | G | A | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2440G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924842 | |||||||
| chr12:2924848 | G | T | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2446G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924848 | |||||||
| chr12:2924850 | C | T | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2448C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924850 | |||||||
| chr12:2924852 | C | T | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2450C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924852 | |||||||
| chr12:2924853 | A | T | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2451A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924853 | |||||||
| chr12:2924854 | A | T | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2452A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924854 | |||||||
| chr12:2924855 | A | T | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2453A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924855 | |||||||
| chr12:2924856 | A | T | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2454A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924856 | |||||||
| chr12:2924857 | A | T | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2455A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924857 | |||||||
| chr12:2924858 | A | T | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2456A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924858 | |||||||
| chr12:2924863 | A | T | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2461A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924863 | |||||||
| chr12:2924864 | A | T | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2462A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924864 | |||||||
| chr12:2924870 | A | G | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2468A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924870 | |||||||
| chr12:2924872 | T | C | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2470T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924872 | |||||||
| chr12:2924874 | A | T | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2472A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924874 | |||||||
| chr12:2924875 | A | G | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2473A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924875 | |||||||
| chr12:2924876 | A | G | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2474A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924876 | |||||||
| chr12:2924877 | A | T | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2475A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924877 | |||||||
| chr12:2924880 | A | C | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2478A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924880 | |||||||
| chr12:2924884 | A | T | 1 | a0001c0001t0001g0350 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.394+2482A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924884 | |||||||
| chr12:2924886 | A | C | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2484A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924886 | |||||||
| chr12:2924887 | A | T | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2485A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924887 | |||||||
| chr12:2924888 | A | G | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2486A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924888 | |||||||
| chr12:2924889 | A | T | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2487A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924889 | |||||||
| chr12:2924890 | A | C | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2488A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924890 | |||||||
| chr12:2924892 | A | C | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2490A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924892 | |||||||
| chr12:2924893 | T | C | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2491T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924893 | |||||||
| chr12:2924894 | A | C | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2492A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924894 | |||||||
| chr12:2924895 | G | A | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2493G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924895 | |||||||
| chr12:2924902 | G | T | 1 | a0001c0001t0002g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+2500G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924902 | |||||||
| chr12:2924952 | C | T | 1 | a0001c0001t0004g0128 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.394+2550C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2924952 | |||||||
| chr12:2925002 | C | A | 1 | a0001c0002t0005g0143 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.394+2600C>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2925002 | |||||||
| chr12:2925055 | C | T | 1 | a0001c0001t0002g0064 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.394+2653C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2925055 | |||||||
| chr12:2925092 | C | T | 1 | a0001c0001t0002g0025 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.394+2690C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2925092 | |||||||
| chr12:2925166 | C | A | 1 | a0001c0001t0002g0085 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.394+2764C>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2925166 | |||||||
| chr12:2925213 | C | T | 1 | a0005c0010t0002g0102 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.394+2811C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2925213 | |||||||
| chr12:2925283 | G | A | 1 | a0001c0001t0002g0090 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.394+2881G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2925283 | |||||||
| chr12:2925318 | G | A | 77 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(74): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.394+2916G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2925318 | |||||||
| chr12:2925324 | C | T | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.394+2922C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2925324 | |||||||
| chr12:2925364 | T | C | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.394+2962T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2925364 | |||||||
| chr12:2925491 | G | A | 1 | a0001c0002t0003g0206 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.394+3089G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2925491 | |||||||
| chr12:2925635 | A | G | 10 | a0001c0001t0004g0015 a0001c0001t0004g0023 a0001c0001t0004g0082 others(7): Show |
10 | HG01943.hp1 HG02055.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.394+3233A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2925635 | |||||||
| chr12:2925709 | G | A | 1 | a0001c0001t0002g0014 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.394+3307G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2925709 | |||||||
| chr12:2925741 | A | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0264 a0001c0001t0001g0298 |
4 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.394+3339A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2925741 | |||||||
| chr12:2925884 | A | G | 211 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(208): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.394+3482A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2925884 | |||||||
| chr12:2925931 | C | T | 2 | a0001c0002t0010g0361 a0001c0002t0010g0363 |
2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.394+3529C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2925931 | |||||||
| chr12:2926404 | C | T | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.395-3844C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2926404 | |||||||
| chr12:2926407 | G | A | 1 | a0001c0001t0017g0117 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.395-3841G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2926407 | |||||||
| chr12:2926465 | A | G | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.395-3783A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2926465 | |||||||
| chr12:2926501 | G | A | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.395-3747G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2926501 | |||||||
| chr12:2926539 | A | G | 1 | a0001c0001t0017g0117 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.395-3709A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2926539 | |||||||
| chr12:2926689 | T | C | 1 | a0001c0001t0002g0042 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.395-3559T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2926689 | |||||||
| chr12:2926729 | C | T | 1 | a0001c0001t0014g0315 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.395-3519C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2926729 | |||||||
| chr12:2926764 | TGTG | T | 224 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(221): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.395-3473_395-3471d others(5): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 2926764 | ||||||
| chr12:2927120 | T | TCATA | 21 | a0001c0001t0002g0014 a0001c0001t0002g0018 a0001c0001t0002g0019 others(18): Show |
21 | HG00735.hp1 HG01070.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.395-3125_395-3122d others(6): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 2927120 | ||||||
| chr12:2927189 | T | C | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.395-3059T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2927189 | |||||||
| chr12:2927200 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.395-3048C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2927200 | |||||||
| chr12:2927231 | C | T | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.395-3017C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2927231 | |||||||
| chr12:2927366 | A | AT | 7 | a0001c0001t0001g0255 a0001c0001t0001g0280 a0001c0001t0001g0281 others(4): Show |
7 | HG02071.hp1 HG02135.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.395-2864dupT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 2927366 | ||||||
| chr12:2927366 | A | ATTTTTTT others(3): Show |
8 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0018 others(5): Show |
8 | HG01169.hp1 HG02922.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.395-2873_395-2864d others(12): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 2927366 | ||||||
| chr12:2927366 | A | ATTTTTTT others(4): Show |
63 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0017 others(60): Show |
65 | HG00544.hp2 HG00639.hp1 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.395-2874_395-2864d others(13): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 2927366 | ||||||
| chr12:2927366 | A | ATTTTTTT others(5): Show |
110 | a0001c0001t0002g0012 a0001c0001t0002g0021 a0001c0001t0002g0022 others(107): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.395-2875_395-2864d others(14): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 2927366 | ||||||
| chr12:2927366 | A | ATTTTTTT others(6): Show |
29 | a0001c0001t0002g0011 a0001c0001t0002g0016 a0001c0001t0002g0029 others(26): Show |
29 | HG00741.hp1 HG01069.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.395-2876_395-2864d others(15): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 2927366 | ||||||
| chr12:2927366 | ATTT | A | 8 | a0001c0002t0010g0358 a0002c0003t0006g0136 a0002c0003t0006g0137 others(5): Show |
8 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.395-2866_395-2864d others(5): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 2927366 | ||||||
| chr12:2927435 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.395-2813C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2927435 | |||||||
| chr12:2927448 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.395-2800C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2927448 | |||||||
| chr12:2927512 | G | A | 1 | a0001c0001t0017g0117 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.395-2736G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2927512 | |||||||
| chr12:2927543 | T | C | 221 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(218): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.395-2705T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2927543 | |||||||
| chr12:2927604 | C | T | 1 | a0001c0001t0017g0117 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.395-2644C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2927604 | |||||||
| chr12:2927613 | A | T | 15 | a0001c0001t0004g0013 a0001c0001t0004g0094 a0001c0001t0004g0122 others(12): Show |
15 | HG01346.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.395-2635A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2927613 | |||||||
| chr12:2927760 | G | A | 2 | a0004c0005t0012g0144 a0004c0005t0012g0145 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.395-2488G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2927760 | |||||||
| chr12:2927819 | T | C | 17 | a0001c0002t0003g0003 a0001c0002t0003g0153 a0001c0002t0003g0154 others(14): Show |
18 | HG00423.hp1 HG01106.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.395-2429T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2927819 | |||||||
| chr12:2927872 | A | G | 1 | a0001c0001t0002g0219 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.395-2376A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2927872 | |||||||
| chr12:2927976 | G | A | 22 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0306 others(19): Show |
22 | HG00423.hp2 HG00741.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.395-2272G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2927976 | |||||||
| chr12:2928084 | T | G | 1 | a0001c0001t0007g0331 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.395-2164T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2928084 | |||||||
| chr12:2928245 | A | G | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.395-2003A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2928245 | |||||||
| chr12:2928461 | C | T | 1 | a0001c0001t0001g0339 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.395-1787C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2928461 | |||||||
| chr12:2928499 | C | T | 1 | a0001c0001t0017g0117 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.395-1749C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2928499 | |||||||
| chr12:2928539 | T | A | 75 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(72): Show |
78 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.395-1709T>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2928539 | |||||||
| chr12:2928771 | T | A | 77 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(74): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.395-1477T>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2928771 | |||||||
| chr12:2928879 | A | G | 1 | a0001c0002t0003g0162 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.395-1369A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2928879 | |||||||
| chr12:2929054 | CT | C | 219 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0278 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.395-1181delT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 2929054 | ||||||
| chr12:2929069 | A | G | 6 | a0001c0002t0005g0112 a0001c0002t0005g0113 a0001c0002t0005g0114 others(3): Show |
6 | HG02615.hp1 HG02886.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.395-1179A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2929069 | |||||||
| chr12:2929178 | A | G | 1 | a0001c0002t0005g0143 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.395-1070A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2929178 | |||||||
| chr12:2929262 | A | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
8 | HG01192.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.395-986A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2929262 | |||||||
| chr12:2929271 | C | G | 1 | a0001c0001t0002g0034 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.395-977C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2929271 | |||||||
| chr12:2929288 | G | T | 99 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(96): Show |
101 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.395-960G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2929288 | |||||||
| chr12:2929340 | A | C | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.395-908A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2929340 | |||||||
| chr12:2929419 | A | G | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.395-829A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2929419 | |||||||
| chr12:2929451 | A | G | 1 | a0001c0002t0003g0180 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.395-797A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2929451 | |||||||
| chr12:2929528 | T | G | 211 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(208): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.395-720T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2929528 | |||||||
| chr12:2929639 | A | G | 99 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(96): Show |
101 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.395-609A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2929639 | |||||||
| chr12:2929640 | T | C | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.395-608T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2929640 | |||||||
| chr12:2929641 | A | G | 1 | a0001c0001t0001g0293 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.395-607A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2929641 | |||||||
| chr12:2929693 | C | T | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.395-555C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2929693 | |||||||
| chr12:2929715 | T | C | 2 | a0001c0001t0001g0333 a0001c0001t0014g0315 |
2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.395-533T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2929715 | |||||||
| chr12:2929751 | C | T | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.395-497C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2929751 | |||||||
| chr12:2929841 | A | G | 1 | a0001c0001t0001g0276 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.395-407A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2929841 | |||||||
| chr12:2929887 | C | G | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.395-361C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2929887 | |||||||
| chr12:2930134 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.395-114T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2930134 | |||||||
| chr12:2930153 | A | G | 221 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(218): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.395-95A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 4/10 | chr12 | 2930153 | |||||||
| chr12:2930383 | T | G | 1 | a0009c0011t0020g0146 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.492+38T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 5/10 | chr12 | 2930383 | |||||||
| chr12:2930428 | A | G | 1 | a0001c0002t0003g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.492+83A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 5/10 | chr12 | 2930428 | |||||||
| chr12:2930430 | T | G | 6 | a0001c0002t0005g0112 a0001c0002t0005g0113 a0001c0002t0005g0114 others(3): Show |
6 | HG02615.hp1 HG02886.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.492+85T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 5/10 | chr12 | 2930430 | |||||||
| chr12:2930547 | C | T | 5 | a0001c0002t0005g0112 a0001c0002t0005g0113 a0001c0002t0005g0114 others(2): Show |
5 | HG02615.hp1 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+202C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 5/10 | chr12 | 2930547 | |||||||
| chr12:2930568 | C | T | 12 | a0001c0001t0001g0233 a0001c0001t0001g0285 a0001c0001t0001g0286 others(9): Show |
12 | HG02074.hp2 HG02523.hp2 HG04184.hp2 others(9): Show |
intron_variant | MODIFIER | c.492+223C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 5/10 | chr12 | 2930568 | |||||||
| chr12:2930613 | C | G | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.492+268C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 5/10 | chr12 | 2930613 | |||||||
| chr12:2930666 | G | A | 7 | a0001c0001t0001g0233 a0001c0001t0001g0285 a0001c0001t0001g0286 others(4): Show |
7 | HG02074.hp2 HG02523.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.492+321G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 5/10 | chr12 | 2930666 | |||||||
| chr12:2930672 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.492+327C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 5/10 | chr12 | 2930672 | |||||||
| chr12:2930712 | C | A | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.493-325C>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 5/10 | chr12 | 2930712 | |||||||
| chr12:2930863 | C | T | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.493-174C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 5/10 | chr12 | 2930863 | |||||||
| chr12:2931329 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.696+89G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2931329 | |||||||
| chr12:2931673 | G | A | 221 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(218): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.696+433G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2931673 | |||||||
| chr12:2931677 | T | C | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.696+437T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2931677 | |||||||
| chr12:2931887 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.696+647C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2931887 | |||||||
| chr12:2931909 | C | T | 221 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(218): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.696+669C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2931909 | |||||||
| chr12:2932015 | A | G | 2 | a0001c0006t0011g0359 a0001c0006t0011g0362 |
2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.696+775A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2932015 | |||||||
| chr12:2932035 | C | G | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.696+795C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2932035 | |||||||
| chr12:2932046 | C | T | 3 | a0001c0001t0002g0012 a0001c0001t0002g0057 a0001c0001t0002g0061 |
3 | HG01256.hp1 HG01934.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.696+806C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2932046 | |||||||
| chr12:2932197 | T | A | 1 | a0001c0001t0001g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.696+957T>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2932197 | |||||||
| chr12:2932229 | A | G | 3 | a0001c0002t0003g0155 a0001c0002t0003g0216 a0008c0012t0003g0169 |
3 | HG01361.hp2 HG01515.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.696+989A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2932229 | |||||||
| chr12:2932258 | CTCTG | C | 5 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0022 others(2): Show |
5 | HG02451.hp2 HG02572.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.696+1024_696+1027d others(6): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 2932258 | ||||||
| chr12:2932319 | G | A | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.696+1079G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2932319 | |||||||
| chr12:2932336 | C | T | 2 | a0004c0005t0012g0144 a0004c0005t0012g0145 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.697-1082C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2932336 | |||||||
| chr12:2932337 | G | A | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.697-1081G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2932337 | |||||||
| chr12:2932384 | G | A | 1 | a0008c0012t0003g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.697-1034G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2932384 | |||||||
| chr12:2932433 | A | G | 2 | a0004c0005t0012g0144 a0004c0005t0012g0145 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.697-985A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2932433 | |||||||
| chr12:2932579 | C | CA | 117 | a0001c0001t0001g0135 a0001c0001t0001g0222 a0001c0001t0001g0225 others(114): Show |
120 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.697-819dupA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 2932579 | ||||||
| chr12:2932579 | C | CAA | 14 | a0001c0001t0002g0054 a0001c0002t0003g0147 a0001c0002t0003g0162 others(11): Show |
14 | HG01175.hp1 HG01433.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.697-820_697-819dup others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 2932579 | ||||||
| chr12:2932579 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0341 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.697-830_697-819del others(12): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 2932579 | ||||||
| chr12:2932822 | A | AT | 9 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0321 others(6): Show |
9 | HG01884.hp1 HG01952.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.697-586dupT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 2932822 | ||||||
| chr12:2932905 | A | G | 2 | a0004c0005t0012g0144 a0004c0005t0012g0145 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.697-513A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2932905 | |||||||
| chr12:2932915 | A | G | 1 | a0001c0001t0002g0090 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.697-503A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2932915 | |||||||
| chr12:2932943 | A | AT | 9 | a0001c0002t0003g0155 a0001c0002t0003g0188 a0001c0002t0003g0190 others(6): Show |
10 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.697-469dupT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 2932943 | ||||||
| chr12:2932947 | T | A | 3 | a0001c0002t0003g0165 a0001c0002t0003g0179 a0001c0002t0003g0197 |
3 | HG02132.hp2 NA18989.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.697-471T>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2932947 | |||||||
| chr12:2932950 | A | T | 76 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(73): Show |
79 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.697-468A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2932950 | |||||||
| chr12:2932999 | A | G | 1 | a0001c0002t0003g0213 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.697-419A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2932999 | |||||||
| chr12:2933035 | T | C | 221 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(218): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.697-383T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2933035 | |||||||
| chr12:2933143 | G | C | 218 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0001 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.697-275G>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2933143 | |||||||
| chr12:2933231 | A | G | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.697-187A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2933231 | |||||||
| chr12:2933237 | T | G | 222 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0295 others(219): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.697-181T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2933237 | |||||||
| chr12:2933306 | T | C | 2 | a0001c0001t0002g0075 a0001c0001t0002g0076 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.697-112T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 6/10 | chr12 | 2933306 | |||||||
| chr12:2933546 | G | C | 1 | a0001c0002t0003g0159 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.809+16G>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 7/10 | chr12 | 2933546 | |||||||
| chr12:2933767 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.809+237A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 7/10 | chr12 | 2933767 | |||||||
| chr12:2933857 | C | T | 1 | a0001c0002t0003g0207 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.809+327C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 7/10 | chr12 | 2933857 | |||||||
| chr12:2934108 | C | T | 4 | a0001c0001t0007g0245 a0001c0001t0007g0246 a0001c0001t0007g0247 others(1): Show |
4 | HG01106.hp1 HG02109.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.810-339C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 7/10 | chr12 | 2934108 | |||||||
| chr12:2934186 | T | A | 2 | a0001c0001t0002g0118 a0001c0001t0002g0119 |
2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.810-261T>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 7/10 | chr12 | 2934186 | |||||||
| chr12:2934234 | G | T | 2 | a0001c0002t0003g0191 a0001c0002t0005g0167 |
2 | NA18963.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.810-213G>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 7/10 | chr12 | 2934234 | |||||||
| chr12:2934359 | A | G | 1 | a0001c0002t0003g0159 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.810-88A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 7/10 | chr12 | 2934359 | |||||||
| chr12:2934631 | G | A | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.924+70G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2934631 | |||||||
| chr12:2934865 | C | T | 1 | a0001c0001t0011g0360 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.924+304C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2934865 | |||||||
| chr12:2934871 | A | G | 2 | a0001c0002t0010g0361 a0001c0002t0010g0363 |
2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.924+310A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2934871 | |||||||
| chr12:2934897 | T | C | 4 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0356 others(1): Show |
4 | HG00642.hp2 HG01261.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.924+336T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2934897 | |||||||
| chr12:2935049 | G | A | 1 | a0001c0002t0003g0211 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.924+488G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2935049 | |||||||
| chr12:2935061 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.924+500C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2935061 | |||||||
| chr12:2935083 | C | T | 4 | a0001c0001t0004g0015 a0001c0001t0004g0107 a0001c0001t0004g0108 others(1): Show |
4 | HG01943.hp1 NA18949.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.924+522C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2935083 | |||||||
| chr12:2935084 | G | A | 1 | a0009c0011t0020g0146 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.924+523G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2935084 | |||||||
| chr12:2935269 | G | A | 10 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 others(7): Show |
10 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.924+708G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2935269 | |||||||
| chr12:2935307 | A | G | 1 | a0001c0001t0004g0110 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.924+746A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2935307 | |||||||
| chr12:2935311 | C | A | 1 | a0001c0002t0003g0151 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.924+750C>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2935311 | |||||||
| chr12:2935594 | C | T | 2 | a0001c0002t0003g0189 a0001c0002t0003g0204 |
2 | HG02683.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.924+1033C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2935594 | |||||||
| chr12:2935702 | G | A | 1 | a0001c0002t0010g0358 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.924+1141G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2935702 | |||||||
| chr12:2935766 | A | C | 15 | a0001c0002t0005g0112 a0001c0002t0005g0113 a0001c0002t0005g0114 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.924+1205A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2935766 | |||||||
| chr12:2935775 | C | T | 1 | a0001c0002t0005g0143 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.924+1214C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2935775 | |||||||
| chr12:2935841 | C | T | 74 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(71): Show |
77 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.924+1280C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2935841 | |||||||
| chr12:2935842 | G | A | 2 | a0004c0005t0012g0144 a0004c0005t0012g0145 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.924+1281G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2935842 | |||||||
| chr12:2935928 | C | G | 2 | a0001c0001t0001g0244 a0001c0001t0001g0252 |
2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.924+1367C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2935928 | |||||||
| chr12:2935989 | A | G | 96 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(93): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.924+1428A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2935989 | |||||||
| chr12:2936013 | T | G | 1 | a0001c0001t0004g0127 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.924+1452T>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2936013 | |||||||
| chr12:2936033 | G | A | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.924+1472G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2936033 | |||||||
| chr12:2936162 | C | A | 2 | a0004c0005t0012g0144 a0004c0005t0012g0145 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.925-1469C>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2936162 | |||||||
| chr12:2936163 | G | A | 2 | a0004c0005t0012g0144 a0004c0005t0012g0145 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.925-1468G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2936163 | |||||||
| chr12:2936185 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
8 | HG01192.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.925-1446G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2936185 | |||||||
| chr12:2936263 | C | A | 78 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(75): Show |
81 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.925-1368C>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2936263 | |||||||
| chr12:2936343 | A | G | 93 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(90): Show |
96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.925-1288A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2936343 | |||||||
| chr12:2936346 | A | C | 96 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(93): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.925-1285A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2936346 | |||||||
| chr12:2936373 | A | T | 1 | a0001c0001t0001g0318 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.925-1258A>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2936373 | |||||||
| chr12:2936477 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.925-1154G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2936477 | |||||||
| chr12:2936493 | G | A | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.925-1138G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2936493 | |||||||
| chr12:2936576 | G | A | 1 | a0001c0001t0002g0048 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.925-1055G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2936576 | |||||||
| chr12:2936579 | TA | T | 84 | a0001c0001t0001g0241 a0001c0001t0001g0303 a0001c0002t0003g0002 others(81): Show |
87 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.925-1036delA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2936579 | ||||||
| chr12:2936653 | G | A | 1 | a0001c0001t0017g0117 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.925-978G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2936653 | |||||||
| chr12:2936681 | G | A | 93 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(90): Show |
96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.925-950G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2936681 | |||||||
| chr12:2936751 | A | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0135 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.925-880A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2936751 | |||||||
| chr12:2936781 | A | C | 77 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(74): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.925-850A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2936781 | |||||||
| chr12:2936797 | TTTAAA | T | 93 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(90): Show |
96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.925-832_925-828del others(5): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2936797 | ||||||
| chr12:2936803 | T | A | 93 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(90): Show |
96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.925-828T>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2936803 | |||||||
| chr12:2936843 | C | T | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.925-788C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2936843 | |||||||
| chr12:2936860 | C | G | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.925-771C>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2936860 | |||||||
| chr12:2936890 | G | A | 93 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(90): Show |
96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.925-741G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2936890 | |||||||
| chr12:2937007 | A | G | 96 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(93): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.925-624A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2937007 | |||||||
| chr12:2937029 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.925-602G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2937029 | |||||||
| chr12:2937071 | A | C | 1 | a0001c0002t0003g0165 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.925-560A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2937071 | |||||||
| chr12:2937104 | C | CA | 15 | a0001c0001t0004g0013 a0001c0001t0004g0094 a0001c0001t0004g0122 others(12): Show |
15 | HG01346.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.925-516dupA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2937104 | ||||||
| chr12:2937157 | T | TTC | 96 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(93): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.925-472_925-471dup others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2937157 | ||||||
| chr12:2937200 | A | AT | 83 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0201 others(80): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.925-400dupT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2937200 | ||||||
| chr12:2937200 | A | ATT | 105 | a0001c0001t0001g0009 a0001c0001t0001g0222 a0001c0001t0001g0224 others(102): Show |
107 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.925-401_925-400dup others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2937200 | ||||||
| chr12:2937200 | A | ATTT | 43 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(40): Show |
43 | HG00558.hp2 HG01070.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.925-402_925-400dup others(3): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2937200 | ||||||
| chr12:2937200 | A | ATTTT | 10 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0002g0019 others(7): Show |
10 | HG01071.hp2 HG02970.hp2 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.925-403_925-400dup others(4): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2937200 | ||||||
| chr12:2937200 | A | ATTTTTTT others(3): Show |
1 | a0002c0003t0006g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.925-409_925-400dup others(10): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2937200 | ||||||
| chr12:2937200 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0004g0108 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.925-410_925-400dup others(11): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2937200 | ||||||
| chr12:2937200 | A | ATTTTTTT others(12): Show |
1 | a0002c0003t0006g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.925-418_925-400dup others(19): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2937200 | ||||||
| chr12:2937200 | A | ATTTTTTT others(13): Show |
2 | a0002c0003t0006g0139 a0002c0003t0006g0141 |
2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.925-419_925-400dup others(20): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2937200 | ||||||
| chr12:2937200 | A | ATTTTTTT others(14): Show |
1 | a0002c0003t0006g0137 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.925-420_925-400dup others(21): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2937200 | ||||||
| chr12:2937200 | A | ATTTTTTT others(17): Show |
1 | a0002c0003t0006g0136 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.925-423_925-400dup others(24): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2937200 | ||||||
| chr12:2937200 | A | ATTTTTTT others(20): Show |
1 | a0002c0003t0006g0138 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.925-426_925-400dup others(27): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2937200 | ||||||
| chr12:2937200 | AT | A | 24 | a0001c0002t0003g0003 a0001c0002t0003g0147 a0001c0002t0003g0152 others(21): Show |
25 | HG00423.hp1 HG01175.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.925-400delT | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2937200 | ||||||
| chr12:2937200 | ATT | A | 57 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0006 others(54): Show |
59 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.925-401_925-400del others(2): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2937200 | ||||||
| chr12:2937200 | ATTTTTTT others(3): Show |
A | 13 | a0001c0001t0004g0013 a0001c0001t0004g0094 a0001c0001t0004g0122 others(10): Show |
13 | HG01346.hp1 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.925-409_925-400del others(10): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2937200 | ||||||
| chr12:2937200 | ATTTTTTT others(5): Show |
A | 1 | a0001c0002t0010g0363 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.925-411_925-400del others(12): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2937200 | ||||||
| chr12:2937200 | ATTTTTTT others(6): Show |
A | 2 | a0001c0002t0010g0358 a0001c0002t0010g0361 |
2 | HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.925-412_925-400del others(13): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2937200 | ||||||
| chr12:2937200 | ATTTTTTT others(9): Show |
A | 1 | a0010c0009t0001g0301 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.925-415_925-400del others(16): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2937200 | ||||||
| chr12:2937200 | ATTTTTTT others(10): Show |
A | 2 | a0001c0001t0001g0287 a0001c0001t0001g0297 |
2 | HG00544.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.925-416_925-400del others(17): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 2937200 | ||||||
| chr12:2937255 | C | T | 77 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(74): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.925-376C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2937255 | |||||||
| chr12:2937256 | G | A | 3 | a0001c0002t0010g0358 a0001c0002t0010g0361 a0001c0002t0010g0363 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.925-375G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2937256 | |||||||
| chr12:2937361 | C | T | 1 | a0001c0002t0003g0195 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.925-270C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2937361 | |||||||
| chr12:2937365 | T | C | 96 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(93): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.925-266T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2937365 | |||||||
| chr12:2937511 | C | T | 5 | a0001c0002t0005g0112 a0001c0002t0005g0113 a0001c0002t0005g0114 others(2): Show |
5 | HG02615.hp1 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.925-120C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2937511 | |||||||
| chr12:2937512 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.925-119G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2937512 | |||||||
| chr12:2937585 | A | G | 1 | a0001c0001t0001g0336 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.925-46A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 8/10 | chr12 | 2937585 | |||||||
| chr12:2937798 | A | AC | 84 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0004 others(81): Show |
87 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1023+70dupC | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 2937798 | ||||||
| chr12:2937799 | C | CA | 12 | a0001c0001t0001g0279 a0001c0001t0001g0294 a0001c0001t0001g0308 others(9): Show |
12 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1023+85dupA | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 2937799 | ||||||
| chr12:2937799 | C | CCAA | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1023+70_1023+71ins others(3): Show |
TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 9/10 | chr12 | 2937799 | |||||||
| chr12:2938300 | G | A | 214 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0271 others(211): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1195+15G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 10/10 | chr12 | 2938300 | |||||||
| chr12:2938389 | A | G | 6 | a0001c0001t0001g0024 a0001c0001t0007g0245 a0001c0001t0007g0246 others(3): Show |
6 | HG01106.hp1 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1195+104A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 10/10 | chr12 | 2938389 | |||||||
| chr12:2938598 | A | C | 2 | a0001c0006t0011g0359 a0001c0006t0011g0362 |
2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1195+313A>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 10/10 | chr12 | 2938598 | |||||||
| chr12:2938627 | T | C | 1 | a0001c0002t0003g0210 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1195+342T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 10/10 | chr12 | 2938627 | |||||||
| chr12:2938698 | C | T | 25 | a0001c0001t0004g0013 a0001c0001t0004g0015 a0001c0001t0004g0023 others(22): Show |
25 | HG01346.hp1 HG01943.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1195+413C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 10/10 | chr12 | 2938698 | |||||||
| chr12:2938727 | G | A | 1 | a0001c0002t0003g0190 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1195+442G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 10/10 | chr12 | 2938727 | |||||||
| chr12:2938731 | T | C | 30 | a0001c0001t0004g0013 a0001c0001t0004g0015 a0001c0001t0004g0023 others(27): Show |
30 | HG01346.hp1 HG01943.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1195+446T>C | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 10/10 | chr12 | 2938731 | |||||||
| chr12:2938875 | C | T | 4 | a0001c0001t0007g0245 a0001c0001t0007g0246 a0001c0001t0007g0247 others(1): Show |
4 | HG01106.hp1 HG02109.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1196-436C>T | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 10/10 | chr12 | 2938875 | |||||||
| chr12:2938878 | A | G | 7 | a0002c0003t0006g0136 a0002c0003t0006g0137 a0002c0003t0006g0138 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1196-433A>G | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 10/10 | chr12 | 2938878 | |||||||
| chr12:2939095 | G | A | 1 | a0001c0001t0004g0128 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1196-216G>A | TULP3 | ENSG00000078246.17 | transcript | ENST00000448120.7 | protein_coding | 10/10 | chr12 | 2939095 |