Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9392 |
| ensemblid | ENSG00000135966.14 |
| hgncid | 16836 |
| symbol | TGFBRAP1 |
| name | transforming growth factor beta receptor associated protein 1 |
| refseq_nuc | NM_004257.6 |
| refseq_prot | NP_004248.2 |
| ensembl_nuc | ENST00000393359.7 |
| ensembl_prot | ENSP00000377027.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 105264414 |
| end | 105329735 |
| strand | - |
| ver | v1.2 |
| region | chr2:105264414-105329735 |
| region5000 | chr2:105259414-105334735 |
| regionname0 | TGFBRAP1_chr2_105264414_105329735 |
| regionname5000 | TGFBRAP1_chr2_105259414_105334735 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 860 | 208 | 51 | 20 | 110 | 6 | 20 | 89 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | MMSIK others(855): Show |
chr2 | 105259414 | 105334735 |
| a0002 | 0/1 | 860 | 168 | 32 | 44 | 57 | 10 | 24 | 40 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | MMSIK others(855): Show |
chr2 | 105259414 | 105334735 |
| a0003 | 0/0 | 860 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | MMSIK others(855): Show |
chr2 | 105259414 | 105334735 |
| a0004 | 0/0 | 860 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | MMSIK others(855): Show |
chr2 | 105259414 | 105334735 |
| a0005 | 0/0 | 860 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | MMSIK others(855): Show |
chr2 | 105259414 | 105334735 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2580 | 110 | 25 | 12 | 62 | 2 | 9 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0001c0003 | 1/0 | 2580 | 69 | 10 | 6 | 38 | 4 | 10 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0001c0006 | 0/0 | 2580 | 12 | 8 | 1 | 2 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0001c0008 | 0/0 | 2580 | 7 | 0 | 0 | 7 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0001c0010 | 0/0 | 2580 | 4 | 3 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0001c0011 | 0/0 | 2580 | 4 | 4 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0001c0016 | 0/0 | 2580 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0001c0021 | 0/0 | 2580 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0002c0002 | 0/0 | 2580 | 69 | 1 | 13 | 38 | 4 | 13 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0002c0004 | 0/1 | 2580 | 48 | 17 | 13 | 7 | 4 | 6 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0002c0005 | 0/0 | 2580 | 24 | 0 | 10 | 8 | 2 | 4 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0002c0007 | 0/0 | 2580 | 9 | 6 | 2 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0002c0009 | 0/0 | 2580 | 7 | 7 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0002c0012 | 0/0 | 2580 | 4 | 0 | 3 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0002c0013 | 0/0 | 2580 | 2 | 0 | 1 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0002c0017 | 0/0 | 2580 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0002c0018 | 0/0 | 2580 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0002c0020 | 0/0 | 2580 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0002c0022 | 0/0 | 2580 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0002c0023 | 0/0 | 2580 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0003c0014 | 0/0 | 2580 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0004c0019 | 0/0 | 2580 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 | ||
| a0005c0015 | 0/0 | 2580 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | ATGAT others(2575): Show |
chr2 | 105259414 | 105334735 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5652 | 95 | 21 | 9 | 56 | 2 | 7 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0001c0001t0005 | 0/0 | 5652 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0001c0001t0012 | 0/0 | 5653 | 4 | 1 | 0 | 2 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5648): Show |
chr2 | 105259414 | 105334735 |
| a0001c0001t0015 | 0/0 | 5652 | 4 | 0 | 3 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0001c0001t0023 | 0/0 | 5652 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0001c0001t0024 | 0/0 | 5680 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5675): Show |
chr2 | 105259414 | 105334735 |
| a0001c0001t0027 | 0/0 | 5638 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5633): Show |
chr2 | 105259414 | 105334735 |
| a0001c0001t0029 | 0/0 | 5652 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0001c0001t0030 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0001c0003t0004 | 1/0 | 5680 | 19 | 0 | 3 | 7 | 2 | 6 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5675): Show |
chr2 | 105259414 | 105334735 |
| a0001c0003t0007 | 0/0 | 5680 | 18 | 8 | 1 | 8 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5675): Show |
chr2 | 105259414 | 105334735 |
| a0001c0003t0008 | 0/0 | 5680 | 10 | 0 | 0 | 10 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5675): Show |
chr2 | 105259414 | 105334735 |
| a0001c0003t0009 | 0/0 | 5680 | 5 | 0 | 1 | 0 | 2 | 2 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5675): Show |
chr2 | 105259414 | 105334735 |
| a0001c0003t0011 | 0/0 | 5652 | 6 | 0 | 0 | 6 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0001c0003t0020 | 0/0 | 5652 | 3 | 0 | 0 | 3 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0001c0003t0024 | 0/0 | 5680 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5675): Show |
chr2 | 105259414 | 105334735 |
| a0001c0003t0026 | 0/0 | 5680 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5675): Show |
chr2 | 105259414 | 105334735 |
| a0001c0003t0034 | 0/0 | 5680 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5675): Show |
chr2 | 105259414 | 105334735 |
| a0001c0003t0039 | 0/0 | 5680 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5675): Show |
chr2 | 105259414 | 105334735 |
| a0001c0003t0040 | 0/0 | 5680 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5675): Show |
chr2 | 105259414 | 105334735 |
| a0001c0003t0041 | 0/0 | 5680 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5675): Show |
chr2 | 105259414 | 105334735 |
| a0001c0003t0043 | 0/0 | 5681 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5676): Show |
chr2 | 105259414 | 105334735 |
| a0001c0006t0001 | 0/0 | 5652 | 6 | 4 | 0 | 1 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0001c0006t0004 | 0/0 | 5680 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5675): Show |
chr2 | 105259414 | 105334735 |
| a0001c0006t0009 | 0/0 | 5680 | 3 | 3 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5675): Show |
chr2 | 105259414 | 105334735 |
| a0001c0006t0012 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5648): Show |
chr2 | 105259414 | 105334735 |
| a0001c0006t0035 | 0/0 | 5680 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5675): Show |
chr2 | 105259414 | 105334735 |
| a0001c0008t0001 | 0/0 | 5652 | 7 | 0 | 0 | 7 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0001c0010t0001 | 0/0 | 5652 | 4 | 3 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0001c0011t0014 | 0/0 | 5652 | 4 | 4 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0001c0016t0001 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0001c0021t0008 | 0/0 | 5680 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5675): Show |
chr2 | 105259414 | 105334735 |
| a0002c0002t0002 | 0/0 | 5652 | 63 | 1 | 13 | 33 | 4 | 12 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0002t0021 | 0/0 | 5652 | 2 | 0 | 0 | 1 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0002t0022 | 0/0 | 5652 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0002t0025 | 0/0 | 5653 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5648): Show |
chr2 | 105259414 | 105334735 |
| a0002c0002t0033 | 0/0 | 5652 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0004t0003 | 0/0 | 5652 | 11 | 4 | 5 | 0 | 2 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0004t0005 | 0/0 | 5652 | 10 | 6 | 0 | 0 | 0 | 4 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0004t0006 | 0/1 | 5652 | 18 | 1 | 6 | 7 | 2 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0004t0013 | 0/0 | 5652 | 4 | 4 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0004t0016 | 0/0 | 5652 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0004t0018 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5648): Show |
chr2 | 105259414 | 105334735 |
| a0002c0004t0028 | 0/0 | 5652 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0004t0031 | 0/0 | 5652 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0004t0032 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0005t0003 | 0/0 | 5652 | 15 | 0 | 5 | 8 | 1 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0005t0010 | 0/0 | 5652 | 7 | 0 | 5 | 0 | 1 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0005t0036 | 0/0 | 5662 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5657): Show |
chr2 | 105259414 | 105334735 |
| a0002c0005t0042 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5648): Show |
chr2 | 105259414 | 105334735 |
| a0002c0007t0003 | 0/0 | 5652 | 3 | 3 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0007t0016 | 0/0 | 5652 | 3 | 0 | 2 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0007t0019 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0007t0037 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0007t0038 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0009t0005 | 0/0 | 5652 | 6 | 6 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0009t0018 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5648): Show |
chr2 | 105259414 | 105334735 |
| a0002c0012t0017 | 0/0 | 5652 | 4 | 0 | 3 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0013t0005 | 0/0 | 5652 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0013t0018 | 0/0 | 5653 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5648): Show |
chr2 | 105259414 | 105334735 |
| a0002c0017t0005 | 0/0 | 5652 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0018t0025 | 0/0 | 5653 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5648): Show |
chr2 | 105259414 | 105334735 |
| a0002c0020t0003 | 0/0 | 5652 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0022t0010 | 0/0 | 5652 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0002c0023t0003 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0003c0014t0019 | 0/0 | 5652 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0004c0019t0011 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| a0005c0015t0001 | 0/0 | 5652 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | GTGAC others(5647): Show |
chr2 | 105259414 | 105334735 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0012g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0012g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0012g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0012g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0015g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0015g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0015g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0023g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0023g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0024g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0027g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0029g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0001t0030g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0004g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0004g0021 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0004g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0004g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0004g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0004g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0004g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0004g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0004g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0004g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0007g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0007g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0007g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0007g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0007g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0007g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0007g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0007g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0007g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0007g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0007g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0007g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0007g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0007g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0007g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0007g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0007g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0008g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0008g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0008g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0008g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0008g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0008g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0008g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0008g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0008g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0009g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0009g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0009g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0009g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0009g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0011g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0011g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0011g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0011g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0011g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0011g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0020g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0020g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0024g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0026g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0026g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0034g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0039g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0040g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0041g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0003t0043g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0006t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0006t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0006t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0006t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0006t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0006t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0006t0004g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0006t0009g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0006t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0006t0012g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0006t0035g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0008t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0008t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0008t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0008t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0008t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0008t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0010t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0010t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0010t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0010t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0011t0014g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0011t0014g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0016t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0001c0021t0008g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0021g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0021g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0022g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0022g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0025g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0002t0033g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0003g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0003g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0003g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0003g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0003g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0003g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0005g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0005g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0005g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0005g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0006g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0006g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0006g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0006g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0006g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0006g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0006g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0006g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0006g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0006g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0013g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0013g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0013g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0013g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0016g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0018g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0028g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0031g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0004t0032g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0010g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0010g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0010g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0010g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0010g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0010g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0010g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0036g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0005t0042g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0007t0003g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0007t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0007t0016g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0007t0016g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0007t0016g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0007t0019g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0007t0037g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0007t0038g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0009t0005g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0009t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0009t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0009t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0009t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0009t0018g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0012t0017g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0012t0017g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0012t0017g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0013t0005g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0013t0018g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0017t0005g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0018t0025g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0020t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0022t0010g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0002c0023t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0003c0014t0019g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0003c0014t0019g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0004c0019t0011g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| a0005c0015t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0133 | EUR | GBR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00140 | hp2 | a0001 | c0003 | t0009 | g0129 | EUR | GBR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0010 | EUR | FIN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00280 | hp2 | a0002 | c0005 | t0003 | g0270 | EUR | FIN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00323 | hp1 | a0001 | c0003 | t0004 | g0284 | EUR | FIN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | FIN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00423 | hp1 | a0002 | c0013 | t0018 | g0248 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0166 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00544 | hp2 | a0001 | c0003 | t0007 | g0298 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00558 | hp2 | a0001 | c0008 | t0001 | g0027 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0160 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00639 | hp1 | a0002 | c0004 | t0006 | g0203 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00639 | hp2 | a0002 | c0012 | t0017 | g0017 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00642 | hp1 | a0002 | c0022 | t0010 | g0275 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0174 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00673 | hp1 | a0001 | c0006 | t0001 | g0159 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00673 | hp2 | a0002 | c0005 | t0003 | g0265 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00735 | hp1 | a0002 | c0005 | t0003 | g0257 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00735 | hp2 | a0002 | c0004 | t0028 | g0214 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00741 | hp1 | a0002 | c0004 | t0006 | g0205 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01070 | hp1 | a0001 | c0001 | t0015 | g0110 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01070 | hp2 | a0002 | c0004 | t0003 | g0341 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01071 | hp1 | a0002 | c0005 | t0003 | g0274 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01071 | hp2 | a0001 | c0001 | t0015 | g0006 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01074 | hp2 | a0002 | c0007 | t0016 | g0334 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0163 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01099 | hp2 | a0001 | c0006 | t0004 | g0345 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01106 | hp1 | a0002 | c0005 | t0010 | g0267 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01109 | hp1 | a0002 | c0005 | t0003 | g0263 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01109 | hp2 | a0002 | c0004 | t0003 | g0347 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0151 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01167 | hp2 | a0001 | c0003 | t0007 | g0022 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01175 | hp1 | a0001 | c0003 | t0004 | g0279 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01192 | hp1 | a0002 | c0004 | t0003 | g0344 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01243 | hp1 | a0001 | c0010 | t0001 | g0047 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0142 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0170 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01257 | hp2 | a0002 | c0005 | t0010 | g0277 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01258 | hp1 | a0002 | c0005 | t0010 | g0276 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0168 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01261 | hp1 | a0002 | c0005 | t0010 | g0256 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01261 | hp2 | a0002 | c0004 | t0006 | g0215 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01346 | hp2 | a0002 | c0004 | t0003 | g0340 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01358 | hp2 | a0001 | c0003 | t0009 | g0031 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01361 | hp1 | a0002 | c0007 | t0016 | g0299 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01361 | hp2 | a0001 | c0003 | t0040 | g0328 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01433 | hp1 | a0002 | c0004 | t0003 | g0342 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0145 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01496 | hp1 | a0001 | c0001 | t0015 | g0006 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01515 | hp1 | a0002 | c0005 | t0010 | g0269 | EUR | IBS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01515 | hp2 | a0002 | c0004 | t0003 | g0025 | EUR | IBS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0013 | EUR | IBS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01516 | hp2 | a0001 | c0003 | t0009 | g0130 | EUR | IBS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01517 | hp1 | a0002 | c0004 | t0003 | g0025 | EUR | IBS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0013 | EUR | IBS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0141 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01928 | hp2 | a0001 | c0003 | t0004 | g0314 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01934 | hp1 | a0002 | c0004 | t0031 | g0211 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0161 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01952 | hp1 | a0002 | c0004 | t0006 | g0014 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01952 | hp2 | a0002 | c0005 | t0003 | g0261 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01975 | hp1 | a0002 | c0012 | t0017 | g0259 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01975 | hp2 | a0002 | c0004 | t0006 | g0014 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0162 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02004 | hp2 | a0002 | c0004 | t0006 | g0207 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02015 | hp1 | a0002 | c0020 | t0003 | g0260 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02015 | hp2 | a0001 | c0003 | t0008 | g0315 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0157 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02040 | hp2 | a0001 | c0001 | t0015 | g0057 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02055 | hp1 | a0001 | c0011 | t0014 | g0002 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02055 | hp2 | a0001 | c0006 | t0012 | g0251 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02056 | hp1 | a0001 | c0003 | t0007 | g0323 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02056 | hp2 | a0002 | c0005 | t0003 | g0255 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02080 | hp2 | a0002 | c0005 | t0003 | g0264 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02083 | hp1 | a0002 | c0004 | t0006 | g0204 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02132 | hp1 | a0002 | c0004 | t0006 | g0213 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0153 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02148 | hp1 | a0002 | c0005 | t0003 | g0253 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CDX | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0152 | EAS | CDX | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CDX | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CDX | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02257 | hp1 | a0002 | c0004 | t0003 | g0024 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02257 | hp2 | a0002 | c0007 | t0003 | g0018 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02258 | hp1 | a0002 | c0007 | t0003 | g0333 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02273 | hp1 | a0002 | c0012 | t0017 | g0017 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02273 | hp2 | a0002 | c0017 | t0005 | g0150 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02280 | hp1 | a0002 | c0007 | t0019 | g0290 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02280 | hp2 | a0001 | c0003 | t0007 | g0325 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02300 | hp2 | a0002 | c0013 | t0005 | g0058 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02451 | hp1 | a0002 | c0004 | t0005 | g0188 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02451 | hp2 | a0002 | c0009 | t0005 | g0056 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0115 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0012 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02602 | hp2 | a0001 | c0003 | t0004 | g0301 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02615 | hp1 | a0001 | c0001 | t0030 | g0068 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02622 | hp1 | a0002 | c0004 | t0032 | g0132 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02622 | hp2 | a0002 | c0023 | t0003 | g0348 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02647 | hp1 | a0001 | c0010 | t0001 | g0048 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02683 | hp2 | a0001 | c0003 | t0009 | g0216 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0158 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02698 | hp2 | a0001 | c0003 | t0009 | g0128 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02717 | hp1 | a0004 | c0019 | t0011 | g0346 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02717 | hp2 | a0002 | c0004 | t0013 | g0195 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02723 | hp1 | a0002 | c0004 | t0013 | g0194 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0180 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02735 | hp2 | a0001 | c0003 | t0004 | g0281 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02738 | hp1 | a0002 | c0007 | t0016 | g0331 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02738 | hp2 | a0002 | c0005 | t0036 | g0242 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02809 | hp1 | a0001 | c0003 | t0007 | g0335 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02809 | hp2 | a0002 | c0009 | t0018 | g0244 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02818 | hp2 | a0002 | c0004 | t0003 | g0024 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02895 | hp1 | a0001 | c0006 | t0001 | g0197 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02895 | hp2 | a0002 | c0009 | t0005 | g0005 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02897 | hp1 | a0002 | c0009 | t0005 | g0063 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02897 | hp2 | a0002 | c0009 | t0005 | g0005 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02922 | hp1 | a0002 | c0007 | t0003 | g0018 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02922 | hp2 | a0003 | c0014 | t0019 | g0336 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02965 | hp2 | a0002 | c0009 | t0005 | g0055 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02970 | hp2 | a0002 | c0007 | t0038 | g0296 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03017 | hp1 | a0001 | c0003 | t0004 | g0327 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03017 | hp2 | a0001 | c0001 | t0029 | g0236 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03041 | hp1 | a0001 | c0003 | t0041 | g0280 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03041 | hp2 | a0002 | c0004 | t0013 | g0185 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03098 | hp1 | a0002 | c0004 | t0018 | g0252 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03098 | hp2 | a0001 | c0001 | t0012 | g0243 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03130 | hp1 | a0001 | c0011 | t0014 | g0043 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03130 | hp2 | a0001 | c0016 | t0001 | g0192 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03139 | hp2 | a0001 | c0011 | t0014 | g0002 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03195 | hp1 | a0001 | c0011 | t0014 | g0002 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03195 | hp2 | a0002 | c0004 | t0013 | g0193 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03209 | hp1 | a0002 | c0004 | t0005 | g0039 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03225 | hp2 | a0001 | c0006 | t0001 | g0199 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03239 | hp2 | a0002 | c0004 | t0006 | g0208 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03453 | hp1 | a0001 | c0010 | t0001 | g0065 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03453 | hp2 | a0002 | c0004 | t0005 | g0042 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03486 | hp1 | a0002 | c0004 | t0005 | g0190 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03486 | hp2 | a0001 | c0006 | t0009 | g0041 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0184 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03490 | hp2 | a0002 | c0004 | t0005 | g0144 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0149 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03540 | hp1 | a0003 | c0014 | t0019 | g0337 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03579 | hp1 | a0001 | c0006 | t0001 | g0198 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03579 | hp2 | a0001 | c0001 | t0023 | g0064 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03654 | hp1 | a0001 | c0003 | t0004 | g0300 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0146 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0181 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03669 | hp2 | a0002 | c0004 | t0005 | g0187 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0165 | SAS | STU | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03688 | hp2 | a0002 | c0005 | t0042 | g0351 | SAS | STU | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03704 | hp2 | a0001 | c0003 | t0034 | g0127 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0134 | SAS | BEB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03831 | hp2 | a0001 | c0006 | t0001 | g0169 | SAS | BEB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03834 | hp2 | a0002 | c0005 | t0010 | g0272 | SAS | BEB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03942 | hp1 | a0001 | c0003 | t0004 | g0332 | SAS | BEB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03942 | hp2 | a0002 | c0002 | t0021 | g0183 | SAS | BEB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG04115 | hp1 | a0002 | c0005 | t0003 | g0262 | SAS | STU | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG04115 | hp2 | a0002 | c0004 | t0016 | g0343 | SAS | STU | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0012 | SAS | BEB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG04184 | hp2 | a0001 | c0003 | t0007 | g0329 | SAS | BEB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG04199 | hp1 | a0001 | c0001 | t0012 | g0249 | SAS | STU | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG04199 | hp2 | a0002 | c0004 | t0005 | g0186 | SAS | STU | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | STU | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0182 | SAS | STU | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG04228 | hp1 | a0001 | c0003 | t0004 | g0021 | SAS | STU | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | STU | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18522 | hp1 | a0001 | c0006 | t0009 | g0004 | AFR | YRI | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18522 | hp2 | a0002 | c0009 | t0005 | g0062 | AFR | YRI | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18612 | hp1 | a0001 | c0003 | t0039 | g0302 | EAS | CHB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0154 | EAS | CHB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18906 | hp1 | a0002 | c0004 | t0005 | g0191 | AFR | YRI | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18941 | hp2 | a0002 | c0005 | t0003 | g0266 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18943 | hp1 | a0002 | c0004 | t0006 | g0206 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18943 | hp2 | a0002 | c0002 | t0022 | g0179 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18944 | hp2 | a0001 | c0003 | t0004 | g0019 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18945 | hp1 | a0001 | c0003 | t0011 | g0306 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18948 | hp1 | a0001 | c0003 | t0008 | g0023 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18948 | hp2 | a0001 | c0006 | t0035 | g0155 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18949 | hp2 | a0001 | c0003 | t0004 | g0283 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18951 | hp1 | a0001 | c0003 | t0020 | g0311 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18952 | hp1 | a0001 | c0003 | t0020 | g0020 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18953 | hp2 | a0001 | c0003 | t0008 | g0287 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18954 | hp2 | a0001 | c0003 | t0007 | g0322 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18961 | hp1 | a0001 | c0003 | t0008 | g0309 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18961 | hp2 | a0001 | c0008 | t0001 | g0029 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18965 | hp2 | a0001 | c0003 | t0008 | g0317 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18968 | hp1 | a0001 | c0003 | t0011 | g0305 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18969 | hp1 | a0002 | c0002 | t0021 | g0172 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18970 | hp2 | a0001 | c0003 | t0004 | g0019 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18973 | hp1 | a0001 | c0003 | t0007 | g0320 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18974 | hp2 | a0001 | c0003 | t0008 | g0312 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18975 | hp2 | a0001 | c0003 | t0011 | g0330 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18977 | hp1 | a0001 | c0008 | t0001 | g0003 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18977 | hp2 | a0001 | c0003 | t0026 | g0350 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18978 | hp1 | a0001 | c0003 | t0007 | g0293 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18978 | hp2 | a0005 | c0015 | t0001 | g0088 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18981 | hp2 | a0001 | c0001 | t0024 | g0117 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18983 | hp1 | a0001 | c0003 | t0008 | g0319 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18989 | hp1 | a0001 | c0001 | t0012 | g0245 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18989 | hp2 | a0002 | c0005 | t0003 | g0258 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18990 | hp2 | a0001 | c0003 | t0007 | g0321 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18991 | hp1 | a0001 | c0003 | t0004 | g0304 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18992 | hp1 | a0001 | c0003 | t0011 | g0282 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18993 | hp1 | a0002 | c0002 | t0025 | g0250 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18993 | hp2 | a0001 | c0021 | t0008 | g0285 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18994 | hp1 | a0002 | c0012 | t0017 | g0310 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18995 | hp1 | a0001 | c0003 | t0008 | g0288 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18997 | hp2 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18998 | hp1 | a0002 | c0002 | t0022 | g0178 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19000 | hp2 | a0001 | c0008 | t0001 | g0030 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19002 | hp1 | a0001 | c0003 | t0011 | g0289 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19003 | hp2 | a0001 | c0003 | t0026 | g0349 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19006 | hp2 | a0001 | c0003 | t0007 | g0292 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19011 | hp1 | a0001 | c0003 | t0024 | g0122 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19011 | hp2 | a0001 | c0008 | t0001 | g0028 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19030 | hp1 | a0002 | c0004 | t0006 | g0202 | AFR | LWK | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19030 | hp2 | a0001 | c0003 | t0007 | g0307 | AFR | LWK | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19043 | hp1 | a0001 | c0003 | t0007 | g0326 | AFR | LWK | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19043 | hp2 | a0001 | c0003 | t0007 | g0294 | AFR | LWK | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19056 | hp1 | a0001 | c0003 | t0011 | g0313 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0171 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19057 | hp2 | a0002 | c0004 | t0006 | g0200 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19060 | hp2 | a0001 | c0003 | t0004 | g0291 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19062 | hp1 | a0002 | c0005 | t0003 | g0271 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19062 | hp2 | a0001 | c0001 | t0012 | g0247 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19064 | hp2 | a0002 | c0002 | t0033 | g0175 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19065 | hp1 | a0001 | c0003 | t0007 | g0316 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19074 | hp1 | a0002 | c0004 | t0006 | g0210 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19077 | hp1 | a0001 | c0003 | t0008 | g0318 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19078 | hp1 | a0001 | c0001 | t0027 | g0069 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19078 | hp2 | a0002 | c0018 | t0025 | g0246 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19079 | hp1 | a0001 | c0003 | t0020 | g0020 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19080 | hp1 | a0002 | c0004 | t0006 | g0212 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19080 | hp2 | a0001 | c0008 | t0001 | g0003 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19081 | hp2 | a0002 | c0004 | t0006 | g0209 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19082 | hp1 | a0002 | c0005 | t0003 | g0254 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19082 | hp2 | a0001 | c0003 | t0004 | g0308 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19084 | hp2 | a0001 | c0003 | t0004 | g0303 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19087 | hp2 | a0001 | c0008 | t0001 | g0026 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19089 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19091 | hp1 | a0002 | c0005 | t0003 | g0273 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19091 | hp2 | a0001 | c0003 | t0008 | g0023 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19240 | hp1 | a0001 | c0003 | t0007 | g0022 | AFR | YRI | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | YRI | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA20129 | hp1 | a0001 | c0001 | t0023 | g0061 | AFR | ASW | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA20129 | hp2 | a0001 | c0010 | t0001 | g0066 | AFR | ASW | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | TSI | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA20752 | hp2 | a0002 | c0004 | t0006 | g0015 | EUR | TSI | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA20805 | hp1 | a0002 | c0004 | t0006 | g0015 | EUR | TSI | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA20805 | hp2 | a0001 | c0003 | t0004 | g0286 | EUR | TSI | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA20905 | hp1 | a0002 | c0004 | t0005 | g0240 | SAS | GIH | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0167 | SAS | GIH | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01123 | hp1 | a0002 | c0005 | t0010 | g0268 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG01123 | hp2 | a0001 | c0003 | t0004 | g0278 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02109 | hp1 | a0001 | c0006 | t0009 | g0004 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02109 | hp2 | a0002 | c0004 | t0005 | g0189 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02486 | hp1 | a0001 | c0003 | t0043 | g0352 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0217 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG02559 | hp2 | a0001 | c0006 | t0001 | g0196 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG03471 | hp2 | a0002 | c0007 | t0037 | g0295 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | USA | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| HG06807 | hp2 | a0002 | c0004 | t0003 | g0338 | AFR | USA | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA20300 | hp1 | a0002 | c0004 | t0003 | g0339 | AFR | USA | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA20300 | hp2 | a0001 | c0003 | t0007 | g0297 | AFR | USA | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| NA21309 | hp2 | a0001 | c0003 | t0007 | g0324 | AFR | LWK | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| homoSapiens | chm13v2 | a0002 | c0004 | t0006 | g0201 | REF | REF | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0004 | g0021 | REF | REF | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:105269504 | T | C | 2 | a0002 a0003 |
169 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
missense_variant | MODERATE | c.2174A>G | p.His725Arg | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/12 | 2302/5680 | 2174/2583 | 725/860 | chr2 | 105269504 | |||
| chr2:105296492 | G | C | 1 | a0003 | 2 | HG02922.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.902C>G | p.Thr301Arg | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/12 | 1030/5680 | 902/2583 | 301/860 | chr2 | 105296492 | |||
| chr2:105307673 | G | A | 1 | a0004 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.629C>T | p.Pro210Leu | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/12 | 757/5680 | 629/2583 | 210/860 | chr2 | 105307673 | |||
| chr2:105308079 | A | T | 1 | a0005 | 1 | NA18978.hp2 | missense_variant | MODERATE | c.223T>A | p.Phe75Ile | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/12 | 351/5680 | 223/2583 | 75/860 | chr2 | 105308079 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:105269292 | A | G | 1 | a0001c0021 | 1 | NA18993.hp2 | synonymous_variant | LOW | c.2386T>C | p.Leu796Leu | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/12 | 2514/5680 | 2386/2583 | 796/860 | chr2 | 105269292 | |||
| chr2:105269416 | C | T | 1 | a0001c0008 | 7 | HG00558.hp2 NA18961.hp2 NA18977.hp1 others(4): Show |
synonymous_variant | LOW | c.2262G>A | p.Leu754Leu | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/12 | 2390/5680 | 2262/2583 | 754/860 | chr2 | 105269416 | |||
| chr2:105269485 | G | A | 1 | a0002c0022 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.2193C>T | p.His731His | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/12 | 2321/5680 | 2193/2583 | 731/860 | chr2 | 105269485 | |||
| chr2:105272892 | G | A | 5 | a0002c0005 a0002c0013 a0002c0017 others(2): Show |
29 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(26): Show |
synonymous_variant | LOW | c.1935C>T | p.Leu645Leu | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/12 | 2063/5680 | 1935/2583 | 645/860 | chr2 | 105272892 | |||
| chr2:105272937 | C | T | 1 | a0001c0010 | 4 | HG01243.hp1 HG02647.hp1 HG03453.hp1 others(1): Show |
synonymous_variant | LOW | c.1890G>A | p.Lys630Lys | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/12 | 2018/5680 | 1890/2583 | 630/860 | chr2 | 105272937 | |||
| chr2:105280546 | G | A | 3 | a0002c0002 a0002c0012 a0002c0018 |
74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
synonymous_variant | LOW | c.1299C>T | p.Asn433Asn | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/12 | 1427/5680 | 1299/2583 | 433/860 | chr2 | 105280546 | |||
| chr2:105298671 | G | A | 7 | a0001c0001 a0001c0008 a0001c0010 others(4): Show |
132 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
synonymous_variant | LOW | c.723C>T | p.Arg241Arg | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/12 | 851/5680 | 723/2583 | 241/860 | chr2 | 105298671 | |||
| chr2:105307807 | C | T | 1 | a0001c0011 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
synonymous_variant | LOW | c.495G>A | p.Ser165Ser | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/12 | 623/5680 | 495/2583 | 165/860 | chr2 | 105307807 | |||
| chr2:105307840 | G | A | 1 | a0001c0011 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
synonymous_variant | LOW | c.462C>T | p.Tyr154Tyr | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/12 | 590/5680 | 462/2583 | 154/860 | chr2 | 105307840 | |||
| chr2:105307909 | C | T | 1 | a0002c0020 | 1 | HG02015.hp1 | synonymous_variant | LOW | c.393G>A | p.Gly131Gly | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/12 | 521/5680 | 393/2583 | 131/860 | chr2 | 105307909 | |||
| chr2:105307966 | C | T | 1 | a0001c0016 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.336G>A | p.Ser112Ser | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/12 | 464/5680 | 336/2583 | 112/860 | chr2 | 105307966 | |||
| chr2:105308053 | A | G | 15 | a0001c0001 a0001c0006 a0001c0008 others(12): Show |
268 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(265): Show |
synonymous_variant | LOW | c.249T>C | p.Arg83Arg | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/12 | 377/5680 | 249/2583 | 83/860 | chr2 | 105308053 | |||
| chr2:105308242 | G | A | 1 | a0002c0023 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.60C>T | p.Gly20Gly | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/12 | 188/5680 | 60/2583 | 20/860 | chr2 | 105308242 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:105264614 | C | A | 1 | a0001c0001t0023 | 2 | HG03579.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2769G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2769 | chr2 | 105264614 | ||||||
| chr2:105264696 | G | A | 1 | a0001c0011t0014 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2687C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2687 | chr2 | 105264696 | ||||||
| chr2:105264914 | C | A | 1 | a0001c0003t0040 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2469G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2469 | chr2 | 105264914 | ||||||
| chr2:105264915 | A | G | 1 | a0001c0011t0014 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2468T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2468 | chr2 | 105264915 | ||||||
| chr2:105265029 | A | G | 5 | a0001c0003t0008 a0001c0003t0026 a0001c0006t0035 others(2): Show |
16 | HG02015.hp2 NA18943.hp2 NA18948.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2354T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2354 | chr2 | 105265029 | ||||||
| chr2:105265090 | T | C | 5 | a0002c0004t0006 a0002c0004t0016 a0002c0004t0028 others(2): Show |
23 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2293A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2293 | chr2 | 105265090 | ||||||
| chr2:105265197 | G | A | 1 | a0001c0001t0029 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2186C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2186 | chr2 | 105265197 | ||||||
| chr2:105265237 | G | A | 1 | a0001c0003t0039 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2146C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2146 | chr2 | 105265237 | ||||||
| chr2:105265274 | T | C | 1 | a0002c0004t0028 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2109A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2109 | chr2 | 105265274 | ||||||
| chr2:105265318 | AATTAGCT others(7): Show |
A | 1 | a0001c0001t0027 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2051_*2064delCACG others(10): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2051 | chr2 | 105265318 | ||||||
| chr2:105265364 | G | A | 1 | a0001c0001t0027 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2019C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2019 | chr2 | 105265364 | ||||||
| chr2:105265383 | C | T | 5 | a0002c0004t0006 a0002c0004t0016 a0002c0004t0028 others(2): Show |
23 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2000G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2000 | chr2 | 105265383 | ||||||
| chr2:105265390 | A | G | 1 | a0001c0011t0014 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1993T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1993 | chr2 | 105265390 | ||||||
| chr2:105265419 | A | T | 1 | a0001c0001t0027 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1964T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1964 | chr2 | 105265419 | ||||||
| chr2:105265426 | G | T | 1 | a0002c0002t0021 | 2 | HG03942.hp2 NA18969.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1957C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1957 | chr2 | 105265426 | ||||||
| chr2:105265547 | G | A | 2 | a0001c0001t0015 a0001c0003t0020 |
7 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1836C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1836 | chr2 | 105265547 | ||||||
| chr2:105265604 | G | A | 5 | a0002c0002t0002 a0002c0002t0025 a0002c0002t0033 others(2): Show |
70 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1779C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1779 | chr2 | 105265604 | ||||||
| chr2:105265889 | A | C | 1 | a0001c0003t0034 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1494T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1494 | chr2 | 105265889 | ||||||
| chr2:105266144 | C | T | 15 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0015 others(12): Show |
137 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*1239G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1239 | chr2 | 105266144 | ||||||
| chr2:105266183 | G | A | 1 | a0001c0006t0035 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1200C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1200 | chr2 | 105266183 | ||||||
| chr2:105266226 | C | T | 14 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0015 others(11): Show |
135 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1157G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1157 | chr2 | 105266226 | ||||||
| chr2:105266256 | A | T | 1 | a0001c0001t0027 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1127T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1127 | chr2 | 105266256 | ||||||
| chr2:105266304 | G | A | 27 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0015 others(24): Show |
182 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*1079C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1079 | chr2 | 105266304 | ||||||
| chr2:105266323 | C | T | 2 | a0002c0005t0010 a0002c0022t0010 |
8 | HG00642.hp1 HG01106.hp1 HG01123.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1060G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1060 | chr2 | 105266323 | ||||||
| chr2:105266411 | T | C | 1 | a0002c0004t0031 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*972A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 972 | chr2 | 105266411 | ||||||
| chr2:105266479 | C | T | 4 | a0002c0004t0013 a0002c0007t0019 a0002c0007t0037 others(1): Show |
8 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*904G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 904 | chr2 | 105266479 | ||||||
| chr2:105266484 | A | G | 1 | a0002c0007t0037 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*899T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 899 | chr2 | 105266484 | ||||||
| chr2:105266536 | T | C | 1 | a0001c0001t0027 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*847A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 847 | chr2 | 105266536 | ||||||
| chr2:105266537 | C | A | 1 | a0001c0001t0027 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*846G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 846 | chr2 | 105266537 | ||||||
| chr2:105266540 | A | T | 1 | a0001c0001t0027 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*843T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 843 | chr2 | 105266540 | ||||||
| chr2:105266578 | G | A | 1 | a0002c0004t0032 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*805C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 805 | chr2 | 105266578 | ||||||
| chr2:105266882 | G | A | 1 | a0002c0007t0038 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*501C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 501 | chr2 | 105266882 | ||||||
| chr2:105266973 | T | C | 1 | a0001c0003t0041 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*410A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 410 | chr2 | 105266973 | ||||||
| chr2:105267029 | G | A | 1 | a0002c0002t0033 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*354C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 354 | chr2 | 105267029 | ||||||
| chr2:105267167 | TTTCCATG others(21): Show |
T | 52 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0012 others(49): Show |
312 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(309): Show |
3_prime_UTR_variant | MODIFIER | c.*188_*215delTGACCA others(22): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 188 | chr2 | 105267167 | ||||||
| chr2:105267344 | A | G | 1 | a0001c0001t0027 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*39T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 39 | chr2 | 105267344 | ||||||
| chr2:105329627 | G | GCGCCGGC others(3): Show |
1 | a0002c0005t0036 | 1 | HG02738.hp2 | 5_prime_UTR_variant | MODIFIER | c.-30_-21dupGGCGCCGG others(2): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/12 | 21327 | chr2 | 105329627 | ||||||
| chr2:105329647 | G | A | 1 | a0001c0003t0026 | 2 | NA18977.hp2 NA19003.hp2 |
5_prime_UTR_variant | MODIFIER | c.-40C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/12 | 21346 | chr2 | 105329647 | ||||||
| chr2:105329667 | G | GC | 9 | a0001c0001t0012 a0001c0003t0043 a0001c0006t0012 others(6): Show |
12 | HG00423.hp1 HG02055.hp2 HG02486.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-61dupG | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/12 | 21367 | chr2 | 105329667 | ||||||
| chr2:105329706 | C | T | 40 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0012 others(37): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
5_prime_UTR_variant | MODIFIER | c.-99G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/12 | 21405 | chr2 | 105329706 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:105267692 | A | G | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2407-133T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105267692 | |||||||
| chr2:105267802 | T | C | 29 | a0001c0001t0001g0016 a0001c0001t0001g0072 a0001c0001t0001g0218 others(26): Show |
30 | HG00408.hp1 HG01192.hp2 HG02135.hp2 others(27): Show |
intron_variant | MODIFIER | c.2407-243A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105267802 | |||||||
| chr2:105267880 | A | G | 4 | a0001c0003t0011g0305 a0001c0003t0011g0306 a0001c0003t0011g0313 others(1): Show |
4 | NA18945.hp1 NA18968.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.2407-321T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105267880 | |||||||
| chr2:105267934 | C | G | 1 | a0002c0002t0002g0012 | 2 | HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2407-375G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105267934 | |||||||
| chr2:105268043 | G | A | 30 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(27): Show |
30 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.2407-484C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268043 | |||||||
| chr2:105268109 | T | G | 1 | a0001c0001t0001g0084 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2407-550A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268109 | |||||||
| chr2:105268262 | G | A | 3 | a0002c0007t0016g0299 a0002c0007t0016g0331 a0002c0007t0016g0334 |
3 | HG01074.hp2 HG01361.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2407-703C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268262 | |||||||
| chr2:105268331 | A | C | 1 | a0002c0004t0006g0202 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2407-772T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268331 | |||||||
| chr2:105268364 | G | A | 2 | a0001c0006t0009g0004 a0001c0006t0009g0041 |
3 | HG02109.hp1 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2407-805C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268364 | |||||||
| chr2:105268678 | G | A | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2406+594C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268678 | |||||||
| chr2:105268737 | A | G | 2 | a0001c0003t0007g0294 a0001c0003t0007g0307 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2406+535T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268737 | |||||||
| chr2:105268777 | A | G | 2 | a0001c0008t0001g0027 a0001c0008t0001g0028 |
2 | HG00558.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2406+495T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268777 | |||||||
| chr2:105268834 | G | A | 2 | a0001c0003t0011g0305 a0001c0003t0011g0313 |
2 | NA18968.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.2406+438C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268834 | |||||||
| chr2:105268852 | C | A | 133 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(130): Show |
137 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.2406+420G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268852 | |||||||
| chr2:105268875 | C | A | 12 | a0002c0004t0003g0024 a0002c0004t0003g0338 a0002c0004t0003g0339 others(9): Show |
14 | HG02257.hp1 HG02451.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.2406+397G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268875 | |||||||
| chr2:105268896 | C | T | 1 | a0001c0003t0007g0321 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2406+376G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268896 | |||||||
| chr2:105268975 | C | T | 30 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(27): Show |
30 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.2406+297G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268975 | |||||||
| chr2:105269007 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2406+265A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105269007 | |||||||
| chr2:105269048 | G | A | 6 | a0001c0003t0011g0282 a0001c0003t0011g0289 a0001c0003t0011g0305 others(3): Show |
6 | NA18945.hp1 NA18968.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.2406+224C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105269048 | |||||||
| chr2:105269052 | A | C | 1 | a0001c0001t0027g0069 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2406+220T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105269052 | |||||||
| chr2:105269056 | G | A | 1 | a0001c0001t0027g0069 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2406+216C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105269056 | |||||||
| chr2:105269114 | C | A | 2 | a0002c0005t0003g0271 a0002c0005t0003g0273 |
2 | NA19062.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2406+158G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105269114 | |||||||
| chr2:105269739 | G | A | 2 | a0001c0006t0009g0004 a0001c0006t0009g0041 |
3 | HG02109.hp1 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1973-34C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105269739 | |||||||
| chr2:105269756 | G | A | 1 | a0002c0002t0002g0156 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1973-51C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105269756 | |||||||
| chr2:105269762 | C | A | 129 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(126): Show |
133 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1973-57G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105269762 | |||||||
| chr2:105269926 | A | G | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1973-221T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105269926 | |||||||
| chr2:105270422 | C | A | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1973-717G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105270422 | |||||||
| chr2:105270604 | T | C | 1 | a0001c0006t0004g0345 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1973-899A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105270604 | |||||||
| chr2:105270699 | C | G | 21 | a0002c0004t0006g0014 a0002c0004t0006g0015 a0002c0004t0006g0200 others(18): Show |
23 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1973-994G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105270699 | |||||||
| chr2:105271019 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0012g0249 |
2 | HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1973-1314C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105271019 | |||||||
| chr2:105271092 | T | C | 90 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(87): Show |
93 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1973-1387A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105271092 | |||||||
| chr2:105271262 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1973-1557A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105271262 | |||||||
| chr2:105271549 | C | G | 1 | a0001c0003t0004g0286 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1972+1306G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105271549 | |||||||
| chr2:105271768 | C | T | 1 | a0001c0003t0004g0314 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1972+1087G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105271768 | |||||||
| chr2:105271835 | C | T | 17 | a0002c0004t0003g0025 a0002c0004t0003g0340 a0002c0004t0003g0341 others(14): Show |
19 | HG01070.hp2 HG01109.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1972+1020G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105271835 | |||||||
| chr2:105271896 | G | A | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1972+959C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105271896 | |||||||
| chr2:105271922 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0121 |
2 | HG00408.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1972+933C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105271922 | |||||||
| chr2:105272037 | G | A | 1 | a0001c0003t0009g0130 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1972+818C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105272037 | |||||||
| chr2:105272382 | C | T | 289 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(286): Show |
312 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.1972+473G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105272382 | |||||||
| chr2:105272452 | C | T | 1 | a0001c0010t0001g0047 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1972+403G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105272452 | |||||||
| chr2:105272626 | C | T | 1 | a0002c0005t0003g0262 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1972+229G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105272626 | |||||||
| chr2:105272628 | T | C | 9 | a0002c0004t0005g0190 a0002c0004t0005g0191 a0002c0007t0038g0296 others(6): Show |
10 | HG02451.hp2 HG02809.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1972+227A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105272628 | |||||||
| chr2:105273105 | C | T | 8 | a0002c0004t0013g0185 a0002c0004t0013g0193 a0002c0004t0013g0194 others(5): Show |
8 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1813-91G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 9/11 | chr2 | 105273105 | |||||||
| chr2:105273204 | A | G | 2 | a0001c0006t0009g0004 a0001c0006t0009g0041 |
3 | HG02109.hp1 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1813-190T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 9/11 | chr2 | 105273204 | |||||||
| chr2:105273226 | C | T | 153 | a0001c0006t0001g0196 a0002c0002t0002g0001 a0002c0002t0002g0007 others(150): Show |
170 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1813-212G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 9/11 | chr2 | 105273226 | |||||||
| chr2:105273227 | A | G | 291 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(288): Show |
315 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.1813-213T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 9/11 | chr2 | 105273227 | |||||||
| chr2:105273236 | G | A | 4 | a0002c0004t0005g0190 a0002c0004t0005g0191 a0002c0009t0005g0005 others(1): Show |
5 | HG02451.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1813-222C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 9/11 | chr2 | 105273236 | |||||||
| chr2:105273347 | C | A | 134 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(131): Show |
138 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1812+197G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 9/11 | chr2 | 105273347 | |||||||
| chr2:105273424 | A | G | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1812+120T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 9/11 | chr2 | 105273424 | |||||||
| chr2:105273513 | C | T | 2 | a0001c0006t0009g0004 a0001c0006t0009g0041 |
3 | HG02109.hp1 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1812+31G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 9/11 | chr2 | 105273513 | |||||||
| chr2:105273735 | C | A | 2 | a0002c0002t0021g0172 a0002c0002t0021g0183 |
2 | HG03942.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1666-45G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105273735 | |||||||
| chr2:105273949 | T | G | 1 | a0002c0002t0002g0180 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1666-259A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105273949 | |||||||
| chr2:105274011 | C | T | 2 | a0001c0006t0009g0004 a0001c0006t0009g0041 |
3 | HG02109.hp1 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1666-321G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274011 | |||||||
| chr2:105274121 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1666-431C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274121 | |||||||
| chr2:105274163 | G | A | 2 | a0001c0006t0009g0004 a0001c0006t0009g0041 |
3 | HG02109.hp1 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1666-473C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274163 | |||||||
| chr2:105274175 | T | C | 134 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(131): Show |
138 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1666-485A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274175 | |||||||
| chr2:105274238 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1666-548C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274238 | |||||||
| chr2:105274321 | C | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(4): Show |
7 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1666-631G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274321 | |||||||
| chr2:105274476 | C | T | 1 | a0002c0004t0006g0210 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1666-786G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274476 | |||||||
| chr2:105274514 | C | T | 291 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(288): Show |
315 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.1666-824G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274514 | |||||||
| chr2:105274579 | C | T | 1 | a0001c0010t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1666-889G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274579 | |||||||
| chr2:105274841 | C | A | 6 | a0001c0003t0009g0031 a0001c0003t0009g0128 a0001c0003t0009g0129 others(3): Show |
6 | HG00140.hp2 HG01358.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1665+719G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274841 | |||||||
| chr2:105274847 | T | G | 6 | a0001c0003t0011g0282 a0001c0003t0011g0289 a0001c0003t0011g0305 others(3): Show |
6 | NA18945.hp1 NA18968.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1665+713A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274847 | |||||||
| chr2:105274894 | C | T | 1 | a0001c0001t0023g0061 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1665+666G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274894 | |||||||
| chr2:105274945 | G | A | 1 | a0001c0006t0001g0159 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1665+615C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274945 | |||||||
| chr2:105275004 | C | A | 2 | a0001c0001t0023g0061 a0001c0001t0023g0064 |
2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1665+556G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105275004 | |||||||
| chr2:105275053 | C | T | 153 | a0001c0006t0001g0196 a0002c0002t0002g0001 a0002c0002t0002g0007 others(150): Show |
170 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1665+507G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105275053 | |||||||
| chr2:105275187 | C | A | 148 | a0001c0006t0001g0196 a0002c0002t0002g0001 a0002c0002t0002g0007 others(145): Show |
164 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1665+373G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105275187 | |||||||
| chr2:105275221 | T | A | 3 | a0002c0002t0002g0166 a0002c0002t0022g0178 a0002c0002t0022g0179 |
3 | HG00544.hp1 NA18943.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1665+339A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105275221 | |||||||
| chr2:105275257 | A | G | 1 | a0001c0001t0001g0222 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1665+303T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105275257 | |||||||
| chr2:105275274 | G | T | 1 | a0002c0002t0021g0172 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1665+286C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105275274 | |||||||
| chr2:105275318 | G | T | 12 | a0002c0004t0003g0024 a0002c0004t0003g0338 a0002c0004t0003g0339 others(9): Show |
14 | HG02257.hp1 HG02451.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.1665+242C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105275318 | |||||||
| chr2:105275516 | C | A | 2 | a0002c0007t0019g0290 a0002c0007t0037g0295 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1665+44G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105275516 | |||||||
| chr2:105275908 | A | T | 1 | a0001c0001t0001g0100 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1522-205T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105275908 | |||||||
| chr2:105276000 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1522-297A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105276000 | |||||||
| chr2:105276163 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1522-460A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105276163 | |||||||
| chr2:105276253 | T | G | 8 | a0002c0004t0013g0185 a0002c0004t0013g0193 a0002c0004t0013g0194 others(5): Show |
8 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1522-550A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105276253 | |||||||
| chr2:105276337 | A | G | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1522-634T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105276337 | |||||||
| chr2:105276392 | C | T | 1 | a0002c0022t0010g0275 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1522-689G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105276392 | |||||||
| chr2:105276399 | A | G | 349 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(346): Show |
376 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.1522-696T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105276399 | |||||||
| chr2:105276695 | G | T | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1521+919C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105276695 | |||||||
| chr2:105276753 | C | T | 8 | a0002c0004t0013g0185 a0002c0004t0013g0193 a0002c0004t0013g0194 others(5): Show |
8 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1521+861G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105276753 | |||||||
| chr2:105276810 | G | A | 126 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(123): Show |
130 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1521+804C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105276810 | |||||||
| chr2:105276990 | G | A | 2 | a0002c0002t0021g0172 a0002c0002t0021g0183 |
2 | HG03942.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1521+624C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105276990 | |||||||
| chr2:105277131 | G | A | 1 | a0001c0008t0001g0028 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1521+483C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105277131 | |||||||
| chr2:105277162 | A | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0096 |
2 | HG01074.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1521+452T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105277162 | |||||||
| chr2:105277205 | T | C | 7 | a0001c0003t0004g0019 a0001c0003t0004g0283 a0001c0003t0004g0303 others(4): Show |
8 | NA18612.hp1 NA18944.hp2 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.1521+409A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105277205 | |||||||
| chr2:105277350 | G | GAA | 5 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0001c0011t0014g0002 others(2): Show |
8 | HG02055.hp1 HG02109.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1521+263_1521+264i others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105277350 | |||||||
| chr2:105277400 | C | G | 5 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0199 others(2): Show |
5 | HG02055.hp2 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1521+214G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105277400 | |||||||
| chr2:105277421 | A | T | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1521+193T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105277421 | |||||||
| chr2:105277478 | C | A | 3 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 |
4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1521+136G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105277478 | |||||||
| chr2:105277749 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | NA19002.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1464-78C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105277749 | |||||||
| chr2:105277770 | T | C | 12 | a0002c0004t0003g0024 a0002c0004t0003g0338 a0002c0004t0003g0339 others(9): Show |
14 | HG02257.hp1 HG02451.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.1464-99A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105277770 | |||||||
| chr2:105277885 | T | G | 2 | a0001c0001t0001g0078 a0001c0001t0012g0249 |
2 | HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1464-214A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105277885 | |||||||
| chr2:105278068 | A | ATG | 23 | a0001c0001t0001g0049 a0001c0001t0001g0070 a0001c0001t0001g0076 others(20): Show |
23 | HG00558.hp2 HG01123.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1464-399_1464-398d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | |||||||
| chr2:105278068 | ATG | A | 45 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(42): Show |
47 | HG00621.hp1 HG01167.hp2 HG01169.hp2 others(44): Show |
intron_variant | MODIFIER | c.1464-399_1464-398d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | |||||||
| chr2:105278068 | ATGTG | A | 18 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0001g0220 others(15): Show |
19 | HG00408.hp1 HG01099.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1464-401_1464-398d others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | |||||||
| chr2:105278068 | ATGTGTG | A | 27 | a0001c0001t0001g0046 a0001c0001t0001g0067 a0001c0001t0001g0080 others(24): Show |
29 | HG01070.hp2 HG01109.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.1464-403_1464-398d others(8): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | |||||||
| chr2:105278068 | ATGTGTGT others(1): Show |
A | 40 | a0001c0011t0014g0002 a0001c0011t0014g0043 a0002c0004t0003g0024 others(37): Show |
43 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1464-405_1464-398d others(10): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | |||||||
| chr2:105278068 | ATGTGTGT others(3): Show |
A | 1 | a0002c0004t0032g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1464-407_1464-398d others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | |||||||
| chr2:105278068 | ATGTGTGT others(5): Show |
A | 11 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 others(8): Show |
12 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.1464-409_1464-398d others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | |||||||
| chr2:105278068 | ATGTGTGT others(7): Show |
A | 23 | a0002c0002t0021g0172 a0002c0002t0021g0183 a0002c0004t0006g0014 others(20): Show |
25 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1464-411_1464-398d others(16): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | |||||||
| chr2:105278068 | ATGTGTGT others(9): Show |
A | 10 | a0002c0002t0002g0007 a0002c0002t0002g0137 a0002c0002t0002g0138 others(7): Show |
11 | HG02004.hp1 HG02040.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.1464-413_1464-398d others(18): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | |||||||
| chr2:105278068 | ATGTGTGT others(11): Show |
A | 51 | a0002c0002t0002g0001 a0002c0002t0002g0008 a0002c0002t0002g0009 others(48): Show |
61 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1464-415_1464-398d others(20): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | |||||||
| chr2:105278068 | ATGTGTGT others(15): Show |
A | 1 | a0002c0005t0003g0274 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1464-419_1464-398d others(24): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | |||||||
| chr2:105278100 | G | T | 7 | a0001c0001t0001g0224 a0001c0003t0011g0282 a0001c0003t0011g0289 others(4): Show |
7 | NA18945.hp1 NA18968.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1464-429C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278100 | |||||||
| chr2:105278103 | T | C | 8 | a0002c0004t0005g0039 a0002c0004t0005g0144 a0002c0004t0005g0186 others(5): Show |
8 | HG02109.hp2 HG02451.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1464-432A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278103 | |||||||
| chr2:105278143 | G | A | 1 | a0002c0004t0032g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1464-472C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278143 | |||||||
| chr2:105278229 | G | A | 1 | a0001c0003t0026g0349 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1464-558C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278229 | |||||||
| chr2:105278281 | T | C | 16 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0199 others(13): Show |
18 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1464-610A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278281 | |||||||
| chr2:105278305 | A | G | 1 | a0002c0002t0002g0153 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1464-634T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278305 | |||||||
| chr2:105278375 | A | C | 1 | a0002c0004t0006g0207 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1464-704T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278375 | |||||||
| chr2:105278517 | C | G | 2 | a0002c0004t0005g0190 a0002c0004t0005g0191 |
2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1464-846G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278517 | |||||||
| chr2:105278537 | G | T | 61 | a0002c0002t0002g0001 a0002c0002t0002g0007 a0002c0002t0002g0008 others(58): Show |
72 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1464-866C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278537 | |||||||
| chr2:105278569 | C | A | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1464-898G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278569 | |||||||
| chr2:105278656 | T | C | 2 | a0001c0006t0001g0196 a0002c0023t0003g0348 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1464-985A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278656 | |||||||
| chr2:105278786 | T | G | 1 | a0002c0007t0016g0334 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1464-1115A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278786 | |||||||
| chr2:105278823 | G | A | 63 | a0002c0002t0002g0001 a0002c0002t0002g0007 a0002c0002t0002g0008 others(60): Show |
74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1464-1152C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278823 | |||||||
| chr2:105278850 | T | C | 2 | a0002c0002t0002g0133 a0002c0002t0002g0146 |
2 | HG00140.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1464-1179A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278850 | |||||||
| chr2:105279132 | A | T | 5 | a0002c0004t0005g0190 a0002c0004t0005g0191 a0002c0007t0038g0296 others(2): Show |
6 | HG02451.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1463+1250T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279132 | |||||||
| chr2:105279227 | G | A | 1 | a0001c0006t0035g0155 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1463+1155C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279227 | |||||||
| chr2:105279228 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1463+1154G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279228 | |||||||
| chr2:105279600 | A | G | 23 | a0001c0011t0014g0002 a0001c0011t0014g0043 a0002c0004t0006g0014 others(20): Show |
27 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1463+782T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279600 | |||||||
| chr2:105279603 | C | CAAGAAGC others(101): Show |
1 | a0002c0004t0006g0205 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1463+778_1463+779i others(110): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279603 | |||||||
| chr2:105279603 | C | CAAGAAGC others(118): Show |
14 | a0002c0004t0006g0015 a0002c0004t0006g0200 a0002c0004t0006g0203 others(11): Show |
15 | HG00639.hp1 HG01074.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.1463+778_1463+779i others(127): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279603 | |||||||
| chr2:105279603 | C | CAAGAAGC others(119): Show |
4 | a0002c0004t0006g0014 a0002c0004t0006g0212 a0002c0004t0006g0215 others(1): Show |
5 | HG00735.hp2 HG01261.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1463+778_1463+779i others(128): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279603 | |||||||
| chr2:105279603 | C | CAAGAAGC others(120): Show |
1 | a0002c0007t0016g0331 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1463+778_1463+779i others(129): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279603 | |||||||
| chr2:105279603 | C | CAAGAAGC others(121): Show |
1 | a0002c0004t0006g0202 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1463+778_1463+779i others(130): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279603 | |||||||
| chr2:105279662 | C | T | 3 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 |
4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463+720G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279662 | |||||||
| chr2:105279679 | T | A | 3 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 |
4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463+703A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279679 | |||||||
| chr2:105279764 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1463+618C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279764 | |||||||
| chr2:105279815 | A | G | 21 | a0002c0004t0006g0014 a0002c0004t0006g0015 a0002c0004t0006g0200 others(18): Show |
23 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1463+567T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279815 | |||||||
| chr2:105279821 | T | G | 17 | a0001c0006t0001g0196 a0002c0004t0003g0025 a0002c0004t0003g0340 others(14): Show |
19 | HG01070.hp2 HG01109.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1463+561A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279821 | |||||||
| chr2:105279840 | C | T | 1 | a0001c0016t0001g0192 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1463+542G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279840 | |||||||
| chr2:105279865 | C | T | 10 | a0002c0005t0003g0274 a0002c0005t0010g0256 a0002c0005t0010g0267 others(7): Show |
10 | HG00642.hp1 HG01071.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.1463+517G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279865 | |||||||
| chr2:105279907 | G | A | 156 | a0001c0006t0001g0196 a0001c0006t0001g0197 a0001c0006t0001g0198 others(153): Show |
173 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1463+475C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279907 | |||||||
| chr2:105279924 | G | GTTAC | 3 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 |
4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463+454_1463+457d others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279924 | |||||||
| chr2:105280053 | TA | T | 7 | a0001c0001t0001g0106 a0001c0001t0001g0124 a0001c0001t0001g0222 others(4): Show |
7 | HG01516.hp2 HG03041.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1463+328delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105280053 | |||||||
| chr2:105280129 | T | G | 1 | a0002c0004t0006g0202 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1463+253A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105280129 | |||||||
| chr2:105280236 | C | A | 16 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0199 others(13): Show |
18 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1463+146G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105280236 | |||||||
| chr2:105280264 | T | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0037 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1463+118A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105280264 | |||||||
| chr2:105280804 | C | T | 345 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(342): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.1122-81G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105280804 | |||||||
| chr2:105280808 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1122-85G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105280808 | |||||||
| chr2:105281062 | C | T | 130 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(127): Show |
134 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1122-339G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281062 | |||||||
| chr2:105281101 | C | T | 63 | a0002c0002t0002g0001 a0002c0002t0002g0007 a0002c0002t0002g0008 others(60): Show |
74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1122-378G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281101 | |||||||
| chr2:105281185 | T | C | 8 | a0002c0004t0013g0185 a0002c0004t0013g0193 a0002c0004t0013g0194 others(5): Show |
8 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1122-462A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281185 | |||||||
| chr2:105281283 | T | G | 290 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(287): Show |
314 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.1122-560A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281283 | |||||||
| chr2:105281319 | G | A | 13 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0199 others(10): Show |
15 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1122-596C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281319 | |||||||
| chr2:105281384 | G | C | 21 | a0002c0004t0006g0014 a0002c0004t0006g0015 a0002c0004t0006g0200 others(18): Show |
23 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1122-661C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281384 | |||||||
| chr2:105281451 | G | A | 1 | a0002c0004t0006g0209 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1122-728C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281451 | |||||||
| chr2:105281453 | C | T | 2 | a0002c0004t0005g0189 a0002c0004t0018g0252 |
2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1122-730G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281453 | |||||||
| chr2:105281507 | T | C | 290 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(287): Show |
314 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.1122-784A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281507 | |||||||
| chr2:105281664 | T | G | 1 | a0002c0004t0032g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1122-941A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281664 | |||||||
| chr2:105281746 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0126 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1122-1023A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281746 | |||||||
| chr2:105281780 | T | G | 2 | a0003c0014t0019g0336 a0003c0014t0019g0337 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1122-1057A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281780 | |||||||
| chr2:105281970 | A | C | 6 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 others(3): Show |
7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1122-1247T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281970 | |||||||
| chr2:105282176 | C | A | 1 | a0001c0001t0001g0038 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1122-1453G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282176 | |||||||
| chr2:105282210 | T | C | 1 | a0002c0020t0003g0260 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1122-1487A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282210 | |||||||
| chr2:105282287 | G | A | 21 | a0002c0004t0006g0014 a0002c0004t0006g0015 a0002c0004t0006g0200 others(18): Show |
23 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1122-1564C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282287 | |||||||
| chr2:105282365 | T | A | 290 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(287): Show |
314 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.1122-1642A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282365 | |||||||
| chr2:105282398 | G | A | 1 | a0002c0002t0002g0156 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1122-1675C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282398 | |||||||
| chr2:105282402 | C | T | 1 | a0002c0002t0002g0136 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1122-1679G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282402 | |||||||
| chr2:105282437 | C | T | 6 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 others(3): Show |
7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1122-1714G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282437 | |||||||
| chr2:105282658 | C | T | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+1658G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282658 | |||||||
| chr2:105282722 | G | C | 1 | a0001c0003t0007g0329 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1121+1594C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282722 | |||||||
| chr2:105282758 | C | T | 1 | a0002c0002t0002g0174 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1121+1558G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282758 | |||||||
| chr2:105282762 | G | C | 1 | a0002c0002t0002g0040 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1121+1554C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282762 | |||||||
| chr2:105282817 | T | C | 13 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0199 others(10): Show |
15 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1121+1499A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282817 | |||||||
| chr2:105282831 | G | A | 1 | a0001c0003t0004g0284 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1121+1485C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282831 | |||||||
| chr2:105282831 | G | GA | 31 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(28): Show |
31 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1121+1484dupT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282831 | |||||||
| chr2:105282831 | GA | G | 183 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(180): Show |
198 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.1121+1484delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282831 | |||||||
| chr2:105282854 | C | T | 6 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 others(3): Show |
7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1121+1462G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282854 | |||||||
| chr2:105282922 | G | A | 1 | a0001c0003t0007g0329 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1121+1394C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282922 | |||||||
| chr2:105282944 | A | G | 1 | a0002c0004t0013g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1121+1372T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282944 | |||||||
| chr2:105283245 | A | C | 30 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(27): Show |
30 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1121+1071T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283245 | |||||||
| chr2:105283267 | T | C | 2 | a0002c0002t0021g0172 a0002c0002t0021g0183 |
2 | HG03942.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1121+1049A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283267 | |||||||
| chr2:105283369 | T | G | 6 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 others(3): Show |
7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1121+947A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283369 | |||||||
| chr2:105283435 | T | G | 1 | a0002c0023t0003g0348 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1121+881A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283435 | |||||||
| chr2:105283487 | T | C | 8 | a0002c0004t0003g0025 a0002c0004t0003g0340 a0002c0004t0003g0341 others(5): Show |
10 | HG01070.hp2 HG01109.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.1121+829A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283487 | |||||||
| chr2:105283504 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1121+812C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283504 | |||||||
| chr2:105283564 | C | T | 1 | a0002c0005t0003g0257 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1121+752G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283564 | |||||||
| chr2:105283573 | A | G | 3 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 |
4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+743T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283573 | |||||||
| chr2:105283677 | C | T | 1 | a0002c0005t0042g0351 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1121+639G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283677 | |||||||
| chr2:105283704 | G | A | 5 | a0002c0005t0003g0270 a0002c0005t0003g0271 a0002c0005t0003g0273 others(2): Show |
5 | HG00280.hp2 HG00423.hp1 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121+612C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283704 | |||||||
| chr2:105283726 | G | A | 6 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 others(3): Show |
7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1121+590C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283726 | |||||||
| chr2:105283809 | C | T | 1 | a0002c0002t0002g0170 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1121+507G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283809 | |||||||
| chr2:105283913 | T | A | 1 | a0001c0001t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1121+403A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283913 | |||||||
| chr2:105284094 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1121+222G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105284094 | |||||||
| chr2:105284237 | C | T | 1 | a0002c0004t0005g0191 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1121+79G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105284237 | |||||||
| chr2:105284413 | G | A | 1 | a0001c0003t0007g0324 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1039-15C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105284413 | |||||||
| chr2:105284430 | G | GA | 5 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0227 others(2): Show |
5 | HG01192.hp2 HG02683.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1039-33dupT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105284430 | |||||||
| chr2:105284433 | T | A | 4 | a0002c0004t0013g0185 a0002c0004t0013g0193 a0002c0004t0013g0194 others(1): Show |
4 | HG02717.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-35A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105284433 | |||||||
| chr2:105284603 | C | T | 8 | a0002c0004t0013g0185 a0002c0004t0013g0193 a0002c0004t0013g0194 others(5): Show |
8 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1039-205G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105284603 | |||||||
| chr2:105284622 | C | G | 63 | a0002c0002t0002g0001 a0002c0002t0002g0007 a0002c0002t0002g0008 others(60): Show |
74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1039-224G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105284622 | |||||||
| chr2:105284650 | G | A | 59 | a0001c0001t0024g0117 a0001c0001t0030g0068 a0001c0003t0004g0019 others(56): Show |
62 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1039-252C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105284650 | |||||||
| chr2:105284722 | G | A | 128 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(125): Show |
132 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1039-324C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105284722 | |||||||
| chr2:105284798 | A | G | 17 | a0002c0004t0003g0025 a0002c0004t0003g0340 a0002c0004t0003g0341 others(14): Show |
19 | HG01070.hp2 HG01109.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1039-400T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105284798 | |||||||
| chr2:105284880 | C | T | 160 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0199 others(157): Show |
180 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1039-482G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105284880 | |||||||
| chr2:105284890 | A | C | 1 | a0002c0002t0002g0136 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1039-492T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105284890 | |||||||
| chr2:105285042 | A | G | 7 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(4): Show |
7 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1039-644T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105285042 | |||||||
| chr2:105285096 | T | C | 188 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(185): Show |
195 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.1039-698A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105285096 | |||||||
| chr2:105285183 | G | C | 1 | a0001c0001t0001g0108 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1039-785C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105285183 | |||||||
| chr2:105285216 | C | T | 77 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0050 others(74): Show |
80 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.1039-818G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105285216 | |||||||
| chr2:105285302 | G | A | 21 | a0002c0004t0006g0014 a0002c0004t0006g0015 a0002c0004t0006g0200 others(18): Show |
23 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1039-904C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105285302 | |||||||
| chr2:105285315 | A | C | 2 | a0003c0014t0019g0336 a0003c0014t0019g0337 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1039-917T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105285315 | |||||||
| chr2:105285451 | A | C | 196 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(193): Show |
206 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.1039-1053T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105285451 | |||||||
| chr2:105285528 | C | T | 6 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 others(3): Show |
7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-1130G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105285528 | |||||||
| chr2:105285798 | T | C | 188 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(185): Show |
195 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.1039-1400A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105285798 | |||||||
| chr2:105285957 | A | G | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-1559T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105285957 | |||||||
| chr2:105286016 | A | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0059 a0001c0001t0001g0060 others(1): Show |
4 | HG00741.hp2 HG01106.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-1618T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105286016 | |||||||
| chr2:105286021 | A | T | 6 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 others(3): Show |
7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-1623T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105286021 | |||||||
| chr2:105286074 | A | G | 9 | a0001c0003t0007g0292 a0001c0003t0007g0293 a0001c0003t0007g0298 others(6): Show |
9 | HG00544.hp2 HG02056.hp1 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039-1676T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105286074 | |||||||
| chr2:105286086 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1039-1688C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105286086 | |||||||
| chr2:105286664 | T | C | 1 | a0002c0004t0006g0213 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1039-2266A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105286664 | |||||||
| chr2:105286946 | T | C | 2 | a0002c0002t0021g0172 a0002c0002t0021g0183 |
2 | HG03942.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1039-2548A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105286946 | |||||||
| chr2:105287156 | G | A | 1 | a0001c0003t0004g0314 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1039-2758C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105287156 | |||||||
| chr2:105287250 | G | A | 1 | a0002c0002t0002g0181 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1039-2852C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105287250 | |||||||
| chr2:105287284 | A | G | 1 | a0002c0005t0003g0258 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1039-2886T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105287284 | |||||||
| chr2:105287392 | AT | A | 6 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 others(3): Show |
7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-2995delA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105287392 | |||||||
| chr2:105287490 | C | T | 1 | a0002c0004t0003g0025 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1039-3092G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105287490 | |||||||
| chr2:105287603 | A | C | 1 | a0001c0016t0001g0192 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1039-3205T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105287603 | |||||||
| chr2:105287846 | T | C | 8 | a0002c0004t0013g0185 a0002c0004t0013g0193 a0002c0004t0013g0194 others(5): Show |
8 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1039-3448A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105287846 | |||||||
| chr2:105288194 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1039-3796C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288194 | |||||||
| chr2:105288205 | T | C | 290 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(287): Show |
314 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.1039-3807A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288205 | |||||||
| chr2:105288320 | G | C | 1 | a0002c0005t0003g0270 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1039-3922C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288320 | |||||||
| chr2:105288352 | G | A | 6 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 others(3): Show |
7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-3954C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288352 | |||||||
| chr2:105288737 | G | A | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-4339C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288737 | |||||||
| chr2:105288742 | A | G | 6 | a0001c0003t0011g0282 a0001c0003t0011g0289 a0001c0003t0011g0305 others(3): Show |
6 | NA18945.hp1 NA18968.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039-4344T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288742 | |||||||
| chr2:105288743 | T | C | 2 | a0003c0014t0019g0336 a0003c0014t0019g0337 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1039-4345A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288743 | |||||||
| chr2:105288797 | C | T | 130 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(127): Show |
134 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1039-4399G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288797 | |||||||
| chr2:105288812 | T | C | 1 | a0002c0018t0025g0246 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1039-4414A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288812 | |||||||
| chr2:105288917 | C | A | 1 | a0002c0009t0005g0055 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1039-4519G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288917 | |||||||
| chr2:105288963 | A | G | 1 | a0002c0004t0005g0186 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1039-4565T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288963 | |||||||
| chr2:105289208 | T | TG | 63 | a0002c0002t0002g0001 a0002c0002t0002g0007 a0002c0002t0002g0008 others(60): Show |
74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1039-4811dupC | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289208 | |||||||
| chr2:105289292 | G | A | 6 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 others(3): Show |
7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-4894C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289292 | |||||||
| chr2:105289402 | G | C | 1 | a0001c0003t0004g0314 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1039-5004C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289402 | |||||||
| chr2:105289411 | A | C | 6 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 others(3): Show |
7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-5013T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289411 | |||||||
| chr2:105289416 | G | A | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-5018C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289416 | |||||||
| chr2:105289507 | ATATGT | A | 63 | a0002c0002t0002g0001 a0002c0002t0002g0007 a0002c0002t0002g0008 others(60): Show |
74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1039-5114_1039-511 others(9): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289507 | |||||||
| chr2:105289661 | C | A | 68 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0199 others(65): Show |
72 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.1039-5263G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289661 | |||||||
| chr2:105289810 | C | A | 21 | a0002c0004t0006g0014 a0002c0004t0006g0015 a0002c0004t0006g0200 others(18): Show |
23 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1039-5412G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289810 | |||||||
| chr2:105289820 | T | C | 8 | a0002c0004t0013g0185 a0002c0004t0013g0193 a0002c0004t0013g0194 others(5): Show |
8 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1039-5422A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289820 | |||||||
| chr2:105289904 | T | A | 1 | a0001c0003t0004g0291 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1039-5506A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289904 | |||||||
| chr2:105289905 | G | A | 1 | a0001c0003t0004g0291 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1039-5507C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289905 | |||||||
| chr2:105289953 | C | G | 30 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(27): Show |
30 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1039-5555G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289953 | |||||||
| chr2:105289990 | G | C | 6 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 others(3): Show |
7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-5592C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289990 | |||||||
| chr2:105290023 | C | G | 290 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(287): Show |
314 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.1039-5625G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290023 | |||||||
| chr2:105290033 | C | A | 1 | a0001c0003t0004g0291 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1039-5635G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290033 | |||||||
| chr2:105290129 | C | T | 61 | a0002c0002t0002g0001 a0002c0002t0002g0007 a0002c0002t0002g0008 others(58): Show |
72 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1039-5731G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290129 | |||||||
| chr2:105290258 | G | A | 6 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 others(3): Show |
7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-5860C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290258 | |||||||
| chr2:105290285 | T | C | 122 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(119): Show |
126 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1039-5887A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290285 | |||||||
| chr2:105290369 | C | A | 17 | a0002c0004t0003g0025 a0002c0004t0003g0340 a0002c0004t0003g0341 others(14): Show |
19 | HG01070.hp2 HG01109.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1039-5971G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290369 | |||||||
| chr2:105290435 | A | ATGAATTC others(18): Show |
1 | a0002c0002t0002g0136 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1038+5920_1038+592 others(29): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290435 | |||||||
| chr2:105290501 | T | C | 61 | a0002c0002t0002g0001 a0002c0002t0002g0007 a0002c0002t0002g0008 others(58): Show |
72 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1038+5855A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290501 | |||||||
| chr2:105290551 | C | T | 6 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 others(3): Show |
7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1038+5805G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290551 | |||||||
| chr2:105290577 | GAGAGAGA others(3): Show |
G | 8 | a0001c0003t0008g0023 a0001c0003t0008g0315 a0001c0003t0008g0317 others(5): Show |
9 | HG00544.hp1 HG02015.hp2 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1038+5769_1038+577 others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290577 | |||||||
| chr2:105290587 | AAG | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0221 a0001c0001t0001g0222 |
4 | NA18950.hp1 NA18960.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+5767_1038+576 others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290587 | |||||||
| chr2:105290591 | G | C | 1 | a0002c0007t0038g0296 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1038+5765C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290591 | |||||||
| chr2:105290599 | G | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0221 a0001c0001t0001g0222 |
4 | NA18950.hp1 NA18960.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+5757C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290599 | |||||||
| chr2:105290605 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0221 a0001c0001t0001g0222 |
4 | NA18950.hp1 NA18960.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+5751T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290605 | |||||||
| chr2:105290608 | A | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0221 a0001c0001t0001g0222 |
4 | NA18950.hp1 NA18960.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+5748T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290608 | |||||||
| chr2:105290610 | A | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0221 a0001c0001t0001g0222 |
4 | NA18950.hp1 NA18960.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+5746T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290610 | |||||||
| chr2:105290612 | A | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0221 a0001c0001t0001g0222 |
4 | NA18950.hp1 NA18960.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+5744T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290612 | |||||||
| chr2:105290613 | GAC | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0221 a0001c0001t0001g0222 |
4 | NA18950.hp1 NA18960.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+5741_1038+574 others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290613 | |||||||
| chr2:105290615 | C | CTG | 21 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0050 others(18): Show |
21 | HG00621.hp1 HG00741.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.1038+5740_1038+574 others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290615 | |||||||
| chr2:105290615 | C | CTGTG | 18 | a0001c0001t0001g0046 a0001c0001t0001g0078 a0001c0001t0001g0085 others(15): Show |
18 | HG00408.hp2 HG01074.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.1038+5740_1038+574 others(8): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290615 | |||||||
| chr2:105290615 | C | CTGTGTG | 50 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(47): Show |
52 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1038+5740_1038+574 others(10): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290615 | |||||||
| chr2:105290615 | C | CTGTGTGT others(1): Show |
13 | a0001c0001t0001g0032 a0001c0001t0001g0051 a0001c0001t0001g0053 others(10): Show |
13 | HG01243.hp1 HG01496.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1038+5740_1038+574 others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290615 | |||||||
| chr2:105290615 | C | CTGTGTGT others(3): Show |
2 | a0001c0001t0005g0115 a0001c0001t0027g0069 |
2 | HG02523.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1038+5740_1038+574 others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290615 | |||||||
| chr2:105290615 | CAGTGTGT others(5): Show |
C | 1 | a0001c0001t0001g0119 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1038+5729_1038+574 others(16): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290615 | |||||||
| chr2:105290616 | A | AGT | 76 | a0001c0003t0004g0301 a0001c0003t0004g0332 a0001c0003t0007g0307 others(73): Show |
90 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1038+5738_1038+573 others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290616 | |||||||
| chr2:105290616 | A | AGTGT | 32 | a0001c0003t0004g0314 a0001c0003t0009g0128 a0001c0003t0009g0130 others(29): Show |
32 | HG00423.hp1 HG01070.hp2 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.1038+5736_1038+573 others(8): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290616 | |||||||
| chr2:105290616 | A | AGTGTGT | 24 | a0001c0003t0009g0031 a0001c0003t0009g0129 a0001c0006t0001g0196 others(21): Show |
25 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.1038+5734_1038+573 others(10): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290616 | |||||||
| chr2:105290616 | A | AGTGTGTG others(1): Show |
13 | a0002c0002t0002g0141 a0002c0002t0002g0145 a0002c0002t0002g0161 others(10): Show |
14 | HG01109.hp2 HG01123.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1038+5732_1038+573 others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290616 | |||||||
| chr2:105290616 | A | AGTGTGTG others(3): Show |
1 | a0002c0004t0003g0342 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1038+5730_1038+573 others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290616 | |||||||
| chr2:105290616 | A | T | 126 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(123): Show |
130 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1038+5740T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290616 | |||||||
| chr2:105290616 | AGT | A | 10 | a0001c0003t0007g0022 a0001c0003t0008g0315 a0001c0003t0041g0280 others(7): Show |
11 | HG01167.hp2 HG02015.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1038+5738_1038+573 others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290616 | |||||||
| chr2:105290616 | AGTGTGT | A | 5 | a0001c0006t0001g0199 a0002c0004t0003g0024 a0002c0004t0003g0338 others(2): Show |
6 | HG02257.hp1 HG02818.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1038+5734_1038+573 others(10): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290616 | |||||||
| chr2:105290616 | AGTGTGTG others(5): Show |
A | 2 | a0001c0021t0008g0285 a0002c0005t0003g0273 |
2 | NA18993.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1038+5728_1038+573 others(16): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290616 | |||||||
| chr2:105290616 | AGTGTGTG others(13): Show |
A | 1 | a0002c0002t0002g0134 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1038+5720_1038+573 others(24): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290616 | |||||||
| chr2:105290653 | G | A | 4 | a0001c0006t0009g0041 a0002c0009t0005g0062 a0002c0009t0005g0063 others(1): Show |
4 | HG02809.hp2 HG02897.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038+5703C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290653 | |||||||
| chr2:105290653 | G | GTA | 2 | a0001c0006t0009g0004 a0002c0004t0005g0042 |
3 | HG02109.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1038+5702_1038+570 others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290653 | |||||||
| chr2:105290724 | G | C | 6 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 others(3): Show |
7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1038+5632C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290724 | |||||||
| chr2:105290777 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1038+5579C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290777 | |||||||
| chr2:105290786 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1038+5570G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290786 | |||||||
| chr2:105290796 | G | C | 130 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(127): Show |
134 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1038+5560C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290796 | |||||||
| chr2:105290831 | C | T | 2 | a0002c0004t0005g0189 a0002c0004t0018g0252 |
2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1038+5525G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290831 | |||||||
| chr2:105291071 | C | T | 29 | a0001c0001t0001g0016 a0001c0001t0001g0072 a0001c0001t0001g0218 others(26): Show |
30 | HG00408.hp1 HG01192.hp2 HG02135.hp2 others(27): Show |
intron_variant | MODIFIER | c.1038+5285G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105291071 | |||||||
| chr2:105291192 | T | A | 14 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(11): Show |
14 | HG00673.hp2 HG00735.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1038+5164A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105291192 | |||||||
| chr2:105291257 | C | T | 1 | a0002c0007t0019g0290 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1038+5099G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105291257 | |||||||
| chr2:105291333 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1038+5023A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105291333 | |||||||
| chr2:105291340 | C | T | 1 | a0002c0004t0006g0208 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1038+5016G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105291340 | |||||||
| chr2:105291479 | G | A | 1 | a0001c0010t0001g0047 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1038+4877C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105291479 | |||||||
| chr2:105291570 | C | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0059 a0001c0001t0001g0060 others(1): Show |
4 | HG00741.hp2 HG01106.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+4786G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105291570 | |||||||
| chr2:105291604 | G | A | 29 | a0001c0001t0001g0016 a0001c0001t0001g0072 a0001c0001t0001g0218 others(26): Show |
30 | HG00408.hp1 HG01192.hp2 HG02135.hp2 others(27): Show |
intron_variant | MODIFIER | c.1038+4752C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105291604 | |||||||
| chr2:105291651 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1038+4705T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105291651 | |||||||
| chr2:105292208 | A | C | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038+4148T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105292208 | |||||||
| chr2:105292225 | C | T | 13 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0199 others(10): Show |
15 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1038+4131G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105292225 | |||||||
| chr2:105292450 | C | T | 4 | a0002c0004t0005g0039 a0002c0004t0005g0188 a0002c0004t0005g0189 others(1): Show |
4 | HG02109.hp2 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+3906G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105292450 | |||||||
| chr2:105292627 | C | A | 8 | a0002c0004t0005g0039 a0002c0004t0005g0144 a0002c0004t0005g0186 others(5): Show |
8 | HG02109.hp2 HG02451.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1038+3729G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105292627 | |||||||
| chr2:105292716 | G | C | 1 | a0001c0001t0001g0108 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1038+3640C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105292716 | |||||||
| chr2:105292969 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1038+3387C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105292969 | |||||||
| chr2:105292979 | G | A | 1 | a0002c0009t0005g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1038+3377C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105292979 | |||||||
| chr2:105292980 | C | T | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | NA18984.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1038+3376G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105292980 | |||||||
| chr2:105293088 | T | C | 1 | a0003c0014t0019g0336 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1038+3268A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105293088 | |||||||
| chr2:105293097 | A | G | 291 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(288): Show |
315 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.1038+3259T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105293097 | |||||||
| chr2:105293102 | G | A | 152 | a0001c0003t0041g0280 a0001c0006t0001g0197 a0001c0006t0001g0198 others(149): Show |
169 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.1038+3254C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105293102 | |||||||
| chr2:105293550 | C | T | 1 | a0002c0005t0003g0274 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1038+2806G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105293550 | |||||||
| chr2:105293737 | C | T | 24 | a0001c0003t0041g0280 a0002c0004t0003g0025 a0002c0004t0003g0340 others(21): Show |
26 | HG01070.hp2 HG01109.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1038+2619G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105293737 | |||||||
| chr2:105293746 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1038+2610G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105293746 | |||||||
| chr2:105293764 | T | C | 1 | a0001c0006t0004g0345 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1038+2592A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105293764 | |||||||
| chr2:105293776 | G | T | 2 | a0001c0001t0001g0229 a0001c0001t0001g0235 |
2 | NA18969.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1038+2580C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105293776 | |||||||
| chr2:105293915 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1038+2441C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105293915 | |||||||
| chr2:105293971 | T | C | 3 | a0001c0001t0001g0046 a0001c0001t0012g0243 a0001c0001t0030g0068 |
3 | HG02559.hp1 HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1038+2385A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105293971 | |||||||
| chr2:105294038 | T | C | 1 | a0002c0007t0038g0296 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1038+2318A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294038 | |||||||
| chr2:105294056 | G | A | 161 | a0001c0003t0041g0280 a0001c0006t0001g0197 a0001c0006t0001g0198 others(158): Show |
181 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.1038+2300C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294056 | |||||||
| chr2:105294141 | T | G | 291 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(288): Show |
315 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.1038+2215A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294141 | |||||||
| chr2:105294205 | C | T | 2 | a0002c0007t0019g0290 a0002c0007t0037g0295 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1038+2151G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294205 | |||||||
| chr2:105294270 | A | C | 1 | a0002c0002t0021g0172 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1038+2086T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294270 | |||||||
| chr2:105294307 | G | GGT | 31 | a0001c0001t0001g0111 a0001c0003t0007g0325 a0001c0003t0007g0326 others(28): Show |
33 | HG00423.hp1 HG01070.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1038+2047_1038+204 others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294307 | |||||||
| chr2:105294307 | G | GGTGT | 109 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(106): Show |
116 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.1038+2045_1038+204 others(8): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294307 | |||||||
| chr2:105294307 | G | GGTGTGT | 36 | a0001c0001t0001g0045 a0001c0001t0001g0067 a0001c0001t0001g0100 others(33): Show |
36 | HG00280.hp2 HG00408.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1038+2043_1038+204 others(10): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294307 | |||||||
| chr2:105294307 | G | GGTGTGTG others(1): Show |
21 | a0001c0001t0023g0061 a0001c0001t0023g0064 a0002c0004t0006g0014 others(18): Show |
23 | HG00639.hp1 HG01074.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1038+2041_1038+204 others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294307 | |||||||
| chr2:105294307 | G | GGTGTGTG others(3): Show |
4 | a0001c0003t0020g0020 a0001c0003t0020g0311 a0002c0004t0006g0208 others(1): Show |
5 | HG01109.hp1 HG03239.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.1038+2039_1038+204 others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294307 | |||||||
| chr2:105294307 | G | GGTGTGTG others(5): Show |
1 | a0001c0001t0012g0243 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1038+2037_1038+204 others(16): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294307 | |||||||
| chr2:105294307 | G | GGTGTGTG others(7): Show |
2 | a0001c0001t0001g0046 a0001c0001t0030g0068 |
2 | HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1038+2035_1038+204 others(18): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294307 | |||||||
| chr2:105294307 | GGTGT | G | 61 | a0002c0002t0002g0001 a0002c0002t0002g0007 a0002c0002t0002g0008 others(58): Show |
72 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1038+2045_1038+204 others(8): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294307 | |||||||
| chr2:105294444 | G | A | 6 | a0002c0004t0013g0185 a0002c0004t0013g0193 a0002c0004t0013g0194 others(3): Show |
6 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+1912C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294444 | |||||||
| chr2:105294481 | A | G | 2 | a0001c0001t0023g0061 a0001c0001t0023g0064 |
2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1038+1875T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294481 | |||||||
| chr2:105294606 | G | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0102 |
2 | HG00621.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.1038+1750C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294606 | |||||||
| chr2:105294801 | C | A | 285 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(282): Show |
307 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.1038+1555G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294801 | |||||||
| chr2:105294917 | CT | C | 33 | a0001c0001t0012g0249 a0001c0006t0001g0197 a0001c0006t0001g0198 others(30): Show |
35 | HG01070.hp2 HG01109.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.1038+1438delA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294917 | |||||||
| chr2:105294933 | C | A | 2 | a0001c0008t0001g0026 a0001c0008t0001g0029 |
2 | NA18961.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1038+1423G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294933 | |||||||
| chr2:105294939 | A | G | 153 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(150): Show |
158 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.1038+1417T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294939 | |||||||
| chr2:105294941 | A | G | 114 | a0001c0001t0012g0249 a0001c0006t0001g0169 a0001c0006t0001g0197 others(111): Show |
128 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.1038+1415T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294941 | |||||||
| chr2:105294976 | C | T | 1 | a0001c0003t0026g0350 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1038+1380G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294976 | |||||||
| chr2:105294978 | T | C | 3 | a0002c0009t0005g0062 a0002c0009t0005g0063 a0002c0009t0018g0244 |
3 | HG02809.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1038+1378A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294978 | |||||||
| chr2:105295028 | C | G | 11 | a0001c0001t0023g0061 a0001c0001t0023g0064 a0001c0006t0001g0197 others(8): Show |
14 | HG02055.hp1 HG02055.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1038+1328G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295028 | |||||||
| chr2:105295145 | A | G | 1 | a0002c0004t0005g0190 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1038+1211T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295145 | |||||||
| chr2:105295448 | G | A | 72 | a0001c0003t0004g0019 a0001c0003t0004g0278 a0001c0003t0004g0279 others(69): Show |
77 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+908C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295448 | |||||||
| chr2:105295681 | G | T | 2 | a0002c0002t0002g0135 a0002c0002t0002g0160 |
2 | HG00621.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1038+675C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295681 | |||||||
| chr2:105295683 | C | T | 2 | a0002c0002t0002g0135 a0002c0002t0002g0160 |
2 | HG00621.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1038+673G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295683 | |||||||
| chr2:105295714 | G | A | 26 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(23): Show |
27 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1038+642C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295714 | |||||||
| chr2:105295803 | C | G | 1 | a0002c0009t0005g0055 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1038+553G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295803 | |||||||
| chr2:105295809 | C | CA | 10 | a0001c0001t0001g0053 a0001c0001t0001g0075 a0001c0001t0001g0076 others(7): Show |
10 | HG00621.hp1 HG01109.hp2 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.1038+546dupT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295809 | |||||||
| chr2:105295809 | CA | C | 126 | a0001c0001t0001g0016 a0001c0001t0001g0045 a0001c0001t0001g0054 others(123): Show |
139 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1038+546delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295809 | |||||||
| chr2:105295809 | CAA | C | 19 | a0002c0004t0006g0014 a0002c0004t0006g0015 a0002c0004t0006g0200 others(16): Show |
21 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1038+545_1038+546d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295809 | |||||||
| chr2:105295868 | C | G | 1 | a0002c0004t0032g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1038+488G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295868 | |||||||
| chr2:105295905 | T | C | 64 | a0001c0006t0001g0159 a0001c0006t0001g0169 a0001c0006t0035g0155 others(61): Show |
74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1038+451A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295905 | |||||||
| chr2:105296178 | G | A | 8 | a0001c0001t0023g0061 a0001c0001t0023g0064 a0002c0009t0005g0005 others(5): Show |
9 | HG02451.hp2 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1038+178C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105296178 | |||||||
| chr2:105296280 | A | G | 1 | a0002c0004t0005g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1038+76T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105296280 | |||||||
| chr2:105296756 | C | CT | 79 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(76): Show |
84 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.884-247dupA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105296756 | |||||||
| chr2:105296756 | C | CTT | 92 | a0001c0001t0001g0016 a0001c0001t0001g0072 a0001c0001t0001g0218 others(89): Show |
102 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.884-248_884-247dup others(2): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105296756 | |||||||
| chr2:105296756 | C | CTTT | 30 | a0001c0001t0001g0224 a0001c0001t0001g0226 a0001c0001t0001g0237 others(27): Show |
33 | HG00280.hp1 HG00639.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.884-249_884-247dup others(3): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105296756 | |||||||
| chr2:105296756 | CT | C | 9 | a0001c0001t0001g0109 a0001c0001t0015g0110 a0001c0003t0041g0280 others(6): Show |
10 | HG01070.hp1 HG01257.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.884-247delA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105296756 | |||||||
| chr2:105297096 | G | A | 3 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 |
4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.884-586C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105297096 | |||||||
| chr2:105297308 | T | A | 1 | a0001c0001t0001g0086 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.884-798A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105297308 | |||||||
| chr2:105297442 | T | G | 2 | a0002c0004t0005g0189 a0002c0004t0018g0252 |
2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.884-932A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105297442 | |||||||
| chr2:105297453 | C | T | 3 | a0001c0001t0001g0080 a0001c0001t0001g0091 a0001c0001t0001g0096 |
3 | HG01074.hp1 HG01346.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.884-943G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105297453 | |||||||
| chr2:105297573 | A | G | 114 | a0001c0006t0001g0159 a0001c0006t0001g0169 a0001c0006t0001g0196 others(111): Show |
128 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.883+938T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105297573 | |||||||
| chr2:105297584 | A | C | 1 | a0001c0003t0007g0022 | 2 | HG01167.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.883+927T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105297584 | |||||||
| chr2:105297913 | G | A | 1 | a0001c0003t0004g0291 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.883+598C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105297913 | |||||||
| chr2:105297976 | A | T | 133 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(130): Show |
140 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.883+535T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105297976 | |||||||
| chr2:105297986 | C | T | 101 | a0001c0006t0001g0159 a0001c0006t0001g0169 a0001c0006t0001g0196 others(98): Show |
113 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.883+525G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105297986 | |||||||
| chr2:105298016 | C | G | 3 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 |
4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.883+495G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105298016 | |||||||
| chr2:105298048 | A | G | 2 | a0002c0009t0005g0005 a0002c0009t0005g0056 |
3 | HG02451.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.883+463T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105298048 | |||||||
| chr2:105298050 | G | A | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.883+461C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105298050 | |||||||
| chr2:105298054 | C | T | 1 | a0002c0004t0005g0144 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.883+457G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105298054 | |||||||
| chr2:105298058 | T | C | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.883+453A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105298058 | |||||||
| chr2:105298217 | T | C | 1 | a0002c0004t0005g0042 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.883+294A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105298217 | |||||||
| chr2:105298329 | C | G | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.883+182G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105298329 | |||||||
| chr2:105298422 | G | A | 2 | a0003c0014t0019g0336 a0003c0014t0019g0337 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.883+89C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105298422 | |||||||
| chr2:105298837 | G | A | 1 | a0002c0004t0006g0208 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.689-132C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105298837 | |||||||
| chr2:105299040 | A | C | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.689-335T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299040 | |||||||
| chr2:105299174 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.689-469C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299174 | |||||||
| chr2:105299174 | G | C | 28 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(25): Show |
29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.689-469C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299174 | |||||||
| chr2:105299254 | C | T | 17 | a0002c0004t0006g0014 a0002c0004t0006g0015 a0002c0004t0006g0200 others(14): Show |
19 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.689-549G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299254 | |||||||
| chr2:105299284 | A | T | 5 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
5 | NA18949.hp1 NA18968.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.689-579T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299284 | |||||||
| chr2:105299368 | A | G | 1 | a0001c0003t0009g0216 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.689-663T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299368 | |||||||
| chr2:105299370 | G | T | 1 | a0002c0007t0003g0333 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.689-665C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299370 | |||||||
| chr2:105299549 | G | A | 5 | a0001c0001t0001g0046 a0001c0001t0001g0067 a0001c0001t0001g0126 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.689-844C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299549 | |||||||
| chr2:105299631 | G | A | 1 | a0002c0004t0006g0202 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.689-926C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299631 | |||||||
| chr2:105299636 | T | C | 17 | a0002c0004t0006g0014 a0002c0004t0006g0015 a0002c0004t0006g0200 others(14): Show |
19 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.689-931A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299636 | |||||||
| chr2:105299781 | C | T | 4 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0199 others(1): Show |
4 | HG02055.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-1076G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299781 | |||||||
| chr2:105300178 | A | T | 275 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(272): Show |
297 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.689-1473T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300178 | |||||||
| chr2:105300252 | G | A | 8 | a0001c0003t0007g0292 a0001c0003t0007g0293 a0001c0003t0007g0298 others(5): Show |
8 | HG00544.hp2 HG02056.hp1 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.689-1547C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300252 | |||||||
| chr2:105300406 | C | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0126 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.689-1701G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300406 | |||||||
| chr2:105300434 | C | CT | 67 | a0001c0003t0004g0291 a0001c0003t0004g0304 a0001c0003t0007g0292 others(64): Show |
77 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.689-1730dupA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300434 | |||||||
| chr2:105300452 | TTTC | T | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.689-1750_689-1748d others(5): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300452 | |||||||
| chr2:105300454 | TC | T | 126 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(123): Show |
129 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.689-1750delG | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300454 | |||||||
| chr2:105300454 | TCC | T | 12 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0074 others(9): Show |
12 | HG02083.hp2 HG02148.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.689-1751_689-1750d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300454 | |||||||
| chr2:105300455 | C | T | 94 | a0001c0006t0001g0159 a0001c0006t0001g0169 a0001c0006t0001g0197 others(91): Show |
109 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.689-1750G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300455 | |||||||
| chr2:105300456 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.689-1751G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300456 | |||||||
| chr2:105300597 | T | G | 1 | a0002c0005t0036g0242 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.689-1892A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300597 | |||||||
| chr2:105300640 | T | C | 10 | a0001c0006t0004g0345 a0002c0004t0003g0025 a0002c0004t0003g0340 others(7): Show |
11 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.689-1935A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300640 | |||||||
| chr2:105301052 | G | A | 17 | a0002c0004t0006g0014 a0002c0004t0006g0015 a0002c0004t0006g0200 others(14): Show |
19 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.689-2347C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301052 | |||||||
| chr2:105301084 | C | G | 4 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0199 others(1): Show |
4 | HG02055.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-2379G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301084 | |||||||
| chr2:105301145 | C | T | 5 | a0001c0006t0001g0196 a0002c0004t0013g0185 a0002c0004t0013g0193 others(2): Show |
5 | HG02559.hp2 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.689-2440G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301145 | |||||||
| chr2:105301154 | G | A | 1 | a0002c0009t0005g0055 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.689-2449C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301154 | |||||||
| chr2:105301226 | A | G | 16 | a0001c0006t0001g0196 a0001c0016t0001g0192 a0002c0004t0005g0039 others(13): Show |
16 | HG02109.hp2 HG02451.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.689-2521T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301226 | |||||||
| chr2:105301444 | A | C | 1 | a0002c0004t0018g0252 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.689-2739T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301444 | |||||||
| chr2:105301512 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.689-2807C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301512 | |||||||
| chr2:105301584 | CA | C | 4 | a0001c0003t0007g0325 a0002c0007t0019g0290 a0002c0007t0037g0295 others(1): Show |
4 | HG02280.hp1 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-2880delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301584 | |||||||
| chr2:105301586 | A | T | 4 | a0001c0003t0007g0325 a0002c0007t0019g0290 a0002c0007t0037g0295 others(1): Show |
4 | HG02280.hp1 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-2881T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301586 | |||||||
| chr2:105301587 | A | C | 4 | a0001c0003t0007g0325 a0002c0007t0019g0290 a0002c0007t0037g0295 others(1): Show |
4 | HG02280.hp1 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-2882T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301587 | |||||||
| chr2:105301609 | G | A | 247 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(244): Show |
268 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.689-2904C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301609 | |||||||
| chr2:105301653 | A | T | 28 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(25): Show |
29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.689-2948T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301653 | |||||||
| chr2:105301672 | T | C | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.689-2967A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301672 | |||||||
| chr2:105301881 | C | T | 1 | a0002c0002t0021g0183 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.689-3176G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301881 | |||||||
| chr2:105301890 | C | G | 1 | a0001c0003t0009g0129 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.689-3185G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301890 | |||||||
| chr2:105301897 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.689-3192A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301897 | |||||||
| chr2:105301999 | T | C | 4 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0199 others(1): Show |
4 | HG02055.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-3294A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301999 | |||||||
| chr2:105302009 | T | TA | 25 | a0001c0003t0004g0279 a0001c0003t0004g0304 a0001c0003t0007g0293 others(22): Show |
28 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.689-3305dupT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302009 | |||||||
| chr2:105302009 | T | TAA | 18 | a0001c0006t0001g0196 a0001c0006t0001g0197 a0001c0006t0001g0198 others(15): Show |
18 | HG02055.hp2 HG02109.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.689-3306_689-3305d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302009 | |||||||
| chr2:105302009 | TA | T | 151 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(148): Show |
158 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.689-3305delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302009 | |||||||
| chr2:105302009 | TAA | T | 7 | a0001c0001t0001g0083 a0001c0001t0001g0104 a0001c0001t0001g0111 others(4): Show |
8 | HG02451.hp2 HG02647.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.689-3306_689-3305d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302009 | |||||||
| chr2:105302140 | A | G | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.689-3435T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302140 | |||||||
| chr2:105302158 | A | G | 2 | a0001c0003t0007g0294 a0001c0003t0007g0307 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.689-3453T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302158 | |||||||
| chr2:105302237 | A | G | 1 | a0004c0019t0011g0346 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.689-3532T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302237 | |||||||
| chr2:105302394 | A | C | 17 | a0002c0004t0006g0014 a0002c0004t0006g0015 a0002c0004t0006g0200 others(14): Show |
19 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.689-3689T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302394 | |||||||
| chr2:105302437 | T | C | 1 | a0002c0004t0006g0202 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.689-3732A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302437 | |||||||
| chr2:105302473 | T | C | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.689-3768A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302473 | |||||||
| chr2:105302482 | A | G | 101 | a0001c0006t0001g0159 a0001c0006t0001g0169 a0001c0006t0001g0196 others(98): Show |
113 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.689-3777T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302482 | |||||||
| chr2:105302487 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.689-3782T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302487 | |||||||
| chr2:105302538 | TA | T | 244 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(241): Show |
265 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.689-3834delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302538 | |||||||
| chr2:105302650 | A | T | 128 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(125): Show |
132 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.689-3945T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302650 | |||||||
| chr2:105302675 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.689-3970A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302675 | |||||||
| chr2:105302686 | C | T | 1 | a0002c0002t0002g0158 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.689-3981G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302686 | |||||||
| chr2:105302886 | A | T | 20 | a0001c0006t0001g0196 a0001c0006t0001g0197 a0001c0006t0001g0198 others(17): Show |
20 | HG02055.hp2 HG02109.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.689-4181T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302886 | |||||||
| chr2:105303081 | G | A | 1 | a0003c0014t0019g0337 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.689-4376C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303081 | |||||||
| chr2:105303149 | C | A | 1 | a0001c0001t0001g0080 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.689-4444G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303149 | |||||||
| chr2:105303259 | G | A | 101 | a0001c0006t0001g0159 a0001c0006t0001g0169 a0001c0006t0001g0196 others(98): Show |
113 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.688+4355C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303259 | |||||||
| chr2:105303295 | C | A | 1 | a0002c0005t0003g0262 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.688+4319G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303295 | |||||||
| chr2:105303357 | C | T | 1 | a0002c0002t0002g0173 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.688+4257G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303357 | |||||||
| chr2:105303431 | G | A | 3 | a0002c0004t0003g0024 a0002c0004t0003g0338 a0002c0004t0003g0339 |
4 | HG02257.hp1 HG02818.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+4183C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303431 | |||||||
| chr2:105303433 | G | C | 2 | a0003c0014t0019g0336 a0003c0014t0019g0337 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.688+4181C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303433 | |||||||
| chr2:105303615 | A | G | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+3999T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303615 | |||||||
| chr2:105303628 | T | G | 8 | a0001c0001t0023g0061 a0001c0001t0023g0064 a0002c0009t0005g0005 others(5): Show |
9 | HG02451.hp2 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.688+3986A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303628 | |||||||
| chr2:105303710 | C | T | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.688+3904G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303710 | |||||||
| chr2:105303754 | C | G | 1 | a0001c0006t0001g0197 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.688+3860G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303754 | |||||||
| chr2:105303754 | C | T | 1 | a0002c0004t0032g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.688+3860G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303754 | |||||||
| chr2:105303828 | C | T | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+3786G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303828 | |||||||
| chr2:105303837 | C | T | 1 | a0001c0006t0001g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.688+3777G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303837 | |||||||
| chr2:105303894 | C | T | 3 | a0001c0016t0001g0192 a0002c0004t0005g0190 a0002c0004t0005g0191 |
3 | HG03130.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.688+3720G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303894 | |||||||
| chr2:105304026 | CTAAAAA | C | 3 | a0002c0009t0005g0005 a0002c0009t0005g0055 a0002c0009t0005g0056 |
4 | HG02451.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+3582_688+3587d others(8): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105304026 | |||||||
| chr2:105304197 | T | C | 1 | a0001c0003t0008g0288 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.688+3417A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105304197 | |||||||
| chr2:105304363 | A | G | 3 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 |
4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+3251T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105304363 | |||||||
| chr2:105304399 | C | T | 2 | a0002c0002t0002g0157 a0002c0002t0002g0241 |
2 | HG02040.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.688+3215G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105304399 | |||||||
| chr2:105304500 | C | T | 321 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(318): Show |
346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.688+3114G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105304500 | |||||||
| chr2:105304507 | G | A | 2 | a0001c0001t0023g0061 a0001c0001t0023g0064 |
2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.688+3107C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105304507 | |||||||
| chr2:105304554 | G | A | 1 | a0002c0007t0016g0334 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.688+3060C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105304554 | |||||||
| chr2:105304762 | G | A | 1 | a0001c0008t0001g0028 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.688+2852C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105304762 | |||||||
| chr2:105304764 | C | T | 1 | a0002c0004t0005g0188 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.688+2850G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105304764 | |||||||
| chr2:105304783 | G | A | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.688+2831C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105304783 | |||||||
| chr2:105305018 | T | C | 1 | a0002c0020t0003g0260 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.688+2596A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105305018 | |||||||
| chr2:105305118 | C | T | 5 | a0001c0001t0023g0061 a0001c0001t0023g0064 a0002c0009t0005g0062 others(2): Show |
5 | HG02809.hp2 HG02897.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.688+2496G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105305118 | |||||||
| chr2:105305322 | C | T | 6 | a0001c0003t0007g0292 a0001c0003t0007g0293 a0001c0003t0007g0320 others(3): Show |
6 | HG02056.hp1 NA18954.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.688+2292G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105305322 | |||||||
| chr2:105305440 | G | C | 1 | a0002c0002t0002g0152 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.688+2174C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105305440 | |||||||
| chr2:105305514 | A | G | 2 | a0002c0009t0005g0063 a0002c0009t0018g0244 |
2 | HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.688+2100T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105305514 | |||||||
| chr2:105305728 | G | A | 128 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(125): Show |
132 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.688+1886C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105305728 | |||||||
| chr2:105305750 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.688+1864G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105305750 | |||||||
| chr2:105306057 | TTTTG | T | 15 | a0001c0006t0001g0196 a0001c0016t0001g0192 a0002c0004t0005g0039 others(12): Show |
15 | HG02109.hp2 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.688+1553_688+1556d others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306057 | |||||||
| chr2:105306061 | G | GT | 4 | a0001c0001t0012g0245 a0001c0006t0009g0004 a0002c0004t0003g0341 others(1): Show |
5 | HG01070.hp2 HG02109.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.688+1552dupA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306061 | |||||||
| chr2:105306066 | T | G | 28 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(25): Show |
29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.688+1548A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306066 | |||||||
| chr2:105306067 | TG | T | 95 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(92): Show |
98 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.688+1546delC | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306067 | |||||||
| chr2:105306068 | G | T | 153 | a0001c0001t0001g0049 a0001c0001t0001g0071 a0001c0001t0001g0073 others(150): Show |
168 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.688+1546C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306068 | |||||||
| chr2:105306068 | GT | G | 20 | a0001c0001t0001g0016 a0001c0001t0001g0124 a0001c0001t0001g0221 others(17): Show |
21 | HG02109.hp2 HG02451.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.688+1545delA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306068 | |||||||
| chr2:105306069 | T | TTG | 85 | a0001c0006t0001g0159 a0001c0006t0001g0169 a0001c0006t0001g0197 others(82): Show |
97 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.688+1544_688+1545i others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306069 | |||||||
| chr2:105306071 | T | G | 1 | a0002c0012t0017g0259 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.688+1543A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306071 | |||||||
| chr2:105306075 | T | G | 4 | a0001c0003t0011g0305 a0001c0003t0011g0306 a0001c0003t0011g0313 others(1): Show |
4 | NA18945.hp1 NA18968.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+1539A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306075 | |||||||
| chr2:105306329 | T | C | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.688+1285A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306329 | |||||||
| chr2:105306335 | T | G | 1 | a0005c0015t0001g0088 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.688+1279A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306335 | |||||||
| chr2:105306336 | A | T | 1 | a0005c0015t0001g0088 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.688+1278T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306336 | |||||||
| chr2:105306341 | C | T | 133 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(130): Show |
140 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.688+1273G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306341 | |||||||
| chr2:105306368 | T | C | 1 | a0001c0003t0009g0129 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.688+1246A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306368 | |||||||
| chr2:105306417 | G | A | 1 | a0001c0003t0008g0319 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.688+1197C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306417 | |||||||
| chr2:105306422 | T | C | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.688+1192A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306422 | |||||||
| chr2:105306545 | C | T | 1 | a0002c0002t0002g0156 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.688+1069G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306545 | |||||||
| chr2:105306623 | C | T | 17 | a0002c0004t0006g0014 a0002c0004t0006g0015 a0002c0004t0006g0200 others(14): Show |
19 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.688+991G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306623 | |||||||
| chr2:105306682 | C | T | 1 | a0002c0005t0003g0262 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.688+932G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306682 | |||||||
| chr2:105306702 | G | T | 3 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 |
4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+912C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306702 | |||||||
| chr2:105306714 | G | A | 1 | a0001c0003t0026g0349 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.688+900C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306714 | |||||||
| chr2:105306791 | T | C | 3 | a0001c0016t0001g0192 a0002c0004t0005g0190 a0002c0004t0005g0191 |
3 | HG03130.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.688+823A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306791 | |||||||
| chr2:105306799 | A | G | 1 | a0002c0005t0003g0261 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.688+815T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306799 | |||||||
| chr2:105306875 | A | G | 4 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0199 others(1): Show |
4 | HG02055.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+739T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306875 | |||||||
| chr2:105306877 | A | G | 1 | a0002c0002t0002g0143 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.688+737T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306877 | |||||||
| chr2:105306914 | T | C | 2 | a0002c0002t0021g0172 a0002c0002t0021g0183 |
2 | HG03942.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.688+700A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306914 | |||||||
| chr2:105307188 | ACT | A | 28 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(25): Show |
29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.688+424_688+425del others(2): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105307188 | |||||||
| chr2:105307514 | G | A | 1 | a0002c0004t0006g0215 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.688+100C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105307514 | |||||||
| chr2:105307534 | G | A | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.688+80C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105307534 | |||||||
| chr2:105307560 | C | T | 28 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(25): Show |
29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.688+54G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105307560 | |||||||
| chr2:105307570 | G | A | 16 | a0001c0006t0001g0196 a0001c0016t0001g0192 a0002c0004t0005g0039 others(13): Show |
16 | HG02109.hp2 HG02451.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.688+44C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105307570 | |||||||
| chr2:105308490 | C | T | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-172G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105308490 | |||||||
| chr2:105308624 | T | C | 101 | a0001c0006t0001g0159 a0001c0006t0001g0169 a0001c0006t0001g0196 others(98): Show |
113 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-17-306A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105308624 | |||||||
| chr2:105308701 | C | T | 3 | a0002c0009t0005g0062 a0002c0009t0005g0063 a0002c0009t0018g0244 |
3 | HG02809.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-17-383G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105308701 | |||||||
| chr2:105308708 | A | G | 37 | a0001c0006t0001g0196 a0001c0006t0001g0197 a0001c0006t0001g0198 others(34): Show |
39 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-17-390T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105308708 | |||||||
| chr2:105308758 | C | T | 1 | a0002c0002t0002g0142 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-17-440G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105308758 | |||||||
| chr2:105308763 | TA | T | 132 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(129): Show |
139 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-17-446delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105308763 | |||||||
| chr2:105308854 | T | C | 64 | a0001c0006t0001g0159 a0001c0006t0001g0169 a0001c0006t0035g0155 others(61): Show |
74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.-17-536A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105308854 | |||||||
| chr2:105309015 | G | A | 1 | a0002c0002t0021g0183 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-17-697C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105309015 | |||||||
| chr2:105309070 | C | T | 5 | a0001c0001t0001g0044 a0001c0001t0001g0087 a0001c0001t0001g0098 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-752G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105309070 | |||||||
| chr2:105309113 | G | A | 1 | a0001c0001t0012g0243 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-17-795C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105309113 | |||||||
| chr2:105309785 | C | G | 28 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(25): Show |
29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-17-1467G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105309785 | |||||||
| chr2:105310118 | T | G | 1 | a0002c0004t0005g0042 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-17-1800A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310118 | |||||||
| chr2:105310183 | G | A | 8 | a0001c0001t0023g0061 a0001c0001t0023g0064 a0002c0009t0005g0005 others(5): Show |
9 | HG02451.hp2 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17-1865C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310183 | |||||||
| chr2:105310417 | T | C | 101 | a0001c0006t0001g0159 a0001c0006t0001g0169 a0001c0006t0001g0196 others(98): Show |
113 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-17-2099A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310417 | |||||||
| chr2:105310484 | C | T | 1 | a0002c0004t0006g0203 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-17-2166G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310484 | |||||||
| chr2:105310569 | T | C | 1 | a0001c0003t0004g0284 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-17-2251A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310569 | |||||||
| chr2:105310706 | A | G | 4 | a0002c0005t0003g0253 a0002c0005t0042g0351 a0002c0012t0017g0017 others(1): Show |
5 | HG00639.hp2 HG01975.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-2388T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310706 | |||||||
| chr2:105310734 | T | C | 4 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0199 others(1): Show |
4 | HG02055.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-2416A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310734 | |||||||
| chr2:105310842 | T | C | 1 | a0002c0002t0002g0040 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-17-2524A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310842 | |||||||
| chr2:105310854 | T | C | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-2536A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310854 | |||||||
| chr2:105310942 | A | G | 1 | a0001c0006t0035g0155 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-17-2624T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310942 | |||||||
| chr2:105310943 | C | T | 28 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(25): Show |
29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-17-2625G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310943 | |||||||
| chr2:105310960 | C | T | 76 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0050 others(73): Show |
78 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.-17-2642G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310960 | |||||||
| chr2:105311145 | T | TA | 11 | a0001c0001t0001g0098 a0001c0001t0001g0116 a0001c0003t0007g0307 others(8): Show |
13 | HG01243.hp1 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-17-2828dupT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311145 | |||||||
| chr2:105311154 | A | C | 64 | a0001c0006t0001g0159 a0001c0006t0001g0169 a0001c0006t0035g0155 others(61): Show |
74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.-17-2836T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311154 | |||||||
| chr2:105311155 | A | C | 103 | a0001c0006t0001g0159 a0001c0006t0001g0169 a0001c0006t0001g0196 others(100): Show |
115 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.-17-2837T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311155 | |||||||
| chr2:105311161 | A | AAC | 28 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(25): Show |
29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-17-2844_-17-2843i others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311161 | |||||||
| chr2:105311162 | C | A | 31 | a0002c0004t0003g0024 a0002c0004t0003g0338 a0002c0004t0003g0339 others(28): Show |
33 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.-17-2844G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311162 | |||||||
| chr2:105311169 | C | A | 3 | a0002c0004t0003g0024 a0002c0004t0003g0338 a0002c0004t0003g0339 |
4 | HG02257.hp1 HG02818.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-2851G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311169 | |||||||
| chr2:105311253 | GT | G | 101 | a0001c0006t0001g0159 a0001c0006t0001g0169 a0001c0006t0001g0196 others(98): Show |
113 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-17-2936delA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311253 | |||||||
| chr2:105311348 | G | A | 20 | a0001c0006t0001g0196 a0001c0006t0001g0197 a0001c0006t0001g0198 others(17): Show |
20 | HG02055.hp2 HG02109.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.-17-3030C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311348 | |||||||
| chr2:105311539 | T | C | 275 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(272): Show |
297 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.-17-3221A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311539 | |||||||
| chr2:105311588 | G | GA | 5 | a0001c0006t0001g0196 a0002c0004t0013g0185 a0002c0004t0013g0193 others(2): Show |
5 | HG02559.hp2 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-3271dupT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311588 | |||||||
| chr2:105311648 | C | T | 1 | a0002c0002t0002g0141 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-17-3330G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311648 | |||||||
| chr2:105311674 | G | A | 1 | a0001c0006t0001g0169 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-17-3356C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311674 | |||||||
| chr2:105311750 | C | A | 8 | a0001c0001t0023g0061 a0001c0001t0023g0064 a0002c0009t0005g0005 others(5): Show |
9 | HG02451.hp2 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17-3432G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311750 | |||||||
| chr2:105312089 | G | C | 2 | a0003c0014t0019g0336 a0003c0014t0019g0337 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-17-3771C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312089 | |||||||
| chr2:105312098 | C | A | 1 | a0002c0013t0005g0058 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-17-3780G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312098 | |||||||
| chr2:105312204 | A | G | 4 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0199 others(1): Show |
4 | HG02055.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-3886T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312204 | |||||||
| chr2:105312303 | A | T | 17 | a0002c0004t0006g0014 a0002c0004t0006g0015 a0002c0004t0006g0200 others(14): Show |
19 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-17-3985T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312303 | |||||||
| chr2:105312447 | A | T | 2 | a0001c0003t0009g0031 a0001c0003t0009g0130 |
2 | HG01358.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-17-4129T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312447 | |||||||
| chr2:105312467 | C | G | 9 | a0001c0006t0004g0345 a0002c0004t0003g0025 a0002c0004t0003g0340 others(6): Show |
10 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-4149G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312467 | |||||||
| chr2:105312554 | G | A | 23 | a0001c0001t0001g0016 a0001c0001t0001g0218 a0001c0001t0001g0219 others(20): Show |
24 | HG00408.hp1 HG01192.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.-17-4236C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312554 | |||||||
| chr2:105312590 | G | A | 2 | a0003c0014t0019g0336 a0003c0014t0019g0337 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-17-4272C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312590 | |||||||
| chr2:105312591 | T | G | 17 | a0002c0004t0006g0014 a0002c0004t0006g0015 a0002c0004t0006g0200 others(14): Show |
19 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-17-4273A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312591 | |||||||
| chr2:105312867 | T | C | 1 | a0002c0004t0032g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-17-4549A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312867 | |||||||
| chr2:105312940 | T | C | 275 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(272): Show |
297 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.-17-4622A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312940 | |||||||
| chr2:105312942 | C | T | 247 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(244): Show |
268 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.-17-4624G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312942 | |||||||
| chr2:105313069 | G | A | 1 | a0001c0003t0009g0130 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-17-4751C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105313069 | |||||||
| chr2:105313125 | G | C | 2 | a0003c0014t0019g0336 a0003c0014t0019g0337 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-17-4807C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105313125 | |||||||
| chr2:105313257 | A | C | 1 | a0001c0001t0001g0016 | 2 | NA19060.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-17-4939T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105313257 | |||||||
| chr2:105313444 | T | C | 278 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(275): Show |
300 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.-17-5126A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105313444 | |||||||
| chr2:105313556 | T | C | 3 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 |
4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-5238A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105313556 | |||||||
| chr2:105313613 | A | G | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-5295T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105313613 | |||||||
| chr2:105313687 | A | G | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-5369T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105313687 | |||||||
| chr2:105313908 | C | G | 101 | a0001c0006t0001g0159 a0001c0006t0001g0169 a0001c0006t0001g0196 others(98): Show |
113 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-17-5590G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105313908 | |||||||
| chr2:105313949 | C | A | 1 | a0002c0009t0005g0062 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-17-5631G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105313949 | |||||||
| chr2:105314082 | G | C | 8 | a0001c0001t0023g0061 a0001c0001t0023g0064 a0002c0009t0005g0005 others(5): Show |
9 | HG02451.hp2 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17-5764C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314082 | |||||||
| chr2:105314249 | C | CT | 18 | a0001c0001t0001g0089 a0001c0003t0004g0291 a0001c0003t0007g0325 others(15): Show |
19 | HG01175.hp2 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.-17-5932dupA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314249 | |||||||
| chr2:105314249 | C | CTT | 14 | a0001c0006t0001g0196 a0002c0004t0005g0186 a0002c0004t0005g0187 others(11): Show |
14 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-17-5933_-17-5932d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314249 | |||||||
| chr2:105314249 | CT | C | 122 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(119): Show |
128 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-17-5932delA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314249 | |||||||
| chr2:105314264 | T | C | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-5946A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314264 | |||||||
| chr2:105314278 | T | A | 1 | a0002c0005t0003g0274 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-17-5960A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314278 | |||||||
| chr2:105314282 | G | A | 23 | a0001c0001t0001g0016 a0001c0001t0001g0218 a0001c0001t0001g0219 others(20): Show |
24 | HG00408.hp1 HG01192.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.-17-5964C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314282 | |||||||
| chr2:105314283 | C | G | 1 | a0002c0004t0006g0202 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-17-5965G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314283 | |||||||
| chr2:105314310 | T | G | 247 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(244): Show |
268 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.-17-5992A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314310 | |||||||
| chr2:105314352 | G | A | 1 | a0002c0002t0002g0170 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-17-6034C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314352 | |||||||
| chr2:105314529 | C | T | 28 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(25): Show |
29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-17-6211G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314529 | |||||||
| chr2:105314531 | T | C | 3 | a0001c0016t0001g0192 a0002c0004t0005g0190 a0002c0004t0005g0191 |
3 | HG03130.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-17-6213A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314531 | |||||||
| chr2:105314628 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-17-6310C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314628 | |||||||
| chr2:105314708 | G | C | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-6390C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314708 | |||||||
| chr2:105314860 | G | A | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-6542C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314860 | |||||||
| chr2:105314949 | C | CA | 52 | a0001c0001t0001g0075 a0001c0001t0001g0125 a0001c0001t0024g0117 others(49): Show |
57 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.-17-6632dupT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314949 | |||||||
| chr2:105314949 | CA | C | 22 | a0001c0001t0001g0081 a0001c0001t0001g0099 a0001c0006t0001g0196 others(19): Show |
22 | HG01169.hp2 HG02109.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.-17-6632delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314949 | |||||||
| chr2:105315018 | ACT | A | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-6702_-17-6701d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105315018 | |||||||
| chr2:105315057 | A | C | 1 | a0002c0002t0002g0153 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-17-6739T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105315057 | |||||||
| chr2:105315236 | G | A | 9 | a0001c0003t0008g0287 a0001c0003t0008g0288 a0001c0003t0008g0309 others(6): Show |
10 | NA18951.hp1 NA18952.hp1 NA18953.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-6918C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105315236 | |||||||
| chr2:105315418 | A | G | 1 | a0001c0003t0011g0289 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-17-7100T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105315418 | |||||||
| chr2:105315609 | C | T | 1 | a0002c0004t0032g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-17-7291G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105315609 | |||||||
| chr2:105315881 | G | T | 10 | a0001c0006t0004g0345 a0002c0004t0003g0025 a0002c0004t0003g0340 others(7): Show |
11 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17-7563C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105315881 | |||||||
| chr2:105315905 | C | T | 2 | a0003c0014t0019g0336 a0003c0014t0019g0337 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-17-7587G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105315905 | |||||||
| chr2:105315923 | A | G | 1 | a0005c0015t0001g0088 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-17-7605T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105315923 | |||||||
| chr2:105316287 | G | C | 1 | a0002c0005t0003g0254 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-17-7969C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316287 | |||||||
| chr2:105316340 | CA | C | 16 | a0001c0001t0001g0239 a0001c0003t0011g0282 a0001c0006t0004g0345 others(13): Show |
18 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-17-8023delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316340 | |||||||
| chr2:105316341 | A | C | 1 | a0002c0002t0002g0143 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-17-8023T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316341 | |||||||
| chr2:105316420 | A | AGT | 34 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0059 others(31): Show |
36 | HG00408.hp2 HG01074.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.-17-8104_-17-8103d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316420 | |||||||
| chr2:105316420 | A | AGTGT | 15 | a0001c0001t0001g0044 a0001c0001t0001g0081 a0001c0001t0001g0082 others(12): Show |
15 | HG00558.hp2 HG00621.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-8106_-17-8103d others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316420 | |||||||
| chr2:105316420 | A | AGTGTGT | 8 | a0001c0001t0001g0049 a0001c0001t0001g0076 a0001c0001t0001g0077 others(5): Show |
8 | HG02300.hp1 HG03704.hp1 NA18989.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-8108_-17-8103d others(8): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316420 | |||||||
| chr2:105316420 | A | AGTGTGTG others(1): Show |
7 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(4): Show |
7 | HG00323.hp1 HG02165.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-8110_-17-8103d others(10): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316420 | |||||||
| chr2:105316420 | A | AGTGTGTG others(5): Show |
1 | a0001c0001t0001g0071 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-17-8114_-17-8103d others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316420 | |||||||
| chr2:105316420 | AGT | A | 6 | a0001c0001t0001g0118 a0001c0001t0023g0064 a0001c0003t0004g0327 others(3): Show |
7 | HG00741.hp2 HG01167.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-8104_-17-8103d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316420 | |||||||
| chr2:105316420 | AGTGT | A | 5 | a0001c0001t0001g0060 a0001c0003t0004g0314 a0001c0003t0004g0332 others(2): Show |
5 | HG01928.hp2 HG03942.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-8106_-17-8103d others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316420 | |||||||
| chr2:105316422 | T | A | 2 | a0002c0004t0005g0189 a0002c0004t0018g0252 |
2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-17-8104A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316422 | |||||||
| chr2:105316446 | TGTGTGTG others(19): Show |
T | 1 | a0002c0009t0005g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-17-8154_-17-8129d others(28): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316446 | |||||||
| chr2:105316452 | TGTGTGTG others(7): Show |
T | 1 | a0001c0001t0001g0099 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-17-8148_-17-8135d others(16): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316452 | |||||||
| chr2:105316454 | TGTGTGTG others(7): Show |
T | 1 | a0002c0002t0002g0010 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-17-8150_-17-8137d others(16): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316454 | |||||||
| chr2:105316454 | TGTGTGTG others(11): Show |
T | 4 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0199 others(1): Show |
4 | HG02055.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-8154_-17-8137d others(20): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316454 | |||||||
| chr2:105316456 | TGTGTGTG others(5): Show |
T | 1 | a0001c0006t0009g0004 | 2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-17-8150_-17-8139d others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316456 | |||||||
| chr2:105316456 | TGTGTGTG others(9): Show |
T | 2 | a0001c0011t0014g0002 a0002c0009t0005g0055 |
2 | HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-17-8154_-17-8139d others(18): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316456 | |||||||
| chr2:105316458 | T | C | 1 | a0002c0009t0005g0056 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-17-8140A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316458 | |||||||
| chr2:105316458 | TGTGTGCG others(3): Show |
T | 3 | a0001c0001t0001g0219 a0001c0001t0001g0237 a0002c0004t0005g0042 |
3 | HG03239.hp1 HG03453.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-17-8150_-17-8141d others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316458 | |||||||
| chr2:105316458 | TGTGTGCG others(5): Show |
T | 1 | a0002c0002t0002g0168 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-17-8152_-17-8141d others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316458 | |||||||
| chr2:105316458 | TGTGTGCG others(7): Show |
T | 2 | a0002c0004t0006g0207 a0002c0004t0028g0214 |
2 | HG00735.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.-17-8154_-17-8141d others(16): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316458 | |||||||
| chr2:105316458 | TGTGTGCG others(9): Show |
T | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
3 | HG02055.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-17-8156_-17-8141d others(18): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316458 | |||||||
| chr2:105316460 | T | C | 2 | a0001c0003t0011g0282 a0002c0009t0005g0056 |
2 | HG02451.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.-17-8142A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316460 | |||||||
| chr2:105316460 | T | TGC | 3 | a0001c0003t0008g0318 a0001c0003t0011g0305 a0001c0003t0011g0330 |
3 | NA18968.hp1 NA18975.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-17-8143_-17-8142i others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316460 | |||||||
| chr2:105316460 | TGTGCGC | T | 3 | a0001c0001t0001g0226 a0001c0001t0001g0230 a0001c0001t0001g0238 |
3 | HG04204.hp1 NA18951.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.-17-8148_-17-8143d others(8): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316460 | |||||||
| chr2:105316460 | TGTGCGCG others(1): Show |
T | 4 | a0001c0001t0001g0218 a0001c0001t0001g0221 a0001c0001t0001g0222 others(1): Show |
4 | HG02683.hp1 HG03017.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-8150_-17-8143d others(10): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316460 | |||||||
| chr2:105316460 | TGTGCGCG others(3): Show |
T | 4 | a0002c0002t0002g0158 a0002c0002t0021g0183 a0002c0005t0003g0255 others(1): Show |
4 | HG01261.hp1 HG02056.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-8152_-17-8143d others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316460 | |||||||
| chr2:105316460 | TGTGCGCG others(5): Show |
T | 6 | a0001c0006t0001g0159 a0002c0002t0002g0135 a0002c0002t0002g0154 others(3): Show |
6 | HG00673.hp1 HG03669.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-8154_-17-8143d others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316460 | |||||||
| chr2:105316462 | T | C | 14 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0038 others(11): Show |
15 | HG00423.hp1 HG00741.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-8144A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | |||||||
| chr2:105316462 | T | TGC | 7 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0037 others(4): Show |
7 | HG02015.hp2 HG02818.hp1 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-8146_-17-8145d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | |||||||
| chr2:105316462 | T | TGCGC | 5 | a0001c0003t0004g0304 a0001c0003t0007g0298 a0001c0003t0007g0323 others(2): Show |
5 | HG00544.hp2 HG01074.hp2 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-8148_-17-8145d others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | |||||||
| chr2:105316462 | T | TGCGCGCG others(3): Show |
1 | a0001c0003t0034g0127 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-17-8154_-17-8145d others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | |||||||
| chr2:105316462 | T | TGTGC | 8 | a0001c0001t0001g0113 a0001c0001t0024g0117 a0001c0003t0004g0021 others(5): Show |
8 | HG00323.hp2 HG01123.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-8145_-17-8144i others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | |||||||
| chr2:105316462 | T | TGTGCGC | 4 | a0001c0003t0004g0308 a0001c0003t0008g0317 a0001c0003t0011g0306 others(1): Show |
4 | NA18945.hp1 NA18965.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-8145_-17-8144i others(8): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | |||||||
| chr2:105316462 | T | TGTGCGCG others(3): Show |
2 | a0001c0003t0009g0129 a0001c0003t0009g0216 |
2 | HG00140.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-17-8145_-17-8144i others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | |||||||
| chr2:105316462 | T | TGTGCGCG others(5): Show |
1 | a0001c0003t0009g0031 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-17-8145_-17-8144i others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | |||||||
| chr2:105316462 | T | TGTGCGCG others(7): Show |
2 | a0001c0003t0007g0335 a0001c0003t0009g0130 |
2 | HG01516.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-17-8145_-17-8144i others(16): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | |||||||
| chr2:105316462 | T | TGTGTGCG others(5): Show |
1 | a0001c0003t0009g0128 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-17-8145_-17-8144i others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | |||||||
| chr2:105316462 | T | TGTGTGCG others(9): Show |
1 | a0002c0007t0037g0295 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-17-8145_-17-8144i others(18): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | |||||||
| chr2:105316462 | T | TGTGTGTG others(3): Show |
2 | a0001c0003t0008g0319 a0001c0003t0024g0122 |
2 | NA18983.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-17-8145_-17-8144i others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | |||||||
| chr2:105316462 | T | TGTGTGTG others(3): Show |
3 | a0001c0003t0007g0297 a0001c0003t0041g0280 a0002c0007t0003g0018 |
3 | HG02922.hp1 HG03041.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-17-8145_-17-8144i others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | |||||||
| chr2:105316462 | T | TGTGTGTG others(5): Show |
2 | a0001c0003t0004g0279 a0001c0003t0043g0352 |
2 | HG01175.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-17-8145_-17-8144i others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | |||||||
| chr2:105316462 | T | TGTGTGTG others(5): Show |
1 | a0001c0003t0026g0349 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-17-8145_-17-8144i others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | |||||||
| chr2:105316462 | T | TGTGTGTG others(7): Show |
1 | a0002c0007t0003g0018 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-17-8145_-17-8144i others(16): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | |||||||
| chr2:105316462 | T | TGTGTGTG others(9): Show |
1 | a0001c0003t0026g0350 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-17-8145_-17-8144i others(18): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | |||||||
| chr2:105316464 | C | T | 168 | a0001c0001t0001g0044 a0001c0001t0001g0050 a0001c0001t0001g0051 others(165): Show |
180 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.-17-8146G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316464 | |||||||
| chr2:105316466 | C | A | 1 | a0002c0004t0006g0015 | 2 | NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-17-8148G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316466 | |||||||
| chr2:105316466 | C | T | 60 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0074 others(57): Show |
63 | HG00423.hp2 HG00558.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.-17-8148G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316466 | |||||||
| chr2:105316467 | GCGCGCGC others(7): Show |
G | 2 | a0002c0012t0017g0017 a0002c0012t0017g0259 |
3 | HG00639.hp2 HG01975.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.-17-8163_-17-8150d others(16): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316467 | |||||||
| chr2:105316468 | C | A | 2 | a0002c0004t0006g0209 a0002c0004t0006g0215 |
2 | HG01261.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-17-8150G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316468 | |||||||
| chr2:105316468 | C | T | 18 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(15): Show |
18 | HG01109.hp1 HG02004.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-8150G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316468 | |||||||
| chr2:105316469 | G | A | 1 | a0001c0003t0004g0314 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-17-8151C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316469 | |||||||
| chr2:105316469 | GCGCGCGC others(5): Show |
G | 16 | a0001c0006t0001g0196 a0002c0004t0003g0339 a0002c0004t0006g0015 others(13): Show |
17 | HG00673.hp2 HG01071.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.-17-8163_-17-8152d others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316469 | |||||||
| chr2:105316470 | C | A | 7 | a0002c0004t0006g0014 a0002c0004t0006g0200 a0002c0004t0006g0202 others(4): Show |
8 | HG00639.hp1 HG00741.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-8152G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316470 | |||||||
| chr2:105316470 | C | T | 9 | a0001c0006t0035g0155 a0002c0002t0002g0007 a0002c0002t0002g0009 others(6): Show |
10 | HG02257.hp1 HG02280.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-8152G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316470 | |||||||
| chr2:105316471 | GCGCGCGC others(3): Show |
G | 31 | a0001c0006t0004g0345 a0002c0002t0002g0011 a0002c0002t0002g0157 others(28): Show |
33 | HG00280.hp2 HG00544.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.-17-8163_-17-8154d others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316471 | |||||||
| chr2:105316472 | C | A | 3 | a0002c0004t0006g0208 a0002c0004t0006g0213 a0002c0004t0031g0211 |
3 | HG01934.hp1 HG02132.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-17-8154G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316472 | |||||||
| chr2:105316473 | G | A | 2 | a0002c0009t0005g0063 a0002c0009t0018g0244 |
2 | HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-17-8155C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316473 | |||||||
| chr2:105316473 | GCGCGCGC others(1): Show |
G | 43 | a0001c0001t0001g0125 a0002c0002t0002g0001 a0002c0002t0002g0008 others(40): Show |
50 | HG00140.hp1 HG00558.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.-17-8163_-17-8156d others(10): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316473 | |||||||
| chr2:105316475 | G | A | 6 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0199 others(3): Show |
6 | HG02055.hp2 HG02895.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-8157C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316475 | |||||||
| chr2:105316475 | GCGCGCA | G | 23 | a0001c0001t0001g0220 a0001c0006t0001g0169 a0001c0006t0009g0041 others(20): Show |
23 | HG00408.hp1 HG00423.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.-17-8163_-17-8158d others(8): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316475 | |||||||
| chr2:105316477 | GCGCA | G | 11 | a0001c0001t0001g0229 a0001c0016t0001g0192 a0002c0002t0002g0012 others(8): Show |
11 | HG02004.hp1 HG02602.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17-8163_-17-8160d others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316477 | |||||||
| chr2:105316478 | C | A | 4 | a0002c0004t0006g0207 a0002c0004t0006g0210 a0002c0004t0006g0212 others(1): Show |
4 | HG00735.hp2 HG02004.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-8160G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316478 | |||||||
| chr2:105316479 | GCA | G | 23 | a0001c0001t0001g0051 a0001c0001t0001g0104 a0001c0001t0001g0105 others(20): Show |
23 | HG01070.hp1 HG02040.hp2 HG02165.hp2 others(20): Show |
intron_variant | MODIFIER | c.-17-8163_-17-8162d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316479 | |||||||
| chr2:105316481 | A | G | 131 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(128): Show |
137 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.-17-8163T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316481 | |||||||
| chr2:105316483 | G | A | 1 | a0002c0022t0010g0275 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-17-8165C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316483 | |||||||
| chr2:105316483 | G | GCGCGCGC others(11): Show |
1 | a0003c0014t0019g0337 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-17-8166_-17-8165i others(20): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316483 | |||||||
| chr2:105316485 | G | A | 27 | a0001c0003t0011g0313 a0002c0005t0003g0253 a0002c0005t0003g0254 others(24): Show |
28 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.-17-8167C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316485 | |||||||
| chr2:105316509 | T | C | 2 | a0002c0009t0005g0005 a0002c0009t0005g0056 |
3 | HG02451.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-17-8191A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316509 | |||||||
| chr2:105316684 | C | A | 1 | a0001c0001t0001g0119 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-17-8366G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316684 | |||||||
| chr2:105316746 | G | A | 1 | a0001c0003t0004g0314 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-17-8428C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316746 | |||||||
| chr2:105316799 | G | C | 2 | a0002c0002t0021g0172 a0002c0002t0021g0183 |
2 | HG03942.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.-17-8481C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316799 | |||||||
| chr2:105316813 | C | CA | 16 | a0002c0004t0006g0014 a0002c0004t0006g0015 a0002c0004t0006g0202 others(13): Show |
18 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-8496dupT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316813 | |||||||
| chr2:105316813 | CA | C | 7 | a0001c0003t0011g0282 a0001c0003t0026g0349 a0002c0004t0013g0185 others(4): Show |
7 | HG02622.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-8496delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316813 | |||||||
| chr2:105316862 | C | G | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-8544G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316862 | |||||||
| chr2:105317080 | C | CTTGTATG others(24): Show |
3 | a0001c0016t0001g0192 a0002c0004t0005g0190 a0002c0004t0005g0191 |
3 | HG03130.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-17-8793_-17-8763d others(33): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317080 | |||||||
| chr2:105317176 | C | A | 2 | a0001c0003t0004g0278 a0001c0003t0004g0279 |
2 | HG01123.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-17-8858G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317176 | |||||||
| chr2:105317176 | C | T | 1 | a0002c0023t0003g0348 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-17-8858G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317176 | |||||||
| chr2:105317201 | G | A | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-8883C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317201 | |||||||
| chr2:105317204 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG00408.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.-17-8886G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317204 | |||||||
| chr2:105317272 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0027g0069 |
2 | NA18950.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.-17-8954T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317272 | |||||||
| chr2:105317329 | C | T | 1 | a0002c0004t0032g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-17-9011G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317329 | |||||||
| chr2:105317368 | C | T | 7 | a0001c0001t0001g0046 a0001c0001t0001g0067 a0001c0001t0001g0126 others(4): Show |
9 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-17-9050G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317368 | |||||||
| chr2:105317369 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG00408.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.-17-9051C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317369 | |||||||
| chr2:105317403 | C | T | 4 | a0002c0002t0002g0007 a0002c0002t0002g0137 a0002c0002t0002g0138 others(1): Show |
5 | NA18941.hp1 NA18981.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-9085G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317403 | |||||||
| chr2:105317434 | C | CA | 11 | a0001c0003t0007g0316 a0001c0003t0007g0323 a0001c0003t0008g0023 others(8): Show |
12 | HG02015.hp2 HG02055.hp2 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.-17-9117dupT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317434 | |||||||
| chr2:105317478 | C | T | 1 | a0002c0002t0002g0136 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-17-9160G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317478 | |||||||
| chr2:105317554 | A | C | 1 | a0002c0002t0002g0135 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-17-9236T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317554 | |||||||
| chr2:105317611 | A | G | 120 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(117): Show |
123 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.-17-9293T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317611 | |||||||
| chr2:105317764 | G | C | 1 | a0002c0007t0003g0333 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-17-9446C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317764 | |||||||
| chr2:105317844 | T | C | 3 | a0002c0004t0005g0186 a0002c0004t0005g0187 a0002c0004t0005g0240 |
3 | HG03669.hp2 HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-17-9526A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317844 | |||||||
| chr2:105317998 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0221 a0001c0001t0001g0222 |
4 | NA18950.hp1 NA18960.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-9680T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317998 | |||||||
| chr2:105318032 | G | C | 1 | a0002c0002t0002g0173 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-17-9714C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105318032 | |||||||
| chr2:105318175 | T | C | 1 | a0001c0001t0023g0064 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-17-9857A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105318175 | |||||||
| chr2:105318354 | C | G | 248 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(245): Show |
269 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.-17-10036G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105318354 | |||||||
| chr2:105318432 | A | C | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-10114T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105318432 | |||||||
| chr2:105318709 | A | G | 28 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(25): Show |
29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-17-10391T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105318709 | |||||||
| chr2:105318804 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-17-10486C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105318804 | |||||||
| chr2:105318822 | G | T | 134 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(131): Show |
141 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.-17-10504C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105318822 | |||||||
| chr2:105319027 | C | A | 3 | a0002c0004t0003g0024 a0002c0004t0003g0338 a0002c0004t0003g0339 |
4 | HG02257.hp1 HG02818.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+10598G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319027 | |||||||
| chr2:105319031 | G | A | 4 | a0001c0003t0007g0320 a0001c0003t0007g0321 a0001c0003t0007g0322 others(1): Show |
4 | HG02056.hp1 NA18954.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+10594C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319031 | |||||||
| chr2:105319065 | T | G | 6 | a0001c0001t0001g0124 a0002c0002t0002g0174 a0002c0004t0003g0339 others(3): Show |
6 | HG00642.hp2 HG01074.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+10560A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319065 | |||||||
| chr2:105319067 | G | T | 1 | a0001c0003t0004g0327 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-18+10558C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319067 | |||||||
| chr2:105319078 | T | TGA | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18+10545_-18+1054 others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319078 | |||||||
| chr2:105319115 | C | T | 1 | a0002c0004t0032g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-18+10510G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319115 | |||||||
| chr2:105319223 | G | A | 1 | a0001c0003t0007g0324 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18+10402C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319223 | |||||||
| chr2:105319337 | C | T | 10 | a0001c0006t0004g0345 a0002c0004t0003g0025 a0002c0004t0003g0340 others(7): Show |
11 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18+10288G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319337 | |||||||
| chr2:105319418 | G | A | 3 | a0001c0016t0001g0192 a0002c0004t0005g0190 a0002c0004t0005g0191 |
3 | HG03130.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-18+10207C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319418 | |||||||
| chr2:105319443 | G | A | 2 | a0001c0008t0001g0027 a0001c0008t0001g0028 |
2 | HG00558.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-18+10182C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319443 | |||||||
| chr2:105319452 | G | A | 1 | a0002c0002t0002g0012 | 2 | HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-18+10173C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319452 | |||||||
| chr2:105319624 | G | A | 2 | a0003c0014t0019g0336 a0003c0014t0019g0337 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-18+10001C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319624 | |||||||
| chr2:105319690 | C | CA | 7 | a0001c0001t0023g0061 a0001c0001t0023g0064 a0001c0001t0029g0236 others(4): Show |
7 | HG02809.hp2 HG02897.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+9934dupT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319690 | |||||||
| chr2:105319690 | CA | C | 117 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(114): Show |
131 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.-18+9934delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319690 | |||||||
| chr2:105319939 | A | C | 2 | a0003c0014t0019g0336 a0003c0014t0019g0337 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-18+9686T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319939 | |||||||
| chr2:105319955 | A | G | 278 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(275): Show |
300 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.-18+9670T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319955 | |||||||
| chr2:105320108 | T | C | 4 | a0001c0010t0001g0047 a0001c0010t0001g0048 a0001c0010t0001g0065 others(1): Show |
4 | HG01243.hp1 HG02647.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+9517A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105320108 | |||||||
| chr2:105320149 | G | A | 3 | a0002c0002t0002g0176 a0002c0002t0002g0177 a0002c0002t0033g0175 |
3 | HG02071.hp2 NA19064.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-18+9476C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105320149 | |||||||
| chr2:105320268 | G | A | 1 | a0001c0008t0001g0029 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-18+9357C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105320268 | |||||||
| chr2:105320552 | T | C | 28 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(25): Show |
29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-18+9073A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105320552 | |||||||
| chr2:105320653 | C | A | 2 | a0002c0002t0022g0178 a0002c0002t0022g0179 |
2 | NA18943.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-18+8972G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105320653 | |||||||
| chr2:105320964 | A | T | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18+8661T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105320964 | |||||||
| chr2:105321027 | C | T | 1 | a0002c0004t0005g0186 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-18+8598G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321027 | |||||||
| chr2:105321069 | T | C | 2 | a0001c0003t0007g0325 a0001c0003t0007g0326 |
2 | HG02280.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-18+8556A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321069 | |||||||
| chr2:105321092 | G | A | 248 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(245): Show |
269 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.-18+8533C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321092 | |||||||
| chr2:105321153 | C | CTTAT | 5 | a0002c0004t0003g0025 a0002c0004t0003g0340 a0002c0004t0005g0186 others(2): Show |
6 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+8468_-18+8471d others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321153 | |||||||
| chr2:105321168 | A | T | 8 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0300 others(5): Show |
8 | HG01123.hp2 HG01175.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18+8457T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321168 | |||||||
| chr2:105321172 | T | A | 262 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0034 others(259): Show |
281 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.-18+8453A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321172 | |||||||
| chr2:105321176 | T | A | 54 | a0001c0006t0001g0196 a0001c0006t0001g0197 a0001c0006t0001g0198 others(51): Show |
59 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.-18+8449A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321176 | |||||||
| chr2:105321176 | T | G | 1 | a0001c0006t0012g0251 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-18+8449A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321176 | |||||||
| chr2:105321291 | T | C | 4 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0199 others(1): Show |
4 | HG02055.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+8334A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321291 | |||||||
| chr2:105321387 | C | T | 1 | a0001c0001t0015g0057 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-18+8238G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321387 | |||||||
| chr2:105321457 | C | T | 1 | a0002c0002t0002g0134 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-18+8168G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321457 | |||||||
| chr2:105321622 | G | A | 1 | a0002c0002t0002g0184 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-18+8003C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321622 | |||||||
| chr2:105321650 | T | C | 276 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(273): Show |
298 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.-18+7975A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321650 | |||||||
| chr2:105321732 | A | C | 1 | a0002c0009t0005g0055 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-18+7893T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321732 | |||||||
| chr2:105321797 | G | T | 3 | a0002c0009t0005g0005 a0002c0009t0005g0055 a0002c0009t0005g0056 |
4 | HG02451.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+7828C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321797 | |||||||
| chr2:105321799 | G | A | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+7826C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321799 | |||||||
| chr2:105321921 | A | C | 248 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(245): Show |
269 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.-18+7704T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321921 | |||||||
| chr2:105322043 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-18+7582T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322043 | |||||||
| chr2:105322243 | TACA | T | 17 | a0002c0004t0006g0014 a0002c0004t0006g0015 a0002c0004t0006g0200 others(14): Show |
19 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-18+7379_-18+7381d others(5): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322243 | |||||||
| chr2:105322350 | T | G | 1 | a0001c0001t0012g0249 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-18+7275A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322350 | |||||||
| chr2:105322452 | C | T | 2 | a0001c0011t0014g0002 a0001c0011t0014g0043 |
4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+7173G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322452 | |||||||
| chr2:105322496 | A | G | 248 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(245): Show |
269 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.-18+7129T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322496 | |||||||
| chr2:105322533 | T | C | 1 | a0001c0003t0007g0335 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-18+7092A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322533 | |||||||
| chr2:105322579 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-18+7046G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322579 | |||||||
| chr2:105322694 | G | C | 28 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(25): Show |
29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-18+6931C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322694 | |||||||
| chr2:105322728 | C | G | 5 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0001c0011t0014g0002 others(2): Show |
8 | HG02055.hp1 HG02109.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+6897G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322728 | |||||||
| chr2:105322780 | C | T | 17 | a0002c0004t0006g0014 a0002c0004t0006g0015 a0002c0004t0006g0200 others(14): Show |
19 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-18+6845G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322780 | |||||||
| chr2:105322841 | A | C | 3 | a0002c0004t0003g0024 a0002c0004t0003g0338 a0002c0004t0003g0339 |
4 | HG02257.hp1 HG02818.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+6784T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322841 | |||||||
| chr2:105322900 | C | G | 2 | a0001c0003t0004g0278 a0001c0003t0004g0279 |
2 | HG01123.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-18+6725G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322900 | |||||||
| chr2:105322912 | C | G | 248 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(245): Show |
269 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.-18+6713G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322912 | |||||||
| chr2:105322973 | C | T | 248 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(245): Show |
269 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.-18+6652G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322973 | |||||||
| chr2:105323212 | C | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | NA18949.hp1 NA18968.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-18+6413G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105323212 | |||||||
| chr2:105323246 | G | C | 5 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0001c0011t0014g0002 others(2): Show |
8 | HG02055.hp1 HG02109.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+6379C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105323246 | |||||||
| chr2:105323473 | A | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | NA18612.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-18+6152T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105323473 | |||||||
| chr2:105323520 | G | T | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18+6105C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105323520 | |||||||
| chr2:105323578 | G | A | 2 | a0003c0014t0019g0336 a0003c0014t0019g0337 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-18+6047C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105323578 | |||||||
| chr2:105323989 | T | C | 248 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(245): Show |
269 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.-18+5636A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105323989 | |||||||
| chr2:105323994 | T | G | 1 | a0001c0001t0001g0237 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-18+5631A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105323994 | |||||||
| chr2:105324002 | C | A | 1 | a0002c0004t0018g0252 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-18+5623G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105324002 | |||||||
| chr2:105324133 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-18+5492C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105324133 | |||||||
| chr2:105324222 | G | A | 28 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(25): Show |
29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-18+5403C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105324222 | |||||||
| chr2:105324482 | G | A | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18+5143C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105324482 | |||||||
| chr2:105324884 | A | G | 1 | a0002c0004t0013g0185 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-18+4741T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105324884 | |||||||
| chr2:105324887 | T | A | 1 | a0002c0023t0003g0348 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-18+4738A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105324887 | |||||||
| chr2:105325173 | A | T | 134 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(131): Show |
141 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.-18+4452T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105325173 | |||||||
| chr2:105325230 | ATGGATGG others(19): Show |
A | 1 | a0001c0001t0001g0126 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-18+4369_-18+4394d others(28): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105325230 | |||||||
| chr2:105325331 | C | A | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18+4294G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105325331 | |||||||
| chr2:105325356 | C | T | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18+4269G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105325356 | |||||||
| chr2:105325466 | A | T | 129 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0033 others(126): Show |
133 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.-18+4159T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105325466 | |||||||
| chr2:105325612 | CTT | C | 17 | a0002c0004t0006g0014 a0002c0004t0006g0015 a0002c0004t0006g0200 others(14): Show |
19 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-18+4011_-18+4012d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105325612 | |||||||
| chr2:105325630 | A | T | 3 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0002c0004t0005g0042 |
4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+3995T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105325630 | |||||||
| chr2:105325632 | C | T | 2 | a0001c0010t0001g0047 a0001c0010t0001g0048 |
2 | HG01243.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-18+3993G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105325632 | |||||||
| chr2:105325793 | C | G | 28 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(25): Show |
29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-18+3832G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105325793 | |||||||
| chr2:105325955 | C | T | 1 | a0002c0005t0003g0253 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-18+3670G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105325955 | |||||||
| chr2:105326055 | T | A | 1 | a0001c0001t0001g0131 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-18+3570A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105326055 | |||||||
| chr2:105326290 | A | T | 2 | a0001c0001t0001g0046 a0001c0001t0012g0243 |
2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-18+3335T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105326290 | |||||||
| chr2:105326620 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-18+3005T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105326620 | |||||||
| chr2:105326668 | G | A | 17 | a0002c0004t0006g0014 a0002c0004t0006g0015 a0002c0004t0006g0200 others(14): Show |
19 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-18+2957C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105326668 | |||||||
| chr2:105326832 | C | T | 3 | a0002c0004t0003g0024 a0002c0004t0003g0338 a0002c0004t0003g0339 |
4 | HG02257.hp1 HG02818.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+2793G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105326832 | |||||||
| chr2:105326900 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-18+2725A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105326900 | |||||||
| chr2:105326981 | T | A | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18+2644A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105326981 | |||||||
| chr2:105326995 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-18+2630G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105326995 | |||||||
| chr2:105327112 | C | G | 64 | a0001c0006t0001g0159 a0001c0006t0001g0169 a0001c0006t0035g0155 others(61): Show |
74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.-18+2513G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327112 | |||||||
| chr2:105327122 | T | C | 101 | a0001c0006t0001g0159 a0001c0006t0001g0169 a0001c0006t0001g0196 others(98): Show |
113 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-18+2503A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327122 | |||||||
| chr2:105327128 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-18+2497G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327128 | |||||||
| chr2:105327218 | A | AT | 13 | a0001c0001t0001g0218 a0001c0006t0004g0345 a0002c0004t0003g0024 others(10): Show |
14 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-18+2406dupA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327218 | |||||||
| chr2:105327375 | G | A | 13 | a0001c0006t0004g0345 a0002c0004t0003g0024 a0002c0004t0003g0025 others(10): Show |
15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18+2250C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327375 | |||||||
| chr2:105327401 | C | T | 1 | a0002c0002t0002g0133 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-18+2224G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327401 | |||||||
| chr2:105327409 | A | T | 10 | a0001c0006t0004g0345 a0002c0004t0003g0025 a0002c0004t0003g0340 others(7): Show |
11 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18+2216T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327409 | |||||||
| chr2:105327438 | C | T | 1 | a0002c0004t0032g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-18+2187G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327438 | |||||||
| chr2:105327442 | C | A | 1 | a0001c0001t0001g0239 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-18+2183G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327442 | |||||||
| chr2:105327590 | C | A | 101 | a0001c0006t0001g0159 a0001c0006t0001g0169 a0001c0006t0001g0196 others(98): Show |
113 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-18+2035G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327590 | |||||||
| chr2:105327688 | G | T | 2 | a0001c0003t0041g0280 a0002c0007t0003g0018 |
3 | HG02257.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-18+1937C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327688 | |||||||
| chr2:105327737 | G | C | 1 | a0001c0003t0009g0216 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-18+1888C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327737 | |||||||
| chr2:105327911 | T | C | 10 | a0001c0006t0004g0345 a0002c0004t0003g0025 a0002c0004t0003g0340 others(7): Show |
11 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18+1714A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327911 | |||||||
| chr2:105328099 | A | G | 5 | a0001c0006t0009g0004 a0001c0006t0009g0041 a0001c0011t0014g0002 others(2): Show |
8 | HG02055.hp1 HG02109.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+1526T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105328099 | |||||||
| chr2:105328166 | C | T | 1 | a0002c0002t0002g0040 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-18+1459G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105328166 | |||||||
| chr2:105328242 | T | C | 1 | a0002c0002t0002g0217 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18+1383A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105328242 | |||||||
| chr2:105328272 | T | C | 10 | a0001c0006t0004g0345 a0002c0004t0003g0025 a0002c0004t0003g0340 others(7): Show |
11 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18+1353A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105328272 | |||||||
| chr2:105328533 | G | A | 23 | a0001c0001t0001g0016 a0001c0001t0001g0218 a0001c0001t0001g0219 others(20): Show |
24 | HG00408.hp1 HG01192.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.-18+1092C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105328533 | |||||||
| chr2:105328609 | A | G | 1 | a0002c0004t0005g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-18+1016T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105328609 | |||||||
| chr2:105328619 | C | G | 2 | a0001c0003t0004g0278 a0001c0003t0004g0279 |
2 | HG01123.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-18+1006G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105328619 | |||||||
| chr2:105328671 | C | T | 7 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(4): Show |
7 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+954G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105328671 | |||||||
| chr2:105329011 | T | C | 2 | a0002c0005t0010g0276 a0002c0005t0010g0277 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-18+614A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105329011 | |||||||
| chr2:105329379 | G | A | 2 | a0001c0008t0001g0003 a0001c0008t0001g0030 |
3 | NA18977.hp1 NA19000.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.-18+246C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105329379 | |||||||
| chr2:105329394 | C | T | 28 | a0002c0005t0003g0253 a0002c0005t0003g0254 a0002c0005t0003g0255 others(25): Show |
29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-18+231G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105329394 | |||||||
| chr2:105329432 | C | A | 1 | a0002c0004t0005g0240 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-18+193G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105329432 | |||||||
| chr2:105329455 | C | A | 1 | a0002c0002t0002g0241 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-18+170G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105329455 | |||||||
| chr2:105329520 | A | G | 1 | a0001c0003t0009g0031 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-18+105T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105329520 | |||||||
| chr2:105329559 | C | T | 6 | a0001c0008t0001g0003 a0001c0008t0001g0026 a0001c0008t0001g0027 others(3): Show |
7 | HG00558.hp2 NA18961.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+66G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105329559 |