Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 121278 |
| ensemblid | ENSG00000139287.13 |
| hgncid | 20692 |
| symbol | TPH2 |
| name | tryptophan hydroxylase 2 |
| refseq_nuc | NM_173353.4 |
| refseq_prot | NP_775489.2 |
| ensembl_nuc | ENST00000333850.4 |
| ensembl_prot | ENSP00000329093.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 71938845 |
| end | 72032440 |
| strand | + |
| ver | v1.2 |
| region | chr12:71938845-72032440 |
| region5000 | chr12:71933845-72037440 |
| regionname0 | TPH2_chr12_71938845_72032440 |
| regionname5000 | TPH2_chr12_71933845_72037440 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 490 | 326 | 94 | 65 | 125 | 12 | 28 | 91 | TPH2_chr12_71933845_72037440 | TPH2 | MQPAM others(485): Show |
chr12 | 71933845 | 72037440 |
| a0002 | 0/0 | 490 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TPH2_chr12_71933845_72037440 | TPH2 | MQPAM others(485): Show |
chr12 | 71933845 | 72037440 |
| a0003 | 0/0 | 490 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | MQPAM others(485): Show |
chr12 | 71933845 | 72037440 |
| a0004 | 0/0 | 490 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | MQPAM others(485): Show |
chr12 | 71933845 | 72037440 |
| a0005 | 0/0 | 490 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | MQPAM others(485): Show |
chr12 | 71933845 | 72037440 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1470 | 145 | 29 | 37 | 63 | 3 | 12 | TPH2_chr12_71933845_72037440 | TPH2 | ATGCA others(1465): Show |
chr12 | 71933845 | 72037440 | ||
| a0001c0002 | 0/1 | 1470 | 104 | 19 | 19 | 48 | 7 | 10 | TPH2_chr12_71933845_72037440 | TPH2 | ATGCA others(1465): Show |
chr12 | 71933845 | 72037440 | ||
| a0001c0003 | 0/0 | 1470 | 46 | 36 | 2 | 5 | 1 | 2 | TPH2_chr12_71933845_72037440 | TPH2 | ATGCA others(1465): Show |
chr12 | 71933845 | 72037440 | ||
| a0001c0004 | 0/0 | 1470 | 31 | 10 | 7 | 9 | 1 | 4 | TPH2_chr12_71933845_72037440 | TPH2 | ATGCA others(1465): Show |
chr12 | 71933845 | 72037440 | ||
| a0002c0005 | 0/0 | 1470 | 3 | 0 | 0 | 3 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | ATGCA others(1465): Show |
chr12 | 71933845 | 72037440 | ||
| a0003c0007 | 0/0 | 1470 | 2 | 1 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | ATGCA others(1465): Show |
chr12 | 71933845 | 72037440 | ||
| a0004c0006 | 0/0 | 1470 | 2 | 0 | 0 | 0 | 2 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | ATGCA others(1465): Show |
chr12 | 71933845 | 72037440 | ||
| a0005c0008 | 0/0 | 1470 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | ATGCA others(1465): Show |
chr12 | 71933845 | 72037440 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2360 | 66 | 26 | 18 | 16 | 1 | 4 | TPH2_chr12_71933845_72037440 | TPH2 | GCATT others(2355): Show |
chr12 | 71933845 | 72037440 |
| a0001c0001t0002 | 0/0 | 2360 | 46 | 1 | 12 | 25 | 2 | 6 | TPH2_chr12_71933845_72037440 | TPH2 | GCATT others(2355): Show |
chr12 | 71933845 | 72037440 |
| a0001c0001t0003 | 0/0 | 2360 | 24 | 2 | 5 | 15 | 0 | 2 | TPH2_chr12_71933845_72037440 | TPH2 | GCATT others(2355): Show |
chr12 | 71933845 | 72037440 |
| a0001c0001t0004 | 0/0 | 2360 | 5 | 0 | 0 | 5 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | GCATT others(2355): Show |
chr12 | 71933845 | 72037440 |
| a0001c0001t0005 | 0/0 | 2360 | 2 | 0 | 1 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | GCATT others(2355): Show |
chr12 | 71933845 | 72037440 |
| a0001c0001t0006 | 0/0 | 2360 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | GCATT others(2355): Show |
chr12 | 71933845 | 72037440 |
| a0001c0001t0008 | 0/0 | 2360 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | GCATT others(2355): Show |
chr12 | 71933845 | 72037440 |
| a0001c0002t0001 | 0/1 | 2360 | 100 | 18 | 19 | 45 | 7 | 10 | TPH2_chr12_71933845_72037440 | TPH2 | GCATT others(2355): Show |
chr12 | 71933845 | 72037440 |
| a0001c0002t0003 | 0/0 | 2360 | 2 | 0 | 0 | 2 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | GCATT others(2355): Show |
chr12 | 71933845 | 72037440 |
| a0001c0002t0005 | 0/0 | 2360 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | GCATT others(2355): Show |
chr12 | 71933845 | 72037440 |
| a0001c0002t0007 | 0/0 | 2360 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | GCATT others(2355): Show |
chr12 | 71933845 | 72037440 |
| a0001c0003t0001 | 0/0 | 2360 | 44 | 36 | 1 | 4 | 1 | 2 | TPH2_chr12_71933845_72037440 | TPH2 | GCATT others(2355): Show |
chr12 | 71933845 | 72037440 |
| a0001c0003t0002 | 0/0 | 2360 | 2 | 0 | 1 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | GCATT others(2355): Show |
chr12 | 71933845 | 72037440 |
| a0001c0004t0001 | 0/0 | 2360 | 23 | 10 | 6 | 6 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | GCATT others(2355): Show |
chr12 | 71933845 | 72037440 |
| a0001c0004t0002 | 0/0 | 2360 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | GCATT others(2355): Show |
chr12 | 71933845 | 72037440 |
| a0001c0004t0003 | 0/0 | 2360 | 7 | 0 | 1 | 2 | 1 | 3 | TPH2_chr12_71933845_72037440 | TPH2 | GCATT others(2355): Show |
chr12 | 71933845 | 72037440 |
| a0002c0005t0001 | 0/0 | 2360 | 3 | 0 | 0 | 3 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | GCATT others(2355): Show |
chr12 | 71933845 | 72037440 |
| a0003c0007t0001 | 0/0 | 2360 | 2 | 1 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | GCATT others(2355): Show |
chr12 | 71933845 | 72037440 |
| a0004c0006t0003 | 0/0 | 2360 | 2 | 0 | 0 | 0 | 2 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | GCATT others(2355): Show |
chr12 | 71933845 | 72037440 |
| a0005c0008t0001 | 0/0 | 2360 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | GCATT others(2355): Show |
chr12 | 71933845 | 72037440 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0236 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0003g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0006g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0001t0008g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0145 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0002t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0001c0004t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0002c0005t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0002c0005t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0002c0005t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0003c0007t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0003c0007t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0004c0006t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0004c0006t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| a0005c0008t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0140 | EUR | GBR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0017 | EUR | GBR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0107 | EUR | GBR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0135 | EUR | GBR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0178 | EUR | FIN | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | FIN | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | CHS | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | CHS | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | CHS | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | CHS | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | CHS | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | CHS | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00558 | hp2 | a0001 | c0002 | t0003 | g0058 | EAS | CHS | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | CHS | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | CHS | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | CHS | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | CHS | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | CHS | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | CHS | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0114 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0161 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0119 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00735 | hp2 | a0001 | c0004 | t0001 | g0205 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0127 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG00738 | hp2 | a0001 | c0004 | t0001 | g0207 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0260 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0198 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0133 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01081 | hp2 | a0001 | c0004 | t0001 | g0275 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01106 | hp1 | a0001 | c0001 | t0008 | g0208 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01106 | hp2 | a0001 | c0004 | t0001 | g0284 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0301 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0243 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01192 | hp1 | a0001 | c0004 | t0001 | g0285 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0240 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0222 | AMR | CLM | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0108 | AMR | CLM | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0172 | AMR | CLM | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | CLM | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01358 | hp2 | a0001 | c0004 | t0003 | g0040 | AMR | CLM | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01361 | hp1 | a0001 | c0004 | t0001 | g0212 | AMR | CLM | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0077 | AMR | CLM | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0248 | AMR | CLM | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01496 | hp1 | a0003 | c0007 | t0001 | g0104 | AMR | CLM | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01515 | hp1 | a0004 | c0006 | t0003 | g0060 | EUR | IBS | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0129 | EUR | IBS | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01517 | hp1 | a0004 | c0006 | t0003 | g0061 | EUR | IBS | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0171 | EUR | IBS | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | ACB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PEL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0271 | AMR | PEL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | PEL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PEL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01975 | hp1 | a0001 | c0003 | t0002 | g0117 | AMR | PEL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0035 | AMR | PEL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0146 | AMR | PEL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | PEL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0170 | EAS | KHV | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02055 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | ACB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | KHV | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02071 | hp2 | a0001 | c0001 | t0006 | g0313 | EAS | KHV | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | KHV | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | KHV | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | KHV | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | KHV | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02135 | hp2 | a0001 | c0003 | t0002 | g0157 | EAS | KHV | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0128 | AFR | ACB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PEL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PEL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02155 | hp1 | a0001 | c0002 | t0005 | g0029 | EAS | CDX | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | CDX | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | CDX | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | CDX | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0091 | AFR | ACB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0227 | AFR | ACB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0162 | AFR | ACB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0191 | AFR | ACB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0239 | AFR | ACB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | PEL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PEL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02572 | hp1 | a0001 | c0004 | t0001 | g0044 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0125 | SAS | PJL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0065 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0197 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02630 | hp1 | a0001 | c0002 | t0007 | g0090 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0237 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0097 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0192 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0155 | SAS | PJL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0134 | SAS | PJL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0228 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02717 | hp2 | a0001 | c0004 | t0001 | g0220 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0074 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0093 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02809 | hp1 | a0005 | c0008 | t0001 | g0073 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0300 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0303 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0158 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0083 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0139 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0095 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0094 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0082 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0047 | AFR | ESN | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0213 | AFR | ESN | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0099 | AFR | ESN | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0113 | SAS | PJL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03017 | hp2 | a0001 | c0004 | t0003 | g0059 | SAS | PJL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03041 | hp2 | a0001 | c0004 | t0001 | g0050 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03098 | hp1 | a0001 | c0004 | t0001 | g0221 | AFR | MSL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03130 | hp1 | a0001 | c0004 | t0001 | g0219 | AFR | ESN | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0088 | AFR | ESN | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0167 | AFR | ESN | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0216 | AFR | ESN | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0063 | AFR | ESN | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | MSL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0070 | AFR | MSL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03225 | hp1 | a0001 | c0004 | t0001 | g0037 | AFR | MSL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | MSL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0089 | AFR | MSL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0241 | AFR | MSL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0179 | SAS | PJL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03491 | hp1 | a0001 | c0004 | t0003 | g0041 | SAS | PJL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0180 | SAS | PJL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0238 | AFR | ESN | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0092 | AFR | ESN | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0103 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | GWD | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03579 | hp1 | a0001 | c0004 | t0001 | g0015 | AFR | MSL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0079 | AFR | MSL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0121 | SAS | PJL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03654 | hp2 | a0001 | c0004 | t0003 | g0039 | SAS | PJL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03831 | hp1 | a0001 | c0004 | t0001 | g0257 | SAS | BEB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0182 | SAS | BEB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | BEB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0136 | SAS | STU | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0156 | SAS | BEB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0234 | SAS | STU | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0195 | SAS | STU | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | STU | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0152 | SAS | STU | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0098 | AFR | YRI | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0087 | AFR | YRI | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | CHB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0064 | AFR | YRI | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | YRI | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18946 | hp2 | a0001 | c0004 | t0003 | g0049 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18960 | hp2 | a0001 | c0003 | t0001 | g0110 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18962 | hp1 | a0002 | c0005 | t0001 | g0012 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18964 | hp1 | a0001 | c0004 | t0003 | g0048 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0294 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18968 | hp1 | a0001 | c0003 | t0001 | g0160 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18968 | hp2 | a0001 | c0004 | t0001 | g0278 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18970 | hp1 | a0001 | c0004 | t0001 | g0302 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18975 | hp2 | a0001 | c0004 | t0001 | g0311 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18990 | hp2 | a0002 | c0005 | t0001 | g0144 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | LWK | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | LWK | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | LWK | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0150 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19070 | hp2 | a0001 | c0004 | t0001 | g0265 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19072 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19080 | hp1 | a0001 | c0002 | t0003 | g0028 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19080 | hp2 | a0001 | c0004 | t0001 | g0249 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19081 | hp1 | a0002 | c0005 | t0001 | g0147 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19084 | hp2 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19085 | hp2 | a0001 | c0004 | t0002 | g0279 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19087 | hp2 | a0001 | c0004 | t0001 | g0273 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | YRI | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA20129 | hp1 | a0001 | c0004 | t0001 | g0038 | AFR | ASW | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | ASW | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA20752 | hp1 | a0001 | c0004 | t0003 | g0024 | EUR | TSI | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0141 | EUR | TSI | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0274 | EUR | TSI | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0166 | EUR | TSI | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0169 | AFR | ACB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0226 | AFR | ACB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0215 | AFR | ACB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0086 | AFR | ACB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0196 | AFR | ACB | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03471 | hp1 | a0003 | c0007 | t0001 | g0105 | AFR | MSL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0080 | AFR | MSL | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0148 | AFR | USA | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0292 | AFR | USA | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0072 | AFR | LWK | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0189 | AFR | LWK | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0145 | REF | REF | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0236 | REF | REF | TPH2_chr12_71933845_72037440 | TPH2 | chr12 | 71933845 | 72037440 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71941584 | C | G | 1 | a0003 | 2 | HG01496.hp1 HG03471.hp1 |
missense_variant&splice_region_variant | MODERATE | c.106C>G | p.Leu36Val | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/11 | 248/2360 | 106/1473 | 36/490 | chr12 | 71941584 | |||
| chr12:71941600 | C | A | 1 | a0002 | 3 | NA18962.hp1 NA18990.hp2 NA19081.hp1 |
missense_variant | MODERATE | c.122C>A | p.Ser41Tyr | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/11 | 264/2360 | 122/1473 | 41/490 | chr12 | 71941600 | |||
| chr12:71941637 | C | A | 1 | a0005 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.159C>A | p.Ser53Arg | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/11 | 301/2360 | 159/1473 | 53/490 | chr12 | 71941637 | |||
| chr12:71972526 | C | T | 1 | a0004 | 2 | HG01515.hp1 HG01517.hp1 |
missense_variant | MODERATE | c.616C>T | p.Pro206Ser | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/11 | 758/2360 | 616/1473 | 206/490 | chr12 | 71972526 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71979082 | A | G | 5 | a0001c0002 a0001c0003 a0002c0005 others(2): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
synonymous_variant | LOW | c.936A>G | p.Pro312Pro | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/11 | 1078/2360 | 936/1473 | 312/490 | chr12 | 71979082 | |||
| chr12:72022455 | A | T | 4 | a0001c0002 a0001c0004 a0002c0005 others(1): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
synonymous_variant | LOW | c.1125A>T | p.Ala375Ala | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/11 | 1267/2360 | 1125/1473 | 375/490 | chr12 | 72022455 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71938935 | A | G | 6 | a0001c0001t0003 a0001c0001t0005 a0001c0002t0003 others(3): Show |
38 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(35): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-52A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/11 | chr12 | 71938935 | |||||||
| chr12:72031844 | G | A | 1 | a0001c0001t0004 | 5 | NA18951.hp2 NA18967.hp1 NA18971.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*149G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 11/11 | 149 | chr12 | 72031844 | ||||||
| chr12:72032119 | C | T | 1 | a0001c0001t0008 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*424C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 11/11 | 424 | chr12 | 72032119 | ||||||
| chr12:72032174 | G | A | 6 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(3): Show |
57 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*479G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 11/11 | 479 | chr12 | 72032174 | ||||||
| chr12:72032340 | G | T | 1 | a0001c0002t0007 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*645G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 11/11 | 645 | chr12 | 72032340 | ||||||
| chr12:72032345 | T | C | 1 | a0001c0001t0006 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*650T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 11/11 | 650 | chr12 | 72032345 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71939123 | T | A | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.105+32T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | chr12 | 71939123 | |||||||
| chr12:71939143 | ATCT | A | 52 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(49): Show |
58 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.105+56_105+58delTC others(1): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 71939143 | ||||||
| chr12:71939365 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.105+274T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | chr12 | 71939365 | |||||||
| chr12:71939393 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.105+302G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | chr12 | 71939393 | |||||||
| chr12:71939395 | C | A | 1 | a0001c0003t0001g0070 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.105+304C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | chr12 | 71939395 | |||||||
| chr12:71939395 | C | CA | 195 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(192): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.105+323dupA | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 71939395 | ||||||
| chr12:71939395 | C | CAA | 18 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0071 others(15): Show |
19 | HG01070.hp1 HG01361.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.105+322_105+323dup others(2): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 71939395 | ||||||
| chr12:71939395 | CA | C | 70 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(67): Show |
74 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.105+323delA | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 71939395 | ||||||
| chr12:71939395 | CAA | C | 10 | a0001c0001t0001g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(7): Show |
10 | HG00621.hp2 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.105+322_105+323del others(2): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 71939395 | ||||||
| chr12:71939415 | T | C | 4 | a0001c0001t0001g0066 a0001c0003t0001g0063 a0001c0003t0001g0064 others(1): Show |
4 | HG02622.hp1 HG03195.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+324T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | chr12 | 71939415 | |||||||
| chr12:71939429 | T | C | 1 | a0001c0001t0003g0023 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.105+338T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | chr12 | 71939429 | |||||||
| chr12:71939790 | G | A | 135 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(132): Show |
145 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.105+699G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | chr12 | 71939790 | |||||||
| chr12:71940011 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.105+920A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | chr12 | 71940011 | |||||||
| chr12:71940190 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.105+1099G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | chr12 | 71940190 | |||||||
| chr12:71940197 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.105+1106C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | chr12 | 71940197 | |||||||
| chr12:71940213 | T | A | 2 | a0001c0001t0003g0025 a0001c0004t0003g0024 |
2 | HG02451.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.105+1122T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | chr12 | 71940213 | |||||||
| chr12:71940704 | C | T | 3 | a0001c0001t0001g0229 a0001c0003t0001g0227 a0001c0003t0001g0228 |
3 | HG02257.hp2 HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.106-880C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | chr12 | 71940704 | |||||||
| chr12:71940903 | G | T | 155 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(152): Show |
167 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.106-681G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | chr12 | 71940903 | |||||||
| chr12:71940908 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.106-676T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | chr12 | 71940908 | |||||||
| chr12:71940976 | G | T | 1 | a0001c0003t0001g0226 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.106-608G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | chr12 | 71940976 | |||||||
| chr12:71941048 | T | A | 14 | a0001c0001t0001g0096 a0001c0002t0007g0090 a0001c0003t0001g0008 others(11): Show |
15 | HG02257.hp1 HG02630.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.106-536T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | chr12 | 71941048 | |||||||
| chr12:71941059 | A | C | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.106-525A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | chr12 | 71941059 | |||||||
| chr12:71941112 | A | G | 2 | a0001c0001t0001g0071 a0001c0003t0001g0072 |
2 | HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.106-472A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | chr12 | 71941112 | |||||||
| chr12:71941222 | C | T | 1 | a0001c0003t0001g0303 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.106-362C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | chr12 | 71941222 | |||||||
| chr12:71941293 | G | T | 308 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(305): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.106-291G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | chr12 | 71941293 | |||||||
| chr12:71941343 | T | C | 1 | a0001c0003t0001g0086 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.106-241T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 1/10 | chr12 | 71941343 | |||||||
| chr12:71941852 | G | C | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.255+119G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71941852 | |||||||
| chr12:71942002 | C | T | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.255+269C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71942002 | |||||||
| chr12:71942014 | A | G | 49 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(46): Show |
55 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.255+281A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71942014 | |||||||
| chr12:71942075 | G | A | 105 | a0001c0001t0001g0009 a0001c0001t0001g0186 a0001c0001t0001g0187 others(102): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.255+342G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71942075 | |||||||
| chr12:71942208 | C | T | 105 | a0001c0001t0001g0009 a0001c0001t0001g0186 a0001c0001t0001g0187 others(102): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.255+475C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71942208 | |||||||
| chr12:71942273 | T | A | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.255+540T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71942273 | |||||||
| chr12:71942441 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.255+708T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71942441 | |||||||
| chr12:71942454 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.255+721C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71942454 | |||||||
| chr12:71942549 | G | C | 7 | a0001c0001t0001g0066 a0001c0001t0001g0071 a0001c0002t0001g0189 others(4): Show |
7 | HG02622.hp1 HG03130.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.255+816G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71942549 | |||||||
| chr12:71942558 | T | C | 14 | a0001c0001t0001g0096 a0001c0001t0001g0190 a0001c0002t0007g0090 others(11): Show |
15 | HG02257.hp1 HG02630.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.255+825T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71942558 | |||||||
| chr12:71942626 | T | A | 14 | a0001c0001t0001g0096 a0001c0001t0001g0190 a0001c0002t0007g0090 others(11): Show |
15 | HG02257.hp1 HG02630.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.255+893T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71942626 | |||||||
| chr12:71942732 | A | G | 95 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0225 others(92): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.255+999A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71942732 | |||||||
| chr12:71942810 | T | A | 2 | a0001c0001t0001g0020 a0001c0003t0001g0086 |
2 | HG02486.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.255+1077T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71942810 | |||||||
| chr12:71942923 | G | A | 14 | a0001c0001t0001g0096 a0001c0001t0001g0190 a0001c0002t0007g0090 others(11): Show |
15 | HG02257.hp1 HG02630.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.255+1190G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71942923 | |||||||
| chr12:71942936 | G | T | 2 | a0003c0007t0001g0104 a0003c0007t0001g0105 |
2 | HG01496.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.255+1203G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71942936 | |||||||
| chr12:71942989 | C | T | 73 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0002g0130 others(70): Show |
76 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.255+1256C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71942989 | |||||||
| chr12:71943017 | A | G | 1 | a0001c0002t0001g0124 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.256-1277A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71943017 | |||||||
| chr12:71943036 | C | T | 7 | a0001c0001t0001g0066 a0001c0001t0001g0071 a0001c0002t0001g0189 others(4): Show |
7 | HG02622.hp1 HG03130.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.256-1258C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71943036 | |||||||
| chr12:71943498 | C | T | 2 | a0001c0001t0002g0312 a0001c0001t0006g0313 |
2 | HG02071.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.256-796C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71943498 | |||||||
| chr12:71943561 | A | T | 1 | a0001c0003t0001g0086 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.256-733A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71943561 | |||||||
| chr12:71943732 | G | T | 4 | a0001c0004t0001g0015 a0001c0004t0001g0219 a0001c0004t0001g0220 others(1): Show |
5 | HG02055.hp2 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.256-562G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71943732 | |||||||
| chr12:71943980 | G | A | 79 | a0001c0001t0001g0019 a0001c0001t0001g0232 a0001c0001t0001g0258 others(76): Show |
83 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.256-314G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71943980 | |||||||
| chr12:71944061 | T | A | 1 | a0001c0002t0001g0125 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.256-233T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 2/10 | chr12 | 71944061 | |||||||
| chr12:71944727 | G | C | 1 | a0001c0001t0001g0026 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.540+41G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71944727 | |||||||
| chr12:71944789 | T | A | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.540+103T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71944789 | |||||||
| chr12:71944848 | A | T | 153 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(150): Show |
165 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.540+162A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71944848 | |||||||
| chr12:71944865 | G | A | 52 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(49): Show |
59 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.540+179G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71944865 | |||||||
| chr12:71944994 | T | C | 5 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
5 | HG01109.hp1 HG02572.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.540+308T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71944994 | |||||||
| chr12:71945226 | A | G | 4 | a0001c0001t0001g0096 a0001c0001t0001g0190 a0001c0003t0001g0097 others(1): Show |
4 | HG02647.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+540A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71945226 | |||||||
| chr12:71945354 | C | T | 2 | a0001c0001t0001g0217 a0001c0002t0001g0216 |
2 | HG01069.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.540+668C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71945354 | |||||||
| chr12:71945500 | G | A | 1 | a0001c0001t0002g0305 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.540+814G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71945500 | |||||||
| chr12:71945673 | C | A | 1 | a0001c0001t0003g0027 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.540+987C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71945673 | |||||||
| chr12:71945768 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.540+1082C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71945768 | |||||||
| chr12:71945801 | C | T | 9 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(6): Show |
9 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.540+1115C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71945801 | |||||||
| chr12:71945815 | G | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0071 a0001c0001t0001g0096 others(1): Show |
4 | HG02486.hp2 HG03130.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+1129G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71945815 | |||||||
| chr12:71946034 | C | T | 1 | a0001c0002t0001g0123 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.540+1348C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71946034 | |||||||
| chr12:71946051 | C | T | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.540+1365C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71946051 | |||||||
| chr12:71946288 | C | G | 2 | a0001c0001t0001g0229 a0001c0003t0001g0228 |
2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.540+1602C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71946288 | |||||||
| chr12:71946293 | G | T | 137 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(134): Show |
149 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.540+1607G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71946293 | |||||||
| chr12:71946303 | A | G | 1 | a0001c0002t0001g0188 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.540+1617A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71946303 | |||||||
| chr12:71946355 | C | T | 9 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(6): Show |
9 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.540+1669C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71946355 | |||||||
| chr12:71946433 | T | C | 1 | a0001c0004t0001g0249 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.540+1747T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71946433 | |||||||
| chr12:71946588 | C | T | 7 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0268 others(4): Show |
7 | HG00423.hp2 HG00558.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.540+1902C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71946588 | |||||||
| chr12:71946785 | C | T | 1 | a0001c0003t0001g0182 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.540+2099C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71946785 | |||||||
| chr12:71947021 | A | C | 2 | a0001c0001t0001g0229 a0001c0003t0001g0228 |
2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.540+2335A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71947021 | |||||||
| chr12:71947128 | C | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
6 | HG02258.hp2 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+2442C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71947128 | |||||||
| chr12:71947267 | T | C | 2 | a0001c0001t0001g0009 a0001c0004t0001g0103 |
3 | HG02280.hp1 HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.541-2321T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71947267 | |||||||
| chr12:71947315 | G | A | 5 | a0001c0001t0001g0229 a0001c0003t0001g0093 a0001c0003t0001g0094 others(2): Show |
5 | HG02717.hp1 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.541-2273G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71947315 | |||||||
| chr12:71947662 | G | T | 3 | a0001c0003t0001g0093 a0001c0003t0001g0094 a0001c0003t0001g0095 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.541-1926G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71947662 | |||||||
| chr12:71947668 | G | A | 4 | a0001c0001t0002g0250 a0001c0001t0002g0306 a0001c0001t0002g0307 others(1): Show |
4 | NA18965.hp1 NA18969.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-1920G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71947668 | |||||||
| chr12:71947703 | C | T | 1 | a0001c0004t0001g0311 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.541-1885C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71947703 | |||||||
| chr12:71947770 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.541-1818G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71947770 | |||||||
| chr12:71947821 | T | C | 5 | a0001c0001t0001g0229 a0001c0003t0001g0093 a0001c0003t0001g0094 others(2): Show |
5 | HG02717.hp1 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.541-1767T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71947821 | |||||||
| chr12:71947961 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.541-1627G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71947961 | |||||||
| chr12:71948092 | C | G | 1 | a0001c0004t0001g0302 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.541-1496C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71948092 | |||||||
| chr12:71948097 | C | G | 2 | a0001c0001t0001g0214 a0001c0003t0001g0213 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.541-1491C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71948097 | |||||||
| chr12:71948164 | T | TTTA | 5 | a0001c0002t0001g0010 a0001c0002t0001g0126 a0001c0002t0001g0127 others(2): Show |
6 | HG00738.hp1 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.541-1406_541-1404d others(5): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 71948164 | ||||||
| chr12:71948504 | C | T | 124 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(121): Show |
133 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.541-1084C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71948504 | |||||||
| chr12:71948550 | T | C | 1 | a0001c0002t0001g0106 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.541-1038T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71948550 | |||||||
| chr12:71948558 | G | A | 2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | NA18942.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.541-1030G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71948558 | |||||||
| chr12:71948709 | C | G | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.541-879C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71948709 | |||||||
| chr12:71948739 | G | A | 2 | a0001c0002t0001g0125 a0001c0002t0001g0195 |
2 | HG02602.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.541-849G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71948739 | |||||||
| chr12:71948867 | G | A | 7 | a0001c0001t0001g0020 a0001c0002t0001g0079 a0001c0003t0001g0063 others(4): Show |
7 | HG02717.hp1 HG02976.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.541-721G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71948867 | |||||||
| chr12:71949098 | T | C | 74 | a0001c0001t0001g0019 a0001c0001t0001g0258 a0001c0001t0001g0259 others(71): Show |
78 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.541-490T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71949098 | |||||||
| chr12:71949416 | T | C | 1 | a0001c0002t0001g0131 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.541-172T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71949416 | |||||||
| chr12:71949463 | T | A | 2 | a0001c0003t0001g0191 a0001c0003t0001g0300 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.541-125T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71949463 | |||||||
| chr12:71949507 | C | T | 37 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(34): Show |
43 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.541-81C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 4/10 | chr12 | 71949507 | |||||||
| chr12:71949882 | C | T | 10 | a0001c0001t0001g0020 a0001c0001t0001g0066 a0001c0001t0001g0071 others(7): Show |
10 | HG02559.hp1 HG02647.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.608+227C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71949882 | |||||||
| chr12:71949887 | T | TTG | 10 | a0001c0001t0001g0020 a0001c0001t0001g0066 a0001c0001t0001g0071 others(7): Show |
10 | HG02559.hp1 HG02647.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.608+234_608+235dup others(2): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71949887 | ||||||
| chr12:71949902 | C | G | 1 | a0001c0002t0001g0181 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.608+247C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71949902 | |||||||
| chr12:71950041 | G | A | 1 | a0001c0002t0001g0132 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.608+386G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71950041 | |||||||
| chr12:71950083 | T | A | 74 | a0001c0001t0001g0019 a0001c0001t0001g0258 a0001c0001t0001g0259 others(71): Show |
78 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.608+428T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71950083 | |||||||
| chr12:71950089 | T | C | 10 | a0001c0001t0001g0020 a0001c0001t0001g0066 a0001c0001t0001g0071 others(7): Show |
10 | HG02559.hp1 HG02647.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.608+434T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71950089 | |||||||
| chr12:71950244 | G | A | 3 | a0001c0001t0001g0096 a0001c0003t0001g0086 a0001c0003t0001g0226 |
3 | HG02109.hp2 HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.608+589G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71950244 | |||||||
| chr12:71950327 | C | T | 10 | a0001c0002t0007g0090 a0001c0003t0001g0008 a0001c0003t0001g0087 others(7): Show |
11 | HG02257.hp1 HG02630.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.608+672C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71950327 | |||||||
| chr12:71950365 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.608+710A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71950365 | |||||||
| chr12:71950650 | C | T | 37 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(34): Show |
43 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.608+995C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71950650 | |||||||
| chr12:71950700 | A | G | 1 | a0001c0002t0001g0181 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.608+1045A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71950700 | |||||||
| chr12:71950763 | C | T | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.608+1108C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71950763 | |||||||
| chr12:71950781 | A | T | 37 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(34): Show |
43 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.608+1126A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71950781 | |||||||
| chr12:71950786 | G | T | 1 | a0001c0001t0001g0210 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.608+1131G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71950786 | |||||||
| chr12:71950838 | C | A | 235 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0066 others(232): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.608+1183C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71950838 | |||||||
| chr12:71950984 | A | G | 1 | a0001c0004t0001g0212 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.608+1329A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71950984 | |||||||
| chr12:71951017 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.608+1362T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71951017 | |||||||
| chr12:71951167 | C | T | 9 | a0001c0001t0001g0066 a0001c0001t0001g0071 a0001c0001t0001g0190 others(6): Show |
9 | HG02559.hp1 HG02647.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.608+1512C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71951167 | |||||||
| chr12:71951224 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.608+1569G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71951224 | |||||||
| chr12:71951325 | G | C | 1 | a0001c0003t0001g0226 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.608+1670G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71951325 | |||||||
| chr12:71951380 | A | T | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.608+1725A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71951380 | |||||||
| chr12:71951603 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.608+1948C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71951603 | |||||||
| chr12:71951702 | A | ATG | 141 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(138): Show |
152 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.608+2069_608+2070d others(4): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71951702 | ||||||
| chr12:71951702 | A | ATGTG | 3 | a0001c0001t0002g0211 a0001c0003t0001g0086 a0001c0004t0001g0249 |
3 | HG02486.hp2 HG04228.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.608+2067_608+2070d others(6): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71951702 | ||||||
| chr12:71951702 | A | ATGTGTG | 9 | a0001c0001t0001g0066 a0001c0001t0001g0071 a0001c0001t0001g0190 others(6): Show |
9 | HG02559.hp1 HG02647.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.608+2065_608+2070d others(8): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71951702 | ||||||
| chr12:71951702 | A | G | 3 | a0001c0003t0001g0072 a0001c0003t0001g0094 a0001c0003t0001g0095 |
3 | HG02896.hp2 HG02897.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.608+2047A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71951702 | |||||||
| chr12:71951790 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.608+2135C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71951790 | |||||||
| chr12:71951824 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.608+2169A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71951824 | |||||||
| chr12:71951827 | A | T | 2 | a0001c0003t0001g0063 a0001c0003t0001g0064 |
2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.608+2172A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71951827 | |||||||
| chr12:71952213 | T | C | 1 | a0001c0003t0001g0072 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.608+2558T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71952213 | |||||||
| chr12:71952355 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.608+2700A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71952355 | |||||||
| chr12:71952367 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.608+2712T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71952367 | |||||||
| chr12:71952435 | G | T | 1 | a0001c0001t0002g0310 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.608+2780G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71952435 | |||||||
| chr12:71952440 | G | A | 5 | a0001c0002t0001g0107 a0001c0002t0001g0133 a0001c0002t0001g0134 others(2): Show |
5 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.608+2785G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71952440 | |||||||
| chr12:71952441 | G | A | 5 | a0001c0002t0001g0107 a0001c0002t0001g0133 a0001c0002t0001g0134 others(2): Show |
5 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.608+2786G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71952441 | |||||||
| chr12:71952641 | A | C | 1 | a0001c0001t0001g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.608+2986A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71952641 | |||||||
| chr12:71952704 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.608+3049G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71952704 | |||||||
| chr12:71952761 | C | A | 1 | a0001c0001t0003g0004 | 2 | HG02602.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.608+3106C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71952761 | |||||||
| chr12:71952823 | A | C | 9 | a0001c0001t0001g0066 a0001c0001t0001g0071 a0001c0001t0001g0190 others(6): Show |
9 | HG02559.hp1 HG02647.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.608+3168A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71952823 | |||||||
| chr12:71952855 | G | A | 2 | a0001c0004t0001g0037 a0001c0004t0001g0038 |
2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.608+3200G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71952855 | |||||||
| chr12:71952868 | C | T | 9 | a0001c0001t0001g0066 a0001c0001t0001g0071 a0001c0001t0001g0190 others(6): Show |
9 | HG02559.hp1 HG02647.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.608+3213C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71952868 | |||||||
| chr12:71953020 | C | G | 122 | a0001c0001t0002g0142 a0001c0001t0002g0143 a0001c0002t0001g0002 others(119): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.608+3365C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71953020 | |||||||
| chr12:71953162 | C | CT | 36 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0186 others(33): Show |
41 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.608+3519dupT | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71953162 | ||||||
| chr12:71953225 | A | G | 5 | a0001c0003t0001g0237 a0001c0003t0001g0238 a0001c0003t0001g0239 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.608+3570A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71953225 | |||||||
| chr12:71953378 | G | T | 1 | a0001c0001t0003g0053 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.608+3723G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71953378 | |||||||
| chr12:71953395 | C | T | 1 | a0001c0002t0001g0177 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.608+3740C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71953395 | |||||||
| chr12:71953841 | G | T | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.608+4186G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71953841 | |||||||
| chr12:71953999 | C | G | 1 | a0001c0002t0001g0198 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.608+4344C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71953999 | |||||||
| chr12:71954021 | G | T | 4 | a0001c0001t0001g0043 a0001c0004t0001g0037 a0001c0004t0001g0038 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.608+4366G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71954021 | |||||||
| chr12:71954176 | C | T | 3 | a0001c0002t0001g0125 a0001c0002t0001g0178 a0001c0002t0001g0195 |
3 | HG00280.hp1 HG02602.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.608+4521C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71954176 | |||||||
| chr12:71954203 | G | A | 4 | a0001c0001t0001g0020 a0001c0002t0001g0215 a0001c0002t0001g0216 others(1): Show |
4 | HG02257.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.608+4548G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71954203 | |||||||
| chr12:71954226 | T | C | 85 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0258 others(82): Show |
89 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.608+4571T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71954226 | |||||||
| chr12:71954385 | G | A | 1 | a0001c0002t0001g0181 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.608+4730G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71954385 | |||||||
| chr12:71954833 | AT | A | 263 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(260): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.608+5188delT | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71954833 | ||||||
| chr12:71954918 | G | T | 247 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(244): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.608+5263G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71954918 | |||||||
| chr12:71955231 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.608+5576T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71955231 | |||||||
| chr12:71955265 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.608+5610C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71955265 | |||||||
| chr12:71955286 | A | G | 3 | a0001c0002t0001g0215 a0001c0002t0001g0216 a0001c0003t0001g0227 |
3 | HG02257.hp2 HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.608+5631A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71955286 | |||||||
| chr12:71955424 | C | T | 3 | a0001c0001t0001g0190 a0001c0001t0001g0214 a0001c0001t0001g0229 |
3 | HG02559.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.608+5769C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71955424 | |||||||
| chr12:71955510 | G | A | 267 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(264): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.608+5855G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71955510 | |||||||
| chr12:71955591 | C | T | 267 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(264): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.608+5936C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71955591 | |||||||
| chr12:71956061 | A | G | 267 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(264): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.608+6406A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71956061 | |||||||
| chr12:71956104 | C | A | 1 | a0001c0002t0001g0126 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.608+6449C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71956104 | |||||||
| chr12:71956246 | T | A | 172 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(169): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.608+6591T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71956246 | |||||||
| chr12:71956377 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0217 a0001c0004t0001g0103 |
4 | HG01069.hp1 HG02280.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.608+6722C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71956377 | |||||||
| chr12:71956407 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.608+6752T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71956407 | |||||||
| chr12:71956468 | C | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.608+6813C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71956468 | |||||||
| chr12:71956469 | TTCCCTCC others(29): Show |
T | 267 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(264): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.608+6850_608+6885d others(38): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71956469 | ||||||
| chr12:71956735 | G | A | 2 | a0001c0002t0001g0137 a0001c0002t0001g0138 |
2 | NA19001.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.608+7080G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71956735 | |||||||
| chr12:71956870 | A | C | 35 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(32): Show |
41 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.608+7215A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71956870 | |||||||
| chr12:71956873 | G | T | 3 | a0001c0001t0001g0190 a0001c0001t0001g0214 a0001c0001t0001g0229 |
3 | HG02559.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.608+7218G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71956873 | |||||||
| chr12:71956887 | G | A | 4 | a0001c0004t0001g0015 a0001c0004t0001g0219 a0001c0004t0001g0220 others(1): Show |
5 | HG02055.hp2 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.608+7232G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71956887 | |||||||
| chr12:71957009 | T | C | 4 | a0001c0004t0001g0015 a0001c0004t0001g0219 a0001c0004t0001g0220 others(1): Show |
5 | HG02055.hp2 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.608+7354T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71957009 | |||||||
| chr12:71957010 | G | A | 265 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(262): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.608+7355G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71957010 | |||||||
| chr12:71957327 | A | AT | 110 | a0001c0001t0001g0021 a0001c0001t0001g0056 a0001c0001t0001g0057 others(107): Show |
117 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.608+7696dupT | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71957327 | ||||||
| chr12:71957327 | A | ATT | 44 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0043 others(41): Show |
48 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.608+7695_608+7696d others(4): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71957327 | ||||||
| chr12:71957327 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.608+7685_608+7696d others(14): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71957327 | ||||||
| chr12:71957327 | AT | A | 16 | a0001c0001t0001g0217 a0001c0002t0001g0079 a0001c0003t0001g0063 others(13): Show |
16 | HG01069.hp1 HG02622.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.608+7696delT | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71957327 | ||||||
| chr12:71957373 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.608+7718G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71957373 | |||||||
| chr12:71957862 | G | A | 1 | a0001c0001t0003g0033 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.608+8207G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71957862 | |||||||
| chr12:71957928 | C | T | 266 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(263): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.608+8273C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71957928 | |||||||
| chr12:71958055 | C | T | 122 | a0001c0001t0002g0142 a0001c0001t0002g0143 a0001c0002t0001g0002 others(119): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.608+8400C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71958055 | |||||||
| chr12:71958080 | T | A | 268 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(265): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.608+8425T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71958080 | |||||||
| chr12:71958085 | G | A | 2 | a0001c0002t0001g0196 a0001c0002t0001g0197 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.608+8430G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71958085 | |||||||
| chr12:71958180 | C | A | 3 | a0001c0002t0001g0007 a0001c0002t0001g0080 a0001c0002t0007g0090 |
4 | HG02630.hp1 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.608+8525C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71958180 | |||||||
| chr12:71958250 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.608+8595G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71958250 | |||||||
| chr12:71958328 | G | C | 267 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(264): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.608+8673G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71958328 | |||||||
| chr12:71958374 | C | T | 3 | a0001c0001t0001g0190 a0001c0001t0001g0214 a0001c0001t0001g0229 |
3 | HG02559.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.608+8719C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71958374 | |||||||
| chr12:71958449 | C | T | 1 | a0001c0002t0001g0119 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.608+8794C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71958449 | |||||||
| chr12:71958482 | C | G | 1 | a0001c0004t0001g0050 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.608+8827C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71958482 | |||||||
| chr12:71958542 | G | A | 247 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(244): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.608+8887G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71958542 | |||||||
| chr12:71958565 | G | A | 1 | a0001c0002t0001g0139 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.608+8910G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71958565 | |||||||
| chr12:71958648 | G | A | 2 | a0001c0001t0001g0043 a0001c0004t0001g0044 |
2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.608+8993G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71958648 | |||||||
| chr12:71958664 | C | T | 1 | a0001c0001t0001g0283 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.608+9009C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71958664 | |||||||
| chr12:71958763 | T | C | 266 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(263): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.608+9108T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71958763 | |||||||
| chr12:71959062 | A | AT | 78 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0258 others(75): Show |
82 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.608+9421dupT | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71959062 | ||||||
| chr12:71959062 | A | ATT | 174 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(171): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.608+9420_608+9421d others(4): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71959062 | ||||||
| chr12:71959062 | A | ATTT | 13 | a0001c0001t0001g0020 a0001c0001t0001g0190 a0001c0001t0001g0225 others(10): Show |
14 | HG01261.hp2 HG01884.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.608+9419_608+9421d others(5): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71959062 | ||||||
| chr12:71959062 | AT | A | 6 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(3): Show |
6 | HG01109.hp1 HG02004.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.608+9421delT | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71959062 | ||||||
| chr12:71959206 | A | G | 271 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(268): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.608+9551A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71959206 | |||||||
| chr12:71959388 | C | T | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.608+9733C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71959388 | |||||||
| chr12:71959390 | C | T | 1 | a0001c0002t0001g0173 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.608+9735C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71959390 | |||||||
| chr12:71959391 | G | A | 16 | a0001c0002t0001g0079 a0001c0002t0001g0215 a0001c0002t0001g0216 others(13): Show |
16 | HG02258.hp2 HG02486.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.608+9736G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71959391 | |||||||
| chr12:71959393 | G | A | 1 | a0001c0003t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.608+9738G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71959393 | |||||||
| chr12:71959477 | A | T | 130 | a0001c0001t0001g0225 a0001c0001t0002g0142 a0001c0001t0002g0143 others(127): Show |
136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.608+9822A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71959477 | |||||||
| chr12:71959735 | G | A | 1 | a0001c0003t0001g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.608+10080G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71959735 | |||||||
| chr12:71959994 | C | T | 14 | a0001c0002t0001g0079 a0001c0002t0001g0215 a0001c0002t0001g0216 others(11): Show |
14 | HG02486.hp1 HG02622.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.608+10339C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71959994 | |||||||
| chr12:71960119 | T | C | 5 | a0001c0003t0001g0237 a0001c0003t0001g0238 a0001c0003t0001g0239 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.608+10464T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71960119 | |||||||
| chr12:71960697 | A | G | 233 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0067 others(230): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.608+11042A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71960697 | |||||||
| chr12:71960798 | T | C | 1 | a0001c0004t0001g0302 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.608+11143T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71960798 | |||||||
| chr12:71961164 | C | G | 2 | a0001c0003t0001g0191 a0001c0003t0001g0300 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.609-11355C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71961164 | |||||||
| chr12:71961399 | A | G | 225 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0067 others(222): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.609-11120A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71961399 | |||||||
| chr12:71961651 | A | G | 5 | a0001c0003t0001g0237 a0001c0003t0001g0238 a0001c0003t0001g0239 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.609-10868A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71961651 | |||||||
| chr12:71961717 | G | T | 3 | a0001c0001t0001g0190 a0001c0001t0001g0214 a0001c0001t0001g0229 |
3 | HG02559.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.609-10802G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71961717 | |||||||
| chr12:71961724 | A | G | 3 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0248 |
3 | HG01261.hp1 HG01433.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.609-10795A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71961724 | |||||||
| chr12:71961762 | T | C | 2 | a0001c0002t0001g0215 a0001c0002t0001g0216 |
2 | HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.609-10757T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71961762 | |||||||
| chr12:71961934 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.609-10585T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71961934 | |||||||
| chr12:71962127 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.609-10392G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71962127 | |||||||
| chr12:71962160 | C | G | 2 | a0001c0002t0001g0215 a0001c0002t0001g0216 |
2 | HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.609-10359C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71962160 | |||||||
| chr12:71962382 | T | C | 1 | a0001c0002t0001g0262 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.609-10137T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71962382 | |||||||
| chr12:71962445 | T | A | 1 | a0001c0003t0001g0099 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.609-10074T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71962445 | |||||||
| chr12:71962449 | G | A | 3 | a0001c0001t0001g0096 a0001c0003t0001g0086 a0001c0003t0001g0226 |
3 | HG02109.hp2 HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.609-10070G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71962449 | |||||||
| chr12:71962487 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.609-10032A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71962487 | |||||||
| chr12:71962534 | G | A | 271 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(268): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.609-9985G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71962534 | |||||||
| chr12:71962583 | A | C | 4 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0097 others(1): Show |
4 | HG02647.hp1 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.609-9936A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71962583 | |||||||
| chr12:71962626 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.609-9893C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71962626 | |||||||
| chr12:71962633 | G | A | 3 | a0001c0001t0001g0096 a0001c0003t0001g0086 a0001c0003t0001g0226 |
3 | HG02109.hp2 HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.609-9886G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71962633 | |||||||
| chr12:71962705 | C | T | 225 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0190 others(222): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.609-9814C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71962705 | |||||||
| chr12:71962796 | GCAACCTC others(1557): Show |
G | 225 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0190 others(222): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.609-9681_609-8118d others(2): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71962796 | ||||||
| chr12:71963116 | T | C | 43 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(40): Show |
49 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.609-9403T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71963116 | |||||||
| chr12:71963175 | C | T | 46 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(43): Show |
52 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.609-9344C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71963175 | |||||||
| chr12:71963206 | T | G | 43 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(40): Show |
49 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.609-9313T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71963206 | |||||||
| chr12:71963255 | C | T | 4 | a0001c0001t0001g0096 a0001c0003t0001g0086 a0001c0003t0001g0226 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.609-9264C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71963255 | |||||||
| chr12:71963443 | C | CATATAT | 4 | a0001c0004t0001g0015 a0001c0004t0001g0219 a0001c0004t0001g0220 others(1): Show |
5 | HG02055.hp2 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.609-9067_609-9062d others(8): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71963443 | ||||||
| chr12:71963535 | A | G | 47 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(44): Show |
53 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.609-8984A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71963535 | |||||||
| chr12:71963586 | G | A | 1 | a0001c0003t0001g0226 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.609-8933G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71963586 | |||||||
| chr12:71963618 | G | A | 1 | a0001c0003t0001g0086 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.609-8901G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71963618 | |||||||
| chr12:71963808 | CA | C | 45 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(42): Show |
51 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.609-8691delA | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71963808 | ||||||
| chr12:71963892 | G | A | 46 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(43): Show |
52 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.609-8627G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71963892 | |||||||
| chr12:71963990 | T | C | 46 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(43): Show |
52 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.609-8529T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71963990 | |||||||
| chr12:71964266 | C | T | 3 | a0001c0001t0001g0096 a0001c0003t0001g0086 a0001c0003t0001g0226 |
3 | HG02109.hp2 HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.609-8253C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71964266 | |||||||
| chr12:71964282 | T | A | 1 | a0001c0001t0001g0224 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.609-8237T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71964282 | |||||||
| chr12:71964312 | G | C | 43 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(40): Show |
49 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.609-8207G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71964312 | |||||||
| chr12:71964386 | G | A | 2 | a0001c0001t0002g0250 a0001c0001t0005g0042 |
2 | NA19001.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.609-8133G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71964386 | |||||||
| chr12:71964431 | C | T | 3 | a0001c0003t0001g0072 a0001c0003t0001g0094 a0001c0003t0001g0095 |
3 | HG02896.hp2 HG02897.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.609-8088C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71964431 | |||||||
| chr12:71964433 | C | T | 1 | a0001c0002t0001g0222 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.609-8086C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71964433 | |||||||
| chr12:71964510 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.609-8009G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71964510 | |||||||
| chr12:71964586 | A | G | 1 | a0001c0003t0001g0170 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.609-7933A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71964586 | |||||||
| chr12:71964709 | T | G | 1 | a0001c0002t0001g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.609-7810T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71964709 | |||||||
| chr12:71964746 | G | T | 2 | a0001c0004t0003g0048 a0001c0004t0003g0049 |
2 | NA18946.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.609-7773G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71964746 | |||||||
| chr12:71964827 | T | A | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.609-7692T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71964827 | |||||||
| chr12:71964990 | A | C | 228 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0096 others(225): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.609-7529A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71964990 | |||||||
| chr12:71965267 | A | G | 303 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(300): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.609-7252A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71965267 | |||||||
| chr12:71965268 | T | C | 4 | a0001c0001t0001g0078 a0001c0001t0001g0081 a0001c0001t0001g0200 others(1): Show |
4 | HG01070.hp1 HG01106.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.609-7251T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71965268 | |||||||
| chr12:71965298 | C | T | 1 | a0001c0001t0003g0004 | 2 | HG02602.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.609-7221C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71965298 | |||||||
| chr12:71965307 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.609-7212G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71965307 | |||||||
| chr12:71965408 | T | C | 3 | a0001c0001t0001g0190 a0001c0001t0001g0214 a0001c0001t0001g0229 |
3 | HG02559.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.609-7111T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71965408 | |||||||
| chr12:71965463 | T | G | 225 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0190 others(222): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.609-7056T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71965463 | |||||||
| chr12:71965535 | G | C | 118 | a0001c0001t0002g0142 a0001c0001t0002g0143 a0001c0002t0001g0002 others(115): Show |
124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.609-6984G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71965535 | |||||||
| chr12:71965579 | C | T | 1 | a0001c0001t0002g0281 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.609-6940C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71965579 | |||||||
| chr12:71965638 | C | G | 271 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(268): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.609-6881C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71965638 | |||||||
| chr12:71965728 | T | C | 4 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0097 others(1): Show |
4 | HG02647.hp1 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.609-6791T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71965728 | |||||||
| chr12:71965796 | G | A | 3 | a0001c0001t0001g0096 a0001c0003t0001g0086 a0001c0003t0001g0226 |
3 | HG02109.hp2 HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.609-6723G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71965796 | |||||||
| chr12:71965858 | T | C | 1 | a0001c0003t0001g0226 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.609-6661T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71965858 | |||||||
| chr12:71965900 | A | G | 4 | a0001c0004t0003g0039 a0001c0004t0003g0040 a0001c0004t0003g0041 others(1): Show |
4 | HG01358.hp2 HG03017.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.609-6619A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71965900 | |||||||
| chr12:71965952 | A | G | 1 | a0001c0001t0002g0299 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.609-6567A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71965952 | |||||||
| chr12:71966250 | C | CT | 19 | a0001c0001t0001g0096 a0001c0002t0001g0079 a0001c0002t0001g0215 others(16): Show |
19 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.609-6258dupT | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71966250 | ||||||
| chr12:71966250 | CT | C | 41 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0186 others(38): Show |
47 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.609-6258delT | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71966250 | ||||||
| chr12:71966438 | G | T | 46 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(43): Show |
52 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.609-6081G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71966438 | |||||||
| chr12:71966484 | A | G | 103 | a0001c0001t0002g0142 a0001c0001t0002g0143 a0001c0002t0001g0002 others(100): Show |
107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.609-6035A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71966484 | |||||||
| chr12:71966541 | G | T | 3 | a0001c0001t0001g0096 a0001c0003t0001g0086 a0001c0003t0001g0226 |
3 | HG02109.hp2 HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.609-5978G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71966541 | |||||||
| chr12:71966542 | C | T | 1 | a0001c0002t0001g0118 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.609-5977C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71966542 | |||||||
| chr12:71966781 | A | G | 1 | a0001c0003t0001g0086 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.609-5738A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71966781 | |||||||
| chr12:71966838 | GTTC | G | 3 | a0001c0001t0001g0096 a0001c0003t0001g0086 a0001c0003t0001g0226 |
3 | HG02109.hp2 HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.609-5676_609-5674d others(5): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71966838 | ||||||
| chr12:71966904 | C | A | 43 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(40): Show |
49 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.609-5615C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71966904 | |||||||
| chr12:71966997 | C | T | 43 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(40): Show |
49 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.609-5522C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71966997 | |||||||
| chr12:71967187 | A | G | 4 | a0001c0004t0001g0015 a0001c0004t0001g0219 a0001c0004t0001g0220 others(1): Show |
5 | HG02055.hp2 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.609-5332A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71967187 | |||||||
| chr12:71967197 | T | C | 3 | a0001c0001t0001g0096 a0001c0003t0001g0086 a0001c0003t0001g0226 |
3 | HG02109.hp2 HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.609-5322T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71967197 | |||||||
| chr12:71967293 | T | C | 3 | a0001c0001t0001g0096 a0001c0003t0001g0086 a0001c0003t0001g0226 |
3 | HG02109.hp2 HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.609-5226T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71967293 | |||||||
| chr12:71967426 | C | T | 271 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(268): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.609-5093C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71967426 | |||||||
| chr12:71967445 | T | C | 1 | a0001c0003t0001g0141 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.609-5074T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71967445 | |||||||
| chr12:71967628 | A | T | 43 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(40): Show |
49 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.609-4891A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71967628 | |||||||
| chr12:71967640 | T | A | 1 | a0001c0002t0001g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.609-4879T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71967640 | |||||||
| chr12:71967651 | T | C | 46 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(43): Show |
52 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.609-4868T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71967651 | |||||||
| chr12:71968008 | C | T | 3 | a0001c0001t0001g0096 a0001c0003t0001g0086 a0001c0003t0001g0226 |
3 | HG02109.hp2 HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.609-4511C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71968008 | |||||||
| chr12:71968009 | T | C | 3 | a0001c0001t0001g0096 a0001c0003t0001g0086 a0001c0003t0001g0226 |
3 | HG02109.hp2 HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.609-4510T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71968009 | |||||||
| chr12:71968028 | A | G | 43 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(40): Show |
49 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.609-4491A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71968028 | |||||||
| chr12:71968148 | T | C | 1 | a0001c0004t0001g0220 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.609-4371T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71968148 | |||||||
| chr12:71968297 | C | T | 1 | a0001c0002t0001g0135 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.609-4222C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71968297 | |||||||
| chr12:71968485 | C | T | 202 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0199 others(199): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.609-4034C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71968485 | |||||||
| chr12:71968598 | G | C | 77 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0258 others(74): Show |
81 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.609-3921G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71968598 | |||||||
| chr12:71968611 | A | G | 3 | a0001c0002t0001g0011 a0001c0003t0001g0192 a0001c0003t0001g0303 |
4 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.609-3908A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71968611 | |||||||
| chr12:71968688 | T | G | 43 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(40): Show |
49 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.609-3831T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71968688 | |||||||
| chr12:71968937 | G | GT | 212 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0096 others(209): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.609-3580dupT | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 71968937 | ||||||
| chr12:71969144 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.609-3375G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71969144 | |||||||
| chr12:71969168 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.609-3351A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71969168 | |||||||
| chr12:71969174 | C | T | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.609-3345C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71969174 | |||||||
| chr12:71969176 | C | T | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.609-3343C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71969176 | |||||||
| chr12:71969209 | G | T | 1 | a0001c0001t0002g0298 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.609-3310G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71969209 | |||||||
| chr12:71969224 | A | G | 1 | a0001c0001t0002g0281 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.609-3295A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71969224 | |||||||
| chr12:71969350 | C | T | 77 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0258 others(74): Show |
81 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.609-3169C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71969350 | |||||||
| chr12:71970211 | C | T | 2 | a0001c0004t0001g0037 a0001c0004t0001g0038 |
2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.609-2308C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71970211 | |||||||
| chr12:71970348 | C | T | 2 | a0001c0004t0001g0037 a0001c0004t0001g0038 |
2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.609-2171C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71970348 | |||||||
| chr12:71970389 | A | T | 152 | a0001c0001t0001g0096 a0001c0001t0001g0190 a0001c0001t0001g0199 others(149): Show |
159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.609-2130A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71970389 | |||||||
| chr12:71970390 | A | C | 152 | a0001c0001t0001g0096 a0001c0001t0001g0190 a0001c0001t0001g0199 others(149): Show |
159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.609-2129A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71970390 | |||||||
| chr12:71970598 | T | C | 43 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(40): Show |
49 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.609-1921T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71970598 | |||||||
| chr12:71970888 | T | C | 76 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0258 others(73): Show |
80 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.609-1631T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71970888 | |||||||
| chr12:71970943 | T | C | 118 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(115): Show |
128 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.609-1576T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71970943 | |||||||
| chr12:71971324 | C | A | 76 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0258 others(73): Show |
80 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.609-1195C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71971324 | |||||||
| chr12:71971489 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.609-1030G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71971489 | |||||||
| chr12:71971541 | A | T | 76 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0258 others(73): Show |
80 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.609-978A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71971541 | |||||||
| chr12:71971610 | C | T | 1 | a0001c0002t0001g0247 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.609-909C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71971610 | |||||||
| chr12:71971614 | A | G | 3 | a0001c0002t0001g0011 a0001c0003t0001g0192 a0001c0003t0001g0303 |
4 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.609-905A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71971614 | |||||||
| chr12:71971693 | C | T | 1 | a0001c0003t0001g0169 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.609-826C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71971693 | |||||||
| chr12:71971699 | C | T | 42 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(39): Show |
48 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.609-820C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71971699 | |||||||
| chr12:71971936 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0217 a0001c0004t0001g0103 |
4 | HG01069.hp1 HG02280.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.609-583A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71971936 | |||||||
| chr12:71971937 | T | A | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.609-582T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71971937 | |||||||
| chr12:71972086 | A | G | 272 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(269): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.609-433A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71972086 | |||||||
| chr12:71972120 | A | G | 42 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(39): Show |
48 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.609-399A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71972120 | |||||||
| chr12:71972161 | G | A | 1 | a0001c0001t0002g0306 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.609-358G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71972161 | |||||||
| chr12:71972193 | T | C | 205 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0190 others(202): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.609-326T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71972193 | |||||||
| chr12:71972338 | T | C | 122 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(119): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.609-181T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71972338 | |||||||
| chr12:71972406 | C | T | 122 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(119): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.609-113C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 5/10 | chr12 | 71972406 | |||||||
| chr12:71972859 | G | A | 44 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(41): Show |
50 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.805+144G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71972859 | |||||||
| chr12:71972859 | G | T | 3 | a0001c0001t0001g0096 a0001c0003t0001g0086 a0001c0003t0001g0226 |
3 | HG02109.hp2 HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.805+144G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71972859 | |||||||
| chr12:71972867 | G | A | 23 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0075 others(20): Show |
25 | HG00140.hp1 HG00438.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.805+152G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71972867 | |||||||
| chr12:71972983 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.805+268G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71972983 | |||||||
| chr12:71973154 | A | G | 272 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(269): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.805+439A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71973154 | |||||||
| chr12:71973279 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.805+564G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71973279 | |||||||
| chr12:71973444 | C | T | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.805+729C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71973444 | |||||||
| chr12:71973504 | G | C | 1 | a0001c0002t0001g0262 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.805+789G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71973504 | |||||||
| chr12:71973546 | A | G | 19 | a0001c0002t0001g0079 a0001c0002t0001g0215 a0001c0002t0001g0216 others(16): Show |
19 | HG02258.hp2 HG02486.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.805+831A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71973546 | |||||||
| chr12:71973607 | G | A | 76 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0258 others(73): Show |
80 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.805+892G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71973607 | |||||||
| chr12:71973611 | C | G | 76 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0258 others(73): Show |
80 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.805+896C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71973611 | |||||||
| chr12:71973640 | A | G | 199 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0199 others(196): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.805+925A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71973640 | |||||||
| chr12:71973675 | T | G | 1 | a0001c0001t0001g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.805+960T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71973675 | |||||||
| chr12:71973694 | C | T | 143 | a0001c0001t0001g0190 a0001c0001t0001g0199 a0001c0002t0001g0002 others(140): Show |
149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.805+979C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71973694 | |||||||
| chr12:71973739 | C | G | 3 | a0001c0001t0001g0190 a0001c0001t0001g0214 a0001c0001t0001g0229 |
3 | HG02559.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.805+1024C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71973739 | |||||||
| chr12:71973875 | A | G | 272 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(269): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.805+1160A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71973875 | |||||||
| chr12:71973946 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.805+1231T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71973946 | |||||||
| chr12:71973951 | G | T | 1 | a0001c0003t0001g0228 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.805+1236G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71973951 | |||||||
| chr12:71973968 | G | A | 4 | a0001c0001t0001g0043 a0001c0004t0001g0037 a0001c0004t0001g0038 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+1253G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71973968 | |||||||
| chr12:71974145 | C | T | 3 | a0001c0002t0001g0011 a0001c0003t0001g0192 a0001c0003t0001g0303 |
4 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+1430C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71974145 | |||||||
| chr12:71974246 | C | T | 1 | a0001c0002t0001g0168 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.805+1531C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71974246 | |||||||
| chr12:71974402 | C | T | 2 | a0001c0002t0001g0132 a0001c0002t0001g0181 |
2 | HG00408.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.805+1687C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71974402 | |||||||
| chr12:71974525 | G | T | 77 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0199 others(74): Show |
81 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.805+1810G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71974525 | |||||||
| chr12:71974535 | CTT | C | 122 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(119): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.805+1821_805+1822d others(4): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71974535 | |||||||
| chr12:71974558 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0084 others(2): Show |
6 | HG02145.hp1 HG02451.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.805+1843C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71974558 | |||||||
| chr12:71974739 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.805+2024T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71974739 | |||||||
| chr12:71974791 | T | G | 218 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0199 others(215): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.805+2076T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71974791 | |||||||
| chr12:71974992 | C | T | 1 | a0001c0002t0001g0167 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.805+2277C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71974992 | |||||||
| chr12:71975013 | G | A | 1 | a0001c0003t0001g0072 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.805+2298G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71975013 | |||||||
| chr12:71975218 | G | A | 2 | a0001c0003t0001g0191 a0001c0003t0001g0300 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.805+2503G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71975218 | |||||||
| chr12:71975275 | G | A | 3 | a0001c0002t0001g0011 a0001c0003t0001g0192 a0001c0003t0001g0303 |
4 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+2560G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71975275 | |||||||
| chr12:71975322 | G | T | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.805+2607G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71975322 | |||||||
| chr12:71975381 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.805+2666C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71975381 | |||||||
| chr12:71975385 | G | T | 272 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(269): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.805+2670G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71975385 | |||||||
| chr12:71975609 | A | G | 2 | a0001c0002t0001g0215 a0001c0002t0001g0216 |
2 | HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.805+2894A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71975609 | |||||||
| chr12:71975793 | G | A | 3 | a0001c0001t0001g0096 a0001c0003t0001g0086 a0001c0003t0001g0226 |
3 | HG02109.hp2 HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.805+3078G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71975793 | |||||||
| chr12:71976228 | A | G | 4 | a0001c0001t0001g0043 a0001c0004t0001g0037 a0001c0004t0001g0038 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-2724A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71976228 | |||||||
| chr12:71976305 | T | G | 122 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(119): Show |
132 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.806-2647T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71976305 | |||||||
| chr12:71976324 | G | A | 1 | a0001c0002t0001g0108 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.806-2628G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71976324 | |||||||
| chr12:71976332 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.806-2620T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71976332 | |||||||
| chr12:71976357 | G | A | 1 | a0001c0004t0001g0050 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.806-2595G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71976357 | |||||||
| chr12:71976388 | T | A | 2 | a0001c0003t0001g0086 a0001c0003t0001g0226 |
2 | HG02109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.806-2564T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71976388 | |||||||
| chr12:71976490 | T | G | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.806-2462T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71976490 | |||||||
| chr12:71976509 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.806-2443A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71976509 | |||||||
| chr12:71976573 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.806-2379G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71976573 | |||||||
| chr12:71976648 | A | T | 1 | a0001c0001t0001g0259 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.806-2304A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71976648 | |||||||
| chr12:71976687 | C | T | 1 | a0001c0002t0001g0166 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.806-2265C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71976687 | |||||||
| chr12:71976941 | G | A | 1 | a0001c0002t0001g0198 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.806-2011G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71976941 | |||||||
| chr12:71976966 | G | A | 43 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(40): Show |
49 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.806-1986G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71976966 | |||||||
| chr12:71976988 | G | C | 2 | a0001c0003t0001g0086 a0001c0003t0001g0226 |
2 | HG02109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.806-1964G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71976988 | |||||||
| chr12:71977093 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.806-1859C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71977093 | |||||||
| chr12:71977155 | G | A | 272 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(269): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.806-1797G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71977155 | |||||||
| chr12:71977330 | T | TA | 8 | a0001c0001t0001g0225 a0001c0001t0003g0030 a0001c0001t0003g0031 others(5): Show |
8 | HG01261.hp2 HG01928.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.806-1621dupA | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 71977330 | ||||||
| chr12:71977448 | T | TAC | 5 | a0001c0001t0001g0020 a0001c0001t0001g0200 a0001c0004t0001g0050 others(2): Show |
5 | HG01106.hp2 HG01192.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.806-1482_806-1481d others(4): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 71977448 | ||||||
| chr12:71977448 | TAC | T | 28 | a0001c0001t0001g0009 a0001c0001t0001g0054 a0001c0001t0001g0055 others(25): Show |
29 | HG01069.hp1 HG01109.hp1 HG02135.hp1 others(26): Show |
intron_variant | MODIFIER | c.806-1482_806-1481d others(4): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 71977448 | ||||||
| chr12:71977470 | C | T | 145 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(142): Show |
152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.806-1482C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71977470 | |||||||
| chr12:71977472 | G | C | 1 | a0001c0001t0001g0259 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.806-1480G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71977472 | |||||||
| chr12:71977480 | C | A | 1 | a0001c0001t0001g0259 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.806-1472C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71977480 | |||||||
| chr12:71978188 | A | G | 1 | a0001c0001t0002g0254 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.806-764A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71978188 | |||||||
| chr12:71978215 | T | TA | 7 | a0001c0002t0001g0079 a0001c0003t0001g0065 a0001c0003t0001g0070 others(4): Show |
7 | HG02622.hp1 HG02717.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.806-724dupA | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 71978215 | ||||||
| chr12:71978215 | TA | T | 45 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(42): Show |
51 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.806-724delA | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 71978215 | ||||||
| chr12:71978292 | G | A | 3 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0004t0001g0257 |
3 | HG03831.hp1 HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.806-660G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71978292 | |||||||
| chr12:71978449 | T | A | 146 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(143): Show |
153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.806-503T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71978449 | |||||||
| chr12:71978617 | G | A | 122 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(119): Show |
132 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.806-335G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71978617 | |||||||
| chr12:71978621 | G | A | 42 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(39): Show |
48 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.806-331G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71978621 | |||||||
| chr12:71978821 | C | T | 146 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(143): Show |
153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.806-131C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71978821 | |||||||
| chr12:71978847 | A | G | 24 | a0001c0002t0001g0011 a0001c0002t0001g0079 a0001c0002t0001g0215 others(21): Show |
25 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.806-105A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 6/10 | chr12 | 71978847 | |||||||
| chr12:71979433 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.941+346C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71979433 | |||||||
| chr12:71979604 | G | T | 2 | a0001c0003t0001g0086 a0001c0003t0001g0226 |
2 | HG02109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.941+517G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71979604 | |||||||
| chr12:71979795 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.941+708G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71979795 | |||||||
| chr12:71979804 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.941+717C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71979804 | |||||||
| chr12:71979860 | G | A | 148 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(145): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.941+773G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71979860 | |||||||
| chr12:71979953 | TACAG | T | 146 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(143): Show |
153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.941+887_941+890del others(4): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71979953 | ||||||
| chr12:71979972 | A | C | 2 | a0001c0003t0001g0086 a0001c0003t0001g0226 |
2 | HG02109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.941+885A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71979972 | |||||||
| chr12:71980025 | C | T | 1 | a0001c0002t0001g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.941+938C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71980025 | |||||||
| chr12:71980074 | G | A | 148 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(145): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.941+987G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71980074 | |||||||
| chr12:71980124 | C | T | 42 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(39): Show |
48 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.941+1037C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71980124 | |||||||
| chr12:71980332 | T | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0026 others(5): Show |
10 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.941+1245T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71980332 | |||||||
| chr12:71980374 | G | A | 1 | a0001c0002t0001g0146 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.941+1287G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71980374 | |||||||
| chr12:71980406 | G | A | 272 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(269): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.941+1319G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71980406 | |||||||
| chr12:71980670 | G | A | 1 | a0001c0002t0001g0109 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.941+1583G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71980670 | |||||||
| chr12:71980750 | C | T | 149 | a0001c0001t0001g0067 a0001c0002t0001g0002 a0001c0002t0001g0007 others(146): Show |
156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.941+1663C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71980750 | |||||||
| chr12:71980857 | C | T | 149 | a0001c0001t0001g0067 a0001c0002t0001g0002 a0001c0002t0001g0007 others(146): Show |
156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.941+1770C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71980857 | |||||||
| chr12:71980938 | A | T | 151 | a0001c0001t0001g0067 a0001c0001t0001g0096 a0001c0001t0001g0199 others(148): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.941+1851A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71980938 | |||||||
| chr12:71980939 | T | A | 149 | a0001c0001t0001g0067 a0001c0002t0001g0002 a0001c0002t0001g0007 others(146): Show |
156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.941+1852T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71980939 | |||||||
| chr12:71980981 | A | C | 149 | a0001c0001t0001g0067 a0001c0002t0001g0002 a0001c0002t0001g0007 others(146): Show |
156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.941+1894A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71980981 | |||||||
| chr12:71981014 | A | G | 149 | a0001c0001t0001g0067 a0001c0002t0001g0002 a0001c0002t0001g0007 others(146): Show |
156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.941+1927A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71981014 | |||||||
| chr12:71981111 | G | T | 149 | a0001c0001t0001g0067 a0001c0002t0001g0002 a0001c0002t0001g0007 others(146): Show |
156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.941+2024G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71981111 | |||||||
| chr12:71981219 | T | C | 123 | a0001c0001t0001g0286 a0001c0002t0001g0002 a0001c0002t0001g0007 others(120): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.941+2132T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71981219 | |||||||
| chr12:71981228 | A | G | 150 | a0001c0001t0001g0067 a0001c0001t0001g0286 a0001c0002t0001g0002 others(147): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.941+2141A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71981228 | |||||||
| chr12:71981597 | C | A | 1 | a0001c0003t0001g0086 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.941+2510C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71981597 | |||||||
| chr12:71981599 | A | G | 4 | a0001c0004t0001g0249 a0001c0004t0001g0278 a0001c0004t0001g0302 others(1): Show |
4 | NA18968.hp2 NA18970.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.941+2512A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71981599 | |||||||
| chr12:71981612 | G | A | 77 | a0001c0001t0001g0019 a0001c0001t0001g0190 a0001c0001t0001g0214 others(74): Show |
81 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.941+2525G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71981612 | |||||||
| chr12:71981695 | T | C | 27 | a0001c0001t0001g0067 a0001c0002t0001g0011 a0001c0002t0001g0079 others(24): Show |
28 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.941+2608T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71981695 | |||||||
| chr12:71981759 | T | G | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.941+2672T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71981759 | |||||||
| chr12:71981966 | G | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0258 a0001c0001t0001g0259 others(4): Show |
8 | HG00438.hp1 HG02165.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.941+2879G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71981966 | |||||||
| chr12:71981968 | G | C | 2 | a0001c0002t0001g0179 a0001c0002t0001g0180 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.941+2881G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71981968 | |||||||
| chr12:71981984 | C | T | 24 | a0001c0002t0001g0011 a0001c0002t0001g0079 a0001c0002t0001g0215 others(21): Show |
25 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.941+2897C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71981984 | |||||||
| chr12:71982013 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.941+2926G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71982013 | |||||||
| chr12:71982015 | A | ATTTTTTT others(8): Show |
1 | a0001c0001t0001g0067 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.941+2931_941+2945d others(17): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(10): Show |
1 | a0001c0003t0001g0226 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.941+2929_941+2945d others(19): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(11): Show |
3 | a0001c0003t0001g0072 a0001c0003t0001g0082 a0001c0003t0001g0086 |
3 | HG02486.hp2 HG02897.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.941+2945_941+2946i others(20): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(12): Show |
10 | a0001c0002t0001g0216 a0001c0003t0001g0065 a0001c0003t0001g0070 others(7): Show |
10 | HG01496.hp1 HG02622.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.941+2945_941+2946i others(21): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(13): Show |
7 | a0001c0002t0001g0079 a0001c0002t0001g0215 a0001c0002t0001g0242 others(4): Show |
7 | HG02486.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.941+2945_941+2946i others(22): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(14): Show |
16 | a0001c0002t0001g0076 a0001c0002t0001g0116 a0001c0002t0001g0138 others(13): Show |
16 | HG01975.hp1 HG02896.hp1 HG06807.hp2 others(13): Show |
intron_variant | MODIFIER | c.941+2945_941+2946i others(23): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(15): Show |
33 | a0001c0002t0001g0010 a0001c0002t0001g0077 a0001c0002t0001g0080 others(30): Show |
34 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.941+2945_941+2946i others(24): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(16): Show |
14 | a0001c0002t0001g0013 a0001c0002t0001g0128 a0001c0002t0001g0131 others(11): Show |
15 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(12): Show |
intron_variant | MODIFIER | c.941+2945_941+2946i others(25): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(17): Show |
13 | a0001c0002t0001g0127 a0001c0002t0001g0161 a0001c0002t0001g0162 others(10): Show |
14 | HG00642.hp2 HG00738.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.941+2945_941+2946i others(26): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(18): Show |
3 | a0001c0002t0001g0195 a0001c0003t0001g0087 a0001c0003t0001g0091 |
3 | HG02257.hp1 HG04204.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.941+2945_941+2946i others(27): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(19): Show |
3 | a0001c0002t0001g0134 a0001c0002t0001g0163 a0001c0002t0001g0164 |
3 | HG00597.hp2 HG00621.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.941+2945_941+2946i others(28): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(20): Show |
1 | a0001c0003t0001g0047 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.941+2945_941+2946i others(29): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(21): Show |
4 | a0001c0003t0001g0089 a0001c0003t0001g0092 a0001c0003t0001g0238 others(1): Show |
4 | HG03486.hp1 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.941+2945_941+2946i others(30): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(23): Show |
1 | a0001c0002t0001g0165 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.941+2945_941+2946i others(32): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(28): Show |
7 | a0001c0002t0001g0012 a0001c0002t0001g0108 a0001c0002t0001g0111 others(4): Show |
7 | HG01257.hp1 HG01975.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.941+2945_941+2946i others(37): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(29): Show |
9 | a0001c0002t0001g0002 a0001c0002t0001g0075 a0001c0002t0001g0106 others(6): Show |
11 | HG00140.hp1 HG00438.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.941+2945_941+2946i others(38): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(30): Show |
4 | a0001c0002t0001g0114 a0001c0002t0001g0122 a0001c0002t0001g0136 others(1): Show |
4 | HG00642.hp1 HG03654.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.941+2945_941+2946i others(39): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(31): Show |
3 | a0001c0002t0001g0115 a0001c0002t0001g0179 a0001c0002t0001g0180 |
3 | HG03490.hp1 HG03492.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.941+2945_941+2946i others(40): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(32): Show |
1 | a0003c0007t0001g0105 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.941+2945_941+2946i others(41): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(33): Show |
1 | a0001c0002t0001g0109 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.941+2945_941+2946i others(42): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(35): Show |
2 | a0001c0003t0001g0237 a0001c0003t0001g0239 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.941+2945_941+2946i others(44): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(36): Show |
2 | a0001c0002t0001g0196 a0001c0003t0001g0240 |
2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.941+2945_941+2946i others(45): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982015 | A | ATTTTTTT others(37): Show |
1 | a0001c0002t0001g0197 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.941+2945_941+2946i others(46): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71982015 | ||||||
| chr12:71982085 | C | T | 149 | a0001c0001t0001g0067 a0001c0002t0001g0002 a0001c0002t0001g0007 others(146): Show |
156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.941+2998C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71982085 | |||||||
| chr12:71982140 | G | A | 149 | a0001c0001t0001g0067 a0001c0002t0001g0002 a0001c0002t0001g0007 others(146): Show |
156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.941+3053G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71982140 | |||||||
| chr12:71982205 | A | G | 78 | a0001c0001t0001g0019 a0001c0001t0001g0190 a0001c0001t0001g0214 others(75): Show |
82 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.941+3118A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71982205 | |||||||
| chr12:71982347 | T | A | 149 | a0001c0001t0001g0067 a0001c0002t0001g0002 a0001c0002t0001g0007 others(146): Show |
156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.941+3260T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71982347 | |||||||
| chr12:71982371 | A | T | 149 | a0001c0001t0001g0067 a0001c0002t0001g0002 a0001c0002t0001g0007 others(146): Show |
156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.941+3284A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71982371 | |||||||
| chr12:71982558 | A | G | 272 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(269): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.941+3471A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71982558 | |||||||
| chr12:71982698 | C | G | 272 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(269): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.941+3611C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71982698 | |||||||
| chr12:71982748 | T | G | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.941+3661T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71982748 | |||||||
| chr12:71982851 | A | G | 148 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(145): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.941+3764A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71982851 | |||||||
| chr12:71982885 | G | A | 1 | a0001c0002t0001g0181 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.941+3798G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71982885 | |||||||
| chr12:71982914 | A | T | 123 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(120): Show |
133 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.941+3827A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71982914 | |||||||
| chr12:71982935 | T | C | 272 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(269): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.941+3848T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71982935 | |||||||
| chr12:71983068 | TA | T | 272 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(269): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.941+3993delA | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71983068 | ||||||
| chr12:71983149 | G | A | 1 | a0001c0003t0001g0110 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.941+4062G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71983149 | |||||||
| chr12:71983283 | G | A | 123 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(120): Show |
133 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.941+4196G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71983283 | |||||||
| chr12:71983377 | A | T | 24 | a0001c0002t0001g0011 a0001c0002t0001g0079 a0001c0002t0001g0215 others(21): Show |
25 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.941+4290A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71983377 | |||||||
| chr12:71983423 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.941+4336A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71983423 | |||||||
| chr12:71983494 | C | T | 2 | a0001c0002t0001g0179 a0001c0002t0001g0180 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.941+4407C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71983494 | |||||||
| chr12:71983532 | G | C | 122 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(119): Show |
132 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.941+4445G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71983532 | |||||||
| chr12:71983697 | T | C | 18 | a0001c0002t0001g0079 a0001c0002t0001g0215 a0001c0002t0001g0216 others(15): Show |
18 | HG02257.hp2 HG02258.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.941+4610T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71983697 | |||||||
| chr12:71983705 | G | A | 2 | a0001c0001t0001g0223 a0001c0004t0001g0257 |
2 | HG03831.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.941+4618G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71983705 | |||||||
| chr12:71983767 | G | C | 1 | a0001c0001t0001g0304 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.941+4680G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71983767 | |||||||
| chr12:71983773 | C | G | 26 | a0001c0002t0001g0011 a0001c0002t0001g0079 a0001c0002t0001g0215 others(23): Show |
27 | HG01884.hp1 HG02109.hp2 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.941+4686C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71983773 | |||||||
| chr12:71983775 | C | CAG | 4 | a0001c0001t0001g0043 a0001c0004t0001g0037 a0001c0004t0001g0038 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.941+4700_941+4701d others(4): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71983775 | ||||||
| chr12:71983775 | C | G | 148 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(145): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.941+4688C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71983775 | |||||||
| chr12:71983803 | G | GAA | 123 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(120): Show |
133 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.941+4718_941+4719d others(4): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71983803 | ||||||
| chr12:71983826 | C | A | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.941+4739C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71983826 | |||||||
| chr12:71983903 | A | G | 272 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(269): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.941+4816A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71983903 | |||||||
| chr12:71984003 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0071 |
2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.941+4916C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71984003 | |||||||
| chr12:71984050 | C | T | 42 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(39): Show |
48 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.941+4963C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71984050 | |||||||
| chr12:71984058 | C | T | 1 | a0001c0002t0001g0165 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.941+4971C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71984058 | |||||||
| chr12:71984109 | A | C | 148 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(145): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.941+5022A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71984109 | |||||||
| chr12:71984134 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.941+5047T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71984134 | |||||||
| chr12:71984138 | A | G | 272 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(269): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.941+5051A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71984138 | |||||||
| chr12:71984161 | A | G | 272 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(269): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.941+5074A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71984161 | |||||||
| chr12:71984271 | C | T | 1 | a0001c0002t0001g0124 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.941+5184C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71984271 | |||||||
| chr12:71984475 | C | T | 5 | a0001c0001t0002g0277 a0001c0001t0004g0018 a0001c0001t0004g0276 others(2): Show |
6 | NA18951.hp2 NA18967.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.941+5388C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71984475 | |||||||
| chr12:71984541 | T | G | 273 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(270): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.941+5454T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71984541 | |||||||
| chr12:71984787 | G | A | 1 | a0001c0002t0001g0262 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.941+5700G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71984787 | |||||||
| chr12:71984819 | T | C | 122 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(119): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.941+5732T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71984819 | |||||||
| chr12:71984935 | C | G | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.941+5848C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71984935 | |||||||
| chr12:71985089 | A | G | 1 | a0001c0004t0001g0275 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.941+6002A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71985089 | |||||||
| chr12:71985143 | A | T | 273 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(270): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.941+6056A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71985143 | |||||||
| chr12:71985255 | C | T | 1 | a0001c0001t0002g0017 | 2 | HG00099.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.941+6168C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71985255 | |||||||
| chr12:71985422 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.941+6335G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71985422 | |||||||
| chr12:71985632 | C | T | 4 | a0001c0004t0003g0039 a0001c0004t0003g0040 a0001c0004t0003g0041 others(1): Show |
4 | HG01358.hp2 HG03017.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.941+6545C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71985632 | |||||||
| chr12:71985706 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.941+6619A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71985706 | |||||||
| chr12:71985774 | T | C | 13 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0002g0142 others(10): Show |
13 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.941+6687T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71985774 | |||||||
| chr12:71985796 | A | G | 3 | a0001c0002t0001g0011 a0001c0003t0001g0192 a0001c0003t0001g0303 |
4 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.941+6709A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71985796 | |||||||
| chr12:71985802 | T | C | 1 | a0001c0003t0001g0065 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.941+6715T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71985802 | |||||||
| chr12:71985995 | A | C | 1 | a0001c0001t0002g0211 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.941+6908A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71985995 | |||||||
| chr12:71986031 | T | C | 1 | a0001c0002t0001g0159 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.941+6944T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71986031 | |||||||
| chr12:71986052 | G | T | 4 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0097 others(1): Show |
4 | HG02647.hp1 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.941+6965G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71986052 | |||||||
| chr12:71986242 | G | T | 266 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(263): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.941+7155G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71986242 | |||||||
| chr12:71986324 | C | T | 1 | a0001c0002t0001g0077 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.941+7237C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71986324 | |||||||
| chr12:71986525 | A | T | 272 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(269): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.941+7438A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71986525 | |||||||
| chr12:71986614 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.941+7527T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71986614 | |||||||
| chr12:71986630 | C | CT | 149 | a0001c0001t0001g0043 a0001c0001t0001g0096 a0001c0001t0001g0199 others(146): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.941+7561dupT | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71986630 | ||||||
| chr12:71986630 | C | CTT | 47 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0186 others(44): Show |
52 | HG00597.hp1 HG00609.hp1 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.941+7560_941+7561d others(4): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71986630 | ||||||
| chr12:71986630 | C | CTTT | 73 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0067 others(70): Show |
77 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.941+7559_941+7561d others(5): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71986630 | ||||||
| chr12:71986685 | C | A | 4 | a0001c0001t0001g0069 a0001c0001t0001g0100 a0001c0001t0001g0101 others(1): Show |
4 | HG01167.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.941+7598C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71986685 | |||||||
| chr12:71986719 | G | A | 36 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0186 others(33): Show |
41 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.941+7632G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71986719 | |||||||
| chr12:71986750 | G | A | 27 | a0001c0001t0001g0043 a0001c0001t0001g0199 a0001c0002t0001g0079 others(24): Show |
28 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.941+7663G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71986750 | |||||||
| chr12:71986841 | G | A | 1 | a0001c0001t0004g0276 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.942-7598G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71986841 | |||||||
| chr12:71987510 | C | T | 1 | a0001c0004t0001g0207 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.942-6929C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71987510 | |||||||
| chr12:71987595 | T | A | 5 | a0001c0001t0002g0277 a0001c0001t0004g0018 a0001c0001t0004g0276 others(2): Show |
6 | NA18951.hp2 NA18967.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.942-6844T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71987595 | |||||||
| chr12:71987620 | G | A | 121 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(118): Show |
127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.942-6819G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71987620 | |||||||
| chr12:71987675 | A | C | 85 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0190 others(82): Show |
90 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.942-6764A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71987675 | |||||||
| chr12:71987724 | T | C | 2 | a0001c0003t0001g0192 a0001c0003t0001g0303 |
2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.942-6715T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71987724 | |||||||
| chr12:71987776 | C | T | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0004t0001g0050 others(1): Show |
4 | HG03041.hp2 HG03831.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.942-6663C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71987776 | |||||||
| chr12:71987844 | C | A | 1 | a0001c0003t0001g0191 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.942-6595C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71987844 | |||||||
| chr12:71987882 | G | C | 1 | a0001c0001t0002g0270 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.942-6557G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71987882 | |||||||
| chr12:71987896 | T | C | 85 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0190 others(82): Show |
90 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.942-6543T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71987896 | |||||||
| chr12:71987900 | C | T | 273 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(270): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.942-6539C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71987900 | |||||||
| chr12:71988026 | G | T | 2 | a0001c0002t0001g0179 a0001c0002t0001g0180 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.942-6413G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71988026 | |||||||
| chr12:71988194 | T | C | 2 | a0003c0007t0001g0104 a0003c0007t0001g0105 |
2 | HG01496.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.942-6245T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71988194 | |||||||
| chr12:71988318 | G | T | 1 | a0001c0003t0001g0086 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.942-6121G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71988318 | |||||||
| chr12:71988380 | G | A | 2 | a0001c0002t0001g0123 a0001c0002t0001g0244 |
2 | NA18969.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.942-6059G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71988380 | |||||||
| chr12:71988414 | A | C | 1 | a0001c0002t0001g0119 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.942-6025A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71988414 | |||||||
| chr12:71988467 | A | G | 103 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0190 others(100): Show |
108 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.942-5972A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71988467 | |||||||
| chr12:71988536 | C | A | 34 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0186 others(31): Show |
39 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.942-5903C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71988536 | |||||||
| chr12:71988549 | G | A | 80 | a0001c0001t0001g0019 a0001c0001t0001g0190 a0001c0001t0001g0214 others(77): Show |
84 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.942-5890G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71988549 | |||||||
| chr12:71988686 | T | G | 34 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0186 others(31): Show |
39 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.942-5753T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71988686 | |||||||
| chr12:71988841 | T | C | 121 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(118): Show |
127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.942-5598T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71988841 | |||||||
| chr12:71988943 | A | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.942-5496A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71988943 | |||||||
| chr12:71989100 | TA | T | 241 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(238): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.942-5318delA | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71989100 | ||||||
| chr12:71989100 | TAA | T | 15 | a0001c0001t0001g0096 a0001c0001t0002g0261 a0001c0001t0002g0270 others(12): Show |
15 | HG00609.hp1 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.942-5319_942-5318d others(4): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71989100 | ||||||
| chr12:71989417 | G | A | 4 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0097 others(1): Show |
4 | HG02647.hp1 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.942-5022G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71989417 | |||||||
| chr12:71989443 | C | T | 2 | a0001c0001t0001g0199 a0001c0003t0001g0226 |
2 | HG01884.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.942-4996C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71989443 | |||||||
| chr12:71989485 | A | G | 103 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0190 others(100): Show |
108 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.942-4954A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71989485 | |||||||
| chr12:71989495 | C | T | 34 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0186 others(31): Show |
39 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.942-4944C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71989495 | |||||||
| chr12:71989529 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0304 |
2 | NA18950.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.942-4910G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71989529 | |||||||
| chr12:71989682 | G | A | 34 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0186 others(31): Show |
39 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.942-4757G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71989682 | |||||||
| chr12:71989780 | G | A | 1 | a0001c0004t0003g0024 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.942-4659G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71989780 | |||||||
| chr12:71989834 | A | G | 258 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(255): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.942-4605A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71989834 | |||||||
| chr12:71989947 | TG | T | 250 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(247): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.942-4490delG | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71989947 | ||||||
| chr12:71989948 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.942-4491G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71989948 | |||||||
| chr12:71989949 | G | C | 17 | a0001c0001t0001g0020 a0001c0002t0001g0079 a0001c0002t0001g0215 others(14): Show |
17 | HG02257.hp2 HG02486.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.942-4490G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71989949 | |||||||
| chr12:71989950 | T | C | 251 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(248): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.942-4489T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71989950 | |||||||
| chr12:71989951 | T | C | 2 | a0001c0002t0001g0107 a0001c0002t0001g0112 |
2 | HG00140.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.942-4488T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71989951 | |||||||
| chr12:71990070 | T | C | 1 | a0001c0001t0003g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.942-4369T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71990070 | |||||||
| chr12:71990156 | G | A | 3 | a0001c0002t0001g0007 a0001c0002t0001g0189 a0001c0002t0007g0090 |
4 | HG02630.hp1 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.942-4283G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71990156 | |||||||
| chr12:71990263 | G | A | 3 | a0001c0003t0001g0072 a0001c0003t0001g0094 a0001c0003t0001g0095 |
3 | HG02896.hp2 HG02897.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.942-4176G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71990263 | |||||||
| chr12:71990349 | G | A | 3 | a0001c0002t0001g0139 a0001c0002t0001g0148 a0001c0003t0001g0169 |
3 | HG02109.hp1 HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.942-4090G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71990349 | |||||||
| chr12:71990415 | C | A | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.942-4024C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71990415 | |||||||
| chr12:71990435 | A | T | 34 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0186 others(31): Show |
39 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.942-4004A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71990435 | |||||||
| chr12:71990562 | T | A | 3 | a0001c0002t0001g0011 a0001c0003t0001g0192 a0001c0003t0001g0303 |
4 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.942-3877T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71990562 | |||||||
| chr12:71990639 | C | G | 1 | a0001c0002t0001g0246 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.942-3800C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71990639 | |||||||
| chr12:71990781 | G | A | 3 | a0001c0002t0001g0011 a0001c0003t0001g0192 a0001c0003t0001g0303 |
4 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.942-3658G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71990781 | |||||||
| chr12:71990931 | C | T | 1 | a0001c0002t0001g0151 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.942-3508C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71990931 | |||||||
| chr12:71991344 | T | A | 2 | a0001c0002t0001g0123 a0001c0002t0001g0244 |
2 | NA18969.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.942-3095T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71991344 | |||||||
| chr12:71991476 | C | T | 1 | a0001c0001t0002g0299 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.942-2963C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71991476 | |||||||
| chr12:71991720 | C | T | 102 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0190 others(99): Show |
107 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.942-2719C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71991720 | |||||||
| chr12:71992081 | A | C | 1 | a0002c0005t0001g0147 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.942-2358A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71992081 | |||||||
| chr12:71992112 | A | G | 23 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0075 others(20): Show |
25 | HG00140.hp1 HG00438.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.942-2327A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71992112 | |||||||
| chr12:71992226 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.942-2213C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71992226 | |||||||
| chr12:71992332 | A | T | 2 | a0001c0003t0001g0094 a0001c0003t0001g0095 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.942-2107A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71992332 | |||||||
| chr12:71992391 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.942-2048G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71992391 | |||||||
| chr12:71992418 | C | G | 121 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(118): Show |
127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.942-2021C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71992418 | |||||||
| chr12:71992477 | G | A | 1 | a0001c0002t0001g0075 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.942-1962G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71992477 | |||||||
| chr12:71992495 | T | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.942-1944T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71992495 | |||||||
| chr12:71992525 | G | A | 34 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0186 others(31): Show |
39 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.942-1914G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71992525 | |||||||
| chr12:71992545 | G | A | 1 | a0001c0004t0001g0037 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.942-1894G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71992545 | |||||||
| chr12:71992614 | GTC | G | 3 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0004t0003g0024 |
3 | HG02970.hp1 NA19240.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.942-1821_942-1820d others(4): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 71992614 | ||||||
| chr12:71992680 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.942-1759C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71992680 | |||||||
| chr12:71992745 | C | T | 1 | a0001c0002t0001g0011 | 2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.942-1694C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71992745 | |||||||
| chr12:71993015 | A | C | 1 | a0001c0001t0002g0017 | 2 | HG00099.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.942-1424A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71993015 | |||||||
| chr12:71993176 | T | G | 84 | a0001c0001t0001g0019 a0001c0001t0001g0190 a0001c0001t0001g0214 others(81): Show |
89 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.942-1263T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71993176 | |||||||
| chr12:71993284 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.942-1155G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71993284 | |||||||
| chr12:71993411 | G | A | 1 | a0001c0003t0001g0047 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.942-1028G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71993411 | |||||||
| chr12:71993562 | C | T | 121 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(118): Show |
127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.942-877C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71993562 | |||||||
| chr12:71993841 | C | T | 1 | a0001c0002t0001g0176 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.942-598C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71993841 | |||||||
| chr12:71994312 | C | T | 27 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0225 others(24): Show |
32 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.942-127C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71994312 | |||||||
| chr12:71994393 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.942-46T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 7/10 | chr12 | 71994393 | |||||||
| chr12:71994594 | G | T | 273 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(270): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1068+29G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71994594 | |||||||
| chr12:71994644 | T | C | 18 | a0001c0002t0001g0079 a0001c0002t0001g0215 a0001c0002t0001g0216 others(15): Show |
18 | HG02257.hp2 HG02258.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1068+79T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71994644 | |||||||
| chr12:71994835 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1068+270C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71994835 | |||||||
| chr12:71994964 | C | T | 18 | a0001c0002t0001g0079 a0001c0002t0001g0215 a0001c0002t0001g0216 others(15): Show |
18 | HG02257.hp2 HG02258.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1068+399C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71994964 | |||||||
| chr12:71994968 | GTGC | G | 80 | a0001c0001t0001g0019 a0001c0001t0001g0190 a0001c0001t0001g0214 others(77): Show |
84 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1068+406_1068+408d others(5): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 71994968 | ||||||
| chr12:71995059 | T | G | 121 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(118): Show |
127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1068+494T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71995059 | |||||||
| chr12:71995079 | A | C | 1 | a0001c0001t0001g0206 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1068+514A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71995079 | |||||||
| chr12:71995123 | C | T | 1 | a0001c0001t0004g0295 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1068+558C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71995123 | |||||||
| chr12:71995296 | T | A | 4 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0097 others(1): Show |
4 | HG02647.hp1 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+731T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71995296 | |||||||
| chr12:71995422 | T | C | 121 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(118): Show |
127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1068+857T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71995422 | |||||||
| chr12:71995476 | T | C | 8 | a0001c0001t0002g0016 a0001c0001t0002g0251 a0001c0001t0002g0252 others(5): Show |
9 | HG00733.hp2 HG01358.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.1068+911T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71995476 | |||||||
| chr12:71995697 | C | T | 2 | a0001c0002t0001g0139 a0001c0002t0001g0148 |
2 | HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1068+1132C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71995697 | |||||||
| chr12:71996053 | C | T | 7 | a0001c0001t0001g0096 a0001c0001t0001g0199 a0001c0003t0001g0226 others(4): Show |
8 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1068+1488C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71996053 | |||||||
| chr12:71996165 | C | T | 124 | a0001c0001t0001g0043 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1068+1600C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71996165 | |||||||
| chr12:71996245 | C | T | 124 | a0001c0001t0001g0043 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1068+1680C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71996245 | |||||||
| chr12:71996260 | A | G | 8 | a0001c0003t0001g0008 a0001c0003t0001g0087 a0001c0003t0001g0089 others(5): Show |
9 | HG02257.hp1 HG02723.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1068+1695A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71996260 | |||||||
| chr12:71996335 | C | G | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1068+1770C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71996335 | |||||||
| chr12:71996503 | G | T | 1 | a0001c0001t0002g0281 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1068+1938G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71996503 | |||||||
| chr12:71996614 | A | G | 1 | a0001c0003t0001g0141 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1068+2049A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71996614 | |||||||
| chr12:71996615 | C | T | 84 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0190 others(81): Show |
89 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1068+2050C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71996615 | |||||||
| chr12:71996674 | G | A | 1 | a0001c0003t0001g0226 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1068+2109G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71996674 | |||||||
| chr12:71996980 | AT | A | 84 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0190 others(81): Show |
89 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1068+2416delT | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71996980 | |||||||
| chr12:71997089 | G | A | 1 | a0001c0004t0001g0037 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1068+2524G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71997089 | |||||||
| chr12:71997184 | G | A | 124 | a0001c0001t0001g0043 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1068+2619G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71997184 | |||||||
| chr12:71997317 | G | A | 118 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(115): Show |
128 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.1068+2752G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71997317 | |||||||
| chr12:71997327 | G | T | 1 | a0001c0002t0001g0242 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1068+2762G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71997327 | |||||||
| chr12:71997338 | A | G | 1 | a0001c0002t0001g0159 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1068+2773A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71997338 | |||||||
| chr12:71997426 | T | G | 4 | a0001c0001t0004g0018 a0001c0001t0004g0276 a0001c0001t0004g0294 others(1): Show |
5 | NA18951.hp2 NA18967.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.1068+2861T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71997426 | |||||||
| chr12:71997513 | G | A | 3 | a0001c0002t0001g0011 a0001c0003t0001g0192 a0001c0003t0001g0303 |
4 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+2948G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71997513 | |||||||
| chr12:71997538 | C | T | 3 | a0001c0002t0001g0011 a0001c0003t0001g0192 a0001c0003t0001g0303 |
4 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+2973C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71997538 | |||||||
| chr12:71997586 | T | C | 1 | a0001c0003t0001g0072 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1068+3021T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71997586 | |||||||
| chr12:71997765 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1068+3200G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71997765 | |||||||
| chr12:71997765 | GA | G | 109 | a0001c0001t0001g0019 a0001c0001t0001g0190 a0001c0001t0001g0214 others(106): Show |
116 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1068+3207delA | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 71997765 | ||||||
| chr12:71997904 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1068+3339T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71997904 | |||||||
| chr12:71998135 | G | A | 31 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0223 others(28): Show |
36 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1068+3570G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71998135 | |||||||
| chr12:71998161 | G | T | 1 | a0001c0001t0001g0067 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1068+3596G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71998161 | |||||||
| chr12:71998219 | C | A | 124 | a0001c0001t0001g0043 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1068+3654C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71998219 | |||||||
| chr12:71998510 | C | A | 272 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(269): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1068+3945C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71998510 | |||||||
| chr12:71998511 | C | A | 1 | a0001c0003t0001g0121 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1068+3946C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71998511 | |||||||
| chr12:71998577 | A | G | 1 | a0001c0002t0001g0077 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1068+4012A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71998577 | |||||||
| chr12:71998934 | T | C | 3 | a0001c0002t0001g0011 a0001c0003t0001g0192 a0001c0003t0001g0303 |
4 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+4369T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71998934 | |||||||
| chr12:71999134 | G | A | 137 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(134): Show |
146 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1068+4569G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71999134 | |||||||
| chr12:71999153 | T | C | 1 | a0001c0002t0005g0029 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1068+4588T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71999153 | |||||||
| chr12:71999349 | A | T | 124 | a0001c0001t0001g0043 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1068+4784A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71999349 | |||||||
| chr12:71999393 | G | C | 3 | a0001c0002t0001g0011 a0001c0003t0001g0192 a0001c0003t0001g0303 |
4 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+4828G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71999393 | |||||||
| chr12:71999400 | A | G | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG00423.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.1068+4835A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71999400 | |||||||
| chr12:71999533 | T | A | 140 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(137): Show |
150 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1068+4968T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71999533 | |||||||
| chr12:71999795 | C | T | 137 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(134): Show |
146 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1068+5230C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71999795 | |||||||
| chr12:71999823 | T | C | 3 | a0001c0003t0001g0082 a0001c0003t0001g0083 a0001c0003t0001g0099 |
3 | HG02895.hp2 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1068+5258T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71999823 | |||||||
| chr12:71999980 | A | G | 2 | a0001c0003t0001g0094 a0001c0003t0001g0095 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1068+5415A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 71999980 | |||||||
| chr12:72000022 | C | T | 3 | a0001c0002t0001g0011 a0001c0003t0001g0192 a0001c0003t0001g0303 |
4 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+5457C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72000022 | |||||||
| chr12:72000117 | G | A | 1 | a0001c0003t0001g0086 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1068+5552G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72000117 | |||||||
| chr12:72000239 | C | T | 8 | a0001c0001t0002g0142 a0001c0001t0002g0233 a0001c0001t0002g0266 others(5): Show |
8 | HG00423.hp2 HG00558.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1068+5674C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72000239 | |||||||
| chr12:72000396 | T | G | 148 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(145): Show |
159 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.1068+5831T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72000396 | |||||||
| chr12:72000502 | C | T | 136 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(133): Show |
145 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1068+5937C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72000502 | |||||||
| chr12:72000519 | C | G | 140 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(137): Show |
150 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1068+5954C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72000519 | |||||||
| chr12:72000710 | C | A | 1 | a0001c0003t0001g0072 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1068+6145C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72000710 | |||||||
| chr12:72000714 | C | T | 4 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0097 others(1): Show |
4 | HG02647.hp1 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+6149C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72000714 | |||||||
| chr12:72000884 | T | C | 1 | a0001c0003t0001g0086 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1068+6319T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72000884 | |||||||
| chr12:72000909 | A | C | 3 | a0001c0002t0001g0011 a0001c0003t0001g0192 a0001c0003t0001g0303 |
4 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+6344A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72000909 | |||||||
| chr12:72000923 | A | G | 1 | a0001c0001t0002g0296 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1068+6358A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72000923 | |||||||
| chr12:72000974 | G | A | 7 | a0001c0001t0001g0096 a0001c0001t0001g0199 a0001c0003t0001g0226 others(4): Show |
8 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1068+6409G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72000974 | |||||||
| chr12:72001301 | G | A | 3 | a0001c0002t0001g0011 a0001c0003t0001g0192 a0001c0003t0001g0303 |
4 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+6736G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72001301 | |||||||
| chr12:72001428 | C | CT | 6 | a0001c0001t0001g0096 a0001c0001t0002g0068 a0001c0001t0002g0253 others(3): Show |
6 | HG01081.hp1 HG01928.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1068+6878dupT | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72001428 | ||||||
| chr12:72001449 | A | G | 148 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(145): Show |
159 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.1068+6884A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72001449 | |||||||
| chr12:72001508 | C | A | 2 | a0001c0003t0001g0094 a0001c0003t0001g0095 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1068+6943C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72001508 | |||||||
| chr12:72001546 | C | T | 4 | a0001c0004t0003g0039 a0001c0004t0003g0040 a0001c0004t0003g0041 others(1): Show |
4 | HG01358.hp2 HG03017.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+6981C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72001546 | |||||||
| chr12:72001925 | G | A | 3 | a0001c0002t0001g0011 a0001c0003t0001g0192 a0001c0003t0001g0303 |
4 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+7360G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72001925 | |||||||
| chr12:72002037 | A | G | 1 | a0001c0003t0001g0086 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1068+7472A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72002037 | |||||||
| chr12:72002081 | G | A | 6 | a0001c0001t0001g0096 a0001c0003t0001g0226 a0001c0004t0001g0015 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1068+7516G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72002081 | |||||||
| chr12:72002325 | G | A | 5 | a0001c0003t0001g0237 a0001c0003t0001g0238 a0001c0003t0001g0239 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1068+7760G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72002325 | |||||||
| chr12:72002405 | A | G | 5 | a0001c0003t0001g0226 a0001c0004t0001g0015 a0001c0004t0001g0219 others(2): Show |
6 | HG02055.hp2 HG02109.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1068+7840A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72002405 | |||||||
| chr12:72002416 | C | T | 1 | a0001c0002t0001g0168 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1068+7851C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72002416 | |||||||
| chr12:72002456 | G | A | 3 | a0001c0002t0001g0011 a0001c0003t0001g0192 a0001c0003t0001g0303 |
4 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+7891G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72002456 | |||||||
| chr12:72002538 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1068+7973G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72002538 | |||||||
| chr12:72002712 | G | A | 91 | a0001c0001t0001g0190 a0001c0001t0001g0199 a0001c0001t0001g0214 others(88): Show |
94 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.1068+8147G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72002712 | |||||||
| chr12:72002723 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1068+8158T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72002723 | |||||||
| chr12:72002757 | C | CT | 98 | a0001c0001t0001g0067 a0001c0001t0001g0096 a0001c0001t0001g0190 others(95): Show |
102 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1068+8205dupT | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72002757 | ||||||
| chr12:72002771 | G | T | 8 | a0001c0003t0001g0008 a0001c0003t0001g0087 a0001c0003t0001g0089 others(5): Show |
9 | HG02257.hp1 HG02723.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1068+8206G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72002771 | |||||||
| chr12:72002779 | G | A | 1 | a0001c0001t0002g0290 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1068+8214G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72002779 | |||||||
| chr12:72002901 | G | A | 98 | a0001c0001t0001g0067 a0001c0001t0001g0096 a0001c0001t0001g0190 others(95): Show |
102 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1068+8336G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72002901 | |||||||
| chr12:72003195 | C | T | 1 | a0001c0001t0004g0294 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1068+8630C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72003195 | |||||||
| chr12:72003216 | C | G | 36 | a0001c0002t0001g0010 a0001c0002t0001g0013 a0001c0002t0001g0077 others(33): Show |
38 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.1068+8651C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72003216 | |||||||
| chr12:72003352 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1068+8787G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72003352 | |||||||
| chr12:72003581 | T | C | 126 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0002t0001g0002 others(123): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1068+9016T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72003581 | |||||||
| chr12:72003726 | A | G | 2 | a0001c0002t0001g0107 a0001c0002t0001g0113 |
2 | HG00140.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1068+9161A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72003726 | |||||||
| chr12:72003826 | T | C | 1 | a0001c0002t0001g0166 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1068+9261T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72003826 | |||||||
| chr12:72003870 | C | T | 3 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 |
3 | HG01109.hp1 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1068+9305C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72003870 | |||||||
| chr12:72003955 | G | T | 8 | a0001c0002t0001g0079 a0001c0002t0001g0215 a0001c0002t0001g0216 others(5): Show |
8 | HG02486.hp1 HG02622.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1068+9390G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72003955 | |||||||
| chr12:72004004 | A | G | 126 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0002t0001g0002 others(123): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1068+9439A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72004004 | |||||||
| chr12:72004008 | C | T | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1068+9443C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72004008 | |||||||
| chr12:72004009 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1068+9444T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72004009 | |||||||
| chr12:72004026 | GCACACAC others(496): Show |
G | 42 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(39): Show |
48 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1068+9463_1068+996 others(4): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72004026 | ||||||
| chr12:72004114 | C | T | 125 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0002t0001g0002 others(122): Show |
131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1068+9549C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72004114 | |||||||
| chr12:72004122 | T | C | 3 | a0001c0002t0001g0139 a0003c0007t0001g0104 a0003c0007t0001g0105 |
3 | HG01496.hp1 HG02896.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1068+9557T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72004122 | |||||||
| chr12:72004337 | C | T | 228 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0067 others(225): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1068+9772C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72004337 | |||||||
| chr12:72004363 | A | G | 125 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0002t0001g0002 others(122): Show |
131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1068+9798A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72004363 | |||||||
| chr12:72004373 | T | C | 228 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0067 others(225): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1068+9808T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72004373 | |||||||
| chr12:72004445 | G | T | 4 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0097 others(1): Show |
4 | HG02647.hp1 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+9880G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72004445 | |||||||
| chr12:72004527 | G | A | 1 | a0001c0002t0001g0146 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1068+9962G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72004527 | |||||||
| chr12:72004545 | T | C | 1 | a0001c0003t0001g0072 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1068+9980T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72004545 | |||||||
| chr12:72004699 | G | A | 5 | a0001c0003t0001g0226 a0001c0004t0001g0015 a0001c0004t0001g0219 others(2): Show |
6 | HG02055.hp2 HG02109.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1068+10134G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72004699 | |||||||
| chr12:72004743 | C | A | 1 | a0001c0002t0001g0174 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1068+10178C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72004743 | |||||||
| chr12:72005078 | G | C | 4 | a0001c0002t0001g0011 a0001c0003t0001g0070 a0001c0003t0001g0192 others(1): Show |
5 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1068+10513G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72005078 | |||||||
| chr12:72005350 | T | C | 1 | a0002c0005t0001g0144 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1068+10785T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72005350 | |||||||
| chr12:72005390 | CAT | C | 126 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0002t0001g0002 others(123): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1068+10830_1068+10 others(8): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72005390 | ||||||
| chr12:72005419 | C | T | 41 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(38): Show |
47 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1068+10854C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72005419 | |||||||
| chr12:72005420 | A | G | 42 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(39): Show |
48 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1068+10855A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72005420 | |||||||
| chr12:72005424 | A | G | 1 | a0001c0003t0001g0169 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1068+10859A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72005424 | |||||||
| chr12:72005765 | C | T | 3 | a0001c0002t0001g0011 a0001c0003t0001g0192 a0001c0003t0001g0303 |
4 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+11200C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72005765 | |||||||
| chr12:72006288 | G | A | 1 | a0001c0004t0001g0050 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1068+11723G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72006288 | |||||||
| chr12:72006318 | A | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0100 a0001c0001t0001g0101 others(1): Show |
4 | HG01167.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+11753A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72006318 | |||||||
| chr12:72006464 | G | A | 2 | a0001c0003t0001g0047 a0001c0003t0001g0227 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1068+11899G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72006464 | |||||||
| chr12:72006518 | G | A | 31 | a0001c0001t0001g0263 a0001c0001t0001g0288 a0001c0001t0001g0289 others(28): Show |
32 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1068+11953G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72006518 | |||||||
| chr12:72006690 | A | G | 7 | a0001c0002t0001g0011 a0001c0003t0001g0072 a0001c0003t0001g0094 others(4): Show |
8 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1068+12125A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72006690 | |||||||
| chr12:72006708 | C | T | 1 | a0001c0001t0004g0294 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1068+12143C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72006708 | |||||||
| chr12:72006836 | A | ATACTATA others(5): Show |
1 | a0001c0002t0001g0243 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1068+12273_1068+12 others(18): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72006836 | ||||||
| chr12:72006849 | T | G | 1 | a0001c0004t0001g0050 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1068+12284T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72006849 | |||||||
| chr12:72006967 | G | A | 16 | a0001c0001t0001g0199 a0001c0002t0001g0079 a0001c0002t0001g0215 others(13): Show |
16 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1068+12402G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72006967 | |||||||
| chr12:72007071 | T | C | 70 | a0001c0001t0001g0263 a0001c0001t0001g0272 a0001c0001t0001g0286 others(67): Show |
73 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1068+12506T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72007071 | |||||||
| chr12:72007181 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1068+12616G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72007181 | |||||||
| chr12:72007229 | C | T | 40 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(37): Show |
46 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.1068+12664C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72007229 | |||||||
| chr12:72007513 | A | C | 7 | a0001c0002t0001g0011 a0001c0003t0001g0072 a0001c0003t0001g0094 others(4): Show |
8 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1068+12948A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72007513 | |||||||
| chr12:72007568 | T | C | 7 | a0001c0002t0001g0011 a0001c0003t0001g0072 a0001c0003t0001g0094 others(4): Show |
8 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1068+13003T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72007568 | |||||||
| chr12:72007746 | C | CT | 7 | a0001c0002t0001g0011 a0001c0003t0001g0072 a0001c0003t0001g0094 others(4): Show |
8 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1068+13192dupT | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72007746 | ||||||
| chr12:72007818 | AG | A | 7 | a0001c0002t0001g0011 a0001c0003t0001g0072 a0001c0003t0001g0094 others(4): Show |
8 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1068+13254delG | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72007818 | |||||||
| chr12:72007859 | C | T | 40 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(37): Show |
46 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.1068+13294C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72007859 | |||||||
| chr12:72007880 | G | A | 2 | a0001c0003t0001g0047 a0001c0003t0001g0227 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1068+13315G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72007880 | |||||||
| chr12:72007893 | C | T | 1 | a0001c0004t0001g0205 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1068+13328C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72007893 | |||||||
| chr12:72007914 | A | G | 3 | a0001c0002t0001g0156 a0001c0002t0001g0161 a0001c0003t0002g0157 |
3 | HG00642.hp2 HG02135.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1068+13349A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72007914 | |||||||
| chr12:72007983 | C | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0258 a0001c0001t0001g0259 others(4): Show |
8 | HG00438.hp1 HG02165.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.1068+13418C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72007983 | |||||||
| chr12:72008090 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1068+13525T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72008090 | |||||||
| chr12:72008119 | C | T | 1 | a0001c0002t0001g0119 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1068+13554C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72008119 | |||||||
| chr12:72008406 | T | C | 132 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0002t0001g0002 others(129): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.1068+13841T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72008406 | |||||||
| chr12:72008436 | T | A | 1 | a0001c0001t0001g0287 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1068+13871T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72008436 | |||||||
| chr12:72008485 | G | A | 2 | a0001c0002t0001g0215 a0001c0002t0001g0216 |
2 | HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1069-13914G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72008485 | |||||||
| chr12:72008532 | G | T | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1069-13867G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72008532 | |||||||
| chr12:72008670 | A | T | 6 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(3): Show |
6 | HG01109.hp1 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1069-13729A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72008670 | |||||||
| chr12:72008716 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1069-13683A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72008716 | |||||||
| chr12:72008816 | G | A | 1 | a0001c0002t0001g0159 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1069-13583G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72008816 | |||||||
| chr12:72009024 | A | G | 5 | a0001c0003t0001g0237 a0001c0003t0001g0238 a0001c0003t0001g0239 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1069-13375A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72009024 | |||||||
| chr12:72009331 | G | A | 42 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(39): Show |
48 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1069-13068G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72009331 | |||||||
| chr12:72009344 | C | T | 7 | a0001c0002t0001g0011 a0001c0003t0001g0072 a0001c0003t0001g0094 others(4): Show |
8 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1069-13055C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72009344 | |||||||
| chr12:72009364 | T | G | 42 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(39): Show |
48 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1069-13035T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72009364 | |||||||
| chr12:72009581 | T | C | 7 | a0001c0002t0001g0011 a0001c0003t0001g0072 a0001c0003t0001g0094 others(4): Show |
8 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1069-12818T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72009581 | |||||||
| chr12:72009683 | T | C | 4 | a0001c0002t0001g0163 a0001c0002t0001g0164 a0001c0002t0001g0165 others(1): Show |
4 | HG00597.hp2 HG00621.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-12716T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72009683 | |||||||
| chr12:72009705 | T | C | 1 | a0001c0004t0001g0265 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1069-12694T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72009705 | |||||||
| chr12:72009752 | T | C | 1 | a0001c0001t0004g0294 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1069-12647T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72009752 | |||||||
| chr12:72010005 | T | C | 7 | a0001c0002t0001g0011 a0001c0003t0001g0072 a0001c0003t0001g0094 others(4): Show |
8 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1069-12394T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72010005 | |||||||
| chr12:72010016 | G | A | 7 | a0001c0002t0001g0011 a0001c0003t0001g0072 a0001c0003t0001g0094 others(4): Show |
8 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1069-12383G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72010016 | |||||||
| chr12:72010030 | T | C | 1 | a0001c0003t0001g0226 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1069-12369T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72010030 | |||||||
| chr12:72010169 | G | A | 42 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(39): Show |
48 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1069-12230G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72010169 | |||||||
| chr12:72010284 | C | T | 4 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0097 others(1): Show |
4 | HG02647.hp1 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-12115C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72010284 | |||||||
| chr12:72010301 | G | T | 8 | a0001c0001t0001g0020 a0001c0002t0001g0011 a0001c0003t0001g0072 others(5): Show |
9 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1069-12098G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72010301 | |||||||
| chr12:72010373 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1069-12026G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72010373 | |||||||
| chr12:72010598 | C | T | 262 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(259): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1069-11801C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72010598 | |||||||
| chr12:72010628 | C | T | 1 | a0001c0002t0001g0122 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1069-11771C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72010628 | |||||||
| chr12:72010657 | G | C | 5 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0097 others(2): Show |
5 | HG02647.hp1 HG02717.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1069-11742G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72010657 | |||||||
| chr12:72010714 | A | C | 42 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(39): Show |
48 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1069-11685A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72010714 | |||||||
| chr12:72011059 | G | C | 42 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(39): Show |
48 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1069-11340G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72011059 | |||||||
| chr12:72011063 | T | C | 1 | a0001c0004t0003g0024 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1069-11336T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72011063 | |||||||
| chr12:72011127 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1069-11272T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72011127 | |||||||
| chr12:72011279 | T | C | 262 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(259): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1069-11120T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72011279 | |||||||
| chr12:72011610 | G | C | 3 | a0001c0001t0002g0068 a0001c0001t0002g0253 a0001c0001t0002g0292 |
3 | HG01928.hp1 HG01934.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1069-10789G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72011610 | |||||||
| chr12:72011758 | C | T | 5 | a0001c0001t0001g0199 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG01884.hp2 HG03041.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.1069-10641C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72011758 | |||||||
| chr12:72011821 | G | C | 42 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(39): Show |
48 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1069-10578G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72011821 | |||||||
| chr12:72012173 | T | TCAACAA | 4 | a0001c0001t0001g0283 a0001c0002t0001g0011 a0001c0003t0001g0192 others(1): Show |
5 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1069-10207_1069-10 others(12): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72012173 | ||||||
| chr12:72012173 | T | TCAACAAC others(2): Show |
31 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(28): Show |
37 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.1069-10210_1069-10 others(15): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72012173 | ||||||
| chr12:72012173 | T | TCAACAAC others(5): Show |
2 | a0001c0001t0001g0223 a0001c0004t0001g0257 |
2 | HG03831.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1069-10213_1069-10 others(18): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72012173 | ||||||
| chr12:72012173 | T | TCAACAAC others(8): Show |
2 | a0001c0001t0001g0020 a0001c0003t0001g0086 |
2 | HG02486.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1069-10216_1069-10 others(21): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72012173 | ||||||
| chr12:72012180 | C | CAACAACA others(20): Show |
8 | a0001c0001t0001g0225 a0001c0001t0003g0030 a0001c0001t0003g0031 others(5): Show |
8 | HG01261.hp2 HG01928.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1069-10202_1069-10 others(33): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72012180 | ||||||
| chr12:72012195 | CAAT | C | 3 | a0001c0003t0001g0072 a0001c0003t0001g0094 a0001c0003t0001g0095 |
3 | HG02896.hp2 HG02897.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1069-10201_1069-10 others(9): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72012195 | ||||||
| chr12:72012198 | T | C | 4 | a0001c0002t0001g0011 a0001c0003t0001g0192 a0001c0003t0001g0303 others(1): Show |
5 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1069-10201T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72012198 | |||||||
| chr12:72012256 | G | A | 167 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(164): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1069-10143G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72012256 | |||||||
| chr12:72012530 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1069-9869C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72012530 | |||||||
| chr12:72012752 | T | C | 175 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(172): Show |
188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1069-9647T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72012752 | |||||||
| chr12:72012943 | C | T | 2 | a0001c0001t0002g0260 a0001c0001t0002g0261 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1069-9456C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72012943 | |||||||
| chr12:72012959 | C | T | 43 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(40): Show |
49 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1069-9440C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72012959 | |||||||
| chr12:72013053 | G | A | 124 | a0001c0001t0001g0043 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-9346G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72013053 | |||||||
| chr12:72013087 | T | C | 42 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(39): Show |
48 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1069-9312T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72013087 | |||||||
| chr12:72013137 | G | T | 1 | a0001c0001t0003g0046 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1069-9262G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72013137 | |||||||
| chr12:72013178 | T | C | 171 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(168): Show |
183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.1069-9221T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72013178 | |||||||
| chr12:72013622 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1069-8777T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72013622 | |||||||
| chr12:72013623 | T | A | 42 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(39): Show |
48 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1069-8776T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72013623 | |||||||
| chr12:72013696 | C | A | 1 | a0001c0002t0001g0181 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1069-8703C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72013696 | |||||||
| chr12:72013697 | A | G | 167 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(164): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1069-8702A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72013697 | |||||||
| chr12:72013921 | T | C | 172 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(169): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.1069-8478T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72013921 | |||||||
| chr12:72013944 | A | G | 42 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(39): Show |
48 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1069-8455A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72013944 | |||||||
| chr12:72013982 | T | C | 4 | a0001c0002t0001g0011 a0001c0003t0001g0192 a0001c0003t0001g0226 others(1): Show |
5 | HG01884.hp1 HG02109.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1069-8417T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72013982 | |||||||
| chr12:72014045 | C | A | 1 | a0001c0001t0003g0033 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1069-8354C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72014045 | |||||||
| chr12:72014045 | C | T | 3 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0283 |
3 | NA18942.hp2 NA19057.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1069-8354C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72014045 | |||||||
| chr12:72014046 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1069-8353G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72014046 | |||||||
| chr12:72014116 | A | G | 1 | a0001c0002t0001g0138 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1069-8283A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72014116 | |||||||
| chr12:72014217 | G | A | 72 | a0001c0001t0001g0190 a0001c0001t0001g0229 a0001c0001t0001g0263 others(69): Show |
75 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1069-8182G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72014217 | |||||||
| chr12:72014395 | C | CT | 139 | a0001c0001t0001g0043 a0001c0002t0001g0002 a0001c0002t0001g0007 others(136): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1069-7991dupT | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72014395 | ||||||
| chr12:72014395 | C | T | 42 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(39): Show |
48 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1069-8004C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72014395 | |||||||
| chr12:72014397 | T | C | 42 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(39): Show |
48 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1069-8002T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72014397 | |||||||
| chr12:72014476 | C | T | 3 | a0001c0001t0001g0067 a0001c0003t0001g0063 a0001c0003t0001g0064 |
3 | HG02055.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1069-7923C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72014476 | |||||||
| chr12:72014477 | G | A | 1 | a0001c0004t0003g0024 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1069-7922G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72014477 | |||||||
| chr12:72014515 | A | C | 308 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(305): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1069-7884A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72014515 | |||||||
| chr12:72014636 | C | A | 1 | a0001c0001t0001g0202 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1069-7763C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72014636 | |||||||
| chr12:72014747 | T | C | 41 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(38): Show |
47 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1069-7652T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72014747 | |||||||
| chr12:72014831 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1069-7568G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72014831 | |||||||
| chr12:72014852 | A | G | 1 | a0001c0002t0001g0155 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1069-7547A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72014852 | |||||||
| chr12:72015039 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1069-7360A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72015039 | |||||||
| chr12:72015135 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1069-7264G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72015135 | |||||||
| chr12:72015144 | G | A | 37 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(34): Show |
43 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.1069-7255G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72015144 | |||||||
| chr12:72015300 | GT | G | 39 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(36): Show |
45 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1069-7089delT | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72015300 | ||||||
| chr12:72015315 | G | GT | 34 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0067 others(31): Show |
35 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1069-7062dupT | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72015315 | ||||||
| chr12:72015315 | GT | G | 15 | a0001c0001t0001g0020 a0001c0001t0002g0296 a0001c0002t0001g0120 others(12): Show |
16 | HG02055.hp2 HG02109.hp2 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.1069-7062delT | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72015315 | ||||||
| chr12:72015315 | GTTTTTTT others(4): Show |
G | 1 | a0001c0002t0001g0112 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1069-7072_1069-706 others(15): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72015315 | ||||||
| chr12:72015383 | G | T | 39 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(36): Show |
45 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1069-7016G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72015383 | |||||||
| chr12:72015533 | A | G | 2 | a0001c0003t0001g0094 a0001c0003t0001g0095 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1069-6866A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72015533 | |||||||
| chr12:72015568 | G | A | 42 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(39): Show |
48 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1069-6831G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72015568 | |||||||
| chr12:72015571 | G | A | 2 | a0001c0003t0001g0072 a0001c0003t0001g0228 |
2 | HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1069-6828G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72015571 | |||||||
| chr12:72015585 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0217 a0001c0004t0001g0103 |
4 | HG01069.hp1 HG02280.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-6814C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72015585 | |||||||
| chr12:72015656 | C | T | 44 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(41): Show |
50 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1069-6743C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72015656 | |||||||
| chr12:72015657 | G | A | 4 | a0001c0001t0001g0232 a0001c0001t0001g0304 a0001c0001t0002g0312 others(1): Show |
4 | HG02071.hp2 HG02074.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-6742G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72015657 | |||||||
| chr12:72015768 | C | T | 40 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(37): Show |
45 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1069-6631C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72015768 | |||||||
| chr12:72015872 | G | T | 2 | a0001c0003t0001g0094 a0001c0003t0001g0095 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1069-6527G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72015872 | |||||||
| chr12:72015918 | C | T | 6 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0086 others(3): Show |
6 | HG02486.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1069-6481C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72015918 | |||||||
| chr12:72016000 | T | C | 131 | a0001c0001t0001g0009 a0001c0001t0001g0043 a0001c0001t0001g0217 others(128): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1069-6399T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72016000 | |||||||
| chr12:72016002 | C | T | 130 | a0001c0001t0001g0009 a0001c0001t0001g0043 a0001c0001t0001g0217 others(127): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.1069-6397C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72016002 | |||||||
| chr12:72016003 | A | C | 1 | a0002c0005t0001g0147 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1069-6396A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72016003 | |||||||
| chr12:72016097 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1069-6302G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72016097 | |||||||
| chr12:72016232 | G | T | 1 | a0001c0002t0001g0106 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1069-6167G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72016232 | |||||||
| chr12:72016241 | T | A | 132 | a0001c0001t0001g0043 a0001c0002t0001g0002 a0001c0002t0001g0007 others(129): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.1069-6158T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72016241 | |||||||
| chr12:72016299 | G | A | 130 | a0001c0001t0001g0043 a0001c0002t0001g0002 a0001c0002t0001g0007 others(127): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.1069-6100G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72016299 | |||||||
| chr12:72016312 | G | A | 1 | a0001c0002t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1069-6087G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72016312 | |||||||
| chr12:72016422 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1069-5977T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72016422 | |||||||
| chr12:72016483 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1069-5916G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72016483 | |||||||
| chr12:72016512 | C | A | 204 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(201): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1069-5887C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72016512 | |||||||
| chr12:72016629 | G | C | 1 | a0001c0001t0001g0043 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1069-5770G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72016629 | |||||||
| chr12:72016706 | T | A | 1 | a0001c0002t0001g0154 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1069-5693T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72016706 | |||||||
| chr12:72016724 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1069-5675C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72016724 | |||||||
| chr12:72016819 | T | A | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1069-5580T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72016819 | |||||||
| chr12:72016965 | G | A | 126 | a0001c0001t0001g0009 a0001c0001t0001g0217 a0001c0002t0001g0002 others(123): Show |
134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.1069-5434G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72016965 | |||||||
| chr12:72017041 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1069-5358T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72017041 | |||||||
| chr12:72017068 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0264 |
2 | HG00438.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1069-5331G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72017068 | |||||||
| chr12:72017189 | T | C | 13 | a0001c0001t0001g0043 a0001c0003t0001g0063 a0001c0003t0001g0064 others(10): Show |
13 | HG02615.hp2 HG02622.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1069-5210T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72017189 | |||||||
| chr12:72017432 | G | T | 157 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0264 others(154): Show |
165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1069-4967G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72017432 | |||||||
| chr12:72017496 | T | C | 5 | a0001c0002t0001g0126 a0001c0002t0001g0127 a0001c0002t0001g0128 others(2): Show |
5 | HG00735.hp2 HG00738.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1069-4903T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72017496 | |||||||
| chr12:72017528 | G | A | 5 | a0001c0003t0001g0237 a0001c0003t0001g0238 a0001c0003t0001g0239 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1069-4871G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72017528 | |||||||
| chr12:72017560 | G | A | 3 | a0001c0001t0002g0201 a0001c0001t0002g0234 a0001c0001t0002g0235 |
3 | HG02698.hp2 HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1069-4839G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72017560 | |||||||
| chr12:72017634 | A | C | 4 | a0001c0001t0001g0199 a0001c0003t0001g0047 a0001c0003t0001g0191 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1069-4765A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72017634 | |||||||
| chr12:72017645 | C | A | 1 | a0001c0003t0001g0086 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1069-4754C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72017645 | |||||||
| chr12:72017689 | T | C | 8 | a0001c0002t0001g0011 a0001c0002t0001g0139 a0001c0002t0001g0158 others(5): Show |
9 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1069-4710T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72017689 | |||||||
| chr12:72017871 | G | T | 5 | a0001c0003t0001g0237 a0001c0003t0001g0238 a0001c0003t0001g0239 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1069-4528G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72017871 | |||||||
| chr12:72018098 | C | G | 1 | a0001c0004t0001g0212 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1069-4301C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72018098 | |||||||
| chr12:72018248 | C | A | 5 | a0001c0003t0001g0237 a0001c0003t0001g0238 a0001c0003t0001g0239 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1069-4151C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72018248 | |||||||
| chr12:72018440 | A | G | 124 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-3959A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72018440 | |||||||
| chr12:72018465 | C | A | 11 | a0001c0001t0001g0043 a0001c0003t0001g0063 a0001c0003t0001g0064 others(8): Show |
11 | HG02615.hp2 HG02622.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1069-3934C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72018465 | |||||||
| chr12:72018492 | G | A | 1 | a0001c0002t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1069-3907G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72018492 | |||||||
| chr12:72018587 | G | T | 124 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-3812G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72018587 | |||||||
| chr12:72018609 | G | A | 8 | a0001c0002t0001g0011 a0001c0002t0001g0139 a0001c0002t0001g0158 others(5): Show |
9 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1069-3790G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72018609 | |||||||
| chr12:72018714 | T | C | 124 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-3685T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72018714 | |||||||
| chr12:72018730 | C | T | 6 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(3): Show |
6 | HG00733.hp1 HG01192.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1069-3669C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72018730 | |||||||
| chr12:72018792 | T | G | 124 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-3607T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72018792 | |||||||
| chr12:72018921 | A | G | 147 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0264 others(144): Show |
154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1069-3478A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72018921 | |||||||
| chr12:72018998 | A | G | 147 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0264 others(144): Show |
154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1069-3401A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72018998 | |||||||
| chr12:72019002 | C | T | 124 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-3397C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72019002 | |||||||
| chr12:72019003 | A | G | 124 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-3396A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72019003 | |||||||
| chr12:72019057 | A | C | 1 | a0001c0002t0001g0124 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1069-3342A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72019057 | |||||||
| chr12:72019118 | T | C | 124 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-3281T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72019118 | |||||||
| chr12:72019119 | C | T | 124 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-3280C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72019119 | |||||||
| chr12:72019229 | T | C | 132 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(129): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.1069-3170T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72019229 | |||||||
| chr12:72019266 | C | A | 1 | a0001c0003t0001g0086 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1069-3133C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72019266 | |||||||
| chr12:72019382 | C | T | 1 | a0001c0002t0001g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1069-3017C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72019382 | |||||||
| chr12:72019390 | A | G | 13 | a0001c0001t0001g0043 a0001c0002t0001g0167 a0001c0003t0001g0063 others(10): Show |
13 | HG02486.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1069-3009A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72019390 | |||||||
| chr12:72019505 | T | C | 1 | a0001c0001t0001g0021 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1069-2894T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72019505 | |||||||
| chr12:72019575 | T | A | 1 | a0001c0003t0001g0097 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1069-2824T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72019575 | |||||||
| chr12:72019582 | C | A | 1 | a0001c0003t0001g0086 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1069-2817C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72019582 | |||||||
| chr12:72019618 | A | T | 8 | a0001c0002t0001g0011 a0001c0002t0001g0139 a0001c0002t0001g0158 others(5): Show |
9 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1069-2781A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72019618 | |||||||
| chr12:72019681 | T | C | 1 | a0001c0004t0001g0285 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1069-2718T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72019681 | |||||||
| chr12:72019820 | G | A | 1 | a0001c0001t0003g0053 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1069-2579G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72019820 | |||||||
| chr12:72019968 | C | A | 1 | a0001c0001t0003g0006 | 2 | HG02004.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1069-2431C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72019968 | |||||||
| chr12:72019983 | C | T | 1 | a0001c0002t0001g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1069-2416C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72019983 | |||||||
| chr12:72019994 | A | C | 1 | a0001c0002t0001g0166 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1069-2405A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72019994 | |||||||
| chr12:72020015 | C | T | 124 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-2384C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72020015 | |||||||
| chr12:72020042 | A | G | 124 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-2357A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72020042 | |||||||
| chr12:72020043 | G | A | 124 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-2356G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72020043 | |||||||
| chr12:72020048 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0264 |
2 | HG00438.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1069-2351T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72020048 | |||||||
| chr12:72020064 | A | C | 1 | a0001c0004t0001g0050 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1069-2335A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72020064 | |||||||
| chr12:72020085 | T | A | 1 | a0001c0004t0001g0212 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1069-2314T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72020085 | |||||||
| chr12:72020152 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0264 |
2 | HG00438.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1069-2247A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72020152 | |||||||
| chr12:72020391 | G | A | 45 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(42): Show |
51 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.1069-2008G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72020391 | |||||||
| chr12:72020510 | C | T | 1 | a0001c0003t0001g0182 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1069-1889C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72020510 | |||||||
| chr12:72020611 | C | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0264 |
2 | HG00438.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1069-1788C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72020611 | |||||||
| chr12:72020616 | G | A | 124 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-1783G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72020616 | |||||||
| chr12:72020653 | A | C | 2 | a0001c0002t0001g0107 a0001c0002t0001g0113 |
2 | HG00140.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1069-1746A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72020653 | |||||||
| chr12:72020677 | G | T | 13 | a0001c0001t0001g0043 a0001c0003t0001g0063 a0001c0003t0001g0064 others(10): Show |
13 | HG02486.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1069-1722G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72020677 | |||||||
| chr12:72020738 | T | C | 124 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-1661T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72020738 | |||||||
| chr12:72020779 | G | T | 1 | a0001c0004t0001g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1069-1620G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72020779 | |||||||
| chr12:72020783 | A | G | 151 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0264 others(148): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1069-1616A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72020783 | |||||||
| chr12:72020825 | GA | G | 8 | a0001c0002t0001g0011 a0001c0002t0001g0139 a0001c0002t0001g0158 others(5): Show |
9 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1069-1566delA | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72020825 | ||||||
| chr12:72020846 | A | T | 1 | a0001c0003t0001g0088 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1069-1553A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72020846 | |||||||
| chr12:72020937 | C | T | 124 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-1462C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72020937 | |||||||
| chr12:72021012 | C | T | 5 | a0001c0002t0001g0075 a0001c0002t0001g0118 a0001c0002t0001g0120 others(2): Show |
5 | HG00438.hp2 NA18939.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1069-1387C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72021012 | |||||||
| chr12:72021024 | AATT | A | 124 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-1368_1069-136 others(7): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72021024 | ||||||
| chr12:72021063 | C | CT | 147 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0264 others(144): Show |
154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1069-1336_1069-133 others(5): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72021063 | |||||||
| chr12:72021078 | T | A | 124 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-1321T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72021078 | |||||||
| chr12:72021090 | C | G | 8 | a0001c0002t0001g0011 a0001c0002t0001g0139 a0001c0002t0001g0158 others(5): Show |
9 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1069-1309C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72021090 | |||||||
| chr12:72021178 | G | A | 8 | a0001c0002t0001g0011 a0001c0002t0001g0139 a0001c0002t0001g0158 others(5): Show |
9 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1069-1221G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72021178 | |||||||
| chr12:72021220 | C | G | 131 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(128): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1069-1179C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72021220 | |||||||
| chr12:72021254 | C | T | 153 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0096 others(150): Show |
160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1069-1145C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72021254 | |||||||
| chr12:72021306 | T | C | 124 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-1093T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72021306 | |||||||
| chr12:72021310 | C | T | 124 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-1089C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72021310 | |||||||
| chr12:72021356 | A | AGT | 19 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0071 others(16): Show |
19 | HG00423.hp1 HG01074.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1069-1004_1069-100 others(6): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72021356 | ||||||
| chr12:72021356 | A | AGTGT | 6 | a0001c0001t0001g0190 a0001c0001t0001g0199 a0001c0001t0002g0142 others(3): Show |
6 | HG01884.hp2 HG01975.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1069-1006_1069-100 others(8): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72021356 | ||||||
| chr12:72021356 | AGT | A | 15 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(12): Show |
15 | HG01109.hp1 HG02109.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1069-1004_1069-100 others(6): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72021356 | ||||||
| chr12:72021356 | AGTGT | A | 8 | a0001c0001t0002g0211 a0001c0001t0003g0004 a0001c0003t0001g0099 others(5): Show |
9 | HG01243.hp1 HG02280.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.1069-1006_1069-100 others(8): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72021356 | ||||||
| chr12:72021356 | AGTGTGT | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0264 a0001c0003t0001g0086 others(1): Show |
4 | HG00438.hp1 HG02486.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-1008_1069-100 others(10): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72021356 | ||||||
| chr12:72021356 | AGTGTGTG others(3): Show |
A | 120 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(117): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1069-1012_1069-100 others(14): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72021356 | ||||||
| chr12:72021356 | AGTGTGTG others(5): Show |
A | 2 | a0001c0002t0001g0140 a0001c0002t0001g0195 |
2 | HG00099.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1069-1014_1069-100 others(16): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72021356 | ||||||
| chr12:72021356 | AGTGTGTG others(7): Show |
A | 1 | a0001c0004t0003g0024 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1069-1016_1069-100 others(18): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72021356 | ||||||
| chr12:72021393 | GTGTA | G | 7 | a0001c0002t0001g0139 a0001c0002t0001g0158 a0001c0002t0001g0215 others(4): Show |
7 | HG01496.hp1 HG02486.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1069-1002_1069-999 others(7): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72021393 | ||||||
| chr12:72021397 | A | G | 1 | a0001c0002t0001g0011 | 2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1069-1002A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72021397 | |||||||
| chr12:72021426 | T | C | 124 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-973T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72021426 | |||||||
| chr12:72021452 | G | GT | 124 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-936dupT | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72021452 | ||||||
| chr12:72021452 | GT | G | 8 | a0001c0002t0001g0011 a0001c0002t0001g0139 a0001c0002t0001g0158 others(5): Show |
9 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1069-936delT | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 72021452 | ||||||
| chr12:72021464 | A | G | 147 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0264 others(144): Show |
154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1069-935A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72021464 | |||||||
| chr12:72021600 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0264 |
2 | HG00438.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1069-799T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72021600 | |||||||
| chr12:72021666 | A | G | 124 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1069-733A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72021666 | |||||||
| chr12:72021675 | A | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0264 |
2 | HG00438.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1069-724A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72021675 | |||||||
| chr12:72021688 | T | C | 2 | a0001c0002t0001g0137 a0001c0002t0001g0138 |
2 | NA19001.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1069-711T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72021688 | |||||||
| chr12:72021815 | T | C | 1 | a0001c0003t0001g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1069-584T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72021815 | |||||||
| chr12:72021933 | A | G | 1 | a0001c0003t0001g0072 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1069-466A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72021933 | |||||||
| chr12:72021978 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0264 |
2 | HG00438.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1069-421C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72021978 | |||||||
| chr12:72022090 | A | T | 145 | a0001c0001t0001g0043 a0001c0002t0001g0002 a0001c0002t0001g0007 others(142): Show |
152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.1069-309A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72022090 | |||||||
| chr12:72022214 | A | G | 6 | a0001c0002t0001g0133 a0001c0002t0001g0134 a0001c0002t0001g0135 others(3): Show |
6 | HG00140.hp2 HG01081.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1069-185A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 8/10 | chr12 | 72022214 | |||||||
| chr12:72022653 | C | A | 1 | a0001c0004t0001g0038 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1164+159C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72022653 | |||||||
| chr12:72022718 | C | T | 1 | a0001c0002t0001g0215 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1164+224C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72022718 | |||||||
| chr12:72022745 | T | C | 2 | a0001c0003t0001g0086 a0001c0003t0001g0088 |
2 | HG02486.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1164+251T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72022745 | |||||||
| chr12:72022763 | G | A | 1 | a0001c0001t0002g0143 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1164+269G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72022763 | |||||||
| chr12:72022844 | G | A | 8 | a0001c0002t0001g0011 a0001c0002t0001g0139 a0001c0002t0001g0158 others(5): Show |
9 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1164+350G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72022844 | |||||||
| chr12:72023087 | A | AT | 8 | a0001c0002t0001g0011 a0001c0002t0001g0139 a0001c0002t0001g0158 others(5): Show |
9 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1164+593_1164+594i others(3): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72023087 | |||||||
| chr12:72023088 | C | T | 48 | a0001c0001t0001g0043 a0001c0001t0001g0297 a0001c0001t0002g0016 others(45): Show |
50 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1164+594C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72023088 | |||||||
| chr12:72023125 | T | G | 1 | a0001c0004t0001g0284 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1164+631T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72023125 | |||||||
| chr12:72023169 | C | T | 1 | a0001c0004t0001g0044 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1164+675C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72023169 | |||||||
| chr12:72023215 | C | T | 1 | a0001c0002t0001g0215 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1164+721C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72023215 | |||||||
| chr12:72023363 | T | C | 1 | a0001c0003t0001g0088 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1164+869T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72023363 | |||||||
| chr12:72023385 | G | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0264 |
2 | HG00438.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1164+891G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72023385 | |||||||
| chr12:72023429 | C | CTTCA | 44 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(41): Show |
50 | HG00597.hp1 HG00609.hp1 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.1164+959_1164+962d others(6): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 72023429 | ||||||
| chr12:72023429 | C | CTTCATTC others(1): Show |
13 | a0001c0001t0001g0043 a0001c0001t0003g0031 a0001c0003t0001g0063 others(10): Show |
13 | HG02300.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1164+955_1164+962d others(10): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 72023429 | ||||||
| chr12:72023495 | G | A | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG00423.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.1164+1001G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72023495 | |||||||
| chr12:72023764 | C | T | 113 | a0001c0002t0001g0002 a0001c0002t0001g0010 a0001c0002t0001g0012 others(110): Show |
117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.1164+1270C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72023764 | |||||||
| chr12:72023778 | C | T | 7 | a0001c0002t0001g0140 a0001c0002t0001g0146 a0001c0002t0001g0171 others(4): Show |
7 | HG00099.hp1 HG01167.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1164+1284C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72023778 | |||||||
| chr12:72023824 | A | AAAAAAAA others(6): Show |
130 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(127): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.1164+1335_1164+134 others(17): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 72023824 | ||||||
| chr12:72023824 | A | AAAAAAAA others(5): Show |
1 | a0001c0004t0001g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1164+1341_1164+134 others(16): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 72023824 | ||||||
| chr12:72023825 | A | AAAAAAAA others(5): Show |
16 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0264 others(13): Show |
16 | HG00438.hp1 HG02486.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1164+1336_1164+134 others(16): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 72023825 | ||||||
| chr12:72023996 | G | A | 6 | a0001c0002t0001g0139 a0001c0002t0001g0158 a0001c0002t0001g0215 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164+1502G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72023996 | |||||||
| chr12:72024041 | C | G | 8 | a0001c0002t0001g0011 a0001c0002t0001g0139 a0001c0002t0001g0158 others(5): Show |
9 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1164+1547C>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72024041 | |||||||
| chr12:72024290 | G | A | 1 | a0001c0001t0002g0130 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1164+1796G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72024290 | |||||||
| chr12:72024315 | C | A | 5 | a0001c0003t0001g0237 a0001c0003t0001g0238 a0001c0003t0001g0239 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1164+1821C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72024315 | |||||||
| chr12:72024367 | T | A | 8 | a0001c0002t0001g0011 a0001c0002t0001g0139 a0001c0002t0001g0158 others(5): Show |
9 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1164+1873T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72024367 | |||||||
| chr12:72024445 | T | A | 21 | a0001c0001t0001g0043 a0001c0002t0001g0011 a0001c0002t0001g0139 others(18): Show |
22 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.1164+1951T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72024445 | |||||||
| chr12:72024490 | G | C | 5 | a0001c0003t0001g0237 a0001c0003t0001g0238 a0001c0003t0001g0239 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1164+1996G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72024490 | |||||||
| chr12:72024564 | C | T | 8 | a0001c0002t0001g0011 a0001c0002t0001g0139 a0001c0002t0001g0158 others(5): Show |
9 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1164+2070C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72024564 | |||||||
| chr12:72024602 | G | A | 5 | a0001c0003t0001g0237 a0001c0003t0001g0238 a0001c0003t0001g0239 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1164+2108G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72024602 | |||||||
| chr12:72024628 | C | T | 11 | a0001c0001t0001g0043 a0001c0003t0001g0063 a0001c0003t0001g0064 others(8): Show |
11 | HG02615.hp2 HG02622.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1164+2134C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72024628 | |||||||
| chr12:72024761 | T | C | 8 | a0001c0002t0001g0011 a0001c0002t0001g0139 a0001c0002t0001g0158 others(5): Show |
9 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1164+2267T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72024761 | |||||||
| chr12:72024814 | C | T | 3 | a0001c0003t0001g0082 a0001c0003t0001g0083 a0001c0003t0001g0099 |
3 | HG02895.hp2 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1164+2320C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72024814 | |||||||
| chr12:72024891 | C | A | 1 | a0001c0002t0001g0245 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1164+2397C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72024891 | |||||||
| chr12:72024997 | C | T | 5 | a0001c0003t0001g0065 a0001c0003t0001g0074 a0001c0003t0001g0082 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1164+2503C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72024997 | |||||||
| chr12:72025047 | C | T | 123 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0010 others(120): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.1164+2553C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72025047 | |||||||
| chr12:72025380 | CAG | C | 3 | a0001c0001t0001g0199 a0001c0003t0001g0047 a0001c0003t0001g0191 |
3 | HG01884.hp2 HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1164+2888_1164+288 others(6): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 72025380 | ||||||
| chr12:72025526 | A | T | 136 | a0001c0001t0001g0066 a0001c0001t0002g0271 a0001c0002t0001g0002 others(133): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1164+3032A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72025526 | |||||||
| chr12:72025631 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0264 a0001c0001t0002g0296 |
3 | HG00438.hp1 NA18967.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1164+3137C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72025631 | |||||||
| chr12:72025663 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1164+3169G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72025663 | |||||||
| chr12:72026203 | A | ATT | 41 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(38): Show |
47 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.1164+3722_1164+372 others(6): Show |
TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 72026203 | ||||||
| chr12:72026265 | T | G | 1 | a0001c0003t0001g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1164+3771T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72026265 | |||||||
| chr12:72026271 | G | A | 39 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(36): Show |
45 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1164+3777G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72026271 | |||||||
| chr12:72026310 | T | G | 1 | a0001c0002t0001g0127 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1164+3816T>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72026310 | |||||||
| chr12:72026380 | G | T | 2 | a0001c0001t0001g0071 a0001c0004t0001g0221 |
2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1164+3886G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72026380 | |||||||
| chr12:72026523 | G | T | 2 | a0001c0001t0001g0194 a0001c0003t0001g0088 |
2 | HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1164+4029G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72026523 | |||||||
| chr12:72026740 | G | T | 8 | a0001c0001t0002g0142 a0001c0001t0002g0233 a0001c0001t0002g0266 others(5): Show |
8 | HG00423.hp2 HG00558.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1164+4246G>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72026740 | |||||||
| chr12:72026917 | A | G | 2 | a0001c0001t0001g0071 a0001c0004t0001g0221 |
2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1165-4341A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72026917 | |||||||
| chr12:72026928 | T | C | 1 | a0001c0001t0002g0310 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1165-4330T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72026928 | |||||||
| chr12:72026962 | G | A | 1 | a0001c0003t0001g0303 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1165-4296G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72026962 | |||||||
| chr12:72027085 | T | C | 2 | a0001c0001t0001g0071 a0001c0004t0001g0221 |
2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1165-4173T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72027085 | |||||||
| chr12:72027119 | A | G | 2 | a0004c0006t0003g0060 a0004c0006t0003g0061 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1165-4139A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72027119 | |||||||
| chr12:72027203 | A | G | 12 | a0001c0001t0001g0071 a0001c0003t0001g0063 a0001c0003t0001g0064 others(9): Show |
12 | HG02622.hp1 HG02647.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1165-4055A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72027203 | |||||||
| chr12:72027220 | G | C | 22 | a0001c0001t0001g0287 a0001c0002t0001g0002 a0001c0002t0001g0012 others(19): Show |
24 | HG00438.hp2 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1165-4038G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72027220 | |||||||
| chr12:72027260 | G | A | 10 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0065 others(7): Show |
10 | HG02622.hp1 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1165-3998G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72027260 | |||||||
| chr12:72027302 | A | G | 1 | a0001c0004t0003g0024 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1165-3956A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72027302 | |||||||
| chr12:72027588 | A | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0217 |
3 | HG01069.hp1 HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1165-3670A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72027588 | |||||||
| chr12:72027612 | T | C | 10 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0065 others(7): Show |
10 | HG02622.hp1 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1165-3646T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72027612 | |||||||
| chr12:72027686 | A | G | 1 | a0001c0002t0001g0153 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1165-3572A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72027686 | |||||||
| chr12:72027721 | G | A | 77 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(74): Show |
85 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.1165-3537G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72027721 | |||||||
| chr12:72027743 | T | C | 2 | a0001c0001t0002g0291 a0001c0001t0002g0299 |
2 | HG02165.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1165-3515T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72027743 | |||||||
| chr12:72027810 | A | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0223 a0001c0001t0001g0264 |
3 | HG00438.hp1 HG03834.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1165-3448A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72027810 | |||||||
| chr12:72027847 | G | A | 81 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(78): Show |
89 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.1165-3411G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72027847 | |||||||
| chr12:72027984 | C | T | 4 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0097 others(1): Show |
4 | HG02647.hp1 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165-3274C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72027984 | |||||||
| chr12:72028062 | C | T | 1 | a0001c0003t0001g0300 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1165-3196C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72028062 | |||||||
| chr12:72028090 | G | A | 10 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0065 others(7): Show |
10 | HG02622.hp1 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1165-3168G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72028090 | |||||||
| chr12:72028163 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0217 |
3 | HG01069.hp1 HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1165-3095C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72028163 | |||||||
| chr12:72028386 | T | C | 8 | a0001c0002t0001g0011 a0001c0002t0001g0139 a0001c0002t0001g0158 others(5): Show |
9 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1165-2872T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72028386 | |||||||
| chr12:72028806 | A | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0264 |
2 | HG00438.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1165-2452A>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72028806 | |||||||
| chr12:72028924 | G | A | 5 | a0001c0002t0001g0013 a0001c0002t0001g0183 a0001c0002t0001g0184 others(2): Show |
6 | NA18954.hp2 NA18961.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.1165-2334G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72028924 | |||||||
| chr12:72029003 | C | T | 3 | a0001c0001t0001g0194 a0001c0003t0001g0088 a0001c0003t0001g0226 |
3 | HG02109.hp2 HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1165-2255C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72029003 | |||||||
| chr12:72029012 | C | T | 2 | a0001c0004t0003g0041 a0001c0004t0003g0059 |
2 | HG03017.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.1165-2246C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72029012 | |||||||
| chr12:72029037 | G | A | 2 | a0001c0002t0001g0127 a0001c0002t0001g0129 |
2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1165-2221G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72029037 | |||||||
| chr12:72029129 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0264 |
2 | HG00438.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1165-2129C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72029129 | |||||||
| chr12:72029153 | G | A | 2 | a0004c0006t0003g0060 a0004c0006t0003g0061 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1165-2105G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72029153 | |||||||
| chr12:72029390 | G | A | 19 | a0001c0001t0001g0043 a0001c0001t0001g0096 a0001c0001t0001g0199 others(16): Show |
19 | HG01884.hp2 HG02257.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1165-1868G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72029390 | |||||||
| chr12:72029396 | C | T | 1 | a0001c0003t0001g0072 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1165-1862C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72029396 | |||||||
| chr12:72029469 | G | C | 1 | a0001c0002t0001g0156 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1165-1789G>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72029469 | |||||||
| chr12:72029490 | G | A | 76 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(73): Show |
83 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.1165-1768G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72029490 | |||||||
| chr12:72029611 | A | G | 1 | a0001c0003t0001g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1165-1647A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72029611 | |||||||
| chr12:72029684 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1165-1574A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72029684 | |||||||
| chr12:72029694 | G | A | 8 | a0001c0002t0001g0011 a0001c0002t0001g0139 a0001c0002t0001g0158 others(5): Show |
9 | HG01496.hp1 HG01884.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1165-1564G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72029694 | |||||||
| chr12:72029700 | A | G | 2 | a0001c0003t0001g0094 a0001c0003t0001g0095 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1165-1558A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72029700 | |||||||
| chr12:72029770 | C | A | 6 | a0001c0001t0001g0199 a0001c0003t0001g0047 a0001c0003t0001g0072 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1165-1488C>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72029770 | |||||||
| chr12:72029904 | G | A | 1 | a0001c0001t0002g0268 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1165-1354G>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72029904 | |||||||
| chr12:72030009 | A | G | 13 | a0001c0001t0001g0066 a0001c0001t0001g0190 a0001c0003t0001g0008 others(10): Show |
14 | HG02257.hp1 HG02572.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1165-1249A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72030009 | |||||||
| chr12:72030148 | C | T | 1 | a0001c0002t0001g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1165-1110C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72030148 | |||||||
| chr12:72030616 | A | G | 3 | a0001c0001t0001g0229 a0001c0003t0001g0192 a0001c0003t0001g0303 |
3 | HG02647.hp2 HG02886.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1165-642A>G | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72030616 | |||||||
| chr12:72030792 | C | T | 4 | a0001c0001t0001g0194 a0001c0001t0002g0296 a0001c0003t0001g0088 others(1): Show |
4 | HG02109.hp2 HG02615.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165-466C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72030792 | |||||||
| chr12:72030916 | C | T | 1 | a0001c0002t0001g0136 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1165-342C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72030916 | |||||||
| chr12:72030942 | T | C | 4 | a0001c0003t0001g0087 a0001c0003t0001g0089 a0001c0003t0001g0093 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165-316T>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72030942 | |||||||
| chr12:72031071 | A | C | 3 | a0001c0001t0002g0068 a0001c0001t0002g0253 a0001c0001t0002g0292 |
3 | HG01928.hp1 HG01934.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1165-187A>C | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72031071 | |||||||
| chr12:72031230 | T | A | 3 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0248 |
3 | HG01261.hp1 HG01433.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1165-28T>A | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 9/10 | chr12 | 72031230 | |||||||
| chr12:72031470 | C | T | 11 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0065 others(8): Show |
11 | HG02486.hp2 HG02622.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1299-51C>T | TPH2 | ENSG00000139287.13 | transcript | ENST00000333850.4 | protein_coding | 10/10 | chr12 | 72031470 |