Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7048 |
| ensemblid | ENSG00000163513.19 |
| hgncid | 11773 |
| symbol | TGFBR2 |
| name | transforming growth factor beta receptor 2 |
| refseq_nuc | NM_003242.6 |
| refseq_prot | NP_003233.4 |
| ensembl_nuc | ENST00000295754.10 |
| ensembl_prot | ENSP00000295754.5 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 30606601 |
| end | 30694142 |
| strand | + |
| ver | v1.2 |
| region | chr3:30606601-30694142 |
| region5000 | chr3:30601601-30699142 |
| regionname0 | TGFBR2_chr3_30606601_30694142 |
| regionname5000 | TGFBR2_chr3_30601601_30699142 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 567 | 379 | 93 | 68 | 154 | 18 | 44 | 113 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | MGRGL others(562): Show |
chr3 | 30601601 | 30699142 |
| a0002 | 0/0 | 567 | 6 | 0 | 0 | 6 | 0 | 0 | 4 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | MGRGL others(562): Show |
chr3 | 30601601 | 30699142 |
| a0003 | 0/0 | 567 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | MGRGL others(562): Show |
chr3 | 30601601 | 30699142 |
| a0004 | 0/0 | 567 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | MGRGL others(562): Show |
chr3 | 30601601 | 30699142 |
| a0005 | 0/0 | 567 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | MGRGL others(562): Show |
chr3 | 30601601 | 30699142 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1701 | 303 | 71 | 65 | 113 | 18 | 34 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ATGGG others(1696): Show |
chr3 | 30601601 | 30699142 | ||
| a0001c0002 | 0/0 | 1701 | 53 | 4 | 0 | 41 | 0 | 8 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ATGGG others(1696): Show |
chr3 | 30601601 | 30699142 | ||
| a0001c0003 | 0/0 | 1701 | 10 | 9 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ATGGG others(1696): Show |
chr3 | 30601601 | 30699142 | ||
| a0001c0004 | 0/0 | 1701 | 9 | 8 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ATGGG others(1696): Show |
chr3 | 30601601 | 30699142 | ||
| a0001c0008 | 0/0 | 1701 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ATGGG others(1696): Show |
chr3 | 30601601 | 30699142 | ||
| a0001c0010 | 0/0 | 1701 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ATGGG others(1696): Show |
chr3 | 30601601 | 30699142 | ||
| a0001c0011 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ATGGG others(1696): Show |
chr3 | 30601601 | 30699142 | ||
| a0001c0012 | 0/0 | 1701 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ATGGG others(1696): Show |
chr3 | 30601601 | 30699142 | ||
| a0002c0005 | 0/0 | 1701 | 6 | 0 | 0 | 6 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ATGGG others(1696): Show |
chr3 | 30601601 | 30699142 | ||
| a0003c0006 | 0/0 | 1701 | 3 | 0 | 0 | 3 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ATGGG others(1696): Show |
chr3 | 30601601 | 30699142 | ||
| a0004c0007 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ATGGG others(1696): Show |
chr3 | 30601601 | 30699142 | ||
| a0005c0009 | 0/0 | 1701 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ATGGG others(1696): Show |
chr3 | 30601601 | 30699142 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4530 | 170 | 12 | 38 | 92 | 9 | 18 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0002 | 0/0 | 4529 | 39 | 5 | 9 | 12 | 4 | 9 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4524): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0003 | 0/0 | 4528 | 14 | 5 | 6 | 0 | 0 | 3 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4523): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0004 | 0/0 | 4532 | 11 | 11 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4527): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0005 | 0/0 | 4530 | 9 | 1 | 0 | 5 | 0 | 3 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0006 | 0/0 | 4528 | 10 | 6 | 4 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4523): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0007 | 0/0 | 4531 | 8 | 7 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4526): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0008 | 0/0 | 4532 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4527): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0009 | 0/1 | 4529 | 7 | 0 | 3 | 0 | 3 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4524): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0010 | 0/0 | 4530 | 2 | 1 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0011 | 0/0 | 4532 | 4 | 3 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4527): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0012 | 0/0 | 4529 | 4 | 1 | 1 | 0 | 1 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4524): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0013 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0014 | 0/0 | 4528 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4523): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0015 | 0/0 | 4532 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4527): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0016 | 0/0 | 4528 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4523): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0017 | 0/0 | 4530 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0018 | 0/0 | 4532 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4527): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0019 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0020 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0022 | 0/0 | 4532 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4527): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0023 | 0/0 | 4530 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0024 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0025 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0026 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0027 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0028 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0031 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0033 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0034 | 0/0 | 4532 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4527): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0040 | 0/0 | 4529 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4524): Show |
chr3 | 30601601 | 30699142 |
| a0001c0001t0041 | 0/0 | 4529 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4524): Show |
chr3 | 30601601 | 30699142 |
| a0001c0002t0001 | 0/0 | 4530 | 39 | 1 | 0 | 32 | 0 | 6 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0002t0002 | 0/0 | 4529 | 3 | 0 | 0 | 3 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4524): Show |
chr3 | 30601601 | 30699142 |
| a0001c0002t0003 | 0/0 | 4528 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4523): Show |
chr3 | 30601601 | 30699142 |
| a0001c0002t0005 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0002t0010 | 0/0 | 4530 | 3 | 0 | 0 | 1 | 0 | 2 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0002t0013 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0002t0029 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0002t0030 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0002t0037 | 0/0 | 4531 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4526): Show |
chr3 | 30601601 | 30699142 |
| a0001c0002t0038 | 0/0 | 4505 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4500): Show |
chr3 | 30601601 | 30699142 |
| a0001c0002t0042 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0003t0001 | 0/0 | 4530 | 3 | 3 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0003t0003 | 0/0 | 4528 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4523): Show |
chr3 | 30601601 | 30699142 |
| a0001c0003t0006 | 0/0 | 4528 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4523): Show |
chr3 | 30601601 | 30699142 |
| a0001c0003t0007 | 0/0 | 4531 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4526): Show |
chr3 | 30601601 | 30699142 |
| a0001c0003t0021 | 0/0 | 4532 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4527): Show |
chr3 | 30601601 | 30699142 |
| a0001c0003t0035 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0003t0039 | 0/0 | 4530 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0004t0003 | 0/0 | 4528 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4523): Show |
chr3 | 30601601 | 30699142 |
| a0001c0004t0008 | 0/0 | 4532 | 5 | 5 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4527): Show |
chr3 | 30601601 | 30699142 |
| a0001c0004t0011 | 0/0 | 4532 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4527): Show |
chr3 | 30601601 | 30699142 |
| a0001c0004t0014 | 0/0 | 4528 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4523): Show |
chr3 | 30601601 | 30699142 |
| a0001c0004t0032 | 0/0 | 4528 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4523): Show |
chr3 | 30601601 | 30699142 |
| a0001c0008t0003 | 0/0 | 4528 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4523): Show |
chr3 | 30601601 | 30699142 |
| a0001c0010t0002 | 0/0 | 4529 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4524): Show |
chr3 | 30601601 | 30699142 |
| a0001c0011t0036 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0001c0012t0002 | 0/0 | 4529 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4524): Show |
chr3 | 30601601 | 30699142 |
| a0002c0005t0001 | 0/0 | 4530 | 4 | 0 | 0 | 4 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0002c0005t0002 | 0/0 | 4529 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4524): Show |
chr3 | 30601601 | 30699142 |
| a0002c0005t0005 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0003c0006t0001 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| a0003c0006t0002 | 0/0 | 4529 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4524): Show |
chr3 | 30601601 | 30699142 |
| a0004c0007t0004 | 0/0 | 4532 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4527): Show |
chr3 | 30601601 | 30699142 |
| a0005c0009t0013 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | ACTCG others(4525): Show |
chr3 | 30601601 | 30699142 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0316 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0001g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0002g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0003g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0004g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0004g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0004g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0004g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0004g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0005g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0005g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0005g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0006g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0006g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0006g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0006g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0006g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0007g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0007g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0007g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0007g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0008g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0008g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0009g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0009g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0009g0163 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0009g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0009g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0009g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0010g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0010g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0011g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0011g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0011g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0011g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0012g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0012g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0012g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0012g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0013g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0014g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0015g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0015g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0016g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0016g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0017g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0017g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0018g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0019g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0020g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0022g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0023g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0024g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0025g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0026g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0027g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0028g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0031g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0033g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0034g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0040g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0001t0041g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0010g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0010g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0010g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0013g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0029g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0030g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0037g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0038g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0002t0042g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0003t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0003t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0003t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0003t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0003t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0003t0007g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0003t0007g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0003t0021g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0003t0035g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0003t0039g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0004t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0004t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0004t0008g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0004t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0004t0008g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0004t0008g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0004t0011g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0004t0014g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0004t0032g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0008t0003g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0010t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0011t0036g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0001c0012t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0002c0005t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0002c0005t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0002c0005t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0002c0005t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0002c0005t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0002c0005t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0003c0006t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0003c0006t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0003c0006t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0004c0007t0004g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| a0005c0009t0013g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0168 | EUR | GBR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | GBR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00140 | hp1 | a0001 | c0001 | t0009 | g0002 | EUR | GBR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0159 | EUR | GBR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00280 | hp1 | a0001 | c0001 | t0023 | g0242 | EUR | FIN | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00280 | hp2 | a0001 | c0001 | t0009 | g0002 | EUR | FIN | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | FIN | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0309 | EUR | FIN | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00558 | hp1 | a0002 | c0005 | t0001 | g0318 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0321 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0356 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00639 | hp2 | a0001 | c0001 | t0010 | g0359 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00673 | hp1 | a0001 | c0002 | t0005 | g0142 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0244 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01106 | hp1 | a0001 | c0001 | t0012 | g0304 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01109 | hp2 | a0001 | c0001 | t0011 | g0010 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01167 | hp2 | a0001 | c0008 | t0003 | g0338 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01243 | hp1 | a0001 | c0003 | t0039 | g0046 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01255 | hp1 | a0001 | c0001 | t0007 | g0348 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0298 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0229 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01257 | hp2 | a0001 | c0001 | t0009 | g0357 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0315 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01258 | hp2 | a0001 | c0001 | t0009 | g0358 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0371 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0011 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0167 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0012 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0072 | EUR | IBS | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | IBS | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01516 | hp1 | a0001 | c0001 | t0012 | g0116 | EUR | IBS | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0314 | EUR | IBS | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0317 | EUR | IBS | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0071 | EUR | IBS | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0349 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0353 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01891 | hp1 | a0001 | c0003 | t0035 | g0026 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01891 | hp2 | a0001 | c0002 | t0038 | g0045 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01934 | hp2 | a0001 | c0004 | t0032 | g0032 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0307 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01952 | hp2 | a0001 | c0001 | t0006 | g0024 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0370 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01981 | hp2 | a0001 | c0001 | t0009 | g0153 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02015 | hp2 | a0001 | c0001 | t0031 | g0103 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02040 | hp1 | a0002 | c0005 | t0001 | g0332 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02055 | hp1 | a0001 | c0001 | t0012 | g0251 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0020 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02132 | hp2 | a0001 | c0002 | t0042 | g0105 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0367 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | CDX | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CDX | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02165 | hp1 | a0001 | c0002 | t0010 | g0101 | EAS | CDX | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02165 | hp2 | a0001 | c0002 | t0030 | g0056 | EAS | CDX | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02257 | hp1 | a0001 | c0001 | t0018 | g0022 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0245 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02258 | hp1 | a0001 | c0004 | t0008 | g0339 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02258 | hp2 | a0001 | c0003 | t0021 | g0354 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02273 | hp2 | a0001 | c0001 | t0006 | g0013 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02280 | hp1 | a0001 | c0001 | t0014 | g0149 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0248 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02300 | hp1 | a0001 | c0001 | t0041 | g0007 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0364 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02602 | hp2 | a0001 | c0001 | t0012 | g0285 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0146 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02615 | hp2 | a0001 | c0001 | t0016 | g0300 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02622 | hp1 | a0001 | c0001 | t0011 | g0042 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02622 | hp2 | a0001 | c0002 | t0037 | g0031 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02630 | hp1 | a0001 | c0001 | t0016 | g0301 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0368 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02683 | hp2 | a0001 | c0012 | t0002 | g0097 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0265 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0360 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0323 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0366 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02723 | hp2 | a0001 | c0004 | t0008 | g0337 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0184 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02809 | hp1 | a0001 | c0001 | t0034 | g0033 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02809 | hp2 | a0001 | c0003 | t0007 | g0352 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0362 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0036 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02886 | hp1 | a0001 | c0004 | t0011 | g0369 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02886 | hp2 | a0001 | c0001 | t0010 | g0365 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0342 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02895 | hp2 | a0001 | c0001 | t0017 | g0292 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0269 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02897 | hp2 | a0001 | c0001 | t0017 | g0291 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02922 | hp1 | a0001 | c0001 | t0022 | g0112 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02965 | hp1 | a0001 | c0003 | t0007 | g0351 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0345 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02976 | hp1 | a0001 | c0001 | t0026 | g0086 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02976 | hp2 | a0001 | c0001 | t0033 | g0008 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0294 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0372 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0021 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0120 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03130 | hp2 | a0001 | c0011 | t0036 | g0047 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03139 | hp2 | a0001 | c0001 | t0025 | g0340 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0363 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03195 | hp2 | a0001 | c0003 | t0003 | g0344 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0041 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03209 | hp2 | a0004 | c0007 | t0004 | g0355 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03225 | hp1 | a0001 | c0001 | t0020 | g0346 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0361 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0329 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0223 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0350 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03486 | hp1 | a0001 | c0001 | t0015 | g0386 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0347 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0016 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0381 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0287 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0017 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0288 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03516 | hp1 | a0001 | c0003 | t0006 | g0040 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0027 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0328 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0380 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0322 | SAS | STU | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0114 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03710 | hp2 | a0001 | c0010 | t0002 | g0290 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0238 | SAS | BEB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0270 | SAS | BEB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0023 | SAS | BEB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03927 | hp2 | a0001 | c0002 | t0010 | g0382 | SAS | BEB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0311 | SAS | BEB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0060 | SAS | BEB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG04115 | hp2 | a0001 | c0002 | t0010 | g0078 | SAS | STU | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0293 | SAS | STU | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | STU | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | STU | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | STU | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0130 | SAS | STU | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | STU | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | YRI | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18522 | hp2 | a0001 | c0004 | t0008 | g0069 | AFR | YRI | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | CHB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18612 | hp2 | a0003 | c0006 | t0002 | g0182 | EAS | CHB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | CHB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | YRI | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18906 | hp2 | a0001 | c0001 | t0040 | g0009 | AFR | YRI | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0379 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18947 | hp2 | a0002 | c0005 | t0002 | g0331 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0376 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18954 | hp1 | a0001 | c0002 | t0013 | g0219 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0025 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18956 | hp2 | a0001 | c0001 | t0005 | g0217 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0320 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0216 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0378 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18977 | hp2 | a0005 | c0009 | t0013 | g0257 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0373 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0385 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0384 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19002 | hp2 | a0001 | c0001 | t0027 | g0156 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19007 | hp1 | a0002 | c0005 | t0001 | g0079 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19009 | hp2 | a0001 | c0001 | t0013 | g0375 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0028 | AFR | LWK | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19030 | hp2 | a0001 | c0001 | t0008 | g0150 | AFR | LWK | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0169 | AFR | LWK | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0343 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19058 | hp2 | a0001 | c0001 | t0024 | g0258 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0383 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19068 | hp1 | a0003 | c0006 | t0001 | g0327 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19070 | hp1 | a0002 | c0005 | t0001 | g0319 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0374 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0377 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19081 | hp1 | a0001 | c0002 | t0029 | g0143 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19086 | hp2 | a0003 | c0006 | t0002 | g0207 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19088 | hp2 | a0002 | c0005 | t0005 | g0176 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19240 | hp1 | a0001 | c0004 | t0014 | g0262 | AFR | YRI | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0037 | AFR | YRI | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | ASW | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ASW | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA20752 | hp1 | a0001 | c0001 | t0009 | g0254 | EUR | TSI | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | TSI | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | TSI | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | GIH | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | GIH | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02109 | hp2 | a0001 | c0001 | t0011 | g0029 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0119 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02486 | hp2 | a0001 | c0001 | t0028 | g0038 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02559 | hp1 | a0001 | c0002 | t0003 | g0341 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG02559 | hp2 | a0001 | c0004 | t0008 | g0043 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03471 | hp1 | a0001 | c0004 | t0003 | g0224 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0035 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG06807 | hp1 | a0001 | c0004 | t0008 | g0125 | AFR | USA | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| HG06807 | hp2 | a0001 | c0001 | t0015 | g0140 | AFR | USA | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA21309 | hp1 | a0001 | c0001 | t0019 | g0305 | AFR | LWK | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | LWK | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0009 | g0163 | REF | REF | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0316 | REF | REF | TGFBR2_chr3_30601601_30699142 | TGFBR2 | chr3 | 30601601 | 30699142 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:30644768 | C | A | 1 | a0004 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.116C>A | p.Thr39Asn | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/7 | 399/4530 | 116/1704 | 39/567 | chr3 | 30644768 | |||
| chr3:30671754 | G | A | 1 | a0003 | 3 | NA18612.hp2 NA19068.hp1 NA19086.hp2 |
missense_variant | MODERATE | c.571G>A | p.Val191Ile | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/7 | 854/4530 | 571/1704 | 191/567 | chr3 | 30671754 | |||
| chr3:30672127 | C | T | 1 | a0002 | 6 | HG00558.hp1 HG02040.hp1 NA18947.hp2 others(3): Show |
missense_variant | MODERATE | c.944C>T | p.Thr315Met | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/7 | 1227/4530 | 944/1704 | 315/567 | chr3 | 30672127 | |||
| chr3:30672391 | G | A | 1 | a0005 | 1 | NA18977.hp2 | missense_variant | MODERATE | c.1208G>A | p.Arg403His | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/7 | 1491/4530 | 1208/1704 | 403/567 | chr3 | 30672391 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:30672182 | A | G | 1 | a0001c0004 | 9 | HG01934.hp2 HG02258.hp1 HG02559.hp2 others(6): Show |
synonymous_variant | LOW | c.999A>G | p.Leu333Leu | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/7 | 1282/4530 | 999/1704 | 333/567 | chr3 | 30672182 | |||
| chr3:30672245 | C | T | 1 | a0001c0012 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.1062C>T | p.Leu354Leu | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/7 | 1345/4530 | 1062/1704 | 354/567 | chr3 | 30672245 | |||
| chr3:30672275 | T | C | 1 | a0001c0008 | 1 | HG01167.hp2 | synonymous_variant | LOW | c.1092T>C | p.Asp364Asp | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/7 | 1375/4530 | 1092/1704 | 364/567 | chr3 | 30672275 | |||
| chr3:30672350 | C | T | 1 | a0001c0002 | 53 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(50): Show |
synonymous_variant | LOW | c.1167C>T | p.Asn389Asn | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/7 | 1450/4530 | 1167/1704 | 389/567 | chr3 | 30672350 | |||
| chr3:30674116 | A | G | 1 | a0001c0003 | 10 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(7): Show |
synonymous_variant | LOW | c.1266A>G | p.Ala422Ala | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/7 | 1549/4530 | 1266/1704 | 422/567 | chr3 | 30674116 | |||
| chr3:30688445 | C | T | 1 | a0001c0011 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.1458C>T | p.Ser486Ser | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/7 | 1741/4530 | 1458/1704 | 486/567 | chr3 | 30688445 | |||
| chr3:30691497 | G | A | 1 | a0001c0010 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.1602G>A | p.Val534Val | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1885/4530 | 1602/1704 | 534/567 | chr3 | 30691497 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:30606691 | G | A | 1 | a0001c0001t0018 | 1 | HG02257.hp1 | 5_prime_UTR_variant | MODIFIER | c.-193G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/7 | 193 | chr3 | 30606691 | ||||||
| chr3:30606742 | C | T | 1 | a0001c0002t0042 | 1 | HG02132.hp2 | 5_prime_UTR_variant | MODIFIER | c.-142C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/7 | 142 | chr3 | 30606742 | ||||||
| chr3:30606756 | C | G | 19 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0011 others(16): Show |
40 | HG00408.hp2 HG00673.hp1 HG01109.hp2 others(37): Show |
5_prime_UTR_variant | MODIFIER | c.-128C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/7 | 128 | chr3 | 30606756 | ||||||
| chr3:30606758 | C | T | 1 | a0001c0001t0016 | 2 | HG02615.hp2 HG02630.hp1 |
5_prime_UTR_variant | MODIFIER | c.-126C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/7 | 126 | chr3 | 30606758 | ||||||
| chr3:30606781 | G | A | 1 | a0001c0001t0019 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-103G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/7 | 103 | chr3 | 30606781 | ||||||
| chr3:30691700 | C | T | 1 | a0001c0001t0031 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*101C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 101 | chr3 | 30691700 | ||||||
| chr3:30691906 | GTT | G | 3 | a0001c0001t0014 a0001c0004t0014 a0001c0004t0032 |
3 | HG01934.hp2 HG02280.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*310_*311delTT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 310 | INFO_REALIGN_3_PRIME | chr3 | 30691906 | |||||
| chr3:30691909 | T | TTA | 11 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(8): Show |
30 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*328_*329dupAT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 330 | INFO_REALIGN_3_PRIME | chr3 | 30691909 | |||||
| chr3:30691909 | TTA | T | 18 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(15): Show |
90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*328_*329delAT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 328 | INFO_REALIGN_3_PRIME | chr3 | 30691909 | |||||
| chr3:30691911 | A | T | 1 | a0001c0002t0001 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*312A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 312 | chr3 | 30691911 | ||||||
| chr3:30691929 | C | A | 2 | a0001c0001t0020 a0001c0001t0033 |
2 | HG02976.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*330C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 330 | chr3 | 30691929 | ||||||
| chr3:30691951 | A | G | 1 | a0001c0002t0030 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*352A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 352 | chr3 | 30691951 | ||||||
| chr3:30692198 | C | A | 2 | a0001c0003t0035 a0001c0011t0036 |
2 | HG01891.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*599C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 599 | chr3 | 30692198 | ||||||
| chr3:30692346 | C | G | 12 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0014 others(9): Show |
35 | HG01074.hp2 HG01106.hp2 HG01167.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*747C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 747 | chr3 | 30692346 | ||||||
| chr3:30692447 | C | T | 1 | a0001c0002t0038 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*848C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 848 | chr3 | 30692447 | ||||||
| chr3:30692474 | A | G | 1 | a0001c0001t0022 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*875A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 875 | chr3 | 30692474 | ||||||
| chr3:30692587 | C | T | 3 | a0001c0001t0013 a0001c0002t0013 a0005c0009t0013 |
3 | NA18954.hp1 NA18977.hp2 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*988C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 988 | chr3 | 30692587 | ||||||
| chr3:30692689 | G | T | 1 | a0001c0002t0038 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1090G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1090 | chr3 | 30692689 | ||||||
| chr3:30692707 | CAACTACA others(18): Show |
C | 1 | a0001c0002t0038 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1109_*1133delAACT others(21): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1109 | chr3 | 30692707 | ||||||
| chr3:30692743 | T | A | 1 | a0001c0002t0038 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1144T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1144 | chr3 | 30692743 | ||||||
| chr3:30692749 | A | G | 1 | a0001c0002t0029 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1150A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1150 | chr3 | 30692749 | ||||||
| chr3:30692953 | C | T | 1 | a0001c0001t0028 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1354C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1354 | chr3 | 30692953 | ||||||
| chr3:30693120 | G | A | 3 | a0001c0001t0007 a0001c0002t0037 a0001c0003t0007 |
11 | HG01255.hp1 HG01884.hp2 HG02622.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1521G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1521 | chr3 | 30693120 | ||||||
| chr3:30693167 | G | A | 1 | a0001c0001t0023 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1568G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1568 | chr3 | 30693167 | ||||||
| chr3:30693171 | A | G | 1 | a0001c0001t0027 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1572A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1572 | chr3 | 30693171 | ||||||
| chr3:30693281 | A | G | 1 | a0001c0002t0038 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1682A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1682 | chr3 | 30693281 | ||||||
| chr3:30693408 | A | G | 16 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0011 others(13): Show |
34 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1809A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1809 | chr3 | 30693408 | ||||||
| chr3:30693432 | A | C | 2 | a0001c0001t0012 a0001c0001t0041 |
5 | HG01106.hp1 HG01516.hp1 HG02055.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1833A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1833 | chr3 | 30693432 | ||||||
| chr3:30693479 | G | A | 3 | a0001c0001t0015 a0001c0001t0018 a0001c0001t0025 |
4 | HG02257.hp1 HG03139.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1880G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1880 | chr3 | 30693479 | ||||||
| chr3:30693485 | G | T | 1 | a0001c0001t0026 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1886G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1886 | chr3 | 30693485 | ||||||
| chr3:30693497 | A | G | 1 | a0001c0002t0038 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1898A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1898 | chr3 | 30693497 | ||||||
| chr3:30693664 | C | T | 1 | a0001c0001t0009 | 6 | HG00140.hp1 HG00280.hp2 HG01257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2065C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 2065 | chr3 | 30693664 | ||||||
| chr3:30693684 | T | A | 12 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0011 others(9): Show |
29 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2085T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 2085 | chr3 | 30693684 | ||||||
| chr3:30693838 | G | GT | 13 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(10): Show |
70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*2248dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 2249 | INFO_REALIGN_3_PRIME | chr3 | 30693838 | |||||
| chr3:30693967 | A | T | 1 | a0001c0011t0036 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2368A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 2368 | chr3 | 30693967 | ||||||
| chr3:30694082 | T | G | 1 | a0001c0003t0035 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2483T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 2483 | chr3 | 30694082 | ||||||
| chr3:30694104 | T | G | 1 | a0001c0001t0024 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2505T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 2505 | chr3 | 30694104 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:30607090 | A | G | 1 | a0001c0001t0015g0386 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.94+113A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607090 | |||||||
| chr3:30607185 | A | G | 12 | a0001c0001t0001g0376 a0001c0001t0001g0377 a0001c0001t0001g0378 others(9): Show |
12 | HG03490.hp2 HG03654.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+208A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607185 | |||||||
| chr3:30607254 | G | A | 1 | a0001c0002t0001g0005 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.94+277G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607254 | |||||||
| chr3:30607286 | A | C | 1 | a0001c0001t0001g0373 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.94+309A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607286 | |||||||
| chr3:30607609 | A | G | 1 | a0001c0001t0002g0372 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.94+632A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607609 | |||||||
| chr3:30607649 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.94+672T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607649 | |||||||
| chr3:30607787 | T | TAA | 4 | a0001c0001t0006g0018 a0001c0001t0006g0019 a0001c0001t0006g0020 others(1): Show |
4 | HG01934.hp2 HG02055.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+814_94+815dupAA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607787 | ||||||
| chr3:30607793 | T | A | 25 | a0001c0001t0004g0030 a0001c0001t0005g0014 a0001c0001t0005g0015 others(22): Show |
25 | HG00408.hp2 HG01109.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.94+816T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607793 | |||||||
| chr3:30607793 | TAAAA | T | 12 | a0001c0001t0001g0376 a0001c0001t0001g0377 a0001c0001t0001g0378 others(9): Show |
12 | HG03490.hp2 HG03654.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+820_94+823delAA others(2): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607793 | ||||||
| chr3:30607795 | A | AAT | 5 | a0001c0001t0004g0030 a0001c0001t0006g0028 a0001c0001t0011g0027 others(2): Show |
5 | HG02109.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+819_94+820insTA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607795 | ||||||
| chr3:30607795 | A | T | 1 | a0001c0004t0032g0032 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.94+818A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607795 | |||||||
| chr3:30607797 | A | T | 6 | a0001c0001t0004g0030 a0001c0001t0006g0028 a0001c0001t0011g0027 others(3): Show |
6 | HG01934.hp2 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+820A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607797 | |||||||
| chr3:30607799 | A | AAAAATAT | 11 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0016 others(8): Show |
11 | HG00408.hp2 HG01109.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.94+823_94+824insAA others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607799 | ||||||
| chr3:30607799 | A | AAT | 10 | a0001c0001t0002g0034 a0001c0001t0002g0039 a0001c0001t0007g0035 others(7): Show |
10 | HG02280.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+835_94+836dupAT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607799 | ||||||
| chr3:30607799 | A | T | 21 | a0001c0001t0001g0006 a0001c0001t0001g0370 a0001c0001t0001g0371 others(18): Show |
21 | HG01192.hp2 HG01261.hp1 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.94+822A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607799 | |||||||
| chr3:30607799 | AAT | A | 6 | a0001c0001t0003g0368 a0001c0001t0005g0364 a0001c0001t0010g0365 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+835_94+836delAT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607799 | ||||||
| chr3:30607800 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0034g0033 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.94+824_94+847delTA others(22): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607800 | |||||||
| chr3:30607801 | T | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0074 others(38): Show |
42 | HG00738.hp2 HG01074.hp1 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.94+824T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607801 | |||||||
| chr3:30607813 | T | A | 12 | a0001c0001t0001g0376 a0001c0001t0001g0377 a0001c0001t0001g0378 others(9): Show |
12 | HG03490.hp2 HG03654.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+836T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607813 | |||||||
| chr3:30607828 | TATATATA others(15): Show |
T | 15 | a0001c0001t0002g0034 a0001c0001t0002g0039 a0001c0001t0004g0044 others(12): Show |
15 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.94+863_94+884delTA others(20): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607828 | ||||||
| chr3:30607848 | T | TA | 12 | a0001c0001t0001g0376 a0001c0001t0001g0377 a0001c0001t0001g0378 others(9): Show |
12 | HG03490.hp2 HG03654.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+874dupA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607848 | ||||||
| chr3:30607850 | A | AAT | 84 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0001g0075 others(81): Show |
85 | HG00408.hp2 HG00738.hp2 HG01074.hp1 others(82): Show |
intron_variant | MODIFIER | c.94+881_94+882dupTA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607850 | ||||||
| chr3:30607865 | AAT | A | 12 | a0001c0001t0001g0376 a0001c0001t0001g0377 a0001c0001t0001g0378 others(9): Show |
12 | HG03490.hp2 HG03654.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+897_94+898delAT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607865 | ||||||
| chr3:30607916 | G | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | NA18967.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.94+939G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607916 | |||||||
| chr3:30607929 | G | C | 18 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(15): Show |
18 | HG00621.hp1 HG02071.hp1 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.94+952G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607929 | |||||||
| chr3:30607946 | A | AT | 8 | a0001c0001t0001g0067 a0001c0001t0001g0360 a0001c0001t0001g0361 others(5): Show |
8 | HG00639.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+981dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607946 | ||||||
| chr3:30608064 | G | T | 11 | a0001c0001t0002g0034 a0001c0001t0002g0039 a0001c0001t0007g0035 others(8): Show |
11 | HG02280.hp2 HG02486.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.94+1087G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608064 | |||||||
| chr3:30608145 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.94+1168G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608145 | |||||||
| chr3:30608173 | G | A | 1 | a0001c0004t0008g0069 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.94+1196G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608173 | |||||||
| chr3:30608344 | C | G | 1 | a0001c0001t0001g0356 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.94+1367C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608344 | |||||||
| chr3:30608345 | C | T | 1 | a0004c0007t0004g0355 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.94+1368C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608345 | |||||||
| chr3:30608362 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.94+1385C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608362 | |||||||
| chr3:30608415 | C | A | 265 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(262): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.94+1438C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608415 | |||||||
| chr3:30608572 | A | G | 278 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(275): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.94+1595A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608572 | |||||||
| chr3:30608590 | G | T | 1 | a0001c0003t0001g0294 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.94+1613G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608590 | |||||||
| chr3:30608612 | G | A | 3 | a0001c0001t0006g0018 a0001c0001t0006g0019 a0001c0001t0006g0020 |
3 | HG02055.hp2 HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.94+1635G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608612 | |||||||
| chr3:30608756 | A | G | 1 | a0001c0001t0002g0293 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.94+1779A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608756 | |||||||
| chr3:30608764 | G | GT | 6 | a0001c0001t0001g0350 a0001c0001t0004g0349 a0001c0001t0007g0353 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+1790dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30608764 | ||||||
| chr3:30608816 | T | A | 1 | a0001c0001t0001g0295 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.94+1839T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608816 | |||||||
| chr3:30608835 | T | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(287): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.94+1858T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608835 | |||||||
| chr3:30608963 | G | A | 14 | a0001c0001t0002g0034 a0001c0001t0002g0039 a0001c0001t0007g0035 others(11): Show |
14 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.94+1986G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608963 | |||||||
| chr3:30609075 | A | G | 8 | a0001c0001t0003g0368 a0001c0001t0005g0364 a0001c0001t0010g0365 others(5): Show |
8 | HG02145.hp1 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+2098A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609075 | |||||||
| chr3:30609100 | G | C | 9 | a0001c0001t0001g0376 a0001c0001t0001g0377 a0001c0001t0001g0378 others(6): Show |
9 | HG03490.hp2 HG03654.hp2 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.94+2123G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609100 | |||||||
| chr3:30609178 | T | C | 2 | a0001c0001t0002g0071 a0001c0001t0002g0072 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.94+2201T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609178 | |||||||
| chr3:30609247 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.94+2270T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609247 | |||||||
| chr3:30609256 | C | T | 12 | a0001c0001t0001g0376 a0001c0001t0001g0377 a0001c0001t0001g0378 others(9): Show |
12 | HG03490.hp2 HG03654.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+2279C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609256 | |||||||
| chr3:30609418 | C | T | 2 | a0001c0001t0002g0381 a0001c0002t0010g0382 |
2 | HG03490.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.94+2441C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609418 | |||||||
| chr3:30609525 | A | G | 1 | a0001c0010t0002g0290 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.94+2548A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609525 | |||||||
| chr3:30609730 | C | A | 1 | a0001c0001t0002g0293 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.94+2753C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609730 | |||||||
| chr3:30609830 | C | T | 11 | a0001c0001t0002g0034 a0001c0001t0002g0039 a0001c0001t0007g0035 others(8): Show |
11 | HG02280.hp2 HG02486.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.94+2853C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609830 | |||||||
| chr3:30609900 | A | G | 2 | a0001c0001t0009g0357 a0001c0001t0009g0358 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.94+2923A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609900 | |||||||
| chr3:30609917 | C | T | 1 | a0001c0002t0001g0343 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.94+2940C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609917 | |||||||
| chr3:30609962 | G | T | 3 | a0001c0001t0001g0289 a0001c0002t0001g0287 a0001c0002t0001g0288 |
3 | HG00741.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.94+2985G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609962 | |||||||
| chr3:30609988 | A | T | 1 | a0001c0001t0001g0286 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.94+3011A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609988 | |||||||
| chr3:30610054 | A | C | 14 | a0001c0001t0002g0034 a0001c0001t0002g0039 a0001c0001t0007g0035 others(11): Show |
14 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.94+3077A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30610054 | |||||||
| chr3:30610146 | G | T | 2 | a0001c0002t0038g0045 a0001c0003t0039g0046 |
2 | HG01243.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.94+3169G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30610146 | |||||||
| chr3:30610295 | T | C | 1 | a0001c0001t0002g0381 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.94+3318T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30610295 | |||||||
| chr3:30610325 | A | AT | 270 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(267): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.94+3357dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30610325 | ||||||
| chr3:30610332 | T | G | 12 | a0001c0001t0001g0376 a0001c0001t0001g0377 a0001c0001t0001g0378 others(9): Show |
12 | HG03490.hp2 HG03654.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+3355T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30610332 | |||||||
| chr3:30610332 | T | TG | 7 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(4): Show |
7 | HG02738.hp2 HG03195.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+3355_94+3356ins others(1): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30610332 | |||||||
| chr3:30610493 | A | T | 1 | a0001c0002t0001g0343 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.94+3516A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30610493 | |||||||
| chr3:30610496 | A | G | 1 | a0001c0001t0012g0285 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.94+3519A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30610496 | |||||||
| chr3:30610553 | T | A | 1 | a0001c0001t0006g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.94+3576T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30610553 | |||||||
| chr3:30610621 | A | C | 1 | a0001c0002t0001g0343 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.94+3644A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30610621 | |||||||
| chr3:30610643 | T | A | 1 | a0001c0001t0001g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.94+3666T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30610643 | |||||||
| chr3:30611045 | A | G | 14 | a0001c0001t0002g0034 a0001c0001t0002g0039 a0001c0001t0007g0035 others(11): Show |
14 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.94+4068A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30611045 | |||||||
| chr3:30611085 | A | T | 1 | a0001c0001t0002g0284 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.94+4108A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30611085 | |||||||
| chr3:30611115 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.94+4138G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30611115 | |||||||
| chr3:30611296 | G | A | 311 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(308): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.94+4319G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30611296 | |||||||
| chr3:30611333 | C | G | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.94+4356C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30611333 | |||||||
| chr3:30611421 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.94+4444G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30611421 | |||||||
| chr3:30611582 | C | CT | 23 | a0001c0001t0001g0082 a0001c0001t0001g0268 a0001c0001t0001g0271 others(20): Show |
23 | HG00597.hp2 HG02027.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.94+4619dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30611582 | ||||||
| chr3:30611613 | AAAGAGAA others(14): Show |
A | 230 | a0001c0001t0001g0006 a0001c0001t0001g0048 a0001c0001t0001g0049 others(227): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.94+4640_94+4660del others(21): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30611613 | ||||||
| chr3:30611790 | G | A | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.94+4813G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30611790 | |||||||
| chr3:30611978 | G | A | 1 | a0001c0001t0002g0293 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.94+5001G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30611978 | |||||||
| chr3:30611995 | C | T | 5 | a0001c0001t0001g0376 a0001c0001t0001g0377 a0001c0001t0001g0378 others(2): Show |
5 | HG03654.hp2 NA18944.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+5018C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30611995 | |||||||
| chr3:30612537 | T | G | 1 | a0001c0001t0001g0109 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.94+5560T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30612537 | |||||||
| chr3:30612609 | A | G | 1 | a0001c0001t0001g0263 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.94+5632A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30612609 | |||||||
| chr3:30612746 | C | CAATT | 289 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(286): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.94+5769_94+5770ins others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30612746 | |||||||
| chr3:30612870 | C | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG00735.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.94+5893C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30612870 | |||||||
| chr3:30612875 | A | T | 7 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0259 others(4): Show |
7 | NA18959.hp1 NA18964.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+5898A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30612875 | |||||||
| chr3:30612939 | C | A | 12 | a0001c0001t0002g0034 a0001c0001t0002g0039 a0001c0001t0007g0035 others(9): Show |
12 | HG02280.hp2 HG02486.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.94+5962C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30612939 | |||||||
| chr3:30613006 | A | T | 1 | a0001c0001t0001g0356 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.94+6029A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30613006 | |||||||
| chr3:30613131 | CT | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.94+6172delT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30613131 | ||||||
| chr3:30613131 | CTT | C | 8 | a0001c0001t0001g0081 a0001c0001t0001g0113 a0001c0001t0001g0115 others(5): Show |
8 | HG01256.hp1 HG01516.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.94+6171_94+6172del others(2): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30613131 | ||||||
| chr3:30613380 | G | A | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0002g0117 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+6403G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30613380 | |||||||
| chr3:30613398 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.94+6421A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30613398 | |||||||
| chr3:30613499 | G | A | 1 | a0001c0001t0002g0293 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.94+6522G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30613499 | |||||||
| chr3:30613502 | C | CTG | 3 | a0001c0001t0001g0383 a0001c0001t0001g0384 a0001c0001t0001g0385 |
3 | NA18990.hp1 NA18999.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.94+6539_94+6540dup others(2): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30613502 | ||||||
| chr3:30613525 | TGA | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(195): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.94+6573_94+6574del others(2): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30613525 | ||||||
| chr3:30613525 | TGAGA | T | 27 | a0001c0001t0001g0376 a0001c0001t0001g0377 a0001c0001t0001g0378 others(24): Show |
27 | HG02055.hp2 HG02280.hp2 HG02486.hp2 others(24): Show |
intron_variant | MODIFIER | c.94+6571_94+6574del others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30613525 | ||||||
| chr3:30613525 | TGAGAGA | T | 14 | a0001c0001t0001g0350 a0001c0001t0003g0119 a0001c0001t0004g0345 others(11): Show |
14 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.94+6569_94+6574del others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30613525 | ||||||
| chr3:30613527 | A | T | 1 | a0001c0001t0001g0232 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.94+6550A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30613527 | |||||||
| chr3:30613532 | G | A | 1 | a0004c0007t0004g0355 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.94+6555G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30613532 | |||||||
| chr3:30613542 | G | C | 5 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0001g0084 others(2): Show |
5 | HG02015.hp1 HG02083.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+6565G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30613542 | |||||||
| chr3:30613627 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.94+6650C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30613627 | |||||||
| chr3:30613629 | G | C | 1 | a0001c0001t0002g0284 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.94+6652G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30613629 | |||||||
| chr3:30613989 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(273): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.94+7012A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30613989 | |||||||
| chr3:30614072 | C | T | 6 | a0001c0001t0004g0030 a0001c0001t0006g0028 a0001c0001t0011g0027 others(3): Show |
6 | HG01934.hp2 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+7095C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30614072 | |||||||
| chr3:30614115 | C | CT | 245 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(242): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.94+7157dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30614115 | ||||||
| chr3:30614115 | CT | C | 13 | a0001c0001t0001g0068 a0001c0001t0001g0296 a0001c0001t0001g0299 others(10): Show |
13 | HG00639.hp2 HG01069.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+7157delT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30614115 | ||||||
| chr3:30614145 | G | C | 2 | a0001c0001t0006g0021 a0001c0004t0014g0262 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.94+7168G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30614145 | |||||||
| chr3:30614202 | T | C | 19 | a0001c0001t0001g0081 a0001c0001t0001g0113 a0001c0001t0002g0034 others(16): Show |
19 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.94+7225T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30614202 | |||||||
| chr3:30614302 | T | A | 2 | a0001c0001t0006g0021 a0001c0004t0014g0262 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.94+7325T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30614302 | |||||||
| chr3:30614364 | T | A | 1 | a0001c0001t0006g0363 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.94+7387T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30614364 | |||||||
| chr3:30614573 | C | T | 29 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(26): Show |
29 | HG02015.hp1 HG02015.hp2 HG02083.hp1 others(26): Show |
intron_variant | MODIFIER | c.94+7596C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30614573 | |||||||
| chr3:30614676 | G | A | 214 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(211): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.94+7699G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30614676 | |||||||
| chr3:30614721 | G | A | 1 | a0001c0001t0006g0363 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.94+7744G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30614721 | |||||||
| chr3:30614982 | C | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(244): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.94+8005C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30614982 | |||||||
| chr3:30615016 | A | T | 2 | a0001c0001t0001g0226 a0001c0001t0002g0225 |
2 | HG02523.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.94+8039A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615016 | |||||||
| chr3:30615081 | C | T | 48 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(45): Show |
48 | HG00408.hp2 HG01109.hp2 HG01358.hp1 others(45): Show |
intron_variant | MODIFIER | c.94+8104C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615081 | |||||||
| chr3:30615114 | A | G | 1 | a0001c0001t0009g0254 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.94+8137A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615114 | |||||||
| chr3:30615147 | A | G | 6 | a0001c0001t0004g0030 a0001c0001t0006g0028 a0001c0001t0011g0027 others(3): Show |
6 | HG01934.hp2 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+8170A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615147 | |||||||
| chr3:30615237 | T | C | 1 | a0001c0001t0003g0229 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.94+8260T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615237 | |||||||
| chr3:30615275 | CCCTGGTA others(5): Show |
C | 12 | a0001c0001t0001g0350 a0001c0001t0004g0345 a0001c0001t0004g0349 others(9): Show |
12 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+8301_94+8312del others(12): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30615275 | ||||||
| chr3:30615289 | C | T | 12 | a0001c0001t0001g0350 a0001c0001t0004g0345 a0001c0001t0004g0349 others(9): Show |
12 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+8312C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615289 | |||||||
| chr3:30615305 | G | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(177): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.94+8328G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615305 | |||||||
| chr3:30615307 | G | A | 6 | a0001c0001t0004g0030 a0001c0001t0006g0028 a0001c0001t0011g0027 others(3): Show |
6 | HG01934.hp2 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+8330G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615307 | |||||||
| chr3:30615353 | C | T | 6 | a0001c0001t0004g0030 a0001c0001t0006g0028 a0001c0001t0011g0027 others(3): Show |
6 | HG01934.hp2 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+8376C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615353 | |||||||
| chr3:30615424 | A | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(244): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.94+8447A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615424 | |||||||
| chr3:30615456 | T | C | 2 | a0001c0001t0006g0021 a0001c0004t0014g0262 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.94+8479T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615456 | |||||||
| chr3:30615588 | A | G | 1 | a0001c0001t0003g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.94+8611A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615588 | |||||||
| chr3:30615746 | A | AT | 247 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(244): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.94+8777dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30615746 | ||||||
| chr3:30615767 | T | A | 1 | a0001c0002t0001g0126 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.94+8790T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615767 | |||||||
| chr3:30615801 | A | G | 2 | a0001c0002t0038g0045 a0001c0003t0039g0046 |
2 | HG01243.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.94+8824A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615801 | |||||||
| chr3:30615833 | A | T | 1 | a0001c0001t0026g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.94+8856A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615833 | |||||||
| chr3:30615883 | A | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(244): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.94+8906A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615883 | |||||||
| chr3:30616189 | T | C | 1 | a0001c0002t0001g0127 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.94+9212T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30616189 | |||||||
| chr3:30616308 | C | T | 3 | a0001c0001t0004g0044 a0001c0001t0026g0086 a0001c0004t0008g0043 |
3 | HG02559.hp2 HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.94+9331C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30616308 | |||||||
| chr3:30616427 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0002g0128 |
2 | HG01255.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.94+9450T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30616427 | |||||||
| chr3:30616438 | T | C | 2 | a0001c0001t0006g0021 a0001c0004t0014g0262 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.94+9461T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30616438 | |||||||
| chr3:30616539 | C | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(244): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.94+9562C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30616539 | |||||||
| chr3:30616603 | T | G | 3 | a0001c0001t0004g0044 a0001c0001t0026g0086 a0001c0004t0008g0043 |
3 | HG02559.hp2 HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.94+9626T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30616603 | |||||||
| chr3:30616658 | A | G | 3 | a0001c0001t0001g0383 a0001c0001t0001g0384 a0001c0001t0001g0385 |
3 | NA18990.hp1 NA18999.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.94+9681A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30616658 | |||||||
| chr3:30616685 | T | C | 2 | a0001c0004t0003g0224 a0001c0004t0008g0125 |
2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+9708T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30616685 | |||||||
| chr3:30616795 | A | G | 1 | a0001c0001t0011g0042 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.94+9818A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30616795 | |||||||
| chr3:30616963 | C | T | 1 | a0001c0001t0007g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.94+9986C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30616963 | |||||||
| chr3:30617023 | T | C | 1 | a0001c0002t0001g0130 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.94+10046T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30617023 | |||||||
| chr3:30617049 | T | A | 295 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(292): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.94+10072T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30617049 | |||||||
| chr3:30617082 | GA | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(188): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.94+10117delA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30617082 | ||||||
| chr3:30617084 | A | G | 2 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
2 | NA18967.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.94+10107A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30617084 | |||||||
| chr3:30617225 | G | A | 38 | a0001c0001t0001g0006 a0001c0001t0001g0068 a0001c0001t0001g0070 others(35): Show |
39 | HG00280.hp1 HG00609.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.94+10248G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30617225 | |||||||
| chr3:30617437 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0022g0112 |
2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.94+10460C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30617437 | |||||||
| chr3:30617627 | C | T | 202 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(199): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.94+10650C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30617627 | |||||||
| chr3:30617697 | C | T | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | NA18965.hp1 NA18999.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.94+10720C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30617697 | |||||||
| chr3:30617759 | C | T | 6 | a0001c0001t0004g0030 a0001c0001t0006g0028 a0001c0001t0011g0027 others(3): Show |
6 | HG01934.hp2 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+10782C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30617759 | |||||||
| chr3:30617760 | G | A | 12 | a0001c0001t0001g0350 a0001c0001t0004g0345 a0001c0001t0004g0349 others(9): Show |
12 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+10783G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30617760 | |||||||
| chr3:30617919 | A | G | 1 | a0004c0007t0004g0355 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.94+10942A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30617919 | |||||||
| chr3:30618112 | T | G | 2 | a0001c0001t0026g0086 a0001c0004t0008g0043 |
2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.94+11135T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30618112 | |||||||
| chr3:30618160 | G | A | 241 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(238): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.94+11183G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30618160 | |||||||
| chr3:30618231 | G | GT | 24 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0106 others(21): Show |
24 | HG01167.hp2 HG02280.hp2 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.94+11270dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30618231 | ||||||
| chr3:30618471 | C | T | 4 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 others(1): Show |
4 | NA18950.hp2 NA18954.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+11494C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30618471 | |||||||
| chr3:30618517 | C | T | 3 | a0001c0001t0001g0383 a0001c0001t0001g0384 a0001c0001t0001g0385 |
3 | NA18990.hp1 NA18999.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.94+11540C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30618517 | |||||||
| chr3:30618532 | G | A | 1 | a0001c0001t0007g0035 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.94+11555G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30618532 | |||||||
| chr3:30618755 | A | G | 1 | a0001c0001t0002g0118 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.94+11778A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30618755 | |||||||
| chr3:30618871 | T | G | 1 | a0001c0001t0001g0356 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.94+11894T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30618871 | |||||||
| chr3:30618909 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.94+11932T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30618909 | |||||||
| chr3:30618937 | A | G | 33 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0080 others(30): Show |
33 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.94+11960A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30618937 | |||||||
| chr3:30619111 | A | G | 1 | a0001c0001t0001g0333 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.94+12134A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619111 | |||||||
| chr3:30619188 | C | T | 134 | a0001c0001t0001g0064 a0001c0001t0001g0073 a0001c0001t0001g0082 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.94+12211C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619188 | |||||||
| chr3:30619238 | C | T | 3 | a0001c0001t0011g0042 a0001c0003t0006g0040 a0001c0011t0036g0047 |
3 | HG02622.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.94+12261C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619238 | |||||||
| chr3:30619239 | G | A | 1 | a0004c0007t0004g0355 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.94+12262G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619239 | |||||||
| chr3:30619277 | A | T | 9 | a0001c0001t0005g0014 a0001c0001t0005g0016 a0001c0001t0005g0017 others(6): Show |
9 | HG00408.hp2 HG01358.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+12300A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619277 | |||||||
| chr3:30619341 | T | C | 2 | a0001c0001t0006g0021 a0001c0004t0014g0262 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.94+12364T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619341 | |||||||
| chr3:30619420 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.94+12443A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619420 | |||||||
| chr3:30619595 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.94+12618A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619595 | |||||||
| chr3:30619677 | C | T | 12 | a0001c0001t0001g0081 a0001c0001t0001g0295 a0001c0001t0001g0329 others(9): Show |
12 | HG01261.hp2 HG03239.hp1 HG03490.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+12700C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619677 | |||||||
| chr3:30619718 | C | T | 145 | a0001c0001t0001g0064 a0001c0001t0001g0073 a0001c0001t0001g0082 others(142): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.94+12741C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619718 | |||||||
| chr3:30619719 | G | A | 1 | a0001c0001t0006g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.94+12742G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619719 | |||||||
| chr3:30619823 | C | G | 1 | a0001c0004t0008g0339 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.94+12846C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619823 | |||||||
| chr3:30619956 | G | C | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(9): Show |
12 | HG00735.hp1 HG01952.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.94+12979G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619956 | |||||||
| chr3:30619961 | GC | G | 140 | a0001c0001t0001g0059 a0001c0001t0001g0064 a0001c0001t0001g0073 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.94+12985delC | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619961 | |||||||
| chr3:30619970 | G | A | 5 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(2): Show |
5 | NA18944.hp2 NA19004.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+12993G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619970 | |||||||
| chr3:30619972 | A | G | 5 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(2): Show |
5 | NA18944.hp2 NA19004.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+12995A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619972 | |||||||
| chr3:30619989 | C | T | 179 | a0001c0001t0001g0059 a0001c0001t0001g0064 a0001c0001t0001g0073 others(176): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.94+13012C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619989 | |||||||
| chr3:30620043 | T | C | 1 | a0004c0007t0004g0355 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.94+13066T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620043 | |||||||
| chr3:30620046 | G | A | 11 | a0001c0001t0005g0014 a0001c0001t0005g0016 a0001c0001t0005g0017 others(8): Show |
11 | HG00408.hp2 HG00639.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.94+13069G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620046 | |||||||
| chr3:30620103 | C | T | 72 | a0001c0001t0001g0006 a0001c0001t0001g0050 a0001c0001t0001g0054 others(69): Show |
74 | HG00280.hp1 HG00621.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.94+13126C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620103 | |||||||
| chr3:30620106 | G | C | 2 | a0001c0001t0003g0119 a0001c0001t0015g0140 |
2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.94+13129G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620106 | |||||||
| chr3:30620119 | G | A | 6 | a0001c0001t0002g0039 a0001c0001t0007g0036 a0001c0001t0007g0037 others(3): Show |
6 | HG02486.hp2 HG02647.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+13142G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620119 | |||||||
| chr3:30620123 | T | C | 5 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
5 | NA18959.hp2 NA19011.hp1 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+13146T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620123 | |||||||
| chr3:30620135 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.94+13158C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620135 | |||||||
| chr3:30620136 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.94+13159G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620136 | |||||||
| chr3:30620143 | C | T | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(9): Show |
12 | HG00735.hp1 HG01952.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.94+13166C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620143 | |||||||
| chr3:30620206 | A | G | 3 | a0001c0001t0001g0081 a0001c0001t0001g0295 a0001c0001t0001g0330 |
3 | HG01261.hp2 HG03540.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.94+13229A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620206 | |||||||
| chr3:30620304 | T | C | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(9): Show |
12 | HG00735.hp1 HG01952.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.94+13327T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620304 | |||||||
| chr3:30620340 | G | A | 9 | a0001c0001t0005g0014 a0001c0001t0005g0016 a0001c0001t0005g0017 others(6): Show |
9 | HG00408.hp2 HG01358.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+13363G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620340 | |||||||
| chr3:30620647 | A | C | 1 | a0001c0004t0014g0262 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.94+13670A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620647 | |||||||
| chr3:30620666 | A | G | 1 | a0001c0001t0002g0194 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.94+13689A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620666 | |||||||
| chr3:30620738 | T | C | 1 | a0001c0001t0007g0035 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.94+13761T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620738 | |||||||
| chr3:30620836 | C | G | 263 | a0001c0001t0001g0006 a0001c0001t0001g0048 a0001c0001t0001g0049 others(260): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.94+13859C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620836 | |||||||
| chr3:30620957 | G | T | 39 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(36): Show |
39 | HG00408.hp2 HG00639.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.94+13980G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620957 | |||||||
| chr3:30620982 | G | A | 2 | a0001c0001t0012g0304 a0001c0001t0041g0007 |
2 | HG01106.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.94+14005G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620982 | |||||||
| chr3:30621062 | A | G | 39 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(36): Show |
39 | HG00408.hp2 HG00639.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.94+14085A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30621062 | |||||||
| chr3:30621168 | A | G | 2 | a0001c0001t0006g0021 a0001c0004t0014g0262 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.94+14191A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30621168 | |||||||
| chr3:30621278 | C | CT | 75 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(72): Show |
75 | HG00558.hp2 HG00673.hp1 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.94+14320dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30621278 | ||||||
| chr3:30621278 | C | CTT | 168 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0064 others(165): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.94+14319_94+14320d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30621278 | ||||||
| chr3:30621278 | C | CTTT | 95 | a0001c0001t0001g0006 a0001c0001t0001g0049 a0001c0001t0001g0050 others(92): Show |
97 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.94+14318_94+14320d others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30621278 | ||||||
| chr3:30621337 | A | C | 3 | a0001c0001t0001g0188 a0001c0001t0001g0193 a0001c0001t0002g0277 |
3 | HG02083.hp2 NA19006.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.94+14360A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30621337 | |||||||
| chr3:30621714 | A | G | 1 | a0001c0001t0001g0255 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.94+14737A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30621714 | |||||||
| chr3:30621894 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.94+14917G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30621894 | |||||||
| chr3:30621938 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.94+14961C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30621938 | |||||||
| chr3:30621958 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(163): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.94+14981A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30621958 | |||||||
| chr3:30622036 | A | G | 3 | a0001c0001t0001g0064 a0001c0002t0001g0063 a0001c0002t0001g0065 |
3 | NA18950.hp1 NA18951.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.94+15059A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622036 | |||||||
| chr3:30622181 | T | A | 3 | a0001c0001t0019g0305 a0001c0004t0008g0337 a0001c0008t0003g0338 |
3 | HG01167.hp2 HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.94+15204T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622181 | |||||||
| chr3:30622422 | A | G | 75 | a0001c0001t0001g0058 a0001c0001t0001g0070 a0001c0001t0001g0073 others(72): Show |
75 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.94+15445A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622422 | |||||||
| chr3:30622495 | A | G | 93 | a0001c0001t0001g0006 a0001c0001t0001g0050 a0001c0001t0001g0051 others(90): Show |
95 | HG00280.hp1 HG00558.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.94+15518A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622495 | |||||||
| chr3:30622537 | C | CA | 9 | a0001c0001t0001g0144 a0001c0001t0001g0256 a0001c0001t0002g0265 others(6): Show |
9 | HG01891.hp2 HG02698.hp2 HG04204.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+15570dupA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30622537 | ||||||
| chr3:30622584 | G | C | 10 | a0001c0001t0006g0363 a0001c0001t0007g0347 a0001c0001t0007g0348 others(7): Show |
10 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+15607G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622584 | |||||||
| chr3:30622588 | G | A | 8 | a0001c0001t0001g0230 a0001c0001t0005g0016 a0001c0001t0005g0017 others(5): Show |
8 | HG01358.hp1 HG01361.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.94+15611G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622588 | |||||||
| chr3:30622656 | C | T | 13 | a0001c0001t0002g0039 a0001c0001t0006g0018 a0001c0001t0006g0019 others(10): Show |
13 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+15679C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622656 | |||||||
| chr3:30622829 | G | A | 137 | a0001c0001t0001g0006 a0001c0001t0001g0050 a0001c0001t0001g0051 others(134): Show |
139 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.94+15852G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622829 | |||||||
| chr3:30622866 | C | T | 1 | a0004c0007t0004g0355 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.94+15889C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622866 | |||||||
| chr3:30622879 | CA | C | 33 | a0001c0001t0001g0006 a0001c0001t0001g0067 a0001c0001t0001g0068 others(30): Show |
33 | HG00280.hp1 HG01074.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.94+15929delA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30622879 | ||||||
| chr3:30622879 | CAA | C | 146 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(143): Show |
148 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(145): Show |
intron_variant | MODIFIER | c.94+15928_94+15929d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30622879 | ||||||
| chr3:30622879 | CAAA | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(143): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.94+15927_94+15929d others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30622879 | ||||||
| chr3:30622879 | CAAAA | C | 7 | a0001c0001t0001g0123 a0001c0001t0001g0221 a0001c0001t0012g0116 others(4): Show |
7 | HG00597.hp1 HG01516.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+15926_94+15929d others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30622879 | ||||||
| chr3:30622879 | CAAAAAAA others(8): Show |
C | 4 | a0001c0001t0001g0189 a0001c0001t0002g0275 a0001c0001t0002g0276 others(1): Show |
4 | HG02040.hp2 HG02135.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+15915_94+15929d others(17): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30622879 | ||||||
| chr3:30622879 | CAAAAAAA others(10): Show |
C | 3 | a0001c0001t0002g0034 a0001c0004t0003g0224 a0001c0004t0008g0125 |
3 | HG02280.hp2 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+15913_94+15929d others(19): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30622879 | ||||||
| chr3:30622879 | CAAAAAAA others(14): Show |
C | 1 | a0001c0002t0001g0185 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.94+15909_94+15929d others(23): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30622879 | ||||||
| chr3:30622883 | A | G | 1 | a0001c0001t0001g0380 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.94+15906A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622883 | |||||||
| chr3:30622913 | GGAAAAA | G | 5 | a0001c0001t0001g0361 a0001c0001t0025g0340 a0001c0003t0021g0354 others(2): Show |
5 | HG02258.hp2 HG03130.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15951_94+15956d others(8): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30622913 | ||||||
| chr3:30622914 | G | A | 1 | a0001c0001t0007g0035 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.94+15937G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622914 | |||||||
| chr3:30622915 | A | G | 1 | a0001c0001t0007g0035 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.94+15938A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622915 | |||||||
| chr3:30622919 | A | G | 1 | a0001c0001t0007g0035 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.94+15942A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622919 | |||||||
| chr3:30623014 | C | T | 1 | a0001c0001t0001g0297 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.94+16037C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623014 | |||||||
| chr3:30623240 | A | C | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | NA19011.hp1 NA19063.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+16263A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623240 | |||||||
| chr3:30623276 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.94+16299A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623276 | |||||||
| chr3:30623372 | T | C | 8 | a0001c0001t0001g0144 a0001c0001t0001g0256 a0001c0001t0002g0265 others(5): Show |
8 | HG02698.hp2 HG04204.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.94+16395T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623372 | |||||||
| chr3:30623398 | G | A | 1 | a0001c0001t0001g0370 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.94+16421G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623398 | |||||||
| chr3:30623445 | T | C | 1 | a0001c0003t0039g0046 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.94+16468T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623445 | |||||||
| chr3:30623619 | G | T | 1 | a0001c0001t0031g0103 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.94+16642G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623619 | |||||||
| chr3:30623692 | G | A | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.94+16715G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623692 | |||||||
| chr3:30623736 | G | A | 93 | a0001c0001t0001g0006 a0001c0001t0001g0050 a0001c0001t0001g0051 others(90): Show |
95 | HG00280.hp1 HG00558.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.94+16759G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623736 | |||||||
| chr3:30623772 | A | G | 5 | a0001c0001t0002g0039 a0001c0001t0007g0036 a0001c0001t0007g0037 others(2): Show |
5 | HG02486.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+16795A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623772 | |||||||
| chr3:30623848 | A | G | 1 | a0001c0001t0005g0023 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.94+16871A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623848 | |||||||
| chr3:30623898 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.94+16921T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623898 | |||||||
| chr3:30624048 | C | A | 154 | a0001c0001t0001g0006 a0001c0001t0001g0050 a0001c0001t0001g0051 others(151): Show |
156 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.94+17071C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624048 | |||||||
| chr3:30624209 | C | T | 1 | a0003c0006t0002g0182 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.94+17232C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624209 | |||||||
| chr3:30624260 | G | C | 4 | a0001c0001t0001g0273 a0001c0001t0002g0267 a0001c0002t0001g0173 others(1): Show |
4 | HG02027.hp1 NA18955.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+17283G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624260 | |||||||
| chr3:30624275 | G | A | 7 | a0001c0001t0001g0144 a0001c0001t0001g0256 a0001c0001t0002g0265 others(4): Show |
7 | HG02698.hp2 NA18959.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+17298G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624275 | |||||||
| chr3:30624382 | C | G | 1 | a0001c0002t0001g0130 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.94+17405C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624382 | |||||||
| chr3:30624390 | G | A | 4 | a0001c0001t0004g0349 a0001c0001t0006g0021 a0001c0001t0011g0010 others(1): Show |
4 | HG01109.hp2 HG01884.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+17413G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624390 | |||||||
| chr3:30624393 | A | G | 9 | a0001c0001t0001g0144 a0001c0001t0001g0256 a0001c0001t0002g0265 others(6): Show |
9 | HG01891.hp2 HG02698.hp2 HG04204.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+17416A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624393 | |||||||
| chr3:30624509 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.94+17532G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624509 | |||||||
| chr3:30624556 | C | G | 1 | a0001c0001t0001g0099 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.94+17579C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624556 | |||||||
| chr3:30624610 | G | A | 42 | a0001c0001t0001g0006 a0001c0001t0001g0050 a0001c0001t0001g0051 others(39): Show |
43 | HG00280.hp1 HG00609.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.94+17633G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624610 | |||||||
| chr3:30624619 | G | GA | 53 | a0001c0001t0001g0109 a0001c0001t0001g0113 a0001c0001t0001g0115 others(50): Show |
53 | HG00408.hp2 HG00639.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.94+17654dupA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30624619 | ||||||
| chr3:30624837 | A | C | 1 | a0001c0001t0001g0181 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.94+17860A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624837 | |||||||
| chr3:30624841 | G | C | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG00738.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.94+17864G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624841 | |||||||
| chr3:30624934 | G | T | 1 | a0001c0001t0001g0350 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.94+17957G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624934 | |||||||
| chr3:30624960 | C | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(169): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.94+17983C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624960 | |||||||
| chr3:30625107 | A | C | 1 | a0001c0001t0005g0025 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.94+18130A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30625107 | |||||||
| chr3:30625174 | A | G | 1 | a0001c0001t0001g0361 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.94+18197A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30625174 | |||||||
| chr3:30625295 | G | A | 1 | a0001c0003t0003g0344 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.94+18318G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30625295 | |||||||
| chr3:30625396 | G | A | 9 | a0001c0001t0001g0144 a0001c0001t0001g0256 a0001c0001t0002g0265 others(6): Show |
9 | HG01891.hp2 HG02698.hp2 HG04204.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+18419G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30625396 | |||||||
| chr3:30625585 | G | T | 11 | a0001c0001t0001g0073 a0001c0001t0002g0124 a0001c0001t0002g0284 others(8): Show |
11 | HG00544.hp2 HG00621.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.94+18608G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30625585 | |||||||
| chr3:30625767 | T | A | 9 | a0001c0001t0001g0144 a0001c0001t0001g0256 a0001c0001t0002g0265 others(6): Show |
9 | HG01891.hp2 HG02698.hp2 HG04204.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+18790T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30625767 | |||||||
| chr3:30625882 | C | T | 3 | a0001c0001t0002g0034 a0001c0004t0003g0224 a0001c0004t0008g0125 |
3 | HG02280.hp2 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.95-18865C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30625882 | |||||||
| chr3:30625930 | C | A | 1 | a0001c0001t0001g0259 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.95-18817C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30625930 | |||||||
| chr3:30625933 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(174): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.95-18814T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30625933 | |||||||
| chr3:30626061 | T | G | 1 | a0001c0001t0025g0340 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.95-18686T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30626061 | |||||||
| chr3:30626070 | A | G | 1 | a0001c0001t0001g0295 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.95-18677A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30626070 | |||||||
| chr3:30626175 | T | A | 1 | a0001c0003t0039g0046 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.95-18572T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30626175 | |||||||
| chr3:30626232 | G | T | 4 | a0001c0001t0010g0365 a0001c0003t0001g0366 a0001c0003t0001g0367 others(1): Show |
4 | HG02145.hp1 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-18515G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30626232 | |||||||
| chr3:30626233 | G | C | 3 | a0001c0001t0006g0018 a0001c0001t0006g0019 a0001c0001t0006g0020 |
3 | HG02055.hp2 HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.95-18514G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30626233 | |||||||
| chr3:30626522 | A | G | 9 | a0001c0001t0002g0039 a0001c0001t0006g0018 a0001c0001t0006g0019 others(6): Show |
9 | HG02055.hp2 HG02258.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-18225A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30626522 | |||||||
| chr3:30626542 | A | G | 1 | a0001c0001t0002g0194 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.95-18205A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30626542 | |||||||
| chr3:30626548 | CAG | C | 4 | a0001c0001t0004g0349 a0001c0001t0006g0021 a0001c0001t0011g0010 others(1): Show |
4 | HG01109.hp2 HG01884.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-18196_95-18195d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30626548 | ||||||
| chr3:30626968 | T | C | 1 | a0001c0001t0003g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.95-17779T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30626968 | |||||||
| chr3:30627171 | G | A | 5 | a0001c0001t0010g0365 a0001c0001t0026g0086 a0001c0003t0001g0366 others(2): Show |
5 | HG02145.hp1 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-17576G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627171 | |||||||
| chr3:30627192 | A | G | 161 | a0001c0001t0001g0006 a0001c0001t0001g0050 a0001c0001t0001g0051 others(158): Show |
163 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.95-17555A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627192 | |||||||
| chr3:30627431 | G | A | 2 | a0001c0001t0001g0326 a0001c0002t0037g0031 |
2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.95-17316G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627431 | |||||||
| chr3:30627447 | G | C | 1 | a0001c0001t0001g0197 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.95-17300G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627447 | |||||||
| chr3:30627454 | A | G | 1 | a0001c0001t0008g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.95-17293A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627454 | |||||||
| chr3:30627739 | A | G | 1 | a0001c0001t0006g0363 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.95-17008A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627739 | |||||||
| chr3:30627759 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.95-16988C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627759 | |||||||
| chr3:30627760 | G | A | 9 | a0001c0001t0001g0144 a0001c0001t0001g0256 a0001c0001t0002g0265 others(6): Show |
9 | HG01891.hp2 HG02698.hp2 HG04204.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-16987G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627760 | |||||||
| chr3:30627821 | TGA | T | 3 | a0001c0001t0002g0034 a0001c0004t0003g0224 a0001c0004t0008g0125 |
3 | HG02280.hp2 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.95-16925_95-16924d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627821 | |||||||
| chr3:30627824 | A | T | 3 | a0001c0001t0002g0034 a0001c0004t0003g0224 a0001c0004t0008g0125 |
3 | HG02280.hp2 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.95-16923A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627824 | |||||||
| chr3:30627866 | G | A | 94 | a0001c0001t0001g0006 a0001c0001t0001g0050 a0001c0001t0001g0051 others(91): Show |
96 | HG00280.hp1 HG00558.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.95-16881G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627866 | |||||||
| chr3:30627882 | T | C | 1 | a0001c0001t0010g0359 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.95-16865T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627882 | |||||||
| chr3:30627911 | C | G | 22 | a0001c0001t0001g0058 a0001c0001t0001g0187 a0001c0001t0001g0263 others(19): Show |
22 | HG00558.hp1 HG00597.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.95-16836C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627911 | |||||||
| chr3:30628112 | C | CT | 169 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(166): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.95-16619dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628112 | ||||||
| chr3:30628112 | C | CTT | 30 | a0001c0001t0002g0039 a0001c0001t0004g0349 a0001c0001t0006g0018 others(27): Show |
30 | HG01109.hp2 HG01243.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.95-16620_95-16619d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628112 | ||||||
| chr3:30628127 | TTA | T | 135 | a0001c0001t0001g0006 a0001c0001t0001g0050 a0001c0001t0001g0051 others(132): Show |
136 | HG00280.hp1 HG00558.hp2 HG00609.hp2 others(133): Show |
intron_variant | MODIFIER | c.95-16619_95-16618d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30628127 | |||||||
| chr3:30628244 | A | G | 10 | a0001c0001t0001g0073 a0001c0001t0001g0144 a0001c0001t0001g0256 others(7): Show |
10 | HG00621.hp2 HG02698.hp2 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-16503A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30628244 | |||||||
| chr3:30628291 | A | G | 43 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(40): Show |
44 | HG00558.hp2 HG01934.hp2 HG02027.hp1 others(41): Show |
intron_variant | MODIFIER | c.95-16456A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30628291 | |||||||
| chr3:30628452 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.95-16295A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30628452 | |||||||
| chr3:30628493 | C | CA | 15 | a0001c0001t0001g0111 a0001c0001t0001g0137 a0001c0001t0001g0144 others(12): Show |
16 | HG00735.hp1 HG00735.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.95-16240dupA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628493 | ||||||
| chr3:30628493 | CA | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(237): Show |
242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.95-16240delA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628493 | ||||||
| chr3:30628528 | G | GT | 66 | a0001c0001t0001g0006 a0001c0001t0001g0067 a0001c0001t0001g0076 others(63): Show |
66 | HG00408.hp2 HG00673.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.95-16194dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628528 | ||||||
| chr3:30628528 | G | GTT | 57 | a0001c0001t0001g0070 a0001c0001t0001g0084 a0001c0001t0001g0135 others(54): Show |
57 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.95-16195_95-16194d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628528 | ||||||
| chr3:30628528 | G | GTTT | 81 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0058 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.95-16196_95-16194d others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628528 | ||||||
| chr3:30628528 | G | GTTTT | 17 | a0001c0001t0001g0049 a0001c0001t0001g0104 a0001c0001t0001g0108 others(14): Show |
17 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-16197_95-16194d others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628528 | ||||||
| chr3:30628528 | GT | G | 15 | a0001c0001t0001g0308 a0001c0001t0001g0361 a0001c0001t0002g0034 others(12): Show |
15 | HG00099.hp1 HG01243.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.95-16194delT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628528 | ||||||
| chr3:30628528 | GTT | G | 6 | a0001c0001t0006g0018 a0001c0001t0006g0019 a0001c0001t0007g0036 others(3): Show |
6 | HG02258.hp1 HG02486.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-16195_95-16194d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628528 | ||||||
| chr3:30628528 | GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0004g0044 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.95-16205_95-16194d others(14): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628528 | ||||||
| chr3:30628529 | T | G | 5 | a0001c0001t0001g0144 a0001c0001t0001g0256 a0001c0001t0002g0265 others(2): Show |
5 | HG02698.hp2 NA18959.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-16218T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30628529 | |||||||
| chr3:30628567 | A | G | 6 | a0001c0001t0001g0144 a0001c0001t0001g0256 a0001c0001t0002g0265 others(3): Show |
6 | HG02698.hp2 NA18959.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-16180A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30628567 | |||||||
| chr3:30628843 | C | T | 4 | a0001c0001t0006g0018 a0001c0001t0006g0019 a0001c0001t0006g0020 others(1): Show |
4 | HG02055.hp2 HG02258.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-15904C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30628843 | |||||||
| chr3:30628933 | G | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(151): Show |
156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.95-15814G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30628933 | |||||||
| chr3:30628975 | C | T | 4 | a0001c0001t0022g0112 a0001c0001t0025g0340 a0001c0001t0034g0033 others(1): Show |
4 | HG02258.hp2 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-15772C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30628975 | |||||||
| chr3:30629399 | AAAG | A | 7 | a0001c0001t0001g0144 a0001c0001t0001g0256 a0001c0001t0002g0265 others(4): Show |
7 | HG02698.hp2 HG04204.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-15342_95-15340d others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30629399 | ||||||
| chr3:30629631 | G | A | 1 | a0004c0007t0004g0355 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.95-15116G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30629631 | |||||||
| chr3:30629692 | G | A | 1 | a0001c0001t0002g0034 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.95-15055G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30629692 | |||||||
| chr3:30630060 | A | G | 4 | a0001c0001t0001g0376 a0001c0001t0001g0377 a0001c0001t0001g0378 others(1): Show |
4 | NA18944.hp1 NA18951.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-14687A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630060 | |||||||
| chr3:30630092 | G | C | 67 | a0001c0001t0001g0141 a0001c0001t0001g0144 a0001c0001t0001g0177 others(64): Show |
67 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.95-14655G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630092 | |||||||
| chr3:30630237 | A | G | 1 | a0001c0002t0037g0031 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.95-14510A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630237 | |||||||
| chr3:30630382 | A | G | 5 | a0001c0001t0002g0039 a0001c0001t0007g0036 a0001c0001t0007g0037 others(2): Show |
5 | HG02486.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-14365A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630382 | |||||||
| chr3:30630557 | T | C | 1 | a0001c0001t0001g0383 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.95-14190T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630557 | |||||||
| chr3:30630587 | C | T | 1 | a0004c0007t0004g0355 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.95-14160C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630587 | |||||||
| chr3:30630764 | G | C | 1 | a0001c0001t0001g0164 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.95-13983G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630764 | |||||||
| chr3:30630765 | A | G | 75 | a0001c0001t0001g0141 a0001c0001t0001g0144 a0001c0001t0001g0177 others(72): Show |
75 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.95-13982A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630765 | |||||||
| chr3:30630775 | C | T | 1 | a0002c0005t0001g0319 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.95-13972C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630775 | |||||||
| chr3:30630793 | G | A | 1 | a0004c0007t0004g0355 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.95-13954G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630793 | |||||||
| chr3:30630836 | A | G | 67 | a0001c0001t0001g0141 a0001c0001t0001g0144 a0001c0001t0001g0177 others(64): Show |
67 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.95-13911A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630836 | |||||||
| chr3:30630870 | C | T | 67 | a0001c0001t0001g0070 a0001c0001t0001g0083 a0001c0001t0001g0098 others(64): Show |
67 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.95-13877C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630870 | |||||||
| chr3:30630879 | A | C | 1 | a0001c0001t0001g0326 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.95-13868A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630879 | |||||||
| chr3:30630963 | A | G | 11 | a0001c0001t0006g0363 a0001c0001t0007g0347 a0001c0001t0007g0348 others(8): Show |
11 | HG00639.hp2 HG01255.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.95-13784A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630963 | |||||||
| chr3:30631009 | G | A | 4 | a0001c0001t0002g0034 a0001c0004t0003g0224 a0001c0004t0008g0125 others(1): Show |
4 | HG02280.hp2 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-13738G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631009 | |||||||
| chr3:30631014 | C | G | 67 | a0001c0001t0001g0141 a0001c0001t0001g0144 a0001c0001t0001g0177 others(64): Show |
67 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.95-13733C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631014 | |||||||
| chr3:30631036 | C | CT | 6 | a0001c0001t0001g0093 a0001c0001t0001g0137 a0001c0001t0001g0170 others(3): Show |
6 | HG01123.hp2 HG01934.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-13689dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30631036 | ||||||
| chr3:30631036 | CT | C | 83 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0058 others(80): Show |
84 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.95-13689delT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30631036 | ||||||
| chr3:30631036 | CTT | C | 151 | a0001c0001t0001g0070 a0001c0001t0001g0083 a0001c0001t0001g0098 others(148): Show |
151 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.95-13690_95-13689d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30631036 | ||||||
| chr3:30631058 | T | A | 2 | a0001c0001t0002g0381 a0001c0002t0010g0382 |
2 | HG03490.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.95-13689T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631058 | |||||||
| chr3:30631105 | G | A | 67 | a0001c0001t0001g0141 a0001c0001t0001g0144 a0001c0001t0001g0177 others(64): Show |
67 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.95-13642G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631105 | |||||||
| chr3:30631143 | T | C | 67 | a0001c0001t0001g0141 a0001c0001t0001g0144 a0001c0001t0001g0177 others(64): Show |
67 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.95-13604T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631143 | |||||||
| chr3:30631197 | A | T | 67 | a0001c0001t0001g0141 a0001c0001t0001g0144 a0001c0001t0001g0177 others(64): Show |
67 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.95-13550A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631197 | |||||||
| chr3:30631214 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.95-13533G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631214 | |||||||
| chr3:30631230 | C | T | 1 | a0001c0001t0002g0249 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.95-13517C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631230 | |||||||
| chr3:30631239 | G | A | 253 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0058 others(250): Show |
255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.95-13508G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631239 | |||||||
| chr3:30631291 | C | T | 1 | a0001c0004t0008g0339 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.95-13456C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631291 | |||||||
| chr3:30631414 | A | C | 67 | a0001c0001t0001g0141 a0001c0001t0001g0144 a0001c0001t0001g0177 others(64): Show |
67 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.95-13333A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631414 | |||||||
| chr3:30631487 | A | G | 3 | a0001c0001t0001g0144 a0001c0001t0001g0256 a0005c0009t0013g0257 |
3 | NA18959.hp1 NA18977.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.95-13260A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631487 | |||||||
| chr3:30631621 | CT | C | 165 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0057 others(162): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.95-13104delT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30631621 | ||||||
| chr3:30631621 | CTT | C | 10 | a0001c0001t0001g0098 a0001c0001t0001g0145 a0001c0001t0001g0236 others(7): Show |
10 | HG00639.hp2 HG01070.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-13105_95-13104d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30631621 | ||||||
| chr3:30631621 | CTTT | C | 47 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0181 others(44): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.95-13106_95-13104d others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30631621 | ||||||
| chr3:30631621 | CTTTT | C | 13 | a0001c0001t0001g0141 a0001c0001t0001g0188 a0001c0001t0001g0189 others(10): Show |
13 | HG00673.hp2 HG02040.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.95-13107_95-13104d others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30631621 | ||||||
| chr3:30631621 | CTTTTTTT others(3): Show |
C | 15 | a0001c0001t0001g0147 a0001c0001t0004g0004 a0001c0001t0004g0030 others(12): Show |
16 | HG01934.hp2 HG02109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.95-13113_95-13104d others(12): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30631621 | ||||||
| chr3:30631626 | T | C | 2 | a0001c0001t0007g0035 a0001c0011t0036g0047 |
2 | HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.95-13121T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631626 | |||||||
| chr3:30631627 | T | C | 1 | a0001c0001t0026g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.95-13120T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631627 | |||||||
| chr3:30631628 | T | C | 3 | a0001c0002t0001g0172 a0001c0002t0001g0183 a0002c0005t0005g0176 |
3 | NA19057.hp1 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.95-13119T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631628 | |||||||
| chr3:30631726 | T | A | 1 | a0001c0002t0001g0238 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.95-13021T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631726 | |||||||
| chr3:30631868 | C | T | 7 | a0001c0001t0001g0144 a0001c0001t0001g0256 a0001c0001t0002g0265 others(4): Show |
7 | HG02698.hp2 HG04204.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-12879C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631868 | |||||||
| chr3:30631878 | C | T | 1 | a0001c0012t0002g0097 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.95-12869C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631878 | |||||||
| chr3:30632020 | T | G | 1 | a0002c0005t0001g0332 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.95-12727T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632020 | |||||||
| chr3:30632187 | A | G | 22 | a0001c0001t0001g0361 a0001c0001t0002g0039 a0001c0001t0006g0018 others(19): Show |
22 | HG00639.hp2 HG01243.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.95-12560A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632187 | |||||||
| chr3:30632228 | C | T | 69 | a0001c0001t0001g0123 a0001c0001t0001g0141 a0001c0001t0001g0144 others(66): Show |
70 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.95-12519C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632228 | |||||||
| chr3:30632291 | G | A | 1 | a0001c0001t0003g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.95-12456G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632291 | |||||||
| chr3:30632373 | C | T | 1 | a0001c0001t0026g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.95-12374C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632373 | |||||||
| chr3:30632397 | A | G | 23 | a0001c0001t0001g0147 a0001c0001t0002g0034 a0001c0001t0004g0004 others(20): Show |
24 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.95-12350A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632397 | |||||||
| chr3:30632513 | A | C | 1 | a0001c0001t0001g0059 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.95-12234A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632513 | |||||||
| chr3:30632558 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.95-12189T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632558 | |||||||
| chr3:30632700 | G | A | 7 | a0001c0001t0002g0034 a0001c0001t0007g0035 a0001c0001t0026g0086 others(4): Show |
7 | HG02280.hp2 HG02723.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-12047G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632700 | |||||||
| chr3:30632762 | C | T | 73 | a0001c0001t0001g0099 a0001c0001t0001g0141 a0001c0001t0001g0177 others(70): Show |
73 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.95-11985C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632762 | |||||||
| chr3:30632941 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.95-11806T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632941 | |||||||
| chr3:30632967 | C | T | 1 | a0001c0001t0003g0119 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.95-11780C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632967 | |||||||
| chr3:30633026 | C | G | 1 | a0001c0003t0021g0354 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.95-11721C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633026 | |||||||
| chr3:30633179 | A | G | 71 | a0001c0001t0001g0099 a0001c0001t0001g0110 a0001c0001t0001g0141 others(68): Show |
71 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.95-11568A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633179 | |||||||
| chr3:30633195 | T | C | 1 | a0001c0004t0008g0337 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.95-11552T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633195 | |||||||
| chr3:30633354 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.95-11393A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633354 | |||||||
| chr3:30633459 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.95-11288A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633459 | |||||||
| chr3:30633492 | C | T | 22 | a0001c0001t0001g0361 a0001c0001t0002g0039 a0001c0001t0006g0018 others(19): Show |
22 | HG00639.hp2 HG01243.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.95-11255C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633492 | |||||||
| chr3:30633541 | T | C | 24 | a0001c0001t0001g0361 a0001c0001t0002g0039 a0001c0001t0006g0018 others(21): Show |
24 | HG00639.hp2 HG01243.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.95-11206T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633541 | |||||||
| chr3:30633562 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(70): Show |
74 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.95-11185C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633562 | |||||||
| chr3:30633659 | C | T | 51 | a0001c0001t0001g0070 a0001c0001t0001g0081 a0001c0001t0001g0098 others(48): Show |
51 | HG00639.hp1 HG00738.hp1 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.95-11088C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633659 | |||||||
| chr3:30633680 | G | A | 1 | a0001c0001t0003g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.95-11067G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633680 | |||||||
| chr3:30633732 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.95-11015T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633732 | |||||||
| chr3:30633818 | C | T | 2 | a0001c0001t0011g0010 a0004c0007t0004g0355 |
2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.95-10929C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633818 | |||||||
| chr3:30633834 | G | A | 257 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(254): Show |
260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.95-10913G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633834 | |||||||
| chr3:30634071 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.95-10676A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634071 | |||||||
| chr3:30634127 | G | A | 11 | a0001c0001t0001g0147 a0001c0001t0004g0004 a0001c0001t0004g0030 others(8): Show |
12 | HG01934.hp2 HG02109.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.95-10620G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634127 | |||||||
| chr3:30634380 | T | C | 15 | a0001c0001t0006g0018 a0001c0001t0006g0019 a0001c0001t0006g0020 others(12): Show |
15 | HG00639.hp2 HG01255.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-10367T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634380 | |||||||
| chr3:30634388 | A | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(181): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.95-10359A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634388 | |||||||
| chr3:30634435 | T | A | 9 | a0001c0001t0002g0039 a0001c0001t0003g0223 a0001c0001t0004g0349 others(6): Show |
9 | HG01884.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-10312T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634435 | |||||||
| chr3:30634465 | T | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(165): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.95-10282T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634465 | |||||||
| chr3:30634508 | G | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(165): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.95-10239G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634508 | |||||||
| chr3:30634525 | G | C | 288 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(285): Show |
291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.95-10222G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634525 | |||||||
| chr3:30634615 | G | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0296 a0001c0001t0001g0325 |
3 | HG01069.hp1 HG01071.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.95-10132G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634615 | |||||||
| chr3:30634851 | G | C | 289 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(286): Show |
292 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.95-9896G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634851 | |||||||
| chr3:30634917 | G | A | 2 | a0001c0001t0006g0011 a0001c0001t0006g0012 |
2 | HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.95-9830G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634917 | |||||||
| chr3:30634929 | T | A | 1 | a0001c0001t0001g0208 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.95-9818T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634929 | |||||||
| chr3:30634954 | C | T | 5 | a0001c0001t0002g0039 a0001c0001t0007g0036 a0001c0001t0007g0037 others(2): Show |
5 | HG02486.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-9793C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634954 | |||||||
| chr3:30635164 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.95-9583T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30635164 | |||||||
| chr3:30635624 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(268): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.95-9123G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30635624 | |||||||
| chr3:30635777 | A | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(155): Show |
159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.95-8970A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30635777 | |||||||
| chr3:30635806 | A | G | 20 | a0001c0001t0001g0187 a0001c0001t0001g0263 a0001c0001t0001g0333 others(17): Show |
20 | HG00544.hp2 HG00673.hp1 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.95-8941A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30635806 | |||||||
| chr3:30635909 | A | G | 2 | a0001c0001t0011g0010 a0004c0007t0004g0355 |
2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.95-8838A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30635909 | |||||||
| chr3:30635957 | A | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0068 a0001c0001t0001g0243 others(2): Show |
5 | HG00280.hp1 HG01074.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-8790A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30635957 | |||||||
| chr3:30635992 | C | A | 257 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0058 others(254): Show |
259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.95-8755C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30635992 | |||||||
| chr3:30636001 | T | C | 9 | a0001c0001t0002g0039 a0001c0001t0003g0223 a0001c0001t0004g0349 others(6): Show |
9 | HG01884.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-8746T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636001 | |||||||
| chr3:30636067 | G | C | 377 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(374): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.95-8680G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636067 | |||||||
| chr3:30636155 | A | ATG | 42 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0080 others(39): Show |
42 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.95-8548_95-8547dup others(2): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | ||||||
| chr3:30636155 | A | ATGTG | 60 | a0001c0001t0001g0001 a0001c0001t0001g0076 a0001c0001t0001g0083 others(57): Show |
61 | HG00558.hp1 HG00609.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.95-8550_95-8547dup others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | ||||||
| chr3:30636155 | A | ATGTGTG | 47 | a0001c0001t0001g0058 a0001c0001t0001g0084 a0001c0001t0001g0099 others(44): Show |
47 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.95-8552_95-8547dup others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | ||||||
| chr3:30636155 | A | ATGTGTGT others(1): Show |
10 | a0001c0001t0001g0129 a0001c0001t0001g0271 a0001c0001t0001g0281 others(7): Show |
10 | HG00140.hp2 HG00597.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-8554_95-8547dup others(8): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | ||||||
| chr3:30636155 | A | ATGTGTGT others(3): Show |
6 | a0001c0001t0001g0082 a0001c0001t0004g0151 a0001c0001t0012g0285 others(3): Show |
6 | HG02109.hp1 HG02602.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-8556_95-8547dup others(10): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | ||||||
| chr3:30636155 | A | ATGTGTGT others(5): Show |
5 | a0001c0001t0001g0064 a0001c0001t0001g0094 a0001c0001t0001g0188 others(2): Show |
5 | NA18950.hp1 NA18966.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-8558_95-8547dup others(12): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | ||||||
| chr3:30636155 | A | G | 1 | a0001c0001t0005g0015 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.95-8592A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636155 | |||||||
| chr3:30636155 | ATG | A | 36 | a0001c0001t0001g0108 a0001c0001t0001g0113 a0001c0001t0001g0145 others(33): Show |
36 | HG01070.hp1 HG01243.hp2 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.95-8548_95-8547del others(2): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | ||||||
| chr3:30636155 | ATGTG | A | 12 | a0001c0001t0001g0089 a0001c0001t0001g0137 a0001c0001t0001g0138 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.95-8550_95-8547del others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | ||||||
| chr3:30636155 | ATGTGTG | A | 96 | a0001c0001t0001g0006 a0001c0001t0001g0050 a0001c0001t0001g0051 others(93): Show |
98 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.95-8552_95-8547del others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | ||||||
| chr3:30636155 | ATGTGTGT others(1): Show |
A | 7 | a0001c0001t0001g0144 a0001c0001t0001g0191 a0001c0001t0001g0250 others(4): Show |
7 | HG01123.hp2 HG03098.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-8554_95-8547del others(8): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | ||||||
| chr3:30636155 | ATGTGTGT others(3): Show |
A | 2 | a0001c0001t0011g0010 a0001c0002t0001g0120 |
2 | HG01109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.95-8556_95-8547del others(10): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | ||||||
| chr3:30636155 | ATGTGTGT others(5): Show |
A | 1 | a0004c0007t0004g0355 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.95-8558_95-8547del others(12): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | ||||||
| chr3:30636155 | ATGTGTGT others(7): Show |
A | 3 | a0001c0002t0038g0045 a0001c0003t0039g0046 a0002c0005t0001g0332 |
3 | HG01243.hp1 HG01891.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.95-8560_95-8547del others(14): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | ||||||
| chr3:30636155 | ATGTGTGT others(9): Show |
A | 2 | a0001c0001t0026g0086 a0001c0004t0008g0337 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.95-8562_95-8547del others(16): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | ||||||
| chr3:30636155 | ATGTGTGT others(11): Show |
A | 3 | a0001c0001t0002g0034 a0001c0004t0003g0224 a0001c0004t0008g0125 |
3 | HG02280.hp2 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.95-8564_95-8547del others(18): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | ||||||
| chr3:30636206 | A | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(268): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.95-8541A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636206 | |||||||
| chr3:30636221 | G | A | 1 | a0001c0001t0023g0242 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.95-8526G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636221 | |||||||
| chr3:30636326 | T | A | 255 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0058 others(252): Show |
257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.95-8421T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636326 | |||||||
| chr3:30636339 | C | T | 5 | a0001c0001t0001g0361 a0001c0001t0006g0018 a0001c0001t0006g0019 others(2): Show |
5 | HG02055.hp2 HG02258.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-8408C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636339 | |||||||
| chr3:30636577 | A | T | 3 | a0001c0001t0006g0018 a0001c0001t0006g0019 a0001c0001t0006g0020 |
3 | HG02055.hp2 HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.95-8170A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636577 | |||||||
| chr3:30636699 | A | T | 5 | a0001c0001t0002g0034 a0001c0004t0003g0224 a0001c0004t0008g0125 others(2): Show |
5 | HG02280.hp2 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-8048A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636699 | |||||||
| chr3:30636722 | A | C | 77 | a0001c0001t0001g0070 a0001c0001t0001g0081 a0001c0001t0001g0098 others(74): Show |
78 | HG00639.hp1 HG00738.hp1 HG01069.hp1 others(75): Show |
intron_variant | MODIFIER | c.95-8025A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636722 | |||||||
| chr3:30636733 | C | CGT | 56 | a0001c0001t0001g0070 a0001c0001t0001g0098 a0001c0001t0001g0109 others(53): Show |
57 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.95-7989_95-7988dup others(2): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636733 | ||||||
| chr3:30636733 | CGT | C | 10 | a0001c0001t0001g0361 a0001c0001t0006g0018 a0001c0001t0006g0019 others(7): Show |
10 | HG02055.hp2 HG02258.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-7989_95-7988del others(2): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636733 | ||||||
| chr3:30636733 | CGTGT | C | 14 | a0001c0001t0001g0147 a0001c0001t0004g0004 a0001c0001t0004g0030 others(11): Show |
15 | HG01934.hp2 HG02109.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-7991_95-7988del others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636733 | ||||||
| chr3:30636790 | C | T | 4 | a0001c0001t0002g0034 a0001c0004t0003g0224 a0001c0004t0008g0125 others(1): Show |
4 | HG02280.hp2 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-7957C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636790 | |||||||
| chr3:30636860 | C | G | 9 | a0001c0001t0001g0090 a0001c0001t0001g0093 a0001c0001t0001g0106 others(6): Show |
9 | HG00558.hp2 HG02132.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-7887C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636860 | |||||||
| chr3:30636861 | G | C | 1 | a0001c0001t0001g0107 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.95-7886G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636861 | |||||||
| chr3:30636895 | T | A | 1 | a0001c0001t0001g0188 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7852T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636895 | |||||||
| chr3:30636908 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0188 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7833_95-7832ins others(14): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636908 | ||||||
| chr3:30636920 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7827C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636920 | |||||||
| chr3:30636921 | A | T | 1 | a0001c0001t0001g0188 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7826A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636921 | |||||||
| chr3:30636922 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7825A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636922 | |||||||
| chr3:30636931 | T | G | 1 | a0001c0001t0001g0188 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7816T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636931 | |||||||
| chr3:30636932 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7815T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636932 | |||||||
| chr3:30636937 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7810A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636937 | |||||||
| chr3:30636953 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7794G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636953 | |||||||
| chr3:30636962 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7785G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636962 | |||||||
| chr3:30636970 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7777A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636970 | |||||||
| chr3:30637021 | G | A | 7 | a0001c0001t0001g0361 a0001c0001t0006g0018 a0001c0001t0006g0019 others(4): Show |
7 | HG02055.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-7726G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30637021 | |||||||
| chr3:30637062 | T | TG | 9 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0353 others(6): Show |
9 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-7684dupG | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30637062 | ||||||
| chr3:30637063 | G | GA | 10 | a0001c0001t0001g0093 a0001c0001t0001g0121 a0001c0001t0001g0161 others(7): Show |
10 | HG01981.hp1 HG02055.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-7668dupA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30637063 | ||||||
| chr3:30637618 | A | G | 1 | a0001c0001t0003g0060 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.95-7129A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30637618 | |||||||
| chr3:30637675 | T | C | 1 | a0001c0001t0024g0258 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.95-7072T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30637675 | |||||||
| chr3:30637727 | G | A | 7 | a0001c0001t0001g0361 a0001c0001t0006g0018 a0001c0001t0006g0019 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-7020G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30637727 | |||||||
| chr3:30637858 | G | A | 2 | a0001c0001t0001g0361 a0001c0001t0004g0146 |
2 | HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.95-6889G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30637858 | |||||||
| chr3:30637876 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.95-6871G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30637876 | |||||||
| chr3:30637885 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.95-6862G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30637885 | |||||||
| chr3:30638066 | A | T | 274 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(271): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.95-6681A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638066 | |||||||
| chr3:30638120 | T | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(271): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.95-6627T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638120 | |||||||
| chr3:30638357 | A | T | 11 | a0001c0001t0001g0147 a0001c0001t0004g0004 a0001c0001t0004g0030 others(8): Show |
12 | HG01934.hp2 HG02109.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.95-6390A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638357 | |||||||
| chr3:30638367 | A | G | 16 | a0001c0001t0001g0361 a0001c0001t0002g0039 a0001c0001t0003g0223 others(13): Show |
16 | HG00639.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.95-6380A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638367 | |||||||
| chr3:30638372 | A | G | 2 | a0001c0001t0011g0010 a0004c0007t0004g0355 |
2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.95-6375A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638372 | |||||||
| chr3:30638391 | A | G | 5 | a0001c0001t0002g0039 a0001c0001t0007g0036 a0001c0001t0007g0037 others(2): Show |
5 | HG02486.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-6356A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638391 | |||||||
| chr3:30638461 | G | A | 16 | a0001c0001t0001g0147 a0001c0001t0004g0004 a0001c0001t0004g0030 others(13): Show |
17 | HG01934.hp2 HG02109.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-6286G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638461 | |||||||
| chr3:30638478 | C | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(162): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.95-6269C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638478 | |||||||
| chr3:30638502 | T | C | 12 | a0001c0001t0001g0123 a0001c0001t0001g0144 a0001c0001t0001g0154 others(9): Show |
13 | HG00140.hp1 HG00280.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.95-6245T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638502 | |||||||
| chr3:30638519 | C | T | 1 | a0001c0002t0001g0238 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.95-6228C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638519 | |||||||
| chr3:30638537 | A | G | 1 | a0001c0002t0001g0173 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.95-6210A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638537 | |||||||
| chr3:30638644 | C | A | 16 | a0001c0001t0001g0147 a0001c0001t0004g0004 a0001c0001t0004g0030 others(13): Show |
17 | HG01934.hp2 HG02109.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-6103C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638644 | |||||||
| chr3:30638690 | T | G | 1 | a0001c0001t0001g0161 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.95-6057T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638690 | |||||||
| chr3:30638878 | T | C | 307 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(304): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.95-5869T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638878 | |||||||
| chr3:30639210 | C | A | 1 | a0001c0012t0002g0097 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.95-5537C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30639210 | |||||||
| chr3:30639379 | G | A | 2 | a0001c0001t0011g0010 a0004c0007t0004g0355 |
2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.95-5368G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30639379 | |||||||
| chr3:30639441 | C | T | 2 | a0001c0001t0011g0010 a0004c0007t0004g0355 |
2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.95-5306C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30639441 | |||||||
| chr3:30639490 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.95-5257G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30639490 | |||||||
| chr3:30639603 | A | G | 70 | a0001c0001t0001g0070 a0001c0001t0001g0081 a0001c0001t0001g0098 others(67): Show |
70 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.95-5144A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30639603 | |||||||
| chr3:30639754 | C | T | 1 | a0001c0001t0004g0044 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.95-4993C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30639754 | |||||||
| chr3:30639982 | T | C | 9 | a0001c0001t0001g0361 a0001c0001t0006g0018 a0001c0001t0006g0019 others(6): Show |
9 | HG00639.hp2 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-4765T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30639982 | |||||||
| chr3:30640055 | A | G | 1 | a0001c0002t0038g0045 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.95-4692A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640055 | |||||||
| chr3:30640134 | C | A | 1 | a0001c0001t0031g0103 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.95-4613C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640134 | |||||||
| chr3:30640153 | A | G | 1 | a0001c0001t0011g0042 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.95-4594A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640153 | |||||||
| chr3:30640224 | G | T | 1 | a0001c0001t0003g0244 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.95-4523G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640224 | |||||||
| chr3:30640330 | G | A | 25 | a0001c0001t0001g0147 a0001c0001t0002g0039 a0001c0001t0003g0223 others(22): Show |
26 | HG01884.hp1 HG01934.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.95-4417G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640330 | |||||||
| chr3:30640436 | G | C | 1 | a0001c0001t0005g0025 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.95-4311G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640436 | |||||||
| chr3:30640617 | G | T | 1 | a0001c0001t0002g0303 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.95-4130G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640617 | |||||||
| chr3:30640625 | A | G | 14 | a0001c0001t0001g0361 a0001c0001t0004g0349 a0001c0001t0006g0018 others(11): Show |
14 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.95-4122A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640625 | |||||||
| chr3:30640658 | T | A | 1 | a0001c0003t0039g0046 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.95-4089T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640658 | |||||||
| chr3:30640658 | TA | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(160): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.95-4082delA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30640658 | ||||||
| chr3:30640750 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(162): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.95-3997A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640750 | |||||||
| chr3:30640761 | A | G | 4 | a0001c0001t0015g0386 a0001c0003t0003g0344 a0001c0003t0006g0040 others(1): Show |
4 | HG01891.hp1 HG03195.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-3986A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640761 | |||||||
| chr3:30641072 | C | A | 1 | a0001c0001t0002g0205 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.95-3675C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641072 | |||||||
| chr3:30641106 | T | C | 3 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0353 |
3 | HG01255.hp1 HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.95-3641T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641106 | |||||||
| chr3:30641139 | G | A | 1 | a0001c0001t0001g0310 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.95-3608G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641139 | |||||||
| chr3:30641447 | G | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(163): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.95-3300G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641447 | |||||||
| chr3:30641455 | T | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(163): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.95-3292T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641455 | |||||||
| chr3:30641485 | G | A | 61 | a0001c0001t0001g0070 a0001c0001t0001g0081 a0001c0001t0001g0098 others(58): Show |
61 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.95-3262G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641485 | |||||||
| chr3:30641506 | G | C | 1 | a0001c0001t0002g0284 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.95-3241G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641506 | |||||||
| chr3:30641542 | C | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(163): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.95-3205C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641542 | |||||||
| chr3:30641573 | G | T | 4 | a0001c0001t0006g0018 a0001c0001t0006g0019 a0001c0001t0006g0020 others(1): Show |
4 | HG02055.hp2 HG02258.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-3174G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641573 | |||||||
| chr3:30641588 | C | A | 1 | a0001c0001t0003g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.95-3159C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641588 | |||||||
| chr3:30641624 | T | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0154 a0001c0001t0009g0002 |
4 | HG00140.hp1 HG00280.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-3123T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641624 | |||||||
| chr3:30641690 | C | G | 5 | a0001c0001t0002g0039 a0001c0001t0007g0036 a0001c0001t0007g0037 others(2): Show |
5 | HG02486.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-3057C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641690 | |||||||
| chr3:30641709 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(163): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.95-3038A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641709 | |||||||
| chr3:30641794 | GTATTA | G | 25 | a0001c0001t0001g0147 a0001c0001t0002g0039 a0001c0001t0003g0223 others(22): Show |
26 | HG01884.hp1 HG01934.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.95-2949_95-2945del others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30641794 | ||||||
| chr3:30641799 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(246): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.95-2948A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641799 | |||||||
| chr3:30641832 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.95-2915C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641832 | |||||||
| chr3:30642003 | C | T | 1 | a0001c0002t0001g0239 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.95-2744C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30642003 | |||||||
| chr3:30642014 | C | T | 61 | a0001c0001t0001g0070 a0001c0001t0001g0081 a0001c0001t0001g0098 others(58): Show |
61 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.95-2733C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30642014 | |||||||
| chr3:30642129 | G | A | 1 | a0001c0001t0007g0269 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.95-2618G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30642129 | |||||||
| chr3:30642320 | G | C | 1 | a0001c0002t0038g0045 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.95-2427G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30642320 | |||||||
| chr3:30642341 | T | C | 2 | a0001c0001t0005g0216 a0001c0001t0005g0217 |
2 | NA18956.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.95-2406T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30642341 | |||||||
| chr3:30642398 | A | G | 8 | a0001c0001t0001g0098 a0001c0001t0001g0218 a0001c0001t0002g0284 others(5): Show |
8 | HG00544.hp1 HG01358.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-2349A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30642398 | |||||||
| chr3:30642549 | A | G | 79 | a0001c0001t0001g0070 a0001c0001t0001g0081 a0001c0001t0001g0098 others(76): Show |
79 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.95-2198A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30642549 | |||||||
| chr3:30642605 | G | A | 185 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0058 others(182): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.95-2142G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30642605 | |||||||
| chr3:30642683 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(176): Show |
181 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.95-2064G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30642683 | |||||||
| chr3:30642904 | C | T | 1 | a0001c0001t0034g0033 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.95-1843C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30642904 | |||||||
| chr3:30643191 | G | A | 275 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(272): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.95-1556G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643191 | |||||||
| chr3:30643303 | T | G | 5 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0181 others(2): Show |
5 | HG00408.hp1 NA18953.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-1444T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643303 | |||||||
| chr3:30643348 | G | C | 11 | a0001c0001t0001g0123 a0001c0001t0001g0144 a0001c0001t0001g0154 others(8): Show |
12 | HG00140.hp1 HG00280.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.95-1399G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643348 | |||||||
| chr3:30643415 | C | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(175): Show |
180 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.95-1332C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643415 | |||||||
| chr3:30643562 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.95-1185C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643562 | |||||||
| chr3:30643574 | G | C | 1 | a0001c0001t0003g0114 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.95-1173G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643574 | |||||||
| chr3:30643577 | T | C | 1 | a0001c0001t0026g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.95-1170T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643577 | |||||||
| chr3:30643608 | A | T | 1 | a0001c0001t0001g0099 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.95-1139A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643608 | |||||||
| chr3:30643636 | T | G | 13 | a0001c0001t0001g0123 a0001c0001t0001g0144 a0001c0001t0001g0154 others(10): Show |
14 | HG00140.hp1 HG00280.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.95-1111T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643636 | |||||||
| chr3:30643824 | A | C | 2 | a0001c0001t0007g0035 a0001c0001t0034g0033 |
2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.95-923A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643824 | |||||||
| chr3:30643946 | G | A | 13 | a0001c0001t0001g0123 a0001c0001t0001g0144 a0001c0001t0001g0154 others(10): Show |
14 | HG00140.hp1 HG00280.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.95-801G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643946 | |||||||
| chr3:30643947 | G | C | 9 | a0001c0001t0002g0034 a0001c0001t0015g0386 a0001c0003t0003g0344 others(6): Show |
9 | HG01891.hp1 HG02280.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-800G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643947 | |||||||
| chr3:30644029 | G | A | 2 | a0001c0001t0007g0035 a0001c0001t0034g0033 |
2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.95-718G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30644029 | |||||||
| chr3:30644123 | G | C | 11 | a0001c0001t0001g0147 a0001c0001t0004g0004 a0001c0001t0004g0030 others(8): Show |
12 | HG01934.hp2 HG02109.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.95-624G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30644123 | |||||||
| chr3:30644128 | A | G | 13 | a0001c0001t0001g0123 a0001c0001t0001g0144 a0001c0001t0001g0154 others(10): Show |
14 | HG00140.hp1 HG00280.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.95-619A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30644128 | |||||||
| chr3:30644196 | G | A | 6 | a0001c0001t0001g0137 a0001c0001t0001g0247 a0001c0001t0002g0231 others(3): Show |
7 | HG00735.hp1 HG01106.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-551G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30644196 | |||||||
| chr3:30644232 | T | C | 2 | a0001c0001t0007g0035 a0001c0001t0034g0033 |
2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.95-515T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30644232 | |||||||
| chr3:30644430 | G | T | 1 | a0001c0001t0004g0328 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.95-317G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30644430 | |||||||
| chr3:30644588 | C | A | 1 | a0001c0004t0008g0339 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.95-159C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30644588 | |||||||
| chr3:30644922 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(189): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
splice_region_variant&intron_variant | LOW | c.263+7A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30644922 | |||||||
| chr3:30644937 | T | C | 1 | a0001c0001t0002g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.263+22T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30644937 | |||||||
| chr3:30645135 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(189): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.263+220T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645135 | |||||||
| chr3:30645155 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(189): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.263+240T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645155 | |||||||
| chr3:30645248 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(189): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.263+333G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645248 | |||||||
| chr3:30645290 | C | G | 13 | a0001c0001t0001g0123 a0001c0001t0001g0144 a0001c0001t0001g0154 others(10): Show |
14 | HG00140.hp1 HG00280.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.263+375C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645290 | |||||||
| chr3:30645332 | G | A | 2 | a0001c0001t0007g0035 a0001c0001t0034g0033 |
2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.263+417G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645332 | |||||||
| chr3:30645405 | T | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(189): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.263+490T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645405 | |||||||
| chr3:30645439 | T | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(189): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.263+524T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645439 | |||||||
| chr3:30645491 | C | CTTTTTTT | 29 | a0001c0001t0001g0123 a0001c0001t0001g0144 a0001c0001t0001g0147 others(26): Show |
31 | HG00140.hp1 HG00280.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.263+582_263+588dup others(7): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30645491 | ||||||
| chr3:30645491 | C | CTTTTTTT others(1): Show |
150 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(147): Show |
151 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.263+581_263+588dup others(8): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30645491 | ||||||
| chr3:30645491 | C | CTTTTTTT others(2): Show |
9 | a0001c0001t0001g0104 a0001c0001t0001g0259 a0001c0001t0002g0124 others(6): Show |
9 | HG01884.hp1 HG03688.hp2 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.263+580_263+588dup others(9): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30645491 | ||||||
| chr3:30645491 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0001g0073 a0001c0001t0003g0223 a0001c0001t0007g0035 others(1): Show |
4 | HG00621.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+579_263+588dup others(10): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30645491 | ||||||
| chr3:30645531 | G | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(176): Show |
181 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.263+616G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645531 | |||||||
| chr3:30645538 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(189): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.263+623T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645538 | |||||||
| chr3:30645590 | T | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(189): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.263+675T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645590 | |||||||
| chr3:30645665 | T | C | 4 | a0001c0001t0001g0376 a0001c0001t0001g0377 a0001c0001t0001g0378 others(1): Show |
4 | NA18944.hp1 NA18951.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+750T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645665 | |||||||
| chr3:30645674 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.263+759C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645674 | |||||||
| chr3:30645770 | G | A | 2 | a0001c0001t0007g0035 a0001c0001t0034g0033 |
2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.263+855G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645770 | |||||||
| chr3:30645781 | C | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(189): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.263+866C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645781 | |||||||
| chr3:30645819 | C | CCTCT | 12 | a0001c0001t0001g0123 a0001c0001t0001g0144 a0001c0001t0001g0154 others(9): Show |
13 | HG00140.hp1 HG00280.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.263+924_263+927dup others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30645819 | ||||||
| chr3:30645819 | C | CCTCTCT | 165 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0058 others(162): Show |
166 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.263+922_263+927dup others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30645819 | ||||||
| chr3:30645819 | C | CCTCTCTC others(1): Show |
11 | a0001c0001t0001g0001 a0001c0001t0001g0087 a0001c0001t0001g0104 others(8): Show |
12 | HG00738.hp2 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.263+920_263+927dup others(8): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30645819 | ||||||
| chr3:30645819 | CCTCT | C | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | NA19011.hp1 NA19063.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+924_263+927del others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30645819 | ||||||
| chr3:30645968 | G | T | 1 | a0001c0001t0004g0349 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.263+1053G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645968 | |||||||
| chr3:30646017 | C | A | 1 | a0001c0001t0005g0015 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.263+1102C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30646017 | |||||||
| chr3:30646062 | A | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(177): Show |
182 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.263+1147A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30646062 | |||||||
| chr3:30646167 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.263+1252T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30646167 | |||||||
| chr3:30646223 | C | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(190): Show |
196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.263+1308C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30646223 | |||||||
| chr3:30646390 | A | G | 2 | a0001c0001t0011g0010 a0004c0007t0004g0355 |
2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.263+1475A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30646390 | |||||||
| chr3:30646477 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(190): Show |
196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.263+1562T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30646477 | |||||||
| chr3:30646532 | G | A | 23 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0077 others(20): Show |
23 | HG02027.hp1 HG02027.hp2 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.263+1617G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30646532 | |||||||
| chr3:30646547 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.263+1632G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30646547 | |||||||
| chr3:30646694 | T | C | 13 | a0001c0001t0001g0073 a0001c0001t0001g0141 a0001c0001t0001g0189 others(10): Show |
13 | HG00408.hp2 HG00621.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.263+1779T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30646694 | |||||||
| chr3:30646903 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.263+1988A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30646903 | |||||||
| chr3:30647019 | G | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(177): Show |
182 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.263+2104G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647019 | |||||||
| chr3:30647148 | C | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(177): Show |
182 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.263+2233C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647148 | |||||||
| chr3:30647241 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(98): Show |
102 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.263+2326C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647241 | |||||||
| chr3:30647265 | T | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(138): Show |
144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.263+2350T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647265 | |||||||
| chr3:30647294 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.263+2379A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647294 | |||||||
| chr3:30647306 | A | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0094 a0001c0001t0001g0271 |
3 | HG00597.hp2 NA18966.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.263+2391A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647306 | |||||||
| chr3:30647362 | A | G | 2 | a0001c0001t0006g0363 a0001c0001t0010g0359 |
2 | HG00639.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.263+2447A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647362 | |||||||
| chr3:30647560 | T | TTTCA | 13 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0181 others(10): Show |
13 | HG00408.hp1 HG00735.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.263+2672_263+2675d others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30647560 | ||||||
| chr3:30647560 | TTTCA | T | 136 | a0001c0001t0001g0064 a0001c0001t0001g0070 a0001c0001t0001g0081 others(133): Show |
136 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.263+2672_263+2675d others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30647560 | ||||||
| chr3:30647564 | A | C | 2 | a0001c0001t0007g0035 a0001c0001t0034g0033 |
2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.263+2649A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647564 | |||||||
| chr3:30647568 | A | C | 2 | a0001c0001t0007g0035 a0001c0001t0034g0033 |
2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.263+2653A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647568 | |||||||
| chr3:30647668 | A | AATT | 111 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(108): Show |
112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.264-2586_264-2584d others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30647668 | ||||||
| chr3:30647702 | A | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(108): Show |
112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.264-2568A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647702 | |||||||
| chr3:30647710 | A | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(108): Show |
112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.264-2560A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647710 | |||||||
| chr3:30647718 | C | G | 30 | a0001c0001t0001g0123 a0001c0001t0001g0144 a0001c0001t0001g0147 others(27): Show |
32 | HG00140.hp1 HG00280.hp2 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.264-2552C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647718 | |||||||
| chr3:30647728 | G | GTGCAA | 13 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0077 others(10): Show |
13 | HG02129.hp1 HG02683.hp2 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.264-2539_264-2535d others(7): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30647728 | ||||||
| chr3:30647737 | C | T | 3 | a0001c0003t0021g0354 a0001c0004t0008g0043 a0001c0004t0008g0069 |
3 | HG02258.hp2 HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.264-2533C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647737 | |||||||
| chr3:30647811 | T | G | 265 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(262): Show |
268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.264-2459T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647811 | |||||||
| chr3:30647894 | G | GT | 3 | a0001c0001t0001g0350 a0001c0003t0007g0351 a0001c0003t0007g0352 |
3 | HG02809.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.264-2375dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30647894 | ||||||
| chr3:30647928 | C | T | 1 | a0001c0001t0003g0270 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.264-2342C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647928 | |||||||
| chr3:30647929 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(94): Show |
98 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.264-2341G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647929 | |||||||
| chr3:30647992 | A | G | 1 | a0001c0001t0001g0306 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.264-2278A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647992 | |||||||
| chr3:30648013 | G | T | 3 | a0001c0003t0001g0366 a0001c0003t0001g0367 a0001c0004t0011g0369 |
3 | HG02145.hp1 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.264-2257G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648013 | |||||||
| chr3:30648020 | T | C | 1 | a0001c0001t0001g0273 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.264-2250T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648020 | |||||||
| chr3:30648026 | A | G | 1 | a0001c0001t0004g0044 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.264-2244A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648026 | |||||||
| chr3:30648105 | T | A | 11 | a0001c0001t0001g0147 a0001c0001t0004g0004 a0001c0001t0004g0030 others(8): Show |
12 | HG01934.hp2 HG02109.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.264-2165T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648105 | |||||||
| chr3:30648263 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(113): Show |
118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.264-2007G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648263 | |||||||
| chr3:30648392 | G | A | 4 | a0001c0001t0020g0346 a0001c0004t0003g0224 a0001c0004t0008g0125 others(1): Show |
4 | HG02723.hp2 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-1878G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648392 | |||||||
| chr3:30648410 | A | G | 1 | a0001c0001t0007g0353 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.264-1860A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648410 | |||||||
| chr3:30648419 | T | TAC | 17 | a0001c0001t0001g0075 a0001c0001t0001g0089 a0001c0001t0001g0092 others(14): Show |
17 | HG00741.hp1 HG00741.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.264-1809_264-1808d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648419 | ||||||
| chr3:30648419 | T | TACAC | 20 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0122 others(17): Show |
21 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.264-1811_264-1808d others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648419 | ||||||
| chr3:30648419 | T | TACACAC | 20 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0083 others(17): Show |
21 | HG00621.hp1 HG00735.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.264-1813_264-1808d others(8): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648419 | ||||||
| chr3:30648419 | T | TACACACA others(1): Show |
18 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0001g0077 others(15): Show |
18 | HG00280.hp1 HG01081.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.264-1815_264-1808d others(10): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648419 | ||||||
| chr3:30648419 | T | TACACACA others(3): Show |
6 | a0001c0001t0001g0074 a0001c0001t0003g0270 a0001c0001t0004g0345 others(3): Show |
6 | HG01884.hp2 HG02970.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-1817_264-1808d others(12): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648419 | ||||||
| chr3:30648419 | T | TACACACA others(9): Show |
3 | a0001c0001t0007g0348 a0001c0001t0034g0033 a0001c0011t0036g0047 |
3 | HG01255.hp1 HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.264-1823_264-1808d others(18): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648419 | ||||||
| chr3:30648419 | TAC | T | 6 | a0001c0001t0001g0081 a0001c0001t0001g0329 a0001c0001t0015g0386 others(3): Show |
6 | HG02630.hp1 HG03195.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-1809_264-1808d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648419 | ||||||
| chr3:30648419 | TACAC | T | 3 | a0001c0001t0001g0384 a0001c0001t0001g0385 a0001c0002t0001g0120 |
3 | HG03130.hp1 NA18990.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.264-1811_264-1808d others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648419 | ||||||
| chr3:30648419 | TACACACA others(5): Show |
T | 17 | a0001c0001t0001g0147 a0001c0001t0002g0034 a0001c0001t0004g0004 others(14): Show |
18 | HG01934.hp2 HG02109.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.264-1819_264-1808d others(14): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648419 | ||||||
| chr3:30648419 | TACACACA others(7): Show |
T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(94): Show |
98 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.264-1821_264-1808d others(16): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648419 | ||||||
| chr3:30648427 | C | CACAA | 4 | a0001c0003t0035g0026 a0001c0004t0003g0224 a0001c0004t0008g0125 others(1): Show |
4 | HG01891.hp1 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-1840_264-1839i others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648427 | ||||||
| chr3:30648460 | A | ACACACAC others(4): Show |
1 | a0001c0001t0019g0305 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.264-1808_264-1807i others(13): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | ||||||
| chr3:30648460 | A | ACACACAC others(8): Show |
2 | a0001c0001t0001g0333 a0001c0002t0042g0105 |
2 | HG02132.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.264-1808_264-1807i others(17): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | ||||||
| chr3:30648460 | A | ACACACAC others(17): Show |
4 | a0001c0001t0001g0253 a0001c0001t0001g0336 a0001c0001t0003g0167 others(1): Show |
4 | HG01192.hp1 HG01358.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-1808_264-1807i others(26): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | ||||||
| chr3:30648460 | A | ACACACAC others(15): Show |
7 | a0001c0001t0001g0121 a0001c0001t0001g0218 a0001c0001t0001g0334 others(4): Show |
7 | HG00544.hp1 HG02738.hp1 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.264-1808_264-1807i others(24): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | ||||||
| chr3:30648460 | A | ACACACAC others(13): Show |
9 | a0001c0001t0001g0263 a0001c0001t0001g0335 a0001c0001t0002g0117 others(6): Show |
9 | HG00544.hp2 HG02135.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.264-1808_264-1807i others(22): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | ||||||
| chr3:30648460 | A | ACACACAC others(11): Show |
11 | a0001c0001t0001g0064 a0001c0001t0001g0084 a0001c0001t0001g0312 others(8): Show |
11 | HG01255.hp2 HG02155.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.264-1808_264-1807i others(20): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | ||||||
| chr3:30648460 | A | ACACACAC others(9): Show |
8 | a0001c0001t0001g0187 a0001c0001t0001g0297 a0001c0001t0001g0313 others(5): Show |
8 | HG01358.hp1 HG01981.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.264-1808_264-1807i others(18): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | ||||||
| chr3:30648460 | A | ACACACAC others(7): Show |
24 | a0001c0001t0001g0068 a0001c0001t0001g0094 a0001c0001t0001g0109 others(21): Show |
24 | HG00597.hp1 HG00639.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.264-1808_264-1807i others(16): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | ||||||
| chr3:30648460 | A | ACACACAC others(5): Show |
18 | a0001c0001t0001g0170 a0001c0001t0001g0271 a0001c0001t0001g0302 others(15): Show |
18 | HG00597.hp2 HG00639.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.264-1808_264-1807i others(14): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | ||||||
| chr3:30648460 | A | ACACACAC others(9): Show |
2 | a0001c0001t0001g0373 a0001c0002t0001g0061 |
2 | NA18982.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.264-1808_264-1807i others(18): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | ||||||
| chr3:30648460 | A | ACACACAC others(3): Show |
15 | a0001c0001t0001g0110 a0001c0001t0001g0237 a0001c0001t0001g0282 others(12): Show |
15 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.264-1808_264-1807i others(12): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | ||||||
| chr3:30648460 | A | ACACACAC others(1): Show |
3 | a0001c0001t0001g0070 a0001c0001t0014g0149 a0001c0002t0029g0143 |
3 | HG01928.hp2 HG02280.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.264-1808_264-1807i others(10): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | ||||||
| chr3:30648460 | A | ACACACAC others(5): Show |
1 | a0001c0002t0001g0162 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.264-1808_264-1807i others(14): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | ||||||
| chr3:30648460 | A | ACACACC | 3 | a0001c0001t0001g0306 a0001c0003t0021g0354 a0001c0004t0008g0339 |
3 | HG02258.hp1 HG02258.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.264-1808_264-1807i others(8): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | ||||||
| chr3:30648460 | A | ACC | 5 | a0001c0001t0001g0296 a0001c0001t0001g0325 a0001c0001t0003g0368 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-1809_264-1808i others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | ||||||
| chr3:30648460 | A | C | 6 | a0001c0001t0001g0081 a0001c0001t0010g0365 a0001c0002t0001g0120 others(3): Show |
6 | HG02145.hp1 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-1810A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648460 | |||||||
| chr3:30648470 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.264-1800G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648470 | |||||||
| chr3:30648534 | T | C | 8 | a0001c0001t0001g0123 a0001c0001t0001g0154 a0001c0001t0001g0236 others(5): Show |
9 | HG00140.hp1 HG00280.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.264-1736T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648534 | |||||||
| chr3:30648576 | G | A | 2 | a0001c0004t0008g0125 a0001c0004t0008g0337 |
2 | HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.264-1694G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648576 | |||||||
| chr3:30648656 | T | C | 1 | a0001c0001t0022g0112 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.264-1614T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648656 | |||||||
| chr3:30648721 | G | A | 2 | a0001c0001t0003g0368 a0001c0001t0016g0300 |
2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.264-1549G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648721 | |||||||
| chr3:30648805 | G | T | 2 | a0001c0001t0006g0021 a0001c0004t0014g0262 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-1465G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648805 | |||||||
| chr3:30648823 | T | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0058 others(93): Show |
97 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.264-1447T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648823 | |||||||
| chr3:30648824 | T | A | 77 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0077 others(74): Show |
77 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.264-1446T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648824 | |||||||
| chr3:30648838 | C | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0058 others(92): Show |
96 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.264-1432C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648838 | |||||||
| chr3:30648901 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0058 others(89): Show |
93 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.264-1369A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648901 | |||||||
| chr3:30648932 | A | G | 189 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(186): Show |
191 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(188): Show |
intron_variant | MODIFIER | c.264-1338A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648932 | |||||||
| chr3:30649013 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.264-1257G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649013 | |||||||
| chr3:30649099 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.264-1171T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649099 | |||||||
| chr3:30649156 | C | T | 2 | a0001c0003t0007g0351 a0001c0003t0007g0352 |
2 | HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.264-1114C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649156 | |||||||
| chr3:30649166 | G | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(89): Show |
93 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.264-1104G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649166 | |||||||
| chr3:30649207 | G | A | 1 | a0001c0001t0002g0194 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.264-1063G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649207 | |||||||
| chr3:30649256 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(93): Show |
97 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.264-1014G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649256 | |||||||
| chr3:30649259 | T | C | 23 | a0001c0001t0001g0113 a0001c0001t0001g0302 a0001c0001t0001g0350 others(20): Show |
23 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.264-1011T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649259 | |||||||
| chr3:30649313 | T | C | 22 | a0001c0001t0001g0113 a0001c0001t0001g0302 a0001c0001t0001g0350 others(19): Show |
22 | HG01109.hp2 HG02145.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.264-957T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649313 | |||||||
| chr3:30649419 | A | G | 79 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0077 others(76): Show |
79 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.264-851A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649419 | |||||||
| chr3:30649586 | C | T | 366 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(363): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(366): Show |
intron_variant | MODIFIER | c.264-684C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649586 | |||||||
| chr3:30649718 | G | A | 1 | a0001c0001t0001g0361 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.264-552G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649718 | |||||||
| chr3:30649815 | A | G | 1 | a0001c0002t0038g0045 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.264-455A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649815 | |||||||
| chr3:30649818 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(93): Show |
97 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.264-452G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649818 | |||||||
| chr3:30649827 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(93): Show |
97 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.264-443G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649827 | |||||||
| chr3:30649846 | C | G | 366 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(363): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(366): Show |
intron_variant | MODIFIER | c.264-424C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649846 | |||||||
| chr3:30649888 | A | G | 1 | a0001c0002t0001g0343 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.264-382A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649888 | |||||||
| chr3:30649949 | T | G | 1 | a0001c0001t0004g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.264-321T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649949 | |||||||
| chr3:30649981 | G | A | 363 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(360): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.264-289G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649981 | |||||||
| chr3:30649999 | C | T | 3 | a0001c0001t0001g0090 a0001c0001t0001g0093 a0001c0001t0001g0106 |
3 | NA18944.hp2 NA19010.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.264-271C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649999 | |||||||
| chr3:30650073 | GA | G | 11 | a0001c0001t0007g0035 a0001c0001t0011g0010 a0001c0001t0034g0033 others(8): Show |
11 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.264-193delA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30650073 | ||||||
| chr3:30650113 | C | A | 2 | a0001c0001t0001g0299 a0001c0001t0001g0324 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.264-157C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30650113 | |||||||
| chr3:30650142 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.264-128G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30650142 | |||||||
| chr3:30650183 | G | A | 1 | a0001c0001t0001g0360 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.264-87G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30650183 | |||||||
| chr3:30650212 | T | C | 1 | a0001c0002t0038g0045 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.264-58T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30650212 | |||||||
| chr3:30650235 | T | G | 3 | a0001c0001t0006g0021 a0001c0004t0014g0262 a0001c0004t0032g0032 |
3 | HG01934.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-35T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30650235 | |||||||
| chr3:30650534 | A | G | 2 | a0001c0003t0003g0344 a0001c0003t0006g0040 |
2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.454+74A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30650534 | |||||||
| chr3:30650626 | G | C | 9 | a0001c0001t0007g0035 a0001c0001t0011g0010 a0001c0001t0034g0033 others(6): Show |
9 | HG01109.hp2 HG02145.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.454+166G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30650626 | |||||||
| chr3:30650708 | T | G | 1 | a0001c0001t0001g0076 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.454+248T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30650708 | |||||||
| chr3:30650727 | T | C | 366 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(363): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(366): Show |
intron_variant | MODIFIER | c.454+267T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30650727 | |||||||
| chr3:30650939 | T | C | 1 | a0001c0003t0035g0026 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.454+479T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30650939 | |||||||
| chr3:30650959 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(93): Show |
97 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.454+499C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30650959 | |||||||
| chr3:30651188 | G | C | 1 | a0001c0001t0003g0248 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.454+728G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651188 | |||||||
| chr3:30651267 | C | G | 3 | a0001c0001t0001g0253 a0001c0001t0001g0370 a0001c0001t0003g0167 |
3 | HG01192.hp1 HG01358.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.454+807C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651267 | |||||||
| chr3:30651274 | C | A | 1 | a0001c0001t0002g0096 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.454+814C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651274 | |||||||
| chr3:30651368 | A | G | 1 | a0001c0001t0001g0360 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.454+908A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651368 | |||||||
| chr3:30651375 | C | T | 12 | a0001c0001t0001g0147 a0001c0001t0002g0034 a0001c0001t0004g0004 others(9): Show |
13 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.454+915C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651375 | |||||||
| chr3:30651436 | A | G | 5 | a0001c0001t0001g0253 a0001c0001t0001g0370 a0001c0001t0002g0128 others(2): Show |
5 | HG01192.hp1 HG01255.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+976A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651436 | |||||||
| chr3:30651496 | C | A | 1 | a0001c0001t0001g0218 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.454+1036C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651496 | |||||||
| chr3:30651603 | A | G | 1 | a0001c0001t0003g0270 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.454+1143A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651603 | |||||||
| chr3:30651766 | A | G | 1 | a0001c0001t0001g0329 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.454+1306A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651766 | |||||||
| chr3:30651779 | C | T | 13 | a0001c0001t0007g0035 a0001c0001t0011g0010 a0001c0001t0034g0033 others(10): Show |
13 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.454+1319C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651779 | |||||||
| chr3:30651989 | T | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0055 a0001c0001t0001g0383 |
3 | HG00621.hp1 HG02071.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.454+1529T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651989 | |||||||
| chr3:30652002 | C | T | 1 | a0001c0011t0036g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.454+1542C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652002 | |||||||
| chr3:30652030 | T | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(210): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.454+1570T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652030 | |||||||
| chr3:30652058 | A | G | 1 | a0001c0001t0006g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.454+1598A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652058 | |||||||
| chr3:30652070 | T | G | 3 | a0001c0001t0006g0021 a0001c0004t0014g0262 a0001c0004t0032g0032 |
3 | HG01934.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.454+1610T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652070 | |||||||
| chr3:30652151 | C | T | 145 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0054 others(142): Show |
146 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.454+1691C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652151 | |||||||
| chr3:30652232 | G | GT | 276 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(273): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.454+1794dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30652232 | ||||||
| chr3:30652232 | G | GTT | 49 | a0001c0001t0001g0051 a0001c0001t0001g0067 a0001c0001t0001g0073 others(46): Show |
49 | HG00544.hp1 HG00621.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.454+1793_454+1794d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30652232 | ||||||
| chr3:30652232 | G | GTTT | 17 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0090 others(14): Show |
17 | HG00558.hp2 HG00738.hp2 HG02132.hp1 others(14): Show |
intron_variant | MODIFIER | c.454+1792_454+1794d others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30652232 | ||||||
| chr3:30652232 | GTTTT | G | 9 | a0001c0001t0001g0049 a0001c0002t0001g0062 a0001c0002t0001g0065 others(6): Show |
9 | HG00544.hp2 HG00597.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.454+1791_454+1794d others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30652232 | ||||||
| chr3:30652549 | G | C | 3 | a0001c0003t0021g0354 a0001c0004t0008g0043 a0001c0004t0008g0069 |
3 | HG02258.hp2 HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.454+2089G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652549 | |||||||
| chr3:30652628 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(95): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.454+2168G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652628 | |||||||
| chr3:30652643 | A | T | 365 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(362): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(365): Show |
intron_variant | MODIFIER | c.454+2183A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652643 | |||||||
| chr3:30652795 | A | G | 2 | a0001c0003t0003g0344 a0001c0003t0006g0040 |
2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.454+2335A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652795 | |||||||
| chr3:30652872 | A | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(94): Show |
98 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.454+2412A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652872 | |||||||
| chr3:30652921 | C | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(96): Show |
100 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.454+2461C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652921 | |||||||
| chr3:30653057 | G | A | 1 | a0001c0001t0002g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.454+2597G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653057 | |||||||
| chr3:30653250 | C | CT | 21 | a0001c0001t0001g0147 a0001c0001t0002g0034 a0001c0001t0004g0004 others(18): Show |
22 | HG02109.hp1 HG02109.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.454+2809dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30653250 | ||||||
| chr3:30653250 | C | CTTT | 15 | a0001c0001t0001g0091 a0001c0001t0001g0110 a0001c0001t0001g0189 others(12): Show |
15 | HG00558.hp2 HG01109.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.454+2807_454+2809d others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30653250 | ||||||
| chr3:30653250 | C | CTTTT | 198 | a0001c0001t0001g0006 a0001c0001t0001g0049 a0001c0001t0001g0051 others(195): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.454+2806_454+2809d others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30653250 | ||||||
| chr3:30653250 | C | CTTTTT | 17 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0074 others(14): Show |
17 | HG01433.hp1 HG02056.hp1 HG02738.hp2 others(14): Show |
intron_variant | MODIFIER | c.454+2805_454+2809d others(7): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30653250 | ||||||
| chr3:30653250 | CTTT | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0058 others(91): Show |
95 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.454+2807_454+2809d others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30653250 | ||||||
| chr3:30653269 | T | G | 3 | a0001c0001t0006g0021 a0001c0004t0014g0262 a0001c0004t0032g0032 |
3 | HG01934.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.454+2809T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653269 | |||||||
| chr3:30653277 | A | T | 1 | a0001c0001t0002g0284 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.454+2817A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653277 | |||||||
| chr3:30653294 | C | T | 1 | a0001c0001t0003g0270 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.454+2834C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653294 | |||||||
| chr3:30653295 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(96): Show |
100 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.454+2835G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653295 | |||||||
| chr3:30653316 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(94): Show |
98 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.454+2856G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653316 | |||||||
| chr3:30653341 | T | C | 28 | a0001c0001t0001g0147 a0001c0001t0001g0361 a0001c0001t0002g0034 others(25): Show |
29 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.454+2881T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653341 | |||||||
| chr3:30653412 | C | T | 1 | a0001c0002t0002g0203 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.454+2952C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653412 | |||||||
| chr3:30653424 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(96): Show |
100 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.454+2964A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653424 | |||||||
| chr3:30653520 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(96): Show |
100 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.454+3060A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653520 | |||||||
| chr3:30653541 | C | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(94): Show |
98 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.454+3081C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653541 | |||||||
| chr3:30653542 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(96): Show |
100 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.454+3082A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653542 | |||||||
| chr3:30653554 | AATGAAAA others(55): Show |
A | 1 | a0001c0002t0001g0274 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.454+3100_454+3161d others(64): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30653554 | ||||||
| chr3:30653599 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(94): Show |
98 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.454+3139G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653599 | |||||||
| chr3:30653660 | G | A | 25 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0091 others(22): Show |
25 | HG00099.hp2 HG00140.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.454+3200G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653660 | |||||||
| chr3:30653737 | A | G | 4 | a0001c0001t0001g0070 a0001c0001t0001g0175 a0001c0001t0001g0296 others(1): Show |
4 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.454+3277A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653737 | |||||||
| chr3:30654585 | A | G | 13 | a0001c0001t0001g0050 a0001c0001t0001g0141 a0001c0001t0001g0279 others(10): Show |
13 | HG00408.hp2 HG00673.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.454+4125A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30654585 | |||||||
| chr3:30654593 | C | T | 1 | a0001c0001t0003g0270 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.454+4133C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30654593 | |||||||
| chr3:30654623 | T | G | 1 | a0001c0001t0004g0004 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.454+4163T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30654623 | |||||||
| chr3:30654759 | T | C | 362 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(359): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.454+4299T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30654759 | |||||||
| chr3:30654782 | C | G | 2 | a0001c0003t0003g0344 a0001c0003t0006g0040 |
2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.454+4322C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30654782 | |||||||
| chr3:30655001 | G | T | 1 | a0001c0002t0013g0219 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.454+4541G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655001 | |||||||
| chr3:30655071 | T | C | 264 | a0001c0001t0001g0006 a0001c0001t0001g0049 a0001c0001t0001g0051 others(261): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.454+4611T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655071 | |||||||
| chr3:30655152 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(95): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.454+4692G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655152 | |||||||
| chr3:30655257 | C | G | 2 | a0001c0001t0001g0333 a0001c0002t0001g0238 |
2 | HG03654.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.454+4797C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655257 | |||||||
| chr3:30655261 | C | T | 3 | a0001c0001t0006g0021 a0001c0004t0014g0262 a0001c0004t0032g0032 |
3 | HG01934.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.454+4801C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655261 | |||||||
| chr3:30655284 | T | C | 1 | a0001c0001t0002g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.454+4824T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655284 | |||||||
| chr3:30655324 | T | C | 331 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(328): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.454+4864T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655324 | |||||||
| chr3:30655357 | A | G | 3 | a0001c0001t0001g0361 a0001c0003t0003g0344 a0001c0003t0006g0040 |
3 | HG03195.hp2 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.454+4897A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655357 | |||||||
| chr3:30655422 | A | C | 1 | a0003c0006t0002g0207 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.454+4962A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655422 | |||||||
| chr3:30655490 | A | T | 3 | a0001c0001t0006g0021 a0001c0004t0014g0262 a0001c0004t0032g0032 |
3 | HG01934.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.454+5030A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655490 | |||||||
| chr3:30655838 | C | G | 365 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(362): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(365): Show |
intron_variant | MODIFIER | c.454+5378C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655838 | |||||||
| chr3:30655945 | C | T | 19 | a0001c0001t0001g0147 a0001c0001t0001g0361 a0001c0001t0002g0034 others(16): Show |
20 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.454+5485C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655945 | |||||||
| chr3:30655965 | TG | T | 13 | a0001c0001t0001g0050 a0001c0001t0001g0141 a0001c0001t0001g0279 others(10): Show |
13 | HG00408.hp2 HG00673.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.454+5509delG | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30655965 | ||||||
| chr3:30656096 | A | T | 1 | a0001c0001t0002g0284 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.454+5636A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656096 | |||||||
| chr3:30656169 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(96): Show |
100 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.454+5709A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656169 | |||||||
| chr3:30656211 | C | G | 1 | a0001c0001t0004g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.454+5751C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656211 | |||||||
| chr3:30656397 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(96): Show |
100 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.454+5937A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656397 | |||||||
| chr3:30656417 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(95): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.454+5957A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656417 | |||||||
| chr3:30656444 | A | G | 117 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0077 others(114): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.454+5984A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656444 | |||||||
| chr3:30656453 | G | A | 5 | a0001c0001t0016g0301 a0001c0004t0003g0224 a0001c0004t0008g0125 others(2): Show |
5 | HG02258.hp1 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+5993G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656453 | |||||||
| chr3:30656484 | A | G | 14 | a0001c0001t0001g0147 a0001c0001t0002g0034 a0001c0001t0004g0004 others(11): Show |
15 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.454+6024A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656484 | |||||||
| chr3:30656567 | G | C | 3 | a0001c0001t0006g0021 a0001c0004t0014g0262 a0001c0004t0032g0032 |
3 | HG01934.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.454+6107G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656567 | |||||||
| chr3:30656599 | G | C | 1 | a0001c0001t0001g0361 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.454+6139G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656599 | |||||||
| chr3:30656604 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(95): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.454+6144G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656604 | |||||||
| chr3:30656623 | G | A | 1 | a0001c0003t0001g0366 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.454+6163G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656623 | |||||||
| chr3:30656671 | A | G | 5 | a0001c0001t0011g0010 a0001c0003t0001g0294 a0001c0003t0001g0366 others(2): Show |
5 | HG01109.hp2 HG02145.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.454+6211A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656671 | |||||||
| chr3:30656678 | T | C | 1 | a0001c0012t0002g0097 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.454+6218T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656678 | |||||||
| chr3:30656800 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.454+6340A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656800 | |||||||
| chr3:30656900 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(95): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.454+6440T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656900 | |||||||
| chr3:30656911 | T | A | 1 | a0001c0002t0001g0130 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.454+6451T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656911 | |||||||
| chr3:30656978 | C | T | 4 | a0001c0001t0012g0116 a0001c0001t0012g0285 a0001c0001t0012g0304 others(1): Show |
4 | HG01106.hp1 HG01516.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.454+6518C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656978 | |||||||
| chr3:30657008 | ATGAAGTG others(7): Show |
A | 1 | a0001c0002t0038g0045 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.454+6553_454+6566d others(16): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30657008 | ||||||
| chr3:30657128 | G | A | 5 | a0001c0001t0001g0361 a0001c0002t0038g0045 a0001c0003t0021g0354 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+6668G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657128 | |||||||
| chr3:30657152 | A | G | 2 | a0001c0003t0003g0344 a0001c0003t0006g0040 |
2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.454+6692A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657152 | |||||||
| chr3:30657277 | C | G | 1 | a0001c0002t0001g0343 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.454+6817C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657277 | |||||||
| chr3:30657290 | G | A | 10 | a0001c0001t0001g0113 a0001c0001t0001g0302 a0001c0001t0001g0350 others(7): Show |
10 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.454+6830G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657290 | |||||||
| chr3:30657310 | G | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(95): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.454+6850G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657310 | |||||||
| chr3:30657323 | G | T | 1 | a0001c0001t0002g0284 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.454+6863G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657323 | |||||||
| chr3:30657329 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(95): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.454+6869G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657329 | |||||||
| chr3:30657408 | G | A | 2 | a0001c0003t0003g0344 a0001c0003t0006g0040 |
2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.454+6948G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657408 | |||||||
| chr3:30657411 | G | A | 5 | a0001c0001t0016g0301 a0001c0004t0003g0224 a0001c0004t0008g0125 others(2): Show |
5 | HG02258.hp1 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+6951G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657411 | |||||||
| chr3:30657425 | G | T | 2 | a0001c0003t0003g0344 a0001c0003t0006g0040 |
2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.454+6965G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657425 | |||||||
| chr3:30657485 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(93): Show |
97 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.454+7025G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657485 | |||||||
| chr3:30657611 | G | A | 2 | a0001c0001t0010g0365 a0001c0001t0025g0340 |
2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.454+7151G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657611 | |||||||
| chr3:30657735 | G | A | 2 | a0001c0003t0003g0344 a0001c0003t0006g0040 |
2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.454+7275G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657735 | |||||||
| chr3:30657798 | A | G | 1 | a0001c0001t0010g0365 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.454+7338A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657798 | |||||||
| chr3:30658290 | T | C | 238 | a0001c0001t0001g0006 a0001c0001t0001g0049 a0001c0001t0001g0051 others(235): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.454+7830T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30658290 | |||||||
| chr3:30658399 | T | C | 20 | a0001c0001t0001g0147 a0001c0001t0002g0034 a0001c0001t0004g0004 others(17): Show |
21 | HG02109.hp1 HG02109.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.454+7939T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30658399 | |||||||
| chr3:30658672 | A | G | 1 | a0001c0002t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.454+8212A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30658672 | |||||||
| chr3:30658925 | T | C | 1 | a0001c0001t0002g0278 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.454+8465T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30658925 | |||||||
| chr3:30658940 | C | T | 99 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0077 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.454+8480C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30658940 | |||||||
| chr3:30658949 | T | C | 239 | a0001c0001t0001g0006 a0001c0001t0001g0049 a0001c0001t0001g0051 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.454+8489T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30658949 | |||||||
| chr3:30659006 | A | G | 239 | a0001c0001t0001g0006 a0001c0001t0001g0049 a0001c0001t0001g0051 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.454+8546A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30659006 | |||||||
| chr3:30659097 | G | T | 1 | a0001c0001t0004g0349 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.454+8637G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30659097 | |||||||
| chr3:30659145 | C | T | 1 | a0001c0001t0002g0194 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.454+8685C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30659145 | |||||||
| chr3:30659210 | T | G | 2 | a0001c0003t0003g0344 a0001c0003t0006g0040 |
2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.454+8750T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30659210 | |||||||
| chr3:30659361 | T | C | 365 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(362): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(365): Show |
intron_variant | MODIFIER | c.454+8901T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30659361 | |||||||
| chr3:30659416 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.454+8956C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30659416 | |||||||
| chr3:30659430 | A | G | 247 | a0001c0001t0001g0006 a0001c0001t0001g0049 a0001c0001t0001g0051 others(244): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.454+8970A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30659430 | |||||||
| chr3:30659682 | C | G | 12 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(9): Show |
12 | NA18959.hp2 NA18960.hp1 NA18975.hp1 others(9): Show |
intron_variant | MODIFIER | c.454+9222C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30659682 | |||||||
| chr3:30660034 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.454+9574C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660034 | |||||||
| chr3:30660079 | T | C | 5 | a0001c0001t0016g0301 a0001c0004t0003g0224 a0001c0004t0008g0125 others(2): Show |
5 | HG02258.hp1 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+9619T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660079 | |||||||
| chr3:30660089 | T | A | 9 | a0001c0001t0001g0081 a0001c0001t0001g0361 a0001c0001t0002g0266 others(6): Show |
9 | HG01934.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.454+9629T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660089 | |||||||
| chr3:30660114 | A | G | 119 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0077 others(116): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.454+9654A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660114 | |||||||
| chr3:30660124 | T | C | 1 | a0001c0001t0001g0326 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.454+9664T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660124 | |||||||
| chr3:30660212 | T | G | 5 | a0001c0001t0016g0301 a0001c0004t0003g0224 a0001c0004t0008g0125 others(2): Show |
5 | HG02258.hp1 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+9752T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660212 | |||||||
| chr3:30660264 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0050 others(108): Show |
113 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.454+9804C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660264 | |||||||
| chr3:30660309 | T | C | 361 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(358): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.454+9849T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660309 | |||||||
| chr3:30660552 | C | T | 12 | a0001c0001t0001g0113 a0001c0001t0001g0302 a0001c0001t0001g0350 others(9): Show |
12 | HG01167.hp2 HG02451.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.454+10092C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660552 | |||||||
| chr3:30660628 | A | T | 1 | a0001c0001t0009g0254 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.454+10168A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660628 | |||||||
| chr3:30660648 | A | G | 366 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(363): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(366): Show |
intron_variant | MODIFIER | c.454+10188A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660648 | |||||||
| chr3:30660660 | A | T | 1 | a0001c0001t0012g0251 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.454+10200A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660660 | |||||||
| chr3:30660720 | G | T | 92 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0058 others(89): Show |
92 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.454+10260G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660720 | |||||||
| chr3:30660853 | T | C | 1 | a0001c0001t0002g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.454+10393T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660853 | |||||||
| chr3:30660975 | G | A | 1 | a0001c0001t0001g0260 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.454+10515G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660975 | |||||||
| chr3:30661073 | T | C | 4 | a0001c0003t0003g0344 a0001c0003t0006g0040 a0001c0003t0007g0351 others(1): Show |
4 | HG02809.hp2 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-10565T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30661073 | |||||||
| chr3:30661119 | C | A | 4 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0353 others(1): Show |
4 | HG00639.hp2 HG01255.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-10519C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30661119 | |||||||
| chr3:30661147 | A | C | 1 | a0001c0001t0001g0361 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.455-10491A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30661147 | |||||||
| chr3:30661151 | C | A | 2 | a0001c0001t0001g0058 a0001c0001t0027g0156 |
2 | NA18977.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.455-10487C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30661151 | |||||||
| chr3:30661151 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.455-10487C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30661151 | |||||||
| chr3:30661293 | ACT | A | 67 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0055 others(64): Show |
67 | HG00544.hp1 HG00621.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.455-10340_455-1033 others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30661293 | ||||||
| chr3:30662026 | C | A | 1 | a0001c0001t0001g0106 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.455-9612C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662026 | |||||||
| chr3:30662045 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.455-9593T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662045 | |||||||
| chr3:30662306 | A | T | 100 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(97): Show |
100 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.455-9332A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662306 | |||||||
| chr3:30662319 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0289 |
2 | HG00741.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.455-9319A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662319 | |||||||
| chr3:30662347 | C | T | 1 | a0001c0001t0004g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.455-9291C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662347 | |||||||
| chr3:30662350 | G | A | 4 | a0001c0001t0011g0010 a0001c0003t0001g0294 a0001c0003t0001g0366 others(1): Show |
4 | HG01109.hp2 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.455-9288G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662350 | |||||||
| chr3:30662438 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.455-9200G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662438 | |||||||
| chr3:30662467 | A | C | 4 | a0001c0001t0001g0361 a0001c0003t0021g0354 a0001c0004t0014g0262 others(1): Show |
4 | HG01934.hp2 HG02258.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-9171A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662467 | |||||||
| chr3:30662515 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0074 others(133): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.455-9123A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662515 | |||||||
| chr3:30662758 | T | C | 1 | a0001c0001t0004g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.455-8880T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662758 | |||||||
| chr3:30662838 | C | T | 1 | a0001c0003t0021g0354 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.455-8800C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662838 | |||||||
| chr3:30662954 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0074 others(146): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.455-8684T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662954 | |||||||
| chr3:30662955 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0074 others(132): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.455-8683A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662955 | |||||||
| chr3:30662984 | G | A | 4 | a0001c0001t0001g0361 a0001c0003t0021g0354 a0001c0004t0014g0262 others(1): Show |
4 | HG01934.hp2 HG02258.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-8654G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662984 | |||||||
| chr3:30663026 | T | C | 2 | a0001c0003t0003g0344 a0001c0003t0006g0040 |
2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.455-8612T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663026 | |||||||
| chr3:30663028 | A | G | 9 | a0001c0003t0003g0344 a0001c0003t0006g0040 a0001c0004t0003g0224 others(6): Show |
9 | HG02258.hp1 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.455-8610A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663028 | |||||||
| chr3:30663127 | A | G | 69 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0055 others(66): Show |
69 | HG00544.hp1 HG00621.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.455-8511A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663127 | |||||||
| chr3:30663184 | C | CTG | 55 | a0001c0001t0001g0064 a0001c0001t0001g0076 a0001c0001t0001g0090 others(52): Show |
55 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.455-8438_455-8437d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30663184 | ||||||
| chr3:30663287 | TA | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0051 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.455-8349delA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30663287 | ||||||
| chr3:30663332 | A | G | 1 | a0001c0001t0001g0361 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.455-8306A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663332 | |||||||
| chr3:30663363 | G | A | 24 | a0001c0001t0001g0111 a0001c0001t0001g0123 a0001c0001t0001g0152 others(21): Show |
26 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.455-8275G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663363 | |||||||
| chr3:30663395 | T | G | 1 | a0001c0003t0003g0344 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.455-8243T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663395 | |||||||
| chr3:30663767 | A | G | 27 | a0001c0001t0001g0147 a0001c0001t0001g0361 a0001c0001t0002g0034 others(24): Show |
28 | HG00639.hp2 HG01243.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.455-7871A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663767 | |||||||
| chr3:30663782 | T | C | 1 | a0001c0002t0001g0062 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.455-7856T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663782 | |||||||
| chr3:30663888 | G | A | 109 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0077 others(106): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.455-7750G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663888 | |||||||
| chr3:30663898 | C | T | 7 | a0001c0004t0003g0224 a0001c0004t0008g0043 a0001c0004t0008g0069 others(4): Show |
7 | HG02258.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.455-7740C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663898 | |||||||
| chr3:30663905 | G | C | 9 | a0001c0003t0003g0344 a0001c0003t0006g0040 a0001c0004t0003g0224 others(6): Show |
9 | HG02258.hp1 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.455-7733G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663905 | |||||||
| chr3:30663972 | C | CT | 108 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0077 others(105): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.455-7660dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30663972 | ||||||
| chr3:30663979 | G | T | 104 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0055 others(101): Show |
105 | HG00544.hp1 HG00621.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.455-7659G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663979 | |||||||
| chr3:30663980 | G | T | 1 | a0001c0002t0038g0045 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.455-7658G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663980 | |||||||
| chr3:30663981 | G | C | 1 | a0001c0003t0035g0026 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.455-7657G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663981 | |||||||
| chr3:30663988 | A | C | 3 | a0003c0006t0001g0327 a0003c0006t0002g0182 a0003c0006t0002g0207 |
3 | NA18612.hp2 NA19068.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.455-7650A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663988 | |||||||
| chr3:30664018 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(101): Show |
105 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.455-7620T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30664018 | |||||||
| chr3:30664149 | A | AT | 155 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(152): Show |
156 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.455-7474dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30664149 | ||||||
| chr3:30664149 | AT | A | 107 | a0001c0001t0001g0006 a0001c0001t0001g0088 a0001c0001t0001g0089 others(104): Show |
110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.455-7474delT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30664149 | ||||||
| chr3:30664274 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.455-7364A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30664274 | |||||||
| chr3:30664346 | A | G | 1 | a0001c0002t0001g0173 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.455-7292A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30664346 | |||||||
| chr3:30664453 | A | C | 1 | a0001c0002t0003g0341 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.455-7185A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30664453 | |||||||
| chr3:30664557 | A | G | 1 | a0001c0001t0004g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.455-7081A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30664557 | |||||||
| chr3:30664682 | G | T | 27 | a0001c0001t0001g0147 a0001c0001t0001g0361 a0001c0001t0002g0034 others(24): Show |
28 | HG00639.hp2 HG01243.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.455-6956G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30664682 | |||||||
| chr3:30664839 | A | G | 1 | a0001c0001t0003g0114 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.455-6799A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30664839 | |||||||
| chr3:30664898 | A | T | 68 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0055 others(65): Show |
68 | HG00544.hp1 HG00621.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.455-6740A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30664898 | |||||||
| chr3:30665362 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0121 |
2 | HG01256.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.455-6276A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30665362 | |||||||
| chr3:30665580 | G | A | 4 | a0001c0001t0001g0361 a0001c0003t0021g0354 a0001c0004t0014g0262 others(1): Show |
4 | HG01934.hp2 HG02258.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-6058G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30665580 | |||||||
| chr3:30665597 | C | T | 1 | a0001c0002t0001g0238 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.455-6041C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30665597 | |||||||
| chr3:30665623 | A | G | 22 | a0001c0001t0001g0147 a0001c0001t0002g0034 a0001c0001t0004g0004 others(19): Show |
23 | HG00639.hp2 HG01243.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.455-6015A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30665623 | |||||||
| chr3:30666252 | G | A | 191 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0054 others(188): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.455-5386G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666252 | |||||||
| chr3:30666270 | T | G | 8 | a0001c0001t0001g0087 a0001c0001t0001g0122 a0001c0001t0001g0129 others(5): Show |
8 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(5): Show |
intron_variant | MODIFIER | c.455-5368T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666270 | |||||||
| chr3:30666510 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.455-5128G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666510 | |||||||
| chr3:30666623 | G | T | 69 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0055 others(66): Show |
69 | HG00544.hp1 HG00621.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.455-5015G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666623 | |||||||
| chr3:30666632 | A | AC | 10 | a0001c0001t0001g0241 a0001c0001t0001g0259 a0001c0001t0001g0302 others(7): Show |
10 | HG00597.hp1 HG01109.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.455-4999dupC | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30666632 | ||||||
| chr3:30666639 | C | A | 9 | a0001c0003t0003g0344 a0001c0003t0006g0040 a0001c0004t0003g0224 others(6): Show |
9 | HG02258.hp1 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.455-4999C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666639 | |||||||
| chr3:30666639 | C | G | 1 | a0001c0002t0042g0105 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.455-4999C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666639 | |||||||
| chr3:30666640 | A | C | 1 | a0001c0001t0005g0023 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.455-4998A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666640 | |||||||
| chr3:30666641 | T | C | 190 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0054 others(187): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.455-4997T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666641 | |||||||
| chr3:30666649 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.455-4989C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666649 | |||||||
| chr3:30666717 | G | A | 1 | a0001c0002t0001g0234 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.455-4921G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666717 | |||||||
| chr3:30666742 | G | A | 2 | a0001c0003t0003g0344 a0001c0003t0006g0040 |
2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.455-4896G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666742 | |||||||
| chr3:30666765 | G | C | 191 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0054 others(188): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.455-4873G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666765 | |||||||
| chr3:30666806 | AT | A | 195 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0054 others(192): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.455-4818delT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30666806 | ||||||
| chr3:30666940 | G | A | 191 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0054 others(188): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.455-4698G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666940 | |||||||
| chr3:30667429 | T | C | 2 | a0001c0001t0001g0087 a0001c0001t0001g0129 |
2 | HG00738.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.455-4209T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30667429 | |||||||
| chr3:30668019 | A | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(158): Show |
162 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.455-3619A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668019 | |||||||
| chr3:30668126 | A | G | 1 | a0001c0001t0004g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.455-3512A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668126 | |||||||
| chr3:30668294 | G | C | 1 | a0001c0002t0010g0078 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.455-3344G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668294 | |||||||
| chr3:30668305 | T | C | 1 | a0001c0001t0010g0365 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.455-3333T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668305 | |||||||
| chr3:30668453 | T | C | 2 | a0001c0003t0007g0351 a0001c0003t0007g0352 |
2 | HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.455-3185T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668453 | |||||||
| chr3:30668524 | C | T | 1 | a0001c0001t0002g0194 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.455-3114C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668524 | |||||||
| chr3:30668568 | T | G | 157 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(154): Show |
157 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.455-3070T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668568 | |||||||
| chr3:30668581 | C | CT | 68 | a0001c0001t0001g0050 a0001c0001t0001g0064 a0001c0001t0001g0076 others(65): Show |
68 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.455-3049dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30668581 | ||||||
| chr3:30668645 | C | T | 82 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0058 others(79): Show |
82 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.455-2993C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668645 | |||||||
| chr3:30668648 | G | A | 68 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0055 others(65): Show |
68 | HG00544.hp1 HG00621.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.455-2990G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668648 | |||||||
| chr3:30668751 | A | G | 68 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0055 others(65): Show |
68 | HG00544.hp1 HG00621.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.455-2887A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668751 | |||||||
| chr3:30668967 | G | C | 1 | a0001c0001t0001g0199 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.455-2671G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668967 | |||||||
| chr3:30668971 | C | T | 1 | a0001c0012t0002g0097 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.455-2667C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668971 | |||||||
| chr3:30669003 | C | T | 26 | a0001c0001t0001g0050 a0001c0001t0001g0141 a0001c0001t0001g0206 others(23): Show |
26 | HG00408.hp2 HG00673.hp2 HG02071.hp2 others(23): Show |
intron_variant | MODIFIER | c.455-2635C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669003 | |||||||
| chr3:30669007 | G | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(194): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.455-2631G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669007 | |||||||
| chr3:30669048 | C | T | 1 | a0001c0004t0008g0337 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.455-2590C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669048 | |||||||
| chr3:30669121 | C | CA | 11 | a0001c0001t0001g0055 a0001c0001t0001g0067 a0001c0001t0001g0121 others(8): Show |
11 | HG00621.hp1 HG01361.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.455-2486dupA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | ||||||
| chr3:30669121 | C | CAA | 8 | a0001c0001t0003g0148 a0001c0001t0006g0018 a0001c0001t0006g0019 others(5): Show |
8 | HG02257.hp1 HG02896.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.455-2487_455-2486d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | ||||||
| chr3:30669121 | C | CAAAAAAA others(5): Show |
1 | a0001c0004t0008g0337 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.455-2497_455-2486d others(14): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | ||||||
| chr3:30669121 | C | CAAAAAAA others(6): Show |
1 | a0001c0004t0011g0369 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.455-2498_455-2486d others(15): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | ||||||
| chr3:30669121 | C | CAAAAAAA others(12): Show |
1 | a0001c0004t0003g0224 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.455-2504_455-2486d others(21): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | ||||||
| chr3:30669121 | CAAA | C | 9 | a0001c0001t0001g0050 a0001c0001t0001g0106 a0001c0001t0002g0265 others(6): Show |
9 | HG02698.hp2 HG02723.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.455-2488_455-2486d others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | ||||||
| chr3:30669121 | CAAAA | C | 25 | a0001c0001t0001g0141 a0001c0001t0001g0147 a0001c0001t0001g0279 others(22): Show |
26 | HG00408.hp2 HG00673.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.455-2489_455-2486d others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | ||||||
| chr3:30669121 | CAAAAAA | C | 6 | a0001c0001t0001g0131 a0001c0001t0004g0146 a0001c0003t0003g0344 others(3): Show |
6 | HG01934.hp2 HG02615.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.455-2491_455-2486d others(8): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | ||||||
| chr3:30669121 | CAAAAAAA | C | 6 | a0001c0001t0001g0240 a0001c0001t0001g0308 a0001c0001t0002g0166 others(3): Show |
6 | HG00099.hp1 HG00741.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.455-2492_455-2486d others(9): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | ||||||
| chr3:30669121 | CAAAAAAA others(1): Show |
C | 69 | a0001c0001t0001g0054 a0001c0001t0001g0064 a0001c0001t0001g0082 others(66): Show |
69 | HG00544.hp2 HG00597.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.455-2493_455-2486d others(10): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | ||||||
| chr3:30669121 | CAAAAAAA others(2): Show |
C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(170): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.455-2494_455-2486d others(11): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | ||||||
| chr3:30669121 | CAAAAAAA others(3): Show |
C | 12 | a0001c0001t0001g0137 a0001c0001t0001g0177 a0001c0001t0001g0181 others(9): Show |
12 | HG00558.hp2 HG01934.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.455-2495_455-2486d others(12): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | ||||||
| chr3:30669153 | G | T | 15 | a0001c0001t0001g0050 a0001c0001t0001g0106 a0001c0001t0001g0141 others(12): Show |
15 | HG00408.hp2 HG00673.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.455-2485G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669153 | |||||||
| chr3:30669221 | C | G | 1 | a0001c0001t0001g0076 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.455-2417C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669221 | |||||||
| chr3:30669273 | A | T | 72 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0058 others(69): Show |
72 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.455-2365A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669273 | |||||||
| chr3:30669325 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.455-2313C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669325 | |||||||
| chr3:30669459 | G | A | 1 | a0001c0003t0001g0367 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.455-2179G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669459 | |||||||
| chr3:30669598 | C | T | 3 | a0001c0003t0001g0294 a0001c0003t0001g0366 a0001c0003t0001g0367 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.455-2040C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669598 | |||||||
| chr3:30669764 | A | G | 70 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0055 others(67): Show |
70 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.455-1874A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669764 | |||||||
| chr3:30669793 | CTT | C | 4 | a0001c0001t0001g0109 a0001c0001t0001g0170 a0001c0001t0001g0237 others(1): Show |
4 | HG00639.hp1 HG01109.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.455-1843_455-1842d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669793 | ||||||
| chr3:30669801 | G | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0064 others(93): Show |
97 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.455-1837G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669801 | |||||||
| chr3:30669801 | GA | G | 70 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0055 others(67): Show |
70 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.455-1833delA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669801 | ||||||
| chr3:30669836 | A | T | 4 | a0001c0001t0001g0058 a0001c0001t0001g0210 a0001c0001t0001g0380 others(1): Show |
4 | HG03654.hp2 NA18977.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-1802A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669836 | |||||||
| chr3:30670185 | C | T | 1 | a0001c0002t0001g0321 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.455-1453C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30670185 | |||||||
| chr3:30670334 | C | A | 1 | a0001c0001t0010g0365 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.455-1304C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30670334 | |||||||
| chr3:30670358 | C | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(102): Show |
108 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.455-1280C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30670358 | |||||||
| chr3:30670389 | A | G | 29 | a0001c0001t0001g0050 a0001c0001t0001g0106 a0001c0001t0001g0141 others(26): Show |
29 | HG00408.hp2 HG00673.hp2 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.455-1249A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30670389 | |||||||
| chr3:30670452 | G | T | 1 | a0001c0001t0001g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.455-1186G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30670452 | |||||||
| chr3:30670636 | C | G | 2 | a0001c0002t0001g0272 a0001c0002t0001g0374 |
2 | NA18955.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.455-1002C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30670636 | |||||||
| chr3:30670852 | C | T | 146 | a0001c0001t0001g0006 a0001c0001t0001g0064 a0001c0001t0001g0074 others(143): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.455-786C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30670852 | |||||||
| chr3:30670968 | C | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(103): Show |
109 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.455-670C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30670968 | |||||||
| chr3:30671335 | A | C | 70 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0055 others(67): Show |
70 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.455-303A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30671335 | |||||||
| chr3:30671634 | T | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(103): Show |
109 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(106): Show |
splice_region_variant&intron_variant | LOW | c.455-4T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30671634 | |||||||
| chr3:30672453 | T | C | 3 | a0001c0001t0001g0306 a0001c0001t0001g0312 a0001c0001t0001g0313 |
3 | NA19066.hp2 NA19083.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1254+16T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30672453 | |||||||
| chr3:30672535 | A | G | 3 | a0001c0004t0008g0043 a0001c0004t0008g0069 a0001c0004t0008g0339 |
3 | HG02258.hp1 HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1254+98A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30672535 | |||||||
| chr3:30672922 | G | A | 1 | a0001c0001t0006g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1254+485G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30672922 | |||||||
| chr3:30672971 | T | A | 5 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0353 others(2): Show |
5 | HG00639.hp2 HG01255.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254+534T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30672971 | |||||||
| chr3:30673094 | A | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0049 others(100): Show |
106 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1254+657A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673094 | |||||||
| chr3:30673099 | T | A | 3 | a0001c0001t0002g0039 a0001c0001t0002g0362 a0001c0001t0008g0169 |
3 | HG02647.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1254+662T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673099 | |||||||
| chr3:30673131 | T | C | 11 | a0001c0001t0001g0326 a0001c0001t0001g0361 a0001c0001t0006g0021 others(8): Show |
11 | HG00639.hp2 HG01255.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1254+694T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673131 | |||||||
| chr3:30673158 | C | A | 14 | a0001c0001t0001g0147 a0001c0001t0002g0034 a0001c0001t0004g0004 others(11): Show |
15 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1254+721C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673158 | |||||||
| chr3:30673173 | A | G | 10 | a0001c0003t0001g0294 a0001c0003t0001g0366 a0001c0003t0001g0367 others(7): Show |
10 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1254+736A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673173 | |||||||
| chr3:30673265 | C | T | 369 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(366): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.1254+828C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673265 | |||||||
| chr3:30673277 | T | C | 2 | a0001c0004t0008g0043 a0001c0004t0008g0069 |
2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1255-828T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673277 | |||||||
| chr3:30673370 | T | G | 1 | a0001c0003t0007g0351 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1255-735T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673370 | |||||||
| chr3:30673572 | CAATTT | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0064 others(147): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1255-526_1255-522d others(7): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 30673572 | ||||||
| chr3:30673603 | G | T | 14 | a0001c0001t0001g0147 a0001c0001t0002g0034 a0001c0001t0004g0004 others(11): Show |
15 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1255-502G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673603 | |||||||
| chr3:30673663 | C | T | 99 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0058 others(96): Show |
101 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.1255-442C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673663 | |||||||
| chr3:30673699 | A | G | 9 | a0001c0004t0003g0224 a0001c0004t0008g0043 a0001c0004t0008g0069 others(6): Show |
9 | HG01934.hp2 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1255-406A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673699 | |||||||
| chr3:30673710 | T | C | 1 | a0001c0001t0001g0309 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1255-395T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673710 | |||||||
| chr3:30673724 | TA | T | 73 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0055 others(70): Show |
73 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.1255-372delA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 30673724 | ||||||
| chr3:30673766 | A | G | 1 | a0001c0001t0004g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1255-339A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673766 | |||||||
| chr3:30673901 | T | C | 1 | a0001c0001t0001g0202 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1255-204T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673901 | |||||||
| chr3:30673923 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0268 |
2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1255-182C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673923 | |||||||
| chr3:30674061 | A | C | 1 | a0001c0001t0002g0165 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1255-44A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30674061 | |||||||
| chr3:30674362 | C | A | 2 | a0001c0004t0014g0262 a0001c0004t0032g0032 |
2 | HG01934.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1396+116C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30674362 | |||||||
| chr3:30674485 | C | T | 73 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0055 others(70): Show |
73 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.1396+239C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30674485 | |||||||
| chr3:30674519 | A | G | 1 | a0001c0001t0001g0191 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1396+273A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30674519 | |||||||
| chr3:30674699 | G | A | 1 | a0001c0001t0004g0349 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1396+453G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30674699 | |||||||
| chr3:30674701 | C | CA | 14 | a0001c0001t0001g0147 a0001c0001t0002g0034 a0001c0001t0004g0004 others(11): Show |
15 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1396+465dupA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30674701 | ||||||
| chr3:30674767 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0064 others(93): Show |
97 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.1396+521G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30674767 | |||||||
| chr3:30674775 | G | A | 4 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 others(1): Show |
4 | HG00408.hp2 NA18950.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396+529G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30674775 | |||||||
| chr3:30674796 | G | C | 53 | a0001c0001t0001g0256 a0001c0002t0001g0005 a0001c0002t0001g0052 others(50): Show |
53 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1396+550G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30674796 | |||||||
| chr3:30674925 | C | T | 1 | a0001c0001t0002g0381 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1396+679C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30674925 | |||||||
| chr3:30675110 | G | A | 107 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0058 others(104): Show |
109 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1396+864G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675110 | |||||||
| chr3:30675158 | G | A | 5 | a0001c0003t0003g0344 a0001c0003t0006g0040 a0001c0003t0007g0351 others(2): Show |
5 | HG02258.hp2 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396+912G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675158 | |||||||
| chr3:30675159 | AC | A | 3 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | NA18950.hp2 NA18983.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1396+914delC | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675159 | |||||||
| chr3:30675393 | C | CT | 147 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(144): Show |
150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1396+1160dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30675393 | ||||||
| chr3:30675393 | C | CTT | 150 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0074 others(147): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1396+1159_1396+116 others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30675393 | ||||||
| chr3:30675418 | G | A | 1 | a0001c0011t0036g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1396+1172G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675418 | |||||||
| chr3:30675451 | A | G | 1 | a0001c0003t0021g0354 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1396+1205A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675451 | |||||||
| chr3:30675480 | G | A | 52 | a0001c0002t0001g0005 a0001c0002t0001g0052 a0001c0002t0001g0053 others(49): Show |
52 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1396+1234G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675480 | |||||||
| chr3:30675503 | C | A | 2 | a0001c0001t0001g0164 a0001c0001t0002g0381 |
2 | HG01433.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1396+1257C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675503 | |||||||
| chr3:30675507 | C | T | 1 | a0001c0001t0025g0340 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1396+1261C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675507 | |||||||
| chr3:30675604 | A | T | 1 | a0001c0001t0006g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1396+1358A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675604 | |||||||
| chr3:30675655 | G | T | 2 | a0001c0004t0014g0262 a0001c0004t0032g0032 |
2 | HG01934.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1396+1409G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675655 | |||||||
| chr3:30675664 | C | T | 13 | a0001c0001t0001g0147 a0001c0001t0002g0034 a0001c0001t0004g0004 others(10): Show |
14 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1396+1418C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675664 | |||||||
| chr3:30675889 | C | T | 1 | a0001c0001t0006g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1396+1643C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675889 | |||||||
| chr3:30675938 | T | G | 16 | a0001c0001t0001g0050 a0001c0001t0001g0106 a0001c0001t0001g0141 others(13): Show |
16 | HG00408.hp2 HG00673.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1396+1692T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675938 | |||||||
| chr3:30676115 | A | G | 1 | a0001c0001t0001g0326 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1396+1869A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30676115 | |||||||
| chr3:30676169 | A | G | 118 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0058 others(115): Show |
120 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1396+1923A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30676169 | |||||||
| chr3:30676466 | C | A | 3 | a0001c0001t0010g0359 a0001c0001t0016g0301 a0001c0003t0003g0344 |
3 | HG00639.hp2 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1396+2220C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30676466 | |||||||
| chr3:30676484 | T | TC | 14 | a0001c0001t0001g0147 a0001c0001t0002g0034 a0001c0001t0004g0004 others(11): Show |
15 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1396+2242dupC | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30676484 | ||||||
| chr3:30676489 | T | C | 2 | a0001c0001t0007g0035 a0001c0011t0036g0047 |
2 | HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1396+2243T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30676489 | |||||||
| chr3:30676809 | G | GAC | 7 | a0001c0003t0035g0026 a0001c0004t0003g0224 a0001c0004t0008g0043 others(4): Show |
7 | HG01891.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1396+2565_1396+256 others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30676809 | ||||||
| chr3:30676825 | T | C | 7 | a0001c0001t0003g0119 a0001c0001t0004g0345 a0001c0001t0008g0150 others(4): Show |
7 | HG02257.hp1 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1396+2579T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30676825 | |||||||
| chr3:30676835 | T | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0230 |
2 | HG01934.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1396+2589T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30676835 | |||||||
| chr3:30676937 | A | C | 297 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(294): Show |
301 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1396+2691A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30676937 | |||||||
| chr3:30677040 | A | G | 27 | a0001c0001t0001g0050 a0001c0001t0001g0106 a0001c0001t0001g0141 others(24): Show |
27 | HG00099.hp1 HG00408.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.1396+2794A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677040 | |||||||
| chr3:30677201 | G | A | 3 | a0001c0001t0001g0371 a0001c0001t0002g0071 a0001c0001t0002g0072 |
3 | HG01261.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1396+2955G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677201 | |||||||
| chr3:30677367 | C | T | 1 | a0001c0001t0020g0346 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1396+3121C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677367 | |||||||
| chr3:30677450 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(173): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.1396+3204G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677450 | |||||||
| chr3:30677459 | A | G | 2 | a0001c0001t0003g0223 a0001c0001t0004g0146 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1396+3213A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677459 | |||||||
| chr3:30677522 | G | C | 2 | a0001c0002t0038g0045 a0001c0011t0036g0047 |
2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1396+3276G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677522 | |||||||
| chr3:30677557 | A | C | 1 | a0001c0001t0001g0279 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1396+3311A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677557 | |||||||
| chr3:30677579 | G | A | 6 | a0001c0001t0014g0149 a0001c0001t0020g0346 a0001c0002t0038g0045 others(3): Show |
6 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1396+3333G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677579 | |||||||
| chr3:30677608 | T | C | 2 | a0001c0001t0003g0223 a0001c0001t0004g0146 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1396+3362T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677608 | |||||||
| chr3:30677636 | G | A | 2 | a0001c0001t0003g0223 a0001c0001t0004g0146 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1396+3390G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677636 | |||||||
| chr3:30677934 | A | G | 3 | a0001c0001t0014g0149 a0001c0004t0014g0262 a0001c0004t0032g0032 |
3 | HG01934.hp2 HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1396+3688A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677934 | |||||||
| chr3:30678050 | A | G | 1 | a0001c0002t0001g0343 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1396+3804A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678050 | |||||||
| chr3:30678269 | C | T | 3 | a0001c0001t0003g0223 a0001c0001t0004g0146 a0001c0001t0006g0021 |
3 | HG02615.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1396+4023C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678269 | |||||||
| chr3:30678280 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(195): Show |
201 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.1396+4034G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678280 | |||||||
| chr3:30678473 | G | A | 1 | a0001c0001t0011g0042 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1396+4227G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678473 | |||||||
| chr3:30678546 | T | TC | 29 | a0001c0001t0001g0050 a0001c0001t0001g0088 a0001c0001t0001g0089 others(26): Show |
29 | HG00280.hp1 HG00741.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.1396+4300_1396+430 others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678546 | |||||||
| chr3:30678546 | T | TCA | 16 | a0001c0001t0001g0210 a0001c0001t0001g0383 a0001c0001t0001g0384 others(13): Show |
16 | HG00639.hp2 HG01167.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.1396+4300_1396+430 others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678546 | |||||||
| chr3:30678546 | T | TCAA | 179 | a0001c0001t0001g0006 a0001c0001t0001g0048 a0001c0001t0001g0049 others(176): Show |
181 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.1396+4300_1396+430 others(7): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678546 | |||||||
| chr3:30678546 | T | TCAAA | 8 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0074 others(5): Show |
9 | HG01074.hp1 HG01099.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1396+4300_1396+430 others(8): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678546 | |||||||
| chr3:30678546 | T | TCAAAA | 5 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0353 others(2): Show |
5 | HG01255.hp1 HG01884.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1396+4300_1396+430 others(9): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678546 | |||||||
| chr3:30678547 | A | C | 54 | a0001c0001t0001g0091 a0001c0001t0001g0094 a0001c0001t0001g0106 others(51): Show |
55 | HG00099.hp1 HG00673.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.1396+4301A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678547 | |||||||
| chr3:30678552 | A | C | 1 | a0001c0001t0004g0349 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1396+4306A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678552 | |||||||
| chr3:30678565 | A | G | 4 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0353 others(1): Show |
4 | HG01255.hp1 HG01884.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396+4319A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678565 | |||||||
| chr3:30678599 | A | G | 3 | a0001c0001t0014g0149 a0001c0004t0014g0262 a0001c0004t0032g0032 |
3 | HG01934.hp2 HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1396+4353A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678599 | |||||||
| chr3:30678644 | G | A | 61 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0092 others(58): Show |
61 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.1396+4398G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678644 | |||||||
| chr3:30678675 | G | C | 1 | a0001c0001t0015g0386 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1396+4429G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678675 | |||||||
| chr3:30678762 | G | C | 1 | a0001c0001t0010g0359 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1396+4516G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678762 | |||||||
| chr3:30678798 | C | A | 3 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | NA18950.hp2 NA18983.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1396+4552C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678798 | |||||||
| chr3:30678812 | G | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(237): Show |
243 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1396+4566G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678812 | |||||||
| chr3:30678950 | C | G | 2 | a0001c0001t0001g0255 a0001c0001t0001g0310 |
2 | NA18970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1396+4704C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678950 | |||||||
| chr3:30678966 | A | C | 1 | a0001c0001t0005g0015 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1396+4720A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678966 | |||||||
| chr3:30679026 | C | G | 2 | a0001c0001t0003g0223 a0001c0001t0004g0146 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1396+4780C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679026 | |||||||
| chr3:30679063 | C | T | 1 | a0001c0001t0010g0359 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1396+4817C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679063 | |||||||
| chr3:30679066 | C | T | 4 | a0001c0001t0001g0095 a0001c0001t0001g0322 a0001c0001t0001g0333 others(1): Show |
4 | HG03491.hp2 HG03654.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396+4820C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679066 | |||||||
| chr3:30679148 | G | T | 1 | a0001c0001t0028g0038 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1396+4902G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679148 | |||||||
| chr3:30679172 | G | A | 4 | a0001c0001t0001g0115 a0001c0001t0001g0121 a0001c0001t0001g0241 others(1): Show |
4 | HG00280.hp1 HG01256.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396+4926G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679172 | |||||||
| chr3:30679338 | G | A | 4 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0353 others(1): Show |
4 | HG01255.hp1 HG01884.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396+5092G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679338 | |||||||
| chr3:30679367 | A | G | 229 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(226): Show |
232 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.1396+5121A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679367 | |||||||
| chr3:30679385 | A | G | 1 | a0001c0001t0002g0096 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1396+5139A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679385 | |||||||
| chr3:30679388 | G | A | 8 | a0001c0001t0006g0021 a0001c0001t0010g0359 a0001c0001t0014g0149 others(5): Show |
8 | HG00639.hp2 HG01891.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.1396+5142G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679388 | |||||||
| chr3:30679468 | G | A | 2 | a0001c0001t0003g0368 a0001c0001t0016g0300 |
2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1396+5222G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679468 | |||||||
| chr3:30679552 | G | C | 6 | a0001c0001t0004g0349 a0001c0004t0008g0043 a0001c0004t0008g0069 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396+5306G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679552 | |||||||
| chr3:30679555 | T | A | 4 | a0001c0001t0001g0326 a0001c0003t0001g0294 a0001c0003t0001g0366 others(1): Show |
4 | HG02145.hp1 HG02723.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1396+5309T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679555 | |||||||
| chr3:30679604 | A | G | 1 | a0001c0001t0002g0278 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1396+5358A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679604 | |||||||
| chr3:30679609 | C | A | 24 | a0001c0001t0001g0091 a0001c0001t0001g0094 a0001c0001t0001g0106 others(21): Show |
24 | HG00099.hp1 HG00673.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1396+5363C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679609 | |||||||
| chr3:30679709 | A | G | 281 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(278): Show |
285 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.1396+5463A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679709 | |||||||
| chr3:30679813 | A | T | 1 | a0001c0002t0010g0382 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1396+5567A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679813 | |||||||
| chr3:30679877 | C | T | 1 | a0001c0002t0042g0105 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1396+5631C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679877 | |||||||
| chr3:30679994 | CG | C | 5 | a0001c0001t0001g0326 a0001c0003t0001g0294 a0001c0003t0001g0366 others(2): Show |
5 | HG02145.hp1 HG02258.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396+5751delG | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30679994 | ||||||
| chr3:30680097 | C | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(241): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1396+5851C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680097 | |||||||
| chr3:30680103 | C | A | 1 | a0001c0001t0001g0206 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1396+5857C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680103 | |||||||
| chr3:30680129 | G | GC | 7 | a0001c0001t0002g0278 a0001c0001t0004g0345 a0001c0001t0008g0150 others(4): Show |
7 | HG02257.hp1 HG02970.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1396+5889dupC | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30680129 | ||||||
| chr3:30680136 | A | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(264): Show |
271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1396+5890A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680136 | |||||||
| chr3:30680177 | C | T | 4 | a0001c0001t0003g0223 a0001c0001t0004g0146 a0001c0002t0037g0031 others(1): Show |
4 | HG02615.hp1 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1396+5931C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680177 | |||||||
| chr3:30680211 | A | T | 287 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(284): Show |
291 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.1396+5965A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680211 | |||||||
| chr3:30680244 | C | A | 23 | a0001c0001t0001g0091 a0001c0001t0001g0094 a0001c0001t0001g0106 others(20): Show |
23 | HG00099.hp1 HG00673.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.1396+5998C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680244 | |||||||
| chr3:30680388 | C | T | 1 | a0001c0003t0035g0026 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1396+6142C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680388 | |||||||
| chr3:30680447 | C | T | 108 | a0001c0001t0001g0006 a0001c0001t0001g0048 a0001c0001t0001g0049 others(105): Show |
110 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1396+6201C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680447 | |||||||
| chr3:30680674 | C | G | 2 | a0001c0001t0003g0223 a0001c0001t0004g0146 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1396+6428C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680674 | |||||||
| chr3:30680726 | T | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(218): Show |
225 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.1396+6480T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680726 | |||||||
| chr3:30680920 | T | G | 287 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(284): Show |
291 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.1396+6674T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680920 | |||||||
| chr3:30680927 | G | C | 2 | a0001c0001t0020g0346 a0001c0011t0036g0047 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1396+6681G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680927 | |||||||
| chr3:30680928 | G | A | 5 | a0001c0004t0008g0043 a0001c0004t0008g0069 a0001c0004t0008g0125 others(2): Show |
5 | HG02258.hp1 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1396+6682G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680928 | |||||||
| chr3:30680937 | G | T | 1 | a0001c0011t0036g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1396+6691G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680937 | |||||||
| chr3:30680943 | G | T | 1 | a0001c0001t0004g0151 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1396+6697G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680943 | |||||||
| chr3:30680986 | G | A | 3 | a0001c0002t0037g0031 a0001c0003t0006g0040 a0001c0003t0021g0354 |
3 | HG02258.hp2 HG02622.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1396+6740G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680986 | |||||||
| chr3:30680998 | C | G | 3 | a0001c0001t0001g0132 a0001c0001t0001g0189 a0002c0005t0005g0176 |
3 | HG02155.hp2 NA18959.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1396+6752C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680998 | |||||||
| chr3:30681009 | G | A | 8 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0353 others(5): Show |
8 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1396+6763G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681009 | |||||||
| chr3:30681015 | A | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0051 a0001c0001t0001g0054 others(117): Show |
121 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.1396+6769A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681015 | |||||||
| chr3:30681159 | T | TG | 140 | a0001c0001t0001g0006 a0001c0001t0001g0048 a0001c0001t0001g0049 others(137): Show |
143 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.1396+6914dupG | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30681159 | ||||||
| chr3:30681160 | G | GA | 20 | a0001c0001t0001g0050 a0001c0001t0001g0188 a0001c0001t0001g0256 others(17): Show |
20 | HG01516.hp2 HG01517.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1396+6935dupA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30681160 | ||||||
| chr3:30681160 | G | GGA | 104 | a0001c0001t0001g0001 a0001c0001t0001g0051 a0001c0001t0001g0054 others(101): Show |
105 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.1396+6914_1396+691 others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681160 | |||||||
| chr3:30681160 | G | GGAA | 24 | a0001c0001t0001g0058 a0001c0001t0001g0094 a0001c0001t0001g0141 others(21): Show |
24 | HG00673.hp2 HG01943.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.1396+6914_1396+691 others(7): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681160 | |||||||
| chr3:30681160 | GAAAAAAA | G | 6 | a0001c0001t0011g0010 a0001c0001t0014g0149 a0001c0002t0037g0031 others(3): Show |
6 | HG01109.hp2 HG01934.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1396+6929_1396+693 others(11): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30681160 | ||||||
| chr3:30681161 | A | G | 4 | a0001c0001t0002g0194 a0001c0002t0001g0212 a0001c0003t0021g0354 others(1): Show |
4 | HG02040.hp1 HG02258.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396+6915A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681161 | |||||||
| chr3:30681168 | A | G | 6 | a0001c0001t0011g0010 a0001c0001t0014g0149 a0001c0002t0037g0031 others(3): Show |
6 | HG01109.hp2 HG01934.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1396+6922A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681168 | |||||||
| chr3:30681246 | G | A | 1 | a0001c0002t0001g0179 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1396+7000G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681246 | |||||||
| chr3:30681282 | C | A | 1 | a0001c0001t0001g0197 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1396+7036C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681282 | |||||||
| chr3:30681297 | G | C | 2 | a0001c0001t0001g0221 a0001c0001t0001g0261 |
2 | NA18964.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1396+7051G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681297 | |||||||
| chr3:30681312 | C | T | 3 | a0001c0001t0014g0149 a0001c0004t0014g0262 a0001c0004t0032g0032 |
3 | HG01934.hp2 HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1396+7066C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681312 | |||||||
| chr3:30681329 | A | G | 1 | a0001c0001t0002g0166 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1397-7055A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681329 | |||||||
| chr3:30681493 | G | C | 1 | a0001c0001t0001g0083 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1397-6891G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681493 | |||||||
| chr3:30681551 | C | T | 1 | a0001c0001t0001g0361 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1397-6833C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681551 | |||||||
| chr3:30681559 | G | A | 4 | a0001c0001t0014g0149 a0001c0003t0006g0040 a0001c0004t0014g0262 others(1): Show |
4 | HG01934.hp2 HG02280.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397-6825G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681559 | |||||||
| chr3:30681562 | C | T | 1 | a0001c0011t0036g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1397-6822C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681562 | |||||||
| chr3:30681638 | G | A | 2 | a0001c0001t0009g0357 a0001c0001t0009g0358 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1397-6746G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681638 | |||||||
| chr3:30681736 | A | G | 1 | a0001c0002t0010g0382 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1397-6648A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681736 | |||||||
| chr3:30681760 | A | G | 7 | a0001c0001t0001g0326 a0001c0001t0003g0223 a0001c0001t0004g0146 others(4): Show |
7 | HG02145.hp1 HG02615.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1397-6624A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681760 | |||||||
| chr3:30681978 | A | G | 265 | a0001c0001t0001g0006 a0001c0001t0001g0048 a0001c0001t0001g0049 others(262): Show |
268 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.1397-6406A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681978 | |||||||
| chr3:30682043 | A | G | 1 | a0001c0001t0004g0349 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1397-6341A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30682043 | |||||||
| chr3:30682272 | A | G | 1 | a0001c0003t0003g0344 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1397-6112A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30682272 | |||||||
| chr3:30682944 | A | G | 89 | a0001c0001t0001g0050 a0001c0001t0001g0076 a0001c0001t0001g0081 others(86): Show |
89 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1397-5440A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30682944 | |||||||
| chr3:30682954 | T | A | 6 | a0001c0001t0008g0150 a0001c0001t0010g0365 a0001c0001t0015g0140 others(3): Show |
6 | HG01891.hp1 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1397-5430T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30682954 | |||||||
| chr3:30683196 | T | C | 9 | a0001c0001t0008g0150 a0001c0001t0010g0359 a0001c0001t0010g0365 others(6): Show |
9 | HG00639.hp2 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1397-5188T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683196 | |||||||
| chr3:30683229 | A | G | 21 | a0001c0001t0001g0094 a0001c0001t0001g0208 a0001c0001t0001g0282 others(18): Show |
21 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1397-5155A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683229 | |||||||
| chr3:30683393 | A | G | 4 | a0001c0001t0014g0149 a0001c0003t0006g0040 a0001c0004t0014g0262 others(1): Show |
4 | HG01934.hp2 HG02280.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397-4991A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683393 | |||||||
| chr3:30683521 | A | T | 1 | a0001c0003t0035g0026 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1397-4863A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683521 | |||||||
| chr3:30683591 | G | A | 4 | a0001c0001t0014g0149 a0001c0003t0006g0040 a0001c0004t0014g0262 others(1): Show |
4 | HG01934.hp2 HG02280.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397-4793G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683591 | |||||||
| chr3:30683721 | A | T | 89 | a0001c0001t0001g0050 a0001c0001t0001g0076 a0001c0001t0001g0081 others(86): Show |
89 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1397-4663A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683721 | |||||||
| chr3:30683799 | T | C | 4 | a0001c0001t0001g0188 a0001c0001t0001g0191 a0001c0001t0001g0193 others(1): Show |
4 | NA19006.hp2 NA19055.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397-4585T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683799 | |||||||
| chr3:30683820 | C | G | 3 | a0001c0001t0001g0107 a0001c0001t0002g0266 a0001c0001t0002g0311 |
3 | HG03834.hp2 HG03942.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1397-4564C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683820 | |||||||
| chr3:30683889 | C | T | 2 | a0001c0001t0002g0071 a0001c0001t0002g0072 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1397-4495C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683889 | |||||||
| chr3:30683892 | C | A | 1 | a0001c0001t0019g0305 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1397-4492C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683892 | |||||||
| chr3:30683898 | G | A | 1 | a0001c0001t0027g0156 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1397-4486G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683898 | |||||||
| chr3:30684021 | G | A | 1 | a0001c0002t0010g0382 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1397-4363G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684021 | |||||||
| chr3:30684042 | A | C | 1 | a0001c0001t0001g0312 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1397-4342A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684042 | |||||||
| chr3:30684153 | T | C | 93 | a0001c0001t0001g0050 a0001c0001t0001g0076 a0001c0001t0001g0081 others(90): Show |
93 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1397-4231T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684153 | |||||||
| chr3:30684284 | G | A | 128 | a0001c0001t0001g0006 a0001c0001t0001g0048 a0001c0001t0001g0049 others(125): Show |
131 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.1397-4100G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684284 | |||||||
| chr3:30684408 | A | G | 1 | a0001c0002t0010g0382 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1397-3976A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684408 | |||||||
| chr3:30684465 | C | T | 1 | a0001c0001t0002g0303 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1397-3919C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684465 | |||||||
| chr3:30684469 | C | T | 3 | a0001c0001t0001g0064 a0001c0002t0001g0127 a0001c0002t0030g0056 |
3 | HG02165.hp2 NA18969.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1397-3915C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684469 | |||||||
| chr3:30684682 | G | A | 1 | a0001c0011t0036g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1397-3702G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684682 | |||||||
| chr3:30684709 | TTGGGAA | T | 12 | a0001c0001t0007g0035 a0001c0001t0007g0036 a0001c0001t0007g0037 others(9): Show |
12 | HG01109.hp2 HG01255.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1397-3673_1397-366 others(10): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30684709 | ||||||
| chr3:30684716 | T | G | 12 | a0001c0001t0007g0035 a0001c0001t0007g0036 a0001c0001t0007g0037 others(9): Show |
12 | HG01109.hp2 HG01255.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1397-3668T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684716 | |||||||
| chr3:30684717 | A | C | 12 | a0001c0001t0007g0035 a0001c0001t0007g0036 a0001c0001t0007g0037 others(9): Show |
12 | HG01109.hp2 HG01255.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1397-3667A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684717 | |||||||
| chr3:30684752 | A | G | 1 | a0001c0001t0008g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1397-3632A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684752 | |||||||
| chr3:30684804 | G | A | 1 | a0001c0001t0003g0244 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1397-3580G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684804 | |||||||
| chr3:30684940 | G | C | 261 | a0001c0001t0001g0006 a0001c0001t0001g0048 a0001c0001t0001g0049 others(258): Show |
264 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.1397-3444G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684940 | |||||||
| chr3:30685027 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1397-3357C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30685027 | |||||||
| chr3:30685094 | A | C | 5 | a0001c0004t0008g0043 a0001c0004t0008g0069 a0001c0004t0008g0125 others(2): Show |
5 | HG02258.hp1 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1397-3290A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30685094 | |||||||
| chr3:30685409 | C | T | 6 | a0001c0004t0008g0043 a0001c0004t0008g0069 a0001c0004t0008g0125 others(3): Show |
6 | HG02258.hp1 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1397-2975C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30685409 | |||||||
| chr3:30685591 | A | G | 2 | a0001c0001t0010g0365 a0001c0003t0035g0026 |
2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1397-2793A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30685591 | |||||||
| chr3:30685592 | G | A | 89 | a0001c0001t0001g0050 a0001c0001t0001g0076 a0001c0001t0001g0081 others(86): Show |
89 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1397-2792G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30685592 | |||||||
| chr3:30686209 | T | C | 8 | a0001c0001t0008g0150 a0001c0001t0010g0359 a0001c0001t0010g0365 others(5): Show |
8 | HG00639.hp2 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1397-2175T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30686209 | |||||||
| chr3:30686284 | G | A | 86 | a0001c0001t0001g0050 a0001c0001t0001g0076 a0001c0001t0001g0081 others(83): Show |
86 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1397-2100G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30686284 | |||||||
| chr3:30686346 | G | A | 11 | a0001c0001t0001g0068 a0001c0001t0001g0247 a0001c0001t0002g0231 others(8): Show |
12 | HG00735.hp1 HG01074.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.1397-2038G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30686346 | |||||||
| chr3:30686471 | A | G | 1 | a0001c0001t0003g0229 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1397-1913A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30686471 | |||||||
| chr3:30686625 | C | T | 1 | a0001c0001t0002g0311 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1397-1759C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30686625 | |||||||
| chr3:30686798 | G | C | 95 | a0001c0001t0001g0050 a0001c0001t0001g0076 a0001c0001t0001g0081 others(92): Show |
95 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1397-1586G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30686798 | |||||||
| chr3:30686819 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1397-1565C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30686819 | |||||||
| chr3:30686858 | A | T | 1 | a0001c0001t0004g0004 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1397-1526A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30686858 | |||||||
| chr3:30687007 | A | C | 1 | a0001c0004t0011g0369 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1397-1377A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687007 | |||||||
| chr3:30687065 | G | A | 1 | a0001c0002t0038g0045 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1397-1319G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687065 | |||||||
| chr3:30687098 | C | A | 89 | a0001c0001t0001g0050 a0001c0001t0001g0076 a0001c0001t0001g0081 others(86): Show |
89 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1397-1286C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687098 | |||||||
| chr3:30687197 | C | T | 92 | a0001c0001t0001g0050 a0001c0001t0001g0076 a0001c0001t0001g0081 others(89): Show |
92 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1397-1187C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687197 | |||||||
| chr3:30687380 | T | G | 237 | a0001c0001t0001g0006 a0001c0001t0001g0048 a0001c0001t0001g0049 others(234): Show |
240 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.1397-1004T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687380 | |||||||
| chr3:30687433 | C | T | 63 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0094 others(60): Show |
63 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1397-951C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687433 | |||||||
| chr3:30687455 | G | A | 3 | a0001c0001t0003g0223 a0001c0001t0004g0146 a0001c0001t0020g0346 |
3 | HG02615.hp1 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1397-929G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687455 | |||||||
| chr3:30687493 | G | T | 3 | a0001c0001t0016g0301 a0001c0001t0034g0033 a0001c0003t0003g0344 |
3 | HG02630.hp1 HG02809.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1397-891G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687493 | |||||||
| chr3:30687504 | A | G | 7 | a0001c0001t0008g0150 a0001c0001t0010g0365 a0001c0001t0015g0140 others(4): Show |
7 | HG01891.hp1 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1397-880A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687504 | |||||||
| chr3:30687647 | C | T | 1 | a0001c0002t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1397-737C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687647 | |||||||
| chr3:30687661 | A | G | 3 | a0001c0001t0003g0223 a0001c0001t0004g0146 a0001c0001t0020g0346 |
3 | HG02615.hp1 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1397-723A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687661 | |||||||
| chr3:30687666 | C | T | 1 | a0001c0001t0001g0380 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1397-718C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687666 | |||||||
| chr3:30687737 | G | C | 247 | a0001c0001t0001g0006 a0001c0001t0001g0048 a0001c0001t0001g0049 others(244): Show |
250 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.1397-647G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687737 | |||||||
| chr3:30687754 | G | A | 90 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0081 others(87): Show |
90 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.1397-630G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687754 | |||||||
| chr3:30687872 | A | T | 4 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0310 others(1): Show |
4 | HG03710.hp1 NA18991.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.1397-512A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687872 | |||||||
| chr3:30688018 | A | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0152 a0001c0002t0010g0382 |
3 | HG00735.hp2 HG01081.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1397-366A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30688018 | |||||||
| chr3:30688144 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0050 others(156): Show |
162 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(159): Show |
intron_variant | MODIFIER | c.1397-240G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30688144 | |||||||
| chr3:30688244 | A | C | 5 | a0001c0001t0015g0140 a0001c0001t0015g0386 a0001c0001t0016g0301 others(2): Show |
5 | HG02257.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1397-140A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30688244 | |||||||
| chr3:30688268 | G | A | 1 | a0001c0003t0006g0040 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1397-116G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30688268 | |||||||
| chr3:30688530 | C | A | 1 | a0001c0002t0001g0062 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1524+19C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30688530 | |||||||
| chr3:30688741 | C | G | 8 | a0001c0001t0008g0150 a0001c0001t0008g0169 a0001c0001t0034g0033 others(5): Show |
8 | HG02258.hp1 HG02559.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1524+230C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30688741 | |||||||
| chr3:30688747 | C | T | 131 | a0001c0001t0001g0048 a0001c0001t0001g0073 a0001c0001t0001g0080 others(128): Show |
132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1524+236C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30688747 | |||||||
| chr3:30689168 | T | C | 1 | a0001c0010t0002g0290 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1524+657T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30689168 | |||||||
| chr3:30689197 | T | C | 27 | a0001c0001t0003g0003 a0001c0001t0003g0060 a0001c0001t0003g0114 others(24): Show |
28 | HG01074.hp2 HG01106.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.1524+686T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30689197 | |||||||
| chr3:30689230 | T | C | 12 | a0001c0001t0007g0035 a0001c0001t0007g0036 a0001c0001t0007g0037 others(9): Show |
12 | HG01109.hp2 HG01255.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1524+719T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30689230 | |||||||
| chr3:30689358 | T | C | 1 | a0001c0001t0003g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1524+847T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30689358 | |||||||
| chr3:30689380 | G | A | 185 | a0001c0001t0001g0048 a0001c0001t0001g0073 a0001c0001t0001g0080 others(182): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1524+869G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30689380 | |||||||
| chr3:30689631 | G | C | 59 | a0001c0001t0001g0104 a0001c0001t0001g0232 a0001c0001t0002g0034 others(56): Show |
60 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.1524+1120G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30689631 | |||||||
| chr3:30689721 | A | G | 3 | a0001c0001t0015g0140 a0001c0001t0015g0386 a0001c0001t0018g0022 |
3 | HG02257.hp1 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1524+1210A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30689721 | |||||||
| chr3:30689729 | C | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0093 |
2 | NA18944.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1524+1218C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30689729 | |||||||
| chr3:30689790 | T | A | 343 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0048 others(340): Show |
347 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.1524+1279T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30689790 | |||||||
| chr3:30690125 | C | T | 1 | a0001c0001t0011g0010 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1525-1295C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30690125 | |||||||
| chr3:30690240 | T | C | 1 | a0001c0003t0039g0046 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1525-1180T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30690240 | |||||||
| chr3:30690377 | C | T | 1 | a0001c0001t0007g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1525-1043C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30690377 | |||||||
| chr3:30690693 | A | G | 68 | a0001c0001t0001g0048 a0001c0001t0001g0073 a0001c0001t0001g0080 others(65): Show |
68 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1525-727A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30690693 | |||||||
| chr3:30690899 | C | T | 9 | a0001c0001t0003g0148 a0001c0001t0006g0018 a0001c0001t0006g0019 others(6): Show |
9 | HG02055.hp2 HG02559.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1525-521C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30690899 | |||||||
| chr3:30691038 | G | A | 128 | a0001c0001t0001g0048 a0001c0001t0001g0073 a0001c0001t0001g0080 others(125): Show |
129 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.1525-382G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30691038 | |||||||
| chr3:30691039 | A | C | 26 | a0001c0001t0004g0004 a0001c0001t0004g0030 a0001c0001t0004g0044 others(23): Show |
27 | HG01884.hp1 HG02109.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1525-381A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30691039 | |||||||
| chr3:30691042 | A | C | 90 | a0001c0001t0001g0048 a0001c0001t0001g0073 a0001c0001t0001g0080 others(87): Show |
90 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.1525-378A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30691042 | |||||||
| chr3:30691208 | G | C | 15 | a0001c0001t0007g0035 a0001c0001t0007g0036 a0001c0001t0007g0037 others(12): Show |
15 | HG01109.hp2 HG01255.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1525-212G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30691208 | |||||||
| chr3:30691252 | A | G | 1 | a0001c0001t0002g0159 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1525-168A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30691252 | |||||||
| chr3:30691329 | C | A | 58 | a0001c0001t0002g0034 a0001c0001t0002g0039 a0001c0001t0002g0071 others(55): Show |
59 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.1525-91C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30691329 | |||||||
| chr3:30691412 | C | T | 1 | a0001c0001t0025g0340 | 1 | HG03139.hp2 | splice_region_variant&intron_variant | LOW | c.1525-8C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30691412 |