Search by Gene
| geneid | 7048 |
|---|---|
| ensemblid | ENSG00000163513.19 |
| hgncid | 11773 |
| symbol | TGFBR2 |
| name | transforming growth factor beta receptor 2 |
| refseq_nuc | NM_003242.6 |
| refseq_prot | NP_003233.4 |
| ensembl_nuc | ENST00000295754.10 |
| ensembl_prot | ENSP00000295754.5 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 30606601 |
| end | 30694142 |
| strand | + |
| ver | v1.2 |
| region | chr3:30606601-30694142 |
| region5000 | chr3:30601601-30699142 |
| regionname0 | TGFBR2_chr3_30606601_30694142 |
| regionname5000 | TGFBR2_chr3_30601601_30699142 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 567 | 379 | 93 | 68 | 154 | 18 | 44 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0002 | 0/0 | 567 | 6 | 0 | 0 | 6 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0003 | 0/0 | 567 | 3 | 0 | 0 | 3 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0004 | 0/0 | 567 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0005 | 0/0 | 567 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1704 | 303 | 71 | 65 | 113 | 18 | 34 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| c0002 | 0/0 | 1704 | 53 | 4 | 0 | 41 | 0 | 8 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| c0003 | 0/0 | 1704 | 10 | 9 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| c0004 | 0/0 | 1704 | 9 | 8 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| c0005 | 0/0 | 1704 | 6 | 0 | 0 | 6 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| c0006 | 0/0 | 1704 | 3 | 0 | 0 | 3 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| c0007 | 0/0 | 1704 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| c0008 | 0/0 | 1704 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| c0009 | 0/0 | 1704 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| c0010 | 0/0 | 1704 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| c0011 | 0/0 | 1704 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| c0012 | 0/0 | 1704 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 2827 | 216 | 16 | 38 | 128 | 9 | 24 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0002 | 0/0 | 2826 | 47 | 5 | 9 | 18 | 4 | 11 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0003 | 0/0 | 2825 | 18 | 8 | 7 | 0 | 0 | 3 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0004 | 0/0 | 2829 | 12 | 12 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0005 | 0/0 | 2827 | 11 | 1 | 0 | 7 | 0 | 3 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0006 | 0/0 | 2825 | 11 | 7 | 4 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0007 | 0/0 | 2828 | 10 | 9 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0008 | 0/0 | 2829 | 7 | 7 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0009 | 0/1 | 2826 | 7 | 0 | 3 | 0 | 3 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0010 | 0/0 | 2827 | 5 | 1 | 1 | 1 | 0 | 2 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0011 | 0/0 | 2829 | 5 | 4 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0012 | 0/0 | 2826 | 4 | 1 | 1 | 0 | 1 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0013 | 0/0 | 2827 | 3 | 0 | 0 | 3 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0014 | 0/0 | 2825 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0015 | 0/0 | 2829 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0016 | 0/0 | 2825 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0017 | 0/0 | 2827 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0018 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0019 | 0/0 | 2827 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0020 | 0/0 | 2827 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0021 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0022 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0023 | 0/0 | 2827 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0024 | 0/0 | 2827 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0025 | 0/0 | 2827 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0026 | 0/0 | 2827 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0027 | 0/0 | 2827 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0028 | 0/0 | 2827 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0029 | 0/0 | 2827 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0030 | 0/0 | 2827 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0031 | 0/0 | 2827 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0032 | 0/0 | 2827 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0033 | 0/0 | 2825 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0034 | 0/0 | 2827 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0035 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0036 | 0/0 | 2827 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0037 | 0/0 | 2827 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0038 | 0/0 | 2828 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0039 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0040 | 0/0 | 2827 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0041 | 0/0 | 2826 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0042 | 0/0 | 2826 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| t0043 | 0/0 | 2827 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0308 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0384 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 303 | 71 | 65 | 113 | 18 | 34 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/0 | 53 | 4 | 0 | 41 | 0 | 8 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0003 | a0001 | c0003 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0004 | a0001 | c0004 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0008 | a0001 | c0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0010 | a0001 | c0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0011 | a0001 | c0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0012 | a0001 | c0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0002c0005 | a0002 | c0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0003c0006 | a0003 | c0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0004c0007 | a0004 | c0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0005c0009 | a0005 | c0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 1/0 | 170 | 12 | 38 | 92 | 9 | 18 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 39 | 5 | 9 | 12 | 4 | 9 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 14 | 5 | 6 | 0 | 0 | 3 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 11 | 11 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 9 | 1 | 0 | 5 | 0 | 3 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 10 | 6 | 4 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0009 | a0001 | c0001 | t0009 | 0/1 | 7 | 0 | 3 | 0 | 3 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0011 | a0001 | c0001 | t0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0015 | a0001 | c0001 | t0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0016 | a0001 | c0001 | t0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0017 | a0001 | c0001 | t0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0018 | a0001 | c0001 | t0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0019 | a0001 | c0001 | t0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0020 | a0001 | c0001 | t0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0022 | a0001 | c0001 | t0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0023 | a0001 | c0001 | t0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0024 | a0001 | c0001 | t0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0025 | a0001 | c0001 | t0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0026 | a0001 | c0001 | t0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0027 | a0001 | c0001 | t0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0028 | a0001 | c0001 | t0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0032 | a0001 | c0001 | t0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0034 | a0001 | c0001 | t0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0035 | a0001 | c0001 | t0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0041 | a0001 | c0001 | t0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0001t0042 | a0001 | c0001 | t0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0002t0001 | a0001 | c0002 | t0001 | 0/0 | 38 | 1 | 0 | 31 | 0 | 6 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0002t0002 | a0001 | c0002 | t0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0002t0003 | a0001 | c0002 | t0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0002t0005 | a0001 | c0002 | t0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0002t0010 | a0001 | c0002 | t0010 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0002t0013 | a0001 | c0002 | t0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0002t0029 | a0001 | c0002 | t0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0002t0030 | a0001 | c0002 | t0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0002t0031 | a0001 | c0002 | t0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0002t0038 | a0001 | c0002 | t0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0002t0039 | a0001 | c0002 | t0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0002t0043 | a0001 | c0002 | t0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0003t0001 | a0001 | c0003 | t0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0003t0003 | a0001 | c0003 | t0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0003t0006 | a0001 | c0003 | t0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0003t0007 | a0001 | c0003 | t0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0003t0021 | a0001 | c0003 | t0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0003t0036 | a0001 | c0003 | t0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0003t0040 | a0001 | c0003 | t0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0004t0003 | a0001 | c0004 | t0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0004t0008 | a0001 | c0004 | t0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0004t0011 | a0001 | c0004 | t0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0004t0014 | a0001 | c0004 | t0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0004t0033 | a0001 | c0004 | t0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0008t0003 | a0001 | c0008 | t0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0010t0002 | a0001 | c0010 | t0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0011t0037 | a0001 | c0011 | t0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0001c0012t0002 | a0001 | c0012 | t0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0002c0005t0001 | a0002 | c0005 | t0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0002c0005t0002 | a0002 | c0005 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0002c0005t0005 | a0002 | c0005 | t0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0003c0006t0001 | a0003 | c0006 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0003c0006t0002 | a0003 | c0006 | t0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0004c0007t0004 | a0004 | c0007 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| a0005c0009t0013 | a0005 | c0009 | t0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 | copy fasta |
| actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0037 | a0001 | c0001 | t0001 | g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0045 | a0001 | c0001 | t0001 | g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0047 | a0001 | c0001 | t0001 | g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0051 | a0001 | c0001 | t0001 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0055 | a0001 | c0001 | t0001 | g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0056 | a0001 | c0001 | t0001 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0058 | a0001 | c0001 | t0001 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0060 | a0001 | c0001 | t0001 | g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0100 | a0001 | c0001 | t0001 | g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0104 | a0001 | c0001 | t0001 | g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0115 | a0001 | c0001 | t0001 | g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0157 | a0001 | c0001 | t0001 | g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0172 | a0001 | c0001 | t0001 | g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0176 | a0001 | c0001 | t0001 | g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0177 | a0001 | c0001 | t0001 | g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0179 | a0001 | c0001 | t0001 | g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0180 | a0001 | c0001 | t0001 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0183 | a0001 | c0001 | t0001 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0189 | a0001 | c0001 | t0001 | g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0190 | a0001 | c0001 | t0001 | g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0191 | a0001 | c0001 | t0001 | g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0192 | a0001 | c0001 | t0001 | g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0193 | a0001 | c0001 | t0001 | g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0194 | a0001 | c0001 | t0001 | g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0195 | a0001 | c0001 | t0001 | g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0197 | a0001 | c0001 | t0001 | g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0199 | a0001 | c0001 | t0001 | g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0200 | a0001 | c0001 | t0001 | g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0201 | a0001 | c0001 | t0001 | g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0204 | a0001 | c0001 | t0001 | g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0206 | a0001 | c0001 | t0001 | g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0208 | a0001 | c0001 | t0001 | g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0210 | a0001 | c0001 | t0001 | g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0214 | a0001 | c0001 | t0001 | g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0215 | a0001 | c0001 | t0001 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0216 | a0001 | c0001 | t0001 | g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0217 | a0001 | c0001 | t0001 | g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0220 | a0001 | c0001 | t0001 | g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0221 | a0001 | c0001 | t0001 | g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0222 | a0001 | c0001 | t0001 | g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0223 | a0001 | c0001 | t0001 | g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0227 | a0001 | c0001 | t0001 | g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0228 | a0001 | c0001 | t0001 | g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0231 | a0001 | c0001 | t0001 | g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0233 | a0001 | c0001 | t0001 | g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0235 | a0001 | c0001 | t0001 | g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0236 | a0001 | c0001 | t0001 | g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0237 | a0001 | c0001 | t0001 | g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0240 | a0001 | c0001 | t0001 | g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0242 | a0001 | c0001 | t0001 | g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0243 | a0001 | c0001 | t0001 | g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0247 | a0001 | c0001 | t0001 | g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0249 | a0001 | c0001 | t0001 | g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0251 | a0001 | c0001 | t0001 | g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0252 | a0001 | c0001 | t0001 | g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0253 | a0001 | c0001 | t0001 | g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0256 | a0001 | c0001 | t0001 | g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0257 | a0001 | c0001 | t0001 | g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0258 | a0001 | c0001 | t0001 | g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0259 | a0001 | c0001 | t0001 | g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0264 | a0001 | c0001 | t0001 | g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0267 | a0001 | c0001 | t0001 | g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0269 | a0001 | c0001 | t0001 | g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0275 | a0001 | c0001 | t0001 | g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0276 | a0001 | c0001 | t0001 | g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0277 | a0001 | c0001 | t0001 | g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0278 | a0001 | c0001 | t0001 | g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0279 | a0001 | c0001 | t0001 | g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0282 | a0001 | c0001 | t0001 | g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0285 | a0001 | c0001 | t0001 | g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0287 | a0001 | c0001 | t0001 | g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0288 | a0001 | c0001 | t0001 | g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0289 | a0001 | c0001 | t0001 | g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0291 | a0001 | c0001 | t0001 | g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0294 | a0001 | c0001 | t0001 | g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0298 | a0001 | c0001 | t0001 | g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0300 | a0001 | c0001 | t0001 | g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0301 | a0001 | c0001 | t0001 | g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0302 | a0001 | c0001 | t0001 | g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0303 | a0001 | c0001 | t0001 | g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0304 | a0001 | c0001 | t0001 | g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0307 | a0001 | c0001 | t0001 | g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0308 | a0001 | c0001 | t0001 | g0308 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0309 | a0001 | c0001 | t0001 | g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0314 | a0001 | c0001 | t0001 | g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0316 | a0001 | c0001 | t0001 | g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0317 | a0001 | c0001 | t0001 | g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0318 | a0001 | c0001 | t0001 | g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0323 | a0001 | c0001 | t0001 | g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0324 | a0001 | c0001 | t0001 | g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0327 | a0001 | c0001 | t0001 | g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0328 | a0001 | c0001 | t0001 | g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0329 | a0001 | c0001 | t0001 | g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0330 | a0001 | c0001 | t0001 | g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0338 | a0001 | c0001 | t0001 | g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0342 | a0001 | c0001 | t0001 | g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0345 | a0001 | c0001 | t0001 | g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0348 | a0001 | c0001 | t0001 | g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0359 | a0001 | c0001 | t0001 | g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0372 | a0001 | c0001 | t0001 | g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0373 | a0001 | c0001 | t0001 | g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0375 | a0001 | c0001 | t0001 | g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0378 | a0001 | c0001 | t0001 | g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0379 | a0001 | c0001 | t0001 | g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0380 | a0001 | c0001 | t0001 | g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0381 | a0001 | c0001 | t0001 | g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0382 | a0001 | c0001 | t0001 | g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0385 | a0001 | c0001 | t0001 | g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0386 | a0001 | c0001 | t0001 | g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0001g0387 | a0001 | c0001 | t0001 | g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0061 | a0001 | c0001 | t0002 | g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0072 | a0001 | c0001 | t0002 | g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0077 | a0001 | c0001 | t0002 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0105 | a0001 | c0001 | t0002 | g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0106 | a0001 | c0001 | t0002 | g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0120 | a0001 | c0001 | t0002 | g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0121 | a0001 | c0001 | t0002 | g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0127 | a0001 | c0001 | t0002 | g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0131 | a0001 | c0001 | t0002 | g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0159 | a0001 | c0001 | t0002 | g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0162 | a0001 | c0001 | t0002 | g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0164 | a0001 | c0001 | t0002 | g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0167 | a0001 | c0001 | t0002 | g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0168 | a0001 | c0001 | t0002 | g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0170 | a0001 | c0001 | t0002 | g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0188 | a0001 | c0001 | t0002 | g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0196 | a0001 | c0001 | t0002 | g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0207 | a0001 | c0001 | t0002 | g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0211 | a0001 | c0001 | t0002 | g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0226 | a0001 | c0001 | t0002 | g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0232 | a0001 | c0001 | t0002 | g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0246 | a0001 | c0001 | t0002 | g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0261 | a0001 | c0001 | t0002 | g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0262 | a0001 | c0001 | t0002 | g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0263 | a0001 | c0001 | t0002 | g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0271 | a0001 | c0001 | t0002 | g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0272 | a0001 | c0001 | t0002 | g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0273 | a0001 | c0001 | t0002 | g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0274 | a0001 | c0001 | t0002 | g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0280 | a0001 | c0001 | t0002 | g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0286 | a0001 | c0001 | t0002 | g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0290 | a0001 | c0001 | t0002 | g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0295 | a0001 | c0001 | t0002 | g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0299 | a0001 | c0001 | t0002 | g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0305 | a0001 | c0001 | t0002 | g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0306 | a0001 | c0001 | t0002 | g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0343 | a0001 | c0001 | t0002 | g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0374 | a0001 | c0001 | t0002 | g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0002g0383 | a0001 | c0001 | t0002 | g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0003g0039 | a0001 | c0001 | t0003 | g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0003g0040 | a0001 | c0001 | t0003 | g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0003g0041 | a0001 | c0001 | t0003 | g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0003g0096 | a0001 | c0001 | t0003 | g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0003g0117 | a0001 | c0001 | t0003 | g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0003g0122 | a0001 | c0001 | t0003 | g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0003g0151 | a0001 | c0001 | t0003 | g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0003g0169 | a0001 | c0001 | t0003 | g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0003g0224 | a0001 | c0001 | t0003 | g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0003g0230 | a0001 | c0001 | t0003 | g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0003g0244 | a0001 | c0001 | t0003 | g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0003g0245 | a0001 | c0001 | t0003 | g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0003g0266 | a0001 | c0001 | t0003 | g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0003g0370 | a0001 | c0001 | t0003 | g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0004g0028 | a0001 | c0001 | t0004 | g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0004g0082 | a0001 | c0001 | t0004 | g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0004g0150 | a0001 | c0001 | t0004 | g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0004g0154 | a0001 | c0001 | t0004 | g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0004g0315 | a0001 | c0001 | t0004 | g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0004g0320 | a0001 | c0001 | t0004 | g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0004g0321 | a0001 | c0001 | t0004 | g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0004g0322 | a0001 | c0001 | t0004 | g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0004g0336 | a0001 | c0001 | t0004 | g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0004g0354 | a0001 | c0001 | t0004 | g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0004g0358 | a0001 | c0001 | t0004 | g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0005g0012 | a0001 | c0001 | t0005 | g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0005g0013 | a0001 | c0001 | t0005 | g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0005g0014 | a0001 | c0001 | t0005 | g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0005g0015 | a0001 | c0001 | t0005 | g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0005g0021 | a0001 | c0001 | t0005 | g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0005g0023 | a0001 | c0001 | t0005 | g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0005g0218 | a0001 | c0001 | t0005 | g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0005g0219 | a0001 | c0001 | t0005 | g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0005g0366 | a0001 | c0001 | t0005 | g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0006g0009 | a0001 | c0001 | t0006 | g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0006g0010 | a0001 | c0001 | t0006 | g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0006g0011 | a0001 | c0001 | t0006 | g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0006g0016 | a0001 | c0001 | t0006 | g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0006g0017 | a0001 | c0001 | t0006 | g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0006g0018 | a0001 | c0001 | t0006 | g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0006g0019 | a0001 | c0001 | t0006 | g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0006g0022 | a0001 | c0001 | t0006 | g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0006g0026 | a0001 | c0001 | t0006 | g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0006g0365 | a0001 | c0001 | t0006 | g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0007g0073 | a0001 | c0001 | t0007 | g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0007g0074 | a0001 | c0001 | t0007 | g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0007g0075 | a0001 | c0001 | t0007 | g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0007g0079 | a0001 | c0001 | t0007 | g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0007g0265 | a0001 | c0001 | t0007 | g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0007g0356 | a0001 | c0001 | t0007 | g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0007g0357 | a0001 | c0001 | t0007 | g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0007g0362 | a0001 | c0001 | t0007 | g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0008g0153 | a0001 | c0001 | t0008 | g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0008g0171 | a0001 | c0001 | t0008 | g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0009g0002 | a0001 | c0001 | t0009 | g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0009g0156 | a0001 | c0001 | t0009 | g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0009g0166 | a0001 | c0001 | t0009 | g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0009g0250 | a0001 | c0001 | t0009 | g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0009g0339 | a0001 | c0001 | t0009 | g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0009g0340 | a0001 | c0001 | t0009 | g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0010g0341 | a0001 | c0001 | t0010 | g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0010g0368 | a0001 | c0001 | t0010 | g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0011g0008 | a0001 | c0001 | t0011 | g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0011g0025 | a0001 | c0001 | t0011 | g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0011g0027 | a0001 | c0001 | t0011 | g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0011g0080 | a0001 | c0001 | t0011 | g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0012g0119 | a0001 | c0001 | t0012 | g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0012g0248 | a0001 | c0001 | t0012 | g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0012g0281 | a0001 | c0001 | t0012 | g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0012g0296 | a0001 | c0001 | t0012 | g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0013g0377 | a0001 | c0001 | t0013 | g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0014g0152 | a0001 | c0001 | t0014 | g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0015g0143 | a0001 | c0001 | t0015 | g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0015g0388 | a0001 | c0001 | t0015 | g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0016g0292 | a0001 | c0001 | t0016 | g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0016g0293 | a0001 | c0001 | t0016 | g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0017g0350 | a0001 | c0001 | t0017 | g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0017g0351 | a0001 | c0001 | t0017 | g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0018g0020 | a0001 | c0001 | t0018 | g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0019g0297 | a0001 | c0001 | t0019 | g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0020g0355 | a0001 | c0001 | t0020 | g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0022g0347 | a0001 | c0001 | t0022 | g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0023g0241 | a0001 | c0001 | t0023 | g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0024g0255 | a0001 | c0001 | t0024 | g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0025g0334 | a0001 | c0001 | t0025 | g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0026g0111 | a0001 | c0001 | t0026 | g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0027g0160 | a0001 | c0001 | t0027 | g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0028g0076 | a0001 | c0001 | t0028 | g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0032g0066 | a0001 | c0001 | t0032 | g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0034g0006 | a0001 | c0001 | t0034 | g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0035g0031 | a0001 | c0001 | t0035 | g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0041g0007 | a0001 | c0001 | t0041 | g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0001t0042g0005 | a0001 | c0001 | t0042 | g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0003 | a0001 | c0002 | t0001 | g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0065 | a0001 | c0002 | t0001 | g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0088 | a0001 | c0002 | t0001 | g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0089 | a0001 | c0002 | t0001 | g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0097 | a0001 | c0002 | t0001 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0098 | a0001 | c0002 | t0001 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0099 | a0001 | c0002 | t0001 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0101 | a0001 | c0002 | t0001 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0102 | a0001 | c0002 | t0001 | g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0123 | a0001 | c0002 | t0001 | g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0129 | a0001 | c0002 | t0001 | g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0130 | a0001 | c0002 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0133 | a0001 | c0002 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0158 | a0001 | c0002 | t0001 | g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0165 | a0001 | c0002 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0173 | a0001 | c0002 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0174 | a0001 | c0002 | t0001 | g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0175 | a0001 | c0002 | t0001 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0181 | a0001 | c0002 | t0001 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0186 | a0001 | c0002 | t0001 | g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0187 | a0001 | c0002 | t0001 | g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0198 | a0001 | c0002 | t0001 | g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0202 | a0001 | c0002 | t0001 | g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0203 | a0001 | c0002 | t0001 | g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0212 | a0001 | c0002 | t0001 | g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0213 | a0001 | c0002 | t0001 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0229 | a0001 | c0002 | t0001 | g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0234 | a0001 | c0002 | t0001 | g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0238 | a0001 | c0002 | t0001 | g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0239 | a0001 | c0002 | t0001 | g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0260 | a0001 | c0002 | t0001 | g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0268 | a0001 | c0002 | t0001 | g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0270 | a0001 | c0002 | t0001 | g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0283 | a0001 | c0002 | t0001 | g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0284 | a0001 | c0002 | t0001 | g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0312 | a0001 | c0002 | t0001 | g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0337 | a0001 | c0002 | t0001 | g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0001g0376 | a0001 | c0002 | t0001 | g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0002g0182 | a0001 | c0002 | t0002 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0002g0205 | a0001 | c0002 | t0002 | g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0002g0313 | a0001 | c0002 | t0002 | g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0003g0335 | a0001 | c0002 | t0003 | g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0005g0145 | a0001 | c0002 | t0005 | g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0010g0108 | a0001 | c0002 | t0010 | g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0010g0346 | a0001 | c0002 | t0010 | g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0010g0384 | a0001 | c0002 | t0010 | g0384 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0013g0036 | a0001 | c0002 | t0013 | g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0029g0146 | a0001 | c0002 | t0029 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0030g0092 | a0001 | c0002 | t0030 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0031g0185 | a0001 | c0002 | t0031 | g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0038g0029 | a0001 | c0002 | t0038 | g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0039g0032 | a0001 | c0002 | t0039 | g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0002t0043g0067 | a0001 | c0002 | t0043 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0003t0001g0352 | a0001 | c0003 | t0001 | g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0003t0001g0367 | a0001 | c0003 | t0001 | g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0003t0001g0369 | a0001 | c0003 | t0001 | g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0003t0003g0353 | a0001 | c0003 | t0003 | g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0003t0006g0078 | a0001 | c0003 | t0006 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0003t0007g0360 | a0001 | c0003 | t0007 | g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0003t0007g0361 | a0001 | c0003 | t0007 | g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0003t0021g0363 | a0001 | c0003 | t0021 | g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0003t0036g0024 | a0001 | c0003 | t0036 | g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0003t0040g0033 | a0001 | c0003 | t0040 | g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0004t0003g0225 | a0001 | c0004 | t0003 | g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0004t0008g0081 | a0001 | c0004 | t0008 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0004t0008g0128 | a0001 | c0004 | t0008 | g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0004t0008g0331 | a0001 | c0004 | t0008 | g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0004t0008g0333 | a0001 | c0004 | t0008 | g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0004t0008g0344 | a0001 | c0004 | t0008 | g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0004t0011g0371 | a0001 | c0004 | t0011 | g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0004t0014g0349 | a0001 | c0004 | t0014 | g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0004t0033g0030 | a0001 | c0004 | t0033 | g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0008t0003g0332 | a0001 | c0008 | t0003 | g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0010t0002g0071 | a0001 | c0010 | t0002 | g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0011t0037g0083 | a0001 | c0011 | t0037 | g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0001c0012t0002g0062 | a0001 | c0012 | t0002 | g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0002c0005t0001g0109 | a0002 | c0005 | t0001 | g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0002c0005t0001g0310 | a0002 | c0005 | t0001 | g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0002c0005t0001g0311 | a0002 | c0005 | t0001 | g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0002c0005t0001g0326 | a0002 | c0005 | t0001 | g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0002c0005t0002g0325 | a0002 | c0005 | t0002 | g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0002c0005t0005g0178 | a0002 | c0005 | t0005 | g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0003c0006t0001g0319 | a0003 | c0006 | t0001 | g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0003c0006t0002g0184 | a0003 | c0006 | t0002 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0003c0006t0002g0209 | a0003 | c0006 | t0002 | g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0004c0007t0004g0364 | a0004 | c0007 | t0004 | g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| a0005c0009t0013g0254 | a0005 | c0009 | t0013 | g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0170 | EUR | GBR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | GBR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00140 | hp1 | a0001 | c0001 | t0009 | g0002 | EUR | GBR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0164 | EUR | GBR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00280 | hp1 | a0001 | c0001 | t0023 | g0241 | EUR | FIN | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00280 | hp2 | a0001 | c0001 | t0009 | g0002 | EUR | FIN | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | FIN | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0301 | EUR | FIN | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00558 | hp1 | a0002 | c0005 | t0001 | g0310 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0312 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00639 | hp2 | a0001 | c0001 | t0010 | g0341 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00673 | hp1 | a0001 | c0002 | t0005 | g0145 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0039 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01106 | hp1 | a0001 | c0001 | t0012 | g0296 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0244 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01109 | hp2 | a0001 | c0001 | t0011 | g0008 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01167 | hp2 | a0001 | c0008 | t0003 | g0332 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01243 | hp1 | a0001 | c0003 | t0040 | g0033 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01255 | hp1 | a0001 | c0001 | t0007 | g0357 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0230 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01257 | hp2 | a0001 | c0001 | t0009 | g0339 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01258 | hp2 | a0001 | c0001 | t0009 | g0340 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0373 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0009 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0169 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0010 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0106 | EUR | IBS | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | IBS | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01516 | hp1 | a0001 | c0001 | t0012 | g0119 | EUR | IBS | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0307 | EUR | IBS | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0309 | EUR | IBS | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0105 | EUR | IBS | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0358 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0362 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01891 | hp1 | a0001 | c0003 | t0036 | g0024 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01891 | hp2 | a0001 | c0002 | t0039 | g0032 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01934 | hp2 | a0001 | c0004 | t0033 | g0030 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01952 | hp2 | a0001 | c0001 | t0006 | g0022 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0372 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01981 | hp2 | a0001 | c0001 | t0009 | g0156 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02015 | hp2 | a0001 | c0001 | t0032 | g0066 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0270 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02040 | hp1 | a0002 | c0005 | t0001 | g0326 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02055 | hp1 | a0001 | c0001 | t0012 | g0248 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02132 | hp2 | a0001 | c0002 | t0043 | g0067 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0369 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | CDX | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CDX | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02165 | hp1 | a0001 | c0002 | t0010 | g0346 | EAS | CDX | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02165 | hp2 | a0001 | c0002 | t0030 | g0092 | EAS | CDX | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02257 | hp1 | a0001 | c0001 | t0018 | g0020 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02258 | hp1 | a0001 | c0004 | t0008 | g0333 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02258 | hp2 | a0001 | c0003 | t0021 | g0363 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02273 | hp2 | a0001 | c0001 | t0006 | g0011 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02280 | hp1 | a0001 | c0001 | t0014 | g0152 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0245 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02300 | hp1 | a0001 | c0001 | t0042 | g0005 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PEL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0366 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02602 | hp2 | a0001 | c0001 | t0012 | g0281 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0150 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02615 | hp2 | a0001 | c0001 | t0016 | g0292 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02622 | hp1 | a0001 | c0001 | t0011 | g0080 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02622 | hp2 | a0001 | c0002 | t0038 | g0029 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02630 | hp1 | a0001 | c0001 | t0016 | g0293 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0370 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0082 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02683 | hp2 | a0001 | c0012 | t0002 | g0062 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0261 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0315 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0367 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02723 | hp2 | a0001 | c0004 | t0008 | g0331 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0186 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02809 | hp1 | a0001 | c0001 | t0035 | g0031 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02809 | hp2 | a0001 | c0003 | t0007 | g0361 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0343 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0074 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02886 | hp1 | a0001 | c0004 | t0011 | g0371 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02886 | hp2 | a0001 | c0001 | t0010 | g0368 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0336 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02895 | hp2 | a0001 | c0001 | t0017 | g0351 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0265 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0320 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0322 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02897 | hp2 | a0001 | c0001 | t0017 | g0350 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02922 | hp1 | a0001 | c0001 | t0022 | g0347 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02965 | hp1 | a0001 | c0003 | t0007 | g0360 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0354 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02976 | hp1 | a0001 | c0001 | t0026 | g0111 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02976 | hp2 | a0001 | c0001 | t0034 | g0006 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0352 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0374 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0123 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03130 | hp2 | a0001 | c0011 | t0037 | g0083 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03139 | hp2 | a0001 | c0001 | t0025 | g0334 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0365 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03195 | hp2 | a0001 | c0003 | t0003 | g0353 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0079 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03209 | hp2 | a0004 | c0007 | t0004 | g0364 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03225 | hp1 | a0001 | c0001 | t0020 | g0355 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0359 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03486 | hp1 | a0001 | c0001 | t0015 | g0388 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0356 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0014 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0383 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0283 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0015 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0284 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03516 | hp1 | a0001 | c0003 | t0006 | g0078 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0025 | AFR | ESN | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0321 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | GWD | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0382 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | STU | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0117 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03710 | hp2 | a0001 | c0010 | t0002 | g0071 | SAS | PJL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0238 | SAS | BEB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0266 | SAS | BEB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0021 | SAS | BEB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03927 | hp2 | a0001 | c0002 | t0010 | g0384 | SAS | BEB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0305 | SAS | BEB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0096 | SAS | BEB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG04115 | hp2 | a0001 | c0002 | t0010 | g0108 | SAS | STU | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0286 | SAS | STU | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | STU | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0262 | SAS | STU | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | STU | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0133 | SAS | STU | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | STU | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | YRI | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18522 | hp2 | a0001 | c0004 | t0008 | g0344 | AFR | YRI | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | CHB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18612 | hp2 | a0003 | c0006 | t0002 | g0184 | EAS | CHB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | CHB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | YRI | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18906 | hp2 | a0001 | c0001 | t0041 | g0007 | AFR | YRI | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0381 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18947 | hp2 | a0002 | c0005 | t0002 | g0325 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0378 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18954 | hp1 | a0001 | c0002 | t0013 | g0036 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18956 | hp2 | a0001 | c0001 | t0005 | g0219 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0313 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0218 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0380 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18977 | hp2 | a0005 | c0009 | t0013 | g0254 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0375 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0387 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0386 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19002 | hp2 | a0001 | c0001 | t0027 | g0160 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19007 | hp1 | a0002 | c0005 | t0001 | g0109 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19009 | hp2 | a0001 | c0001 | t0013 | g0377 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0026 | AFR | LWK | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19030 | hp2 | a0001 | c0001 | t0008 | g0153 | AFR | LWK | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | LWK | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0171 | AFR | LWK | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0337 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19057 | hp1 | a0001 | c0002 | t0031 | g0185 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19058 | hp2 | a0001 | c0001 | t0024 | g0255 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0385 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19068 | hp1 | a0003 | c0006 | t0001 | g0319 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19070 | hp1 | a0002 | c0005 | t0001 | g0311 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0376 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0379 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19081 | hp1 | a0001 | c0002 | t0029 | g0146 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19086 | hp2 | a0003 | c0006 | t0002 | g0209 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19088 | hp2 | a0002 | c0005 | t0005 | g0178 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19240 | hp1 | a0001 | c0004 | t0014 | g0349 | AFR | YRI | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0075 | AFR | YRI | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | ASW | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ASW | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA20752 | hp1 | a0001 | c0001 | t0009 | g0250 | EUR | TSI | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0064 | EUR | TSI | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | TSI | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | GIH | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | GIH | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0154 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02109 | hp2 | a0001 | c0001 | t0011 | g0027 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02486 | hp2 | a0001 | c0001 | t0028 | g0076 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02559 | hp1 | a0001 | c0002 | t0003 | g0335 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG02559 | hp2 | a0001 | c0004 | t0008 | g0081 | AFR | ACB | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03471 | hp1 | a0001 | c0004 | t0003 | g0225 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0073 | AFR | MSL | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG06807 | hp1 | a0001 | c0004 | t0008 | g0128 | AFR | USA | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| HG06807 | hp2 | a0001 | c0001 | t0015 | g0143 | AFR | USA | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA21309 | hp1 | a0001 | c0001 | t0019 | g0297 | AFR | LWK | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | LWK | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0009 | g0166 | REF | REF | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0308 | REF | REF | TGFBR2_chr3_30601601_30699142 | TGFBR2 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:30644768
|
C | A | 1 | a0004 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.116C>A | p.Thr39Asn | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/7 | 399/4530 | 116/1704 | 39/567 | chr3 | 30644768 | ||
| chr3:30671754
|
G | A | 1 | a0003 | 3 | NA18612.hp2 NA19068.hp1 NA19086.hp2 |
missense_variant | MODERATE | c.571G>A | p.Val191Ile | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/7 | 854/4530 | 571/1704 | 191/567 | chr3 | 30671754 | ||
| chr3:30672127
|
C | T | 1 | a0002 | 6 | HG00558.hp1 HG02040.hp1 NA18947.hp2 others(3): Show |
missense_variant | MODERATE | c.944C>T | p.Thr315Met | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/7 | 1227/4530 | 944/1704 | 315/567 | chr3 | 30672127 | ||
| chr3:30672391
|
G | A | 1 | a0005 | 1 | NA18977.hp2 | missense_variant | MODERATE | c.1208G>A | p.Arg403His | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/7 | 1491/4530 | 1208/1704 | 403/567 | chr3 | 30672391 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:30672182
|
A | G | 1 | a0001c0004 | 9 | HG01934.hp2 HG02258.hp1 HG02559.hp2 others(6): Show |
synonymous_variant | LOW | c.999A>G | p.Leu333Leu | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/7 | 1282/4530 | 999/1704 | 333/567 | chr3 | 30672182 | ||
| chr3:30672245
|
C | T | 1 | a0001c0012 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.1062C>T | p.Leu354Leu | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/7 | 1345/4530 | 1062/1704 | 354/567 | chr3 | 30672245 | ||
| chr3:30672275
|
T | C | 1 | a0001c0008 | 1 | HG01167.hp2 | synonymous_variant | LOW | c.1092T>C | p.Asp364Asp | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/7 | 1375/4530 | 1092/1704 | 364/567 | chr3 | 30672275 | ||
| chr3:30672350
|
C | T | 1 | a0001c0002 | 53 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(50): Show |
synonymous_variant | LOW | c.1167C>T | p.Asn389Asn | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/7 | 1450/4530 | 1167/1704 | 389/567 | chr3 | 30672350 | ||
| chr3:30674116
|
A | G | 1 | a0001c0003 | 10 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(7): Show |
synonymous_variant | LOW | c.1266A>G | p.Ala422Ala | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/7 | 1549/4530 | 1266/1704 | 422/567 | chr3 | 30674116 | ||
| chr3:30688445
|
C | T | 1 | a0001c0011 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.1458C>T | p.Ser486Ser | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/7 | 1741/4530 | 1458/1704 | 486/567 | chr3 | 30688445 | ||
| chr3:30691497
|
G | A | 1 | a0001c0010 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.1602G>A | p.Val534Val | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1885/4530 | 1602/1704 | 534/567 | chr3 | 30691497 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:30606691
|
G | A | 1 | a0001c0001t0018 | 1 | HG02257.hp1 | 5_prime_UTR_variant | MODIFIER | c.-193G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/7 | 193 | chr3 | 30606691 | |||||
| chr3:30606742
|
C | T | 1 | a0001c0002t0043 | 1 | HG02132.hp2 | 5_prime_UTR_variant | MODIFIER | c.-142C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/7 | 142 | chr3 | 30606742 | |||||
| chr3:30606756
|
C | G | 19 | a0001c0001t0005a0001c0001t0006a0001c0001t0011others(16): Show | 40 | HG00408.hp2 HG00673.hp1 HG01109.hp2 others(37): Show |
5_prime_UTR_variant | MODIFIER | c.-128C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/7 | 128 | chr3 | 30606756 | |||||
| chr3:30606758
|
C | T | 1 | a0001c0001t0016 | 2 | HG02615.hp2 HG02630.hp1 |
5_prime_UTR_variant | MODIFIER | c.-126C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/7 | 126 | chr3 | 30606758 | |||||
| chr3:30606781
|
G | A | 1 | a0001c0001t0019 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-103G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/7 | 103 | chr3 | 30606781 | |||||
| chr3:30691700
|
C | T | 1 | a0001c0001t0032 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*101C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 101 | chr3 | 30691700 | |||||
| chr3:30691906
|
GTT | G | 3 | a0001c0001t0014a0001c0004t0014a0001c0004t0033 | 3 | HG01934.hp2 HG02280.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*310_*311delTT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 310 | INFO_REALIGN_3_PRIME | chr3 | 30691906 | ||||
| chr3:30691909
|
T | TTA | 11 | a0001c0001t0004a0001c0001t0008a0001c0001t0011others(8): Show | 30 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*328_*329dupAT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 330 | INFO_REALIGN_3_PRIME | chr3 | 30691909 | ||||
| chr3:30691909
|
TTA | T | 18 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(15): Show | 91 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*328_*329delAT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 328 | INFO_REALIGN_3_PRIME | chr3 | 30691909 | ||||
| chr3:30691911
|
A | T | 1 | a0001c0002t0031 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*312A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 312 | chr3 | 30691911 | |||||
| chr3:30691929
|
C | A | 2 | a0001c0001t0020a0001c0001t0034 | 2 | HG02976.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*330C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 330 | chr3 | 30691929 | |||||
| chr3:30691951
|
A | G | 1 | a0001c0002t0030 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*352A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 352 | chr3 | 30691951 | |||||
| chr3:30692198
|
C | A | 2 | a0001c0003t0036a0001c0011t0037 | 2 | HG01891.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*599C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 599 | chr3 | 30692198 | |||||
| chr3:30692346
|
C | G | 12 | a0001c0001t0003a0001c0001t0006a0001c0001t0014others(9): Show | 35 | HG01074.hp2 HG01106.hp2 HG01167.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*747C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 747 | chr3 | 30692346 | |||||
| chr3:30692447
|
C | T | 1 | a0001c0002t0039 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*848C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 848 | chr3 | 30692447 | |||||
| chr3:30692474
|
A | G | 1 | a0001c0001t0022 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*875A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 875 | chr3 | 30692474 | |||||
| chr3:30692587
|
C | T | 3 | a0001c0001t0013a0001c0002t0013a0005c0009t0013 | 3 | NA18954.hp1 NA18977.hp2 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*988C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 988 | chr3 | 30692587 | |||||
| chr3:30692689
|
G | T | 1 | a0001c0002t0039 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1090G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1090 | chr3 | 30692689 | |||||
| chr3:30692707
|
CAACTACA others(18): Show |
C | 1 | a0001c0002t0039 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1109_*1133delAACT others(21): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1109 | chr3 | 30692707 | |||||
| chr3:30692743
|
T | A | 1 | a0001c0002t0039 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1144T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1144 | chr3 | 30692743 | |||||
| chr3:30692749
|
A | G | 1 | a0001c0002t0029 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1150A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1150 | chr3 | 30692749 | |||||
| chr3:30692953
|
C | T | 1 | a0001c0001t0028 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1354C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1354 | chr3 | 30692953 | |||||
| chr3:30693120
|
G | A | 3 | a0001c0001t0007a0001c0002t0038a0001c0003t0007 | 11 | HG01255.hp1 HG01884.hp2 HG02622.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1521G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1521 | chr3 | 30693120 | |||||
| chr3:30693167
|
G | A | 1 | a0001c0001t0023 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1568G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1568 | chr3 | 30693167 | |||||
| chr3:30693171
|
A | G | 1 | a0001c0001t0027 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1572A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1572 | chr3 | 30693171 | |||||
| chr3:30693281
|
A | G | 1 | a0001c0002t0039 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1682A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1682 | chr3 | 30693281 | |||||
| chr3:30693408
|
A | G | 16 | a0001c0001t0004a0001c0001t0010a0001c0001t0011others(13): Show | 34 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1809A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1809 | chr3 | 30693408 | |||||
| chr3:30693432
|
A | C | 2 | a0001c0001t0012a0001c0001t0042 | 5 | HG01106.hp1 HG01516.hp1 HG02055.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1833A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1833 | chr3 | 30693432 | |||||
| chr3:30693479
|
G | A | 3 | a0001c0001t0015a0001c0001t0018a0001c0001t0025 | 4 | HG02257.hp1 HG03139.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1880G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1880 | chr3 | 30693479 | |||||
| chr3:30693485
|
G | T | 1 | a0001c0001t0026 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1886G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1886 | chr3 | 30693485 | |||||
| chr3:30693497
|
A | G | 1 | a0001c0002t0039 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1898A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 1898 | chr3 | 30693497 | |||||
| chr3:30693664
|
C | T | 1 | a0001c0001t0009 | 7 | HG00140.hp1 HG00280.hp2 HG01257.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2065C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 2065 | chr3 | 30693664 | |||||
| chr3:30693684
|
T | A | 12 | a0001c0001t0004a0001c0001t0010a0001c0001t0011others(9): Show | 29 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2085T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 2085 | chr3 | 30693684 | |||||
| chr3:30693838
|
G | GT | 13 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(10): Show | 71 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*2248dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 2249 | INFO_REALIGN_3_PRIME | chr3 | 30693838 | ||||
| chr3:30693967
|
A | T | 1 | a0001c0011t0037 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2368A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 2368 | chr3 | 30693967 | |||||
| chr3:30694082
|
T | G | 1 | a0001c0003t0036 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2483T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 2483 | chr3 | 30694082 | |||||
| chr3:30694104
|
T | G | 1 | a0001c0001t0024 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2505T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 7/7 | 2505 | chr3 | 30694104 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:30607090
|
A | G | 1 | a0001c0001t0015g0388 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.94+113A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607090 | ||||||
| chr3:30607185
|
A | G | 12 | a0001c0001t0001g0378a0001c0001t0001g0379a0001c0001t0001g0380others(9): Show | 12 | HG03490.hp2 HG03654.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+208A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607185 | ||||||
| chr3:30607254
|
G | A | 1 | a0001c0002t0001g0003 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.94+277G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607254 | ||||||
| chr3:30607286
|
A | C | 1 | a0001c0001t0001g0375 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.94+309A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607286 | ||||||
| chr3:30607609
|
A | G | 1 | a0001c0001t0002g0374 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.94+632A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607609 | ||||||
| chr3:30607649
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.94+672T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607649 | ||||||
| chr3:30607787
|
T | TAA | 4 | a0001c0001t0006g0016a0001c0001t0006g0017a0001c0001t0006g0018others(1): Show | 4 | HG01934.hp2 HG02055.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+814_94+815dupAA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607787 | |||||
| chr3:30607793
|
T | A | 25 | a0001c0001t0004g0028a0001c0001t0005g0012a0001c0001t0005g0013others(22): Show | 25 | HG00408.hp2 HG01109.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.94+816T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607793 | ||||||
| chr3:30607793
|
TAAAA | T | 12 | a0001c0001t0001g0378a0001c0001t0001g0379a0001c0001t0001g0380others(9): Show | 12 | HG03490.hp2 HG03654.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+820_94+823delAA others(2): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607793 | |||||
| chr3:30607795
|
A | AAT | 5 | a0001c0001t0004g0028a0001c0001t0006g0026a0001c0001t0011g0025others(2): Show | 5 | HG02109.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+819_94+820insTA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607795 | |||||
| chr3:30607795
|
A | T | 1 | a0001c0004t0033g0030 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.94+818A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607795 | ||||||
| chr3:30607797
|
A | T | 6 | a0001c0001t0004g0028a0001c0001t0006g0026a0001c0001t0011g0025others(3): Show | 6 | HG01934.hp2 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+820A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607797 | ||||||
| chr3:30607799
|
A | AAAAATAT | 11 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(8): Show | 11 | HG00408.hp2 HG01109.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.94+823_94+824insAA others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607799 | |||||
| chr3:30607799
|
A | AAT | 10 | a0001c0001t0002g0072a0001c0001t0002g0077a0001c0001t0007g0073others(7): Show | 10 | HG02280.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+835_94+836dupAT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607799 | |||||
| chr3:30607799
|
A | T | 21 | a0001c0001t0001g0004a0001c0001t0001g0372a0001c0001t0001g0373others(18): Show | 21 | HG01192.hp2 HG01261.hp1 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.94+822A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607799 | ||||||
| chr3:30607799
|
AAT | A | 6 | a0001c0001t0003g0370a0001c0001t0005g0366a0001c0001t0010g0368others(3): Show | 6 | HG02145.hp1 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+835_94+836delAT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607799 | |||||
| chr3:30607800
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0035g0031 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.94+824_94+847delTA others(22): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607800 | ||||||
| chr3:30607801
|
T | A | 41 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(38): Show | 42 | HG00738.hp2 HG01074.hp1 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.94+824T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607801 | ||||||
| chr3:30607813
|
T | A | 12 | a0001c0001t0001g0378a0001c0001t0001g0379a0001c0001t0001g0380others(9): Show | 12 | HG03490.hp2 HG03654.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+836T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607813 | ||||||
| chr3:30607828
|
TATATATA others(15): Show |
T | 15 | a0001c0001t0002g0072a0001c0001t0002g0077a0001c0001t0004g0082others(12): Show | 15 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.94+863_94+884delTA others(20): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607828 | |||||
| chr3:30607848
|
T | TA | 12 | a0001c0001t0001g0378a0001c0001t0001g0379a0001c0001t0001g0380others(9): Show | 12 | HG03490.hp2 HG03654.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+874dupA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607848 | |||||
| chr3:30607850
|
A | AAT | 84 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(81): Show | 85 | HG00408.hp2 HG00738.hp2 HG01074.hp1 others(82): Show |
intron_variant | MODIFIER | c.94+881_94+882dupTA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607850 | |||||
| chr3:30607865
|
AAT | A | 12 | a0001c0001t0001g0378a0001c0001t0001g0379a0001c0001t0001g0380others(9): Show | 12 | HG03490.hp2 HG03654.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+897_94+898delAT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607865 | |||||
| chr3:30607916
|
G | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | NA18967.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.94+939G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607916 | ||||||
| chr3:30607929
|
G | C | 18 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0090others(15): Show | 18 | HG00621.hp1 HG02071.hp1 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.94+952G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30607929 | ||||||
| chr3:30607946
|
A | AT | 8 | a0001c0001t0001g0043a0001c0001t0001g0103a0001c0001t0001g0342others(5): Show | 8 | HG00639.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+981dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30607946 | |||||
| chr3:30608064
|
G | T | 11 | a0001c0001t0002g0072a0001c0001t0002g0077a0001c0001t0007g0073others(8): Show | 11 | HG02280.hp2 HG02486.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.94+1087G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608064 | ||||||
| chr3:30608145
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.94+1168G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608145 | ||||||
| chr3:30608173
|
G | A | 1 | a0001c0004t0008g0344 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.94+1196G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608173 | ||||||
| chr3:30608344
|
C | G | 1 | a0001c0001t0001g0338 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.94+1367C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608344 | ||||||
| chr3:30608345
|
C | T | 1 | a0004c0007t0004g0364 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.94+1368C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608345 | ||||||
| chr3:30608362
|
C | A | 1 | a0001c0001t0001g0104 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.94+1385C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608362 | ||||||
| chr3:30608415
|
C | A | 267 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(264): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.94+1438C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608415 | ||||||
| chr3:30608572
|
A | G | 280 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(277): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.94+1595A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608572 | ||||||
| chr3:30608590
|
G | T | 1 | a0001c0003t0001g0352 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.94+1613G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608590 | ||||||
| chr3:30608612
|
G | A | 3 | a0001c0001t0006g0016a0001c0001t0006g0017a0001c0001t0006g0018 | 3 | HG02055.hp2 HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.94+1635G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608612 | ||||||
| chr3:30608756
|
A | G | 1 | a0001c0001t0002g0286 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.94+1779A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608756 | ||||||
| chr3:30608764
|
G | GT | 6 | a0001c0001t0001g0359a0001c0001t0004g0358a0001c0001t0007g0362others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+1790dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30608764 | |||||
| chr3:30608816
|
T | A | 1 | a0001c0001t0001g0287 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.94+1839T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608816 | ||||||
| chr3:30608835
|
T | C | 292 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.94+1858T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608835 | ||||||
| chr3:30608963
|
G | A | 14 | a0001c0001t0002g0072a0001c0001t0002g0077a0001c0001t0007g0073others(11): Show | 14 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.94+1986G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30608963 | ||||||
| chr3:30609075
|
A | G | 8 | a0001c0001t0003g0370a0001c0001t0005g0366a0001c0001t0010g0368others(5): Show | 8 | HG02145.hp1 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+2098A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609075 | ||||||
| chr3:30609100
|
G | C | 9 | a0001c0001t0001g0378a0001c0001t0001g0379a0001c0001t0001g0380others(6): Show | 9 | HG03490.hp2 HG03654.hp2 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.94+2123G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609100 | ||||||
| chr3:30609178
|
T | C | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.94+2201T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609178 | ||||||
| chr3:30609247
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.94+2270T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609247 | ||||||
| chr3:30609256
|
C | T | 12 | a0001c0001t0001g0378a0001c0001t0001g0379a0001c0001t0001g0380others(9): Show | 12 | HG03490.hp2 HG03654.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+2279C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609256 | ||||||
| chr3:30609418
|
C | T | 2 | a0001c0001t0002g0383a0001c0002t0010g0384 | 2 | HG03490.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.94+2441C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609418 | ||||||
| chr3:30609525
|
A | G | 1 | a0001c0010t0002g0071 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.94+2548A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609525 | ||||||
| chr3:30609730
|
C | A | 1 | a0001c0001t0002g0286 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.94+2753C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609730 | ||||||
| chr3:30609830
|
C | T | 11 | a0001c0001t0002g0072a0001c0001t0002g0077a0001c0001t0007g0073others(8): Show | 11 | HG02280.hp2 HG02486.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.94+2853C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609830 | ||||||
| chr3:30609900
|
A | G | 2 | a0001c0001t0009g0339a0001c0001t0009g0340 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.94+2923A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609900 | ||||||
| chr3:30609917
|
C | T | 1 | a0001c0002t0001g0337 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.94+2940C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609917 | ||||||
| chr3:30609962
|
G | T | 3 | a0001c0001t0001g0285a0001c0002t0001g0283a0001c0002t0001g0284 | 3 | HG00741.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.94+2985G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609962 | ||||||
| chr3:30609988
|
A | T | 1 | a0001c0001t0001g0282 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.94+3011A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30609988 | ||||||
| chr3:30610054
|
A | C | 14 | a0001c0001t0002g0072a0001c0001t0002g0077a0001c0001t0007g0073others(11): Show | 14 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.94+3077A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30610054 | ||||||
| chr3:30610146
|
G | T | 2 | a0001c0002t0039g0032a0001c0003t0040g0033 | 2 | HG01243.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.94+3169G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30610146 | ||||||
| chr3:30610295
|
T | C | 1 | a0001c0001t0002g0383 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.94+3318T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30610295 | ||||||
| chr3:30610325
|
A | AT | 272 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(269): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.94+3357dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30610325 | |||||
| chr3:30610332
|
T | G | 12 | a0001c0001t0001g0378a0001c0001t0001g0379a0001c0001t0001g0380others(9): Show | 12 | HG03490.hp2 HG03654.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+3355T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30610332 | ||||||
| chr3:30610332
|
T | TG | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG02738.hp2 HG03195.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+3355_94+3356ins others(1): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30610332 | ||||||
| chr3:30610493
|
A | T | 1 | a0001c0002t0001g0337 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.94+3516A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30610493 | ||||||
| chr3:30610496
|
A | G | 1 | a0001c0001t0012g0281 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.94+3519A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30610496 | ||||||
| chr3:30610553
|
T | A | 1 | a0001c0001t0006g0019 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.94+3576T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30610553 | ||||||
| chr3:30610621
|
A | C | 1 | a0001c0002t0001g0337 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.94+3644A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30610621 | ||||||
| chr3:30610643
|
T | A | 1 | a0001c0001t0001g0048 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.94+3666T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30610643 | ||||||
| chr3:30611045
|
A | G | 14 | a0001c0001t0002g0072a0001c0001t0002g0077a0001c0001t0007g0073others(11): Show | 14 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.94+4068A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30611045 | ||||||
| chr3:30611085
|
A | T | 1 | a0001c0001t0002g0280 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.94+4108A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30611085 | ||||||
| chr3:30611115
|
G | A | 1 | a0001c0001t0001g0345 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.94+4138G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30611115 | ||||||
| chr3:30611296
|
G | A | 313 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(310): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.94+4319G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30611296 | ||||||
| chr3:30611333
|
C | G | 2 | a0001c0001t0001g0278a0001c0001t0001g0279 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.94+4356C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30611333 | ||||||
| chr3:30611421
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.94+4444G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30611421 | ||||||
| chr3:30611582
|
C | CT | 23 | a0001c0001t0001g0110a0001c0001t0001g0264a0001c0001t0001g0267others(20): Show | 23 | HG00597.hp2 HG02027.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.94+4619dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30611582 | |||||
| chr3:30611613
|
AAAGAGAA others(14): Show |
A | 232 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0035others(229): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.94+4640_94+4660del others(21): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30611613 | |||||
| chr3:30611790
|
G | A | 2 | a0001c0001t0001g0278a0001c0001t0001g0279 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.94+4813G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30611790 | ||||||
| chr3:30611978
|
G | A | 1 | a0001c0001t0002g0286 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.94+5001G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30611978 | ||||||
| chr3:30611995
|
C | T | 5 | a0001c0001t0001g0378a0001c0001t0001g0379a0001c0001t0001g0380others(2): Show | 5 | HG03654.hp2 NA18944.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+5018C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30611995 | ||||||
| chr3:30612537
|
T | G | 1 | a0001c0001t0001g0114 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.94+5560T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30612537 | ||||||
| chr3:30612609
|
A | G | 1 | a0001c0001t0001g0259 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.94+5632A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30612609 | ||||||
| chr3:30612746
|
C | CAATT | 291 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(288): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.94+5769_94+5770ins others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30612746 | ||||||
| chr3:30612870
|
C | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG00735.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.94+5893C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30612870 | ||||||
| chr3:30612875
|
A | T | 7 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0256others(4): Show | 7 | NA18959.hp1 NA18964.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+5898A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30612875 | ||||||
| chr3:30612939
|
C | A | 12 | a0001c0001t0002g0072a0001c0001t0002g0077a0001c0001t0007g0073others(9): Show | 12 | HG02280.hp2 HG02486.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.94+5962C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30612939 | ||||||
| chr3:30613006
|
A | T | 1 | a0001c0001t0001g0338 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.94+6029A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30613006 | ||||||
| chr3:30613131
|
CT | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(235): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.94+6172delT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30613131 | |||||
| chr3:30613131
|
CTT | C | 8 | a0001c0001t0001g0118a0001c0001t0001g0345a0001c0001t0001g0348others(5): Show | 8 | HG01256.hp1 HG01516.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.94+6171_94+6172del others(2): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30613131 | |||||
| chr3:30613380
|
G | A | 4 | a0001c0001t0001g0278a0001c0001t0001g0279a0001c0001t0002g0120others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+6403G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30613380 | ||||||
| chr3:30613398
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.94+6421A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30613398 | ||||||
| chr3:30613499
|
G | A | 1 | a0001c0001t0002g0286 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.94+6522G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30613499 | ||||||
| chr3:30613502
|
C | CTG | 3 | a0001c0001t0001g0385a0001c0001t0001g0386a0001c0001t0001g0387 | 3 | NA18990.hp1 NA18999.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.94+6539_94+6540dup others(2): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30613502 | |||||
| chr3:30613525
|
TGA | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(196): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.94+6573_94+6574del others(2): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30613525 | |||||
| chr3:30613525
|
TGAGA | T | 27 | a0001c0001t0001g0378a0001c0001t0001g0379a0001c0001t0001g0380others(24): Show | 27 | HG02055.hp2 HG02280.hp2 HG02486.hp2 others(24): Show |
intron_variant | MODIFIER | c.94+6571_94+6574del others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30613525 | |||||
| chr3:30613525
|
TGAGAGA | T | 14 | a0001c0001t0001g0359a0001c0001t0003g0122a0001c0001t0004g0354others(11): Show | 14 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.94+6569_94+6574del others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30613525 | |||||
| chr3:30613527
|
A | T | 1 | a0001c0001t0001g0251 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.94+6550A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30613527 | ||||||
| chr3:30613532
|
G | A | 1 | a0004c0007t0004g0364 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.94+6555G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30613532 | ||||||
| chr3:30613542
|
G | C | 5 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(2): Show | 5 | HG02015.hp1 HG02083.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+6565G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30613542 | ||||||
| chr3:30613627
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.94+6650C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30613627 | ||||||
| chr3:30613629
|
G | C | 1 | a0001c0001t0002g0280 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.94+6652G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30613629 | ||||||
| chr3:30613989
|
A | G | 277 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0044others(274): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.94+7012A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30613989 | ||||||
| chr3:30614072
|
C | T | 6 | a0001c0001t0004g0028a0001c0001t0006g0026a0001c0001t0011g0025others(3): Show | 6 | HG01934.hp2 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+7095C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30614072 | ||||||
| chr3:30614115
|
C | CT | 246 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0044others(243): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.94+7157dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30614115 | |||||
| chr3:30614115
|
CT | C | 13 | a0001c0001t0001g0034a0001c0001t0001g0288a0001c0001t0001g0291others(10): Show | 13 | HG00639.hp2 HG01069.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+7157delT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30614115 | |||||
| chr3:30614145
|
G | C | 2 | a0001c0001t0006g0019a0001c0004t0014g0349 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.94+7168G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30614145 | ||||||
| chr3:30614202
|
T | C | 19 | a0001c0001t0001g0345a0001c0001t0001g0348a0001c0001t0002g0072others(16): Show | 19 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.94+7225T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30614202 | ||||||
| chr3:30614302
|
T | A | 2 | a0001c0001t0006g0019a0001c0004t0014g0349 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.94+7325T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30614302 | ||||||
| chr3:30614364
|
T | A | 1 | a0001c0001t0006g0365 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.94+7387T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30614364 | ||||||
| chr3:30614573
|
C | T | 29 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(26): Show | 29 | HG02015.hp1 HG02015.hp2 HG02083.hp1 others(26): Show |
intron_variant | MODIFIER | c.94+7596C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30614573 | ||||||
| chr3:30614676
|
G | A | 215 | a0001c0001t0001g0035a0001c0001t0001g0084a0001c0001t0001g0085others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.94+7699G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30614676 | ||||||
| chr3:30614721
|
G | A | 1 | a0001c0001t0006g0365 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.94+7744G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30614721 | ||||||
| chr3:30614982
|
C | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0052others(245): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.94+8005C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30614982 | ||||||
| chr3:30615016
|
A | T | 2 | a0001c0001t0001g0227a0001c0001t0002g0226 | 2 | HG02523.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.94+8039A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615016 | ||||||
| chr3:30615081
|
C | T | 48 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(45): Show | 48 | HG00408.hp2 HG01109.hp2 HG01358.hp1 others(45): Show |
intron_variant | MODIFIER | c.94+8104C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615081 | ||||||
| chr3:30615114
|
A | G | 1 | a0001c0001t0009g0250 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.94+8137A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615114 | ||||||
| chr3:30615147
|
A | G | 6 | a0001c0001t0004g0028a0001c0001t0006g0026a0001c0001t0011g0025others(3): Show | 6 | HG01934.hp2 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+8170A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615147 | ||||||
| chr3:30615237
|
T | C | 1 | a0001c0001t0003g0230 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.94+8260T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615237 | ||||||
| chr3:30615275
|
CCCTGGTA others(5): Show |
C | 12 | a0001c0001t0001g0359a0001c0001t0004g0354a0001c0001t0004g0358others(9): Show | 12 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+8301_94+8312del others(12): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30615275 | |||||
| chr3:30615289
|
C | T | 12 | a0001c0001t0001g0359a0001c0001t0004g0354a0001c0001t0004g0358others(9): Show | 12 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+8312C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615289 | ||||||
| chr3:30615305
|
G | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0052others(178): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.94+8328G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615305 | ||||||
| chr3:30615307
|
G | A | 6 | a0001c0001t0004g0028a0001c0001t0006g0026a0001c0001t0011g0025others(3): Show | 6 | HG01934.hp2 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+8330G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615307 | ||||||
| chr3:30615353
|
C | T | 6 | a0001c0001t0004g0028a0001c0001t0006g0026a0001c0001t0011g0025others(3): Show | 6 | HG01934.hp2 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+8376C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615353 | ||||||
| chr3:30615424
|
A | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0052others(245): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.94+8447A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615424 | ||||||
| chr3:30615456
|
T | C | 2 | a0001c0001t0006g0019a0001c0004t0014g0349 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.94+8479T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615456 | ||||||
| chr3:30615588
|
A | G | 1 | a0001c0001t0003g0224 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.94+8611A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615588 | ||||||
| chr3:30615746
|
A | AT | 248 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0052others(245): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.94+8777dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30615746 | |||||
| chr3:30615767
|
T | A | 1 | a0001c0002t0001g0129 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.94+8790T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615767 | ||||||
| chr3:30615801
|
A | G | 2 | a0001c0002t0039g0032a0001c0003t0040g0033 | 2 | HG01243.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.94+8824A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615801 | ||||||
| chr3:30615833
|
A | T | 1 | a0001c0001t0026g0111 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.94+8856A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615833 | ||||||
| chr3:30615883
|
A | T | 248 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0052others(245): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.94+8906A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30615883 | ||||||
| chr3:30616189
|
T | C | 1 | a0001c0002t0001g0130 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.94+9212T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30616189 | ||||||
| chr3:30616308
|
C | T | 3 | a0001c0001t0004g0082a0001c0001t0026g0111a0001c0004t0008g0081 | 3 | HG02559.hp2 HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.94+9331C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30616308 | ||||||
| chr3:30616427
|
T | C | 2 | a0001c0001t0001g0132a0001c0001t0002g0131 | 2 | HG01255.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.94+9450T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30616427 | ||||||
| chr3:30616438
|
T | C | 2 | a0001c0001t0006g0019a0001c0004t0014g0349 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.94+9461T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30616438 | ||||||
| chr3:30616539
|
C | T | 248 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0052others(245): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.94+9562C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30616539 | ||||||
| chr3:30616603
|
T | G | 3 | a0001c0001t0004g0082a0001c0001t0026g0111a0001c0004t0008g0081 | 3 | HG02559.hp2 HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.94+9626T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30616603 | ||||||
| chr3:30616658
|
A | G | 3 | a0001c0001t0001g0385a0001c0001t0001g0386a0001c0001t0001g0387 | 3 | NA18990.hp1 NA18999.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.94+9681A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30616658 | ||||||
| chr3:30616685
|
T | C | 2 | a0001c0004t0003g0225a0001c0004t0008g0128 | 2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+9708T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30616685 | ||||||
| chr3:30616795
|
A | G | 1 | a0001c0001t0011g0080 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.94+9818A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30616795 | ||||||
| chr3:30616963
|
C | T | 1 | a0001c0001t0007g0079 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.94+9986C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30616963 | ||||||
| chr3:30617023
|
T | C | 1 | a0001c0002t0001g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.94+10046T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30617023 | ||||||
| chr3:30617049
|
T | A | 296 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0044others(293): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.94+10072T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30617049 | ||||||
| chr3:30617082
|
GA | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0052others(189): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.94+10117delA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30617082 | |||||
| chr3:30617084
|
A | G | 2 | a0001c0001t0001g0275a0001c0001t0001g0276 | 2 | NA18967.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.94+10107A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30617084 | ||||||
| chr3:30617225
|
G | A | 39 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0037others(36): Show | 39 | HG00280.hp1 HG00609.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.94+10248G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30617225 | ||||||
| chr3:30617437
|
C | T | 2 | a0001c0001t0001g0348a0001c0001t0022g0347 | 2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.94+10460C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30617437 | ||||||
| chr3:30617627
|
C | T | 203 | a0001c0001t0001g0035a0001c0001t0001g0084a0001c0001t0001g0085others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.94+10650C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30617627 | ||||||
| chr3:30617697
|
C | T | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | NA18965.hp1 NA18999.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.94+10720C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30617697 | ||||||
| chr3:30617759
|
C | T | 6 | a0001c0001t0004g0028a0001c0001t0006g0026a0001c0001t0011g0025others(3): Show | 6 | HG01934.hp2 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+10782C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30617759 | ||||||
| chr3:30617760
|
G | A | 12 | a0001c0001t0001g0359a0001c0001t0004g0354a0001c0001t0004g0358others(9): Show | 12 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+10783G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30617760 | ||||||
| chr3:30617919
|
A | G | 1 | a0004c0007t0004g0364 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.94+10942A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30617919 | ||||||
| chr3:30618112
|
T | G | 2 | a0001c0001t0026g0111a0001c0004t0008g0081 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.94+11135T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30618112 | ||||||
| chr3:30618160
|
G | A | 242 | a0001c0001t0001g0035a0001c0001t0001g0084a0001c0001t0001g0085others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.94+11183G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30618160 | ||||||
| chr3:30618231
|
G | GT | 24 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0085others(21): Show | 24 | HG01167.hp2 HG02280.hp2 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.94+11270dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30618231 | |||||
| chr3:30618471
|
C | T | 4 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0330others(1): Show | 4 | NA18950.hp2 NA18954.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+11494C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30618471 | ||||||
| chr3:30618517
|
C | T | 3 | a0001c0001t0001g0385a0001c0001t0001g0386a0001c0001t0001g0387 | 3 | NA18990.hp1 NA18999.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.94+11540C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30618517 | ||||||
| chr3:30618532
|
G | A | 1 | a0001c0001t0007g0073 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.94+11555G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30618532 | ||||||
| chr3:30618755
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.94+11778A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30618755 | ||||||
| chr3:30618871
|
T | G | 1 | a0001c0001t0001g0338 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.94+11894T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30618871 | ||||||
| chr3:30618909
|
T | C | 1 | a0001c0001t0001g0345 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.94+11932T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30618909 | ||||||
| chr3:30618937
|
A | G | 33 | a0001c0001t0001g0048a0001c0001t0001g0084a0001c0001t0001g0085others(30): Show | 33 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.94+11960A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30618937 | ||||||
| chr3:30619111
|
A | G | 1 | a0001c0001t0001g0327 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.94+12134A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619111 | ||||||
| chr3:30619188
|
C | T | 135 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0100others(132): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.94+12211C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619188 | ||||||
| chr3:30619238
|
C | T | 3 | a0001c0001t0011g0080a0001c0003t0006g0078a0001c0011t0037g0083 | 3 | HG02622.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.94+12261C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619238 | ||||||
| chr3:30619239
|
G | A | 1 | a0004c0007t0004g0364 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.94+12262G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619239 | ||||||
| chr3:30619277
|
A | T | 9 | a0001c0001t0005g0012a0001c0001t0005g0014a0001c0001t0005g0015others(6): Show | 9 | HG00408.hp2 HG01358.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+12300A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619277 | ||||||
| chr3:30619341
|
T | C | 2 | a0001c0001t0006g0019a0001c0004t0014g0349 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.94+12364T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619341 | ||||||
| chr3:30619420
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.94+12443A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619420 | ||||||
| chr3:30619595
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.94+12618A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619595 | ||||||
| chr3:30619677
|
C | T | 12 | a0001c0001t0001g0287a0001c0001t0001g0323a0001c0001t0001g0324others(9): Show | 12 | HG01261.hp2 HG03239.hp1 HG03490.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+12700C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619677 | ||||||
| chr3:30619718
|
C | T | 146 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0100others(143): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.94+12741C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619718 | ||||||
| chr3:30619719
|
G | A | 1 | a0001c0001t0006g0019 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.94+12742G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619719 | ||||||
| chr3:30619823
|
C | G | 1 | a0001c0004t0008g0333 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.94+12846C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619823 | ||||||
| chr3:30619956
|
G | C | 12 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(9): Show | 12 | HG00735.hp1 HG01952.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.94+12979G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619956 | ||||||
| chr3:30619961
|
GC | G | 141 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0095others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.94+12985delC | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619961 | ||||||
| chr3:30619970
|
G | A | 5 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(2): Show | 5 | NA18944.hp2 NA19004.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+12993G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619970 | ||||||
| chr3:30619972
|
A | G | 5 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(2): Show | 5 | NA18944.hp2 NA19004.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+12995A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619972 | ||||||
| chr3:30619989
|
C | T | 180 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0095others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.94+13012C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30619989 | ||||||
| chr3:30620043
|
T | C | 1 | a0004c0007t0004g0364 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.94+13066T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620043 | ||||||
| chr3:30620046
|
G | A | 11 | a0001c0001t0005g0012a0001c0001t0005g0014a0001c0001t0005g0015others(8): Show | 11 | HG00408.hp2 HG00639.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.94+13069G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620046 | ||||||
| chr3:30620103
|
C | T | 74 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0037others(71): Show | 74 | HG00280.hp1 HG00621.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.94+13126C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620103 | ||||||
| chr3:30620106
|
G | C | 2 | a0001c0001t0003g0122a0001c0001t0015g0143 | 2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.94+13129G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620106 | ||||||
| chr3:30620119
|
G | A | 6 | a0001c0001t0002g0077a0001c0001t0007g0074a0001c0001t0007g0075others(3): Show | 6 | HG02486.hp2 HG02647.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+13142G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620119 | ||||||
| chr3:30620123
|
T | C | 5 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(2): Show | 5 | NA18959.hp2 NA19011.hp1 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+13146T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620123 | ||||||
| chr3:30620135
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.94+13158C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620135 | ||||||
| chr3:30620136
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.94+13159G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620136 | ||||||
| chr3:30620143
|
C | T | 12 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(9): Show | 12 | HG00735.hp1 HG01952.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.94+13166C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620143 | ||||||
| chr3:30620206
|
A | G | 3 | a0001c0001t0001g0287a0001c0001t0001g0324a0001c0001t0001g0345 | 3 | HG01261.hp2 HG03540.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.94+13229A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620206 | ||||||
| chr3:30620304
|
T | C | 12 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(9): Show | 12 | HG00735.hp1 HG01952.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.94+13327T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620304 | ||||||
| chr3:30620340
|
G | A | 9 | a0001c0001t0005g0012a0001c0001t0005g0014a0001c0001t0005g0015others(6): Show | 9 | HG00408.hp2 HG01358.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+13363G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620340 | ||||||
| chr3:30620647
|
A | C | 1 | a0001c0004t0014g0349 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.94+13670A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620647 | ||||||
| chr3:30620666
|
A | G | 1 | a0001c0001t0002g0196 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.94+13689A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620666 | ||||||
| chr3:30620738
|
T | C | 1 | a0001c0001t0007g0073 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.94+13761T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620738 | ||||||
| chr3:30620836
|
C | G | 266 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0035others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.94+13859C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620836 | ||||||
| chr3:30620957
|
G | T | 39 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(36): Show | 39 | HG00408.hp2 HG00639.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.94+13980G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620957 | ||||||
| chr3:30620982
|
G | A | 2 | a0001c0001t0012g0296a0001c0001t0042g0005 | 2 | HG01106.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.94+14005G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30620982 | ||||||
| chr3:30621062
|
A | G | 39 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(36): Show | 39 | HG00408.hp2 HG00639.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.94+14085A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30621062 | ||||||
| chr3:30621168
|
A | G | 2 | a0001c0001t0006g0019a0001c0004t0014g0349 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.94+14191A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30621168 | ||||||
| chr3:30621278
|
C | CT | 75 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(72): Show | 75 | HG00558.hp2 HG00673.hp1 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.94+14320dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30621278 | |||||
| chr3:30621278
|
C | CTT | 169 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(166): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.94+14319_94+14320d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30621278 | |||||
| chr3:30621278
|
C | CTTT | 97 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0037others(94): Show | 97 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.94+14318_94+14320d others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30621278 | |||||
| chr3:30621337
|
A | C | 3 | a0001c0001t0001g0190a0001c0001t0001g0195a0001c0001t0002g0273 | 3 | HG02083.hp2 NA19006.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.94+14360A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30621337 | ||||||
| chr3:30621714
|
A | G | 1 | a0001c0001t0001g0252 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.94+14737A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30621714 | ||||||
| chr3:30621894
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.94+14917G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30621894 | ||||||
| chr3:30621938
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.94+14961C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30621938 | ||||||
| chr3:30621958
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(164): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.94+14981A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30621958 | ||||||
| chr3:30622036
|
A | G | 3 | a0001c0001t0001g0100a0001c0002t0001g0099a0001c0002t0001g0101 | 3 | NA18950.hp1 NA18951.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.94+15059A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622036 | ||||||
| chr3:30622181
|
T | A | 3 | a0001c0001t0019g0297a0001c0004t0008g0331a0001c0008t0003g0332 | 3 | HG01167.hp2 HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.94+15204T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622181 | ||||||
| chr3:30622422
|
A | G | 75 | a0001c0001t0001g0094a0001c0001t0001g0104a0001c0001t0001g0107others(72): Show | 75 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.94+15445A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622422 | ||||||
| chr3:30622495
|
A | G | 95 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0038others(92): Show | 95 | HG00280.hp1 HG00558.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.94+15518A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622495 | ||||||
| chr3:30622537
|
C | CA | 9 | a0001c0001t0001g0147a0001c0001t0001g0253a0001c0001t0002g0261others(6): Show | 9 | HG01891.hp2 HG02698.hp2 HG04204.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+15570dupA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30622537 | |||||
| chr3:30622584
|
G | C | 10 | a0001c0001t0006g0365a0001c0001t0007g0356a0001c0001t0007g0357others(7): Show | 10 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+15607G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622584 | ||||||
| chr3:30622588
|
G | A | 8 | a0001c0001t0001g0231a0001c0001t0005g0014a0001c0001t0005g0015others(5): Show | 8 | HG01358.hp1 HG01361.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.94+15611G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622588 | ||||||
| chr3:30622656
|
C | T | 13 | a0001c0001t0002g0077a0001c0001t0006g0016a0001c0001t0006g0017others(10): Show | 13 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+15679C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622656 | ||||||
| chr3:30622829
|
G | A | 139 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0038others(136): Show | 139 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.94+15852G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622829 | ||||||
| chr3:30622866
|
C | T | 1 | a0004c0007t0004g0364 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.94+15889C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622866 | ||||||
| chr3:30622879
|
CA | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0037others(30): Show | 33 | HG00280.hp1 HG01074.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.94+15929delA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30622879 | |||||
| chr3:30622879
|
CAA | C | 148 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(145): Show | 148 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(145): Show |
intron_variant | MODIFIER | c.94+15928_94+15929d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30622879 | |||||
| chr3:30622879
|
CAAA | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(144): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.94+15927_94+15929d others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30622879 | |||||
| chr3:30622879
|
CAAAA | C | 7 | a0001c0001t0001g0126a0001c0001t0001g0222a0001c0001t0012g0119others(4): Show | 7 | HG00597.hp1 HG01516.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+15926_94+15929d others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30622879 | |||||
| chr3:30622879
|
CAAAAAAA others(8): Show |
C | 4 | a0001c0001t0001g0191a0001c0001t0002g0271a0001c0001t0002g0272others(1): Show | 4 | HG02040.hp2 HG02135.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+15915_94+15929d others(17): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30622879 | |||||
| chr3:30622879
|
CAAAAAAA others(10): Show |
C | 3 | a0001c0001t0002g0072a0001c0004t0003g0225a0001c0004t0008g0128 | 3 | HG02280.hp2 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+15913_94+15929d others(19): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30622879 | |||||
| chr3:30622879
|
CAAAAAAA others(14): Show |
C | 1 | a0001c0002t0001g0187 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.94+15909_94+15929d others(23): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30622879 | |||||
| chr3:30622883
|
A | G | 1 | a0001c0001t0001g0382 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.94+15906A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622883 | ||||||
| chr3:30622913
|
GGAAAAA | G | 5 | a0001c0001t0001g0342a0001c0001t0025g0334a0001c0003t0021g0363others(2): Show | 5 | HG02258.hp2 HG03130.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15951_94+15956d others(8): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30622913 | |||||
| chr3:30622914
|
G | A | 1 | a0001c0001t0007g0073 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.94+15937G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622914 | ||||||
| chr3:30622915
|
A | G | 1 | a0001c0001t0007g0073 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.94+15938A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622915 | ||||||
| chr3:30622919
|
A | G | 1 | a0001c0001t0007g0073 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.94+15942A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30622919 | ||||||
| chr3:30623014
|
C | T | 1 | a0001c0001t0001g0289 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.94+16037C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623014 | ||||||
| chr3:30623240
|
A | C | 4 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 4 | NA19011.hp1 NA19063.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+16263A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623240 | ||||||
| chr3:30623276
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.94+16299A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623276 | ||||||
| chr3:30623372
|
T | C | 8 | a0001c0001t0001g0147a0001c0001t0001g0253a0001c0001t0002g0261others(5): Show | 8 | HG02698.hp2 HG04204.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.94+16395T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623372 | ||||||
| chr3:30623398
|
G | A | 1 | a0001c0001t0001g0372 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.94+16421G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623398 | ||||||
| chr3:30623445
|
T | C | 1 | a0001c0003t0040g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.94+16468T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623445 | ||||||
| chr3:30623619
|
G | T | 1 | a0001c0001t0032g0066 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.94+16642G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623619 | ||||||
| chr3:30623692
|
G | A | 2 | a0001c0001t0001g0278a0001c0001t0001g0279 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.94+16715G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623692 | ||||||
| chr3:30623736
|
G | A | 95 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0038others(92): Show | 95 | HG00280.hp1 HG00558.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.94+16759G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623736 | ||||||
| chr3:30623772
|
A | G | 5 | a0001c0001t0002g0077a0001c0001t0007g0074a0001c0001t0007g0075others(2): Show | 5 | HG02486.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+16795A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623772 | ||||||
| chr3:30623848
|
A | G | 1 | a0001c0001t0005g0021 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.94+16871A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623848 | ||||||
| chr3:30623898
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.94+16921T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30623898 | ||||||
| chr3:30624048
|
C | A | 156 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0038others(153): Show | 156 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.94+17071C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624048 | ||||||
| chr3:30624209
|
C | T | 1 | a0003c0006t0002g0184 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.94+17232C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624209 | ||||||
| chr3:30624260
|
G | C | 4 | a0001c0001t0001g0269a0001c0001t0002g0263a0001c0002t0001g0175others(1): Show | 4 | HG02027.hp1 NA18955.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+17283G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624260 | ||||||
| chr3:30624275
|
G | A | 7 | a0001c0001t0001g0147a0001c0001t0001g0253a0001c0001t0002g0261others(4): Show | 7 | HG02698.hp2 NA18959.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+17298G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624275 | ||||||
| chr3:30624382
|
C | G | 1 | a0001c0002t0001g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.94+17405C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624382 | ||||||
| chr3:30624390
|
G | A | 4 | a0001c0001t0004g0358a0001c0001t0006g0019a0001c0001t0011g0008others(1): Show | 4 | HG01109.hp2 HG01884.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+17413G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624390 | ||||||
| chr3:30624393
|
A | G | 9 | a0001c0001t0001g0147a0001c0001t0001g0253a0001c0001t0002g0261others(6): Show | 9 | HG01891.hp2 HG02698.hp2 HG04204.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+17416A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624393 | ||||||
| chr3:30624509
|
G | A | 1 | a0001c0001t0001g0298 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.94+17532G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624509 | ||||||
| chr3:30624556
|
C | G | 1 | a0001c0001t0001g0063 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.94+17579C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624556 | ||||||
| chr3:30624610
|
G | A | 43 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0038others(40): Show | 43 | HG00280.hp1 HG00609.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.94+17633G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624610 | ||||||
| chr3:30624619
|
G | GA | 53 | a0001c0001t0001g0043a0001c0001t0001g0114a0001c0001t0001g0118others(50): Show | 53 | HG00408.hp2 HG00639.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.94+17654dupA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30624619 | |||||
| chr3:30624837
|
A | C | 1 | a0001c0001t0001g0183 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.94+17860A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624837 | ||||||
| chr3:30624841
|
G | C | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG00738.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.94+17864G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624841 | ||||||
| chr3:30624934
|
G | T | 1 | a0001c0001t0001g0359 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.94+17957G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624934 | ||||||
| chr3:30624960
|
C | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(170): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.94+17983C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30624960 | ||||||
| chr3:30625107
|
A | C | 1 | a0001c0001t0005g0023 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.94+18130A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30625107 | ||||||
| chr3:30625174
|
A | G | 1 | a0001c0001t0001g0342 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.94+18197A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30625174 | ||||||
| chr3:30625295
|
G | A | 1 | a0001c0003t0003g0353 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.94+18318G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30625295 | ||||||
| chr3:30625396
|
G | A | 9 | a0001c0001t0001g0147a0001c0001t0001g0253a0001c0001t0002g0261others(6): Show | 9 | HG01891.hp2 HG02698.hp2 HG04204.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+18419G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30625396 | ||||||
| chr3:30625585
|
G | T | 11 | a0001c0001t0001g0107a0001c0001t0002g0127a0001c0001t0002g0280others(8): Show | 11 | HG00544.hp2 HG00621.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.94+18608G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30625585 | ||||||
| chr3:30625767
|
T | A | 9 | a0001c0001t0001g0147a0001c0001t0001g0253a0001c0001t0002g0261others(6): Show | 9 | HG01891.hp2 HG02698.hp2 HG04204.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+18790T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30625767 | ||||||
| chr3:30625882
|
C | T | 3 | a0001c0001t0002g0072a0001c0004t0003g0225a0001c0004t0008g0128 | 3 | HG02280.hp2 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.95-18865C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30625882 | ||||||
| chr3:30625930
|
C | A | 1 | a0001c0001t0001g0256 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.95-18817C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30625930 | ||||||
| chr3:30625933
|
T | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(175): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.95-18814T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30625933 | ||||||
| chr3:30626061
|
T | G | 1 | a0001c0001t0025g0334 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.95-18686T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30626061 | ||||||
| chr3:30626070
|
A | G | 1 | a0001c0001t0001g0287 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.95-18677A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30626070 | ||||||
| chr3:30626175
|
T | A | 1 | a0001c0003t0040g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.95-18572T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30626175 | ||||||
| chr3:30626232
|
G | T | 4 | a0001c0001t0010g0368a0001c0003t0001g0367a0001c0003t0001g0369others(1): Show | 4 | HG02145.hp1 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-18515G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30626232 | ||||||
| chr3:30626233
|
G | C | 3 | a0001c0001t0006g0016a0001c0001t0006g0017a0001c0001t0006g0018 | 3 | HG02055.hp2 HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.95-18514G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30626233 | ||||||
| chr3:30626522
|
A | G | 9 | a0001c0001t0002g0077a0001c0001t0006g0016a0001c0001t0006g0017others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-18225A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30626522 | ||||||
| chr3:30626542
|
A | G | 1 | a0001c0001t0002g0196 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.95-18205A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30626542 | ||||||
| chr3:30626548
|
CAG | C | 4 | a0001c0001t0004g0358a0001c0001t0006g0019a0001c0001t0011g0008others(1): Show | 4 | HG01109.hp2 HG01884.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-18196_95-18195d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30626548 | |||||
| chr3:30626968
|
T | C | 1 | a0001c0001t0003g0224 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.95-17779T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30626968 | ||||||
| chr3:30627171
|
G | A | 5 | a0001c0001t0010g0368a0001c0001t0026g0111a0001c0003t0001g0367others(2): Show | 5 | HG02145.hp1 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-17576G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627171 | ||||||
| chr3:30627192
|
A | G | 163 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0038others(160): Show | 163 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.95-17555A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627192 | ||||||
| chr3:30627431
|
G | A | 2 | a0001c0001t0001g0318a0001c0002t0038g0029 | 2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.95-17316G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627431 | ||||||
| chr3:30627447
|
G | C | 1 | a0001c0001t0001g0199 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.95-17300G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627447 | ||||||
| chr3:30627454
|
A | G | 1 | a0001c0001t0008g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.95-17293A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627454 | ||||||
| chr3:30627739
|
A | G | 1 | a0001c0001t0006g0365 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.95-17008A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627739 | ||||||
| chr3:30627759
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.95-16988C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627759 | ||||||
| chr3:30627760
|
G | A | 9 | a0001c0001t0001g0147a0001c0001t0001g0253a0001c0001t0002g0261others(6): Show | 9 | HG01891.hp2 HG02698.hp2 HG04204.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-16987G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627760 | ||||||
| chr3:30627821
|
TGA | T | 3 | a0001c0001t0002g0072a0001c0004t0003g0225a0001c0004t0008g0128 | 3 | HG02280.hp2 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.95-16925_95-16924d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627821 | ||||||
| chr3:30627824
|
A | T | 3 | a0001c0001t0002g0072a0001c0004t0003g0225a0001c0004t0008g0128 | 3 | HG02280.hp2 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.95-16923A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627824 | ||||||
| chr3:30627866
|
G | A | 96 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0038others(93): Show | 96 | HG00280.hp1 HG00558.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.95-16881G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627866 | ||||||
| chr3:30627882
|
T | C | 1 | a0001c0001t0010g0341 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.95-16865T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627882 | ||||||
| chr3:30627911
|
C | G | 22 | a0001c0001t0001g0094a0001c0001t0001g0189a0001c0001t0001g0259others(19): Show | 22 | HG00558.hp1 HG00597.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.95-16836C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30627911 | ||||||
| chr3:30628112
|
C | CT | 170 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(167): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.95-16619dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628112 | |||||
| chr3:30628112
|
C | CTT | 30 | a0001c0001t0002g0077a0001c0001t0004g0358a0001c0001t0006g0016others(27): Show | 30 | HG01109.hp2 HG01243.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.95-16620_95-16619d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628112 | |||||
| chr3:30628127
|
TTA | T | 136 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0038others(133): Show | 136 | HG00280.hp1 HG00558.hp2 HG00609.hp2 others(133): Show |
intron_variant | MODIFIER | c.95-16619_95-16618d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30628127 | ||||||
| chr3:30628244
|
A | G | 10 | a0001c0001t0001g0107a0001c0001t0001g0147a0001c0001t0001g0253others(7): Show | 10 | HG00621.hp2 HG02698.hp2 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-16503A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30628244 | ||||||
| chr3:30628291
|
A | G | 44 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(41): Show | 44 | HG00558.hp2 HG01934.hp2 HG02027.hp1 others(41): Show |
intron_variant | MODIFIER | c.95-16456A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30628291 | ||||||
| chr3:30628452
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.95-16295A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30628452 | ||||||
| chr3:30628493
|
C | CA | 16 | a0001c0001t0001g0116a0001c0001t0001g0140a0001c0001t0001g0147others(13): Show | 16 | HG00735.hp1 HG00735.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.95-16240dupA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628493 | |||||
| chr3:30628493
|
CA | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(238): Show | 243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.95-16240delA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628493 | |||||
| chr3:30628528
|
G | GT | 66 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0043others(63): Show | 66 | HG00408.hp2 HG00673.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.95-16194dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628528 | |||||
| chr3:30628528
|
G | GTT | 57 | a0001c0001t0001g0050a0001c0001t0001g0104a0001c0001t0001g0138others(54): Show | 57 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.95-16195_95-16194d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628528 | |||||
| chr3:30628528
|
G | GTTT | 82 | a0001c0001t0001g0001a0001c0001t0001g0042a0001c0001t0001g0048others(79): Show | 84 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.95-16196_95-16194d others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628528 | |||||
| chr3:30628528
|
G | GTTTT | 17 | a0001c0001t0001g0035a0001c0001t0001g0070a0001c0001t0001g0085others(14): Show | 17 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-16197_95-16194d others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628528 | |||||
| chr3:30628528
|
GT | G | 15 | a0001c0001t0001g0300a0001c0001t0001g0342a0001c0001t0002g0072others(12): Show | 15 | HG00099.hp1 HG01243.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.95-16194delT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628528 | |||||
| chr3:30628528
|
GTT | G | 6 | a0001c0001t0006g0016a0001c0001t0006g0017a0001c0001t0007g0074others(3): Show | 6 | HG02258.hp1 HG02486.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-16195_95-16194d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628528 | |||||
| chr3:30628528
|
GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0004g0082 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.95-16205_95-16194d others(14): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30628528 | |||||
| chr3:30628529
|
T | G | 5 | a0001c0001t0001g0147a0001c0001t0001g0253a0001c0001t0002g0261others(2): Show | 5 | HG02698.hp2 NA18959.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-16218T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30628529 | ||||||
| chr3:30628567
|
A | G | 6 | a0001c0001t0001g0147a0001c0001t0001g0253a0001c0001t0002g0261others(3): Show | 6 | HG02698.hp2 NA18959.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-16180A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30628567 | ||||||
| chr3:30628843
|
C | T | 4 | a0001c0001t0006g0016a0001c0001t0006g0017a0001c0001t0006g0018others(1): Show | 4 | HG02055.hp2 HG02258.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-15904C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30628843 | ||||||
| chr3:30628933
|
G | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(152): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.95-15814G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30628933 | ||||||
| chr3:30628975
|
C | T | 4 | a0001c0001t0022g0347a0001c0001t0025g0334a0001c0001t0035g0031others(1): Show | 4 | HG02258.hp2 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-15772C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30628975 | ||||||
| chr3:30629399
|
AAAG | A | 7 | a0001c0001t0001g0147a0001c0001t0001g0253a0001c0001t0002g0261others(4): Show | 7 | HG02698.hp2 HG04204.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-15342_95-15340d others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30629399 | |||||
| chr3:30629631
|
G | A | 1 | a0004c0007t0004g0364 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.95-15116G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30629631 | ||||||
| chr3:30629692
|
G | A | 1 | a0001c0001t0002g0072 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.95-15055G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30629692 | ||||||
| chr3:30630060
|
A | G | 4 | a0001c0001t0001g0378a0001c0001t0001g0379a0001c0001t0001g0380others(1): Show | 4 | NA18944.hp1 NA18951.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-14687A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630060 | ||||||
| chr3:30630092
|
G | C | 67 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0001t0001g0179others(64): Show | 67 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.95-14655G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630092 | ||||||
| chr3:30630237
|
A | G | 1 | a0001c0002t0038g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.95-14510A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630237 | ||||||
| chr3:30630382
|
A | G | 5 | a0001c0001t0002g0077a0001c0001t0007g0074a0001c0001t0007g0075others(2): Show | 5 | HG02486.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-14365A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630382 | ||||||
| chr3:30630557
|
T | C | 1 | a0001c0001t0001g0385 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.95-14190T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630557 | ||||||
| chr3:30630587
|
C | T | 1 | a0004c0007t0004g0364 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.95-14160C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630587 | ||||||
| chr3:30630764
|
G | C | 1 | a0001c0001t0001g0035 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.95-13983G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630764 | ||||||
| chr3:30630765
|
A | G | 75 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0001t0001g0179others(72): Show | 75 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.95-13982A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630765 | ||||||
| chr3:30630775
|
C | T | 1 | a0002c0005t0001g0311 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.95-13972C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630775 | ||||||
| chr3:30630793
|
G | A | 1 | a0004c0007t0004g0364 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.95-13954G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630793 | ||||||
| chr3:30630836
|
A | G | 67 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0001t0001g0179others(64): Show | 67 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.95-13911A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630836 | ||||||
| chr3:30630870
|
C | T | 67 | a0001c0001t0001g0043a0001c0001t0001g0049a0001c0001t0001g0104others(64): Show | 67 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.95-13877C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630870 | ||||||
| chr3:30630879
|
A | C | 1 | a0001c0001t0001g0318 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.95-13868A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630879 | ||||||
| chr3:30630963
|
A | G | 11 | a0001c0001t0006g0365a0001c0001t0007g0356a0001c0001t0007g0357others(8): Show | 11 | HG00639.hp2 HG01255.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.95-13784A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30630963 | ||||||
| chr3:30631009
|
G | A | 4 | a0001c0001t0002g0072a0001c0004t0003g0225a0001c0004t0008g0128others(1): Show | 4 | HG02280.hp2 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-13738G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631009 | ||||||
| chr3:30631014
|
C | G | 67 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0001t0001g0179others(64): Show | 67 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.95-13733C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631014 | ||||||
| chr3:30631036
|
C | CT | 6 | a0001c0001t0001g0058a0001c0001t0001g0140a0001c0001t0001g0172others(3): Show | 6 | HG01123.hp2 HG01934.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-13689dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30631036 | |||||
| chr3:30631036
|
CT | C | 84 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0048others(81): Show | 85 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.95-13689delT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30631036 | |||||
| chr3:30631036
|
CTT | C | 151 | a0001c0001t0001g0043a0001c0001t0001g0049a0001c0001t0001g0104others(148): Show | 151 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.95-13690_95-13689d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30631036 | |||||
| chr3:30631058
|
T | A | 2 | a0001c0001t0002g0383a0001c0002t0010g0384 | 2 | HG03490.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.95-13689T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631058 | ||||||
| chr3:30631105
|
G | A | 67 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0001t0001g0179others(64): Show | 67 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.95-13642G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631105 | ||||||
| chr3:30631143
|
T | C | 67 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0001t0001g0179others(64): Show | 67 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.95-13604T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631143 | ||||||
| chr3:30631197
|
A | T | 67 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0001t0001g0179others(64): Show | 67 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.95-13550A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631197 | ||||||
| chr3:30631214
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.95-13533G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631214 | ||||||
| chr3:30631230
|
C | T | 1 | a0001c0001t0002g0246 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.95-13517C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631230 | ||||||
| chr3:30631239
|
G | A | 255 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0043others(252): Show | 256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.95-13508G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631239 | ||||||
| chr3:30631291
|
C | T | 1 | a0001c0004t0008g0333 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.95-13456C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631291 | ||||||
| chr3:30631414
|
A | C | 67 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0001t0001g0179others(64): Show | 67 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.95-13333A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631414 | ||||||
| chr3:30631487
|
A | G | 3 | a0001c0001t0001g0147a0001c0001t0001g0253a0005c0009t0013g0254 | 3 | NA18959.hp1 NA18977.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.95-13260A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631487 | ||||||
| chr3:30631621
|
CT | C | 166 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0042others(163): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.95-13104delT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30631621 | |||||
| chr3:30631621
|
CTT | C | 10 | a0001c0001t0001g0112a0001c0001t0001g0148a0001c0001t0001g0236others(7): Show | 10 | HG00639.hp2 HG01070.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-13105_95-13104d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30631621 | |||||
| chr3:30631621
|
CTTT | C | 47 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0183others(44): Show | 47 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.95-13106_95-13104d others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30631621 | |||||
| chr3:30631621
|
CTTTT | C | 13 | a0001c0001t0001g0144a0001c0001t0001g0190a0001c0001t0001g0191others(10): Show | 13 | HG00673.hp2 HG02040.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.95-13107_95-13104d others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30631621 | |||||
| chr3:30631621
|
CTTTTTTT others(3): Show |
C | 16 | a0001c0001t0001g0149a0001c0001t0004g0028a0001c0001t0004g0315others(13): Show | 16 | HG01934.hp2 HG02109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.95-13113_95-13104d others(12): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30631621 | |||||
| chr3:30631626
|
T | C | 2 | a0001c0001t0007g0073a0001c0011t0037g0083 | 2 | HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.95-13121T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631626 | ||||||
| chr3:30631627
|
T | C | 1 | a0001c0001t0026g0111 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.95-13120T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631627 | ||||||
| chr3:30631628
|
T | C | 3 | a0001c0002t0001g0174a0001c0002t0031g0185a0002c0005t0005g0178 | 3 | NA19057.hp1 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.95-13119T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631628 | ||||||
| chr3:30631726
|
T | A | 1 | a0001c0002t0001g0238 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.95-13021T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631726 | ||||||
| chr3:30631868
|
C | T | 7 | a0001c0001t0001g0147a0001c0001t0001g0253a0001c0001t0002g0261others(4): Show | 7 | HG02698.hp2 HG04204.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-12879C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631868 | ||||||
| chr3:30631878
|
C | T | 1 | a0001c0012t0002g0062 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.95-12869C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30631878 | ||||||
| chr3:30632020
|
T | G | 1 | a0002c0005t0001g0326 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.95-12727T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632020 | ||||||
| chr3:30632187
|
A | G | 22 | a0001c0001t0001g0342a0001c0001t0002g0077a0001c0001t0006g0016others(19): Show | 22 | HG00639.hp2 HG01243.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.95-12560A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632187 | ||||||
| chr3:30632228
|
C | T | 70 | a0001c0001t0001g0126a0001c0001t0001g0144a0001c0001t0001g0147others(67): Show | 71 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.95-12519C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632228 | ||||||
| chr3:30632291
|
G | A | 1 | a0001c0001t0003g0224 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.95-12456G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632291 | ||||||
| chr3:30632373
|
C | T | 1 | a0001c0001t0026g0111 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.95-12374C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632373 | ||||||
| chr3:30632397
|
A | G | 24 | a0001c0001t0001g0149a0001c0001t0002g0072a0001c0001t0004g0028others(21): Show | 24 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.95-12350A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632397 | ||||||
| chr3:30632513
|
A | C | 1 | a0001c0001t0001g0095 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.95-12234A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632513 | ||||||
| chr3:30632558
|
T | G | 1 | a0001c0001t0001g0112 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.95-12189T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632558 | ||||||
| chr3:30632700
|
G | A | 7 | a0001c0001t0002g0072a0001c0001t0007g0073a0001c0001t0026g0111others(4): Show | 7 | HG02280.hp2 HG02723.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-12047G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632700 | ||||||
| chr3:30632762
|
C | T | 73 | a0001c0001t0001g0063a0001c0001t0001g0144a0001c0001t0001g0179others(70): Show | 73 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.95-11985C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632762 | ||||||
| chr3:30632941
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.95-11806T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632941 | ||||||
| chr3:30632967
|
C | T | 1 | a0001c0001t0003g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.95-11780C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30632967 | ||||||
| chr3:30633026
|
C | G | 1 | a0001c0003t0021g0363 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.95-11721C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633026 | ||||||
| chr3:30633179
|
A | G | 71 | a0001c0001t0001g0063a0001c0001t0001g0115a0001c0001t0001g0144others(68): Show | 71 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.95-11568A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633179 | ||||||
| chr3:30633195
|
T | C | 1 | a0001c0004t0008g0331 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.95-11552T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633195 | ||||||
| chr3:30633354
|
A | G | 1 | a0001c0001t0001g0253 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.95-11393A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633354 | ||||||
| chr3:30633459
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.95-11288A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633459 | ||||||
| chr3:30633492
|
C | T | 22 | a0001c0001t0001g0342a0001c0001t0002g0077a0001c0001t0006g0016others(19): Show | 22 | HG00639.hp2 HG01243.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.95-11255C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633492 | ||||||
| chr3:30633541
|
T | C | 24 | a0001c0001t0001g0342a0001c0001t0002g0077a0001c0001t0006g0016others(21): Show | 24 | HG00639.hp2 HG01243.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.95-11206T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633541 | ||||||
| chr3:30633562
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(71): Show | 75 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.95-11185C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633562 | ||||||
| chr3:30633659
|
C | T | 51 | a0001c0001t0001g0043a0001c0001t0001g0104a0001c0001t0001g0112others(48): Show | 51 | HG00639.hp1 HG00738.hp1 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.95-11088C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633659 | ||||||
| chr3:30633680
|
G | A | 1 | a0001c0001t0003g0224 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.95-11067G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633680 | ||||||
| chr3:30633732
|
T | C | 1 | a0001c0001t0001g0054 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.95-11015T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633732 | ||||||
| chr3:30633818
|
C | T | 2 | a0001c0001t0011g0008a0004c0007t0004g0364 | 2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.95-10929C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633818 | ||||||
| chr3:30633834
|
G | A | 259 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(256): Show | 261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.95-10913G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30633834 | ||||||
| chr3:30634071
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.95-10676A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634071 | ||||||
| chr3:30634127
|
G | A | 12 | a0001c0001t0001g0149a0001c0001t0004g0028a0001c0001t0004g0315others(9): Show | 12 | HG01934.hp2 HG02109.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.95-10620G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634127 | ||||||
| chr3:30634380
|
T | C | 15 | a0001c0001t0006g0016a0001c0001t0006g0017a0001c0001t0006g0018others(12): Show | 15 | HG00639.hp2 HG01255.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-10367T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634380 | ||||||
| chr3:30634388
|
A | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(182): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.95-10359A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634388 | ||||||
| chr3:30634435
|
T | A | 9 | a0001c0001t0002g0077a0001c0001t0003g0224a0001c0001t0004g0358others(6): Show | 9 | HG01884.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-10312T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634435 | ||||||
| chr3:30634465
|
T | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(166): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.95-10282T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634465 | ||||||
| chr3:30634508
|
G | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(166): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.95-10239G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634508 | ||||||
| chr3:30634525
|
G | C | 290 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(287): Show | 292 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.95-10222G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634525 | ||||||
| chr3:30634615
|
G | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0288a0001c0001t0001g0317 | 3 | HG01069.hp1 HG01071.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.95-10132G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634615 | ||||||
| chr3:30634851
|
G | C | 291 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(288): Show | 293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.95-9896G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634851 | ||||||
| chr3:30634917
|
G | A | 2 | a0001c0001t0006g0009a0001c0001t0006g0010 | 2 | HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.95-9830G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634917 | ||||||
| chr3:30634929
|
T | A | 1 | a0001c0001t0001g0210 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.95-9818T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634929 | ||||||
| chr3:30634954
|
C | T | 5 | a0001c0001t0002g0077a0001c0001t0007g0074a0001c0001t0007g0075others(2): Show | 5 | HG02486.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-9793C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30634954 | ||||||
| chr3:30635164
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.95-9583T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30635164 | ||||||
| chr3:30635329
|
G | T | 1 | a0001c0001t0009g0166 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.95-9418G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30635329 | ||||||
| chr3:30635624
|
G | A | 273 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(270): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.95-9123G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30635624 | ||||||
| chr3:30635777
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(155): Show | 159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.95-8970A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30635777 | ||||||
| chr3:30635806
|
A | G | 20 | a0001c0001t0001g0189a0001c0001t0001g0259a0001c0001t0001g0327others(17): Show | 20 | HG00544.hp2 HG00673.hp1 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.95-8941A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30635806 | ||||||
| chr3:30635909
|
A | G | 2 | a0001c0001t0011g0008a0004c0007t0004g0364 | 2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.95-8838A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30635909 | ||||||
| chr3:30635957
|
A | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0038others(2): Show | 5 | HG00280.hp1 HG01074.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-8790A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30635957 | ||||||
| chr3:30635992
|
C | A | 259 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0043others(256): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.95-8755C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30635992 | ||||||
| chr3:30636001
|
T | C | 9 | a0001c0001t0002g0077a0001c0001t0003g0224a0001c0001t0004g0358others(6): Show | 9 | HG01884.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-8746T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636001 | ||||||
| chr3:30636067
|
G | C | 380 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(377): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.95-8680G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636067 | ||||||
| chr3:30636155
|
A | ATG | 42 | a0001c0001t0001g0043a0001c0001t0001g0048a0001c0001t0001g0084others(39): Show | 42 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.95-8548_95-8547dup others(2): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | |||||
| chr3:30636155
|
A | ATGTG | 60 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0049others(57): Show | 61 | HG00558.hp1 HG00609.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.95-8550_95-8547dup others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | |||||
| chr3:30636155
|
A | ATGTGTG | 47 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0050others(44): Show | 47 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.95-8552_95-8547dup others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | |||||
| chr3:30636155
|
A | ATGTGTGT others(1): Show |
10 | a0001c0001t0001g0132a0001c0001t0001g0267a0001c0001t0001g0277others(7): Show | 10 | HG00140.hp2 HG00597.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-8554_95-8547dup others(8): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | |||||
| chr3:30636155
|
A | ATGTGTGT others(3): Show |
6 | a0001c0001t0001g0110a0001c0001t0004g0154a0001c0001t0012g0281others(3): Show | 6 | HG02109.hp1 HG02602.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-8556_95-8547dup others(10): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | |||||
| chr3:30636155
|
A | ATGTGTGT others(5): Show |
5 | a0001c0001t0001g0059a0001c0001t0001g0100a0001c0001t0001g0190others(2): Show | 5 | NA18950.hp1 NA18966.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-8558_95-8547dup others(12): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | |||||
| chr3:30636155
|
A | G | 1 | a0001c0001t0005g0013 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.95-8592A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636155 | ||||||
| chr3:30636155
|
ATG | A | 36 | a0001c0001t0001g0070a0001c0001t0001g0148a0001c0001t0001g0172others(33): Show | 36 | HG01070.hp1 HG01243.hp2 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.95-8548_95-8547del others(2): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | |||||
| chr3:30636155
|
ATGTG | A | 12 | a0001c0001t0001g0054a0001c0001t0001g0140a0001c0001t0001g0141others(9): Show | 12 | HG01070.hp2 HG01071.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.95-8550_95-8547del others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | |||||
| chr3:30636155
|
ATGTGTG | A | 98 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0037others(95): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.95-8552_95-8547del others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | |||||
| chr3:30636155
|
ATGTGTGT others(1): Show |
A | 7 | a0001c0001t0001g0147a0001c0001t0001g0193a0001c0001t0001g0247others(4): Show | 7 | HG01123.hp2 HG03098.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-8554_95-8547del others(8): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | |||||
| chr3:30636155
|
ATGTGTGT others(3): Show |
A | 2 | a0001c0001t0011g0008a0001c0002t0001g0123 | 2 | HG01109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.95-8556_95-8547del others(10): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | |||||
| chr3:30636155
|
ATGTGTGT others(5): Show |
A | 1 | a0004c0007t0004g0364 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.95-8558_95-8547del others(12): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | |||||
| chr3:30636155
|
ATGTGTGT others(7): Show |
A | 3 | a0001c0002t0039g0032a0001c0003t0040g0033a0002c0005t0001g0326 | 3 | HG01243.hp1 HG01891.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.95-8560_95-8547del others(14): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | |||||
| chr3:30636155
|
ATGTGTGT others(9): Show |
A | 2 | a0001c0001t0026g0111a0001c0004t0008g0331 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.95-8562_95-8547del others(16): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | |||||
| chr3:30636155
|
ATGTGTGT others(11): Show |
A | 3 | a0001c0001t0002g0072a0001c0004t0003g0225a0001c0004t0008g0128 | 3 | HG02280.hp2 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.95-8564_95-8547del others(18): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636155 | |||||
| chr3:30636206
|
A | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(270): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.95-8541A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636206 | ||||||
| chr3:30636221
|
G | A | 1 | a0001c0001t0023g0241 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.95-8526G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636221 | ||||||
| chr3:30636326
|
T | A | 257 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0043others(254): Show | 258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.95-8421T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636326 | ||||||
| chr3:30636339
|
C | T | 5 | a0001c0001t0001g0342a0001c0001t0006g0016a0001c0001t0006g0017others(2): Show | 5 | HG02055.hp2 HG02258.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-8408C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636339 | ||||||
| chr3:30636577
|
A | T | 3 | a0001c0001t0006g0016a0001c0001t0006g0017a0001c0001t0006g0018 | 3 | HG02055.hp2 HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.95-8170A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636577 | ||||||
| chr3:30636699
|
A | T | 5 | a0001c0001t0002g0072a0001c0004t0003g0225a0001c0004t0008g0128others(2): Show | 5 | HG02280.hp2 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-8048A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636699 | ||||||
| chr3:30636722
|
A | C | 78 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0104others(75): Show | 78 | HG00639.hp1 HG00738.hp1 HG01069.hp1 others(75): Show |
intron_variant | MODIFIER | c.95-8025A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636722 | ||||||
| chr3:30636733
|
C | CGT | 57 | a0001c0001t0001g0042a0001c0001t0001g0104a0001c0001t0001g0112others(54): Show | 58 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.95-7989_95-7988dup others(2): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636733 | |||||
| chr3:30636733
|
CGT | C | 10 | a0001c0001t0001g0342a0001c0001t0006g0016a0001c0001t0006g0017others(7): Show | 10 | HG02055.hp2 HG02258.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-7989_95-7988del others(2): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636733 | |||||
| chr3:30636733
|
CGTGT | C | 15 | a0001c0001t0001g0149a0001c0001t0004g0028a0001c0001t0004g0150others(12): Show | 15 | HG01934.hp2 HG02109.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-7991_95-7988del others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636733 | |||||
| chr3:30636790
|
C | T | 4 | a0001c0001t0002g0072a0001c0004t0003g0225a0001c0004t0008g0128others(1): Show | 4 | HG02280.hp2 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-7957C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636790 | ||||||
| chr3:30636860
|
C | G | 9 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0068others(6): Show | 9 | HG00558.hp2 HG02132.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-7887C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636860 | ||||||
| chr3:30636861
|
G | C | 1 | a0001c0001t0001g0069 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.95-7886G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636861 | ||||||
| chr3:30636895
|
T | A | 1 | a0001c0001t0001g0190 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7852T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636895 | ||||||
| chr3:30636908
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0190 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7833_95-7832ins others(14): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30636908 | |||||
| chr3:30636920
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7827C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636920 | ||||||
| chr3:30636921
|
A | T | 1 | a0001c0001t0001g0190 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7826A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636921 | ||||||
| chr3:30636922
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7825A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636922 | ||||||
| chr3:30636931
|
T | G | 1 | a0001c0001t0001g0190 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7816T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636931 | ||||||
| chr3:30636932
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7815T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636932 | ||||||
| chr3:30636937
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7810A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636937 | ||||||
| chr3:30636953
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7794G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636953 | ||||||
| chr3:30636962
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7785G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636962 | ||||||
| chr3:30636970
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.95-7777A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30636970 | ||||||
| chr3:30637021
|
G | A | 7 | a0001c0001t0001g0342a0001c0001t0006g0016a0001c0001t0006g0017others(4): Show | 7 | HG02055.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-7726G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30637021 | ||||||
| chr3:30637062
|
T | TG | 9 | a0001c0001t0007g0356a0001c0001t0007g0357a0001c0001t0007g0362others(6): Show | 9 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-7684dupG | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30637062 | |||||
| chr3:30637063
|
G | GA | 10 | a0001c0001t0001g0058a0001c0001t0001g0124a0001c0001t0001g0163others(7): Show | 10 | HG01981.hp1 HG02055.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-7668dupA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30637063 | |||||
| chr3:30637618
|
A | G | 1 | a0001c0001t0003g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.95-7129A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30637618 | ||||||
| chr3:30637675
|
T | C | 1 | a0001c0001t0024g0255 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.95-7072T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30637675 | ||||||
| chr3:30637727
|
G | A | 7 | a0001c0001t0001g0342a0001c0001t0006g0016a0001c0001t0006g0017others(4): Show | 7 | HG01109.hp2 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-7020G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30637727 | ||||||
| chr3:30637858
|
G | A | 2 | a0001c0001t0001g0342a0001c0001t0004g0150 | 2 | HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.95-6889G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30637858 | ||||||
| chr3:30637876
|
G | C | 1 | a0001c0001t0001g0155 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.95-6871G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30637876 | ||||||
| chr3:30637885
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.95-6862G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30637885 | ||||||
| chr3:30638066
|
A | T | 276 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(273): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.95-6681A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638066 | ||||||
| chr3:30638120
|
T | C | 276 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(273): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.95-6627T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638120 | ||||||
| chr3:30638357
|
A | T | 12 | a0001c0001t0001g0149a0001c0001t0004g0028a0001c0001t0004g0315others(9): Show | 12 | HG01934.hp2 HG02109.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.95-6390A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638357 | ||||||
| chr3:30638367
|
A | G | 16 | a0001c0001t0001g0342a0001c0001t0002g0077a0001c0001t0003g0224others(13): Show | 16 | HG00639.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.95-6380A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638367 | ||||||
| chr3:30638372
|
A | G | 2 | a0001c0001t0011g0008a0004c0007t0004g0364 | 2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.95-6375A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638372 | ||||||
| chr3:30638391
|
A | G | 5 | a0001c0001t0002g0077a0001c0001t0007g0074a0001c0001t0007g0075others(2): Show | 5 | HG02486.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-6356A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638391 | ||||||
| chr3:30638461
|
G | A | 17 | a0001c0001t0001g0149a0001c0001t0004g0028a0001c0001t0004g0150others(14): Show | 17 | HG01934.hp2 HG02109.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-6286G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638461 | ||||||
| chr3:30638478
|
C | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(163): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.95-6269C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638478 | ||||||
| chr3:30638502
|
T | C | 13 | a0001c0001t0001g0126a0001c0001t0001g0147a0001c0001t0001g0157others(10): Show | 14 | HG00140.hp1 HG00280.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.95-6245T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638502 | ||||||
| chr3:30638519
|
C | T | 1 | a0001c0002t0001g0238 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.95-6228C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638519 | ||||||
| chr3:30638537
|
A | G | 1 | a0001c0002t0001g0175 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.95-6210A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638537 | ||||||
| chr3:30638644
|
C | A | 17 | a0001c0001t0001g0149a0001c0001t0004g0028a0001c0001t0004g0150others(14): Show | 17 | HG01934.hp2 HG02109.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-6103C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638644 | ||||||
| chr3:30638690
|
T | G | 1 | a0001c0001t0001g0163 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.95-6057T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638690 | ||||||
| chr3:30638878
|
T | C | 309 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(306): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.95-5869T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30638878 | ||||||
| chr3:30639210
|
C | A | 1 | a0001c0012t0002g0062 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.95-5537C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30639210 | ||||||
| chr3:30639379
|
G | A | 2 | a0001c0001t0011g0008a0004c0007t0004g0364 | 2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.95-5368G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30639379 | ||||||
| chr3:30639441
|
C | T | 2 | a0001c0001t0011g0008a0004c0007t0004g0364 | 2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.95-5306C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30639441 | ||||||
| chr3:30639490
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.95-5257G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30639490 | ||||||
| chr3:30639603
|
A | G | 70 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0104others(67): Show | 70 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.95-5144A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30639603 | ||||||
| chr3:30639754
|
C | T | 1 | a0001c0001t0004g0082 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.95-4993C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30639754 | ||||||
| chr3:30639982
|
T | C | 9 | a0001c0001t0001g0342a0001c0001t0006g0016a0001c0001t0006g0017others(6): Show | 9 | HG00639.hp2 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-4765T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30639982 | ||||||
| chr3:30640055
|
A | G | 1 | a0001c0002t0039g0032 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.95-4692A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640055 | ||||||
| chr3:30640134
|
C | A | 1 | a0001c0001t0032g0066 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.95-4613C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640134 | ||||||
| chr3:30640153
|
A | G | 1 | a0001c0001t0011g0080 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.95-4594A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640153 | ||||||
| chr3:30640224
|
G | T | 1 | a0001c0001t0003g0039 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.95-4523G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640224 | ||||||
| chr3:30640330
|
G | A | 26 | a0001c0001t0001g0149a0001c0001t0002g0077a0001c0001t0003g0224others(23): Show | 26 | HG01884.hp1 HG01934.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.95-4417G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640330 | ||||||
| chr3:30640436
|
G | C | 1 | a0001c0001t0005g0023 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.95-4311G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640436 | ||||||
| chr3:30640617
|
G | T | 1 | a0001c0001t0002g0295 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.95-4130G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640617 | ||||||
| chr3:30640625
|
A | G | 14 | a0001c0001t0001g0342a0001c0001t0004g0358a0001c0001t0006g0016others(11): Show | 14 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.95-4122A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640625 | ||||||
| chr3:30640658
|
T | A | 1 | a0001c0003t0040g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.95-4089T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640658 | ||||||
| chr3:30640658
|
TA | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(161): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.95-4082delA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30640658 | |||||
| chr3:30640750
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(163): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.95-3997A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640750 | ||||||
| chr3:30640761
|
A | G | 4 | a0001c0001t0015g0388a0001c0003t0003g0353a0001c0003t0006g0078others(1): Show | 4 | HG01891.hp1 HG03195.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-3986A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30640761 | ||||||
| chr3:30641072
|
C | A | 1 | a0001c0001t0002g0207 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.95-3675C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641072 | ||||||
| chr3:30641106
|
T | C | 3 | a0001c0001t0007g0356a0001c0001t0007g0357a0001c0001t0007g0362 | 3 | HG01255.hp1 HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.95-3641T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641106 | ||||||
| chr3:30641139
|
G | A | 1 | a0001c0001t0001g0304 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.95-3608G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641139 | ||||||
| chr3:30641447
|
G | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(164): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.95-3300G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641447 | ||||||
| chr3:30641455
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(164): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.95-3292T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641455 | ||||||
| chr3:30641485
|
G | A | 61 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0104others(58): Show | 61 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.95-3262G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641485 | ||||||
| chr3:30641506
|
G | C | 1 | a0001c0001t0002g0280 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.95-3241G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641506 | ||||||
| chr3:30641542
|
C | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(164): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.95-3205C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641542 | ||||||
| chr3:30641573
|
G | T | 4 | a0001c0001t0006g0016a0001c0001t0006g0017a0001c0001t0006g0018others(1): Show | 4 | HG02055.hp2 HG02258.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-3174G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641573 | ||||||
| chr3:30641588
|
C | A | 1 | a0001c0001t0003g0224 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.95-3159C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641588 | ||||||
| chr3:30641624
|
T | A | 4 | a0001c0001t0001g0126a0001c0001t0001g0157a0001c0001t0009g0002others(1): Show | 5 | HG00140.hp1 HG00280.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-3123T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641624 | ||||||
| chr3:30641690
|
C | G | 5 | a0001c0001t0002g0077a0001c0001t0007g0074a0001c0001t0007g0075others(2): Show | 5 | HG02486.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-3057C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641690 | ||||||
| chr3:30641709
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(164): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.95-3038A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641709 | ||||||
| chr3:30641794
|
GTATTA | G | 26 | a0001c0001t0001g0149a0001c0001t0002g0077a0001c0001t0003g0224others(23): Show | 26 | HG01884.hp1 HG01934.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.95-2949_95-2945del others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 30641794 | |||||
| chr3:30641799
|
A | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(247): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.95-2948A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641799 | ||||||
| chr3:30641832
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.95-2915C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30641832 | ||||||
| chr3:30642003
|
C | T | 1 | a0001c0002t0001g0239 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.95-2744C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30642003 | ||||||
| chr3:30642014
|
C | T | 61 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0104others(58): Show | 61 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.95-2733C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30642014 | ||||||
| chr3:30642129
|
G | A | 1 | a0001c0001t0007g0265 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.95-2618G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30642129 | ||||||
| chr3:30642320
|
G | C | 1 | a0001c0002t0039g0032 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.95-2427G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30642320 | ||||||
| chr3:30642341
|
T | C | 2 | a0001c0001t0005g0218a0001c0001t0005g0219 | 2 | NA18956.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.95-2406T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30642341 | ||||||
| chr3:30642398
|
A | G | 8 | a0001c0001t0001g0112a0001c0001t0001g0220a0001c0001t0002g0280others(5): Show | 8 | HG00544.hp1 HG01358.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-2349A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30642398 | ||||||
| chr3:30642549
|
A | G | 79 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0104others(76): Show | 79 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.95-2198A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30642549 | ||||||
| chr3:30642605
|
G | A | 187 | a0001c0001t0001g0035a0001c0001t0001g0046a0001c0001t0001g0048others(184): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.95-2142G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30642605 | ||||||
| chr3:30642683
|
G | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(177): Show | 181 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.95-2064G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30642683 | ||||||
| chr3:30642904
|
C | T | 1 | a0001c0001t0035g0031 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.95-1843C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30642904 | ||||||
| chr3:30643191
|
G | A | 277 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(274): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.95-1556G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643191 | ||||||
| chr3:30643303
|
T | G | 5 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0183others(2): Show | 5 | HG00408.hp1 NA18953.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-1444T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643303 | ||||||
| chr3:30643348
|
G | C | 12 | a0001c0001t0001g0126a0001c0001t0001g0147a0001c0001t0001g0157others(9): Show | 13 | HG00140.hp1 HG00280.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.95-1399G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643348 | ||||||
| chr3:30643415
|
C | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(176): Show | 180 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.95-1332C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643415 | ||||||
| chr3:30643562
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.95-1185C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643562 | ||||||
| chr3:30643574
|
G | C | 1 | a0001c0001t0003g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.95-1173G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643574 | ||||||
| chr3:30643577
|
T | C | 1 | a0001c0001t0026g0111 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.95-1170T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643577 | ||||||
| chr3:30643608
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.95-1139A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643608 | ||||||
| chr3:30643636
|
T | G | 14 | a0001c0001t0001g0126a0001c0001t0001g0147a0001c0001t0001g0157others(11): Show | 15 | HG00140.hp1 HG00280.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-1111T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643636 | ||||||
| chr3:30643824
|
A | C | 2 | a0001c0001t0007g0073a0001c0001t0035g0031 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.95-923A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643824 | ||||||
| chr3:30643946
|
G | A | 14 | a0001c0001t0001g0126a0001c0001t0001g0147a0001c0001t0001g0157others(11): Show | 15 | HG00140.hp1 HG00280.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-801G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643946 | ||||||
| chr3:30643947
|
G | C | 9 | a0001c0001t0002g0072a0001c0001t0015g0388a0001c0003t0003g0353others(6): Show | 9 | HG01891.hp1 HG02280.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-800G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30643947 | ||||||
| chr3:30644029
|
G | A | 2 | a0001c0001t0007g0073a0001c0001t0035g0031 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.95-718G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30644029 | ||||||
| chr3:30644123
|
G | C | 12 | a0001c0001t0001g0149a0001c0001t0004g0028a0001c0001t0004g0315others(9): Show | 12 | HG01934.hp2 HG02109.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.95-624G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30644123 | ||||||
| chr3:30644128
|
A | G | 14 | a0001c0001t0001g0126a0001c0001t0001g0147a0001c0001t0001g0157others(11): Show | 15 | HG00140.hp1 HG00280.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-619A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30644128 | ||||||
| chr3:30644196
|
G | A | 7 | a0001c0001t0001g0140a0001c0001t0001g0243a0001c0001t0002g0232others(4): Show | 7 | HG00735.hp1 HG01106.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-551G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30644196 | ||||||
| chr3:30644232
|
T | C | 2 | a0001c0001t0007g0073a0001c0001t0035g0031 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.95-515T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30644232 | ||||||
| chr3:30644430
|
G | T | 1 | a0001c0001t0004g0321 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.95-317G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30644430 | ||||||
| chr3:30644588
|
C | A | 1 | a0001c0004t0008g0333 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.95-159C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 1/6 | chr3 | 30644588 | ||||||
| chr3:30644922
|
A | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(191): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
splice_region_variant&intron_variant | LOW | c.263+7A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30644922 | ||||||
| chr3:30644937
|
T | C | 1 | a0001c0001t0002g0262 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.263+22T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30644937 | ||||||
| chr3:30645135
|
T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(191): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.263+220T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645135 | ||||||
| chr3:30645155
|
T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(191): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.263+240T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645155 | ||||||
| chr3:30645248
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(191): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.263+333G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645248 | ||||||
| chr3:30645290
|
C | G | 14 | a0001c0001t0001g0126a0001c0001t0001g0147a0001c0001t0001g0157others(11): Show | 15 | HG00140.hp1 HG00280.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.263+375C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645290 | ||||||
| chr3:30645332
|
G | A | 2 | a0001c0001t0007g0073a0001c0001t0035g0031 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.263+417G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645332 | ||||||
| chr3:30645405
|
T | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(191): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.263+490T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645405 | ||||||
| chr3:30645439
|
T | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(191): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.263+524T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645439 | ||||||
| chr3:30645491
|
C | CTTTTTTT | 31 | a0001c0001t0001g0126a0001c0001t0001g0147a0001c0001t0001g0149others(28): Show | 32 | HG00140.hp1 HG00280.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.263+582_263+588dup others(7): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30645491 | |||||
| chr3:30645491
|
C | CTTTTTTT others(1): Show |
150 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(147): Show | 151 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.263+581_263+588dup others(8): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30645491 | |||||
| chr3:30645491
|
C | CTTTTTTT others(2): Show |
9 | a0001c0001t0001g0113a0001c0001t0001g0256a0001c0001t0002g0127others(6): Show | 9 | HG01884.hp1 HG03688.hp2 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.263+580_263+588dup others(9): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30645491 | |||||
| chr3:30645491
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0001g0107a0001c0001t0003g0224a0001c0001t0007g0073others(1): Show | 4 | HG00621.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+579_263+588dup others(10): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30645491 | |||||
| chr3:30645531
|
G | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(177): Show | 181 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.263+616G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645531 | ||||||
| chr3:30645538
|
T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(191): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.263+623T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645538 | ||||||
| chr3:30645590
|
T | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(191): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.263+675T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645590 | ||||||
| chr3:30645665
|
T | C | 4 | a0001c0001t0001g0378a0001c0001t0001g0379a0001c0001t0001g0380others(1): Show | 4 | NA18944.hp1 NA18951.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+750T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645665 | ||||||
| chr3:30645674
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.263+759C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645674 | ||||||
| chr3:30645770
|
G | A | 2 | a0001c0001t0007g0073a0001c0001t0035g0031 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.263+855G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645770 | ||||||
| chr3:30645781
|
C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(191): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.263+866C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645781 | ||||||
| chr3:30645819
|
C | CCTCT | 12 | a0001c0001t0001g0126a0001c0001t0001g0147a0001c0001t0001g0157others(9): Show | 13 | HG00140.hp1 HG00280.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.263+924_263+927dup others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30645819 | |||||
| chr3:30645819
|
C | CCTCTCT | 166 | a0001c0001t0001g0035a0001c0001t0001g0046a0001c0001t0001g0048others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.263+922_263+927dup others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30645819 | |||||
| chr3:30645819
|
C | CCTCTCTC others(1): Show |
11 | a0001c0001t0001g0001a0001c0001t0001g0052a0001c0001t0001g0113others(8): Show | 12 | HG00738.hp2 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.263+920_263+927dup others(8): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30645819 | |||||
| chr3:30645819
|
CCTCT | C | 4 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 4 | NA19011.hp1 NA19063.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+924_263+927del others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30645819 | |||||
| chr3:30645968
|
G | T | 1 | a0001c0001t0004g0358 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.263+1053G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30645968 | ||||||
| chr3:30646017
|
C | A | 1 | a0001c0001t0005g0013 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.263+1102C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30646017 | ||||||
| chr3:30646062
|
A | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(178): Show | 182 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.263+1147A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30646062 | ||||||
| chr3:30646167
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.263+1252T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30646167 | ||||||
| chr3:30646223
|
C | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(192): Show | 197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.263+1308C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30646223 | ||||||
| chr3:30646390
|
A | G | 2 | a0001c0001t0011g0008a0004c0007t0004g0364 | 2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.263+1475A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30646390 | ||||||
| chr3:30646477
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(192): Show | 197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.263+1562T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30646477 | ||||||
| chr3:30646532
|
G | A | 23 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0047others(20): Show | 23 | HG02027.hp1 HG02027.hp2 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.263+1617G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30646532 | ||||||
| chr3:30646547
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.263+1632G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30646547 | ||||||
| chr3:30646694
|
T | C | 13 | a0001c0001t0001g0107a0001c0001t0001g0144a0001c0001t0001g0191others(10): Show | 13 | HG00408.hp2 HG00621.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.263+1779T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30646694 | ||||||
| chr3:30646903
|
A | G | 1 | a0001c0001t0001g0324 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.263+1988A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30646903 | ||||||
| chr3:30647019
|
G | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(178): Show | 182 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.263+2104G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647019 | ||||||
| chr3:30647148
|
C | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(178): Show | 182 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.263+2233C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647148 | ||||||
| chr3:30647241
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(98): Show | 102 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.263+2326C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647241 | ||||||
| chr3:30647265
|
T | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(140): Show | 145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.263+2350T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647265 | ||||||
| chr3:30647294
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.263+2379A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647294 | ||||||
| chr3:30647306
|
A | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0110a0001c0001t0001g0267 | 3 | HG00597.hp2 NA18966.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.263+2391A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647306 | ||||||
| chr3:30647362
|
A | G | 2 | a0001c0001t0006g0365a0001c0001t0010g0341 | 2 | HG00639.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.263+2447A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647362 | ||||||
| chr3:30647560
|
T | TTTCA | 13 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0183others(10): Show | 13 | HG00408.hp1 HG00735.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.263+2672_263+2675d others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30647560 | |||||
| chr3:30647560
|
TTTCA | T | 136 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0049others(133): Show | 136 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.263+2672_263+2675d others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30647560 | |||||
| chr3:30647564
|
A | C | 2 | a0001c0001t0007g0073a0001c0001t0035g0031 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.263+2649A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647564 | ||||||
| chr3:30647568
|
A | C | 2 | a0001c0001t0007g0073a0001c0001t0035g0031 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.263+2653A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647568 | ||||||
| chr3:30647668
|
A | AATT | 111 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(108): Show | 112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.264-2586_264-2584d others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30647668 | |||||
| chr3:30647702
|
A | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(108): Show | 112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.264-2568A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647702 | ||||||
| chr3:30647710
|
A | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(108): Show | 112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.264-2560A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647710 | ||||||
| chr3:30647718
|
C | G | 32 | a0001c0001t0001g0126a0001c0001t0001g0147a0001c0001t0001g0149others(29): Show | 33 | HG00140.hp1 HG00280.hp2 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.264-2552C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647718 | ||||||
| chr3:30647728
|
G | GTGCAA | 13 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0047others(10): Show | 13 | HG02129.hp1 HG02683.hp2 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.264-2539_264-2535d others(7): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30647728 | |||||
| chr3:30647737
|
C | T | 3 | a0001c0003t0021g0363a0001c0004t0008g0081a0001c0004t0008g0344 | 3 | HG02258.hp2 HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.264-2533C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647737 | ||||||
| chr3:30647811
|
T | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0042others(264): Show | 269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.264-2459T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647811 | ||||||
| chr3:30647894
|
G | GT | 3 | a0001c0001t0001g0359a0001c0003t0007g0360a0001c0003t0007g0361 | 3 | HG02809.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.264-2375dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30647894 | |||||
| chr3:30647928
|
C | T | 1 | a0001c0001t0003g0266 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.264-2342C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647928 | ||||||
| chr3:30647929
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(94): Show | 98 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.264-2341G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647929 | ||||||
| chr3:30647992
|
A | G | 1 | a0001c0001t0001g0298 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.264-2278A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30647992 | ||||||
| chr3:30648013
|
G | T | 3 | a0001c0003t0001g0367a0001c0003t0001g0369a0001c0004t0011g0371 | 3 | HG02145.hp1 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.264-2257G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648013 | ||||||
| chr3:30648020
|
T | C | 1 | a0001c0001t0001g0269 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.264-2250T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648020 | ||||||
| chr3:30648026
|
A | G | 1 | a0001c0001t0004g0082 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.264-2244A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648026 | ||||||
| chr3:30648105
|
T | A | 12 | a0001c0001t0001g0149a0001c0001t0004g0028a0001c0001t0004g0315others(9): Show | 12 | HG01934.hp2 HG02109.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.264-2165T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648105 | ||||||
| chr3:30648263
|
G | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0048others(114): Show | 119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.264-2007G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648263 | ||||||
| chr3:30648392
|
G | A | 4 | a0001c0001t0020g0355a0001c0004t0003g0225a0001c0004t0008g0128others(1): Show | 4 | HG02723.hp2 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-1878G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648392 | ||||||
| chr3:30648410
|
A | G | 1 | a0001c0001t0007g0362 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.264-1860A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648410 | ||||||
| chr3:30648419
|
T | TAC | 17 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0057others(14): Show | 17 | HG00741.hp1 HG00741.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.264-1809_264-1808d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648419 | |||||
| chr3:30648419
|
T | TACAC | 21 | a0001c0001t0001g0035a0001c0001t0001g0086a0001c0001t0001g0090others(18): Show | 22 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.264-1811_264-1808d others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648419 | |||||
| chr3:30648419
|
T | TACACAC | 21 | a0001c0001t0001g0049a0001c0001t0001g0091a0001c0001t0001g0095others(18): Show | 21 | HG00621.hp1 HG00735.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.264-1813_264-1808d others(8): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648419 | |||||
| chr3:30648419
|
T | TACACACA others(1): Show |
18 | a0001c0001t0001g0038a0001c0001t0001g0047a0001c0001t0001g0087others(15): Show | 18 | HG00280.hp1 HG01081.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.264-1815_264-1808d others(10): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648419 | |||||
| chr3:30648419
|
T | TACACACA others(3): Show |
6 | a0001c0001t0001g0044a0001c0001t0003g0266a0001c0001t0004g0354others(3): Show | 6 | HG01884.hp2 HG02970.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-1817_264-1808d others(12): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648419 | |||||
| chr3:30648419
|
T | TACACACA others(9): Show |
3 | a0001c0001t0007g0357a0001c0001t0035g0031a0001c0011t0037g0083 | 3 | HG01255.hp1 HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.264-1823_264-1808d others(18): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648419 | |||||
| chr3:30648419
|
TAC | T | 6 | a0001c0001t0001g0323a0001c0001t0001g0345a0001c0001t0015g0388others(3): Show | 6 | HG02630.hp1 HG03195.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-1809_264-1808d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648419 | |||||
| chr3:30648419
|
TACAC | T | 3 | a0001c0001t0001g0386a0001c0001t0001g0387a0001c0002t0001g0123 | 3 | HG03130.hp1 NA18990.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.264-1811_264-1808d others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648419 | |||||
| chr3:30648419
|
TACACACA others(5): Show |
T | 18 | a0001c0001t0001g0149a0001c0001t0002g0072a0001c0001t0004g0028others(15): Show | 18 | HG01934.hp2 HG02109.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.264-1819_264-1808d others(14): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648419 | |||||
| chr3:30648419
|
TACACACA others(7): Show |
T | 97 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0048others(94): Show | 98 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.264-1821_264-1808d others(16): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648419 | |||||
| chr3:30648427
|
C | CACAA | 4 | a0001c0003t0036g0024a0001c0004t0003g0225a0001c0004t0008g0128others(1): Show | 4 | HG01891.hp1 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-1840_264-1839i others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648427 | |||||
| chr3:30648460
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0019g0297 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.264-1808_264-1807i others(13): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | |||||
| chr3:30648460
|
A | ACACACAC others(8): Show |
2 | a0001c0001t0001g0327a0001c0002t0043g0067 | 2 | HG02132.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.264-1808_264-1807i others(17): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | |||||
| chr3:30648460
|
A | ACACACAC others(17): Show |
4 | a0001c0001t0001g0042a0001c0001t0001g0330a0001c0001t0003g0169others(1): Show | 4 | HG01192.hp1 HG01358.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-1808_264-1807i others(26): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | |||||
| chr3:30648460
|
A | ACACACAC others(15): Show |
7 | a0001c0001t0001g0124a0001c0001t0001g0220a0001c0001t0001g0328others(4): Show | 7 | HG00544.hp1 HG02738.hp1 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.264-1808_264-1807i others(24): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | |||||
| chr3:30648460
|
A | ACACACAC others(13): Show |
9 | a0001c0001t0001g0259a0001c0001t0001g0329a0001c0001t0002g0120others(6): Show | 9 | HG00544.hp2 HG02135.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.264-1808_264-1807i others(22): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | |||||
| chr3:30648460
|
A | ACACACAC others(11): Show |
11 | a0001c0001t0001g0050a0001c0001t0001g0100a0001c0001t0001g0302others(8): Show | 11 | HG01255.hp2 HG02155.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.264-1808_264-1807i others(20): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | |||||
| chr3:30648460
|
A | ACACACAC others(9): Show |
8 | a0001c0001t0001g0043a0001c0001t0001g0189a0001c0001t0001g0289others(5): Show | 8 | HG01358.hp1 HG01981.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.264-1808_264-1807i others(18): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | |||||
| chr3:30648460
|
A | ACACACAC others(7): Show |
24 | a0001c0001t0001g0034a0001c0001t0001g0059a0001c0001t0001g0114others(21): Show | 24 | HG00597.hp1 HG00639.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.264-1808_264-1807i others(16): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | |||||
| chr3:30648460
|
A | ACACACAC others(5): Show |
18 | a0001c0001t0001g0172a0001c0001t0001g0267a0001c0001t0001g0294others(15): Show | 18 | HG00597.hp2 HG00639.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.264-1808_264-1807i others(14): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | |||||
| chr3:30648460
|
A | ACACACAC others(9): Show |
2 | a0001c0001t0001g0375a0001c0002t0001g0097 | 2 | NA18982.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.264-1808_264-1807i others(18): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | |||||
| chr3:30648460
|
A | ACACACAC others(3): Show |
15 | a0001c0001t0001g0115a0001c0001t0001g0237a0001c0001t0001g0278others(12): Show | 15 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.264-1808_264-1807i others(12): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | |||||
| chr3:30648460
|
A | ACACACAC others(1): Show |
3 | a0001c0001t0001g0104a0001c0001t0014g0152a0001c0002t0029g0146 | 3 | HG01928.hp2 HG02280.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.264-1808_264-1807i others(10): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | |||||
| chr3:30648460
|
A | ACACACAC others(5): Show |
1 | a0001c0002t0001g0165 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.264-1808_264-1807i others(14): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | |||||
| chr3:30648460
|
A | ACACACC | 3 | a0001c0001t0001g0298a0001c0003t0021g0363a0001c0004t0008g0333 | 3 | HG02258.hp1 HG02258.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.264-1808_264-1807i others(8): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | |||||
| chr3:30648460
|
A | ACC | 5 | a0001c0001t0001g0288a0001c0001t0001g0317a0001c0001t0003g0370others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-1809_264-1808i others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30648460 | |||||
| chr3:30648460
|
A | C | 6 | a0001c0001t0001g0345a0001c0001t0010g0368a0001c0002t0001g0123others(3): Show | 6 | HG02145.hp1 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-1810A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648460 | ||||||
| chr3:30648470
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.264-1800G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648470 | ||||||
| chr3:30648534
|
T | C | 9 | a0001c0001t0001g0126a0001c0001t0001g0157a0001c0001t0001g0236others(6): Show | 10 | HG00140.hp1 HG00280.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.264-1736T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648534 | ||||||
| chr3:30648576
|
G | A | 2 | a0001c0004t0008g0128a0001c0004t0008g0331 | 2 | HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.264-1694G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648576 | ||||||
| chr3:30648656
|
T | C | 1 | a0001c0001t0022g0347 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.264-1614T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648656 | ||||||
| chr3:30648721
|
G | A | 2 | a0001c0001t0003g0370a0001c0001t0016g0292 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.264-1549G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648721 | ||||||
| chr3:30648805
|
G | T | 2 | a0001c0001t0006g0019a0001c0004t0014g0349 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-1465G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648805 | ||||||
| chr3:30648823
|
T | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(93): Show | 97 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.264-1447T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648823 | ||||||
| chr3:30648824
|
T | A | 77 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0044others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.264-1446T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648824 | ||||||
| chr3:30648838
|
C | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(92): Show | 96 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.264-1432C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648838 | ||||||
| chr3:30648901
|
A | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(89): Show | 93 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.264-1369A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648901 | ||||||
| chr3:30648932
|
A | G | 191 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(188): Show | 191 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(188): Show |
intron_variant | MODIFIER | c.264-1338A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30648932 | ||||||
| chr3:30649013
|
G | T | 1 | a0001c0001t0001g0172 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.264-1257G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649013 | ||||||
| chr3:30649099
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.264-1171T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649099 | ||||||
| chr3:30649156
|
C | T | 2 | a0001c0003t0007g0360a0001c0003t0007g0361 | 2 | HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.264-1114C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649156 | ||||||
| chr3:30649166
|
G | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(89): Show | 93 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.264-1104G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649166 | ||||||
| chr3:30649207
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.264-1063G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649207 | ||||||
| chr3:30649256
|
G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 97 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.264-1014G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649256 | ||||||
| chr3:30649259
|
T | C | 23 | a0001c0001t0001g0043a0001c0001t0001g0294a0001c0001t0001g0348others(20): Show | 23 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.264-1011T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649259 | ||||||
| chr3:30649313
|
T | C | 22 | a0001c0001t0001g0043a0001c0001t0001g0294a0001c0001t0001g0348others(19): Show | 22 | HG01109.hp2 HG02145.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.264-957T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649313 | ||||||
| chr3:30649419
|
A | G | 79 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0044others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.264-851A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649419 | ||||||
| chr3:30649586
|
C | T | 368 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(365): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(366): Show |
intron_variant | MODIFIER | c.264-684C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649586 | ||||||
| chr3:30649718
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.264-552G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649718 | ||||||
| chr3:30649815
|
A | G | 1 | a0001c0002t0039g0032 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.264-455A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649815 | ||||||
| chr3:30649818
|
G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 97 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.264-452G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649818 | ||||||
| chr3:30649827
|
G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 97 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.264-443G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649827 | ||||||
| chr3:30649846
|
C | G | 368 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(365): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(366): Show |
intron_variant | MODIFIER | c.264-424C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649846 | ||||||
| chr3:30649888
|
A | G | 1 | a0001c0002t0001g0337 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.264-382A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649888 | ||||||
| chr3:30649949
|
T | G | 1 | a0001c0001t0004g0150 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.264-321T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649949 | ||||||
| chr3:30649981
|
G | A | 365 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(362): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.264-289G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649981 | ||||||
| chr3:30649999
|
C | T | 3 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0068 | 3 | NA18944.hp2 NA19010.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.264-271C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30649999 | ||||||
| chr3:30650073
|
GA | G | 11 | a0001c0001t0007g0073a0001c0001t0011g0008a0001c0001t0035g0031others(8): Show | 11 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.264-193delA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 30650073 | |||||
| chr3:30650113
|
C | A | 2 | a0001c0001t0001g0291a0001c0001t0001g0316 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.264-157C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30650113 | ||||||
| chr3:30650142
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.264-128G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30650142 | ||||||
| chr3:30650183
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.264-87G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30650183 | ||||||
| chr3:30650212
|
T | C | 1 | a0001c0002t0039g0032 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.264-58T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30650212 | ||||||
| chr3:30650235
|
T | G | 3 | a0001c0001t0006g0019a0001c0004t0014g0349a0001c0004t0033g0030 | 3 | HG01934.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-35T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 2/6 | chr3 | 30650235 | ||||||
| chr3:30650534
|
A | G | 2 | a0001c0003t0003g0353a0001c0003t0006g0078 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.454+74A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30650534 | ||||||
| chr3:30650626
|
G | C | 9 | a0001c0001t0007g0073a0001c0001t0011g0008a0001c0001t0035g0031others(6): Show | 9 | HG01109.hp2 HG02145.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.454+166G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30650626 | ||||||
| chr3:30650708
|
T | G | 1 | a0001c0001t0001g0046 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.454+248T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30650708 | ||||||
| chr3:30650727
|
T | C | 368 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(365): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(366): Show |
intron_variant | MODIFIER | c.454+267T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30650727 | ||||||
| chr3:30650939
|
T | C | 1 | a0001c0003t0036g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.454+479T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30650939 | ||||||
| chr3:30650959
|
C | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 97 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.454+499C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30650959 | ||||||
| chr3:30651188
|
G | C | 1 | a0001c0001t0003g0245 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.454+728G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651188 | ||||||
| chr3:30651267
|
C | G | 3 | a0001c0001t0001g0042a0001c0001t0001g0372a0001c0001t0003g0169 | 3 | HG01192.hp1 HG01358.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.454+807C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651267 | ||||||
| chr3:30651274
|
C | A | 1 | a0001c0001t0002g0061 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.454+814C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651274 | ||||||
| chr3:30651368
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.454+908A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651368 | ||||||
| chr3:30651375
|
C | T | 13 | a0001c0001t0001g0149a0001c0001t0002g0072a0001c0001t0004g0028others(10): Show | 13 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.454+915C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651375 | ||||||
| chr3:30651436
|
A | G | 5 | a0001c0001t0001g0042a0001c0001t0001g0372a0001c0001t0002g0131others(2): Show | 5 | HG01192.hp1 HG01255.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+976A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651436 | ||||||
| chr3:30651496
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.454+1036C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651496 | ||||||
| chr3:30651603
|
A | G | 1 | a0001c0001t0003g0266 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.454+1143A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651603 | ||||||
| chr3:30651766
|
A | G | 1 | a0001c0001t0001g0323 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.454+1306A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651766 | ||||||
| chr3:30651779
|
C | T | 13 | a0001c0001t0007g0073a0001c0001t0011g0008a0001c0001t0035g0031others(10): Show | 13 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.454+1319C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651779 | ||||||
| chr3:30651989
|
T | C | 3 | a0001c0001t0001g0087a0001c0001t0001g0091a0001c0001t0001g0385 | 3 | HG00621.hp1 HG02071.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.454+1529T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30651989 | ||||||
| chr3:30652002
|
C | T | 1 | a0001c0011t0037g0083 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.454+1542C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652002 | ||||||
| chr3:30652030
|
T | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.454+1570T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652030 | ||||||
| chr3:30652058
|
A | G | 1 | a0001c0001t0006g0019 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.454+1598A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652058 | ||||||
| chr3:30652070
|
T | G | 3 | a0001c0001t0006g0019a0001c0004t0014g0349a0001c0004t0033g0030 | 3 | HG01934.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.454+1610T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652070 | ||||||
| chr3:30652151
|
C | T | 146 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0049others(143): Show | 146 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.454+1691C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652151 | ||||||
| chr3:30652232
|
G | GT | 278 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(275): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.454+1794dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30652232 | |||||
| chr3:30652232
|
G | GTT | 49 | a0001c0001t0001g0087a0001c0001t0001g0103a0001c0001t0001g0107others(46): Show | 49 | HG00544.hp1 HG00621.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.454+1793_454+1794d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30652232 | |||||
| chr3:30652232
|
G | GTTT | 17 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0058others(14): Show | 17 | HG00558.hp2 HG00738.hp2 HG02132.hp1 others(14): Show |
intron_variant | MODIFIER | c.454+1792_454+1794d others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30652232 | |||||
| chr3:30652232
|
GTTTT | G | 9 | a0001c0001t0001g0085a0001c0002t0001g0065a0001c0002t0001g0098others(6): Show | 9 | HG00544.hp2 HG00597.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.454+1791_454+1794d others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30652232 | |||||
| chr3:30652549
|
G | C | 3 | a0001c0003t0021g0363a0001c0004t0008g0081a0001c0004t0008g0344 | 3 | HG02258.hp2 HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.454+2089G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652549 | ||||||
| chr3:30652628
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(95): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.454+2168G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652628 | ||||||
| chr3:30652643
|
A | T | 367 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(364): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(365): Show |
intron_variant | MODIFIER | c.454+2183A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652643 | ||||||
| chr3:30652795
|
A | G | 2 | a0001c0003t0003g0353a0001c0003t0006g0078 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.454+2335A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652795 | ||||||
| chr3:30652872
|
A | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(94): Show | 98 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.454+2412A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652872 | ||||||
| chr3:30652921
|
C | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(96): Show | 100 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.454+2461C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30652921 | ||||||
| chr3:30653057
|
G | A | 1 | a0001c0001t0002g0262 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.454+2597G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653057 | ||||||
| chr3:30653250
|
C | CT | 22 | a0001c0001t0001g0149a0001c0001t0002g0072a0001c0001t0004g0028others(19): Show | 22 | HG02109.hp1 HG02109.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.454+2809dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30653250 | |||||
| chr3:30653250
|
C | CTTT | 15 | a0001c0001t0001g0056a0001c0001t0001g0115a0001c0001t0001g0191others(12): Show | 15 | HG00558.hp2 HG01109.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.454+2807_454+2809d others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30653250 | |||||
| chr3:30653250
|
C | CTTTT | 199 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0038others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.454+2806_454+2809d others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30653250 | |||||
| chr3:30653250
|
C | CTTTTT | 17 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0001g0058others(14): Show | 17 | HG01433.hp1 HG02056.hp1 HG02738.hp2 others(14): Show |
intron_variant | MODIFIER | c.454+2805_454+2809d others(7): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30653250 | |||||
| chr3:30653250
|
CTTT | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(91): Show | 95 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.454+2807_454+2809d others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30653250 | |||||
| chr3:30653269
|
T | G | 3 | a0001c0001t0006g0019a0001c0004t0014g0349a0001c0004t0033g0030 | 3 | HG01934.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.454+2809T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653269 | ||||||
| chr3:30653277
|
A | T | 1 | a0001c0001t0002g0280 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.454+2817A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653277 | ||||||
| chr3:30653294
|
C | T | 1 | a0001c0001t0003g0266 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.454+2834C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653294 | ||||||
| chr3:30653295
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(96): Show | 100 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.454+2835G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653295 | ||||||
| chr3:30653316
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(94): Show | 98 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.454+2856G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653316 | ||||||
| chr3:30653341
|
T | C | 29 | a0001c0001t0001g0149a0001c0001t0001g0342a0001c0001t0002g0072others(26): Show | 29 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.454+2881T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653341 | ||||||
| chr3:30653412
|
C | T | 1 | a0001c0002t0002g0205 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.454+2952C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653412 | ||||||
| chr3:30653424
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(96): Show | 100 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.454+2964A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653424 | ||||||
| chr3:30653520
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(96): Show | 100 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.454+3060A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653520 | ||||||
| chr3:30653541
|
C | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(94): Show | 98 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.454+3081C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653541 | ||||||
| chr3:30653542
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(96): Show | 100 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.454+3082A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653542 | ||||||
| chr3:30653554
|
AATGAAAA others(55): Show |
A | 1 | a0001c0002t0001g0270 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.454+3100_454+3161d others(64): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30653554 | |||||
| chr3:30653599
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(94): Show | 98 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.454+3139G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653599 | ||||||
| chr3:30653660
|
G | A | 25 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0001g0056others(22): Show | 25 | HG00099.hp2 HG00140.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.454+3200G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653660 | ||||||
| chr3:30653737
|
A | G | 4 | a0001c0001t0001g0104a0001c0001t0001g0177a0001c0001t0001g0288others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.454+3277A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30653737 | ||||||
| chr3:30654585
|
A | G | 13 | a0001c0001t0001g0086a0001c0001t0001g0144a0001c0001t0001g0275others(10): Show | 13 | HG00408.hp2 HG00673.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.454+4125A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30654585 | ||||||
| chr3:30654593
|
C | T | 1 | a0001c0001t0003g0266 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.454+4133C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30654593 | ||||||
| chr3:30654623
|
T | G | 2 | a0001c0001t0004g0320a0001c0001t0004g0322 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.454+4163T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30654623 | ||||||
| chr3:30654759
|
T | C | 364 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(361): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.454+4299T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30654759 | ||||||
| chr3:30654782
|
C | G | 2 | a0001c0003t0003g0353a0001c0003t0006g0078 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.454+4322C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30654782 | ||||||
| chr3:30655001
|
G | T | 1 | a0001c0002t0013g0036 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.454+4541G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655001 | ||||||
| chr3:30655071
|
T | C | 266 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0038others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.454+4611T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655071 | ||||||
| chr3:30655152
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(95): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.454+4692G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655152 | ||||||
| chr3:30655257
|
C | G | 2 | a0001c0001t0001g0327a0001c0002t0001g0238 | 2 | HG03654.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.454+4797C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655257 | ||||||
| chr3:30655261
|
C | T | 3 | a0001c0001t0006g0019a0001c0004t0014g0349a0001c0004t0033g0030 | 3 | HG01934.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.454+4801C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655261 | ||||||
| chr3:30655284
|
T | C | 1 | a0001c0001t0002g0262 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.454+4824T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655284 | ||||||
| chr3:30655324
|
T | C | 332 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(329): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.454+4864T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655324 | ||||||
| chr3:30655357
|
A | G | 3 | a0001c0001t0001g0342a0001c0003t0003g0353a0001c0003t0006g0078 | 3 | HG03195.hp2 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.454+4897A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655357 | ||||||
| chr3:30655422
|
A | C | 1 | a0003c0006t0002g0209 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.454+4962A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655422 | ||||||
| chr3:30655490
|
A | T | 3 | a0001c0001t0006g0019a0001c0004t0014g0349a0001c0004t0033g0030 | 3 | HG01934.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.454+5030A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655490 | ||||||
| chr3:30655838
|
C | G | 367 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(364): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(365): Show |
intron_variant | MODIFIER | c.454+5378C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655838 | ||||||
| chr3:30655945
|
C | T | 20 | a0001c0001t0001g0149a0001c0001t0001g0342a0001c0001t0002g0072others(17): Show | 20 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.454+5485C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30655945 | ||||||
| chr3:30655965
|
TG | T | 13 | a0001c0001t0001g0086a0001c0001t0001g0144a0001c0001t0001g0275others(10): Show | 13 | HG00408.hp2 HG00673.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.454+5509delG | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30655965 | |||||
| chr3:30656096
|
A | T | 1 | a0001c0001t0002g0280 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.454+5636A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656096 | ||||||
| chr3:30656169
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(96): Show | 100 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.454+5709A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656169 | ||||||
| chr3:30656211
|
C | G | 1 | a0001c0001t0004g0150 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.454+5751C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656211 | ||||||
| chr3:30656397
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(96): Show | 100 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.454+5937A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656397 | ||||||
| chr3:30656417
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(95): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.454+5957A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656417 | ||||||
| chr3:30656444
|
A | G | 118 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0043others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.454+5984A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656444 | ||||||
| chr3:30656453
|
G | A | 5 | a0001c0001t0016g0293a0001c0004t0003g0225a0001c0004t0008g0128others(2): Show | 5 | HG02258.hp1 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+5993G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656453 | ||||||
| chr3:30656484
|
A | G | 15 | a0001c0001t0001g0149a0001c0001t0002g0072a0001c0001t0004g0028others(12): Show | 15 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.454+6024A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656484 | ||||||
| chr3:30656567
|
G | C | 3 | a0001c0001t0006g0019a0001c0004t0014g0349a0001c0004t0033g0030 | 3 | HG01934.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.454+6107G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656567 | ||||||
| chr3:30656599
|
G | C | 1 | a0001c0001t0001g0342 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.454+6139G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656599 | ||||||
| chr3:30656604
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(95): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.454+6144G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656604 | ||||||
| chr3:30656623
|
G | A | 1 | a0001c0003t0001g0367 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.454+6163G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656623 | ||||||
| chr3:30656671
|
A | G | 5 | a0001c0001t0011g0008a0001c0003t0001g0352a0001c0003t0001g0367others(2): Show | 5 | HG01109.hp2 HG02145.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.454+6211A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656671 | ||||||
| chr3:30656678
|
T | C | 1 | a0001c0012t0002g0062 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.454+6218T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656678 | ||||||
| chr3:30656800
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.454+6340A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656800 | ||||||
| chr3:30656900
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(95): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.454+6440T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656900 | ||||||
| chr3:30656911
|
T | A | 1 | a0001c0002t0001g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.454+6451T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656911 | ||||||
| chr3:30656978
|
C | T | 4 | a0001c0001t0012g0119a0001c0001t0012g0281a0001c0001t0012g0296others(1): Show | 4 | HG01106.hp1 HG01516.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.454+6518C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30656978 | ||||||
| chr3:30657008
|
ATGAAGTG others(7): Show |
A | 1 | a0001c0002t0039g0032 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.454+6553_454+6566d others(16): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30657008 | |||||
| chr3:30657128
|
G | A | 5 | a0001c0001t0001g0342a0001c0002t0039g0032a0001c0003t0021g0363others(2): Show | 5 | HG01891.hp2 HG02258.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+6668G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657128 | ||||||
| chr3:30657152
|
A | G | 2 | a0001c0003t0003g0353a0001c0003t0006g0078 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.454+6692A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657152 | ||||||
| chr3:30657277
|
C | G | 1 | a0001c0002t0001g0337 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.454+6817C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657277 | ||||||
| chr3:30657290
|
G | A | 10 | a0001c0001t0001g0043a0001c0001t0001g0294a0001c0001t0001g0348others(7): Show | 10 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.454+6830G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657290 | ||||||
| chr3:30657310
|
G | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(95): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.454+6850G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657310 | ||||||
| chr3:30657323
|
G | T | 1 | a0001c0001t0002g0280 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.454+6863G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657323 | ||||||
| chr3:30657329
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(95): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.454+6869G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657329 | ||||||
| chr3:30657408
|
G | A | 2 | a0001c0003t0003g0353a0001c0003t0006g0078 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.454+6948G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657408 | ||||||
| chr3:30657411
|
G | A | 5 | a0001c0001t0016g0293a0001c0004t0003g0225a0001c0004t0008g0128others(2): Show | 5 | HG02258.hp1 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+6951G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657411 | ||||||
| chr3:30657425
|
G | T | 2 | a0001c0003t0003g0353a0001c0003t0006g0078 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.454+6965G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657425 | ||||||
| chr3:30657485
|
G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 97 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.454+7025G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657485 | ||||||
| chr3:30657611
|
G | A | 2 | a0001c0001t0010g0368a0001c0001t0025g0334 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.454+7151G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657611 | ||||||
| chr3:30657735
|
G | A | 2 | a0001c0003t0003g0353a0001c0003t0006g0078 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.454+7275G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657735 | ||||||
| chr3:30657798
|
A | G | 1 | a0001c0001t0010g0368 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.454+7338A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30657798 | ||||||
| chr3:30658290
|
T | C | 239 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0038others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.454+7830T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30658290 | ||||||
| chr3:30658399
|
T | C | 21 | a0001c0001t0001g0149a0001c0001t0002g0072a0001c0001t0004g0028others(18): Show | 21 | HG02109.hp1 HG02109.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.454+7939T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30658399 | ||||||
| chr3:30658672
|
A | G | 1 | a0001c0002t0001g0123 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.454+8212A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30658672 | ||||||
| chr3:30658925
|
T | C | 1 | a0001c0001t0002g0274 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.454+8465T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30658925 | ||||||
| chr3:30658940
|
C | T | 99 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0043others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.454+8480C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30658940 | ||||||
| chr3:30658949
|
T | C | 240 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0038others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.454+8489T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30658949 | ||||||
| chr3:30659006
|
A | G | 240 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0038others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.454+8546A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30659006 | ||||||
| chr3:30659097
|
G | T | 1 | a0001c0001t0004g0358 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.454+8637G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30659097 | ||||||
| chr3:30659145
|
C | T | 1 | a0001c0001t0002g0196 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.454+8685C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30659145 | ||||||
| chr3:30659210
|
T | G | 2 | a0001c0003t0003g0353a0001c0003t0006g0078 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.454+8750T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30659210 | ||||||
| chr3:30659361
|
T | C | 367 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(364): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(365): Show |
intron_variant | MODIFIER | c.454+8901T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30659361 | ||||||
| chr3:30659416
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.454+8956C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30659416 | ||||||
| chr3:30659430
|
A | G | 248 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0038others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.454+8970A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30659430 | ||||||
| chr3:30659682
|
C | G | 12 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(9): Show | 12 | NA18959.hp2 NA18960.hp1 NA18975.hp1 others(9): Show |
intron_variant | MODIFIER | c.454+9222C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30659682 | ||||||
| chr3:30660034
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.454+9574C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660034 | ||||||
| chr3:30660079
|
T | C | 5 | a0001c0001t0016g0293a0001c0004t0003g0225a0001c0004t0008g0128others(2): Show | 5 | HG02258.hp1 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+9619T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660079 | ||||||
| chr3:30660089
|
T | A | 9 | a0001c0001t0001g0342a0001c0001t0001g0345a0001c0001t0002g0262others(6): Show | 9 | HG01934.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.454+9629T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660089 | ||||||
| chr3:30660114
|
A | G | 120 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0038others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.454+9654A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660114 | ||||||
| chr3:30660124
|
T | C | 1 | a0001c0001t0001g0318 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.454+9664T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660124 | ||||||
| chr3:30660212
|
T | G | 5 | a0001c0001t0016g0293a0001c0004t0003g0225a0001c0004t0008g0128others(2): Show | 5 | HG02258.hp1 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+9752T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660212 | ||||||
| chr3:30660264
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(109): Show | 113 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.454+9804C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660264 | ||||||
| chr3:30660309
|
T | C | 363 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(360): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.454+9849T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660309 | ||||||
| chr3:30660552
|
C | T | 12 | a0001c0001t0001g0043a0001c0001t0001g0294a0001c0001t0001g0348others(9): Show | 12 | HG01167.hp2 HG02451.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.454+10092C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660552 | ||||||
| chr3:30660628
|
A | T | 1 | a0001c0001t0009g0250 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.454+10168A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660628 | ||||||
| chr3:30660648
|
A | G | 368 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(365): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(366): Show |
intron_variant | MODIFIER | c.454+10188A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660648 | ||||||
| chr3:30660660
|
A | T | 1 | a0001c0001t0012g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.454+10200A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660660 | ||||||
| chr3:30660720
|
G | T | 92 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0046others(89): Show | 92 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.454+10260G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660720 | ||||||
| chr3:30660853
|
T | C | 1 | a0001c0001t0002g0262 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.454+10393T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660853 | ||||||
| chr3:30660975
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.454+10515G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30660975 | ||||||
| chr3:30661073
|
T | C | 4 | a0001c0003t0003g0353a0001c0003t0006g0078a0001c0003t0007g0360others(1): Show | 4 | HG02809.hp2 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-10565T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30661073 | ||||||
| chr3:30661119
|
C | A | 4 | a0001c0001t0007g0356a0001c0001t0007g0357a0001c0001t0007g0362others(1): Show | 4 | HG00639.hp2 HG01255.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-10519C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30661119 | ||||||
| chr3:30661147
|
A | C | 1 | a0001c0001t0001g0342 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.455-10491A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30661147 | ||||||
| chr3:30661151
|
C | A | 2 | a0001c0001t0001g0094a0001c0001t0027g0160 | 2 | NA18977.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.455-10487C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30661151 | ||||||
| chr3:30661151
|
C | T | 1 | a0001c0001t0001g0287 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.455-10487C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30661151 | ||||||
| chr3:30661293
|
ACT | A | 67 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0087others(64): Show | 67 | HG00544.hp1 HG00621.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.455-10340_455-1033 others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30661293 | |||||
| chr3:30662026
|
C | A | 1 | a0001c0001t0001g0068 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.455-9612C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662026 | ||||||
| chr3:30662045
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.455-9593T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662045 | ||||||
| chr3:30662306
|
A | T | 100 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0048others(97): Show | 100 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.455-9332A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662306 | ||||||
| chr3:30662319
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0285 | 2 | HG00741.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.455-9319A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662319 | ||||||
| chr3:30662347
|
C | T | 1 | a0001c0001t0004g0150 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.455-9291C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662347 | ||||||
| chr3:30662350
|
G | A | 4 | a0001c0001t0011g0008a0001c0003t0001g0352a0001c0003t0001g0367others(1): Show | 4 | HG01109.hp2 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.455-9288G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662350 | ||||||
| chr3:30662438
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.455-9200G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662438 | ||||||
| chr3:30662467
|
A | C | 4 | a0001c0001t0001g0342a0001c0003t0021g0363a0001c0004t0014g0349others(1): Show | 4 | HG01934.hp2 HG02258.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-9171A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662467 | ||||||
| chr3:30662515
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0037others(136): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.455-9123A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662515 | ||||||
| chr3:30662758
|
T | C | 1 | a0001c0001t0004g0150 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.455-8880T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662758 | ||||||
| chr3:30662838
|
C | T | 1 | a0001c0003t0021g0363 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.455-8800C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662838 | ||||||
| chr3:30662954
|
T | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0037others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.455-8684T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662954 | ||||||
| chr3:30662955
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0037others(135): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.455-8683A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662955 | ||||||
| chr3:30662984
|
G | A | 4 | a0001c0001t0001g0342a0001c0003t0021g0363a0001c0004t0014g0349others(1): Show | 4 | HG01934.hp2 HG02258.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-8654G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30662984 | ||||||
| chr3:30663026
|
T | C | 2 | a0001c0003t0003g0353a0001c0003t0006g0078 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.455-8612T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663026 | ||||||
| chr3:30663028
|
A | G | 9 | a0001c0003t0003g0353a0001c0003t0006g0078a0001c0004t0003g0225others(6): Show | 9 | HG02258.hp1 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.455-8610A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663028 | ||||||
| chr3:30663127
|
A | G | 69 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0087others(66): Show | 69 | HG00544.hp1 HG00621.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.455-8511A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663127 | ||||||
| chr3:30663184
|
C | CTG | 55 | a0001c0001t0001g0046a0001c0001t0001g0055a0001c0001t0001g0058others(52): Show | 55 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.455-8438_455-8437d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30663184 | |||||
| chr3:30663287
|
TA | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0037others(218): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.455-8349delA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30663287 | |||||
| chr3:30663332
|
A | G | 1 | a0001c0001t0001g0342 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.455-8306A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663332 | ||||||
| chr3:30663363
|
G | A | 26 | a0001c0001t0001g0038a0001c0001t0001g0116a0001c0001t0001g0126others(23): Show | 27 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.455-8275G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663363 | ||||||
| chr3:30663395
|
T | G | 1 | a0001c0003t0003g0353 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.455-8243T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663395 | ||||||
| chr3:30663767
|
A | G | 28 | a0001c0001t0001g0149a0001c0001t0001g0342a0001c0001t0002g0072others(25): Show | 28 | HG00639.hp2 HG01243.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.455-7871A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663767 | ||||||
| chr3:30663782
|
T | C | 1 | a0001c0002t0001g0098 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.455-7856T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663782 | ||||||
| chr3:30663888
|
G | A | 111 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0038others(108): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.455-7750G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663888 | ||||||
| chr3:30663898
|
C | T | 7 | a0001c0004t0003g0225a0001c0004t0008g0081a0001c0004t0008g0128others(4): Show | 7 | HG02258.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.455-7740C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663898 | ||||||
| chr3:30663905
|
G | C | 9 | a0001c0003t0003g0353a0001c0003t0006g0078a0001c0004t0003g0225others(6): Show | 9 | HG02258.hp1 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.455-7733G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663905 | ||||||
| chr3:30663972
|
C | CT | 110 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0038others(107): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.455-7660dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30663972 | |||||
| chr3:30663979
|
G | T | 105 | a0001c0001t0001g0042a0001c0001t0001g0087a0001c0001t0001g0090others(102): Show | 105 | HG00544.hp1 HG00621.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.455-7659G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663979 | ||||||
| chr3:30663980
|
G | T | 1 | a0001c0002t0039g0032 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.455-7658G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663980 | ||||||
| chr3:30663981
|
G | C | 1 | a0001c0003t0036g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.455-7657G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663981 | ||||||
| chr3:30663988
|
A | C | 3 | a0003c0006t0001g0319a0003c0006t0002g0184a0003c0006t0002g0209 | 3 | NA18612.hp2 NA19068.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.455-7650A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30663988 | ||||||
| chr3:30664018
|
T | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(101): Show | 105 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.455-7620T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30664018 | ||||||
| chr3:30664149
|
A | AT | 155 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(152): Show | 156 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.455-7474dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30664149 | |||||
| chr3:30664149
|
AT | A | 110 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0038others(107): Show | 111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.455-7474delT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30664149 | |||||
| chr3:30664274
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.455-7364A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30664274 | ||||||
| chr3:30664346
|
A | G | 1 | a0001c0002t0001g0175 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.455-7292A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30664346 | ||||||
| chr3:30664453
|
A | C | 1 | a0001c0002t0003g0335 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.455-7185A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30664453 | ||||||
| chr3:30664557
|
A | G | 1 | a0001c0001t0004g0150 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.455-7081A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30664557 | ||||||
| chr3:30664682
|
G | T | 28 | a0001c0001t0001g0149a0001c0001t0001g0342a0001c0001t0002g0072others(25): Show | 28 | HG00639.hp2 HG01243.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.455-6956G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30664682 | ||||||
| chr3:30664839
|
A | G | 1 | a0001c0001t0003g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.455-6799A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30664839 | ||||||
| chr3:30664898
|
A | T | 68 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0087others(65): Show | 68 | HG00544.hp1 HG00621.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.455-6740A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30664898 | ||||||
| chr3:30665362
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0124 | 2 | HG01256.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.455-6276A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30665362 | ||||||
| chr3:30665580
|
G | A | 4 | a0001c0001t0001g0342a0001c0003t0021g0363a0001c0004t0014g0349others(1): Show | 4 | HG01934.hp2 HG02258.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-6058G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30665580 | ||||||
| chr3:30665597
|
C | T | 1 | a0001c0002t0001g0238 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.455-6041C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30665597 | ||||||
| chr3:30665623
|
A | G | 23 | a0001c0001t0001g0149a0001c0001t0002g0072a0001c0001t0004g0028others(20): Show | 23 | HG00639.hp2 HG01243.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.455-6015A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30665623 | ||||||
| chr3:30666252
|
G | A | 193 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0038others(190): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.455-5386G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666252 | ||||||
| chr3:30666270
|
T | G | 8 | a0001c0001t0001g0052a0001c0001t0001g0125a0001c0001t0001g0132others(5): Show | 8 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(5): Show |
intron_variant | MODIFIER | c.455-5368T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666270 | ||||||
| chr3:30666510
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.455-5128G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666510 | ||||||
| chr3:30666623
|
G | T | 69 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0087others(66): Show | 69 | HG00544.hp1 HG00621.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.455-5015G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666623 | ||||||
| chr3:30666632
|
A | AC | 10 | a0001c0001t0001g0240a0001c0001t0001g0256a0001c0001t0001g0294others(7): Show | 10 | HG00597.hp1 HG01109.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.455-4999dupC | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30666632 | |||||
| chr3:30666639
|
C | A | 9 | a0001c0003t0003g0353a0001c0003t0006g0078a0001c0004t0003g0225others(6): Show | 9 | HG02258.hp1 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.455-4999C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666639 | ||||||
| chr3:30666639
|
C | G | 1 | a0001c0002t0043g0067 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.455-4999C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666639 | ||||||
| chr3:30666640
|
A | C | 1 | a0001c0001t0005g0021 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.455-4998A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666640 | ||||||
| chr3:30666641
|
T | C | 192 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0038others(189): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.455-4997T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666641 | ||||||
| chr3:30666649
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.455-4989C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666649 | ||||||
| chr3:30666717
|
G | A | 1 | a0001c0002t0001g0234 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.455-4921G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666717 | ||||||
| chr3:30666742
|
G | A | 2 | a0001c0003t0003g0353a0001c0003t0006g0078 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.455-4896G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666742 | ||||||
| chr3:30666765
|
G | C | 193 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0038others(190): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.455-4873G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666765 | ||||||
| chr3:30666806
|
AT | A | 197 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0038others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.455-4818delT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30666806 | |||||
| chr3:30666940
|
G | A | 193 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0038others(190): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.455-4698G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30666940 | ||||||
| chr3:30667429
|
T | C | 2 | a0001c0001t0001g0052a0001c0001t0001g0132 | 2 | HG00738.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.455-4209T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30667429 | ||||||
| chr3:30668019
|
A | T | 161 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(158): Show | 162 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.455-3619A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668019 | ||||||
| chr3:30668126
|
A | G | 1 | a0001c0001t0004g0150 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.455-3512A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668126 | ||||||
| chr3:30668294
|
G | C | 1 | a0001c0002t0010g0108 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.455-3344G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668294 | ||||||
| chr3:30668305
|
T | C | 1 | a0001c0001t0010g0368 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.455-3333T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668305 | ||||||
| chr3:30668453
|
T | C | 2 | a0001c0003t0007g0360a0001c0003t0007g0361 | 2 | HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.455-3185T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668453 | ||||||
| chr3:30668524
|
C | T | 1 | a0001c0001t0002g0196 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.455-3114C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668524 | ||||||
| chr3:30668568
|
T | G | 157 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0046others(154): Show | 157 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.455-3070T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668568 | ||||||
| chr3:30668581
|
C | CT | 68 | a0001c0001t0001g0046a0001c0001t0001g0055a0001c0001t0001g0058others(65): Show | 68 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.455-3049dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30668581 | |||||
| chr3:30668645
|
C | T | 82 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0048others(79): Show | 82 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.455-2993C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668645 | ||||||
| chr3:30668648
|
G | A | 68 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0087others(65): Show | 68 | HG00544.hp1 HG00621.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.455-2990G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668648 | ||||||
| chr3:30668751
|
A | G | 68 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0087others(65): Show | 68 | HG00544.hp1 HG00621.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.455-2887A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668751 | ||||||
| chr3:30668967
|
G | C | 1 | a0001c0001t0001g0201 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.455-2671G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668967 | ||||||
| chr3:30668971
|
C | T | 1 | a0001c0012t0002g0062 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.455-2667C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30668971 | ||||||
| chr3:30669003
|
C | T | 26 | a0001c0001t0001g0086a0001c0001t0001g0144a0001c0001t0001g0208others(23): Show | 26 | HG00408.hp2 HG00673.hp2 HG02071.hp2 others(23): Show |
intron_variant | MODIFIER | c.455-2635C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669003 | ||||||
| chr3:30669007
|
G | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(196): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.455-2631G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669007 | ||||||
| chr3:30669048
|
C | T | 1 | a0001c0004t0008g0331 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.455-2590C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669048 | ||||||
| chr3:30669121
|
C | CA | 11 | a0001c0001t0001g0091a0001c0001t0001g0103a0001c0001t0001g0124others(8): Show | 11 | HG00621.hp1 HG01361.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.455-2486dupA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | |||||
| chr3:30669121
|
C | CAA | 8 | a0001c0001t0003g0151a0001c0001t0006g0016a0001c0001t0006g0017others(5): Show | 8 | HG02257.hp1 HG02896.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.455-2487_455-2486d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | |||||
| chr3:30669121
|
C | CAAAAAAA others(5): Show |
1 | a0001c0004t0008g0331 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.455-2497_455-2486d others(14): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | |||||
| chr3:30669121
|
C | CAAAAAAA others(6): Show |
1 | a0001c0004t0011g0371 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.455-2498_455-2486d others(15): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | |||||
| chr3:30669121
|
C | CAAAAAAA others(12): Show |
1 | a0001c0004t0003g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.455-2504_455-2486d others(21): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | |||||
| chr3:30669121
|
CAAA | C | 9 | a0001c0001t0001g0068a0001c0001t0001g0086a0001c0001t0002g0261others(6): Show | 9 | HG02698.hp2 HG02723.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.455-2488_455-2486d others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | |||||
| chr3:30669121
|
CAAAA | C | 26 | a0001c0001t0001g0144a0001c0001t0001g0149a0001c0001t0001g0275others(23): Show | 26 | HG00408.hp2 HG00673.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.455-2489_455-2486d others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | |||||
| chr3:30669121
|
CAAAAAA | C | 6 | a0001c0001t0001g0134a0001c0001t0004g0150a0001c0003t0003g0353others(3): Show | 6 | HG01934.hp2 HG02615.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.455-2491_455-2486d others(8): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | |||||
| chr3:30669121
|
CAAAAAAA | C | 6 | a0001c0001t0001g0037a0001c0001t0001g0300a0001c0001t0002g0168others(3): Show | 6 | HG00099.hp1 HG00741.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.455-2492_455-2486d others(9): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | |||||
| chr3:30669121
|
CAAAAAAA others(1): Show |
C | 69 | a0001c0001t0001g0043a0001c0001t0001g0053a0001c0001t0001g0054others(66): Show | 69 | HG00544.hp2 HG00597.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.455-2493_455-2486d others(10): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | |||||
| chr3:30669121
|
CAAAAAAA others(2): Show |
C | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(172): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.455-2494_455-2486d others(11): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | |||||
| chr3:30669121
|
CAAAAAAA others(3): Show |
C | 12 | a0001c0001t0001g0140a0001c0001t0001g0179a0001c0001t0001g0183others(9): Show | 12 | HG00558.hp2 HG01934.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.455-2495_455-2486d others(12): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669121 | |||||
| chr3:30669153
|
G | T | 15 | a0001c0001t0001g0068a0001c0001t0001g0086a0001c0001t0001g0144others(12): Show | 15 | HG00408.hp2 HG00673.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.455-2485G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669153 | ||||||
| chr3:30669221
|
C | G | 1 | a0001c0001t0001g0046 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.455-2417C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669221 | ||||||
| chr3:30669273
|
A | T | 72 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0048others(69): Show | 72 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.455-2365A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669273 | ||||||
| chr3:30669325
|
C | G | 1 | a0001c0001t0001g0116 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.455-2313C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669325 | ||||||
| chr3:30669459
|
G | A | 1 | a0001c0003t0001g0369 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.455-2179G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669459 | ||||||
| chr3:30669598
|
C | T | 3 | a0001c0003t0001g0352a0001c0003t0001g0367a0001c0003t0001g0369 | 3 | HG02145.hp1 HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.455-2040C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669598 | ||||||
| chr3:30669764
|
A | G | 70 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0051others(67): Show | 70 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.455-1874A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669764 | ||||||
| chr3:30669793
|
CTT | C | 4 | a0001c0001t0001g0114a0001c0001t0001g0172a0001c0001t0001g0237others(1): Show | 4 | HG00639.hp1 HG01109.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.455-1843_455-1842d others(4): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669793 | |||||
| chr3:30669801
|
G | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0037others(93): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.455-1837G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669801 | ||||||
| chr3:30669801
|
GA | G | 70 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0051others(67): Show | 70 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.455-1833delA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 30669801 | |||||
| chr3:30669836
|
A | T | 4 | a0001c0001t0001g0094a0001c0001t0001g0216a0001c0001t0001g0382others(1): Show | 4 | HG03654.hp2 NA18977.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-1802A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30669836 | ||||||
| chr3:30670185
|
C | T | 1 | a0001c0002t0001g0312 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.455-1453C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30670185 | ||||||
| chr3:30670334
|
C | A | 1 | a0001c0001t0010g0368 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.455-1304C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30670334 | ||||||
| chr3:30670358
|
C | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(104): Show | 109 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.455-1280C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30670358 | ||||||
| chr3:30670389
|
A | G | 29 | a0001c0001t0001g0068a0001c0001t0001g0086a0001c0001t0001g0144others(26): Show | 29 | HG00408.hp2 HG00673.hp2 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.455-1249A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30670389 | ||||||
| chr3:30670452
|
G | T | 1 | a0001c0001t0001g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.455-1186G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30670452 | ||||||
| chr3:30670636
|
C | G | 2 | a0001c0002t0001g0268a0001c0002t0001g0376 | 2 | NA18955.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.455-1002C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30670636 | ||||||
| chr3:30670852
|
C | T | 146 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0038others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.455-786C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30670852 | ||||||
| chr3:30670968
|
C | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(105): Show | 110 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.455-670C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30670968 | ||||||
| chr3:30671335
|
A | C | 70 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0051others(67): Show | 70 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.455-303A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30671335 | ||||||
| chr3:30671634
|
T | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(105): Show | 110 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
splice_region_variant&intron_variant | LOW | c.455-4T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 3/6 | chr3 | 30671634 | ||||||
| chr3:30672453
|
T | C | 3 | a0001c0001t0001g0298a0001c0001t0001g0302a0001c0001t0001g0303 | 3 | NA19066.hp2 NA19083.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1254+16T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30672453 | ||||||
| chr3:30672535
|
A | G | 3 | a0001c0004t0008g0081a0001c0004t0008g0333a0001c0004t0008g0344 | 3 | HG02258.hp1 HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1254+98A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30672535 | ||||||
| chr3:30672922
|
G | A | 1 | a0001c0001t0006g0019 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1254+485G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30672922 | ||||||
| chr3:30672971
|
T | A | 5 | a0001c0001t0007g0356a0001c0001t0007g0357a0001c0001t0007g0362others(2): Show | 5 | HG00639.hp2 HG01255.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254+534T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30672971 | ||||||
| chr3:30673094
|
A | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(102): Show | 107 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1254+657A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673094 | ||||||
| chr3:30673099
|
T | A | 3 | a0001c0001t0002g0077a0001c0001t0002g0343a0001c0001t0008g0171 | 3 | HG02647.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1254+662T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673099 | ||||||
| chr3:30673131
|
T | C | 11 | a0001c0001t0001g0318a0001c0001t0001g0342a0001c0001t0006g0019others(8): Show | 11 | HG00639.hp2 HG01255.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1254+694T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673131 | ||||||
| chr3:30673158
|
C | A | 15 | a0001c0001t0001g0149a0001c0001t0002g0072a0001c0001t0004g0028others(12): Show | 15 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1254+721C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673158 | ||||||
| chr3:30673173
|
A | G | 10 | a0001c0003t0001g0352a0001c0003t0001g0367a0001c0003t0001g0369others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1254+736A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673173 | ||||||
| chr3:30673265
|
C | T | 372 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(369): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.1254+828C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673265 | ||||||
| chr3:30673277
|
T | C | 2 | a0001c0004t0008g0081a0001c0004t0008g0344 | 2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1255-828T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673277 | ||||||
| chr3:30673370
|
T | G | 1 | a0001c0003t0007g0360 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1255-735T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673370 | ||||||
| chr3:30673572
|
CAATTT | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0037others(147): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1255-526_1255-522d others(7): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 30673572 | |||||
| chr3:30673603
|
G | T | 15 | a0001c0001t0001g0149a0001c0001t0002g0072a0001c0001t0004g0028others(12): Show | 15 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1255-502G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673603 | ||||||
| chr3:30673663
|
C | T | 101 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0046others(98): Show | 102 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1255-442C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673663 | ||||||
| chr3:30673699
|
A | G | 9 | a0001c0004t0003g0225a0001c0004t0008g0081a0001c0004t0008g0128others(6): Show | 9 | HG01934.hp2 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1255-406A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673699 | ||||||
| chr3:30673710
|
T | C | 1 | a0001c0001t0001g0301 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1255-395T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673710 | ||||||
| chr3:30673724
|
TA | T | 73 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0051others(70): Show | 73 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.1255-372delA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 30673724 | |||||
| chr3:30673766
|
A | G | 1 | a0001c0001t0004g0150 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1255-339A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673766 | ||||||
| chr3:30673901
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1255-204T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673901 | ||||||
| chr3:30673923
|
C | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0264 | 2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1255-182C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30673923 | ||||||
| chr3:30674061
|
A | C | 1 | a0001c0001t0002g0167 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1255-44A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 4/6 | chr3 | 30674061 | ||||||
| chr3:30674362
|
C | A | 2 | a0001c0004t0014g0349a0001c0004t0033g0030 | 2 | HG01934.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1396+116C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30674362 | ||||||
| chr3:30674485
|
C | T | 73 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0051others(70): Show | 73 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.1396+239C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30674485 | ||||||
| chr3:30674519
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1396+273A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30674519 | ||||||
| chr3:30674699
|
G | A | 1 | a0001c0001t0004g0358 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1396+453G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30674699 | ||||||
| chr3:30674701
|
C | CA | 15 | a0001c0001t0001g0149a0001c0001t0002g0072a0001c0001t0004g0028others(12): Show | 15 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1396+465dupA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30674701 | |||||
| chr3:30674767
|
G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0037others(93): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.1396+521G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30674767 | ||||||
| chr3:30674775
|
G | A | 4 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0330others(1): Show | 4 | HG00408.hp2 NA18950.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396+529G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30674775 | ||||||
| chr3:30674796
|
G | C | 53 | a0001c0001t0001g0253a0001c0002t0001g0003a0001c0002t0001g0065others(50): Show | 53 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1396+550G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30674796 | ||||||
| chr3:30674925
|
C | T | 1 | a0001c0001t0002g0383 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1396+679C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30674925 | ||||||
| chr3:30675110
|
G | A | 109 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0046others(106): Show | 110 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1396+864G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675110 | ||||||
| chr3:30675158
|
G | A | 5 | a0001c0003t0003g0353a0001c0003t0006g0078a0001c0003t0007g0360others(2): Show | 5 | HG02258.hp2 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396+912G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675158 | ||||||
| chr3:30675159
|
AC | A | 3 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0330 | 3 | NA18950.hp2 NA18983.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1396+914delC | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675159 | ||||||
| chr3:30675393
|
C | CT | 150 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0046others(147): Show | 151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1396+1160dupT | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30675393 | |||||
| chr3:30675393
|
C | CTT | 150 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0037others(147): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1396+1159_1396+116 others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30675393 | |||||
| chr3:30675418
|
G | A | 1 | a0001c0011t0037g0083 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1396+1172G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675418 | ||||||
| chr3:30675451
|
A | G | 1 | a0001c0003t0021g0363 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1396+1205A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675451 | ||||||
| chr3:30675480
|
G | A | 52 | a0001c0002t0001g0003a0001c0002t0001g0065a0001c0002t0001g0088others(49): Show | 52 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1396+1234G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675480 | ||||||
| chr3:30675503
|
C | A | 2 | a0001c0001t0001g0035a0001c0001t0002g0383 | 2 | HG01433.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1396+1257C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675503 | ||||||
| chr3:30675507
|
C | T | 1 | a0001c0001t0025g0334 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1396+1261C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675507 | ||||||
| chr3:30675604
|
A | T | 1 | a0001c0001t0006g0019 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1396+1358A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675604 | ||||||
| chr3:30675655
|
G | T | 2 | a0001c0004t0014g0349a0001c0004t0033g0030 | 2 | HG01934.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1396+1409G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675655 | ||||||
| chr3:30675664
|
C | T | 14 | a0001c0001t0001g0149a0001c0001t0002g0072a0001c0001t0004g0028others(11): Show | 14 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1396+1418C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675664 | ||||||
| chr3:30675889
|
C | T | 1 | a0001c0001t0006g0017 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1396+1643C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675889 | ||||||
| chr3:30675938
|
T | G | 16 | a0001c0001t0001g0068a0001c0001t0001g0086a0001c0001t0001g0144others(13): Show | 16 | HG00408.hp2 HG00673.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1396+1692T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30675938 | ||||||
| chr3:30676115
|
A | G | 1 | a0001c0001t0001g0318 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1396+1869A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30676115 | ||||||
| chr3:30676169
|
A | G | 120 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0046others(117): Show | 121 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.1396+1923A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30676169 | ||||||
| chr3:30676466
|
C | A | 3 | a0001c0001t0010g0341a0001c0001t0016g0293a0001c0003t0003g0353 | 3 | HG00639.hp2 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1396+2220C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30676466 | ||||||
| chr3:30676484
|
T | TC | 15 | a0001c0001t0001g0149a0001c0001t0002g0072a0001c0001t0004g0028others(12): Show | 15 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1396+2242dupC | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30676484 | |||||
| chr3:30676489
|
T | C | 2 | a0001c0001t0007g0073a0001c0011t0037g0083 | 2 | HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1396+2243T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30676489 | ||||||
| chr3:30676809
|
G | GAC | 7 | a0001c0003t0036g0024a0001c0004t0003g0225a0001c0004t0008g0081others(4): Show | 7 | HG01891.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1396+2565_1396+256 others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30676809 | |||||
| chr3:30676825
|
T | C | 7 | a0001c0001t0003g0122a0001c0001t0004g0354a0001c0001t0008g0153others(4): Show | 7 | HG02257.hp1 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1396+2579T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30676825 | ||||||
| chr3:30676835
|
T | C | 2 | a0001c0001t0001g0140a0001c0001t0001g0231 | 2 | HG01934.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1396+2589T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30676835 | ||||||
| chr3:30676937
|
A | C | 300 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(297): Show | 302 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1396+2691A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30676937 | ||||||
| chr3:30677040
|
A | G | 27 | a0001c0001t0001g0068a0001c0001t0001g0086a0001c0001t0001g0144others(24): Show | 27 | HG00099.hp1 HG00408.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.1396+2794A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677040 | ||||||
| chr3:30677201
|
G | A | 3 | a0001c0001t0001g0373a0001c0001t0002g0105a0001c0001t0002g0106 | 3 | HG01261.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1396+2955G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677201 | ||||||
| chr3:30677367
|
C | T | 1 | a0001c0001t0020g0355 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1396+3121C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677367 | ||||||
| chr3:30677450
|
G | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(175): Show | 180 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1396+3204G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677450 | ||||||
| chr3:30677459
|
A | G | 2 | a0001c0001t0003g0224a0001c0001t0004g0150 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1396+3213A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677459 | ||||||
| chr3:30677522
|
G | C | 2 | a0001c0002t0039g0032a0001c0011t0037g0083 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1396+3276G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677522 | ||||||
| chr3:30677557
|
A | C | 1 | a0001c0001t0001g0275 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1396+3311A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677557 | ||||||
| chr3:30677579
|
G | A | 6 | a0001c0001t0014g0152a0001c0001t0020g0355a0001c0002t0039g0032others(3): Show | 6 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1396+3333G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677579 | ||||||
| chr3:30677608
|
T | C | 2 | a0001c0001t0003g0224a0001c0001t0004g0150 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1396+3362T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677608 | ||||||
| chr3:30677636
|
G | A | 2 | a0001c0001t0003g0224a0001c0001t0004g0150 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1396+3390G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677636 | ||||||
| chr3:30677934
|
A | G | 3 | a0001c0001t0014g0152a0001c0004t0014g0349a0001c0004t0033g0030 | 3 | HG01934.hp2 HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1396+3688A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30677934 | ||||||
| chr3:30678050
|
A | G | 1 | a0001c0002t0001g0337 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1396+3804A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678050 | ||||||
| chr3:30678269
|
C | T | 3 | a0001c0001t0003g0224a0001c0001t0004g0150a0001c0001t0006g0019 | 3 | HG02615.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1396+4023C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678269 | ||||||
| chr3:30678280
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(197): Show | 202 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.1396+4034G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678280 | ||||||
| chr3:30678473
|
G | A | 1 | a0001c0001t0011g0080 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1396+4227G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678473 | ||||||
| chr3:30678546
|
T | TC | 29 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0086others(26): Show | 29 | HG00280.hp1 HG00741.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.1396+4300_1396+430 others(5): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678546 | ||||||
| chr3:30678546
|
T | TCA | 16 | a0001c0001t0001g0216a0001c0001t0001g0385a0001c0001t0001g0386others(13): Show | 16 | HG00639.hp2 HG01167.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.1396+4300_1396+430 others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678546 | ||||||
| chr3:30678546
|
T | TCAA | 181 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0035others(178): Show | 182 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.1396+4300_1396+430 others(7): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678546 | ||||||
| chr3:30678546
|
T | TCAAA | 8 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0090others(5): Show | 9 | HG01074.hp1 HG01099.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1396+4300_1396+430 others(8): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678546 | ||||||
| chr3:30678546
|
T | TCAAAA | 5 | a0001c0001t0007g0356a0001c0001t0007g0357a0001c0001t0007g0362others(2): Show | 5 | HG01255.hp1 HG01884.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1396+4300_1396+430 others(9): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678546 | ||||||
| chr3:30678547
|
A | C | 55 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0068others(52): Show | 55 | HG00099.hp1 HG00673.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.1396+4301A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678547 | ||||||
| chr3:30678552
|
A | C | 1 | a0001c0001t0004g0358 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1396+4306A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678552 | ||||||
| chr3:30678565
|
A | G | 4 | a0001c0001t0007g0356a0001c0001t0007g0357a0001c0001t0007g0362others(1): Show | 4 | HG01255.hp1 HG01884.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396+4319A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678565 | ||||||
| chr3:30678599
|
A | G | 3 | a0001c0001t0014g0152a0001c0004t0014g0349a0001c0004t0033g0030 | 3 | HG01934.hp2 HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1396+4353A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678599 | ||||||
| chr3:30678644
|
G | A | 61 | a0001c0001t0001g0057a0001c0001t0001g0069a0001c0001t0001g0094others(58): Show | 61 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.1396+4398G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678644 | ||||||
| chr3:30678675
|
G | C | 1 | a0001c0001t0015g0388 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1396+4429G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678675 | ||||||
| chr3:30678762
|
G | C | 1 | a0001c0001t0010g0341 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1396+4516G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678762 | ||||||
| chr3:30678798
|
C | A | 3 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0330 | 3 | NA18950.hp2 NA18983.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1396+4552C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678798 | ||||||
| chr3:30678812
|
G | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(239): Show | 244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1396+4566G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678812 | ||||||
| chr3:30678950
|
C | G | 2 | a0001c0001t0001g0252a0001c0001t0001g0304 | 2 | NA18970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1396+4704C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678950 | ||||||
| chr3:30678966
|
A | C | 1 | a0001c0001t0005g0013 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1396+4720A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30678966 | ||||||
| chr3:30679026
|
C | G | 2 | a0001c0001t0003g0224a0001c0001t0004g0150 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1396+4780C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679026 | ||||||
| chr3:30679063
|
C | T | 1 | a0001c0001t0010g0341 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1396+4817C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679063 | ||||||
| chr3:30679066
|
C | T | 4 | a0001c0001t0001g0060a0001c0001t0001g0314a0001c0001t0001g0327others(1): Show | 4 | HG03491.hp2 HG03654.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396+4820C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679066 | ||||||
| chr3:30679148
|
G | T | 1 | a0001c0001t0028g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1396+4902G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679148 | ||||||
| chr3:30679172
|
G | A | 4 | a0001c0001t0001g0118a0001c0001t0001g0124a0001c0001t0001g0240others(1): Show | 4 | HG00280.hp1 HG01256.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396+4926G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679172 | ||||||
| chr3:30679338
|
G | A | 4 | a0001c0001t0007g0356a0001c0001t0007g0357a0001c0001t0007g0362others(1): Show | 4 | HG01255.hp1 HG01884.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396+5092G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679338 | ||||||
| chr3:30679367
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(228): Show | 233 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.1396+5121A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679367 | ||||||
| chr3:30679385
|
A | G | 1 | a0001c0001t0002g0061 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1396+5139A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679385 | ||||||
| chr3:30679388
|
G | A | 8 | a0001c0001t0006g0019a0001c0001t0010g0341a0001c0001t0014g0152others(5): Show | 8 | HG00639.hp2 HG01891.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.1396+5142G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679388 | ||||||
| chr3:30679468
|
G | A | 2 | a0001c0001t0003g0370a0001c0001t0016g0292 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1396+5222G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679468 | ||||||
| chr3:30679552
|
G | C | 6 | a0001c0001t0004g0358a0001c0004t0008g0081a0001c0004t0008g0128others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396+5306G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679552 | ||||||
| chr3:30679555
|
T | A | 4 | a0001c0001t0001g0318a0001c0003t0001g0352a0001c0003t0001g0367others(1): Show | 4 | HG02145.hp1 HG02723.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1396+5309T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679555 | ||||||
| chr3:30679604
|
A | G | 1 | a0001c0001t0002g0274 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1396+5358A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679604 | ||||||
| chr3:30679609
|
C | A | 24 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0068others(21): Show | 24 | HG00099.hp1 HG00673.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1396+5363C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679609 | ||||||
| chr3:30679709
|
A | G | 284 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(281): Show | 286 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.1396+5463A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679709 | ||||||
| chr3:30679813
|
A | T | 1 | a0001c0002t0010g0384 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1396+5567A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679813 | ||||||
| chr3:30679877
|
C | T | 1 | a0001c0002t0043g0067 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1396+5631C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30679877 | ||||||
| chr3:30679994
|
CG | C | 5 | a0001c0001t0001g0318a0001c0003t0001g0352a0001c0003t0001g0367others(2): Show | 5 | HG02145.hp1 HG02258.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396+5751delG | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30679994 | |||||
| chr3:30680097
|
C | T | 246 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(243): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1396+5851C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680097 | ||||||
| chr3:30680103
|
C | A | 1 | a0001c0001t0001g0208 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1396+5857C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680103 | ||||||
| chr3:30680129
|
G | GC | 7 | a0001c0001t0002g0274a0001c0001t0004g0354a0001c0001t0008g0153others(4): Show | 7 | HG02257.hp1 HG02970.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1396+5889dupC | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30680129 | |||||
| chr3:30680136
|
A | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(267): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1396+5890A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680136 | ||||||
| chr3:30680177
|
C | T | 4 | a0001c0001t0003g0224a0001c0001t0004g0150a0001c0002t0038g0029others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1396+5931C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680177 | ||||||
| chr3:30680211
|
A | T | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(287): Show | 292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1396+5965A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680211 | ||||||
| chr3:30680244
|
C | A | 23 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0068others(20): Show | 23 | HG00099.hp1 HG00673.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.1396+5998C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680244 | ||||||
| chr3:30680388
|
C | T | 1 | a0001c0003t0036g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1396+6142C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680388 | ||||||
| chr3:30680447
|
C | T | 110 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0042others(107): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1396+6201C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680447 | ||||||
| chr3:30680674
|
C | G | 2 | a0001c0001t0003g0224a0001c0001t0004g0150 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1396+6428C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680674 | ||||||
| chr3:30680726
|
T | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(221): Show | 226 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.1396+6480T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680726 | ||||||
| chr3:30680920
|
T | G | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(287): Show | 292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1396+6674T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680920 | ||||||
| chr3:30680927
|
G | C | 2 | a0001c0001t0020g0355a0001c0011t0037g0083 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1396+6681G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680927 | ||||||
| chr3:30680928
|
G | A | 5 | a0001c0004t0008g0081a0001c0004t0008g0128a0001c0004t0008g0331others(2): Show | 5 | HG02258.hp1 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1396+6682G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680928 | ||||||
| chr3:30680937
|
G | T | 1 | a0001c0011t0037g0083 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1396+6691G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680937 | ||||||
| chr3:30680943
|
G | T | 1 | a0001c0001t0004g0154 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1396+6697G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680943 | ||||||
| chr3:30680986
|
G | A | 3 | a0001c0002t0038g0029a0001c0003t0006g0078a0001c0003t0021g0363 | 3 | HG02258.hp2 HG02622.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1396+6740G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680986 | ||||||
| chr3:30680998
|
C | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0191a0002c0005t0005g0178 | 3 | HG02155.hp2 NA18959.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1396+6752C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30680998 | ||||||
| chr3:30681009
|
G | A | 8 | a0001c0001t0007g0356a0001c0001t0007g0357a0001c0001t0007g0362others(5): Show | 8 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1396+6763G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681009 | ||||||
| chr3:30681015
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(117): Show | 121 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.1396+6769A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681015 | ||||||
| chr3:30681159
|
T | TG | 143 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0042others(140): Show | 144 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.1396+6914dupG | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30681159 | |||||
| chr3:30681160
|
G | GA | 20 | a0001c0001t0001g0043a0001c0001t0001g0086a0001c0001t0001g0190others(17): Show | 20 | HG01516.hp2 HG01517.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1396+6935dupA | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30681160 | |||||
| chr3:30681160
|
G | GGA | 104 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(101): Show | 105 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.1396+6914_1396+691 others(6): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681160 | ||||||
| chr3:30681160
|
G | GGAA | 24 | a0001c0001t0001g0059a0001c0001t0001g0094a0001c0001t0001g0144others(21): Show | 24 | HG00673.hp2 HG01943.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.1396+6914_1396+691 others(7): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681160 | ||||||
| chr3:30681160
|
GAAAAAAA | G | 6 | a0001c0001t0011g0008a0001c0001t0014g0152a0001c0002t0038g0029others(3): Show | 6 | HG01109.hp2 HG01934.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1396+6929_1396+693 others(11): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30681160 | |||||
| chr3:30681161
|
A | G | 4 | a0001c0001t0002g0196a0001c0002t0001g0213a0001c0003t0021g0363others(1): Show | 4 | HG02040.hp1 HG02258.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396+6915A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681161 | ||||||
| chr3:30681168
|
A | G | 6 | a0001c0001t0011g0008a0001c0001t0014g0152a0001c0002t0038g0029others(3): Show | 6 | HG01109.hp2 HG01934.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1396+6922A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681168 | ||||||
| chr3:30681246
|
G | A | 1 | a0001c0002t0001g0181 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1396+7000G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681246 | ||||||
| chr3:30681282
|
C | A | 1 | a0001c0001t0001g0199 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1396+7036C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681282 | ||||||
| chr3:30681297
|
G | C | 2 | a0001c0001t0001g0222a0001c0001t0001g0258 | 2 | NA18964.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1396+7051G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681297 | ||||||
| chr3:30681312
|
C | T | 3 | a0001c0001t0014g0152a0001c0004t0014g0349a0001c0004t0033g0030 | 3 | HG01934.hp2 HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1396+7066C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681312 | ||||||
| chr3:30681329
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1397-7055A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681329 | ||||||
| chr3:30681493
|
G | C | 1 | a0001c0001t0001g0049 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1397-6891G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681493 | ||||||
| chr3:30681551
|
C | T | 1 | a0001c0001t0001g0342 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1397-6833C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681551 | ||||||
| chr3:30681559
|
G | A | 4 | a0001c0001t0014g0152a0001c0003t0006g0078a0001c0004t0014g0349others(1): Show | 4 | HG01934.hp2 HG02280.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397-6825G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681559 | ||||||
| chr3:30681562
|
C | T | 1 | a0001c0011t0037g0083 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1397-6822C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681562 | ||||||
| chr3:30681638
|
G | A | 2 | a0001c0001t0009g0339a0001c0001t0009g0340 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1397-6746G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681638 | ||||||
| chr3:30681736
|
A | G | 1 | a0001c0002t0010g0384 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1397-6648A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681736 | ||||||
| chr3:30681760
|
A | G | 7 | a0001c0001t0001g0318a0001c0001t0003g0224a0001c0001t0004g0150others(4): Show | 7 | HG02145.hp1 HG02615.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1397-6624A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681760 | ||||||
| chr3:30681978
|
A | G | 268 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0042others(265): Show | 269 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.1397-6406A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30681978 | ||||||
| chr3:30682043
|
A | G | 1 | a0001c0001t0004g0358 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1397-6341A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30682043 | ||||||
| chr3:30682272
|
A | G | 1 | a0001c0003t0003g0353 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1397-6112A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30682272 | ||||||
| chr3:30682944
|
A | G | 89 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0055others(86): Show | 89 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1397-5440A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30682944 | ||||||
| chr3:30682954
|
T | A | 6 | a0001c0001t0008g0153a0001c0001t0010g0368a0001c0001t0015g0143others(3): Show | 6 | HG01891.hp1 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1397-5430T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30682954 | ||||||
| chr3:30683196
|
T | C | 9 | a0001c0001t0008g0153a0001c0001t0010g0341a0001c0001t0010g0368others(6): Show | 9 | HG00639.hp2 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1397-5188T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683196 | ||||||
| chr3:30683229
|
A | G | 21 | a0001c0001t0001g0059a0001c0001t0001g0210a0001c0001t0001g0278others(18): Show | 21 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1397-5155A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683229 | ||||||
| chr3:30683393
|
A | G | 4 | a0001c0001t0014g0152a0001c0003t0006g0078a0001c0004t0014g0349others(1): Show | 4 | HG01934.hp2 HG02280.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397-4991A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683393 | ||||||
| chr3:30683521
|
A | T | 1 | a0001c0003t0036g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1397-4863A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683521 | ||||||
| chr3:30683591
|
G | A | 4 | a0001c0001t0014g0152a0001c0003t0006g0078a0001c0004t0014g0349others(1): Show | 4 | HG01934.hp2 HG02280.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397-4793G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683591 | ||||||
| chr3:30683721
|
A | T | 89 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0055others(86): Show | 89 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1397-4663A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683721 | ||||||
| chr3:30683799
|
T | C | 4 | a0001c0001t0001g0190a0001c0001t0001g0193a0001c0001t0001g0195others(1): Show | 4 | NA19006.hp2 NA19055.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397-4585T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683799 | ||||||
| chr3:30683820
|
C | G | 3 | a0001c0001t0001g0069a0001c0001t0002g0262a0001c0001t0002g0305 | 3 | HG03834.hp2 HG03942.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1397-4564C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683820 | ||||||
| chr3:30683889
|
C | T | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1397-4495C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683889 | ||||||
| chr3:30683892
|
C | A | 1 | a0001c0001t0019g0297 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1397-4492C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683892 | ||||||
| chr3:30683898
|
G | A | 1 | a0001c0001t0027g0160 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1397-4486G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30683898 | ||||||
| chr3:30684021
|
G | A | 1 | a0001c0002t0010g0384 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1397-4363G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684021 | ||||||
| chr3:30684042
|
A | C | 1 | a0001c0001t0001g0302 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1397-4342A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684042 | ||||||
| chr3:30684153
|
T | C | 93 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0055others(90): Show | 93 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1397-4231T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684153 | ||||||
| chr3:30684284
|
G | A | 131 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0042others(128): Show | 132 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.1397-4100G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684284 | ||||||
| chr3:30684408
|
A | G | 1 | a0001c0002t0010g0384 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1397-3976A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684408 | ||||||
| chr3:30684465
|
C | T | 1 | a0001c0001t0002g0295 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1397-3919C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684465 | ||||||
| chr3:30684469
|
C | T | 3 | a0001c0001t0001g0100a0001c0002t0001g0130a0001c0002t0030g0092 | 3 | HG02165.hp2 NA18969.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1397-3915C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684469 | ||||||
| chr3:30684682
|
G | A | 1 | a0001c0011t0037g0083 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1397-3702G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684682 | ||||||
| chr3:30684709
|
TTGGGAA | T | 12 | a0001c0001t0007g0073a0001c0001t0007g0074a0001c0001t0007g0075others(9): Show | 12 | HG01109.hp2 HG01255.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1397-3673_1397-366 others(10): Show |
TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 30684709 | |||||
| chr3:30684716
|
T | G | 12 | a0001c0001t0007g0073a0001c0001t0007g0074a0001c0001t0007g0075others(9): Show | 12 | HG01109.hp2 HG01255.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1397-3668T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684716 | ||||||
| chr3:30684717
|
A | C | 12 | a0001c0001t0007g0073a0001c0001t0007g0074a0001c0001t0007g0075others(9): Show | 12 | HG01109.hp2 HG01255.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1397-3667A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684717 | ||||||
| chr3:30684752
|
A | G | 1 | a0001c0001t0008g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1397-3632A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684752 | ||||||
| chr3:30684804
|
G | A | 1 | a0001c0001t0003g0039 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1397-3580G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684804 | ||||||
| chr3:30684940
|
G | C | 264 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0042others(261): Show | 265 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1397-3444G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30684940 | ||||||
| chr3:30685027
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1397-3357C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30685027 | ||||||
| chr3:30685094
|
A | C | 5 | a0001c0004t0008g0081a0001c0004t0008g0128a0001c0004t0008g0331others(2): Show | 5 | HG02258.hp1 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1397-3290A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30685094 | ||||||
| chr3:30685409
|
C | T | 6 | a0001c0004t0008g0081a0001c0004t0008g0128a0001c0004t0008g0331others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1397-2975C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30685409 | ||||||
| chr3:30685591
|
A | G | 2 | a0001c0001t0010g0368a0001c0003t0036g0024 | 2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1397-2793A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30685591 | ||||||
| chr3:30685592
|
G | A | 89 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0055others(86): Show | 89 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1397-2792G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30685592 | ||||||
| chr3:30686209
|
T | C | 8 | a0001c0001t0008g0153a0001c0001t0010g0341a0001c0001t0010g0368others(5): Show | 8 | HG00639.hp2 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1397-2175T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30686209 | ||||||
| chr3:30686284
|
G | A | 86 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0055others(83): Show | 86 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1397-2100G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30686284 | ||||||
| chr3:30686346
|
G | A | 12 | a0001c0001t0001g0034a0001c0001t0001g0243a0001c0001t0002g0232others(9): Show | 12 | HG00735.hp1 HG01074.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.1397-2038G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30686346 | ||||||
| chr3:30686471
|
A | G | 1 | a0001c0001t0003g0230 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1397-1913A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30686471 | ||||||
| chr3:30686625
|
C | T | 1 | a0001c0001t0002g0305 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1397-1759C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30686625 | ||||||
| chr3:30686798
|
G | C | 95 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0055others(92): Show | 95 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1397-1586G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30686798 | ||||||
| chr3:30686819
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1397-1565C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30686819 | ||||||
| chr3:30686858
|
A | T | 2 | a0001c0001t0004g0320a0001c0001t0004g0322 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1397-1526A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30686858 | ||||||
| chr3:30687007
|
A | C | 1 | a0001c0004t0011g0371 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1397-1377A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687007 | ||||||
| chr3:30687065
|
G | A | 1 | a0001c0002t0039g0032 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1397-1319G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687065 | ||||||
| chr3:30687098
|
C | A | 89 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0055others(86): Show | 89 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1397-1286C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687098 | ||||||
| chr3:30687197
|
C | T | 92 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0055others(89): Show | 92 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1397-1187C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687197 | ||||||
| chr3:30687380
|
T | G | 240 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0042others(237): Show | 241 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.1397-1004T>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687380 | ||||||
| chr3:30687433
|
C | T | 63 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0059others(60): Show | 63 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1397-951C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687433 | ||||||
| chr3:30687455
|
G | A | 3 | a0001c0001t0003g0224a0001c0001t0004g0150a0001c0001t0020g0355 | 3 | HG02615.hp1 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1397-929G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687455 | ||||||
| chr3:30687493
|
G | T | 3 | a0001c0001t0016g0293a0001c0001t0035g0031a0001c0003t0003g0353 | 3 | HG02630.hp1 HG02809.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1397-891G>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687493 | ||||||
| chr3:30687504
|
A | G | 7 | a0001c0001t0008g0153a0001c0001t0010g0368a0001c0001t0015g0143others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1397-880A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687504 | ||||||
| chr3:30687647
|
C | T | 1 | a0001c0002t0001g0123 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1397-737C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687647 | ||||||
| chr3:30687661
|
A | G | 3 | a0001c0001t0003g0224a0001c0001t0004g0150a0001c0001t0020g0355 | 3 | HG02615.hp1 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1397-723A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687661 | ||||||
| chr3:30687666
|
C | T | 1 | a0001c0001t0001g0382 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1397-718C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687666 | ||||||
| chr3:30687737
|
G | C | 250 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0037others(247): Show | 251 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.1397-647G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687737 | ||||||
| chr3:30687754
|
G | A | 90 | a0001c0001t0001g0037a0001c0001t0001g0043a0001c0001t0001g0055others(87): Show | 90 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.1397-630G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687754 | ||||||
| chr3:30687872
|
A | T | 4 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0304others(1): Show | 4 | HG03710.hp1 NA18991.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.1397-512A>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30687872 | ||||||
| chr3:30688018
|
A | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0155a0001c0002t0010g0384 | 3 | HG00735.hp2 HG01081.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1397-366A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30688018 | ||||||
| chr3:30688144
|
G | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0035others(158): Show | 162 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(159): Show |
intron_variant | MODIFIER | c.1397-240G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30688144 | ||||||
| chr3:30688244
|
A | C | 5 | a0001c0001t0015g0143a0001c0001t0015g0388a0001c0001t0016g0293others(2): Show | 5 | HG02257.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1397-140A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30688244 | ||||||
| chr3:30688268
|
G | A | 1 | a0001c0003t0006g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1397-116G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 5/6 | chr3 | 30688268 | ||||||
| chr3:30688530
|
C | A | 1 | a0001c0002t0001g0098 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1524+19C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30688530 | ||||||
| chr3:30688741
|
C | G | 8 | a0001c0001t0008g0153a0001c0001t0008g0171a0001c0001t0035g0031others(5): Show | 8 | HG02258.hp1 HG02559.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1524+230C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30688741 | ||||||
| chr3:30688747
|
C | T | 132 | a0001c0001t0001g0037a0001c0001t0001g0043a0001c0001t0001g0048others(129): Show | 132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1524+236C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30688747 | ||||||
| chr3:30689168
|
T | C | 1 | a0001c0010t0002g0071 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1524+657T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30689168 | ||||||
| chr3:30689197
|
T | C | 28 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0003g0041others(25): Show | 28 | HG01074.hp2 HG01106.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.1524+686T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30689197 | ||||||
| chr3:30689230
|
T | C | 12 | a0001c0001t0007g0073a0001c0001t0007g0074a0001c0001t0007g0075others(9): Show | 12 | HG01109.hp2 HG01255.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1524+719T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30689230 | ||||||
| chr3:30689358
|
T | C | 1 | a0001c0001t0003g0224 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1524+847T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30689358 | ||||||
| chr3:30689380
|
G | A | 187 | a0001c0001t0001g0037a0001c0001t0001g0043a0001c0001t0001g0048others(184): Show | 188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1524+869G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30689380 | ||||||
| chr3:30689631
|
G | C | 60 | a0001c0001t0001g0113a0001c0001t0001g0251a0001c0001t0002g0061others(57): Show | 61 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.1524+1120G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30689631 | ||||||
| chr3:30689721
|
A | G | 3 | a0001c0001t0015g0143a0001c0001t0015g0388a0001c0001t0018g0020 | 3 | HG02257.hp1 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1524+1210A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30689721 | ||||||
| chr3:30689729
|
C | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0058 | 2 | NA18944.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1524+1218C>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30689729 | ||||||
| chr3:30689790
|
T | A | 346 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0034others(343): Show | 348 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.1524+1279T>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30689790 | ||||||
| chr3:30690125
|
C | T | 1 | a0001c0001t0011g0008 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1525-1295C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30690125 | ||||||
| chr3:30690240
|
T | C | 1 | a0001c0003t0040g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1525-1180T>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30690240 | ||||||
| chr3:30690377
|
C | T | 1 | a0001c0001t0007g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1525-1043C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30690377 | ||||||
| chr3:30690693
|
A | G | 68 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0055others(65): Show | 68 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1525-727A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30690693 | ||||||
| chr3:30690899
|
C | T | 9 | a0001c0001t0003g0151a0001c0001t0006g0016a0001c0001t0006g0017others(6): Show | 9 | HG02055.hp2 HG02559.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1525-521C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30690899 | ||||||
| chr3:30691038
|
G | A | 129 | a0001c0001t0001g0037a0001c0001t0001g0043a0001c0001t0001g0048others(126): Show | 129 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.1525-382G>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30691038 | ||||||
| chr3:30691039
|
A | C | 27 | a0001c0001t0004g0028a0001c0001t0004g0082a0001c0001t0004g0150others(24): Show | 27 | HG01884.hp1 HG02109.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1525-381A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30691039 | ||||||
| chr3:30691042
|
A | C | 90 | a0001c0001t0001g0037a0001c0001t0001g0043a0001c0001t0001g0048others(87): Show | 90 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.1525-378A>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30691042 | ||||||
| chr3:30691208
|
G | C | 15 | a0001c0001t0007g0073a0001c0001t0007g0074a0001c0001t0007g0075others(12): Show | 15 | HG01109.hp2 HG01255.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1525-212G>C | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30691208 | ||||||
| chr3:30691252
|
A | G | 1 | a0001c0001t0002g0164 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1525-168A>G | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30691252 | ||||||
| chr3:30691329
|
C | A | 59 | a0001c0001t0002g0061a0001c0001t0002g0072a0001c0001t0002g0077others(56): Show | 60 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.1525-91C>A | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30691329 | ||||||
| chr3:30691412
|
C | T | 1 | a0001c0001t0025g0334 | 1 | HG03139.hp2 | splice_region_variant&intron_variant | LOW | c.1525-8C>T | TGFBR2 | ENSG00000163513.19 | transcript | ENST00000295754.10 | protein_coding | 6/6 | chr3 | 30691412 |