| geneid | 3482 |
|---|---|
| ensemblid | ENSG00000197081.16 |
| hgncid | 5467 |
| symbol | IGF2R |
| name | insulin like growth factor 2 receptor |
| refseq_nuc | NM_000876.4 |
| refseq_prot | NP_000867.3 |
| ensembl_nuc | ENST00000356956.6 |
| ensembl_prot | ENSP00000349437.1 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 159969082 |
| end | 160111504 |
| strand | + |
| ver | v1.2 |
| region | chr6:159969082-160111504 |
| region5000 | chr6:159964082-160116504 |
| regionname0 | IGF2R_chr6_159969082_160111504 |
| regionname5000 | IGF2R_chr6_159964082_160116504 |
| 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 | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 2491 | 148 | 35 | 31 | 47 | 12 | 22 | 39 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002 | 0/0 | 2491 | 47 | 0 | 9 | 36 | 0 | 2 | 28 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003 | 0/0 | 2491 | 23 | 11 | 0 | 7 | 0 | 5 | 6 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0004 | 0/0 | 2491 | 18 | 0 | 1 | 11 | 0 | 6 | 8 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0005 | 1/0 | 2491 | 14 | 1 | 9 | 1 | 1 | 1 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0006 | 0/0 | 2491 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0007 | 0/0 | 2491 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0008 | 0/0 | 2491 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0009 | 0/0 | 2491 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0010 | 0/0 | 2491 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0011 | 0/0 | 2491 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0012 | 0/0 | 2491 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0013 | 0/0 | 2491 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0014 | 0/0 | 2491 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0015 | 0/0 | 2491 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0016 | 0/0 | 2491 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0017 | 0/0 | 2491 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0018 | 0/0 | 2491 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0019 | 0/0 | 2491 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0020 | 0/0 | 2491 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0021 | 0/0 | 2491 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0022 | 0/0 | 2491 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0023 | 0/0 | 2491 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0024 | 0/0 | 2491 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0025 | 0/0 | 2491 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0026 | 0/0 | 2491 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0027 | 0/0 | 2491 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0028 | 0/0 | 2491 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0029 | 0/0 | 2491 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0030 | 0/0 | 2491 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0031 | 0/0 | 2491 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0032 | 0/0 | 2491 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0033 | 0/0 | 2491 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0034 | 0/0 | 2491 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0035 | 0/0 | 2491 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0036 | 0/0 | 2491 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0037 | 0/0 | 2491 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 7476 | 49 | 7 | 17 | 10 | 6 | 9 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0002 | 0/1 | 7476 | 43 | 16 | 9 | 7 | 4 | 6 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0003 | 0/0 | 7476 | 39 | 0 | 9 | 28 | 0 | 2 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0004 | 0/0 | 7476 | 22 | 3 | 4 | 10 | 2 | 3 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0005 | 0/0 | 7476 | 15 | 1 | 0 | 14 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0006 | 0/0 | 7476 | 14 | 0 | 1 | 9 | 0 | 4 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0007 | 0/0 | 7476 | 14 | 6 | 0 | 6 | 0 | 2 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0008 | 0/0 | 7476 | 10 | 1 | 7 | 0 | 1 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0009 | 0/0 | 7476 | 8 | 2 | 0 | 5 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0010 | 0/0 | 7476 | 5 | 5 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0011 | 0/0 | 7476 | 4 | 4 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0012 | 0/0 | 7476 | 4 | 4 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0013 | 0/0 | 7476 | 4 | 4 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0014 | 0/0 | 7476 | 3 | 3 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0015 | 0/0 | 7476 | 3 | 0 | 0 | 3 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0016 | 0/0 | 7476 | 3 | 3 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0017 | 0/0 | 7476 | 3 | 0 | 0 | 3 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0018 | 0/0 | 7476 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0019 | 0/0 | 7476 | 2 | 0 | 2 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0020 | 1/0 | 7476 | 2 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0021 | 0/0 | 7476 | 2 | 0 | 0 | 0 | 1 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0022 | 0/0 | 7476 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0023 | 0/0 | 7476 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0024 | 0/0 | 7476 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0025 | 0/0 | 7476 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0026 | 0/0 | 7476 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0027 | 0/0 | 7476 | 2 | 0 | 1 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0028 | 0/0 | 7476 | 2 | 0 | 0 | 2 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0029 | 0/0 | 7476 | 2 | 0 | 0 | 2 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0030 | 0/0 | 7476 | 2 | 0 | 0 | 1 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0031 | 0/0 | 7476 | 2 | 1 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0032 | 0/0 | 7476 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0033 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0034 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0035 | 0/0 | 7476 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0036 | 0/0 | 7476 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0037 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0038 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0039 | 0/0 | 7476 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0040 | 0/0 | 7476 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0041 | 0/0 | 7476 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0042 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0043 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0044 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0045 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0046 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0047 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0048 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0049 | 0/0 | 7476 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0050 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0051 | 0/0 | 7476 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0052 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0053 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0054 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0055 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0056 | 0/0 | 7476 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0057 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0058 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0059 | 0/0 | 7476 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0060 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0061 | 0/0 | 7476 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0062 | 0/0 | 7476 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0063 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0064 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0065 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0066 | 0/0 | 7476 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0067 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0068 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| c0069 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| thapid | grch38chm13v2 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 6584 | 43 | 0 | 9 | 34 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0002 | 0/0 | 6584 | 38 | 2 | 14 | 12 | 2 | 8 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0003 | 0/0 | 6584 | 28 | 2 | 4 | 16 | 0 | 6 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0004 | 0/0 | 6580 | 14 | 0 | 0 | 12 | 0 | 2 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0005 | 0/0 | 6580 | 13 | 1 | 7 | 0 | 1 | 4 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0006 | 0/0 | 6585 | 12 | 4 | 2 | 5 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0007 | 0/1 | 6582 | 9 | 4 | 2 | 0 | 1 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0008 | 0/0 | 6584 | 8 | 0 | 1 | 6 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0009 | 0/0 | 6585 | 7 | 3 | 0 | 0 | 0 | 4 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0010 | 0/0 | 6586 | 6 | 6 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0011 | 0/0 | 6587 | 6 | 6 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0012 | 0/0 | 6580 | 5 | 2 | 0 | 3 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0013 | 1/0 | 6586 | 5 | 0 | 3 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0014 | 0/0 | 6582 | 4 | 0 | 0 | 2 | 0 | 2 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0015 | 0/0 | 6582 | 4 | 3 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0016 | 0/0 | 6583 | 3 | 3 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0017 | 0/0 | 6584 | 3 | 3 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0018 | 0/0 | 6582 | 3 | 3 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0019 | 0/0 | 6582 | 3 | 2 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0020 | 0/0 | 6586 | 3 | 0 | 0 | 3 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0021 | 0/0 | 6584 | 3 | 0 | 1 | 0 | 2 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0022 | 0/0 | 6584 | 3 | 3 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0023 | 0/0 | 6586 | 3 | 1 | 1 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0024 | 0/0 | 6580 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0025 | 0/0 | 6582 | 2 | 0 | 0 | 2 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0026 | 0/0 | 6585 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0027 | 0/0 | 6582 | 2 | 1 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0028 | 0/0 | 6586 | 2 | 1 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0029 | 0/0 | 6582 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0030 | 0/0 | 6586 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0031 | 0/0 | 6582 | 2 | 0 | 0 | 0 | 1 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0032 | 0/0 | 6584 | 2 | 0 | 1 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0033 | 0/0 | 6584 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0034 | 0/0 | 6586 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0035 | 0/0 | 6582 | 2 | 0 | 2 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0036 | 0/0 | 6582 | 2 | 0 | 2 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0037 | 0/0 | 6580 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0038 | 0/0 | 6580 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0039 | 0/0 | 6580 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0040 | 0/0 | 6580 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0041 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0042 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0043 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0044 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0045 | 0/0 | 6584 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0046 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0047 | 0/0 | 6580 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0048 | 0/0 | 6584 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0049 | 0/0 | 6584 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0050 | 0/0 | 6585 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0051 | 0/0 | 6616 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0052 | 0/0 | 6581 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0053 | 0/0 | 6588 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0054 | 0/0 | 6587 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0055 | 0/0 | 6578 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0056 | 0/0 | 6582 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0057 | 0/0 | 6582 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0058 | 0/0 | 6582 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0059 | 0/0 | 6582 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0060 | 0/0 | 6582 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0061 | 0/0 | 6584 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0062 | 0/0 | 6584 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0063 | 0/0 | 6584 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0064 | 0/0 | 6584 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0065 | 0/0 | 6586 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0066 | 0/0 | 6586 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0067 | 0/0 | 6586 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0068 | 0/0 | 6586 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0069 | 0/0 | 6584 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0070 | 0/0 | 6590 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0071 | 0/0 | 6586 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0072 | 0/0 | 6591 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0073 | 0/0 | 6580 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0074 | 0/0 | 6582 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0075 | 0/0 | 6583 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0076 | 0/0 | 6583 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0077 | 0/0 | 6585 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0078 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0079 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0080 | 0/0 | 6584 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0081 | 0/0 | 6584 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0082 | 0/0 | 6581 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0083 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0084 | 0/0 | 6584 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0085 | 0/0 | 6587 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0086 | 0/0 | 6586 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0087 | 0/0 | 6590 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0088 | 0/0 | 6582 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0089 | 0/0 | 6582 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0090 | 0/0 | 6584 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0091 | 0/0 | 6586 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0092 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0093 | 0/0 | 6584 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| t0094 | 0/0 | 6580 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0056 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0059 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| achapid | 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 7476 | 49 | 7 | 17 | 10 | 6 | 9 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002 | 0/1 | 7476 | 43 | 16 | 9 | 7 | 4 | 6 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0004 | 0/0 | 7476 | 22 | 3 | 4 | 10 | 2 | 3 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0005 | 0/0 | 7476 | 15 | 1 | 0 | 14 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0009 | 0/0 | 7476 | 8 | 2 | 0 | 5 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0024 | 0/0 | 7476 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0034 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0036 | 0/0 | 7476 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0037 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0039 | 0/0 | 7476 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0045 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0046 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0049 | 0/0 | 7476 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0056 | 0/0 | 7476 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0069 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002c0003 | 0/0 | 7476 | 39 | 0 | 9 | 28 | 0 | 2 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002c0015 | 0/0 | 7476 | 3 | 0 | 0 | 3 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002c0028 | 0/0 | 7476 | 2 | 0 | 0 | 2 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002c0047 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002c0052 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002c0057 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0007 | 0/0 | 7476 | 14 | 6 | 0 | 6 | 0 | 2 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0012 | 0/0 | 7476 | 4 | 4 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0030 | 0/0 | 7476 | 2 | 0 | 0 | 1 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0058 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0059 | 0/0 | 7476 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0066 | 0/0 | 7476 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0004c0006 | 0/0 | 7476 | 14 | 0 | 1 | 9 | 0 | 4 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0004c0029 | 0/0 | 7476 | 2 | 0 | 0 | 2 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0004c0061 | 0/0 | 7476 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0004c0062 | 0/0 | 7476 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0005c0008 | 0/0 | 7476 | 10 | 1 | 7 | 0 | 1 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0005c0020 | 1/0 | 7476 | 2 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0005c0027 | 0/0 | 7476 | 2 | 0 | 1 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0006c0010 | 0/0 | 7476 | 5 | 5 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0006c0025 | 0/0 | 7476 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0007c0014 | 0/0 | 7476 | 3 | 3 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0007c0018 | 0/0 | 7476 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0008c0011 | 0/0 | 7476 | 4 | 4 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0008c0043 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0009c0013 | 0/0 | 7476 | 4 | 4 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0010c0016 | 0/0 | 7476 | 3 | 3 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0011c0017 | 0/0 | 7476 | 3 | 0 | 0 | 3 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0012c0031 | 0/0 | 7476 | 2 | 1 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0013c0026 | 0/0 | 7476 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0014c0022 | 0/0 | 7476 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0015c0023 | 0/0 | 7476 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0016c0019 | 0/0 | 7476 | 2 | 0 | 2 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0017c0021 | 0/0 | 7476 | 2 | 0 | 0 | 0 | 1 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0018c0032 | 0/0 | 7476 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0019c0068 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0020c0041 | 0/0 | 7476 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0021c0044 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0022c0042 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0023c0035 | 0/0 | 7476 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0024c0051 | 0/0 | 7476 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0025c0053 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0026c0054 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0027c0055 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0028c0050 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0029c0038 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0030c0040 | 0/0 | 7476 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0031c0048 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0032c0065 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0033c0064 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0034c0063 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0035c0060 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0036c0067 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0037c0033 | 0/0 | 7476 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 14059 | 4 | 0 | 0 | 4 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0001t0002 | 0/0 | 14059 | 5 | 0 | 3 | 0 | 0 | 2 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0001t0003 | 0/0 | 14059 | 7 | 1 | 3 | 1 | 0 | 2 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0001t0005 | 0/0 | 14055 | 9 | 0 | 5 | 0 | 1 | 3 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0001t0006 | 0/0 | 14060 | 5 | 1 | 0 | 4 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0001t0008 | 0/0 | 14059 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0001t0010 | 0/0 | 14061 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0001t0013 | 0/0 | 14061 | 3 | 0 | 2 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0001t0014 | 0/0 | 14057 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0001t0021 | 0/0 | 14059 | 3 | 0 | 1 | 0 | 2 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0001t0026 | 0/0 | 14060 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0001t0030 | 0/0 | 14061 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0001t0032 | 0/0 | 14059 | 2 | 0 | 1 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0001t0035 | 0/0 | 14057 | 2 | 0 | 2 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0001t0043 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0001t0069 | 0/0 | 14059 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0001t0085 | 0/0 | 14062 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0002 | 0/0 | 14059 | 3 | 0 | 1 | 2 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0003 | 0/0 | 14059 | 3 | 0 | 0 | 3 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0006 | 0/0 | 14060 | 2 | 0 | 1 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0007 | 0/1 | 14057 | 9 | 4 | 2 | 0 | 1 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0009 | 0/0 | 14060 | 3 | 0 | 0 | 0 | 0 | 3 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0010 | 0/0 | 14061 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0015 | 0/0 | 14057 | 3 | 3 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0018 | 0/0 | 14057 | 3 | 3 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0023 | 0/0 | 14061 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0027 | 0/0 | 14057 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0028 | 0/0 | 14061 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0036 | 0/0 | 14057 | 2 | 0 | 2 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0039 | 0/0 | 14055 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0050 | 0/0 | 14060 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0056 | 0/0 | 14057 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0058 | 0/0 | 14057 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0067 | 0/0 | 14061 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0071 | 0/0 | 14061 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0080 | 0/0 | 14059 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0082 | 0/0 | 14056 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0088 | 0/0 | 14057 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0090 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0002t0091 | 0/0 | 14061 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0004t0001 | 0/0 | 14059 | 2 | 0 | 1 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0004t0002 | 0/0 | 14059 | 4 | 0 | 2 | 1 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0004t0003 | 0/0 | 14059 | 5 | 0 | 0 | 4 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0004t0020 | 0/0 | 14061 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0004t0027 | 0/0 | 14057 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0004t0034 | 0/0 | 14061 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0004t0044 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0004t0046 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0004t0048 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0004t0051 | 0/0 | 14091 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0004t0065 | 0/0 | 14061 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0004t0066 | 0/0 | 14061 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0004t0081 | 0/0 | 14059 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0004t0084 | 0/0 | 14059 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0005t0004 | 0/0 | 14055 | 10 | 0 | 0 | 10 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0005t0012 | 0/0 | 14055 | 4 | 1 | 0 | 3 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0005t0092 | 0/0 | 14062 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0009t0001 | 0/0 | 14059 | 2 | 0 | 0 | 2 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0009t0002 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0009t0005 | 0/0 | 14055 | 2 | 1 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0009t0008 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0009t0023 | 0/0 | 14061 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0009t0028 | 0/0 | 14061 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0024t0024 | 0/0 | 14055 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0024t0070 | 0/0 | 14065 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0034t0006 | 0/0 | 14060 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0036t0047 | 0/0 | 14055 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0037t0002 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0039t0045 | 0/0 | 14059 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0045t0057 | 0/0 | 14057 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0046t0054 | 0/0 | 14062 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0049t0004 | 0/0 | 14055 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0056t0003 | 0/0 | 14059 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0001c0069t0052 | 0/0 | 14056 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002c0003t0001 | 0/0 | 14059 | 28 | 0 | 8 | 20 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002c0003t0008 | 0/0 | 14059 | 3 | 0 | 1 | 2 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002c0003t0014 | 0/0 | 14057 | 2 | 0 | 0 | 0 | 0 | 2 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002c0003t0020 | 0/0 | 14061 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002c0003t0060 | 0/0 | 14057 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002c0003t0061 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002c0003t0063 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002c0003t0064 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002c0003t0077 | 0/0 | 14060 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002c0015t0001 | 0/0 | 14059 | 2 | 0 | 0 | 2 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002c0015t0014 | 0/0 | 14057 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002c0028t0001 | 0/0 | 14059 | 2 | 0 | 0 | 2 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002c0047t0008 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002c0052t0008 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0002c0057t0001 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0007t0001 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0007t0003 | 0/0 | 14059 | 3 | 0 | 0 | 2 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0007t0004 | 0/0 | 14055 | 2 | 0 | 0 | 2 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0007t0006 | 0/0 | 14060 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0007t0009 | 0/0 | 14060 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0007t0022 | 0/0 | 14059 | 3 | 3 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0007t0023 | 0/0 | 14061 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0007t0075 | 0/0 | 14058 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0007t0079 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0012t0006 | 0/0 | 14060 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0012t0009 | 0/0 | 14060 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0030t0004 | 0/0 | 14055 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0030t0025 | 0/0 | 14057 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0058t0076 | 0/0 | 14058 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0059t0055 | 0/0 | 14053 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0003c0066t0053 | 0/0 | 14063 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0004c0006t0002 | 0/0 | 14059 | 9 | 0 | 1 | 5 | 0 | 3 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0004c0006t0003 | 0/0 | 14059 | 3 | 0 | 0 | 3 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0004c0006t0049 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0004c0006t0087 | 0/0 | 14065 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0004c0029t0003 | 0/0 | 14059 | 2 | 0 | 0 | 2 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0004c0061t0003 | 0/0 | 14059 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0004c0062t0002 | 0/0 | 14059 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0005c0008t0002 | 0/0 | 14059 | 7 | 0 | 5 | 0 | 1 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0005c0008t0013 | 0/0 | 14061 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0005c0008t0083 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0005c0008t0093 | 0/0 | 14059 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0005c0020t0002 | 0/0 | 14059 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0005c0020t0013 | 1/0 | 14061 | 1 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0005c0027t0003 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0005c0027t0006 | 0/0 | 14060 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0006c0010t0002 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0006c0010t0011 | 0/0 | 14062 | 3 | 3 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0006c0010t0072 | 0/0 | 14066 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0006c0025t0009 | 0/0 | 14060 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0006c0025t0059 | 0/0 | 14057 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0007c0014t0011 | 0/0 | 14062 | 3 | 3 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0007c0018t0019 | 0/0 | 14057 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0008c0011t0017 | 0/0 | 14059 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0008c0011t0030 | 0/0 | 14061 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0008c0011t0078 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0008c0043t0017 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0009c0013t0010 | 0/0 | 14061 | 4 | 4 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0010c0016t0016 | 0/0 | 14058 | 3 | 3 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0011c0017t0002 | 0/0 | 14059 | 2 | 0 | 0 | 2 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0011c0017t0086 | 0/0 | 14061 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0012c0031t0019 | 0/0 | 14057 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0012c0031t0089 | 0/0 | 14057 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0013c0026t0029 | 0/0 | 14057 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0014c0022t0038 | 0/0 | 14055 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0014c0022t0040 | 0/0 | 14055 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0015c0023t0037 | 0/0 | 14055 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0015c0023t0094 | 0/0 | 14055 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0016c0019t0005 | 0/0 | 14055 | 2 | 0 | 2 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0017c0021t0031 | 0/0 | 14057 | 2 | 0 | 0 | 0 | 1 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0018c0032t0033 | 0/0 | 14059 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0019c0068t0012 | 0/0 | 14055 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0020c0041t0002 | 0/0 | 14059 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0021c0044t0074 | 0/0 | 14057 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0022c0042t0024 | 0/0 | 14055 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0023c0035t0003 | 0/0 | 14059 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0024c0051t0015 | 0/0 | 14057 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0025c0053t0062 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0026c0054t0001 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0027c0055t0020 | 0/0 | 14061 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0028c0050t0025 | 0/0 | 14057 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0029c0038t0003 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0030c0040t0002 | 0/0 | 14059 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0031c0048t0002 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0032c0065t0041 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0033c0064t0068 | 0/0 | 14061 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0034c0063t0008 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0035c0060t0042 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0036c0067t0034 | 0/0 | 14061 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| a0037c0033t0073 | 0/0 | 14055 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | copy fasta | chr6 | 159964082 | 160116504 |
| actghapid | 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0005g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0006g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0006g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0006g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0006g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0006g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0008g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0010g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0013g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0013g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0013g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0014g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0021g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0021g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0021g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0026g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0026g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0030g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0032g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0032g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0035g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0035g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0043g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0069g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0001t0085g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0006g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0006g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0007g0056 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0007g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0007g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0007g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0007g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0009g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0009g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0009g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0010g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0015g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0015g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0015g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0018g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0018g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0018g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0023g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0027g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0028g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0036g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0036g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0039g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0050g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0056g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0058g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0067g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0071g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0080g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0082g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0088g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0090g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0002t0091g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0020g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0027g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0034g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0044g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0046g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0048g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0051g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0065g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0066g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0081g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0004t0084g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0005t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0005t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0005t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0005t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0005t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0005t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0005t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0005t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0005t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0005t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0005t0012g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0005t0012g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0005t0012g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0005t0012g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0005t0092g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0009t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0009t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0009t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0009t0005g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0009t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0009t0008g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0009t0023g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0009t0028g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0024t0024g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0024t0070g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0034t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0036t0047g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0037t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0039t0045g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0045t0057g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0046t0054g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0049t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0056t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0001c0069t0052g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0008g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0008g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0008g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0014g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0014g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0020g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0060g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0061g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0063g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0064g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0003t0077g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0015t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0015t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0015t0014g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0028t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0028t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0047t0008g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0052t0008g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0002c0057t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0007t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0007t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0007t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0007t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0007t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0007t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0007t0006g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0007t0009g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0007t0022g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0007t0022g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0007t0022g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0007t0023g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0007t0075g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0007t0079g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0012t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0012t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0012t0009g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0012t0009g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0030t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0030t0025g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0058t0076g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0059t0055g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0003c0066t0053g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0004c0006t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0004c0006t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0004c0006t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0004c0006t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0004c0006t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0004c0006t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0004c0006t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0004c0006t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0004c0006t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0004c0006t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0004c0006t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0004c0006t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0004c0006t0049g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0004c0006t0087g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0004c0029t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0004c0029t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0004c0061t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0004c0062t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0005c0008t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0005c0008t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0005c0008t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0005c0008t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0005c0008t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0005c0008t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0005c0008t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0005c0008t0013g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0005c0008t0083g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0005c0008t0093g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0005c0020t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0005c0020t0013g0059 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0005c0027t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0005c0027t0006g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0006c0010t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0006c0010t0011g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0006c0010t0011g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0006c0010t0011g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0006c0010t0072g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0006c0025t0009g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0006c0025t0059g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0007c0014t0011g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0007c0014t0011g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0007c0014t0011g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0007c0018t0019g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0007c0018t0019g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0008c0011t0017g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0008c0011t0017g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0008c0011t0030g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0008c0011t0078g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0008c0043t0017g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0009c0013t0010g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0009c0013t0010g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0009c0013t0010g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0009c0013t0010g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0010c0016t0016g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0010c0016t0016g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0010c0016t0016g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0011c0017t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0011c0017t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0011c0017t0086g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0012c0031t0019g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0012c0031t0089g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0013c0026t0029g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0013c0026t0029g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0014c0022t0038g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0014c0022t0040g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0015c0023t0037g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0015c0023t0094g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0016c0019t0005g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0016c0019t0005g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0017c0021t0031g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0017c0021t0031g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0018c0032t0033g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0018c0032t0033g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0019c0068t0012g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0020c0041t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0021c0044t0074g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0022c0042t0024g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0023c0035t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0024c0051t0015g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0025c0053t0062g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0026c0054t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0027c0055t0020g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0028c0050t0025g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0029c0038t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0030c0040t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0031c0048t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0032c0065t0041g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0033c0064t0068g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0034c0063t0008g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0035c0060t0042g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0036c0067t0034g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| a0037c0033t0073g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0085 | g0294 | EUR | GBR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00140 | hp2 | a0001 | c0002 | t0007 | g0091 | EUR | GBR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00280 | hp1 | a0001 | c0001 | t0013 | g0006 | EUR | FIN | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00280 | hp2 | a0001 | c0001 | t0032 | g0040 | EUR | FIN | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0119 | EUR | FIN | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00323 | hp2 | a0001 | c0002 | t0082 | g0007 | EUR | FIN | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00408 | hp1 | a0028 | c0050 | t0025 | g0227 | EAS | CHS | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00408 | hp2 | a0001 | c0002 | t0090 | g0133 | EAS | CHS | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00423 | hp1 | a0003 | c0030 | t0025 | g0257 | EAS | CHS | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00423 | hp2 | a0002 | c0003 | t0001 | g0277 | EAS | CHS | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00438 | hp1 | a0002 | c0028 | t0001 | g0262 | EAS | CHS | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00438 | hp2 | a0002 | c0052 | t0008 | g0023 | EAS | CHS | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00544 | hp1 | a0001 | c0009 | t0028 | g0229 | EAS | CHS | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | CHS | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00597 | hp1 | a0004 | c0006 | t0002 | g0073 | EAS | CHS | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00597 | hp2 | a0001 | c0004 | t0065 | g0200 | EAS | CHS | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00621 | hp1 | a0033 | c0064 | t0068 | g0221 | EAS | CHS | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00621 | hp2 | a0002 | c0003 | t0020 | g0278 | EAS | CHS | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00639 | hp1 | a0030 | c0040 | t0002 | g0291 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00639 | hp2 | a0004 | c0006 | t0002 | g0075 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00642 | hp1 | a0001 | c0002 | t0036 | g0290 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00642 | hp2 | a0023 | c0035 | t0003 | g0245 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00733 | hp1 | a0005 | c0008 | t0002 | g0032 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00733 | hp2 | a0001 | c0002 | t0007 | g0060 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00735 | hp1 | a0001 | c0002 | t0007 | g0061 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0114 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00738 | hp1 | a0001 | c0004 | t0002 | g0065 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00738 | hp2 | a0024 | c0051 | t0015 | g0097 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00741 | hp1 | a0005 | c0008 | t0013 | g0104 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0030 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01081 | hp1 | a0001 | c0004 | t0002 | g0064 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01106 | hp1 | a0001 | c0002 | t0023 | g0101 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01106 | hp2 | a0005 | c0027 | t0006 | g0155 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01109 | hp1 | a0012 | c0031 | t0019 | g0165 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0246 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01168 | hp1 | a0002 | c0003 | t0001 | g0191 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01168 | hp2 | a0001 | c0001 | t0013 | g0146 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01169 | hp1 | a0001 | c0001 | t0035 | g0113 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01169 | hp2 | a0001 | c0001 | t0013 | g0145 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01175 | hp1 | a0005 | c0020 | t0002 | g0031 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01175 | hp2 | a0001 | c0002 | t0080 | g0054 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01192 | hp1 | a0002 | c0003 | t0008 | g0148 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01192 | hp2 | a0001 | c0001 | t0032 | g0041 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01243 | hp1 | a0001 | c0004 | t0027 | g0287 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01255 | hp1 | a0005 | c0008 | t0093 | g0295 | AMR | CLM | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0120 | AMR | CLM | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01258 | hp1 | a0001 | c0002 | t0088 | g0063 | AMR | CLM | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01258 | hp2 | a0002 | c0003 | t0001 | g0001 | AMR | CLM | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | CLM | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01261 | hp2 | a0005 | c0008 | t0002 | g0033 | AMR | CLM | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01346 | hp1 | a0005 | c0008 | t0002 | g0077 | AMR | CLM | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0100 | AMR | CLM | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01358 | hp1 | a0002 | c0003 | t0001 | g0212 | AMR | CLM | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01358 | hp2 | a0001 | c0036 | t0047 | g0248 | AMR | CLM | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01361 | hp1 | a0005 | c0008 | t0002 | g0029 | AMR | CLM | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0249 | AMR | CLM | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01433 | hp1 | a0001 | c0002 | t0036 | g0289 | AMR | CLM | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01433 | hp2 | a0001 | c0002 | t0006 | g0198 | AMR | CLM | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01496 | hp1 | a0002 | c0003 | t0001 | g0001 | AMR | CLM | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01496 | hp2 | a0005 | c0008 | t0002 | g0296 | AMR | CLM | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01515 | hp1 | a0001 | c0001 | t0021 | g0045 | EUR | IBS | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01515 | hp2 | a0005 | c0008 | t0002 | g0099 | EUR | IBS | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01517 | hp1 | a0001 | c0001 | t0021 | g0046 | EUR | IBS | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01517 | hp2 | a0001 | c0002 | t0006 | g0197 | EUR | IBS | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01884 | hp1 | a0010 | c0016 | t0016 | g0169 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01884 | hp2 | a0001 | c0009 | t0005 | g0144 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01891 | hp1 | a0001 | c0002 | t0007 | g0055 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01891 | hp2 | a0006 | c0010 | t0002 | g0010 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0256 | AMR | PEL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01934 | hp2 | a0001 | c0001 | t0035 | g0053 | AMR | PEL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01943 | hp1 | a0002 | c0003 | t0001 | g0193 | AMR | PEL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01943 | hp2 | a0016 | c0019 | t0005 | g0138 | AMR | PEL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01952 | hp1 | a0002 | c0003 | t0001 | g0189 | AMR | PEL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01952 | hp2 | a0016 | c0019 | t0005 | g0118 | AMR | PEL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01975 | hp1 | a0002 | c0003 | t0001 | g0188 | AMR | PEL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01975 | hp2 | a0001 | c0001 | t0021 | g0044 | AMR | PEL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01981 | hp1 | a0002 | c0003 | t0001 | g0175 | AMR | PEL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0117 | AMR | PEL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02040 | hp1 | a0004 | c0006 | t0003 | g0216 | EAS | KHV | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02040 | hp2 | a0002 | c0003 | t0008 | g0085 | EAS | KHV | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02055 | hp1 | a0013 | c0026 | t0029 | g0149 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02055 | hp2 | a0001 | c0004 | t0034 | g0126 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02132 | hp1 | a0002 | c0003 | t0001 | g0255 | EAS | KHV | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02132 | hp2 | a0001 | c0037 | t0002 | g0079 | EAS | KHV | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02135 | hp1 | a0002 | c0003 | t0001 | g0199 | EAS | KHV | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02145 | hp1 | a0006 | c0025 | t0009 | g0139 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02145 | hp2 | a0001 | c0034 | t0006 | g0035 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02155 | hp1 | a0002 | c0015 | t0014 | g0298 | EAS | CDX | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02155 | hp2 | a0001 | c0004 | t0001 | g0222 | EAS | CDX | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02165 | hp1 | a0001 | c0002 | t0091 | g0292 | EAS | CDX | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02165 | hp2 | a0004 | c0006 | t0003 | g0217 | EAS | CDX | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02257 | hp1 | a0001 | c0005 | t0012 | g0167 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02257 | hp2 | a0001 | c0002 | t0007 | g0058 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02258 | hp1 | a0003 | c0058 | t0076 | g0070 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02258 | hp2 | a0001 | c0002 | t0015 | g0009 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02280 | hp1 | a0010 | c0016 | t0016 | g0150 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02280 | hp2 | a0007 | c0018 | t0019 | g0238 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0115 | AMR | PEL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02293 | hp2 | a0001 | c0004 | t0001 | g0240 | AMR | PEL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02451 | hp1 | a0001 | c0001 | t0043 | g0036 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02451 | hp2 | a0003 | c0012 | t0006 | g0284 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02572 | hp1 | a0018 | c0032 | t0033 | g0086 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02572 | hp2 | a0001 | c0004 | t0046 | g0273 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02602 | hp1 | a0001 | c0056 | t0003 | g0154 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02602 | hp2 | a0001 | c0002 | t0050 | g0242 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02630 | hp1 | a0001 | c0001 | t0026 | g0269 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02630 | hp2 | a0006 | c0010 | t0011 | g0122 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02647 | hp1 | a0009 | c0013 | t0010 | g0160 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02647 | hp2 | a0001 | c0002 | t0039 | g0233 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0116 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02683 | hp2 | a0004 | c0006 | t0087 | g0081 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02698 | hp1 | a0001 | c0002 | t0067 | g0247 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02723 | hp1 | a0003 | c0007 | t0022 | g0106 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02723 | hp2 | a0008 | c0011 | t0017 | g0152 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02735 | hp1 | a0003 | c0059 | t0055 | g0171 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02735 | hp2 | a0001 | c0001 | t0069 | g0232 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02738 | hp1 | a0001 | c0004 | t0003 | g0210 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02738 | hp2 | a0004 | c0006 | t0002 | g0128 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02818 | hp1 | a0018 | c0032 | t0033 | g0087 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02818 | hp2 | a0003 | c0012 | t0009 | g0088 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02886 | hp1 | a0003 | c0007 | t0079 | g0137 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02886 | hp2 | a0001 | c0001 | t0026 | g0268 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02895 | hp1 | a0007 | c0014 | t0011 | g0092 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02895 | hp2 | a0008 | c0011 | t0078 | g0008 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02896 | hp1 | a0009 | c0013 | t0010 | g0159 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02896 | hp2 | a0007 | c0014 | t0011 | g0094 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02897 | hp1 | a0007 | c0014 | t0011 | g0093 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02897 | hp2 | a0009 | c0013 | t0010 | g0158 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02922 | hp1 | a0001 | c0001 | t0030 | g0105 | AFR | ESN | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02922 | hp2 | a0008 | c0011 | t0030 | g0124 | AFR | ESN | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02965 | hp1 | a0001 | c0046 | t0054 | g0281 | AFR | ESN | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02965 | hp2 | a0006 | c0010 | t0011 | g0123 | AFR | ESN | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02976 | hp1 | a0001 | c0002 | t0071 | g0194 | AFR | ESN | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02976 | hp2 | a0021 | c0044 | t0074 | g0111 | AFR | ESN | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03041 | hp1 | a0006 | c0025 | t0059 | g0288 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03041 | hp2 | a0001 | c0002 | t0018 | g0236 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03098 | hp1 | a0003 | c0007 | t0022 | g0107 | AFR | MSL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03098 | hp2 | a0022 | c0042 | t0024 | g0151 | AFR | MSL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03130 | hp1 | a0006 | c0010 | t0072 | g0196 | AFR | ESN | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03130 | hp2 | a0003 | c0012 | t0009 | g0095 | AFR | ESN | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03139 | hp1 | a0006 | c0010 | t0011 | g0125 | AFR | ESN | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03139 | hp2 | a0003 | c0012 | t0006 | g0285 | AFR | ESN | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03195 | hp1 | a0036 | c0067 | t0034 | g0110 | AFR | ESN | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03195 | hp2 | a0037 | c0033 | t0073 | g0140 | AFR | ESN | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03209 | hp1 | a0014 | c0022 | t0040 | g0270 | AFR | MSL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03209 | hp2 | a0010 | c0016 | t0016 | g0170 | AFR | MSL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03225 | hp1 | a0001 | c0004 | t0044 | g0153 | AFR | MSL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03225 | hp2 | a0001 | c0002 | t0027 | g0052 | AFR | MSL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03239 | hp1 | a0001 | c0002 | t0009 | g0047 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03239 | hp2 | a0003 | c0007 | t0009 | g0048 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03453 | hp1 | a0008 | c0011 | t0017 | g0195 | AFR | MSL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03453 | hp2 | a0001 | c0069 | t0052 | g0164 | AFR | MSL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03486 | hp1 | a0003 | c0007 | t0075 | g0147 | AFR | MSL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03486 | hp2 | a0001 | c0002 | t0028 | g0034 | AFR | MSL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03490 | hp1 | a0001 | c0002 | t0009 | g0102 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0230 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03492 | hp1 | a0001 | c0002 | t0007 | g0066 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03492 | hp2 | a0001 | c0002 | t0009 | g0103 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03516 | hp1 | a0001 | c0009 | t0002 | g0068 | AFR | ESN | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03516 | hp2 | a0001 | c0002 | t0015 | g0127 | AFR | ESN | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03540 | hp1 | a0001 | c0002 | t0007 | g0089 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03540 | hp2 | a0009 | c0013 | t0010 | g0161 | AFR | GWD | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | MSL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03579 | hp2 | a0003 | c0007 | t0022 | g0108 | AFR | MSL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03654 | hp1 | a0004 | c0006 | t0002 | g0071 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03654 | hp2 | a0001 | c0004 | t0081 | g0112 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03669 | hp1 | a0004 | c0006 | t0002 | g0130 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03669 | hp2 | a0001 | c0004 | t0066 | g0174 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03688 | hp1 | a0001 | c0001 | t0008 | g0042 | SAS | STU | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03688 | hp2 | a0017 | c0021 | t0031 | g0004 | SAS | STU | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03710 | hp1 | a0002 | c0003 | t0014 | g0173 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03710 | hp2 | a0001 | c0009 | t0005 | g0143 | SAS | PJL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03831 | hp1 | a0005 | c0008 | t0002 | g0051 | SAS | BEB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03831 | hp2 | a0001 | c0039 | t0045 | g0228 | SAS | BEB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03834 | hp1 | a0004 | c0061 | t0003 | g0266 | SAS | BEB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0293 | SAS | BEB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0028 | SAS | BEB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03927 | hp2 | a0002 | c0003 | t0014 | g0177 | SAS | BEB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03942 | hp1 | a0003 | c0030 | t0004 | g0049 | SAS | BEB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03942 | hp2 | a0003 | c0066 | t0053 | g0162 | SAS | BEB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG04115 | hp1 | a0003 | c0007 | t0003 | g0172 | SAS | STU | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0231 | SAS | STU | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG04204 | hp1 | a0001 | c0049 | t0004 | g0090 | SAS | STU | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG04204 | hp2 | a0004 | c0062 | t0002 | g0050 | SAS | STU | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG04228 | hp1 | a0020 | c0041 | t0002 | g0013 | SAS | STU | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0121 | SAS | STU | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18522 | hp1 | a0032 | c0065 | t0041 | g0283 | AFR | YRI | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18522 | hp2 | a0001 | c0002 | t0058 | g0234 | AFR | YRI | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18906 | hp1 | a0003 | c0007 | t0023 | g0109 | AFR | YRI | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18906 | hp2 | a0015 | c0023 | t0094 | g0096 | AFR | YRI | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18942 | hp1 | a0001 | c0005 | t0004 | g0027 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18942 | hp2 | a0002 | c0003 | t0001 | g0241 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18943 | hp1 | a0001 | c0004 | t0003 | g0190 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18943 | hp2 | a0001 | c0005 | t0004 | g0014 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18945 | hp1 | a0001 | c0005 | t0004 | g0026 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18946 | hp1 | a0002 | c0003 | t0063 | g0207 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18946 | hp2 | a0001 | c0005 | t0004 | g0083 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18948 | hp1 | a0002 | c0003 | t0001 | g0260 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18948 | hp2 | a0001 | c0005 | t0012 | g0184 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18950 | hp1 | a0002 | c0003 | t0064 | g0213 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18950 | hp2 | a0001 | c0005 | t0004 | g0012 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18951 | hp1 | a0001 | c0004 | t0002 | g0132 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18951 | hp2 | a0034 | c0063 | t0008 | g0076 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18952 | hp1 | a0025 | c0053 | t0062 | g0166 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18952 | hp2 | a0002 | c0003 | t0001 | g0204 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18954 | hp1 | a0001 | c0009 | t0008 | g0011 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18954 | hp2 | a0001 | c0004 | t0003 | g0203 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18959 | hp1 | a0003 | c0007 | t0004 | g0074 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18959 | hp2 | a0027 | c0055 | t0020 | g0183 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18960 | hp1 | a0002 | c0003 | t0001 | g0179 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18960 | hp2 | a0005 | c0027 | t0003 | g0003 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18963 | hp1 | a0004 | c0006 | t0002 | g0082 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18963 | hp2 | a0003 | c0007 | t0006 | g0272 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18964 | hp1 | a0001 | c0009 | t0001 | g0181 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18964 | hp2 | a0003 | c0007 | t0001 | g0205 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18967 | hp1 | a0001 | c0001 | t0014 | g0300 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18967 | hp2 | a0002 | c0003 | t0061 | g0182 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0299 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18970 | hp2 | a0011 | c0017 | t0002 | g0015 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18972 | hp1 | a0031 | c0048 | t0002 | g0069 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18972 | hp2 | a0004 | c0006 | t0002 | g0080 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18974 | hp1 | a0002 | c0003 | t0001 | g0202 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18974 | hp2 | a0001 | c0001 | t0006 | g0308 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18977 | hp1 | a0001 | c0004 | t0051 | g0178 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18977 | hp2 | a0004 | c0006 | t0002 | g0084 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18979 | hp1 | a0001 | c0004 | t0020 | g0253 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18979 | hp2 | a0003 | c0007 | t0003 | g0254 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18980 | hp1 | a0001 | c0005 | t0092 | g0025 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18980 | hp2 | a0001 | c0001 | t0006 | g0244 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18982 | hp1 | a0002 | c0028 | t0001 | g0263 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18982 | hp2 | a0001 | c0002 | t0003 | g0303 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18983 | hp1 | a0004 | c0029 | t0003 | g0180 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18983 | hp2 | a0004 | c0006 | t0003 | g0176 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18985 | hp2 | a0004 | c0006 | t0002 | g0072 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18987 | hp1 | a0001 | c0009 | t0001 | g0211 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18987 | hp2 | a0001 | c0005 | t0004 | g0022 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18990 | hp1 | a0001 | c0004 | t0048 | g0259 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18990 | hp2 | a0002 | c0003 | t0001 | g0186 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18992 | hp1 | a0004 | c0006 | t0049 | g0226 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18992 | hp2 | a0002 | c0003 | t0001 | g0251 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18994 | hp1 | a0002 | c0003 | t0077 | g0134 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18994 | hp2 | a0001 | c0004 | t0003 | g0223 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18997 | hp1 | a0003 | c0007 | t0004 | g0078 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18997 | hp2 | a0002 | c0047 | t0008 | g0135 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18998 | hp1 | a0001 | c0005 | t0004 | g0018 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18998 | hp2 | a0001 | c0004 | t0003 | g0192 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18999 | hp1 | a0002 | c0003 | t0001 | g0225 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA18999 | hp2 | a0001 | c0005 | t0012 | g0258 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19000 | hp1 | a0002 | c0003 | t0001 | g0218 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19004 | hp1 | a0002 | c0003 | t0001 | g0208 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19004 | hp2 | a0001 | c0005 | t0004 | g0024 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19007 | hp1 | a0001 | c0001 | t0006 | g0219 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19007 | hp2 | a0002 | c0003 | t0001 | g0220 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19009 | hp1 | a0001 | c0002 | t0003 | g0302 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19009 | hp2 | a0002 | c0003 | t0001 | g0265 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19011 | hp1 | a0011 | c0017 | t0002 | g0017 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19011 | hp2 | a0002 | c0003 | t0008 | g0136 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19030 | hp1 | a0001 | c0024 | t0070 | g0282 | AFR | LWK | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19030 | hp2 | a0012 | c0031 | t0089 | g0067 | AFR | LWK | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19043 | hp1 | a0001 | c0002 | t0010 | g0168 | AFR | LWK | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19043 | hp2 | a0001 | c0002 | t0018 | g0237 | AFR | LWK | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19058 | hp1 | a0004 | c0029 | t0003 | g0185 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19058 | hp2 | a0002 | c0015 | t0001 | g0252 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19060 | hp1 | a0001 | c0005 | t0004 | g0019 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19062 | hp1 | a0002 | c0015 | t0001 | g0280 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19062 | hp2 | a0002 | c0003 | t0001 | g0276 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19064 | hp1 | a0001 | c0009 | t0023 | g0131 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19064 | hp2 | a0026 | c0054 | t0001 | g0214 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19066 | hp1 | a0002 | c0003 | t0060 | g0215 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19066 | hp2 | a0001 | c0005 | t0004 | g0021 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19084 | hp1 | a0011 | c0017 | t0086 | g0016 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19084 | hp2 | a0002 | c0057 | t0001 | g0243 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19085 | hp1 | a0001 | c0001 | t0006 | g0264 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19085 | hp2 | a0002 | c0003 | t0001 | g0224 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19087 | hp1 | a0002 | c0003 | t0001 | g0271 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19087 | hp2 | a0001 | c0005 | t0012 | g0209 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19088 | hp1 | a0002 | c0003 | t0001 | g0206 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19088 | hp2 | a0001 | c0002 | t0003 | g0306 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19090 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19090 | hp2 | a0003 | c0007 | t0003 | g0261 | EAS | JPT | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19240 | hp1 | a0019 | c0068 | t0012 | g0279 | AFR | YRI | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA19240 | hp2 | a0007 | c0018 | t0019 | g0239 | AFR | YRI | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA20129 | hp1 | a0001 | c0002 | t0007 | g0057 | AFR | ASW | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA20129 | hp2 | a0001 | c0024 | t0024 | g0201 | AFR | ASW | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA20752 | hp1 | a0001 | c0002 | t0056 | g0156 | EUR | TSI | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA20752 | hp2 | a0017 | c0021 | t0031 | g0005 | EUR | TSI | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA20805 | hp1 | a0001 | c0004 | t0084 | g0098 | EUR | TSI | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA20805 | hp2 | a0001 | c0004 | t0002 | g0129 | EUR | TSI | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02109 | hp1 | a0001 | c0002 | t0015 | g0163 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02109 | hp2 | a0014 | c0022 | t0038 | g0275 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02486 | hp1 | a0013 | c0026 | t0029 | g0297 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02486 | hp2 | a0005 | c0008 | t0083 | g0039 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02559 | hp1 | a0001 | c0001 | t0010 | g0157 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG02559 | hp2 | a0035 | c0060 | t0042 | g0267 | AFR | ACB | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03471 | hp1 | a0008 | c0043 | t0017 | g0038 | AFR | MSL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0274 | AFR | MSL | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG06807 | hp1 | a0029 | c0038 | t0003 | g0286 | AFR | USA | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| HG06807 | hp2 | a0015 | c0023 | t0037 | g0309 | AFR | USA | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA21309 | hp1 | a0001 | c0002 | t0018 | g0235 | AFR | LWK | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| NA21309 | hp2 | a0001 | c0045 | t0057 | g0250 | AFR | LWK | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0007 | g0056 | REF | REF | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| homoSapiens_grch38 | hp1 | a0005 | c0020 | t0013 | g0059 | REF | REF | IGF2R_chr6_159964082_160116504 | IGF2R | chr6 | 159964082 | 160116504 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:160024618
|
A | G | 1 | a0018 | 2 | HG02572.hp1 HG02818.hp1 |
missense_variant | MODERATE | c.560A>G | p.Asn187Ser | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 5/48 | 725/14061 | 560/7476 | 187/2491 | chr6 | 160024618 | ||
| chr6:160027229
|
G | A | 1 | a0037 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.691G>A | p.Gly231Ser | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 6/48 | 856/14061 | 691/7476 | 231/2491 | chr6 | 160027229 | ||
| chr6:160027230
|
G | A | 1 | a0007 | 5 | HG02280.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
missense_variant | MODERATE | c.692G>A | p.Gly231Asp | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 6/48 | 857/14061 | 692/7476 | 231/2491 | chr6 | 160027230 | ||
| chr6:160027232
|
A | G | 2 | a0012a0019 | 3 | HG01109.hp1 NA19030.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.694A>G | p.Thr232Ala | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 6/48 | 859/14061 | 694/7476 | 232/2491 | chr6 | 160027232 | ||
| chr6:160027283
|
C | T | 2 | a0009a0036 | 5 | HG02647.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
missense_variant | MODERATE | c.745C>T | p.Arg249Trp | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 6/48 | 910/14061 | 745/7476 | 249/2491 | chr6 | 160027283 | ||
| chr6:160027292
|
C | G | 7 | a0003a0004a0011others(4): Show | 48 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(45): Show |
missense_variant | MODERATE | c.754C>G | p.Leu252Val | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 6/48 | 919/14061 | 754/7476 | 252/2491 | chr6 | 160027292 | ||
| chr6:160040682
|
G | A | 1 | a0035 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.1438G>A | p.Gly480Arg | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/48 | 1603/14061 | 1438/7476 | 480/2491 | chr6 | 160040682 | ||
| chr6:160046591
|
C | T | 1 | a0013 | 2 | HG02055.hp1 HG02486.hp1 |
missense_variant | MODERATE | c.1997C>T | p.Pro666Leu | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 15/48 | 2162/14061 | 1997/7476 | 666/2491 | chr6 | 160046591 | ||
| chr6:160048478
|
C | G | 1 | a0017 | 2 | HG03688.hp2 NA20752.hp2 |
missense_variant | MODERATE | c.2449C>G | p.Leu817Val | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 18/48 | 2614/14061 | 2449/7476 | 817/2491 | chr6 | 160048478 | ||
| chr6:160048512
|
C | T | 1 | a0020 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.2483C>T | p.Ser828Leu | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 18/48 | 2648/14061 | 2483/7476 | 828/2491 | chr6 | 160048512 | ||
| chr6:160050524
|
G | A | 1 | a0016 | 2 | HG01943.hp2 HG01952.hp2 |
missense_variant | MODERATE | c.2566G>A | p.Gly856Ser | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/48 | 2731/14061 | 2566/7476 | 856/2491 | chr6 | 160050524 | ||
| chr6:160058998
|
G | C | 1 | a0031 | 1 | NA18972.hp1 | missense_variant | MODERATE | c.2991G>C | p.Lys997Asn | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 22/48 | 3156/14061 | 2991/7476 | 997/2491 | chr6 | 160058998 | ||
| chr6:160061560
|
C | T | 2 | a0006a0007 | 12 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(9): Show |
missense_variant | MODERATE | c.3320C>T | p.Thr1107Met | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 24/48 | 3485/14061 | 3320/7476 | 1107/2491 | chr6 | 160061560 | ||
| chr6:160061617
|
A | G | 1 | a0030 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.3377A>G | p.Asn1126Ser | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 24/48 | 3542/14061 | 3377/7476 | 1126/2491 | chr6 | 160061617 | ||
| chr6:160061897
|
C | G | 2 | a0021a0032 | 2 | HG02976.hp2 NA18522.hp1 |
missense_variant | MODERATE | c.3551C>G | p.Thr1184Ser | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 25/48 | 3716/14061 | 3551/7476 | 1184/2491 | chr6 | 160061897 | ||
| chr6:160061927
|
C | T | 1 | a0011 | 3 | NA18970.hp2 NA19011.hp1 NA19084.hp1 |
missense_variant&splice_region_variant | MODERATE | c.3581C>T | p.Ser1194Leu | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 25/48 | 3746/14061 | 3581/7476 | 1194/2491 | chr6 | 160061927 | ||
| chr6:160064518
|
G | A | 3 | a0014a0022a0037 | 4 | HG02109.hp2 HG03098.hp2 HG03195.hp2 others(1): Show |
missense_variant | MODERATE | c.4004G>A | p.Arg1335His | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 28/48 | 4169/14061 | 4004/7476 | 1335/2491 | chr6 | 160064518 | ||
| chr6:160073377
|
A | G | 34 | a0001a0002a0003others(31): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
missense_variant | MODERATE | c.4855A>G | p.Arg1619Gly | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 34/48 | 5020/14061 | 4855/7476 | 1619/2491 | chr6 | 160073377 | ||
| chr6:160073896
|
A | G | 1 | a0010 | 3 | HG01884.hp1 HG02280.hp1 HG03209.hp2 |
missense_variant | MODERATE | c.5087A>G | p.Gln1696Arg | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/48 | 5252/14061 | 5087/7476 | 1696/2491 | chr6 | 160073896 | ||
| chr6:160075935
|
C | T | 1 | a0036 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.5255C>T | p.Ala1752Val | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/48 | 5420/14061 | 5255/7476 | 1752/2491 | chr6 | 160075935 | ||
| chr6:160078349
|
C | T | 1 | a0008 | 5 | HG02723.hp2 HG02895.hp2 HG02922.hp2 others(2): Show |
missense_variant | MODERATE | c.5465C>T | p.Thr1822Met | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 37/48 | 5630/14061 | 5465/7476 | 1822/2491 | chr6 | 160078349 | ||
| chr6:160079593
|
C | T | 1 | a0033 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.5492C>T | p.Ser1831Leu | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 38/48 | 5657/14061 | 5492/7476 | 1831/2491 | chr6 | 160079593 | ||
| chr6:160079596
|
G | A | 2 | a0013a0015 | 4 | HG02055.hp1 HG02486.hp1 HG06807.hp2 others(1): Show |
missense_variant | MODERATE | c.5495G>A | p.Arg1832His | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 38/48 | 5660/14061 | 5495/7476 | 1832/2491 | chr6 | 160079596 | ||
| chr6:160080143
|
G | A | 3 | a0022a0023a0037 | 3 | HG00642.hp2 HG03098.hp2 HG03195.hp2 |
missense_variant | MODERATE | c.5701G>A | p.Val1901Ile | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/48 | 5866/14061 | 5701/7476 | 1901/2491 | chr6 | 160080143 | ||
| chr6:160080166
|
A | G | 1 | a0029 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.5724A>G | p.Ile1908Met | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/48 | 5889/14061 | 5724/7476 | 1908/2491 | chr6 | 160080166 | ||
| chr6:160083984
|
G | C | 1 | a0028 | 1 | HG00408.hp1 | missense_variant | MODERATE | c.5868G>C | p.Lys1956Asn | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 40/48 | 6033/14061 | 5868/7476 | 1956/2491 | chr6 | 160083984 | ||
| chr6:160084175
|
A | G | 6 | a0002a0025a0026others(3): Show | 52 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(49): Show |
missense_variant | MODERATE | c.6059A>G | p.Asn2020Ser | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 40/48 | 6224/14061 | 6059/7476 | 2020/2491 | chr6 | 160084175 | ||
| chr6:160090023
|
A | G | 1 | a0027 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.6575A>G | p.Asn2192Ser | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/48 | 6740/14061 | 6575/7476 | 2192/2491 | chr6 | 160090023 | ||
| chr6:160102544
|
G | A | 1 | a0024 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.6868G>A | p.Gly2290Arg | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 46/48 | 7033/14061 | 6868/7476 | 2290/2491 | chr6 | 160102544 | ||
| chr6:160102598
|
G | A | 1 | a0019 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.6922G>A | p.Ala2308Thr | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 46/48 | 7087/14061 | 6922/7476 | 2308/2491 | chr6 | 160102598 | ||
| chr6:160103793
|
A | G | 1 | a0026 | 1 | NA19064.hp2 | missense_variant | MODERATE | c.7043A>G | p.Asn2348Ser | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 47/48 | 7208/14061 | 7043/7476 | 2348/2491 | chr6 | 160103793 | ||
| chr6:160104984
|
C | T | 1 | a0025 | 1 | NA18952.hp1 | missense_variant | MODERATE | c.7376C>T | p.Ala2459Val | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 7541/14061 | 7376/7476 | 2459/2491 | chr6 | 160104984 | ||
| chr6:160111503
|
A | G | 1 | a0001 | 1 | HG03669.hp2 | splice_region_variant | LOW | c.*6419A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | chr6 | 160111503 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:159969357
|
C | T | 1 | a0001c0069 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.111C>T | p.Ser37Ser | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/48 | 276/14061 | 111/7476 | 37/2491 | chr6 | 159969357 | ||
| chr6:160032709
|
C | T | 1 | a0002c0028 | 2 | HG00438.hp1 NA18982.hp1 |
synonymous_variant | LOW | c.1041C>T | p.Ser347Ser | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 8/48 | 1206/14061 | 1041/7476 | 347/2491 | chr6 | 160032709 | ||
| chr6:160032946
|
A | G | 32 | a0001c0004a0001c0009a0001c0049others(29): Show | 135 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
synonymous_variant | LOW | c.1050A>G | p.Ser350Ser | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 9/48 | 1215/14061 | 1050/7476 | 350/2491 | chr6 | 160032946 | ||
| chr6:160034518
|
C | T | 1 | a0002c0057 | 1 | NA19084.hp2 | synonymous_variant | LOW | c.1311C>T | p.Thr437Thr | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/48 | 1476/14061 | 1311/7476 | 437/2491 | chr6 | 160034518 | ||
| chr6:160043257
|
G | A | 34 | a0001c0004a0001c0009a0001c0049others(31): Show | 143 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(140): Show |
synonymous_variant | LOW | c.1590G>A | p.Gly530Gly | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/48 | 1755/14061 | 1590/7476 | 530/2491 | chr6 | 160043257 | ||
| chr6:160046592
|
G | A | 1 | a0004c0061 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.1998G>A | p.Pro666Pro | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 15/48 | 2163/14061 | 1998/7476 | 666/2491 | chr6 | 160046592 | ||
| chr6:160047246
|
A | G | 45 | a0001c0002a0001c0004a0001c0005others(42): Show | 192 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(189): Show |
synonymous_variant | LOW | c.2139A>G | p.Thr713Thr | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 16/48 | 2304/14061 | 2139/7476 | 713/2491 | chr6 | 160047246 | ||
| chr6:160048510
|
A | G | 1 | a0032c0065 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.2481A>G | p.Ala827Ala | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 18/48 | 2646/14061 | 2481/7476 | 827/2491 | chr6 | 160048510 | ||
| chr6:160050583
|
C | T | 1 | a0001c0046 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.2625C>T | p.Cys875Cys | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/48 | 2790/14061 | 2625/7476 | 875/2491 | chr6 | 160050583 | ||
| chr6:160061757
|
C | T | 1 | a0001c0045 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.3411C>T | p.Ser1137Ser | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 25/48 | 3576/14061 | 3411/7476 | 1137/2491 | chr6 | 160061757 | ||
| chr6:160068372
|
G | A | 2 | a0001c0034a0003c0012 | 5 | HG02145.hp2 HG02451.hp2 HG02818.hp2 others(2): Show |
synonymous_variant | LOW | c.4239G>A | p.Pro1413Pro | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 30/48 | 4404/14061 | 4239/7476 | 1413/2491 | chr6 | 160068372 | ||
| chr6:160072802
|
G | A | 5 | a0001c0005a0001c0049a0003c0030others(2): Show | 21 | HG00423.hp1 HG01109.hp1 HG02257.hp1 others(18): Show |
synonymous_variant | LOW | c.4608G>A | p.Ala1536Ala | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 33/48 | 4773/14061 | 4608/7476 | 1536/2491 | chr6 | 160072802 | ||
| chr6:160073283
|
C | T | 1 | a0003c0058 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.4761C>T | p.Val1587Val | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 34/48 | 4926/14061 | 4761/7476 | 1587/2491 | chr6 | 160073283 | ||
| chr6:160073358
|
C | T | 1 | a0001c0039 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.4836C>T | p.Phe1612Phe | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 34/48 | 5001/14061 | 4836/7476 | 1612/2491 | chr6 | 160073358 | ||
| chr6:160079780
|
C | T | 1 | a0032c0065 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.5679C>T | p.Cys1893Cys | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 38/48 | 5844/14061 | 5679/7476 | 1893/2491 | chr6 | 160079780 | ||
| chr6:160084128
|
C | T | 1 | a0015c0023 | 2 | HG06807.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.6012C>T | p.Asp2004Asp | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 40/48 | 6177/14061 | 6012/7476 | 2004/2491 | chr6 | 160084128 | ||
| chr6:160084167
|
C | G | 68 | a0001c0001a0001c0002a0001c0004others(65): Show | 308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
synonymous_variant | LOW | c.6051C>G | p.Leu2017Leu | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 40/48 | 6216/14061 | 6051/7476 | 2017/2491 | chr6 | 160084167 | ||
| chr6:160089173
|
T | C | 1 | a0001c0036 | 1 | HG01358.hp2 | synonymous_variant | LOW | c.6387T>C | p.Pro2129Pro | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 43/48 | 6552/14061 | 6387/7476 | 2129/2491 | chr6 | 160089173 | ||
| chr6:160089197
|
G | C | 1 | a0004c0029 | 2 | NA18983.hp1 NA19058.hp1 |
synonymous_variant | LOW | c.6411G>C | p.Gly2137Gly | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 43/48 | 6576/14061 | 6411/7476 | 2137/2491 | chr6 | 160089197 | ||
| chr6:160096449
|
C | T | 23 | a0001c0005a0001c0024a0001c0049others(20): Show | 88 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(85): Show |
synonymous_variant | LOW | c.6666C>T | p.Leu2222Leu | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/48 | 6831/14061 | 6666/7476 | 2222/2491 | chr6 | 160096449 | ||
| chr6:160103779
|
T | C | 2 | a0013c0026a0015c0023 | 4 | HG02055.hp1 HG02486.hp1 HG06807.hp2 others(1): Show |
synonymous_variant | LOW | c.7029T>C | p.Cys2343Cys | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 47/48 | 7194/14061 | 7029/7476 | 2343/2491 | chr6 | 160103779 | ||
| chr6:160104676
|
G | C | 1 | a0001c0037 | 1 | HG02132.hp2 | splice_region_variant&synonymous_variant | LOW | c.7068G>C | p.Val2356Val | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 7233/14061 | 7068/7476 | 2356/2491 | chr6 | 160104676 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:159969199
|
T | G | 1 | a0015c0023t0037 | 1 | HG06807.hp2 | 5_prime_UTR_variant | MODIFIER | c.-48T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/48 | 48 | chr6 | 159969199 | |||||
| chr6:159969209
|
T | C | 88 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(85): Show | 159 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(156): Show |
5_prime_UTR_variant | MODIFIER | c.-38T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/48 | 38 | chr6 | 159969209 | |||||
| chr6:159969239
|
C | G | 2 | a0001c0002t0071a0006c0010t0072 | 2 | HG02976.hp1 HG03130.hp1 |
5_prime_UTR_variant | MODIFIER | c.-8C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/48 | 8 | chr6 | 159969239 | |||||
| chr6:159969241
|
G | C | 1 | a0014c0022t0038 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-6G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/48 | 6 | chr6 | 159969241 | |||||
| chr6:160105307
|
C | T | 1 | a0001c0024t0070 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*223C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 223 | chr6 | 160105307 | |||||
| chr6:160105417
|
G | T | 1 | a0001c0001t0069 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*333G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 333 | chr6 | 160105417 | |||||
| chr6:160105506
|
G | GA | 11 | a0001c0002t0039a0001c0024t0024a0002c0003t0077others(8): Show | 13 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*431dupA | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 432 | INFO_REALIGN_3_PRIME | chr6 | 160105506 | ||||
| chr6:160105606
|
G | A | 10 | a0001c0005t0004a0001c0005t0012a0001c0024t0070others(7): Show | 23 | HG00408.hp1 HG00423.hp1 HG02257.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*522G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 522 | chr6 | 160105606 | |||||
| chr6:160105654
|
T | G | 1 | a0013c0026t0029 | 2 | HG02055.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*570T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 570 | chr6 | 160105654 | |||||
| chr6:160105692
|
GCACA | G | 8 | a0001c0005t0004a0001c0005t0012a0001c0049t0004others(5): Show | 21 | HG00408.hp1 HG00423.hp1 HG02257.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*614_*617delACAC | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 614 | INFO_REALIGN_3_PRIME | chr6 | 160105692 | ||||
| chr6:160105727
|
C | T | 3 | a0013c0026t0029a0015c0023t0037a0015c0023t0094 | 4 | HG02055.hp1 HG02486.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*643C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 643 | chr6 | 160105727 | |||||
| chr6:160105742
|
C | T | 1 | a0005c0008t0093 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*658C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 658 | chr6 | 160105742 | |||||
| chr6:160105802
|
C | T | 1 | a0033c0064t0068 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*718C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 718 | chr6 | 160105802 | |||||
| chr6:160105872
|
TCAAA | T | 61 | a0001c0001t0001a0001c0001t0008a0001c0001t0014others(58): Show | 115 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*792_*795delACAA | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 792 | INFO_REALIGN_3_PRIME | chr6 | 160105872 | ||||
| chr6:160105903
|
GTT | G | 3 | a0008c0011t0017a0008c0011t0078a0008c0043t0017 | 4 | HG02723.hp2 HG02895.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*821_*822delTT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 821 | INFO_REALIGN_3_PRIME | chr6 | 160105903 | ||||
| chr6:160105905
|
T | G | 2 | a0001c0001t0030a0008c0011t0030 | 2 | HG02922.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*821T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 821 | chr6 | 160105905 | |||||
| chr6:160105905
|
T | TTG | 22 | a0001c0001t0001a0001c0001t0008a0001c0002t0090others(19): Show | 58 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*854_*855dupTG | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 856 | INFO_REALIGN_3_PRIME | chr6 | 160105905 | ||||
| chr6:160105905
|
T | TTGTG | 16 | a0001c0002t0023a0001c0002t0028a0001c0002t0067others(13): Show | 16 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*852_*855dupTGTG | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 856 | INFO_REALIGN_3_PRIME | chr6 | 160105905 | ||||
| chr6:160105905
|
T | TTGTGTG | 3 | a0001c0046t0054a0006c0010t0011a0007c0014t0011 | 7 | HG02630.hp2 HG02895.hp1 HG02896.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*850_*855dupTGTGTG | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 856 | INFO_REALIGN_3_PRIME | chr6 | 160105905 | ||||
| chr6:160105905
|
T | TTGTGTGT others(3): Show |
1 | a0006c0010t0072 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*846_*855dupTGTGTG others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 856 | INFO_REALIGN_3_PRIME | chr6 | 160105905 | ||||
| chr6:160105905
|
TTG | T | 76 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(73): Show | 156 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*854_*855delTG | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 854 | INFO_REALIGN_3_PRIME | chr6 | 160105905 | ||||
| chr6:160105905
|
TTGTG | T | 2 | a0003c0059t0055a0017c0021t0031 | 3 | HG02735.hp1 HG03688.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*852_*855delTGTG | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 852 | INFO_REALIGN_3_PRIME | chr6 | 160105905 | ||||
| chr6:160106143
|
C | T | 2 | a0014c0022t0038a0014c0022t0040 | 2 | HG02109.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1059C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 1059 | chr6 | 160106143 | |||||
| chr6:160106148
|
C | A | 7 | a0001c0002t0007a0001c0002t0018a0001c0002t0036others(4): Show | 18 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1064C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 1064 | chr6 | 160106148 | |||||
| chr6:160106183
|
T | TGGGCGGG others(25): Show |
1 | a0001c0004t0051 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1100_*1131dupGGGC others(28): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 1132 | INFO_REALIGN_3_PRIME | chr6 | 160106183 | ||||
| chr6:160106197
|
G | A | 1 | a0001c0002t0058 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1113G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 1113 | chr6 | 160106197 | |||||
| chr6:160106207
|
A | G | 1 | a0011c0017t0086 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1123A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 1123 | chr6 | 160106207 | |||||
| chr6:160106219
|
C | T | 1 | a0001c0002t0039 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1135C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 1135 | chr6 | 160106219 | |||||
| chr6:160106229
|
G | A | 9 | a0001c0002t0039a0001c0024t0024a0003c0007t0079others(6): Show | 9 | HG02109.hp2 HG02559.hp2 HG02647.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1145G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 1145 | chr6 | 160106229 | |||||
| chr6:160106248
|
G | A | 1 | a0001c0001t0043 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1164G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 1164 | chr6 | 160106248 | |||||
| chr6:160106395
|
G | T | 1 | a0037c0033t0073 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1311G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 1311 | chr6 | 160106395 | |||||
| chr6:160106556
|
G | C | 1 | a0001c0002t0090 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1472G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 1472 | chr6 | 160106556 | |||||
| chr6:160106664
|
T | C | 1 | a0013c0026t0029 | 2 | HG02055.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1580T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 1580 | chr6 | 160106664 | |||||
| chr6:160106669
|
G | A | 1 | a0001c0002t0080 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1585G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 1585 | chr6 | 160106669 | |||||
| chr6:160106709
|
G | C | 1 | a0014c0022t0040 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1625G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 1625 | chr6 | 160106709 | |||||
| chr6:160106720
|
G | A | 4 | a0001c0002t0091a0001c0004t0065a0001c0004t0066others(1): Show | 4 | HG00597.hp2 HG02165.hp1 HG03669.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1636G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 1636 | chr6 | 160106720 | |||||
| chr6:160106740
|
C | G | 5 | a0001c0046t0054a0001c0069t0052a0006c0010t0011others(2): Show | 9 | HG02630.hp2 HG02895.hp1 HG02896.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1656C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 1656 | chr6 | 160106740 | |||||
| chr6:160106744
|
C | T | 1 | a0002c0003t0064 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1660C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 1660 | chr6 | 160106744 | |||||
| chr6:160107025
|
T | C | 66 | a0001c0001t0001a0001c0001t0008a0001c0001t0014others(63): Show | 134 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*1941T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 1941 | chr6 | 160107025 | |||||
| chr6:160107033
|
C | G | 3 | a0003c0007t0075a0003c0058t0076a0010c0016t0016 | 5 | HG01884.hp1 HG02258.hp1 HG02280.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1949C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 1949 | chr6 | 160107033 | |||||
| chr6:160107068
|
C | G | 1 | a0001c0004t0084 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1984C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 1984 | chr6 | 160107068 | |||||
| chr6:160107201
|
G | C | 8 | a0001c0002t0071a0001c0004t0034a0001c0004t0044others(5): Show | 9 | HG01109.hp1 HG02055.hp2 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2117G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 2117 | chr6 | 160107201 | |||||
| chr6:160107205
|
T | C | 3 | a0002c0003t0060a0002c0003t0061a0002c0003t0064 | 3 | NA18950.hp1 NA18967.hp2 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2121T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 2121 | chr6 | 160107205 | |||||
| chr6:160107274
|
C | T | 1 | a0001c0002t0050 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2190C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 2190 | chr6 | 160107274 | |||||
| chr6:160107602
|
T | G | 3 | a0001c0001t0021a0001c0001t0032a0001c0039t0045 | 6 | HG00280.hp2 HG01192.hp2 HG01515.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2518T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 2518 | chr6 | 160107602 | |||||
| chr6:160107623
|
C | T | 1 | a0006c0025t0059 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2539C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 2539 | chr6 | 160107623 | |||||
| chr6:160107670
|
A | C | 1 | a0003c0058t0076 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2586A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 2586 | chr6 | 160107670 | |||||
| chr6:160107836
|
T | C | 1 | a0001c0004t0081 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2752T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 2752 | chr6 | 160107836 | |||||
| chr6:160107852
|
C | G | 1 | a0001c0002t0067 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2768C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 2768 | chr6 | 160107852 | |||||
| chr6:160108088
|
C | T | 1 | a0001c0001t0021 | 3 | HG01515.hp1 HG01517.hp1 HG01975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3004C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 3004 | chr6 | 160108088 | |||||
| chr6:160108160
|
C | T | 1 | a0001c0001t0026 | 2 | HG02630.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3076C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 3076 | chr6 | 160108160 | |||||
| chr6:160108202
|
G | A | 5 | a0001c0046t0054a0001c0069t0052a0006c0010t0011others(2): Show | 9 | HG02630.hp2 HG02895.hp1 HG02896.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3118G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 3118 | chr6 | 160108202 | |||||
| chr6:160108205
|
T | A | 4 | a0001c0004t0046a0003c0007t0022a0003c0007t0079others(1): Show | 6 | HG02559.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3121T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 3121 | chr6 | 160108205 | |||||
| chr6:160108382
|
T | G | 1 | a0001c0004t0065 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3298T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 3298 | chr6 | 160108382 | |||||
| chr6:160108389
|
A | C | 34 | a0001c0001t0001a0001c0001t0008a0001c0001t0014others(31): Show | 82 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*3305A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 3305 | chr6 | 160108389 | |||||
| chr6:160108624
|
ATTCCT | A | 7 | a0001c0002t0039a0001c0024t0024a0014c0022t0038others(4): Show | 7 | HG02109.hp2 HG02647.hp2 HG02976.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3552_*3556delTCCT others(1): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 3552 | INFO_REALIGN_3_PRIME | chr6 | 160108624 | ||||
| chr6:160108649
|
CTCTT | C | 6 | a0001c0001t0005a0001c0001t0035a0001c0002t0082others(3): Show | 17 | HG00323.hp1 HG00323.hp2 HG00735.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3576_*3579delTTTC | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 3576 | INFO_REALIGN_3_PRIME | chr6 | 160108649 | ||||
| chr6:160108658
|
TCTTTC | T | 5 | a0001c0046t0054a0001c0069t0052a0006c0010t0011others(2): Show | 9 | HG02630.hp2 HG02895.hp1 HG02896.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3579_*3583delCCTT others(1): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 3579 | INFO_REALIGN_3_PRIME | chr6 | 160108658 | ||||
| chr6:160108663
|
C | T | 63 | a0001c0001t0001a0001c0001t0008a0001c0001t0014others(60): Show | 127 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*3579C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 3579 | chr6 | 160108663 | |||||
| chr6:160108701
|
C | T | 1 | a0013c0026t0029 | 2 | HG02055.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3617C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 3617 | chr6 | 160108701 | |||||
| chr6:160108752
|
G | A | 1 | a0001c0024t0070 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3668G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 3668 | chr6 | 160108752 | |||||
| chr6:160108778
|
G | A | 34 | a0001c0001t0001a0001c0001t0008a0001c0001t0014others(31): Show | 82 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*3694G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 3694 | chr6 | 160108778 | |||||
| chr6:160108829
|
C | T | 1 | a0018c0032t0033 | 2 | HG02572.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3745C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 3745 | chr6 | 160108829 | |||||
| chr6:160108843
|
C | T | 1 | a0001c0004t0048 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3759C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 3759 | chr6 | 160108843 | |||||
| chr6:160109472
|
T | C | 1 | a0001c0002t0088 | 1 | HG01258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4388T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 4388 | chr6 | 160109472 | |||||
| chr6:160109594
|
T | C | 68 | a0001c0001t0001a0001c0001t0008a0001c0001t0014others(65): Show | 136 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*4510T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 4510 | chr6 | 160109594 | |||||
| chr6:160109605
|
C | T | 1 | a0001c0001t0085 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4521C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 4521 | chr6 | 160109605 | |||||
| chr6:160109890
|
A | G | 5 | a0001c0046t0054a0001c0069t0052a0006c0010t0011others(2): Show | 9 | HG02630.hp2 HG02895.hp1 HG02896.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4806A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 4806 | chr6 | 160109890 | |||||
| chr6:160109949
|
G | C | 1 | a0001c0036t0047 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4865G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 4865 | chr6 | 160109949 | |||||
| chr6:160110007
|
G | A | 1 | a0018c0032t0033 | 2 | HG02572.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4923G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 4923 | chr6 | 160110007 | |||||
| chr6:160110411
|
A | G | 34 | a0001c0001t0001a0001c0001t0008a0001c0001t0014others(31): Show | 82 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*5327A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 5327 | chr6 | 160110411 | |||||
| chr6:160110469
|
C | T | 2 | a0001c0002t0088a0001c0045t0057 | 2 | HG01258.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5385C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 5385 | chr6 | 160110469 | |||||
| chr6:160110743
|
A | G | 34 | a0001c0001t0001a0001c0001t0008a0001c0001t0014others(31): Show | 82 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*5659A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 5659 | chr6 | 160110743 | |||||
| chr6:160110793
|
A | G | 1 | a0005c0008t0083 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5709A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 5709 | chr6 | 160110793 | |||||
| chr6:160111043
|
G | A | 9 | a0001c0005t0004a0001c0005t0012a0001c0049t0004others(6): Show | 22 | HG00408.hp1 HG00423.hp1 HG02257.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*5959G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 5959 | chr6 | 160111043 | |||||
| chr6:160111237
|
G | GT | 15 | a0001c0001t0006a0001c0001t0026a0001c0001t0085others(12): Show | 25 | HG00140.hp1 HG00323.hp2 HG01106.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*6163dupT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 6164 | INFO_REALIGN_3_PRIME | chr6 | 160111237 | ||||
| chr6:160111303
|
C | T | 32 | a0001c0001t0001a0001c0001t0008a0001c0001t0014others(29): Show | 79 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*6219C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 6219 | chr6 | 160111303 | |||||
| chr6:160111413
|
A | G | 1 | a0025c0053t0062 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6329A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 48/48 | 6329 | chr6 | 160111413 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:159969398
|
G | A | 2 | a0002c0003t0001g0002a0005c0027t0003g0003 | 2 | NA18960.hp2 NA19090.hp1 |
splice_region_variant&intron_variant | LOW | c.149+3G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159969398 | ||||||
| chr6:159969571
|
G | C | 24 | a0001c0001t0013g0006a0001c0002t0002g0020a0001c0002t0015g0009others(21): Show | 24 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.149+176G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159969571 | ||||||
| chr6:159969574
|
C | G | 1 | a0015c0023t0037g0309 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.149+179C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159969574 | ||||||
| chr6:159969608
|
G | C | 1 | a0001c0001t0005g0028 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.149+213G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159969608 | ||||||
| chr6:159969721
|
C | T | 11 | a0001c0001t0001g0301a0001c0001t0001g0304a0001c0001t0001g0305others(8): Show | 11 | HG02135.hp2 HG02155.hp1 NA18945.hp2 others(8): Show |
intron_variant | MODIFIER | c.149+326C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159969721 | ||||||
| chr6:159969751
|
G | A | 5 | a0001c0002t0002g0030a0005c0008t0002g0029a0005c0008t0002g0032others(2): Show | 5 | HG00733.hp1 HG00741.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+356G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159969751 | ||||||
| chr6:159969886
|
G | C | 5 | a0001c0001t0003g0037a0001c0001t0043g0036a0001c0002t0028g0034others(2): Show | 5 | HG02145.hp2 HG02451.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+491G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159969886 | ||||||
| chr6:159969899
|
C | A | 5 | a0001c0001t0003g0037a0001c0001t0043g0036a0001c0002t0028g0034others(2): Show | 5 | HG02145.hp2 HG02451.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+504C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159969899 | ||||||
| chr6:159969939
|
A | G | 9 | a0001c0001t0002g0293a0001c0001t0085g0294a0001c0002t0036g0289others(6): Show | 9 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.149+544A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159969939 | ||||||
| chr6:159969954
|
A | T | 3 | a0001c0004t0027g0287a0006c0025t0059g0288a0029c0038t0003g0286 | 3 | HG01243.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.149+559A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159969954 | ||||||
| chr6:159969956
|
A | ATT | 9 | a0001c0001t0002g0293a0001c0001t0085g0294a0001c0002t0036g0289others(6): Show | 9 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.149+565_149+566dup others(2): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159969956 | |||||
| chr6:159969956
|
A | T | 149 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(146): Show | 150 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.149+561A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159969956 | ||||||
| chr6:159969974
|
CT | C | 3 | a0001c0002t0056g0156a0001c0056t0003g0154a0005c0027t0006g0155 | 3 | HG01106.hp2 HG02602.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.149+583delT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159969974 | |||||
| chr6:159970157
|
C | T | 16 | a0001c0001t0002g0293a0001c0001t0085g0294a0001c0002t0036g0289others(13): Show | 16 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.149+762C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159970157 | ||||||
| chr6:159970166
|
TTC | T | 10 | a0001c0001t0002g0043a0001c0001t0005g0028a0001c0001t0008g0042others(7): Show | 10 | HG00280.hp2 HG01081.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.149+772_149+773del others(2): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159970166 | ||||||
| chr6:159970350
|
TGTTACTT others(6): Show |
T | 1 | a0002c0015t0001g0280 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.149+978_149+990del others(13): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159970350 | |||||
| chr6:159970455
|
T | G | 1 | a0001c0001t0010g0157 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.149+1060T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159970455 | ||||||
| chr6:159970456
|
C | G | 1 | a0001c0001t0010g0157 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.149+1061C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159970456 | ||||||
| chr6:159970677
|
C | T | 17 | a0001c0002t0002g0020a0001c0005t0004g0012a0001c0005t0004g0014others(14): Show | 17 | HG00438.hp2 HG00544.hp2 HG04228.hp1 others(14): Show |
intron_variant | MODIFIER | c.149+1282C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159970677 | ||||||
| chr6:159970752
|
A | G | 4 | a0008c0011t0017g0152a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG02723.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+1357A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159970752 | ||||||
| chr6:159970899
|
G | A | 10 | a0001c0002t0028g0034a0001c0034t0006g0035a0008c0011t0017g0152others(7): Show | 10 | HG02145.hp2 HG02280.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.149+1504G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159970899 | ||||||
| chr6:159970993
|
A | G | 168 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(165): Show | 169 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.149+1598A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159970993 | ||||||
| chr6:159971005
|
C | G | 168 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(165): Show | 169 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.149+1610C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159971005 | ||||||
| chr6:159971080
|
A | C | 2 | a0002c0003t0001g0277a0002c0003t0020g0278 | 2 | HG00423.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.149+1685A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159971080 | ||||||
| chr6:159971146
|
T | G | 2 | a0001c0069t0052g0164a0012c0031t0019g0165 | 2 | HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.149+1751T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159971146 | ||||||
| chr6:159971548
|
T | C | 11 | a0001c0001t0002g0293a0001c0001t0085g0294a0001c0002t0036g0289others(8): Show | 11 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.149+2153T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159971548 | ||||||
| chr6:159971787
|
A | T | 4 | a0001c0005t0004g0024a0001c0005t0004g0026a0001c0005t0004g0027others(1): Show | 4 | NA18942.hp1 NA18945.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+2392A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159971787 | ||||||
| chr6:159971813
|
TATTATAT others(9): Show |
T | 1 | a0025c0053t0062g0166 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.149+2420_149+2435d others(18): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159971813 | |||||
| chr6:159971866
|
A | C | 1 | a0003c0007t0075g0147 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.149+2471A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159971866 | ||||||
| chr6:159972145
|
T | C | 11 | a0001c0001t0002g0293a0001c0001t0085g0294a0001c0002t0036g0289others(8): Show | 11 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.149+2750T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159972145 | ||||||
| chr6:159972146
|
C | T | 13 | a0001c0001t0003g0037a0001c0001t0043g0036a0001c0002t0028g0034others(10): Show | 13 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.149+2751C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159972146 | ||||||
| chr6:159972354
|
A | C | 168 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(165): Show | 169 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.149+2959A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159972354 | ||||||
| chr6:159972394
|
T | C | 1 | a0006c0025t0059g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.149+2999T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159972394 | ||||||
| chr6:159972482
|
C | G | 4 | a0001c0001t0013g0145a0001c0001t0013g0146a0001c0009t0005g0143others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+3087C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159972482 | ||||||
| chr6:159972778
|
C | T | 1 | a0001c0004t0044g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.149+3383C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159972778 | ||||||
| chr6:159972828
|
C | T | 11 | a0001c0001t0002g0293a0001c0001t0085g0294a0001c0002t0036g0289others(8): Show | 11 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.149+3433C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159972828 | ||||||
| chr6:159972838
|
T | A | 104 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0230others(101): Show | 105 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.149+3443T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159972838 | ||||||
| chr6:159972889
|
GT | G | 11 | a0001c0001t0002g0293a0001c0001t0085g0294a0001c0002t0036g0289others(8): Show | 11 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.149+3502delT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159972889 | |||||
| chr6:159973059
|
G | C | 2 | a0001c0002t0010g0168a0001c0005t0012g0167 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.149+3664G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159973059 | ||||||
| chr6:159973061
|
C | A | 13 | a0001c0001t0003g0037a0001c0001t0043g0036a0001c0002t0028g0034others(10): Show | 13 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.149+3666C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159973061 | ||||||
| chr6:159973159
|
G | A | 3 | a0003c0007t0009g0048a0003c0030t0004g0049a0004c0062t0002g0050 | 3 | HG03239.hp2 HG03942.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.149+3764G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159973159 | ||||||
| chr6:159973186
|
A | G | 3 | a0001c0001t0003g0037a0001c0001t0043g0036a0008c0043t0017g0038 | 3 | HG02451.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.149+3791A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159973186 | ||||||
| chr6:159973215
|
A | G | 93 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(90): Show | 94 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.149+3820A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159973215 | ||||||
| chr6:159973698
|
A | G | 85 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(82): Show | 86 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.149+4303A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159973698 | ||||||
| chr6:159973853
|
T | C | 3 | a0001c0001t0003g0037a0001c0001t0043g0036a0008c0043t0017g0038 | 3 | HG02451.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.149+4458T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159973853 | ||||||
| chr6:159973863
|
A | G | 1 | a0001c0001t0002g0142 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.149+4468A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159973863 | ||||||
| chr6:159974034
|
G | T | 1 | a0001c0001t0002g0141 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.149+4639G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159974034 | ||||||
| chr6:159974190
|
G | GTATCTCA others(23): Show |
1 | a0025c0053t0062g0166 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.149+4796_149+4825d others(32): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159974190 | |||||
| chr6:159974254
|
ATCTTT | A | 4 | a0001c0001t0013g0006a0001c0002t0082g0007a0017c0021t0031g0004others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+4864_149+4868d others(7): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159974254 | |||||
| chr6:159974270
|
A | G | 1 | a0012c0031t0019g0165 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.149+4875A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159974270 | ||||||
| chr6:159974383
|
G | C | 1 | a0003c0059t0055g0171 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.149+4988G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159974383 | ||||||
| chr6:159974600
|
A | G | 147 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(144): Show | 148 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.149+5205A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159974600 | ||||||
| chr6:159974604
|
A | C | 1 | a0002c0003t0001g0276 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.149+5209A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159974604 | ||||||
| chr6:159974685
|
A | G | 1 | a0016c0019t0005g0138 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.149+5290A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159974685 | ||||||
| chr6:159975016
|
G | A | 5 | a0001c0024t0070g0282a0008c0011t0017g0152a0010c0016t0016g0150others(2): Show | 5 | HG02280.hp1 HG02723.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+5621G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159975016 | ||||||
| chr6:159975022
|
C | A | 1 | a0002c0003t0014g0173 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.149+5627C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159975022 | ||||||
| chr6:159975113
|
T | C | 1 | a0001c0001t0010g0157 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.149+5718T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159975113 | ||||||
| chr6:159975128
|
C | T | 1 | a0002c0057t0001g0243 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.149+5733C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159975128 | ||||||
| chr6:159975152
|
C | T | 1 | a0003c0059t0055g0171 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.149+5757C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159975152 | ||||||
| chr6:159975323
|
T | C | 94 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0230others(91): Show | 95 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.149+5928T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159975323 | ||||||
| chr6:159975362
|
C | T | 2 | a0001c0002t0050g0242a0002c0003t0001g0241 | 2 | HG02602.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.149+5967C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159975362 | ||||||
| chr6:159975382
|
C | T | 3 | a0001c0002t0010g0168a0001c0005t0012g0167a0003c0007t0079g0137 | 3 | HG02257.hp1 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.149+5987C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159975382 | ||||||
| chr6:159975495
|
A | G | 94 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0230others(91): Show | 95 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.149+6100A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159975495 | ||||||
| chr6:159975543
|
T | C | 2 | a0017c0021t0031g0004a0017c0021t0031g0005 | 2 | HG03688.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.149+6148T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159975543 | ||||||
| chr6:159975652
|
G | GA | 5 | a0001c0001t0005g0028a0001c0001t0006g0244a0001c0002t0036g0289others(2): Show | 5 | HG00642.hp1 HG01433.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+6266dupA | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159975652 | |||||
| chr6:159975682
|
A | ATT | 7 | a0001c0001t0003g0037a0001c0001t0043g0036a0002c0003t0014g0173others(4): Show | 7 | HG02451.hp1 HG02451.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.149+6289_149+6290d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159975682 | |||||
| chr6:159975684
|
T | A | 7 | a0001c0002t0028g0034a0001c0034t0006g0035a0009c0013t0010g0158others(4): Show | 7 | HG01109.hp1 HG02145.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+6289T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159975684 | ||||||
| chr6:159975684
|
T | TTA | 88 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0230others(85): Show | 89 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.149+6306_149+6307d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159975684 | |||||
| chr6:159975684
|
T | TTATA | 4 | a0001c0004t0044g0153a0005c0008t0002g0296a0005c0008t0093g0295others(1): Show | 4 | HG01255.hp1 HG01496.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+6304_149+6307d others(6): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159975684 | |||||
| chr6:159975684
|
T | TTTTATA | 7 | a0001c0002t0010g0168a0001c0005t0012g0167a0001c0024t0070g0282others(4): Show | 7 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.149+6290_149+6291i others(8): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159975684 | |||||
| chr6:159975686
|
A | T | 1 | a0001c0001t0010g0157 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.149+6291A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159975686 | ||||||
| chr6:159975701
|
T | A | 1 | a0001c0046t0054g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.149+6306T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159975701 | ||||||
| chr6:159975701
|
T | TATATATA others(5): Show |
2 | a0010c0016t0016g0169a0010c0016t0016g0170 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.149+6307_149+6308i others(14): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159975701 | |||||
| chr6:159975705
|
G | A | 94 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0230others(91): Show | 95 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.149+6310G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159975705 | ||||||
| chr6:159975733
|
G | A | 1 | a0001c0002t0027g0052 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.149+6338G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159975733 | ||||||
| chr6:159975742
|
TTA | T | 10 | a0001c0001t0003g0037a0001c0001t0010g0157a0001c0001t0043g0036others(7): Show | 10 | HG02145.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.149+6357_149+6358d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159975742 | |||||
| chr6:159975849
|
G | A | 1 | a0012c0031t0019g0165 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.149+6454G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159975849 | ||||||
| chr6:159976028
|
T | G | 94 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0230others(91): Show | 95 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.149+6633T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159976028 | ||||||
| chr6:159976079
|
T | C | 4 | a0008c0011t0017g0152a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG02723.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+6684T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159976079 | ||||||
| chr6:159976086
|
G | C | 1 | a0001c0004t0066g0174 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.149+6691G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159976086 | ||||||
| chr6:159976168
|
G | T | 10 | a0001c0001t0002g0293a0001c0001t0085g0294a0001c0002t0036g0289others(7): Show | 10 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.149+6773G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159976168 | ||||||
| chr6:159976323
|
T | G | 2 | a0001c0004t0051g0178a0002c0003t0001g0179 | 2 | NA18960.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.149+6928T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159976323 | ||||||
| chr6:159976377
|
G | A | 1 | a0001c0009t0023g0131 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.149+6982G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159976377 | ||||||
| chr6:159976445
|
T | TGTTTTGT others(17): Show |
1 | a0001c0001t0035g0053 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.149+7051_149+7074d others(26): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159976445 | |||||
| chr6:159976510
|
C | G | 93 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0230others(90): Show | 94 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.149+7115C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159976510 | ||||||
| chr6:159976621
|
A | G | 93 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0230others(90): Show | 94 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.149+7226A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159976621 | ||||||
| chr6:159976681
|
C | T | 291 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(288): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.149+7286C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159976681 | ||||||
| chr6:159976696
|
A | G | 1 | a0001c0004t0001g0240 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.149+7301A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159976696 | ||||||
| chr6:159976865
|
G | C | 1 | a0001c0002t0080g0054 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.149+7470G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159976865 | ||||||
| chr6:159977004
|
T | C | 93 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0230others(90): Show | 94 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.149+7609T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159977004 | ||||||
| chr6:159977031
|
G | A | 4 | a0001c0009t0002g0068a0003c0058t0076g0070a0012c0031t0089g0067others(1): Show | 4 | HG02258.hp1 HG03516.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+7636G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159977031 | ||||||
| chr6:159977298
|
C | T | 93 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0230others(90): Show | 94 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.149+7903C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159977298 | ||||||
| chr6:159977450
|
C | T | 3 | a0001c0002t0010g0168a0001c0005t0012g0167a0003c0007t0079g0137 | 3 | HG02257.hp1 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.149+8055C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159977450 | ||||||
| chr6:159977451
|
G | A | 17 | a0001c0002t0002g0020a0001c0005t0004g0012a0001c0005t0004g0014others(14): Show | 17 | HG00438.hp2 HG00544.hp2 HG04228.hp1 others(14): Show |
intron_variant | MODIFIER | c.149+8056G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159977451 | ||||||
| chr6:159977496
|
T | TC | 115 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0037others(112): Show | 116 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.149+8102dupC | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159977496 | |||||
| chr6:159977674
|
C | T | 93 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0230others(90): Show | 94 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.149+8279C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159977674 | ||||||
| chr6:159977766
|
A | G | 92 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0230others(89): Show | 93 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.149+8371A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159977766 | ||||||
| chr6:159977808
|
T | TTTGTAGG others(23): Show |
2 | a0012c0031t0019g0165a0025c0053t0062g0166 | 2 | HG01109.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.149+8516_149+8545d others(32): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159977808 | |||||
| chr6:159977808
|
TTTGTAGG others(23): Show |
T | 5 | a0001c0004t0002g0129a0001c0005t0004g0022a0002c0052t0008g0023others(2): Show | 5 | HG00438.hp2 HG03669.hp1 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+8516_149+8545d others(32): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159977808 | |||||
| chr6:159977896
|
G | C | 1 | a0001c0069t0052g0164 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.149+8501G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159977896 | ||||||
| chr6:159978143
|
T | C | 2 | a0001c0002t0028g0034a0001c0034t0006g0035 | 2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.149+8748T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159978143 | ||||||
| chr6:159978155
|
G | A | 1 | a0001c0009t0001g0181 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.149+8760G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159978155 | ||||||
| chr6:159978160
|
T | G | 6 | a0001c0002t0028g0034a0001c0034t0006g0035a0009c0013t0010g0158others(3): Show | 6 | HG02145.hp2 HG02647.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+8765T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159978160 | ||||||
| chr6:159978310
|
T | C | 1 | a0002c0003t0001g0175 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.149+8915T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159978310 | ||||||
| chr6:159978375
|
C | G | 116 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0230others(113): Show | 117 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.149+8980C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159978375 | ||||||
| chr6:159978692
|
C | T | 1 | a0001c0004t0066g0174 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.149+9297C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159978692 | ||||||
| chr6:159978735
|
C | T | 2 | a0001c0001t0006g0274a0014c0022t0038g0275 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.149+9340C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159978735 | ||||||
| chr6:159978863
|
G | A | 17 | a0001c0005t0004g0083a0001c0037t0002g0079a0002c0003t0008g0085others(14): Show | 17 | HG00597.hp1 HG00639.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.149+9468G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159978863 | ||||||
| chr6:159978892
|
C | T | 3 | a0001c0001t0021g0044a0001c0001t0021g0045a0001c0001t0021g0046 | 3 | HG01515.hp1 HG01517.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.149+9497C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159978892 | ||||||
| chr6:159978893
|
A | T | 3 | a0001c0004t0044g0153a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.149+9498A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159978893 | ||||||
| chr6:159978915
|
G | A | 6 | a0001c0001t0003g0246a0001c0001t0003g0249a0001c0002t0067g0247others(3): Show | 6 | HG00642.hp2 HG01109.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+9520G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159978915 | ||||||
| chr6:159978941
|
C | T | 10 | a0001c0002t0015g0127a0001c0002t0015g0163a0001c0002t0027g0052others(7): Show | 10 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.149+9546C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159978941 | ||||||
| chr6:159978971
|
AG | A | 90 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(87): Show | 91 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.149+9581delG | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159978971 | |||||
| chr6:159978995
|
C | T | 1 | a0012c0031t0019g0165 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.149+9600C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159978995 | ||||||
| chr6:159978996
|
G | A | 1 | a0002c0003t0061g0182 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.149+9601G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159978996 | ||||||
| chr6:159979023
|
G | A | 1 | a0001c0004t0066g0174 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.149+9628G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159979023 | ||||||
| chr6:159979108
|
C | T | 3 | a0001c0046t0054g0281a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.149+9713C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159979108 | ||||||
| chr6:159979115
|
A | G | 36 | a0001c0001t0002g0293a0001c0001t0005g0114a0001c0001t0005g0115others(33): Show | 36 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.149+9720A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159979115 | ||||||
| chr6:159979164
|
A | G | 128 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(125): Show | 129 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.149+9769A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159979164 | ||||||
| chr6:159979547
|
G | A | 3 | a0001c0001t0003g0037a0001c0001t0043g0036a0008c0043t0017g0038 | 3 | HG02451.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.149+10152G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159979547 | ||||||
| chr6:159979589
|
T | C | 18 | a0001c0001t0003g0037a0001c0001t0043g0036a0001c0002t0015g0127others(15): Show | 18 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.149+10194T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159979589 | ||||||
| chr6:159979672
|
C | G | 86 | a0001c0001t0001g0187a0001c0001t0003g0037a0001c0001t0003g0230others(83): Show | 87 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.149+10277C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159979672 | ||||||
| chr6:159979754
|
G | A | 98 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(95): Show | 99 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.149+10359G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159979754 | ||||||
| chr6:159979801
|
G | A | 1 | a0002c0015t0001g0280 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.149+10406G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159979801 | ||||||
| chr6:159979996
|
G | A | 15 | a0001c0001t0002g0293a0001c0001t0013g0006a0001c0001t0085g0294others(12): Show | 15 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.149+10601G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159979996 | ||||||
| chr6:159980042
|
G | A | 1 | a0001c0001t0013g0006 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.149+10647G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980042 | ||||||
| chr6:159980044
|
G | A | 2 | a0001c0001t0001g0187a0002c0003t0001g0186 | 2 | NA18985.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.149+10649G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980044 | ||||||
| chr6:159980050
|
G | A | 3 | a0010c0016t0016g0150a0019c0068t0012g0279a0022c0042t0024g0151 | 3 | HG02280.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.149+10655G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980050 | ||||||
| chr6:159980073
|
C | T | 1 | a0001c0002t0088g0063 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.149+10678C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980073 | ||||||
| chr6:159980138
|
ACCGCTGC others(241): Show |
A | 1 | a0001c0001t0005g0028 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.149+10745_150-1079 others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980138 | |||||
| chr6:159980183
|
A | AAAAG | 10 | a0001c0001t0003g0256a0001c0001t0005g0119a0001c0001t0013g0145others(7): Show | 10 | HG00323.hp1 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.149+10841_149+1084 others(8): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980183 | |||||
| chr6:159980183
|
A | AAAAGAAA others(1): Show |
4 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0002t0036g0289others(1): Show | 4 | HG01433.hp1 HG01952.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+10837_149+1084 others(12): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980183 | |||||
| chr6:159980183
|
A | AAAAGAAA others(5): Show |
1 | a0001c0001t0005g0115 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.149+10833_149+1084 others(16): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980183 | |||||
| chr6:159980183
|
A | AAAAGAAA others(9): Show |
1 | a0001c0001t0005g0114 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.149+10829_149+1084 others(20): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980183 | |||||
| chr6:159980183
|
A | AAAAGAAA others(13): Show |
1 | a0001c0001t0035g0113 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.149+10825_149+1084 others(24): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980183 | |||||
| chr6:159980183
|
AAAAG | A | 23 | a0001c0001t0002g0142a0001c0001t0003g0037a0001c0001t0043g0036others(20): Show | 23 | HG00741.hp2 HG01175.hp2 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.149+10841_149+1084 others(8): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980183 | |||||
| chr6:159980183
|
AAAAGAAA others(1): Show |
A | 28 | a0001c0001t0002g0141a0001c0001t0005g0100a0001c0002t0009g0102others(25): Show | 28 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.149+10837_149+1084 others(12): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980183 | |||||
| chr6:159980183
|
AAAAGAAA others(5): Show |
A | 11 | a0001c0002t0027g0052a0001c0005t0004g0083a0001c0037t0002g0079others(8): Show | 11 | HG01884.hp1 HG02132.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.149+10833_149+1084 others(16): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980183 | |||||
| chr6:159980183
|
AAAAGAAA others(9): Show |
A | 21 | a0001c0002t0002g0020a0001c0002t0015g0009a0001c0005t0004g0012others(18): Show | 21 | HG00544.hp2 HG02258.hp2 HG02895.hp2 others(18): Show |
intron_variant | MODIFIER | c.149+10829_149+1084 others(20): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980183 | |||||
| chr6:159980183
|
AAAAGAAA others(13): Show |
A | 13 | a0001c0001t0008g0042a0001c0002t0028g0034a0001c0034t0006g0035others(10): Show | 13 | HG02040.hp2 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.149+10825_149+1084 others(24): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980183 | |||||
| chr6:159980183
|
AAAAGAAA others(17): Show |
A | 7 | a0001c0004t0003g0190a0001c0004t0003g0192a0001c0004t0044g0153others(4): Show | 7 | HG01168.hp1 HG01943.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+10821_149+1084 others(28): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980183 | |||||
| chr6:159980183
|
AAAAGAAA others(21): Show |
A | 80 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(77): Show | 81 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.149+10817_149+1084 others(32): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980183 | |||||
| chr6:159980200
|
A | AAAGAAAG others(33): Show |
5 | a0013c0026t0029g0149a0013c0026t0029g0297a0014c0022t0038g0275others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+10812_149+1081 others(44): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980200 | |||||
| chr6:159980200
|
A | AAAGAAAG others(41): Show |
3 | a0001c0001t0006g0274a0001c0001t0026g0268a0001c0001t0026g0269 | 3 | HG02630.hp1 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.149+10812_149+1081 others(52): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980200 | |||||
| chr6:159980200
|
A | G | 12 | a0001c0001t0002g0293a0001c0001t0013g0006a0001c0001t0085g0294others(9): Show | 12 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.149+10805A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980200 | ||||||
| chr6:159980202
|
A | AGAAGGAA others(137): Show |
2 | a0001c0001t0003g0307a0001c0002t0003g0306 | 2 | NA19060.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.149+10810_149+1081 others(148): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980202 | |||||
| chr6:159980205
|
A | AAGAGAGA others(81): Show |
1 | a0001c0001t0002g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.149+10813_149+1081 others(92): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980205 | |||||
| chr6:159980206
|
A | AGAAAGAA others(85): Show |
1 | a0003c0007t0075g0147 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.149+10822_149+1082 others(96): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980206 | |||||
| chr6:159980206
|
A | AGAAGGAA others(145): Show |
1 | a0001c0001t0001g0305 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.149+10814_149+1081 others(156): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980206 | |||||
| chr6:159980206
|
A | G | 2 | a0001c0001t0003g0307a0001c0002t0003g0306 | 2 | NA19060.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.149+10811A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980206 | ||||||
| chr6:159980208
|
A | AAAGGAAG others(45): Show |
2 | a0001c0004t0027g0287a0035c0060t0042g0267 | 2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.149+10816_149+1081 others(56): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980208 | |||||
| chr6:159980208
|
A | AAAGGAAG others(53): Show |
1 | a0029c0038t0003g0286 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.149+10816_149+1081 others(64): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980208 | |||||
| chr6:159980208
|
A | G | 20 | a0001c0001t0002g0293a0001c0001t0006g0274a0001c0001t0013g0006others(17): Show | 20 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.149+10813A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980208 | ||||||
| chr6:159980210
|
A | AGAAGGAA others(85): Show |
1 | a0003c0007t0079g0137 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.149+10818_149+1081 others(96): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980210 | |||||
| chr6:159980210
|
A | AGAAGGAA others(137): Show |
1 | a0001c0002t0003g0303 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.149+10818_149+1081 others(148): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980210 | |||||
| chr6:159980210
|
A | AGAAGGAA others(149): Show |
1 | a0001c0001t0001g0304 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.149+10818_149+1081 others(160): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980210 | |||||
| chr6:159980210
|
A | G | 4 | a0001c0001t0001g0305a0001c0001t0003g0307a0001c0002t0003g0306others(1): Show | 4 | HG02976.hp2 NA18945.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+10815A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980210 | ||||||
| chr6:159980211
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.149+10816G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980211 | ||||||
| chr6:159980213
|
A | G | 1 | a0001c0001t0002g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.149+10818A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980213 | ||||||
| chr6:159980214
|
A | AGAAAGAA others(142): Show |
1 | a0003c0007t0003g0261 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.149+10832_149+1083 others(153): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980214 | |||||
| chr6:159980214
|
A | AGAAAGAA others(153): Show |
1 | a0003c0007t0006g0272 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.149+10830_149+1083 others(164): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980214 | |||||
| chr6:159980214
|
A | AGAAGGAA others(149): Show |
1 | a0002c0003t0001g0265 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.149+10822_149+1082 others(160): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980214 | |||||
| chr6:159980214
|
A | AGAAGGAA others(161): Show |
1 | a0001c0002t0003g0302 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.149+10822_149+1082 others(172): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980214 | |||||
| chr6:159980214
|
A | AGAAGGGA others(105): Show |
1 | a0004c0061t0003g0266 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.149+10822_149+1082 others(116): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980214 | |||||
| chr6:159980214
|
A | G | 5 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0003g0307others(2): Show | 5 | NA18945.hp2 NA18982.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+10819A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980214 | ||||||
| chr6:159980215
|
G | GAAAGAAA others(188): Show |
1 | a0002c0015t0001g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.149+10844_149+1084 others(199): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980215 | |||||
| chr6:159980215
|
G | GAAAGAAA others(85): Show |
1 | a0003c0030t0025g0257 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.149+10838_149+1083 others(96): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980215 | |||||
| chr6:159980215
|
G | GAAAGAAA others(93): Show |
1 | a0001c0005t0012g0258 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.149+10838_149+1083 others(104): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980215 | |||||
| chr6:159980215
|
G | GAAAGAAA others(86): Show |
1 | a0002c0015t0014g0298 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.149+10834_149+1083 others(97): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980215 | |||||
| chr6:159980215
|
G | GAAAGAAA others(109): Show |
1 | a0002c0015t0001g0280 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.149+10834_149+1083 others(120): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980215 | |||||
| chr6:159980215
|
G | GAAAGAAA others(81): Show |
1 | a0002c0028t0001g0262 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.149+10830_149+1083 others(92): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980215 | |||||
| chr6:159980215
|
G | GAAAGAAA others(89): Show |
1 | a0002c0028t0001g0263 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.149+10830_149+1083 others(100): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980215 | |||||
| chr6:159980215
|
G | GAAGGAAG others(77): Show |
1 | a0001c0001t0001g0301 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.149+10822_149+1082 others(88): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980215 | |||||
| chr6:159980216
|
A | G | 23 | a0001c0001t0002g0293a0001c0001t0006g0274a0001c0001t0013g0006others(20): Show | 23 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.149+10821A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980216 | ||||||
| chr6:159980217
|
A | G | 1 | a0001c0001t0002g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.149+10822A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980217 | ||||||
| chr6:159980218
|
A | AGAAAGAA others(93): Show |
1 | a0037c0033t0073g0140 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.149+10830_149+1083 others(104): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980218 | |||||
| chr6:159980218
|
A | AGAAGGAA others(101): Show |
1 | a0001c0001t0006g0308 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.149+10826_149+1082 others(112): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980218 | |||||
| chr6:159980218
|
A | AGAAGGAA others(133): Show |
1 | a0001c0002t0002g0299 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.149+10826_149+1082 others(144): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980218 | |||||
| chr6:159980218
|
A | AGAAGGAA others(141): Show |
1 | a0001c0001t0014g0300 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.149+10826_149+1082 others(152): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980218 | |||||
| chr6:159980218
|
A | AGAAGGAA others(153): Show |
1 | a0001c0001t0006g0264 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.149+10826_149+1082 others(164): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980218 | |||||
| chr6:159980218
|
A | G | 10 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0003g0307others(7): Show | 10 | HG02976.hp2 HG03486.hp1 HG03834.hp1 others(7): Show |
intron_variant | MODIFIER | c.149+10823A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980218 | ||||||
| chr6:159980219
|
G | GAAAGAAA others(607): Show |
1 | a0002c0003t0001g0251 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.149+10844_149+1084 others(618): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980219 | |||||
| chr6:159980219
|
G | GAAAGAAA others(433): Show |
1 | a0025c0053t0062g0166 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.149+10844_149+1084 others(444): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980219 | |||||
| chr6:159980219
|
G | GAAAGAAA others(329): Show |
1 | a0001c0004t0020g0253 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.149+10844_149+1084 others(340): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980219 | |||||
| chr6:159980219
|
G | GAAAGAAA others(353): Show |
1 | a0003c0007t0003g0254 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.149+10844_149+1084 others(364): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980219 | |||||
| chr6:159980222
|
A | AGAAGGAA others(113): Show |
1 | a0001c0001t0006g0244 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.149+10830_149+1083 others(124): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980222 | |||||
| chr6:159980222
|
A | G | 17 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0003g0307others(14): Show | 17 | HG02886.hp1 HG03098.hp1 HG03195.hp1 others(14): Show |
intron_variant | MODIFIER | c.149+10827A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980222 | ||||||
| chr6:159980224
|
A | AAAGGAAG others(177): Show |
1 | a0001c0001t0005g0121 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.149+10832_149+1083 others(188): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980224 | |||||
| chr6:159980224
|
A | G | 23 | a0001c0001t0002g0293a0001c0001t0006g0274a0001c0001t0013g0006others(20): Show | 23 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.149+10829A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980224 | ||||||
| chr6:159980226
|
A | AGAAAGAA others(314): Show |
1 | a0001c0001t0035g0053 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.149+10844_149+1084 others(325): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980226 | |||||
| chr6:159980226
|
A | AGAAGAAG others(131): Show |
1 | a0002c0003t0001g0276 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.149+10834_149+1083 others(142): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980226 | |||||
| chr6:159980226
|
A | AGAAGGAA others(93): Show |
1 | a0002c0003t0001g0260 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.149+10834_149+1083 others(104): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980226 | |||||
| chr6:159980226
|
A | AGAAGGAA others(97): Show |
1 | a0001c0004t0048g0259 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.149+10834_149+1083 others(108): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980226 | |||||
| chr6:159980226
|
A | AGAAGGAA others(121): Show |
1 | a0002c0003t0001g0271 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.149+10834_149+1083 others(132): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980226 | |||||
| chr6:159980226
|
A | G | 14 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0003g0307others(11): Show | 14 | HG02976.hp2 HG03834.hp1 NA18945.hp2 others(11): Show |
intron_variant | MODIFIER | c.149+10831A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980226 | ||||||
| chr6:159980227
|
G | GAAAGAAA others(259): Show |
1 | a0018c0032t0033g0086 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.149+10844_149+1084 others(270): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980227 | |||||
| chr6:159980227
|
G | GAAAGAAA others(244): Show |
1 | a0018c0032t0033g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.149+10844_149+1084 others(255): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980227 | |||||
| chr6:159980227
|
G | GAAAGAAA others(242): Show |
1 | a0006c0025t0009g0139 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.149+10844_149+1084 others(253): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980227 | |||||
| chr6:159980227
|
G | GAAGGAAA others(78): Show |
1 | a0003c0007t0022g0107 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.149+10834_149+1083 others(89): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980227 | |||||
| chr6:159980227
|
G | GAAGGAAA others(86): Show |
1 | a0003c0007t0022g0108 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.149+10834_149+1083 others(97): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980227 | |||||
| chr6:159980227
|
G | GAAGGAAA others(94): Show |
2 | a0001c0001t0030g0105a0001c0004t0002g0129 | 2 | HG02922.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.149+10834_149+1083 others(105): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980227 | |||||
| chr6:159980227
|
G | GAAGGAAA others(102): Show |
1 | a0003c0007t0023g0109 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.149+10834_149+1083 others(113): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980227 | |||||
| chr6:159980227
|
G | GAAGGAAA others(110): Show |
1 | a0036c0067t0034g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.149+10834_149+1083 others(121): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980227 | |||||
| chr6:159980227
|
G | GAAGGAAA others(118): Show |
1 | a0003c0007t0022g0106 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.149+10834_149+1083 others(129): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980227 | |||||
| chr6:159980228
|
A | AAAGGAAG others(157): Show |
1 | a0001c0001t0005g0120 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.149+10836_149+1083 others(168): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980228 | |||||
| chr6:159980228
|
A | G | 1 | a0001c0001t0005g0121 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.149+10833A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980228 | ||||||
| chr6:159980230
|
A | AGAAGGAA others(82): Show |
1 | a0021c0044t0074g0111 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.149+10838_149+1083 others(93): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980230 | |||||
| chr6:159980230
|
A | G | 20 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0003g0307others(17): Show | 20 | HG02723.hp1 HG02922.hp1 HG03098.hp1 others(17): Show |
intron_variant | MODIFIER | c.149+10835A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980230 | ||||||
| chr6:159980231
|
G | GGAAGAAA others(93): Show |
1 | a0001c0002t0091g0292 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.149+10836_149+1083 others(104): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980231 | ||||||
| chr6:159980231
|
G | GGAAGAAA others(112): Show |
3 | a0001c0001t0013g0006a0017c0021t0031g0004a0017c0021t0031g0005 | 3 | HG00280.hp1 HG03688.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.149+10836_149+1083 others(123): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980231 | ||||||
| chr6:159980231
|
G | GGAAGAAA others(107): Show |
1 | a0001c0002t0082g0007 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.149+10836_149+1083 others(118): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980231 | ||||||
| chr6:159980231
|
G | GGAAGAAA others(80): Show |
3 | a0001c0001t0002g0293a0005c0008t0002g0296a0005c0008t0093g0295 | 3 | HG01255.hp1 HG01496.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.149+10836_149+1083 others(91): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980231 | ||||||
| chr6:159980231
|
G | GGAAGAAA others(75): Show |
1 | a0001c0004t0081g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.149+10836_149+1083 others(86): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980231 | ||||||
| chr6:159980231
|
G | GGAAGAAA others(70): Show |
1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.149+10836_149+1083 others(81): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980231 | ||||||
| chr6:159980231
|
G | GGAAGGAA others(67): Show |
2 | a0001c0001t0085g0294a0030c0040t0002g0291 | 2 | HG00140.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.149+10836_149+1083 others(78): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980231 | ||||||
| chr6:159980232
|
A | G | 13 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0006g0274others(10): Show | 13 | HG01243.hp1 HG01255.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.149+10837A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980232 | ||||||
| chr6:159980234
|
A | G | 5 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0003g0307others(2): Show | 5 | NA18945.hp2 NA18967.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+10839A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980234 | ||||||
| chr6:159980236
|
A | AAAGAAAG others(359): Show |
1 | a0023c0035t0003g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.149+10844_149+1084 others(370): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980236 | |||||
| chr6:159980236
|
A | AAAGGAAG others(189): Show |
1 | a0001c0049t0004g0090 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.149+10845_149+1084 others(200): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980236 | |||||
| chr6:159980236
|
A | G | 2 | a0001c0001t0005g0120a0001c0001t0005g0121 | 2 | HG01255.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.149+10841A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980236 | ||||||
| chr6:159980238
|
A | AGAAAGAA others(206): Show |
1 | a0002c0003t0001g0255 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.149+10844_149+1084 others(217): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159980238 | |||||
| chr6:159980240
|
G | A | 16 | a0001c0001t0002g0293a0001c0001t0013g0006a0001c0001t0085g0294others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(13): Show |
intron_variant | MODIFIER | c.149+10845G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980240 | ||||||
| chr6:159980241
|
T | A | 15 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0030g0105others(12): Show | 15 | HG00642.hp2 HG01255.hp2 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.149+10846T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980241 | ||||||
| chr6:159980242
|
A | AGAAAGAA others(221): Show |
1 | a0003c0066t0053g0162 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.149+10847_149+1084 others(232): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980242 | ||||||
| chr6:159980243
|
C | A | 1 | a0003c0066t0053g0162 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.149+10848C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980243 | ||||||
| chr6:159980245
|
T | A | 1 | a0003c0066t0053g0162 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.149+10850T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980245 | ||||||
| chr6:159980247
|
G | A | 1 | a0003c0066t0053g0162 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.149+10852G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980247 | ||||||
| chr6:159980254
|
C | T | 14 | a0001c0001t0002g0293a0001c0001t0013g0006a0001c0001t0085g0294others(11): Show | 14 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.149+10859C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980254 | ||||||
| chr6:159980284
|
A | G | 83 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(80): Show | 84 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.149+10889A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980284 | ||||||
| chr6:159980314
|
T | C | 1 | a0001c0046t0054g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.150-10870T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980314 | ||||||
| chr6:159980339
|
T | C | 1 | a0023c0035t0003g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.150-10845T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980339 | ||||||
| chr6:159980443
|
C | T | 1 | a0006c0025t0059g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.150-10741C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980443 | ||||||
| chr6:159980531
|
G | A | 4 | a0009c0013t0010g0158a0009c0013t0010g0159a0009c0013t0010g0160others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-10653G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980531 | ||||||
| chr6:159980630
|
G | A | 13 | a0001c0001t0013g0006a0001c0001t0085g0294a0001c0002t0010g0168others(10): Show | 13 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.150-10554G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980630 | ||||||
| chr6:159980639
|
A | C | 3 | a0007c0014t0011g0092a0007c0014t0011g0093a0007c0014t0011g0094 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.150-10545A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980639 | ||||||
| chr6:159980712
|
T | C | 1 | a0001c0002t0002g0299 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.150-10472T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159980712 | ||||||
| chr6:159981265
|
G | C | 2 | a0001c0002t0010g0168a0001c0005t0012g0167 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.150-9919G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159981265 | ||||||
| chr6:159981283
|
G | A | 28 | a0001c0001t0003g0037a0001c0001t0043g0036a0001c0002t0002g0020others(25): Show | 28 | HG00438.hp2 HG00544.hp2 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.150-9901G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159981283 | ||||||
| chr6:159981313
|
C | G | 90 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(87): Show | 91 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.150-9871C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159981313 | ||||||
| chr6:159981338
|
A | AGT | 4 | a0006c0025t0059g0288a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-9834_150-9833d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159981338 | |||||
| chr6:159981426
|
G | A | 2 | a0001c0004t0046g0273a0012c0031t0019g0165 | 2 | HG01109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.150-9758G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159981426 | ||||||
| chr6:159981586
|
G | C | 5 | a0001c0001t0002g0141a0001c0001t0005g0100a0001c0004t0084g0098others(2): Show | 5 | HG00738.hp2 HG01243.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-9598G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159981586 | ||||||
| chr6:159981673
|
G | A | 12 | a0001c0001t0002g0293a0001c0001t0013g0006a0001c0001t0085g0294others(9): Show | 12 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.150-9511G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159981673 | ||||||
| chr6:159981674
|
G | T | 4 | a0006c0025t0059g0288a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-9510G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159981674 | ||||||
| chr6:159981712
|
T | C | 17 | a0001c0002t0002g0020a0001c0005t0004g0012a0001c0005t0004g0014others(14): Show | 17 | HG00438.hp2 HG00544.hp2 HG04228.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-9472T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159981712 | ||||||
| chr6:159981800
|
C | T | 17 | a0001c0002t0002g0020a0001c0005t0004g0012a0001c0005t0004g0014others(14): Show | 17 | HG00438.hp2 HG00544.hp2 HG04228.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-9384C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159981800 | ||||||
| chr6:159981835
|
T | C | 1 | a0006c0025t0059g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.150-9349T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159981835 | ||||||
| chr6:159982065
|
C | G | 1 | a0001c0009t0005g0143 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.150-9119C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159982065 | ||||||
| chr6:159982161
|
C | T | 3 | a0003c0012t0006g0284a0003c0012t0006g0285a0032c0065t0041g0283 | 3 | HG02451.hp2 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.150-9023C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159982161 | ||||||
| chr6:159982210
|
C | T | 1 | a0001c0004t0066g0174 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.150-8974C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159982210 | ||||||
| chr6:159982331
|
G | A | 28 | a0001c0001t0003g0037a0001c0001t0043g0036a0001c0002t0002g0020others(25): Show | 28 | HG00438.hp2 HG00544.hp2 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.150-8853G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159982331 | ||||||
| chr6:159982340
|
T | C | 1 | a0001c0004t0044g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.150-8844T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159982340 | ||||||
| chr6:159982355
|
CTTGAATA others(5): Show |
C | 1 | a0001c0046t0054g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.150-8826_150-8815d others(14): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159982355 | |||||
| chr6:159982370
|
A | C | 1 | a0003c0030t0025g0257 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.150-8814A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159982370 | ||||||
| chr6:159982485
|
G | A | 2 | a0001c0004t0046g0273a0012c0031t0019g0165 | 2 | HG01109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.150-8699G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159982485 | ||||||
| chr6:159982524
|
T | A | 86 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(83): Show | 87 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.150-8660T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159982524 | ||||||
| chr6:159982595
|
G | A | 1 | a0002c0003t0001g0265 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.150-8589G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159982595 | ||||||
| chr6:159982617
|
C | T | 2 | a0010c0016t0016g0169a0010c0016t0016g0170 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.150-8567C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159982617 | ||||||
| chr6:159982756
|
C | T | 86 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(83): Show | 87 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.150-8428C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159982756 | ||||||
| chr6:159983012
|
C | T | 28 | a0001c0001t0003g0037a0001c0001t0043g0036a0001c0002t0002g0020others(25): Show | 28 | HG00438.hp2 HG00544.hp2 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.150-8172C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159983012 | ||||||
| chr6:159983166
|
C | T | 1 | a0002c0003t0001g0193 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.150-8018C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159983166 | ||||||
| chr6:159983179
|
C | G | 4 | a0006c0025t0059g0288a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-8005C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159983179 | ||||||
| chr6:159983204
|
C | T | 1 | a0001c0002t0002g0020 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.150-7980C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159983204 | ||||||
| chr6:159983487
|
A | C | 7 | a0001c0002t0018g0235a0001c0002t0018g0236a0001c0002t0018g0237others(4): Show | 7 | HG02280.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.150-7697A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159983487 | ||||||
| chr6:159983518
|
C | T | 17 | a0001c0002t0002g0020a0001c0005t0004g0012a0001c0005t0004g0014others(14): Show | 17 | HG00438.hp2 HG00544.hp2 HG04228.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-7666C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159983518 | ||||||
| chr6:159983727
|
G | A | 4 | a0001c0002t0071g0194a0006c0010t0072g0196a0008c0011t0017g0152others(1): Show | 4 | HG02723.hp2 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.150-7457G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159983727 | ||||||
| chr6:159983800
|
T | C | 20 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0005g0100others(17): Show | 20 | HG00408.hp2 HG00733.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.150-7384T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159983800 | ||||||
| chr6:159983903
|
A | G | 2 | a0001c0002t0010g0168a0001c0005t0012g0167 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.150-7281A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159983903 | ||||||
| chr6:159984057
|
A | G | 152 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0037others(149): Show | 153 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.150-7127A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159984057 | ||||||
| chr6:159984132
|
T | C | 4 | a0006c0025t0059g0288a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-7052T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159984132 | ||||||
| chr6:159984157
|
T | C | 2 | a0001c0004t0046g0273a0012c0031t0019g0165 | 2 | HG01109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.150-7027T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159984157 | ||||||
| chr6:159984210
|
G | A | 1 | a0006c0025t0059g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.150-6974G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159984210 | ||||||
| chr6:159984367
|
A | G | 152 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0037others(149): Show | 153 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.150-6817A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159984367 | ||||||
| chr6:159984392
|
G | A | 86 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(83): Show | 87 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.150-6792G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159984392 | ||||||
| chr6:159984392
|
G | T | 6 | a0001c0002t0028g0034a0001c0034t0006g0035a0009c0013t0010g0158others(3): Show | 6 | HG02145.hp2 HG02647.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-6792G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159984392 | ||||||
| chr6:159984393
|
T | C | 6 | a0001c0002t0028g0034a0001c0034t0006g0035a0009c0013t0010g0158others(3): Show | 6 | HG02145.hp2 HG02647.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-6791T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159984393 | ||||||
| chr6:159984419
|
CCACTCAC others(5): Show |
C | 3 | a0001c0001t0003g0230a0001c0001t0003g0231a0001c0001t0069g0232 | 3 | HG02735.hp2 HG03490.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.150-6764_150-6753d others(14): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159984419 | ||||||
| chr6:159984494
|
G | A | 1 | a0018c0032t0033g0086 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.150-6690G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159984494 | ||||||
| chr6:159984558
|
A | G | 1 | a0002c0003t0001g0179 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.150-6626A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159984558 | ||||||
| chr6:159984590
|
G | A | 5 | a0001c0024t0070g0282a0006c0025t0059g0288a0010c0016t0016g0150others(2): Show | 5 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-6594G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159984590 | ||||||
| chr6:159984774
|
C | T | 1 | a0001c0004t0044g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.150-6410C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159984774 | ||||||
| chr6:159984936
|
A | G | 8 | a0001c0001t0001g0305a0001c0001t0003g0307a0001c0001t0006g0308others(5): Show | 8 | NA18945.hp2 NA18967.hp1 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.150-6248A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159984936 | ||||||
| chr6:159984959
|
A | G | 1 | a0013c0026t0029g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.150-6225A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159984959 | ||||||
| chr6:159984985
|
G | A | 4 | a0001c0001t0006g0244a0001c0001t0006g0264a0002c0003t0001g0276others(1): Show | 4 | NA18980.hp2 NA19058.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-6199G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159984985 | ||||||
| chr6:159985003
|
C | T | 4 | a0006c0025t0059g0288a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-6181C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159985003 | ||||||
| chr6:159985013
|
A | G | 2 | a0010c0016t0016g0169a0010c0016t0016g0170 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.150-6171A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159985013 | ||||||
| chr6:159985458
|
T | C | 4 | a0006c0025t0059g0288a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-5726T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159985458 | ||||||
| chr6:159985630
|
T | C | 22 | a0001c0005t0004g0083a0001c0005t0012g0184a0001c0037t0002g0079others(19): Show | 22 | HG00597.hp1 HG00639.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.150-5554T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159985630 | ||||||
| chr6:159985724
|
C | G | 3 | a0010c0016t0016g0150a0019c0068t0012g0279a0022c0042t0024g0151 | 3 | HG02280.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.150-5460C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159985724 | ||||||
| chr6:159985786
|
T | C | 4 | a0006c0025t0059g0288a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-5398T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159985786 | ||||||
| chr6:159985816
|
G | A | 7 | a0001c0001t0002g0293a0001c0001t0085g0294a0001c0002t0091g0292others(4): Show | 7 | HG00140.hp1 HG00639.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-5368G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159985816 | ||||||
| chr6:159985910
|
A | C | 1 | a0001c0004t0044g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.150-5274A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159985910 | ||||||
| chr6:159986100
|
C | T | 1 | a0001c0002t0015g0163 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.150-5084C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986100 | ||||||
| chr6:159986232
|
C | CT | 7 | a0001c0001t0002g0142a0001c0001t0003g0037a0001c0001t0043g0036others(4): Show | 7 | HG01261.hp1 HG01261.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-4935dupT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159986232 | |||||
| chr6:159986232
|
CT | C | 84 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(81): Show | 85 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.150-4935delT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159986232 | |||||
| chr6:159986309
|
G | A | 1 | a0005c0008t0013g0104 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.150-4875G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986309 | ||||||
| chr6:159986310
|
C | A | 1 | a0005c0008t0013g0104 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.150-4874C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986310 | ||||||
| chr6:159986342
|
G | A | 1 | a0001c0002t0039g0233 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.150-4842G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986342 | ||||||
| chr6:159986402
|
T | G | 2 | a0001c0004t0002g0132a0001c0046t0054g0281 | 2 | HG02965.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.150-4782T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986402 | ||||||
| chr6:159986402
|
T | TTG | 34 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0003g0246others(31): Show | 34 | HG00408.hp2 HG00642.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.150-4754_150-4753d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159986402 | |||||
| chr6:159986402
|
T | TTGTG | 7 | a0001c0002t0009g0047a0001c0004t0020g0253a0001c0049t0004g0090others(4): Show | 7 | HG03239.hp1 HG03239.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-4756_150-4753d others(6): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159986402 | |||||
| chr6:159986402
|
TTGTG | T | 4 | a0001c0001t0026g0268a0001c0001t0026g0269a0014c0022t0040g0270others(1): Show | 4 | HG02630.hp1 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.150-4756_150-4753d others(6): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159986402 | |||||
| chr6:159986403
|
TG | T | 3 | a0010c0016t0016g0150a0019c0068t0012g0279a0022c0042t0024g0151 | 3 | HG02280.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.150-4780delG | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986403 | ||||||
| chr6:159986404
|
G | T | 11 | a0001c0005t0012g0258a0002c0003t0001g0251a0002c0003t0001g0255others(8): Show | 11 | HG00423.hp1 HG00438.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.150-4780G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986404 | ||||||
| chr6:159986406
|
G | T | 5 | a0002c0003t0001g0271a0003c0007t0006g0272a0010c0016t0016g0150others(2): Show | 5 | HG02280.hp1 HG03098.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-4778G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986406 | ||||||
| chr6:159986427
|
TGTG | T | 3 | a0001c0001t0003g0037a0001c0001t0043g0036a0008c0043t0017g0038 | 3 | HG02451.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.150-4756_150-4754d others(5): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986427 | ||||||
| chr6:159986428
|
GTGT | G | 11 | a0001c0001t0002g0293a0001c0001t0013g0006a0001c0001t0085g0294others(8): Show | 11 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(8): Show |
intron_variant | MODIFIER | c.150-4754_150-4752d others(5): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159986428 | |||||
| chr6:159986430
|
GT | G | 89 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(86): Show | 90 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.150-4738delT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159986430 | |||||
| chr6:159986430
|
GTTT | G | 25 | a0001c0002t0002g0020a0001c0002t0010g0168a0001c0002t0015g0009others(22): Show | 25 | HG00438.hp2 HG00544.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.150-4740_150-4738d others(5): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159986430 | |||||
| chr6:159986431
|
T | TG | 15 | a0001c0001t0002g0043a0001c0001t0005g0028a0001c0001t0008g0042others(12): Show | 15 | HG00280.hp2 HG00597.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.150-4753_150-4752i others(3): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986431 | ||||||
| chr6:159986431
|
T | TGTG | 21 | a0001c0001t0005g0114a0001c0001t0005g0115a0001c0001t0005g0116others(18): Show | 21 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.150-4753_150-4752i others(5): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986431 | ||||||
| chr6:159986432
|
T | G | 12 | a0001c0002t0007g0091a0001c0004t0002g0132a0001c0009t0005g0144others(9): Show | 12 | HG00140.hp2 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.150-4752T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986432 | ||||||
| chr6:159986433
|
T | G | 105 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(102): Show | 106 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.150-4751T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986433 | ||||||
| chr6:159986434
|
T | G | 3 | a0002c0003t0014g0177a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG03209.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.150-4750T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986434 | ||||||
| chr6:159986435
|
T | G | 83 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(80): Show | 84 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.150-4749T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986435 | ||||||
| chr6:159986436
|
T | G | 1 | a0002c0003t0014g0177 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.150-4748T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986436 | ||||||
| chr6:159986437
|
T | G | 72 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(69): Show | 73 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.150-4747T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986437 | ||||||
| chr6:159986438
|
T | G | 1 | a0002c0003t0014g0177 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.150-4746T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986438 | ||||||
| chr6:159986439
|
T | G | 7 | a0001c0002t0006g0197a0001c0002t0006g0198a0001c0039t0045g0228others(4): Show | 7 | HG01433.hp2 HG01517.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-4745T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986439 | ||||||
| chr6:159986441
|
T | G | 3 | a0001c0002t0006g0197a0001c0002t0006g0198a0001c0046t0054g0281 | 3 | HG01433.hp2 HG01517.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.150-4743T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986441 | ||||||
| chr6:159986525
|
C | T | 4 | a0006c0025t0059g0288a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-4659C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986525 | ||||||
| chr6:159986562
|
A | G | 3 | a0010c0016t0016g0150a0019c0068t0012g0279a0022c0042t0024g0151 | 3 | HG02280.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.150-4622A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986562 | ||||||
| chr6:159986588
|
A | G | 3 | a0010c0016t0016g0150a0019c0068t0012g0279a0022c0042t0024g0151 | 3 | HG02280.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.150-4596A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986588 | ||||||
| chr6:159986642
|
C | A | 1 | a0001c0002t0082g0007 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.150-4542C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986642 | ||||||
| chr6:159986677
|
T | A | 6 | a0001c0002t0090g0133a0001c0004t0002g0132a0001c0009t0023g0131others(3): Show | 6 | HG00408.hp2 NA18951.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-4507T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986677 | ||||||
| chr6:159986683
|
A | T | 12 | a0001c0001t0002g0293a0001c0001t0013g0006a0001c0001t0085g0294others(9): Show | 12 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.150-4501A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159986683 | ||||||
| chr6:159986740
|
CT | C | 112 | a0001c0001t0001g0187a0001c0001t0002g0141a0001c0001t0002g0142others(109): Show | 113 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.150-4431delT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159986740 | |||||
| chr6:159987038
|
C | A | 4 | a0006c0025t0059g0288a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-4146C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159987038 | ||||||
| chr6:159987191
|
G | A | 10 | a0001c0001t0030g0105a0001c0004t0002g0129a0003c0007t0022g0106others(7): Show | 10 | HG02723.hp1 HG02886.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.150-3993G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159987191 | ||||||
| chr6:159987293
|
G | T | 12 | a0001c0001t0002g0293a0001c0001t0013g0006a0001c0001t0085g0294others(9): Show | 12 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.150-3891G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159987293 | ||||||
| chr6:159987296
|
C | T | 2 | a0001c0001t0005g0100a0005c0008t0002g0099 | 2 | HG01346.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.150-3888C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159987296 | ||||||
| chr6:159987427
|
T | C | 4 | a0006c0025t0059g0288a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-3757T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159987427 | ||||||
| chr6:159987432
|
C | T | 1 | a0001c0004t0044g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.150-3752C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159987432 | ||||||
| chr6:159987536
|
C | T | 3 | a0001c0001t0003g0037a0001c0001t0043g0036a0008c0043t0017g0038 | 3 | HG02451.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.150-3648C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159987536 | ||||||
| chr6:159987552
|
C | T | 1 | a0015c0023t0094g0096 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.150-3632C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159987552 | ||||||
| chr6:159987595
|
C | T | 288 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(285): Show | 289 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.150-3589C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159987595 | ||||||
| chr6:159987682
|
G | A | 1 | a0001c0046t0054g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.150-3502G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159987682 | ||||||
| chr6:159987714
|
A | G | 1 | a0028c0050t0025g0227 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.150-3470A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159987714 | ||||||
| chr6:159987720
|
C | T | 4 | a0001c0002t0071g0194a0006c0010t0072g0196a0008c0011t0017g0152others(1): Show | 4 | HG02723.hp2 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.150-3464C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159987720 | ||||||
| chr6:159987729
|
A | G | 2 | a0005c0008t0002g0296a0005c0008t0093g0295 | 2 | HG01255.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.150-3455A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159987729 | ||||||
| chr6:159987788
|
T | C | 1 | a0001c0004t0044g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.150-3396T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159987788 | ||||||
| chr6:159988020
|
A | G | 7 | a0001c0001t0002g0293a0001c0001t0085g0294a0001c0002t0091g0292others(4): Show | 7 | HG00140.hp1 HG00639.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-3164A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159988020 | ||||||
| chr6:159988036
|
C | G | 124 | a0001c0001t0001g0187a0001c0001t0003g0037a0001c0001t0003g0230others(121): Show | 125 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.150-3148C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159988036 | ||||||
| chr6:159988084
|
A | G | 1 | a0002c0003t0014g0177 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.150-3100A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159988084 | ||||||
| chr6:159988297
|
C | T | 1 | a0001c0001t0002g0062 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.150-2887C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159988297 | ||||||
| chr6:159988381
|
G | C | 9 | a0001c0002t0015g0127a0001c0002t0015g0163a0001c0002t0027g0052others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.150-2803G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159988381 | ||||||
| chr6:159988383
|
T | C | 160 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0037others(157): Show | 161 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.150-2801T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159988383 | ||||||
| chr6:159988406
|
G | C | 1 | a0002c0003t0014g0177 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.150-2778G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159988406 | ||||||
| chr6:159988507
|
C | T | 2 | a0001c0004t0046g0273a0012c0031t0019g0165 | 2 | HG01109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.150-2677C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159988507 | ||||||
| chr6:159988512
|
C | CA | 19 | a0001c0001t0003g0246a0001c0001t0005g0115a0001c0001t0006g0244others(16): Show | 19 | HG00423.hp1 HG01106.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.150-2648dupA | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159988512 | |||||
| chr6:159988512
|
CA | C | 84 | a0001c0001t0001g0187a0001c0001t0003g0037a0001c0001t0003g0230others(81): Show | 85 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.150-2648delA | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159988512 | |||||
| chr6:159988512
|
CAAAAAAA others(3): Show |
C | 1 | a0004c0006t0049g0226 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.150-2657_150-2648d others(12): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159988512 | |||||
| chr6:159988559
|
C | T | 2 | a0001c0002t0010g0168a0001c0005t0012g0167 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.150-2625C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159988559 | ||||||
| chr6:159988734
|
G | T | 1 | a0012c0031t0019g0165 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.150-2450G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159988734 | ||||||
| chr6:159988862
|
G | T | 4 | a0001c0001t0013g0006a0001c0002t0082g0007a0017c0021t0031g0004others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-2322G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159988862 | ||||||
| chr6:159988962
|
A | G | 1 | a0006c0025t0059g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.150-2222A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159988962 | ||||||
| chr6:159989061
|
C | T | 2 | a0010c0016t0016g0169a0010c0016t0016g0170 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.150-2123C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159989061 | ||||||
| chr6:159989177
|
C | T | 7 | a0001c0001t0002g0293a0001c0001t0085g0294a0001c0002t0091g0292others(4): Show | 7 | HG00140.hp1 HG00639.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-2007C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159989177 | ||||||
| chr6:159989225
|
G | A | 1 | a0001c0024t0024g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.150-1959G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159989225 | ||||||
| chr6:159989233
|
C | T | 1 | a0005c0008t0013g0104 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.150-1951C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159989233 | ||||||
| chr6:159989298
|
G | C | 1 | a0004c0006t0002g0075 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.150-1886G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159989298 | ||||||
| chr6:159989299
|
T | C | 13 | a0001c0001t0003g0246a0001c0001t0003g0249a0001c0001t0003g0256others(10): Show | 13 | HG00642.hp2 HG00741.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.150-1885T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159989299 | ||||||
| chr6:159989308
|
A | G | 4 | a0006c0025t0059g0288a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-1876A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159989308 | ||||||
| chr6:159989334
|
G | C | 1 | a0001c0005t0004g0012 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.150-1850G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159989334 | ||||||
| chr6:159989425
|
A | C | 2 | a0003c0012t0009g0088a0003c0012t0009g0095 | 2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.150-1759A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159989425 | ||||||
| chr6:159989466
|
T | A | 112 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(109): Show | 113 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.150-1718T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159989466 | ||||||
| chr6:159989545
|
C | A | 4 | a0006c0025t0059g0288a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-1639C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159989545 | ||||||
| chr6:159989555
|
G | C | 1 | a0001c0004t0002g0129 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.150-1629G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159989555 | ||||||
| chr6:159989664
|
T | G | 1 | a0001c0004t0044g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.150-1520T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159989664 | ||||||
| chr6:159989671
|
A | G | 1 | a0006c0010t0072g0196 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.150-1513A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159989671 | ||||||
| chr6:159989712
|
C | T | 5 | a0001c0002t0071g0194a0001c0024t0024g0201a0006c0010t0072g0196others(2): Show | 5 | HG02723.hp2 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-1472C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159989712 | ||||||
| chr6:159989742
|
A | G | 4 | a0006c0025t0059g0288a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-1442A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159989742 | ||||||
| chr6:159989822
|
T | C | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.150-1362T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159989822 | ||||||
| chr6:159989888
|
G | A | 2 | a0001c0024t0070g0282a0006c0025t0059g0288 | 2 | HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.150-1296G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159989888 | ||||||
| chr6:159990040
|
C | G | 2 | a0003c0012t0006g0284a0003c0012t0006g0285 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.150-1144C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159990040 | ||||||
| chr6:159990050
|
A | C | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.150-1134A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159990050 | ||||||
| chr6:159990235
|
A | G | 290 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(287): Show | 291 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.150-949A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159990235 | ||||||
| chr6:159990242
|
T | C | 1 | a0001c0069t0052g0164 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.150-942T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159990242 | ||||||
| chr6:159990264
|
C | T | 2 | a0001c0002t0010g0168a0001c0005t0012g0167 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.150-920C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159990264 | ||||||
| chr6:159990268
|
T | C | 1 | a0006c0025t0059g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.150-916T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159990268 | ||||||
| chr6:159990353
|
G | A | 1 | a0002c0003t0001g0202 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.150-831G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159990353 | ||||||
| chr6:159990438
|
A | G | 2 | a0001c0046t0054g0281a0001c0069t0052g0164 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.150-746A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159990438 | ||||||
| chr6:159990465
|
C | T | 11 | a0001c0001t0003g0037a0001c0001t0043g0036a0001c0002t0056g0156others(8): Show | 11 | HG00738.hp1 HG01081.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.150-719C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159990465 | ||||||
| chr6:159990489
|
C | T | 2 | a0001c0009t0002g0068a0012c0031t0089g0067 | 2 | HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.150-695C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159990489 | ||||||
| chr6:159990499
|
C | G | 1 | a0001c0004t0044g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.150-685C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159990499 | ||||||
| chr6:159990652
|
CAG | C | 7 | a0001c0001t0003g0037a0001c0001t0043g0036a0006c0025t0059g0288others(4): Show | 7 | HG02280.hp1 HG02451.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-529_150-528del others(2): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr6 | 159990652 | |||||
| chr6:159990672
|
C | T | 2 | a0011c0017t0002g0015a0011c0017t0086g0016 | 2 | NA18970.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.150-512C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159990672 | ||||||
| chr6:159990693
|
G | A | 78 | a0001c0001t0001g0187a0001c0001t0003g0037a0001c0001t0003g0230others(75): Show | 79 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.150-491G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159990693 | ||||||
| chr6:159990715
|
C | T | 13 | a0001c0001t0002g0293a0001c0001t0013g0006a0001c0001t0085g0294others(10): Show | 13 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.150-469C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159990715 | ||||||
| chr6:159990737
|
C | T | 2 | a0001c0004t0046g0273a0012c0031t0019g0165 | 2 | HG01109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.150-447C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159990737 | ||||||
| chr6:159990774
|
C | T | 8 | a0001c0001t0006g0274a0001c0001t0026g0268a0001c0001t0026g0269others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.150-410C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159990774 | ||||||
| chr6:159990927
|
C | T | 10 | a0001c0001t0030g0105a0001c0004t0002g0129a0003c0007t0022g0106others(7): Show | 10 | HG02723.hp1 HG02886.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.150-257C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159990927 | ||||||
| chr6:159990933
|
C | T | 160 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0037others(157): Show | 161 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.150-251C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159990933 | ||||||
| chr6:159991156
|
T | G | 4 | a0006c0025t0059g0288a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-28T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 1/47 | chr6 | 159991156 | ||||||
| chr6:159991461
|
T | C | 3 | a0007c0014t0011g0092a0007c0014t0011g0093a0007c0014t0011g0094 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.289+138T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159991461 | ||||||
| chr6:159991609
|
A | C | 24 | a0001c0002t0010g0168a0001c0005t0004g0083a0001c0005t0012g0167others(21): Show | 24 | HG00597.hp1 HG00639.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.289+286A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159991609 | ||||||
| chr6:159991610
|
T | TA | 24 | a0001c0002t0010g0168a0001c0005t0004g0083a0001c0005t0012g0167others(21): Show | 24 | HG00597.hp1 HG00639.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.289+287_289+288ins others(1): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159991610 | ||||||
| chr6:159991858
|
G | A | 4 | a0006c0025t0059g0288a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+535G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159991858 | ||||||
| chr6:159992042
|
G | A | 8 | a0001c0001t0013g0145a0001c0001t0013g0146a0001c0002t0007g0066others(5): Show | 8 | HG00642.hp1 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.289+719G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159992042 | ||||||
| chr6:159992358
|
T | C | 1 | a0001c0002t0009g0047 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.289+1035T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159992358 | ||||||
| chr6:159992427
|
C | G | 4 | a0006c0025t0059g0288a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+1104C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159992427 | ||||||
| chr6:159992507
|
T | G | 116 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(113): Show | 117 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.289+1184T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159992507 | ||||||
| chr6:159992598
|
T | TCA | 44 | a0001c0001t0005g0121a0001c0002t0002g0020a0001c0002t0007g0066others(41): Show | 44 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.289+1306_289+1307d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 159992598 | |||||
| chr6:159992598
|
T | TCACACAC others(3): Show |
1 | a0019c0068t0012g0279 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.289+1298_289+1307d others(12): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 159992598 | |||||
| chr6:159992598
|
TCA | T | 105 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0037others(102): Show | 106 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.289+1306_289+1307d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 159992598 | |||||
| chr6:159992598
|
TCACA | T | 29 | a0001c0002t0010g0168a0001c0004t0065g0200a0001c0005t0004g0083others(26): Show | 29 | HG00597.hp1 HG00597.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.289+1304_289+1307d others(6): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 159992598 | |||||
| chr6:159992603
|
C | T | 3 | a0001c0009t0001g0181a0002c0003t0001g0224a0002c0003t0001g0225 | 3 | NA18964.hp1 NA18999.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.289+1280C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159992603 | ||||||
| chr6:159992631
|
A | C | 1 | a0006c0025t0059g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.289+1308A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159992631 | ||||||
| chr6:159992637
|
C | T | 1 | a0001c0049t0004g0090 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.289+1314C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159992637 | ||||||
| chr6:159992639
|
C | A | 1 | a0006c0025t0059g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.289+1316C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159992639 | ||||||
| chr6:159993032
|
C | T | 2 | a0001c0002t0010g0168a0001c0005t0012g0167 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.289+1709C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159993032 | ||||||
| chr6:159993162
|
A | T | 3 | a0010c0016t0016g0150a0019c0068t0012g0279a0022c0042t0024g0151 | 3 | HG02280.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.289+1839A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159993162 | ||||||
| chr6:159993423
|
A | G | 2 | a0010c0016t0016g0150a0022c0042t0024g0151 | 2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.289+2100A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159993423 | ||||||
| chr6:159993572
|
G | A | 17 | a0001c0002t0002g0020a0001c0005t0004g0012a0001c0005t0004g0014others(14): Show | 17 | HG00438.hp2 HG00544.hp2 HG04228.hp1 others(14): Show |
intron_variant | MODIFIER | c.289+2249G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159993572 | ||||||
| chr6:159993746
|
T | C | 4 | a0006c0025t0059g0288a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+2423T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159993746 | ||||||
| chr6:159993783
|
A | G | 1 | a0001c0002t0015g0163 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.289+2460A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159993783 | ||||||
| chr6:159993985
|
A | AT | 28 | a0001c0001t0001g0301a0001c0001t0001g0304a0001c0001t0003g0037others(25): Show | 28 | HG00280.hp1 HG00323.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.289+2687dupT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 159993985 | |||||
| chr6:159993985
|
A | ATT | 11 | a0001c0001t0002g0293a0001c0001t0085g0294a0001c0002t0010g0168others(8): Show | 11 | HG00140.hp1 HG00639.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.289+2686_289+2687d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 159993985 | |||||
| chr6:159993985
|
A | ATTT | 21 | a0001c0002t0002g0020a0001c0002t0015g0009a0001c0002t0058g0234others(18): Show | 21 | HG00544.hp2 HG02258.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.289+2685_289+2687d others(5): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 159993985 | |||||
| chr6:159993985
|
A | ATTTT | 69 | a0001c0001t0003g0230a0001c0001t0006g0219a0001c0001t0030g0105others(66): Show | 70 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.289+2684_289+2687d others(6): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 159993985 | |||||
| chr6:159993985
|
A | ATTTTT | 16 | a0001c0001t0001g0187a0001c0001t0003g0231a0001c0004t0003g0223others(13): Show | 16 | HG00544.hp1 HG00621.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.289+2683_289+2687d others(7): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 159993985 | |||||
| chr6:159993985
|
ATTTTT | A | 6 | a0001c0002t0028g0034a0001c0034t0006g0035a0009c0013t0010g0158others(3): Show | 6 | HG02145.hp2 HG02647.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.289+2683_289+2687d others(7): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 159993985 | |||||
| chr6:159993985
|
ATTTTTTT others(1): Show |
A | 22 | a0001c0005t0004g0083a0001c0005t0012g0184a0001c0037t0002g0079others(19): Show | 22 | HG00597.hp1 HG00639.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.289+2680_289+2687d others(10): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 159993985 | |||||
| chr6:159994129
|
C | G | 1 | a0001c0046t0054g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.289+2806C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159994129 | ||||||
| chr6:159994309
|
T | C | 112 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(109): Show | 113 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.289+2986T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159994309 | ||||||
| chr6:159994429
|
G | T | 4 | a0006c0025t0059g0288a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+3106G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159994429 | ||||||
| chr6:159994510
|
T | C | 1 | a0001c0002t0018g0235 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.289+3187T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159994510 | ||||||
| chr6:159994522
|
C | T | 1 | a0001c0002t0082g0007 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.289+3199C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159994522 | ||||||
| chr6:159994592
|
C | A | 2 | a0001c0002t0010g0168a0001c0005t0012g0167 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.289+3269C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159994592 | ||||||
| chr6:159994612
|
T | A | 26 | a0001c0002t0002g0020a0001c0002t0015g0009a0001c0002t0028g0034others(23): Show | 26 | HG00438.hp2 HG00544.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.289+3289T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159994612 | ||||||
| chr6:159995008
|
T | C | 162 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0037others(159): Show | 163 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.289+3685T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159995008 | ||||||
| chr6:159995072
|
A | G | 112 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(109): Show | 113 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.289+3749A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159995072 | ||||||
| chr6:159995164
|
T | A | 1 | a0002c0003t0014g0177 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.289+3841T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159995164 | ||||||
| chr6:159995171
|
C | T | 2 | a0010c0016t0016g0169a0010c0016t0016g0170 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.289+3848C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159995171 | ||||||
| chr6:159995243
|
A | G | 160 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0037others(157): Show | 161 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.289+3920A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159995243 | ||||||
| chr6:159995318
|
G | GT | 13 | a0001c0001t0003g0246a0001c0001t0003g0249a0001c0001t0003g0256others(10): Show | 13 | HG00642.hp2 HG00741.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.289+4000dupT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 159995318 | |||||
| chr6:159995335
|
G | T | 88 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(85): Show | 89 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.289+4012G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159995335 | ||||||
| chr6:159995738
|
G | A | 7 | a0001c0001t0003g0037a0001c0001t0013g0006a0001c0001t0043g0036others(4): Show | 7 | HG00280.hp1 HG00323.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.289+4415G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159995738 | ||||||
| chr6:159995798
|
A | G | 1 | a0001c0009t0008g0011 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.289+4475A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159995798 | ||||||
| chr6:159995851
|
A | G | 2 | a0010c0016t0016g0169a0010c0016t0016g0170 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.289+4528A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159995851 | ||||||
| chr6:159995895
|
CT | C | 140 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0037others(137): Show | 141 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.289+4592delT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 159995895 | |||||
| chr6:159995895
|
CTT | C | 35 | a0001c0002t0002g0020a0001c0002t0015g0009a0001c0002t0028g0034others(32): Show | 35 | HG00438.hp2 HG00544.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.289+4591_289+4592d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 159995895 | |||||
| chr6:159995916
|
A | G | 1 | a0002c0003t0008g0136 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.289+4593A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159995916 | ||||||
| chr6:159996008
|
T | C | 5 | a0001c0002t0071g0194a0001c0024t0024g0201a0006c0010t0072g0196others(2): Show | 5 | HG02723.hp2 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.289+4685T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159996008 | ||||||
| chr6:159996173
|
G | C | 10 | a0001c0002t0009g0047a0003c0007t0003g0172a0003c0007t0003g0254others(7): Show | 10 | HG00621.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.289+4850G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159996173 | ||||||
| chr6:159996190
|
G | A | 7 | a0001c0001t0002g0293a0001c0001t0085g0294a0001c0002t0091g0292others(4): Show | 7 | HG00140.hp1 HG00639.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.289+4867G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159996190 | ||||||
| chr6:159996555
|
C | T | 1 | a0001c0069t0052g0164 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.289+5232C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159996555 | ||||||
| chr6:159996682
|
G | A | 2 | a0001c0005t0012g0184a0027c0055t0020g0183 | 2 | NA18948.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.289+5359G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159996682 | ||||||
| chr6:159996784
|
A | G | 1 | a0006c0025t0059g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.289+5461A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159996784 | ||||||
| chr6:159996814
|
C | T | 1 | a0001c0001t0001g0304 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.289+5491C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159996814 | ||||||
| chr6:159996891
|
C | T | 1 | a0001c0005t0004g0027 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.289+5568C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159996891 | ||||||
| chr6:159996949
|
C | T | 1 | a0001c0004t0003g0192 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.289+5626C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159996949 | ||||||
| chr6:159996987
|
G | C | 6 | a0001c0002t0028g0034a0001c0034t0006g0035a0009c0013t0010g0158others(3): Show | 6 | HG02145.hp2 HG02647.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.289+5664G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159996987 | ||||||
| chr6:159996997
|
C | T | 1 | a0001c0002t0003g0306 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.289+5674C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159996997 | ||||||
| chr6:159997018
|
G | A | 7 | a0001c0001t0003g0037a0001c0001t0013g0006a0001c0001t0043g0036others(4): Show | 7 | HG00280.hp1 HG00323.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.289+5695G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159997018 | ||||||
| chr6:159997032
|
A | C | 4 | a0006c0025t0059g0288a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+5709A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159997032 | ||||||
| chr6:159997243
|
C | T | 1 | a0002c0003t0014g0173 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.289+5920C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159997243 | ||||||
| chr6:159997346
|
T | C | 2 | a0010c0016t0016g0169a0010c0016t0016g0170 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.289+6023T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159997346 | ||||||
| chr6:159997540
|
C | T | 1 | a0002c0003t0060g0215 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.289+6217C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159997540 | ||||||
| chr6:159997553
|
T | C | 1 | a0001c0046t0054g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.289+6230T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159997553 | ||||||
| chr6:159997556
|
A | G | 4 | a0006c0025t0059g0288a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+6233A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159997556 | ||||||
| chr6:159997649
|
C | T | 2 | a0001c0002t0010g0168a0001c0005t0012g0167 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.289+6326C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159997649 | ||||||
| chr6:159997674
|
C | T | 1 | a0001c0001t0006g0264 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.289+6351C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159997674 | ||||||
| chr6:159997691
|
G | C | 7 | a0001c0002t0018g0235a0001c0002t0018g0236a0001c0002t0018g0237others(4): Show | 7 | HG02280.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.289+6368G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159997691 | ||||||
| chr6:159997693
|
T | G | 4 | a0006c0025t0059g0288a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+6370T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159997693 | ||||||
| chr6:159997740
|
C | T | 20 | a0001c0002t0002g0020a0001c0002t0015g0009a0001c0004t0044g0153others(17): Show | 20 | HG00438.hp2 HG00544.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.289+6417C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159997740 | ||||||
| chr6:159997950
|
T | G | 1 | a0001c0001t0006g0264 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.289+6627T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159997950 | ||||||
| chr6:159998030
|
A | G | 10 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0003g0307others(7): Show | 10 | HG02155.hp1 NA18945.hp2 NA18967.hp1 others(7): Show |
intron_variant | MODIFIER | c.289+6707A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159998030 | ||||||
| chr6:159998225
|
A | T | 20 | a0001c0002t0002g0020a0001c0002t0015g0009a0001c0004t0044g0153others(17): Show | 20 | HG00438.hp2 HG00544.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.289+6902A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159998225 | ||||||
| chr6:159998270
|
G | A | 2 | a0002c0003t0001g0002a0005c0027t0003g0003 | 2 | NA18960.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.289+6947G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159998270 | ||||||
| chr6:159998763
|
A | T | 2 | a0001c0001t0003g0230a0001c0001t0003g0231 | 2 | HG03490.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.289+7440A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159998763 | ||||||
| chr6:159998807
|
C | G | 6 | a0001c0002t0010g0168a0001c0005t0012g0167a0006c0025t0059g0288others(3): Show | 6 | HG02257.hp1 HG02280.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.289+7484C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159998807 | ||||||
| chr6:159998878
|
T | C | 1 | a0001c0004t0081g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.289+7555T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159998878 | ||||||
| chr6:159998992
|
A | G | 2 | a0001c0005t0004g0021a0002c0052t0008g0023 | 2 | HG00438.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.289+7669A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159998992 | ||||||
| chr6:159999180
|
A | G | 7 | a0001c0009t0001g0211a0002c0003t0001g0001a0002c0003t0001g0199others(4): Show | 8 | HG00408.hp1 HG01258.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.289+7857A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159999180 | ||||||
| chr6:159999181
|
C | T | 1 | a0004c0061t0003g0266 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.289+7858C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159999181 | ||||||
| chr6:159999187
|
A | G | 1 | a0019c0068t0012g0279 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.289+7864A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159999187 | ||||||
| chr6:159999202
|
C | G | 2 | a0005c0008t0002g0296a0005c0008t0093g0295 | 2 | HG01255.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.289+7879C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159999202 | ||||||
| chr6:159999293
|
T | G | 111 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(108): Show | 112 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.289+7970T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159999293 | ||||||
| chr6:159999474
|
C | T | 161 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0037others(158): Show | 162 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.289+8151C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159999474 | ||||||
| chr6:159999673
|
A | G | 112 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(109): Show | 113 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.289+8350A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159999673 | ||||||
| chr6:159999832
|
A | T | 111 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(108): Show | 112 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.289+8509A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159999832 | ||||||
| chr6:159999980
|
A | G | 161 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0037others(158): Show | 162 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.289+8657A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 159999980 | ||||||
| chr6:160000033
|
G | T | 1 | a0017c0021t0031g0005 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.289+8710G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160000033 | ||||||
| chr6:160000163
|
G | A | 1 | a0001c0005t0004g0014 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.289+8840G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160000163 | ||||||
| chr6:160000231
|
C | A | 23 | a0001c0005t0004g0083a0001c0005t0012g0184a0001c0037t0002g0079others(20): Show | 23 | HG00597.hp1 HG00639.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.290-8779C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160000231 | ||||||
| chr6:160000362
|
A | G | 2 | a0001c0004t0046g0273a0012c0031t0019g0165 | 2 | HG01109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.290-8648A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160000362 | ||||||
| chr6:160000631
|
G | T | 7 | a0001c0001t0002g0293a0001c0001t0085g0294a0001c0002t0091g0292others(4): Show | 7 | HG00140.hp1 HG00639.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.290-8379G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160000631 | ||||||
| chr6:160000665
|
C | T | 111 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(108): Show | 112 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.290-8345C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160000665 | ||||||
| chr6:160000728
|
G | GT | 92 | a0001c0001t0001g0301a0001c0001t0003g0230a0001c0001t0003g0256others(89): Show | 93 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.290-8257dupT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 160000728 | |||||
| chr6:160000728
|
G | GTT | 58 | a0001c0001t0001g0187a0001c0001t0003g0231a0001c0001t0005g0100others(55): Show | 58 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.290-8258_290-8257d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 160000728 | |||||
| chr6:160000728
|
G | GTTT | 6 | a0001c0002t0002g0020a0001c0004t0044g0153a0001c0005t0004g0019others(3): Show | 6 | HG00544.hp2 HG02738.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.290-8259_290-8257d others(5): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 160000728 | |||||
| chr6:160000728
|
G | GTTTTTTT others(5): Show |
1 | a0009c0013t0010g0158 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.290-8268_290-8257d others(14): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 160000728 | |||||
| chr6:160000728
|
G | GTTTTTTT others(6): Show |
2 | a0009c0013t0010g0159a0009c0013t0010g0161 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.290-8269_290-8257d others(15): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 160000728 | |||||
| chr6:160000728
|
G | GTTTTTTT others(7): Show |
3 | a0001c0002t0028g0034a0001c0034t0006g0035a0009c0013t0010g0160 | 3 | HG02145.hp2 HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.290-8270_290-8257d others(16): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 160000728 | |||||
| chr6:160000728
|
G | GTTTTTTT others(29): Show |
1 | a0001c0004t0046g0273 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.290-8257_290-8256i others(38): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 160000728 | |||||
| chr6:160000728
|
GTT | G | 12 | a0001c0001t0002g0293a0001c0001t0003g0037a0001c0001t0013g0006others(9): Show | 12 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.290-8258_290-8257d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 160000728 | |||||
| chr6:160000735
|
T | TTTTTTTT others(5): Show |
3 | a0001c0002t0010g0168a0001c0005t0012g0167a0006c0025t0059g0288 | 3 | HG02257.hp1 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.290-8264_290-8263i others(14): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 160000735 | |||||
| chr6:160000777
|
C | A | 1 | a0001c0001t0002g0293 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.290-8233C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160000777 | ||||||
| chr6:160000883
|
C | T | 1 | a0001c0004t0044g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.290-8127C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160000883 | ||||||
| chr6:160001079
|
C | T | 1 | a0001c0004t0065g0200 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.290-7931C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160001079 | ||||||
| chr6:160001095
|
G | A | 1 | a0002c0003t0020g0278 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.290-7915G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160001095 | ||||||
| chr6:160001116
|
G | A | 1 | a0006c0010t0002g0010 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.290-7894G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160001116 | ||||||
| chr6:160001167
|
C | T | 111 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(108): Show | 112 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.290-7843C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160001167 | ||||||
| chr6:160001183
|
C | T | 15 | a0001c0001t0002g0293a0001c0001t0003g0037a0001c0001t0013g0006others(12): Show | 15 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.290-7827C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160001183 | ||||||
| chr6:160001219
|
A | G | 1 | a0001c0046t0054g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.290-7791A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160001219 | ||||||
| chr6:160001507
|
C | T | 1 | a0002c0003t0001g0199 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.290-7503C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160001507 | ||||||
| chr6:160001585
|
G | A | 3 | a0001c0002t0010g0168a0001c0005t0012g0167a0006c0025t0059g0288 | 3 | HG02257.hp1 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.290-7425G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160001585 | ||||||
| chr6:160001659
|
A | G | 3 | a0001c0002t0010g0168a0001c0005t0012g0167a0006c0025t0059g0288 | 3 | HG02257.hp1 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.290-7351A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160001659 | ||||||
| chr6:160001669
|
A | G | 2 | a0003c0007t0004g0074a0003c0007t0004g0078 | 2 | NA18959.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.290-7341A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160001669 | ||||||
| chr6:160001727
|
A | G | 1 | a0001c0056t0003g0154 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.290-7283A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160001727 | ||||||
| chr6:160001753
|
A | G | 111 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(108): Show | 112 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.290-7257A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160001753 | ||||||
| chr6:160001786
|
C | T | 3 | a0001c0002t0010g0168a0001c0005t0012g0167a0006c0025t0059g0288 | 3 | HG02257.hp1 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.290-7224C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160001786 | ||||||
| chr6:160002045
|
A | G | 9 | a0001c0001t0030g0105a0001c0004t0002g0129a0003c0007t0022g0106others(6): Show | 9 | HG02723.hp1 HG02886.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.290-6965A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160002045 | ||||||
| chr6:160002382
|
A | G | 5 | a0001c0001t0021g0044a0001c0001t0021g0045a0001c0001t0021g0046others(2): Show | 5 | HG00280.hp2 HG01192.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.290-6628A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160002382 | ||||||
| chr6:160002408
|
G | C | 161 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0037others(158): Show | 162 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.290-6602G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160002408 | ||||||
| chr6:160002461
|
T | C | 1 | a0001c0039t0045g0228 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.290-6549T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160002461 | ||||||
| chr6:160002495
|
C | T | 1 | a0004c0006t0002g0084 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.290-6515C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160002495 | ||||||
| chr6:160002590
|
G | T | 4 | a0009c0013t0010g0158a0009c0013t0010g0159a0009c0013t0010g0160others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-6420G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160002590 | ||||||
| chr6:160002822
|
T | C | 1 | a0006c0025t0059g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.290-6188T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160002822 | ||||||
| chr6:160003082
|
C | T | 110 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(107): Show | 111 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.290-5928C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160003082 | ||||||
| chr6:160003246
|
T | G | 1 | a0001c0046t0054g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.290-5764T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160003246 | ||||||
| chr6:160003544
|
A | G | 3 | a0010c0016t0016g0150a0019c0068t0012g0279a0022c0042t0024g0151 | 3 | HG02280.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.290-5466A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160003544 | ||||||
| chr6:160003728
|
T | C | 2 | a0001c0002t0036g0289a0001c0002t0036g0290 | 2 | HG00642.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.290-5282T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160003728 | ||||||
| chr6:160003780
|
A | T | 110 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(107): Show | 111 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.290-5230A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160003780 | ||||||
| chr6:160003869
|
T | C | 113 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(110): Show | 114 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.290-5141T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160003869 | ||||||
| chr6:160003923
|
CTTGAG | C | 110 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(107): Show | 111 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.290-5081_290-5077d others(7): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 160003923 | |||||
| chr6:160004215
|
T | C | 113 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(110): Show | 114 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.290-4795T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160004215 | ||||||
| chr6:160004352
|
G | A | 1 | a0004c0029t0003g0180 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.290-4658G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160004352 | ||||||
| chr6:160004447
|
C | G | 1 | a0003c0007t0003g0172 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.290-4563C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160004447 | ||||||
| chr6:160004572
|
A | G | 113 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(110): Show | 114 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.290-4438A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160004572 | ||||||
| chr6:160004651
|
G | A | 2 | a0010c0016t0016g0169a0010c0016t0016g0170 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.290-4359G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160004651 | ||||||
| chr6:160004666
|
G | A | 1 | a0001c0002t0082g0007 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.290-4344G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160004666 | ||||||
| chr6:160004671
|
G | A | 2 | a0001c0004t0046g0273a0012c0031t0019g0165 | 2 | HG01109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.290-4339G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160004671 | ||||||
| chr6:160004801
|
G | A | 3 | a0010c0016t0016g0150a0019c0068t0012g0279a0022c0042t0024g0151 | 3 | HG02280.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.290-4209G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160004801 | ||||||
| chr6:160004868
|
A | G | 1 | a0023c0035t0003g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.290-4142A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160004868 | ||||||
| chr6:160004937
|
C | T | 22 | a0001c0005t0004g0083a0001c0005t0012g0184a0001c0037t0002g0079others(19): Show | 22 | HG00597.hp1 HG00639.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.290-4073C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160004937 | ||||||
| chr6:160004975
|
A | T | 3 | a0001c0002t0015g0009a0001c0004t0044g0153a0008c0011t0078g0008 | 3 | HG02258.hp2 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.290-4035A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160004975 | ||||||
| chr6:160005035
|
T | G | 3 | a0001c0002t0010g0168a0001c0005t0012g0167a0006c0025t0059g0288 | 3 | HG02257.hp1 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.290-3975T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160005035 | ||||||
| chr6:160005157
|
A | G | 3 | a0010c0016t0016g0150a0019c0068t0012g0279a0022c0042t0024g0151 | 3 | HG02280.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.290-3853A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160005157 | ||||||
| chr6:160005195
|
A | G | 1 | a0002c0047t0008g0135 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.290-3815A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160005195 | ||||||
| chr6:160005248
|
G | A | 1 | a0005c0020t0002g0031 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.290-3762G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160005248 | ||||||
| chr6:160005252
|
C | T | 2 | a0001c0002t0091g0292a0001c0004t0081g0112 | 2 | HG02165.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.290-3758C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160005252 | ||||||
| chr6:160005401
|
C | T | 4 | a0003c0007t0022g0107a0003c0007t0022g0108a0003c0007t0023g0109others(1): Show | 4 | HG02886.hp1 HG03098.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-3609C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160005401 | ||||||
| chr6:160005424
|
C | T | 15 | a0001c0001t0002g0142a0001c0001t0005g0100a0001c0002t0002g0030others(12): Show | 15 | HG00733.hp1 HG00733.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.290-3586C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160005424 | ||||||
| chr6:160005427
|
T | G | 88 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(85): Show | 89 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.290-3583T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160005427 | ||||||
| chr6:160005459
|
C | T | 1 | a0002c0003t0001g0189 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.290-3551C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160005459 | ||||||
| chr6:160005531
|
G | A | 1 | a0001c0046t0054g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.290-3479G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160005531 | ||||||
| chr6:160005590
|
C | T | 2 | a0001c0002t0036g0289a0001c0002t0036g0290 | 2 | HG00642.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.290-3420C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160005590 | ||||||
| chr6:160005728
|
C | G | 5 | a0001c0009t0002g0068a0002c0003t0008g0148a0003c0058t0076g0070others(2): Show | 5 | HG01192.hp1 HG02258.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.290-3282C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160005728 | ||||||
| chr6:160005762
|
A | G | 5 | a0001c0004t0034g0126a0006c0010t0002g0010a0006c0010t0011g0123others(2): Show | 5 | HG01891.hp2 HG02055.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.290-3248A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160005762 | ||||||
| chr6:160005912
|
C | T | 2 | a0010c0016t0016g0169a0010c0016t0016g0170 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.290-3098C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160005912 | ||||||
| chr6:160005916
|
C | T | 1 | a0001c0005t0004g0083 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.290-3094C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160005916 | ||||||
| chr6:160005920
|
G | A | 2 | a0001c0004t0002g0064a0001c0004t0002g0065 | 2 | HG00738.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.290-3090G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160005920 | ||||||
| chr6:160005982
|
G | A | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.290-3028G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160005982 | ||||||
| chr6:160006035
|
C | A | 1 | a0001c0004t0065g0200 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.290-2975C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160006035 | ||||||
| chr6:160006061
|
C | T | 1 | a0012c0031t0019g0165 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.290-2949C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160006061 | ||||||
| chr6:160006179
|
C | T | 23 | a0001c0005t0004g0083a0001c0005t0012g0184a0001c0037t0002g0079others(20): Show | 23 | HG00597.hp1 HG00639.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.290-2831C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160006179 | ||||||
| chr6:160006206
|
T | TC | 114 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(111): Show | 115 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.290-2798dupC | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 160006206 | |||||
| chr6:160006217
|
G | A | 1 | a0002c0003t0001g0202 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.290-2793G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160006217 | ||||||
| chr6:160006219
|
C | G | 1 | a0001c0001t0005g0115 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.290-2791C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160006219 | ||||||
| chr6:160006225
|
C | G | 1 | a0005c0008t0002g0033 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.290-2785C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160006225 | ||||||
| chr6:160006229
|
C | G | 1 | a0002c0028t0001g0262 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.290-2781C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160006229 | ||||||
| chr6:160006244
|
C | T | 1 | a0021c0044t0074g0111 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.290-2766C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160006244 | ||||||
| chr6:160006277
|
C | A | 23 | a0001c0005t0004g0083a0001c0005t0012g0184a0001c0037t0002g0079others(20): Show | 23 | HG00597.hp1 HG00639.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.290-2733C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160006277 | ||||||
| chr6:160006411
|
G | A | 2 | a0001c0009t0005g0143a0001c0009t0005g0144 | 2 | HG01884.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.290-2599G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160006411 | ||||||
| chr6:160006423
|
C | CGGAGCTG others(10): Show |
4 | a0001c0046t0054g0281a0010c0016t0016g0150a0019c0068t0012g0279others(1): Show | 4 | HG02280.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-2558_290-2542d others(19): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 160006423 | |||||
| chr6:160006423
|
CGGAGCTG others(10): Show |
C | 25 | a0001c0005t0004g0083a0001c0005t0012g0184a0001c0037t0002g0079others(22): Show | 25 | HG00597.hp1 HG00639.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.290-2558_290-2542d others(19): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 160006423 | |||||
| chr6:160006454
|
C | A | 1 | a0001c0001t0010g0157 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.290-2556C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160006454 | ||||||
| chr6:160006479
|
A | T | 114 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(111): Show | 115 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.290-2531A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160006479 | ||||||
| chr6:160006612
|
G | C | 111 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(108): Show | 112 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.290-2398G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160006612 | ||||||
| chr6:160006803
|
C | T | 1 | a0001c0001t0006g0244 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.290-2207C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160006803 | ||||||
| chr6:160006850
|
T | C | 111 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(108): Show | 112 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.290-2160T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160006850 | ||||||
| chr6:160006914
|
A | AT | 92 | a0001c0001t0003g0230a0001c0001t0003g0231a0001c0001t0006g0219others(89): Show | 93 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.290-2081dupT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 160006914 | |||||
| chr6:160006945
|
C | CA | 152 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0037others(149): Show | 153 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.290-2053dupA | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 160006945 | |||||
| chr6:160006945
|
C | CAA | 8 | a0001c0002t0028g0034a0001c0004t0003g0223a0001c0034t0006g0035others(5): Show | 8 | HG02145.hp2 HG02647.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.290-2054_290-2053d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 160006945 | |||||
| chr6:160007042
|
G | A | 114 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(111): Show | 115 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.290-1968G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160007042 | ||||||
| chr6:160007091
|
T | A | 6 | a0001c0002t0028g0034a0001c0034t0006g0035a0009c0013t0010g0158others(3): Show | 6 | HG02145.hp2 HG02647.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.290-1919T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160007091 | ||||||
| chr6:160007105
|
T | C | 120 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(117): Show | 121 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.290-1905T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160007105 | ||||||
| chr6:160007250
|
T | C | 2 | a0001c0001t0002g0043a0001c0001t0005g0028 | 2 | HG01081.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.290-1760T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160007250 | ||||||
| chr6:160007376
|
G | T | 161 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0037others(158): Show | 162 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.290-1634G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160007376 | ||||||
| chr6:160007517
|
C | T | 26 | a0001c0002t0002g0020a0001c0002t0015g0009a0001c0002t0028g0034others(23): Show | 26 | HG00438.hp2 HG00544.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.290-1493C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160007517 | ||||||
| chr6:160007529
|
T | A | 15 | a0001c0001t0002g0293a0001c0001t0003g0037a0001c0001t0013g0006others(12): Show | 15 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.290-1481T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160007529 | ||||||
| chr6:160007567
|
T | G | 1 | a0003c0059t0055g0171 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.290-1443T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160007567 | ||||||
| chr6:160007590
|
A | G | 20 | a0001c0002t0002g0020a0001c0002t0015g0009a0001c0004t0044g0153others(17): Show | 20 | HG00438.hp2 HG00544.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.290-1420A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160007590 | ||||||
| chr6:160007607
|
T | C | 1 | a0006c0025t0059g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.290-1403T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160007607 | ||||||
| chr6:160007811
|
C | T | 91 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(88): Show | 92 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.290-1199C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160007811 | ||||||
| chr6:160007826
|
G | A | 114 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(111): Show | 115 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.290-1184G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160007826 | ||||||
| chr6:160007914
|
T | A | 1 | a0004c0006t0003g0176 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.290-1096T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160007914 | ||||||
| chr6:160007973
|
G | A | 1 | a0001c0002t0002g0020 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.290-1037G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160007973 | ||||||
| chr6:160008014
|
T | G | 1 | a0006c0025t0059g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.290-996T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160008014 | ||||||
| chr6:160008215
|
C | G | 1 | a0002c0003t0001g0265 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.290-795C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160008215 | ||||||
| chr6:160008268
|
A | G | 1 | a0002c0003t0014g0177 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.290-742A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160008268 | ||||||
| chr6:160008271
|
TC | T | 3 | a0010c0016t0016g0150a0019c0068t0012g0279a0022c0042t0024g0151 | 3 | HG02280.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.290-737delC | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr6 | 160008271 | |||||
| chr6:160008325
|
A | G | 1 | a0002c0003t0014g0177 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.290-685A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160008325 | ||||||
| chr6:160008659
|
C | T | 3 | a0010c0016t0016g0150a0019c0068t0012g0279a0022c0042t0024g0151 | 3 | HG02280.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.290-351C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160008659 | ||||||
| chr6:160008660
|
G | A | 2 | a0001c0002t0036g0289a0001c0002t0036g0290 | 2 | HG00642.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.290-350G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160008660 | ||||||
| chr6:160008674
|
G | T | 1 | a0001c0001t0005g0120 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.290-336G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160008674 | ||||||
| chr6:160008705
|
A | G | 49 | a0001c0001t0001g0301a0001c0001t0001g0304a0001c0001t0001g0305others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG01192.hp1 others(46): Show |
intron_variant | MODIFIER | c.290-305A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160008705 | ||||||
| chr6:160008756
|
G | A | 1 | a0001c0004t0003g0210 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.290-254G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160008756 | ||||||
| chr6:160008774
|
C | G | 1 | a0001c0001t0001g0301 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.290-236C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160008774 | ||||||
| chr6:160008851
|
A | G | 117 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(114): Show | 118 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.290-159A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 2/47 | chr6 | 160008851 | ||||||
| chr6:160009167
|
T | TA | 24 | a0001c0002t0002g0020a0001c0002t0015g0009a0001c0004t0044g0153others(21): Show | 24 | HG00438.hp2 HG00544.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.414+44dupA | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr6 | 160009167 | |||||
| chr6:160009178
|
A | T | 3 | a0001c0002t0010g0168a0001c0005t0012g0167a0006c0025t0059g0288 | 3 | HG02257.hp1 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.414+44A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | chr6 | 160009178 | ||||||
| chr6:160009180
|
G | A | 3 | a0010c0016t0016g0150a0019c0068t0012g0279a0022c0042t0024g0151 | 3 | HG02280.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.414+46G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | chr6 | 160009180 | ||||||
| chr6:160009227
|
G | A | 1 | a0001c0002t0080g0054 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.414+93G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | chr6 | 160009227 | ||||||
| chr6:160009559
|
G | A | 88 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(85): Show | 89 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.414+425G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | chr6 | 160009559 | ||||||
| chr6:160009569
|
G | A | 3 | a0003c0012t0006g0284a0003c0012t0006g0285a0032c0065t0041g0283 | 3 | HG02451.hp2 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.414+435G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | chr6 | 160009569 | ||||||
| chr6:160009585
|
C | T | 1 | a0003c0007t0003g0254 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.414+451C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | chr6 | 160009585 | ||||||
| chr6:160009624
|
A | C | 172 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0037others(169): Show | 173 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.414+490A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | chr6 | 160009624 | ||||||
| chr6:160009968
|
G | A | 1 | a0003c0007t0009g0048 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.415-719G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | chr6 | 160009968 | ||||||
| chr6:160009985
|
C | CTTAA | 169 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0037others(166): Show | 170 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.415-702_415-701ins others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | chr6 | 160009985 | ||||||
| chr6:160009986
|
C | A | 169 | a0001c0001t0001g0187a0001c0001t0002g0293a0001c0001t0003g0037others(166): Show | 170 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.415-701C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | chr6 | 160009986 | ||||||
| chr6:160010075
|
T | G | 1 | a0002c0003t0008g0085 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.415-612T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | chr6 | 160010075 | ||||||
| chr6:160010094
|
C | T | 1 | a0003c0007t0075g0147 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.415-593C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | chr6 | 160010094 | ||||||
| chr6:160010340
|
T | C | 1 | a0001c0002t0050g0242 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.415-347T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | chr6 | 160010340 | ||||||
| chr6:160010348
|
G | A | 75 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0231others(72): Show | 76 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.415-339G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | chr6 | 160010348 | ||||||
| chr6:160010404
|
A | T | 7 | a0001c0002t0010g0168a0001c0002t0071g0194a0001c0005t0012g0167others(4): Show | 7 | HG02257.hp1 HG02723.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-283A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | chr6 | 160010404 | ||||||
| chr6:160010440
|
G | C | 1 | a0002c0015t0014g0298 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.415-247G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | chr6 | 160010440 | ||||||
| chr6:160010550
|
A | G | 4 | a0009c0013t0010g0158a0009c0013t0010g0159a0009c0013t0010g0160others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.415-137A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | chr6 | 160010550 | ||||||
| chr6:160010552
|
T | A | 4 | a0009c0013t0010g0158a0009c0013t0010g0159a0009c0013t0010g0160others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.415-135T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | chr6 | 160010552 | ||||||
| chr6:160010568
|
C | G | 1 | a0005c0008t0002g0033 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.415-119C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | chr6 | 160010568 | ||||||
| chr6:160010603
|
A | G | 1 | a0001c0004t0046g0273 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.415-84A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | chr6 | 160010603 | ||||||
| chr6:160010672
|
A | AT | 6 | a0001c0004t0002g0129a0003c0007t0022g0107a0003c0007t0022g0108others(3): Show | 6 | HG02886.hp1 HG03098.hp1 HG03486.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.415-6dupT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr6 | 160010672 | |||||
| chr6:160010870
|
G | A | 2 | a0001c0009t0002g0068a0003c0058t0076g0070 | 2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.513+85G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160010870 | ||||||
| chr6:160011213
|
T | C | 1 | a0001c0004t0003g0203 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.513+428T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160011213 | ||||||
| chr6:160011241
|
T | C | 21 | a0001c0002t0002g0020a0001c0002t0009g0047a0001c0005t0004g0012others(18): Show | 21 | HG00544.hp2 HG03239.hp1 HG03942.hp2 others(18): Show |
intron_variant | MODIFIER | c.513+456T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160011241 | ||||||
| chr6:160011299
|
T | A | 21 | a0001c0001t0003g0037a0001c0001t0003g0246a0001c0001t0003g0249others(18): Show | 21 | HG00280.hp1 HG00642.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.513+514T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160011299 | ||||||
| chr6:160011431
|
A | G | 6 | a0001c0004t0065g0200a0001c0005t0012g0209a0001c0009t0001g0181others(3): Show | 6 | HG00597.hp2 NA18950.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+646A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160011431 | ||||||
| chr6:160011509
|
G | T | 3 | a0001c0046t0054g0281a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.513+724G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160011509 | ||||||
| chr6:160011551
|
G | GT | 126 | a0001c0001t0001g0304a0001c0001t0002g0141a0001c0001t0002g0142others(123): Show | 127 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.513+783dupT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160011551 | |||||
| chr6:160011551
|
G | GTT | 23 | a0001c0001t0003g0246a0001c0001t0003g0249a0001c0004t0001g0240others(20): Show | 23 | HG00544.hp1 HG01106.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.513+782_513+783dup others(2): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160011551 | |||||
| chr6:160011551
|
GT | G | 38 | a0001c0001t0002g0062a0001c0001t0003g0230a0001c0001t0003g0231others(35): Show | 38 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.513+783delT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160011551 | |||||
| chr6:160011603
|
C | T | 1 | a0008c0011t0078g0008 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.513+818C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160011603 | ||||||
| chr6:160011780
|
C | T | 3 | a0014c0022t0040g0270a0015c0023t0037g0309a0015c0023t0094g0096 | 3 | HG03209.hp1 HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.513+995C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160011780 | ||||||
| chr6:160011817
|
A | G | 191 | a0001c0001t0002g0062a0001c0001t0003g0037a0001c0001t0003g0230others(188): Show | 192 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.513+1032A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160011817 | ||||||
| chr6:160011826
|
T | C | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.513+1041T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160011826 | ||||||
| chr6:160012113
|
T | C | 1 | a0001c0001t0002g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.513+1328T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012113 | ||||||
| chr6:160012342
|
A | G | 1 | a0001c0004t0001g0240 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.513+1557A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012342 | ||||||
| chr6:160012402
|
C | T | 196 | a0001c0001t0002g0062a0001c0001t0003g0037a0001c0001t0003g0230others(193): Show | 197 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.513+1617C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012402 | ||||||
| chr6:160012569
|
G | T | 1 | a0001c0049t0004g0090 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.513+1784G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012569 | ||||||
| chr6:160012745
|
T | TATATATA others(8): Show |
1 | a0001c0004t0048g0259 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.513+1960_513+1961i others(17): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012745 | ||||||
| chr6:160012745
|
T | TTATATAC others(11): Show |
2 | a0002c0003t0001g0002a0005c0027t0003g0003 | 2 | NA18960.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.513+1966_513+1967i others(20): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012745 | |||||
| chr6:160012745
|
T | TTATATAT others(3): Show |
4 | a0001c0004t0002g0132a0002c0003t0001g0265a0002c0003t0008g0148others(1): Show | 4 | HG01192.hp1 NA18951.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+1970_513+1979d others(12): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012745 | |||||
| chr6:160012745
|
T | TTATATAT others(5): Show |
12 | a0001c0009t0005g0144a0001c0009t0028g0229a0002c0003t0001g0001others(9): Show | 13 | HG00438.hp1 HG00544.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.513+1968_513+1979d others(14): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012745 | |||||
| chr6:160012745
|
T | TTATATAT others(7): Show |
10 | a0001c0002t0028g0034a0001c0004t0020g0253a0001c0004t0066g0174others(7): Show | 10 | HG00408.hp1 HG01981.hp1 HG03486.hp2 others(7): Show |
intron_variant | MODIFIER | c.513+1966_513+1979d others(16): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012745 | |||||
| chr6:160012745
|
T | TTATATAT others(45): Show |
4 | a0009c0013t0010g0158a0009c0013t0010g0159a0009c0013t0010g0160others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+1974_513+1975i others(54): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012745 | |||||
| chr6:160012745
|
T | TTATATAT others(9): Show |
17 | a0001c0004t0001g0222a0001c0004t0003g0190a0001c0004t0046g0273others(14): Show | 17 | HG00423.hp2 HG00597.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.513+1964_513+1979d others(18): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012745 | |||||
| chr6:160012745
|
T | TTATATAT others(11): Show |
8 | a0001c0004t0003g0203a0001c0004t0027g0287a0001c0004t0034g0126others(5): Show | 8 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.513+1962_513+1979d others(20): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012745 | |||||
| chr6:160012745
|
T | TTATATAT others(13): Show |
7 | a0001c0009t0001g0181a0001c0009t0001g0211a0002c0003t0001g0179others(4): Show | 7 | HG01106.hp2 NA18946.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.513+1979_513+1980i others(22): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012745 | |||||
| chr6:160012745
|
T | TTATATAT others(15): Show |
5 | a0001c0004t0003g0223a0001c0004t0051g0178a0002c0003t0008g0085others(2): Show | 5 | HG00438.hp2 HG02040.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+1979_513+1980i others(24): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012745 | |||||
| chr6:160012745
|
T | TTATATAT others(17): Show |
2 | a0001c0034t0006g0035a0001c0056t0003g0154 | 2 | HG02145.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.513+1979_513+1980i others(26): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012745 | |||||
| chr6:160012745
|
T | TTATATAT others(19): Show |
4 | a0001c0004t0044g0153a0002c0003t0001g0199a0002c0047t0008g0135others(1): Show | 4 | HG02135.hp1 HG03225.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+1979_513+1980i others(28): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012745 | |||||
| chr6:160012745
|
T | TTATATAT others(25): Show |
2 | a0001c0004t0002g0065a0002c0003t0014g0177 | 2 | HG00738.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.513+1979_513+1980i others(34): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012745 | |||||
| chr6:160012745
|
T | TTATATAT others(27): Show |
1 | a0002c0003t0001g0241 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.513+1979_513+1980i others(36): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012745 | |||||
| chr6:160012745
|
T | TTATATAT others(29): Show |
1 | a0002c0003t0001g0206 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.513+1979_513+1980i others(38): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012745 | |||||
| chr6:160012745
|
T | TTATATAT others(35): Show |
1 | a0001c0004t0002g0064 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.513+1979_513+1980i others(44): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012745 | |||||
| chr6:160012745
|
T | TTATATTT others(29): Show |
1 | a0001c0004t0003g0210 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.513+1965_513+1966i others(38): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012745 | |||||
| chr6:160012745
|
T | TTATTTAT others(25): Show |
1 | a0001c0049t0004g0090 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.513+1963_513+1964i others(34): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012745 | |||||
| chr6:160012745
|
TTA | T | 3 | a0014c0022t0040g0270a0015c0023t0037g0309a0015c0023t0094g0096 | 3 | HG03209.hp1 HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.513+1978_513+1979d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012745 | |||||
| chr6:160012762
|
TA | T | 3 | a0001c0001t0030g0105a0006c0010t0072g0196a0010c0016t0016g0150 | 3 | HG02280.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.513+1978delA | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012762 | ||||||
| chr6:160012763
|
A | ATAT | 9 | a0001c0002t0002g0030a0001c0002t0007g0060a0005c0008t0002g0029others(6): Show | 9 | HG00733.hp1 HG00733.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.513+1979_513+1980i others(5): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012763 | |||||
| chr6:160012763
|
A | T | 10 | a0001c0002t0015g0127a0001c0002t0015g0163a0001c0002t0027g0052others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.513+1978A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012763 | ||||||
| chr6:160012763
|
AT | A | 25 | a0001c0001t0002g0293a0001c0001t0003g0256a0001c0001t0010g0157others(22): Show | 25 | HG00408.hp2 HG00741.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.513+1993delT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012763 | |||||
| chr6:160012763
|
ATTTT | A | 59 | a0001c0001t0002g0062a0001c0001t0003g0037a0001c0001t0003g0230others(56): Show | 59 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.513+1990_513+1993d others(6): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012763 | |||||
| chr6:160012763
|
ATTTTTT | A | 25 | a0001c0001t0003g0246a0001c0001t0003g0249a0001c0001t0013g0006others(22): Show | 25 | HG00280.hp1 HG00642.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.513+1988_513+1993d others(8): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012763 | |||||
| chr6:160012763
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0009t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.513+1984_513+1993d others(12): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160012763 | |||||
| chr6:160012764
|
T | TA | 10 | a0001c0001t0006g0219a0001c0001t0006g0274a0001c0001t0026g0268others(7): Show | 10 | HG00642.hp1 HG01433.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.513+1979_513+1980i others(3): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012764 | ||||||
| chr6:160012765
|
T | A | 147 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(144): Show | 148 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.513+1980T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012765 | ||||||
| chr6:160012766
|
T | A | 21 | a0001c0001t0002g0293a0001c0001t0003g0256a0001c0001t0006g0219others(18): Show | 21 | HG00408.hp2 HG01106.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.513+1981T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012766 | ||||||
| chr6:160012767
|
T | A | 115 | a0001c0001t0001g0187a0001c0001t0001g0304a0001c0001t0001g0305others(112): Show | 116 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.513+1982T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012767 | ||||||
| chr6:160012768
|
T | A | 8 | a0001c0001t0002g0293a0001c0001t0006g0274a0001c0001t0026g0268others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.513+1983T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012768 | ||||||
| chr6:160012769
|
T | A | 151 | a0001c0001t0001g0187a0001c0001t0002g0062a0001c0001t0003g0037others(148): Show | 152 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.513+1984T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012769 | ||||||
| chr6:160012770
|
T | A | 2 | a0001c0001t0006g0274a0014c0022t0038g0275 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.513+1985T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012770 | ||||||
| chr6:160012771
|
T | A | 137 | a0001c0001t0003g0037a0001c0001t0003g0246a0001c0001t0003g0249others(134): Show | 138 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.513+1986T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012771 | ||||||
| chr6:160012771
|
T | G | 18 | a0001c0001t0032g0040a0001c0001t0032g0041a0001c0002t0002g0030others(15): Show | 18 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.513+1986T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012771 | ||||||
| chr6:160012773
|
T | A | 133 | a0001c0001t0003g0037a0001c0001t0003g0246a0001c0001t0003g0249others(130): Show | 134 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.513+1988T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012773 | ||||||
| chr6:160012775
|
T | A | 90 | a0001c0002t0010g0168a0001c0002t0028g0034a0001c0004t0001g0222others(87): Show | 91 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.513+1990T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012775 | ||||||
| chr6:160012775
|
T | G | 101 | a0001c0001t0001g0187a0001c0001t0002g0043a0001c0001t0002g0062others(98): Show | 101 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.513+1990T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012775 | ||||||
| chr6:160012777
|
T | A | 85 | a0001c0002t0028g0034a0001c0004t0001g0222a0001c0004t0001g0240others(82): Show | 86 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.513+1992T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012777 | ||||||
| chr6:160012779
|
G | A | 84 | a0001c0002t0028g0034a0001c0004t0001g0222a0001c0004t0001g0240others(81): Show | 85 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.513+1994G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012779 | ||||||
| chr6:160012779
|
G | T | 2 | a0001c0002t0082g0007a0010c0016t0016g0170 | 2 | HG00323.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.513+1994G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012779 | ||||||
| chr6:160012816
|
G | A | 38 | a0001c0001t0002g0062a0001c0001t0003g0230a0001c0001t0003g0231others(35): Show | 38 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.513+2031G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012816 | ||||||
| chr6:160012950
|
T | G | 1 | a0001c0001t0005g0100 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.513+2165T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012950 | ||||||
| chr6:160012961
|
G | A | 41 | a0001c0001t0002g0062a0001c0001t0003g0230a0001c0001t0003g0231others(38): Show | 41 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.513+2176G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160012961 | ||||||
| chr6:160013227
|
A | G | 1 | a0006c0025t0059g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.513+2442A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160013227 | ||||||
| chr6:160013284
|
T | C | 1 | a0001c0004t0003g0210 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.513+2499T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160013284 | ||||||
| chr6:160013410
|
T | TA | 17 | a0001c0001t0001g0304a0001c0001t0032g0041a0001c0002t0007g0056others(14): Show | 17 | HG00597.hp2 HG00738.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.513+2648dupA | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160013410 | |||||
| chr6:160013410
|
TA | T | 52 | a0001c0001t0002g0062a0001c0001t0003g0230a0001c0001t0003g0231others(49): Show | 52 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.513+2648delA | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160013410 | |||||
| chr6:160013410
|
TAA | T | 9 | a0001c0037t0002g0079a0003c0007t0003g0172a0003c0007t0003g0254others(6): Show | 9 | HG00621.hp1 HG02132.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.513+2647_513+2648d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160013410 | |||||
| chr6:160013581
|
C | T | 1 | a0004c0006t0002g0073 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.513+2796C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160013581 | ||||||
| chr6:160013683
|
C | A | 3 | a0003c0012t0006g0284a0003c0012t0006g0285a0032c0065t0041g0283 | 3 | HG02451.hp2 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.513+2898C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160013683 | ||||||
| chr6:160014015
|
A | G | 2 | a0001c0002t0018g0235a0001c0002t0039g0233 | 2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.513+3230A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160014015 | ||||||
| chr6:160014317
|
G | A | 3 | a0006c0025t0009g0139a0018c0032t0033g0086a0018c0032t0033g0087 | 3 | HG02145.hp1 HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.513+3532G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160014317 | ||||||
| chr6:160014421
|
A | G | 1 | a0016c0019t0005g0138 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.513+3636A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160014421 | ||||||
| chr6:160014537
|
T | G | 193 | a0001c0001t0002g0062a0001c0001t0003g0037a0001c0001t0003g0230others(190): Show | 194 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.513+3752T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160014537 | ||||||
| chr6:160014897
|
G | A | 94 | a0001c0002t0010g0168a0001c0002t0028g0034a0001c0004t0001g0222others(91): Show | 95 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.513+4112G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160014897 | ||||||
| chr6:160015171
|
T | C | 52 | a0001c0001t0002g0062a0001c0001t0003g0230a0001c0001t0003g0231others(49): Show | 52 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.513+4386T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160015171 | ||||||
| chr6:160015917
|
G | A | 1 | a0006c0025t0059g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.513+5132G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160015917 | ||||||
| chr6:160015920
|
A | C | 92 | a0001c0001t0002g0062a0001c0001t0003g0037a0001c0001t0003g0230others(89): Show | 92 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.513+5135A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160015920 | ||||||
| chr6:160015941
|
A | G | 4 | a0009c0013t0010g0158a0009c0013t0010g0159a0009c0013t0010g0160others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+5156A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160015941 | ||||||
| chr6:160015985
|
C | T | 1 | a0028c0050t0025g0227 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.513+5200C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160015985 | ||||||
| chr6:160016100
|
C | G | 1 | a0003c0030t0004g0049 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.513+5315C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160016100 | ||||||
| chr6:160016315
|
G | A | 85 | a0001c0001t0002g0062a0001c0001t0003g0037a0001c0001t0003g0230others(82): Show | 85 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.513+5530G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160016315 | ||||||
| chr6:160016848
|
A | G | 5 | a0001c0002t0006g0197a0001c0002t0006g0198a0001c0002t0009g0102others(2): Show | 5 | HG01433.hp2 HG01517.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+6063A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160016848 | ||||||
| chr6:160017039
|
CT | C | 3 | a0004c0006t0002g0071a0004c0006t0002g0072a0004c0006t0002g0073 | 3 | HG00597.hp1 HG03654.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.513+6255delT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160017039 | ||||||
| chr6:160017467
|
T | C | 2 | a0010c0016t0016g0169a0010c0016t0016g0170 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.513+6682T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160017467 | ||||||
| chr6:160017632
|
A | G | 1 | a0001c0024t0024g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.513+6847A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160017632 | ||||||
| chr6:160017698
|
C | G | 204 | a0001c0001t0002g0062a0001c0001t0003g0037a0001c0001t0003g0230others(201): Show | 205 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.514-6874C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160017698 | ||||||
| chr6:160017924
|
C | T | 3 | a0007c0014t0011g0092a0007c0014t0011g0093a0007c0014t0011g0094 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.514-6648C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160017924 | ||||||
| chr6:160017960
|
A | G | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.514-6612A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160017960 | ||||||
| chr6:160018270
|
G | T | 1 | a0001c0001t0005g0121 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.514-6302G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160018270 | ||||||
| chr6:160018499
|
C | T | 3 | a0014c0022t0040g0270a0015c0023t0037g0309a0015c0023t0094g0096 | 3 | HG03209.hp1 HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.514-6073C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160018499 | ||||||
| chr6:160018602
|
C | A | 3 | a0004c0006t0002g0071a0004c0006t0002g0072a0004c0006t0002g0073 | 3 | HG00597.hp1 HG03654.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.514-5970C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160018602 | ||||||
| chr6:160018693
|
G | A | 3 | a0001c0002t0036g0289a0001c0002t0036g0290a0001c0002t0056g0156 | 3 | HG00642.hp1 HG01433.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.514-5879G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160018693 | ||||||
| chr6:160018748
|
G | A | 45 | a0001c0001t0002g0062a0001c0001t0003g0230a0001c0001t0003g0231others(42): Show | 45 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.514-5824G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160018748 | ||||||
| chr6:160019100
|
A | G | 6 | a0001c0037t0002g0079a0003c0007t0003g0172a0003c0007t0003g0254others(3): Show | 6 | HG00621.hp1 HG02132.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.514-5472A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160019100 | ||||||
| chr6:160019124
|
C | A | 1 | a0001c0004t0001g0240 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.514-5448C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160019124 | ||||||
| chr6:160019140
|
A | C | 48 | a0001c0001t0002g0062a0001c0001t0003g0230a0001c0001t0003g0231others(45): Show | 48 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.514-5432A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160019140 | ||||||
| chr6:160019556
|
C | A | 4 | a0009c0013t0010g0158a0009c0013t0010g0159a0009c0013t0010g0160others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-5016C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160019556 | ||||||
| chr6:160019619
|
C | T | 3 | a0007c0014t0011g0092a0007c0014t0011g0093a0007c0014t0011g0094 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.514-4953C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160019619 | ||||||
| chr6:160019643
|
G | C | 1 | a0004c0006t0003g0216 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.514-4929G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160019643 | ||||||
| chr6:160019659
|
A | G | 1 | a0005c0008t0002g0051 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.514-4913A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160019659 | ||||||
| chr6:160019702
|
T | A | 41 | a0001c0001t0002g0062a0001c0001t0003g0230a0001c0001t0003g0231others(38): Show | 41 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.514-4870T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160019702 | ||||||
| chr6:160019793
|
T | A | 3 | a0014c0022t0040g0270a0015c0023t0037g0309a0015c0023t0094g0096 | 3 | HG03209.hp1 HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.514-4779T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160019793 | ||||||
| chr6:160019851
|
C | T | 44 | a0001c0001t0002g0062a0001c0001t0003g0230a0001c0001t0003g0231others(41): Show | 44 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.514-4721C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160019851 | ||||||
| chr6:160019931
|
A | G | 2 | a0001c0001t0006g0244a0001c0001t0006g0264 | 2 | NA18980.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.514-4641A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160019931 | ||||||
| chr6:160020124
|
A | G | 1 | a0005c0008t0002g0033 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.514-4448A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160020124 | ||||||
| chr6:160020249
|
A | G | 2 | a0001c0002t0010g0168a0001c0005t0012g0167 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.514-4323A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160020249 | ||||||
| chr6:160020333
|
A | G | 45 | a0001c0001t0002g0062a0001c0001t0003g0230a0001c0001t0003g0231others(42): Show | 45 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.514-4239A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160020333 | ||||||
| chr6:160020376
|
G | A | 2 | a0001c0001t0005g0117a0008c0011t0030g0124 | 2 | HG01981.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.514-4196G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160020376 | ||||||
| chr6:160020635
|
A | G | 3 | a0014c0022t0040g0270a0015c0023t0037g0309a0015c0023t0094g0096 | 3 | HG03209.hp1 HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.514-3937A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160020635 | ||||||
| chr6:160020642
|
A | G | 1 | a0002c0003t0061g0182 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.514-3930A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160020642 | ||||||
| chr6:160020745
|
C | T | 1 | a0003c0030t0004g0049 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.514-3827C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160020745 | ||||||
| chr6:160020900
|
A | G | 4 | a0009c0013t0010g0158a0009c0013t0010g0159a0009c0013t0010g0160others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-3672A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160020900 | ||||||
| chr6:160021220
|
A | G | 2 | a0010c0016t0016g0169a0010c0016t0016g0170 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.514-3352A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160021220 | ||||||
| chr6:160021444
|
G | T | 1 | a0004c0029t0003g0180 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.514-3128G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160021444 | ||||||
| chr6:160021485
|
CTAATGCT others(11): Show |
C | 1 | a0001c0009t0008g0011 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.514-3081_514-3064d others(20): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160021485 | |||||
| chr6:160021509
|
G | A | 2 | a0010c0016t0016g0169a0010c0016t0016g0170 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.514-3063G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160021509 | ||||||
| chr6:160021606
|
A | T | 45 | a0001c0001t0002g0062a0001c0001t0003g0230a0001c0001t0003g0231others(42): Show | 45 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.514-2966A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160021606 | ||||||
| chr6:160021607
|
A | T | 1 | a0004c0006t0002g0084 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.514-2965A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160021607 | ||||||
| chr6:160021674
|
T | C | 1 | a0003c0007t0003g0172 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.514-2898T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160021674 | ||||||
| chr6:160021742
|
G | A | 89 | a0001c0001t0002g0062a0001c0001t0003g0037a0001c0001t0003g0230others(86): Show | 89 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.514-2830G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160021742 | ||||||
| chr6:160021894
|
G | A | 3 | a0001c0001t0021g0044a0001c0001t0021g0045a0001c0001t0021g0046 | 3 | HG01515.hp1 HG01517.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.514-2678G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160021894 | ||||||
| chr6:160021901
|
A | T | 8 | a0001c0004t0003g0223a0002c0003t0001g0175a0002c0003t0001g0188others(5): Show | 8 | HG01168.hp1 HG01943.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.514-2671A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160021901 | ||||||
| chr6:160021971
|
G | A | 3 | a0001c0002t0010g0168a0001c0005t0012g0167a0001c0024t0024g0201 | 3 | HG02257.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.514-2601G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160021971 | ||||||
| chr6:160022013
|
A | AACAC | 4 | a0001c0002t0071g0194a0006c0010t0072g0196a0010c0016t0016g0169others(1): Show | 4 | HG01884.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-2534_514-2531d others(6): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160022013 | |||||
| chr6:160022013
|
A | AACACAC | 79 | a0001c0002t0028g0034a0001c0004t0001g0240a0001c0004t0002g0064others(76): Show | 80 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.514-2536_514-2531d others(8): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160022013 | |||||
| chr6:160022013
|
A | AACACACA others(1): Show |
14 | a0001c0002t0010g0168a0001c0004t0001g0222a0001c0004t0002g0132others(11): Show | 14 | HG02155.hp2 HG02257.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.514-2538_514-2531d others(10): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160022013 | |||||
| chr6:160022013
|
A | AACACACA others(3): Show |
4 | a0002c0003t0001g0206a0003c0012t0006g0284a0003c0012t0006g0285others(1): Show | 4 | HG02451.hp2 HG03139.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-2540_514-2531d others(12): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160022013 | |||||
| chr6:160022013
|
A | AACACACA others(5): Show |
4 | a0001c0024t0070g0282a0014c0022t0040g0270a0015c0023t0037g0309others(1): Show | 4 | HG03209.hp1 HG06807.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-2542_514-2531d others(14): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160022013 | |||||
| chr6:160022013
|
A | AACACACA others(7): Show |
3 | a0003c0030t0004g0049a0004c0006t0087g0081a0034c0063t0008g0076 | 3 | HG02683.hp2 HG03942.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.514-2544_514-2531d others(16): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160022013 | |||||
| chr6:160022013
|
A | AACACACA others(9): Show |
5 | a0001c0001t0003g0230a0001c0001t0003g0231a0001c0001t0069g0232others(2): Show | 5 | HG02735.hp2 HG03490.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-2546_514-2531d others(18): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160022013 | |||||
| chr6:160022013
|
A | AACACACA others(11): Show |
17 | a0003c0007t0001g0205a0003c0007t0003g0261a0003c0007t0006g0272others(14): Show | 17 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.514-2548_514-2531d others(20): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160022013 | |||||
| chr6:160022013
|
A | AACACACA others(13): Show |
9 | a0001c0001t0030g0105a0003c0007t0003g0254a0003c0007t0022g0106others(6): Show | 9 | HG02165.hp2 HG02723.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.514-2550_514-2531d others(22): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160022013 | |||||
| chr6:160022013
|
A | AACACACA others(15): Show |
4 | a0001c0001t0002g0062a0003c0007t0004g0074a0003c0012t0009g0088others(1): Show | 4 | HG00621.hp1 HG02698.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-2552_514-2531d others(24): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160022013 | |||||
| chr6:160022013
|
A | AACACACA others(17): Show |
6 | a0001c0037t0002g0079a0003c0007t0003g0172a0003c0007t0004g0078others(3): Show | 6 | HG02040.hp1 HG02132.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.514-2554_514-2531d others(26): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160022013 | |||||
| chr6:160022013
|
A | AACACACA others(19): Show |
2 | a0003c0007t0009g0048a0003c0007t0075g0147 | 2 | HG03239.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.514-2556_514-2531d others(28): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160022013 | |||||
| chr6:160022013
|
A | AACACACA others(27): Show |
1 | a0004c0062t0002g0050 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.514-2531_514-2530i others(36): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160022013 | |||||
| chr6:160022013
|
AACACACA others(3): Show |
A | 2 | a0001c0002t0009g0102a0001c0002t0009g0103 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.514-2540_514-2531d others(12): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160022013 | |||||
| chr6:160022020
|
A | ACACACC | 39 | a0001c0001t0003g0037a0001c0001t0003g0246a0001c0001t0003g0249others(36): Show | 39 | HG00280.hp1 HG00544.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.514-2547_514-2546i others(8): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160022020 | |||||
| chr6:160022041
|
C | CACACACA others(16): Show |
1 | a0004c0006t0002g0130 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.514-2531_514-2530i others(25): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160022041 | ||||||
| chr6:160022358
|
A | G | 9 | a0001c0004t0027g0287a0001c0004t0084g0098a0001c0009t0002g0068others(6): Show | 9 | HG00738.hp2 HG01192.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.514-2214A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160022358 | ||||||
| chr6:160022396
|
A | G | 84 | a0001c0002t0028g0034a0001c0004t0001g0222a0001c0004t0001g0240others(81): Show | 85 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.514-2176A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160022396 | ||||||
| chr6:160022829
|
C | T | 55 | a0001c0001t0002g0062a0001c0001t0003g0230a0001c0001t0003g0231others(52): Show | 55 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.514-1743C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160022829 | ||||||
| chr6:160022979
|
A | G | 52 | a0001c0001t0002g0062a0001c0001t0003g0230a0001c0001t0003g0231others(49): Show | 52 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.514-1593A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160022979 | ||||||
| chr6:160023263
|
C | T | 1 | a0002c0003t0008g0085 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.514-1309C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160023263 | ||||||
| chr6:160023444
|
G | T | 1 | a0001c0004t0046g0273 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.514-1128G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160023444 | ||||||
| chr6:160023488
|
A | G | 4 | a0002c0003t0001g0202a0002c0003t0001g0204a0002c0003t0001g0208others(1): Show | 4 | NA18952.hp2 NA18974.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-1084A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160023488 | ||||||
| chr6:160023960
|
C | A | 46 | a0001c0001t0002g0062a0001c0001t0003g0230a0001c0001t0003g0231others(43): Show | 46 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.514-612C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160023960 | ||||||
| chr6:160024000
|
G | C | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.514-572G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160024000 | ||||||
| chr6:160024044
|
G | A | 1 | a0006c0025t0059g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.514-528G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160024044 | ||||||
| chr6:160024175
|
A | T | 1 | a0001c0004t0001g0240 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.514-397A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160024175 | ||||||
| chr6:160024236
|
ATAGC | A | 8 | a0001c0001t0002g0043a0001c0001t0005g0028a0001c0001t0005g0116others(5): Show | 8 | HG00323.hp1 HG00323.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-332_514-329del others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr6 | 160024236 | |||||
| chr6:160024317
|
G | C | 46 | a0001c0001t0002g0062a0001c0001t0003g0230a0001c0001t0003g0231others(43): Show | 46 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.514-255G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160024317 | ||||||
| chr6:160024461
|
G | A | 94 | a0001c0001t0005g0114a0001c0001t0005g0115a0001c0001t0005g0117others(91): Show | 95 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.514-111G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160024461 | ||||||
| chr6:160024537
|
T | G | 1 | a0006c0025t0059g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.514-35T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160024537 | ||||||
| chr6:160024563
|
C | A | 3 | a0007c0014t0011g0092a0007c0014t0011g0093a0007c0014t0011g0094 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.514-9C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 4/47 | chr6 | 160024563 | ||||||
| chr6:160024761
|
A | G | 59 | a0001c0001t0001g0187a0001c0001t0001g0304a0001c0001t0001g0305others(56): Show | 59 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.646+57A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 5/47 | chr6 | 160024761 | ||||||
| chr6:160024998
|
C | T | 3 | a0007c0014t0011g0092a0007c0014t0011g0093a0007c0014t0011g0094 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.646+294C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 5/47 | chr6 | 160024998 | ||||||
| chr6:160025051
|
G | C | 11 | a0001c0002t0002g0020a0001c0005t0004g0012a0001c0005t0004g0018others(8): Show | 11 | HG00544.hp2 NA18942.hp1 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.646+347G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 5/47 | chr6 | 160025051 | ||||||
| chr6:160025127
|
T | G | 2 | a0003c0007t0004g0074a0003c0007t0004g0078 | 2 | NA18959.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.646+423T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 5/47 | chr6 | 160025127 | ||||||
| chr6:160025299
|
C | A | 1 | a0021c0044t0074g0111 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.646+595C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 5/47 | chr6 | 160025299 | ||||||
| chr6:160025566
|
A | G | 50 | a0001c0001t0002g0062a0001c0001t0003g0230a0001c0001t0003g0231others(47): Show | 50 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.646+862A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 5/47 | chr6 | 160025566 | ||||||
| chr6:160025985
|
G | A | 204 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0003g0037others(201): Show | 205 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.647-1200G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 5/47 | chr6 | 160025985 | ||||||
| chr6:160026053
|
G | T | 1 | a0001c0001t0002g0062 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.647-1132G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 5/47 | chr6 | 160026053 | ||||||
| chr6:160026127
|
G | A | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.647-1058G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 5/47 | chr6 | 160026127 | ||||||
| chr6:160026501
|
C | G | 1 | a0002c0003t0077g0134 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.647-684C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 5/47 | chr6 | 160026501 | ||||||
| chr6:160026507
|
C | T | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.647-678C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 5/47 | chr6 | 160026507 | ||||||
| chr6:160026956
|
A | G | 218 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0003g0037others(215): Show | 219 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.647-229A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 5/47 | chr6 | 160026956 | ||||||
| chr6:160026965
|
C | T | 2 | a0001c0002t0010g0168a0001c0005t0012g0167 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.647-220C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 5/47 | chr6 | 160026965 | ||||||
| chr6:160026975
|
C | G | 6 | a0001c0001t0021g0044a0001c0001t0021g0045a0001c0001t0021g0046others(3): Show | 6 | HG00280.hp2 HG01192.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.647-210C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 5/47 | chr6 | 160026975 | ||||||
| chr6:160027033
|
G | A | 1 | a0001c0001t0035g0053 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.647-152G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 5/47 | chr6 | 160027033 | ||||||
| chr6:160027141
|
A | G | 1 | a0003c0059t0055g0171 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.647-44A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 5/47 | chr6 | 160027141 | ||||||
| chr6:160027430
|
G | A | 36 | a0003c0007t0001g0205a0003c0007t0003g0172a0003c0007t0003g0254others(33): Show | 36 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.776+116G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 6/47 | chr6 | 160027430 | ||||||
| chr6:160027631
|
C | T | 3 | a0001c0004t0002g0064a0001c0004t0002g0065a0008c0011t0078g0008 | 3 | HG00738.hp1 HG01081.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.776+317C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 6/47 | chr6 | 160027631 | ||||||
| chr6:160027824
|
G | A | 2 | a0001c0004t0001g0222a0002c0057t0001g0243 | 2 | HG02155.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.776+510G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 6/47 | chr6 | 160027824 | ||||||
| chr6:160027951
|
T | G | 1 | a0001c0004t0084g0098 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.776+637T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 6/47 | chr6 | 160027951 | ||||||
| chr6:160028239
|
C | T | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.776+925C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 6/47 | chr6 | 160028239 | ||||||
| chr6:160028389
|
G | A | 1 | a0001c0002t0090g0133 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.776+1075G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 6/47 | chr6 | 160028389 | ||||||
| chr6:160028559
|
C | A | 1 | a0001c0009t0023g0131 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.777-991C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 6/47 | chr6 | 160028559 | ||||||
| chr6:160029267
|
A | T | 47 | a0003c0007t0001g0205a0003c0007t0003g0172a0003c0007t0003g0254others(44): Show | 47 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.777-283A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 6/47 | chr6 | 160029267 | ||||||
| chr6:160029369
|
CT | C | 86 | a0001c0002t0028g0034a0001c0004t0001g0222a0001c0004t0001g0240others(83): Show | 87 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.777-169delT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr6 | 160029369 | |||||
| chr6:160029370
|
T | C | 46 | a0003c0007t0001g0205a0003c0007t0003g0172a0003c0007t0003g0254others(43): Show | 46 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.777-180T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 6/47 | chr6 | 160029370 | ||||||
| chr6:160029398
|
C | G | 1 | a0002c0003t0014g0173 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.777-152C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 6/47 | chr6 | 160029398 | ||||||
| chr6:160029457
|
C | G | 1 | a0006c0025t0059g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.777-93C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 6/47 | chr6 | 160029457 | ||||||
| chr6:160029489
|
A | G | 1 | a0002c0003t0001g0188 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.777-61A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 6/47 | chr6 | 160029489 | ||||||
| chr6:160029717
|
C | T | 2 | a0001c0001t0003g0230a0001c0001t0003g0231 | 2 | HG03490.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.882+62C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | chr6 | 160029717 | ||||||
| chr6:160029804
|
AAGCTTCC others(6): Show |
A | 1 | a0001c0002t0028g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.882+156_882+168del others(13): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr6 | 160029804 | |||||
| chr6:160029889
|
G | A | 1 | a0004c0006t0002g0130 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.882+234G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | chr6 | 160029889 | ||||||
| chr6:160030186
|
G | A | 2 | a0001c0004t0002g0132a0001c0009t0023g0131 | 2 | NA18951.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.882+531G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | chr6 | 160030186 | ||||||
| chr6:160030366
|
C | T | 93 | a0001c0004t0001g0222a0001c0004t0001g0240a0001c0004t0002g0064others(90): Show | 94 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.882+711C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | chr6 | 160030366 | ||||||
| chr6:160030561
|
G | C | 1 | a0002c0003t0001g0241 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.882+906G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | chr6 | 160030561 | ||||||
| chr6:160030639
|
CAGGCGGT | C | 75 | a0001c0004t0001g0222a0001c0004t0001g0240a0001c0004t0002g0064others(72): Show | 76 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.882+987_882+993del others(7): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr6 | 160030639 | |||||
| chr6:160030643
|
C | T | 1 | a0001c0024t0024g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.882+988C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | chr6 | 160030643 | ||||||
| chr6:160030822
|
G | GT | 44 | a0001c0001t0014g0300a0001c0002t0010g0168a0001c0004t0020g0253others(41): Show | 44 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.882+1185dupT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr6 | 160030822 | |||||
| chr6:160031116
|
A | G | 1 | a0001c0004t0003g0210 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.883-1435A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | chr6 | 160031116 | ||||||
| chr6:160031125
|
A | T | 93 | a0001c0004t0001g0222a0001c0004t0001g0240a0001c0004t0002g0064others(90): Show | 94 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.883-1426A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | chr6 | 160031125 | ||||||
| chr6:160031198
|
A | C | 1 | a0001c0004t0034g0126 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.883-1353A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | chr6 | 160031198 | ||||||
| chr6:160031554
|
T | C | 1 | a0001c0005t0004g0022 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.883-997T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | chr6 | 160031554 | ||||||
| chr6:160031619
|
G | C | 88 | a0001c0004t0001g0222a0001c0004t0001g0240a0001c0004t0002g0064others(85): Show | 89 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.883-932G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | chr6 | 160031619 | ||||||
| chr6:160031825
|
G | A | 4 | a0001c0002t0010g0168a0001c0005t0012g0167a0001c0024t0024g0201others(1): Show | 4 | HG02257.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-726G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | chr6 | 160031825 | ||||||
| chr6:160031873
|
G | T | 1 | a0012c0031t0019g0165 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.883-678G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | chr6 | 160031873 | ||||||
| chr6:160031981
|
G | T | 4 | a0001c0002t0010g0168a0001c0005t0012g0167a0001c0024t0024g0201others(1): Show | 4 | HG02257.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-570G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | chr6 | 160031981 | ||||||
| chr6:160032088
|
A | G | 2 | a0004c0006t0003g0216a0004c0006t0003g0217 | 2 | HG02040.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.883-463A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | chr6 | 160032088 | ||||||
| chr6:160032131
|
C | A | 5 | a0009c0013t0010g0158a0009c0013t0010g0159a0009c0013t0010g0160others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-420C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | chr6 | 160032131 | ||||||
| chr6:160032205
|
A | G | 1 | a0001c0069t0052g0164 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.883-346A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | chr6 | 160032205 | ||||||
| chr6:160032288
|
A | G | 1 | a0002c0003t0014g0173 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.883-263A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | chr6 | 160032288 | ||||||
| chr6:160032529
|
T | G | 88 | a0001c0004t0001g0222a0001c0004t0001g0240a0001c0004t0002g0064others(85): Show | 89 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.883-22T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | chr6 | 160032529 | ||||||
| chr6:160032537
|
A | G | 4 | a0001c0002t0010g0168a0001c0005t0012g0167a0001c0024t0024g0201others(1): Show | 4 | HG02257.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-14A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 7/47 | chr6 | 160032537 | ||||||
| chr6:160033116
|
A | G | 1 | a0014c0022t0038g0275 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1211+9A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 9/47 | chr6 | 160033116 | ||||||
| chr6:160033210
|
C | T | 1 | a0001c0069t0052g0164 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1211+103C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 9/47 | chr6 | 160033210 | ||||||
| chr6:160033390
|
C | G | 3 | a0014c0022t0040g0270a0015c0023t0037g0309a0015c0023t0094g0096 | 3 | HG03209.hp1 HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1211+283C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 9/47 | chr6 | 160033390 | ||||||
| chr6:160033520
|
C | A | 59 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0003g0037others(56): Show | 59 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.1211+413C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 9/47 | chr6 | 160033520 | ||||||
| chr6:160033520
|
C | T | 5 | a0001c0046t0054g0281a0014c0022t0040g0270a0015c0023t0037g0309others(2): Show | 5 | HG02965.hp1 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1211+413C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 9/47 | chr6 | 160033520 | ||||||
| chr6:160034187
|
C | T | 1 | a0003c0007t0003g0254 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1212-232C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 9/47 | chr6 | 160034187 | ||||||
| chr6:160034188
|
G | A | 1 | a0016c0019t0005g0138 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1212-231G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 9/47 | chr6 | 160034188 | ||||||
| chr6:160034222
|
G | A | 88 | a0001c0004t0001g0222a0001c0004t0001g0240a0001c0004t0002g0064others(85): Show | 89 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1212-197G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 9/47 | chr6 | 160034222 | ||||||
| chr6:160034272
|
T | C | 1 | a0010c0016t0016g0150 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1212-147T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 9/47 | chr6 | 160034272 | ||||||
| chr6:160034311
|
G | A | 4 | a0001c0002t0010g0168a0001c0005t0012g0167a0001c0024t0024g0201others(1): Show | 4 | HG02257.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1212-108G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 9/47 | chr6 | 160034311 | ||||||
| chr6:160034944
|
A | G | 15 | a0001c0001t0002g0043a0001c0001t0005g0028a0001c0001t0005g0100others(12): Show | 15 | HG00323.hp1 HG00735.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.1315+422A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160034944 | ||||||
| chr6:160034981
|
T | C | 1 | a0001c0001t0005g0120 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1315+459T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160034981 | ||||||
| chr6:160034988
|
A | G | 210 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0003g0037others(207): Show | 211 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.1315+466A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160034988 | ||||||
| chr6:160035001
|
G | A | 1 | a0001c0009t0005g0143 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1315+479G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160035001 | ||||||
| chr6:160035030
|
C | T | 5 | a0009c0013t0010g0158a0009c0013t0010g0159a0009c0013t0010g0160others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315+508C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160035030 | ||||||
| chr6:160035088
|
C | T | 1 | a0011c0017t0002g0017 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1315+566C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160035088 | ||||||
| chr6:160035131
|
C | T | 73 | a0001c0004t0001g0222a0001c0004t0001g0240a0001c0004t0002g0064others(70): Show | 74 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1315+609C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160035131 | ||||||
| chr6:160035251
|
G | A | 5 | a0001c0001t0006g0274a0001c0001t0026g0268a0001c0001t0026g0269others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1315+729G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160035251 | ||||||
| chr6:160035381
|
A | C | 1 | a0001c0002t0007g0055 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1315+859A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160035381 | ||||||
| chr6:160035632
|
G | T | 1 | a0001c0004t0044g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1315+1110G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160035632 | ||||||
| chr6:160035711
|
G | A | 1 | a0001c0001t0014g0300 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1315+1189G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160035711 | ||||||
| chr6:160035717
|
A | G | 4 | a0001c0002t0010g0168a0001c0005t0012g0167a0001c0024t0024g0201others(1): Show | 4 | HG02257.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1315+1195A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160035717 | ||||||
| chr6:160036070
|
G | A | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1315+1548G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160036070 | ||||||
| chr6:160036209
|
C | G | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1315+1687C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160036209 | ||||||
| chr6:160036275
|
C | T | 1 | a0001c0002t0007g0091 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1315+1753C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160036275 | ||||||
| chr6:160036444
|
C | A | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1315+1922C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160036444 | ||||||
| chr6:160036621
|
T | C | 11 | a0001c0001t0005g0114a0001c0001t0005g0115a0001c0001t0005g0116others(8): Show | 11 | HG00323.hp1 HG00735.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.1315+2099T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160036621 | ||||||
| chr6:160036634
|
C | T | 1 | a0005c0008t0083g0039 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1315+2112C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160036634 | ||||||
| chr6:160036871
|
A | G | 5 | a0007c0014t0011g0092a0007c0014t0011g0093a0007c0014t0011g0094others(2): Show | 5 | HG02280.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315+2349A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160036871 | ||||||
| chr6:160036873
|
T | A | 2 | a0001c0002t0028g0034a0001c0034t0006g0035 | 2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1315+2351T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160036873 | ||||||
| chr6:160037058
|
T | A | 1 | a0001c0004t0003g0210 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1315+2536T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160037058 | ||||||
| chr6:160037148
|
G | A | 5 | a0009c0013t0010g0158a0009c0013t0010g0159a0009c0013t0010g0160others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315+2626G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160037148 | ||||||
| chr6:160037616
|
G | C | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1316-2944G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160037616 | ||||||
| chr6:160037655
|
T | A | 6 | a0001c0024t0024g0201a0001c0046t0054g0281a0014c0022t0040g0270others(3): Show | 6 | HG02965.hp1 HG02976.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1316-2905T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160037655 | ||||||
| chr6:160037670
|
G | C | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1316-2890G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160037670 | ||||||
| chr6:160037725
|
T | C | 85 | a0001c0004t0001g0222a0001c0004t0001g0240a0001c0004t0002g0064others(82): Show | 86 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1316-2835T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160037725 | ||||||
| chr6:160038068
|
G | A | 1 | a0001c0005t0012g0258 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1316-2492G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160038068 | ||||||
| chr6:160038083
|
T | C | 2 | a0001c0002t0010g0168a0001c0005t0012g0167 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1316-2477T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160038083 | ||||||
| chr6:160038159
|
A | G | 28 | a0003c0007t0001g0205a0003c0007t0003g0261a0003c0007t0004g0074others(25): Show | 28 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.1316-2401A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160038159 | ||||||
| chr6:160038173
|
G | T | 40 | a0003c0007t0001g0205a0003c0007t0003g0172a0003c0007t0003g0254others(37): Show | 40 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1316-2387G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160038173 | ||||||
| chr6:160038189
|
G | A | 1 | a0021c0044t0074g0111 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1316-2371G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160038189 | ||||||
| chr6:160038217
|
G | C | 3 | a0003c0012t0006g0284a0003c0012t0006g0285a0032c0065t0041g0283 | 3 | HG02451.hp2 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1316-2343G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160038217 | ||||||
| chr6:160038697
|
A | G | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1316-1863A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160038697 | ||||||
| chr6:160038726
|
G | A | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1316-1834G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160038726 | ||||||
| chr6:160038732
|
G | A | 1 | a0002c0003t0001g0175 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1316-1828G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160038732 | ||||||
| chr6:160038797
|
AC | A | 4 | a0009c0013t0010g0158a0009c0013t0010g0159a0009c0013t0010g0160others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1316-1761delC | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr6 | 160038797 | |||||
| chr6:160038838
|
A | G | 5 | a0009c0013t0010g0158a0009c0013t0010g0159a0009c0013t0010g0160others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1316-1722A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160038838 | ||||||
| chr6:160038864
|
C | A | 1 | a0001c0004t0046g0273 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1316-1696C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160038864 | ||||||
| chr6:160038969
|
T | A | 1 | a0001c0045t0057g0250 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1316-1591T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160038969 | ||||||
| chr6:160039050
|
C | G | 139 | a0001c0002t0010g0168a0001c0004t0001g0222a0001c0004t0001g0240others(136): Show | 140 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1316-1510C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160039050 | ||||||
| chr6:160039077
|
A | G | 1 | a0001c0046t0054g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1316-1483A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160039077 | ||||||
| chr6:160039107
|
T | C | 2 | a0001c0004t0002g0064a0001c0004t0002g0065 | 2 | HG00738.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1316-1453T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160039107 | ||||||
| chr6:160039189
|
A | G | 2 | a0002c0003t0008g0085a0002c0003t0063g0207 | 2 | HG02040.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1316-1371A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160039189 | ||||||
| chr6:160039330
|
G | A | 127 | a0001c0004t0001g0222a0001c0004t0001g0240a0001c0004t0002g0064others(124): Show | 128 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.1316-1230G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160039330 | ||||||
| chr6:160039584
|
A | G | 4 | a0001c0002t0010g0168a0001c0005t0012g0167a0001c0024t0024g0201others(1): Show | 4 | HG02257.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1316-976A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160039584 | ||||||
| chr6:160040016
|
A | G | 2 | a0001c0002t0010g0168a0001c0005t0012g0167 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1316-544A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160040016 | ||||||
| chr6:160040016
|
A | T | 1 | a0004c0062t0002g0050 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1316-544A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160040016 | ||||||
| chr6:160040043
|
G | A | 1 | a0003c0012t0009g0095 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1316-517G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160040043 | ||||||
| chr6:160040053
|
A | G | 135 | a0001c0004t0001g0222a0001c0004t0001g0240a0001c0004t0002g0064others(132): Show | 136 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1316-507A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160040053 | ||||||
| chr6:160040187
|
G | T | 3 | a0001c0005t0004g0021a0001c0005t0004g0083a0001c0005t0012g0258 | 3 | NA18946.hp2 NA18999.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1316-373G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160040187 | ||||||
| chr6:160040302
|
A | G | 149 | a0001c0002t0010g0168a0001c0004t0001g0222a0001c0004t0001g0240others(146): Show | 150 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1316-258A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160040302 | ||||||
| chr6:160040436
|
C | A | 1 | a0020c0041t0002g0013 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1316-124C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160040436 | ||||||
| chr6:160040494
|
G | T | 1 | a0002c0015t0001g0280 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1316-66G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160040494 | ||||||
| chr6:160040521
|
C | G | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1316-39C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 10/47 | chr6 | 160040521 | ||||||
| chr6:160040761
|
T | C | 3 | a0001c0004t0027g0287a0001c0004t0084g0098a0024c0051t0015g0097 | 3 | HG00738.hp2 HG01243.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1480+37T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160040761 | ||||||
| chr6:160040788
|
C | T | 1 | a0022c0042t0024g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1480+64C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160040788 | ||||||
| chr6:160040807
|
T | C | 23 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(20): Show | 23 | HG02055.hp1 HG02135.hp2 HG02155.hp1 others(20): Show |
intron_variant | MODIFIER | c.1480+83T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160040807 | ||||||
| chr6:160040899
|
GAA | G | 53 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0003g0037others(50): Show | 53 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1480+177_1480+178d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | INFO_REALIGN_3_PRIME | chr6 | 160040899 | |||||
| chr6:160041114
|
C | T | 1 | a0019c0068t0012g0279 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1480+390C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160041114 | ||||||
| chr6:160041192
|
T | C | 1 | a0001c0001t0006g0244 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1480+468T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160041192 | ||||||
| chr6:160041252
|
T | TG | 88 | a0001c0004t0001g0222a0001c0004t0001g0240a0001c0004t0002g0064others(85): Show | 89 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1480+535dupG | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | INFO_REALIGN_3_PRIME | chr6 | 160041252 | |||||
| chr6:160041397
|
C | T | 3 | a0001c0002t0010g0168a0001c0005t0012g0167a0001c0024t0070g0282 | 3 | HG02257.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1480+673C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160041397 | ||||||
| chr6:160041421
|
G | A | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1480+697G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160041421 | ||||||
| chr6:160041424
|
T | C | 3 | a0014c0022t0040g0270a0015c0023t0037g0309a0015c0023t0094g0096 | 3 | HG03209.hp1 HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1480+700T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160041424 | ||||||
| chr6:160041441
|
A | C | 1 | a0001c0001t0005g0119 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1480+717A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160041441 | ||||||
| chr6:160041590
|
T | A | 1 | a0008c0011t0078g0008 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1480+866T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160041590 | ||||||
| chr6:160041659
|
C | G | 1 | a0001c0005t0012g0209 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1480+935C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160041659 | ||||||
| chr6:160041814
|
G | A | 1 | a0012c0031t0089g0067 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1480+1090G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160041814 | ||||||
| chr6:160041840
|
G | A | 10 | a0001c0004t0001g0240a0001c0004t0003g0190a0001c0004t0003g0203others(7): Show | 10 | HG02293.hp2 HG03710.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.1480+1116G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160041840 | ||||||
| chr6:160041908
|
A | G | 1 | a0005c0020t0002g0031 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1480+1184A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160041908 | ||||||
| chr6:160041910
|
C | G | 1 | a0004c0029t0003g0185 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1480+1186C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160041910 | ||||||
| chr6:160041947
|
C | T | 3 | a0017c0021t0031g0004a0017c0021t0031g0005a0021c0044t0074g0111 | 3 | HG02976.hp2 HG03688.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1481-1201C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160041947 | ||||||
| chr6:160041996
|
C | CT | 136 | a0001c0001t0035g0113a0001c0002t0002g0020a0001c0004t0001g0222others(133): Show | 137 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.1481-1140dupT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | INFO_REALIGN_3_PRIME | chr6 | 160041996 | |||||
| chr6:160042075
|
A | G | 140 | a0001c0004t0001g0222a0001c0004t0001g0240a0001c0004t0002g0064others(137): Show | 141 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.1481-1073A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160042075 | ||||||
| chr6:160042076
|
C | T | 1 | a0003c0012t0006g0285 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1481-1072C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160042076 | ||||||
| chr6:160042378
|
C | T | 2 | a0003c0012t0006g0284a0003c0012t0006g0285 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1481-770C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160042378 | ||||||
| chr6:160042395
|
G | T | 16 | a0001c0002t0015g0009a0001c0002t0015g0127a0001c0002t0015g0163others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1481-753G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160042395 | ||||||
| chr6:160042435
|
C | A | 1 | a0001c0001t0035g0053 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1481-713C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160042435 | ||||||
| chr6:160042477
|
C | T | 1 | a0002c0003t0001g0206 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1481-671C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160042477 | ||||||
| chr6:160042659
|
A | G | 3 | a0001c0002t0010g0168a0001c0005t0012g0167a0001c0024t0024g0201 | 3 | HG02257.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1481-489A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160042659 | ||||||
| chr6:160042695
|
G | A | 1 | a0001c0001t0030g0105 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1481-453G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160042695 | ||||||
| chr6:160042765
|
C | T | 1 | a0004c0029t0003g0180 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1481-383C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160042765 | ||||||
| chr6:160042774
|
C | T | 1 | a0036c0067t0034g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1481-374C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160042774 | ||||||
| chr6:160042828
|
T | C | 1 | a0001c0001t0026g0269 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1481-320T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160042828 | ||||||
| chr6:160042904
|
G | A | 9 | a0001c0001t0002g0142a0001c0001t0003g0246a0001c0001t0003g0249others(6): Show | 9 | HG00642.hp2 HG01109.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1481-244G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160042904 | ||||||
| chr6:160042956
|
T | A | 2 | a0001c0002t0010g0168a0001c0005t0012g0167 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1481-192T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160042956 | ||||||
| chr6:160042974
|
C | T | 3 | a0001c0001t0003g0037a0001c0001t0043g0036a0008c0043t0017g0038 | 3 | HG02451.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1481-174C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160042974 | ||||||
| chr6:160043019
|
G | A | 1 | a0004c0006t0002g0073 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1481-129G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160043019 | ||||||
| chr6:160043078
|
C | T | 1 | a0001c0004t0034g0126 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1481-70C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 11/47 | chr6 | 160043078 | ||||||
| chr6:160043365
|
C | T | 1 | a0002c0003t0001g0179 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1621+77C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | chr6 | 160043365 | ||||||
| chr6:160043523
|
G | A | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1621+235G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | chr6 | 160043523 | ||||||
| chr6:160043552
|
T | G | 1 | a0001c0002t0002g0030 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1621+264T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | chr6 | 160043552 | ||||||
| chr6:160043620
|
A | G | 1 | a0001c0002t0067g0247 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1621+332A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | chr6 | 160043620 | ||||||
| chr6:160043712
|
C | T | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1621+424C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | chr6 | 160043712 | ||||||
| chr6:160043912
|
A | G | 20 | a0001c0002t0015g0009a0001c0002t0015g0127a0001c0002t0015g0163others(17): Show | 20 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1622-602A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | chr6 | 160043912 | ||||||
| chr6:160043953
|
T | C | 2 | a0018c0032t0033g0086a0018c0032t0033g0087 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1622-561T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | chr6 | 160043953 | ||||||
| chr6:160044022
|
T | C | 223 | a0001c0001t0002g0043a0001c0001t0002g0141a0001c0001t0002g0142others(220): Show | 224 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.1622-492T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | chr6 | 160044022 | ||||||
| chr6:160044033
|
C | T | 1 | a0001c0002t0023g0101 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1622-481C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | chr6 | 160044033 | ||||||
| chr6:160044245
|
G | T | 1 | a0001c0002t0015g0163 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1622-269G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | chr6 | 160044245 | ||||||
| chr6:160044258
|
C | T | 1 | a0001c0001t0003g0037 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1622-256C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | chr6 | 160044258 | ||||||
| chr6:160044259
|
G | A | 132 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(129): Show | 132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1622-255G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | chr6 | 160044259 | ||||||
| chr6:160044345
|
A | T | 13 | a0001c0001t0006g0274a0001c0002t0071g0194a0003c0007t0023g0109others(10): Show | 13 | HG01884.hp1 HG02630.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1622-169A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | chr6 | 160044345 | ||||||
| chr6:160044348
|
C | T | 3 | a0001c0024t0024g0201a0003c0007t0079g0137a0035c0060t0042g0267 | 3 | HG02559.hp2 HG02886.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1622-166C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | chr6 | 160044348 | ||||||
| chr6:160044370
|
G | T | 2 | a0003c0007t0079g0137a0035c0060t0042g0267 | 2 | HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1622-144G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | chr6 | 160044370 | ||||||
| chr6:160044383
|
C | T | 1 | a0027c0055t0020g0183 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1622-131C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | chr6 | 160044383 | ||||||
| chr6:160044387
|
A | G | 13 | a0003c0012t0009g0088a0007c0014t0011g0092a0007c0014t0011g0093others(10): Show | 13 | HG02647.hp1 HG02723.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.1622-127A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | chr6 | 160044387 | ||||||
| chr6:160044389
|
G | T | 189 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(186): Show | 190 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.1622-125G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | chr6 | 160044389 | ||||||
| chr6:160044424
|
C | T | 86 | a0001c0001t0002g0062a0001c0001t0002g0141a0001c0001t0002g0293others(83): Show | 87 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1622-90C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | chr6 | 160044424 | ||||||
| chr6:160044432
|
CT | C | 14 | a0001c0001t0002g0293a0001c0002t0010g0168a0001c0005t0012g0167others(11): Show | 14 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1622-72delT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr6 | 160044432 | |||||
| chr6:160044434
|
T | G | 8 | a0001c0001t0026g0268a0001c0001t0026g0269a0001c0002t0028g0034others(5): Show | 8 | HG02145.hp2 HG02630.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1622-80T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | chr6 | 160044434 | ||||||
| chr6:160044454
|
TTGTC | T | 72 | a0001c0001t0002g0043a0001c0001t0002g0141a0001c0001t0002g0142others(69): Show | 72 | HG00140.hp2 HG00544.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.1622-57_1622-54del others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr6 | 160044454 | |||||
| chr6:160044458
|
C | T | 1 | a0007c0018t0019g0239 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1622-56C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 12/47 | chr6 | 160044458 | ||||||
| chr6:160044721
|
T | G | 191 | a0001c0001t0002g0043a0001c0001t0002g0141a0001c0001t0002g0293others(188): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1765+64T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 13/47 | chr6 | 160044721 | ||||||
| chr6:160044904
|
G | A | 9 | a0006c0010t0002g0010a0006c0010t0011g0122a0006c0010t0011g0123others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1765+247G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 13/47 | chr6 | 160044904 | ||||||
| chr6:160044921
|
G | A | 3 | a0001c0001t0006g0274a0001c0001t0026g0268a0001c0001t0026g0269 | 3 | HG02630.hp1 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1765+264G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 13/47 | chr6 | 160044921 | ||||||
| chr6:160044931
|
C | T | 1 | a0014c0022t0038g0275 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1765+274C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 13/47 | chr6 | 160044931 | ||||||
| chr6:160045071
|
C | A | 16 | a0001c0001t0002g0062a0001c0001t0002g0293a0001c0001t0003g0230others(13): Show | 16 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.1765+414C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 13/47 | chr6 | 160045071 | ||||||
| chr6:160045140
|
A | G | 1 | a0004c0006t0049g0226 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1765+483A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 13/47 | chr6 | 160045140 | ||||||
| chr6:160045280
|
C | T | 2 | a0003c0012t0006g0284a0003c0012t0006g0285 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1766-465C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 13/47 | chr6 | 160045280 | ||||||
| chr6:160045296
|
T | A | 1 | a0002c0047t0008g0135 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1766-449T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 13/47 | chr6 | 160045296 | ||||||
| chr6:160045375
|
A | G | 2 | a0002c0003t0001g0002a0002c0003t0001g0179 | 2 | NA18960.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1766-370A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 13/47 | chr6 | 160045375 | ||||||
| chr6:160045386
|
T | G | 1 | a0002c0047t0008g0135 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1766-359T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 13/47 | chr6 | 160045386 | ||||||
| chr6:160045462
|
A | G | 1 | a0011c0017t0002g0017 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1766-283A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 13/47 | chr6 | 160045462 | ||||||
| chr6:160045557
|
T | C | 2 | a0001c0024t0024g0201a0036c0067t0034g0110 | 2 | HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1766-188T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 13/47 | chr6 | 160045557 | ||||||
| chr6:160045649
|
T | A | 1 | a0001c0001t0005g0120 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1766-96T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 13/47 | chr6 | 160045649 | ||||||
| chr6:160045983
|
A | T | 1 | a0002c0015t0001g0280 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1903+101A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 14/47 | chr6 | 160045983 | ||||||
| chr6:160046055
|
C | T | 50 | a0002c0003t0001g0001a0002c0003t0001g0002a0002c0003t0001g0175others(47): Show | 51 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1903+173C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 14/47 | chr6 | 160046055 | ||||||
| chr6:160046211
|
A | G | 5 | a0001c0002t0006g0197a0001c0002t0006g0198a0005c0008t0002g0033others(2): Show | 5 | HG01261.hp2 HG01346.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1904-287A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 14/47 | chr6 | 160046211 | ||||||
| chr6:160046248
|
T | C | 3 | a0006c0025t0059g0288a0007c0018t0019g0238a0007c0018t0019g0239 | 3 | HG02280.hp2 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1904-250T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 14/47 | chr6 | 160046248 | ||||||
| chr6:160046374
|
C | A | 1 | a0028c0050t0025g0227 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1904-124C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 14/47 | chr6 | 160046374 | ||||||
| chr6:160046826
|
C | G | 2 | a0001c0001t0002g0141a0001c0001t0003g0256 | 2 | HG01243.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.2051+181C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 15/47 | chr6 | 160046826 | ||||||
| chr6:160046858
|
T | C | 268 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(265): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.2051+213T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 15/47 | chr6 | 160046858 | ||||||
| chr6:160046953
|
T | C | 3 | a0012c0031t0019g0165a0012c0031t0089g0067a0019c0068t0012g0279 | 3 | HG01109.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2052-206T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 15/47 | chr6 | 160046953 | ||||||
| chr6:160046988
|
T | G | 6 | a0001c0001t0003g0037a0001c0009t0002g0068a0009c0013t0010g0158others(3): Show | 6 | HG02647.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2052-171T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 15/47 | chr6 | 160046988 | ||||||
| chr6:160047069
|
C | T | 1 | a0003c0030t0025g0257 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2052-90C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 15/47 | chr6 | 160047069 | ||||||
| chr6:160047148
|
G | A | 23 | a0001c0002t0002g0020a0001c0002t0010g0168a0001c0005t0004g0012others(20): Show | 23 | HG00423.hp1 HG00544.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.2052-11G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 15/47 | chr6 | 160047148 | ||||||
| chr6:160047351
|
T | C | 189 | a0001c0002t0002g0020a0001c0002t0002g0030a0001c0002t0002g0299others(186): Show | 190 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.2229+15T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 16/47 | chr6 | 160047351 | ||||||
| chr6:160047398
|
A | G | 1 | a0001c0002t0090g0133 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2229+62A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 16/47 | chr6 | 160047398 | ||||||
| chr6:160047521
|
A | G | 50 | a0002c0003t0001g0001a0002c0003t0001g0002a0002c0003t0001g0175others(47): Show | 51 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.2229+185A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 16/47 | chr6 | 160047521 | ||||||
| chr6:160047637
|
G | A | 72 | a0001c0024t0024g0201a0001c0024t0070g0282a0002c0003t0001g0001others(69): Show | 73 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.2230-155G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 16/47 | chr6 | 160047637 | ||||||
| chr6:160047674
|
T | C | 1 | a0006c0025t0059g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2230-118T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 16/47 | chr6 | 160047674 | ||||||
| chr6:160047915
|
A | G | 3 | a0001c0024t0024g0201a0003c0007t0075g0147a0036c0067t0034g0110 | 3 | HG03195.hp1 HG03486.hp1 NA20129.hp2 |
splice_region_variant&intron_variant | LOW | c.2345+8A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 17/47 | chr6 | 160047915 | ||||||
| chr6:160048067
|
T | A | 189 | a0001c0002t0002g0020a0001c0002t0002g0030a0001c0002t0002g0299others(186): Show | 190 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.2345+160T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 17/47 | chr6 | 160048067 | ||||||
| chr6:160048117
|
G | A | 186 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(183): Show | 187 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.2345+210G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 17/47 | chr6 | 160048117 | ||||||
| chr6:160048233
|
G | C | 2 | a0001c0001t0021g0045a0001c0001t0021g0046 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2346-142G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 17/47 | chr6 | 160048233 | ||||||
| chr6:160048863
|
G | T | 67 | a0002c0003t0001g0001a0002c0003t0001g0002a0002c0003t0001g0175others(64): Show | 68 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.2514+320G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 18/47 | chr6 | 160048863 | ||||||
| chr6:160048915
|
C | G | 6 | a0001c0001t0021g0044a0001c0001t0021g0045a0001c0001t0021g0046others(3): Show | 6 | HG00280.hp2 HG01192.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.2514+372C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 18/47 | chr6 | 160048915 | ||||||
| chr6:160049002
|
G | A | 2 | a0001c0002t0007g0091a0032c0065t0041g0283 | 2 | HG00140.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2514+459G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 18/47 | chr6 | 160049002 | ||||||
| chr6:160049054
|
G | T | 1 | a0017c0021t0031g0005 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2514+511G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 18/47 | chr6 | 160049054 | ||||||
| chr6:160049360
|
C | T | 4 | a0014c0022t0038g0275a0014c0022t0040g0270a0022c0042t0024g0151others(1): Show | 4 | HG02109.hp2 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2514+817C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 18/47 | chr6 | 160049360 | ||||||
| chr6:160049476
|
G | A | 1 | a0001c0002t0007g0066 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2514+933G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 18/47 | chr6 | 160049476 | ||||||
| chr6:160049525
|
C | T | 1 | a0004c0006t0002g0128 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2515-948C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 18/47 | chr6 | 160049525 | ||||||
| chr6:160049725
|
A | G | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2515-748A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 18/47 | chr6 | 160049725 | ||||||
| chr6:160049795
|
T | C | 1 | a0001c0001t0069g0232 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2515-678T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 18/47 | chr6 | 160049795 | ||||||
| chr6:160049848
|
G | A | 22 | a0001c0002t0010g0168a0001c0005t0004g0012a0001c0005t0004g0014others(19): Show | 22 | HG00423.hp1 HG01109.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2515-625G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 18/47 | chr6 | 160049848 | ||||||
| chr6:160049974
|
C | G | 56 | a0001c0024t0024g0201a0002c0003t0001g0001a0002c0003t0001g0002others(53): Show | 57 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.2515-499C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 18/47 | chr6 | 160049974 | ||||||
| chr6:160050027
|
C | T | 1 | a0032c0065t0041g0283 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2515-446C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 18/47 | chr6 | 160050027 | ||||||
| chr6:160050159
|
T | G | 68 | a0001c0024t0024g0201a0002c0003t0001g0001a0002c0003t0001g0002others(65): Show | 69 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.2515-314T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 18/47 | chr6 | 160050159 | ||||||
| chr6:160050163
|
A | G | 5 | a0001c0004t0003g0192a0003c0007t0001g0205a0003c0007t0004g0074others(2): Show | 5 | NA18959.hp1 NA18963.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.2515-310A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 18/47 | chr6 | 160050163 | ||||||
| chr6:160050278
|
C | T | 1 | a0001c0009t0001g0181 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2515-195C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 18/47 | chr6 | 160050278 | ||||||
| chr6:160050720
|
C | T | 51 | a0002c0003t0001g0001a0002c0003t0001g0002a0002c0003t0001g0175others(48): Show | 52 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.2694+68C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160050720 | ||||||
| chr6:160050886
|
C | T | 3 | a0001c0002t0071g0194a0001c0004t0034g0126a0001c0004t0044g0153 | 3 | HG02055.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2694+234C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160050886 | ||||||
| chr6:160051000
|
T | G | 90 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(87): Show | 90 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.2694+348T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160051000 | ||||||
| chr6:160051070
|
A | G | 2 | a0002c0003t0008g0136a0002c0003t0077g0134 | 2 | NA18994.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.2694+418A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160051070 | ||||||
| chr6:160051152
|
C | G | 1 | a0001c0045t0057g0250 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2694+500C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160051152 | ||||||
| chr6:160051382
|
C | T | 3 | a0006c0025t0059g0288a0007c0018t0019g0238a0007c0018t0019g0239 | 3 | HG02280.hp2 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2694+730C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160051382 | ||||||
| chr6:160051456
|
G | A | 1 | a0001c0046t0054g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2694+804G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160051456 | ||||||
| chr6:160051515
|
T | G | 28 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.2694+863T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160051515 | ||||||
| chr6:160051521
|
A | G | 1 | a0004c0061t0003g0266 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2694+869A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160051521 | ||||||
| chr6:160051793
|
C | T | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2694+1141C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160051793 | ||||||
| chr6:160051802
|
T | A | 43 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(40): Show | 43 | HG00544.hp2 HG00738.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.2694+1150T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160051802 | ||||||
| chr6:160051884
|
C | G | 2 | a0021c0044t0074g0111a0032c0065t0041g0283 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2694+1232C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160051884 | ||||||
| chr6:160051967
|
T | C | 4 | a0001c0002t0071g0194a0001c0004t0034g0126a0001c0004t0044g0153others(1): Show | 4 | HG02055.hp2 HG02258.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2694+1315T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160051967 | ||||||
| chr6:160052025
|
C | T | 5 | a0008c0011t0017g0152a0008c0011t0017g0195a0008c0011t0030g0124others(2): Show | 5 | HG02723.hp2 HG02895.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2694+1373C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160052025 | ||||||
| chr6:160052202
|
T | G | 1 | a0036c0067t0034g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2694+1550T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160052202 | ||||||
| chr6:160052242
|
G | C | 1 | a0003c0007t0075g0147 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2694+1590G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160052242 | ||||||
| chr6:160052559
|
TC | T | 3 | a0006c0025t0059g0288a0007c0018t0019g0238a0007c0018t0019g0239 | 3 | HG02280.hp2 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2694+1908delC | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160052559 | ||||||
| chr6:160052596
|
A | T | 4 | a0013c0026t0029g0149a0013c0026t0029g0297a0015c0023t0037g0309others(1): Show | 4 | HG02055.hp1 HG02486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2694+1944A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160052596 | ||||||
| chr6:160052766
|
A | G | 22 | a0001c0002t0010g0168a0001c0005t0004g0012a0001c0005t0004g0014others(19): Show | 22 | HG00423.hp1 HG01109.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2694+2114A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160052766 | ||||||
| chr6:160053112
|
C | T | 2 | a0001c0001t0026g0268a0001c0001t0026g0269 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2694+2460C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160053112 | ||||||
| chr6:160053113
|
G | A | 2 | a0001c0046t0054g0281a0001c0069t0052g0164 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2694+2461G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160053113 | ||||||
| chr6:160053164
|
A | G | 5 | a0001c0034t0006g0035a0003c0012t0006g0284a0003c0012t0006g0285others(2): Show | 5 | HG02145.hp2 HG02451.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2694+2512A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160053164 | ||||||
| chr6:160053181
|
A | G | 1 | a0002c0003t0014g0173 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2694+2529A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160053181 | ||||||
| chr6:160053229
|
T | G | 1 | a0001c0004t0066g0174 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2694+2577T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160053229 | ||||||
| chr6:160053278
|
G | C | 2 | a0001c0046t0054g0281a0001c0069t0052g0164 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2694+2626G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160053278 | ||||||
| chr6:160053278
|
G | T | 56 | a0001c0024t0024g0201a0002c0003t0001g0001a0002c0003t0001g0002others(53): Show | 57 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.2694+2626G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160053278 | ||||||
| chr6:160053315
|
A | G | 1 | a0003c0066t0053g0162 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2694+2663A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160053315 | ||||||
| chr6:160053497
|
A | C | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2694+2845A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160053497 | ||||||
| chr6:160053790
|
C | T | 1 | a0032c0065t0041g0283 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2695-2634C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160053790 | ||||||
| chr6:160053829
|
A | G | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2695-2595A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160053829 | ||||||
| chr6:160053918
|
A | G | 1 | a0008c0011t0078g0008 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2695-2506A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160053918 | ||||||
| chr6:160054317
|
T | A | 3 | a0002c0003t0001g0224a0002c0003t0001g0225a0002c0015t0001g0280 | 3 | NA18999.hp1 NA19062.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2695-2107T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160054317 | ||||||
| chr6:160054468
|
G | T | 5 | a0001c0002t0010g0168a0001c0005t0012g0167a0012c0031t0019g0165others(2): Show | 5 | HG01109.hp1 HG02257.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.2695-1956G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160054468 | ||||||
| chr6:160054520
|
A | G | 3 | a0001c0002t0015g0127a0001c0002t0027g0052a0001c0002t0058g0234 | 3 | HG03225.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2695-1904A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160054520 | ||||||
| chr6:160054525
|
A | G | 1 | a0032c0065t0041g0283 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2695-1899A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160054525 | ||||||
| chr6:160054651
|
A | G | 1 | a0003c0007t0075g0147 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2695-1773A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160054651 | ||||||
| chr6:160054805
|
T | C | 3 | a0010c0016t0016g0150a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2695-1619T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160054805 | ||||||
| chr6:160055104
|
C | T | 2 | a0013c0026t0029g0149a0013c0026t0029g0297 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2695-1320C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160055104 | ||||||
| chr6:160055105
|
A | G | 9 | a0006c0010t0002g0010a0006c0010t0011g0122a0006c0010t0011g0123others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2695-1319A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160055105 | ||||||
| chr6:160055235
|
A | G | 261 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(258): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.2695-1189A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160055235 | ||||||
| chr6:160055456
|
G | A | 1 | a0001c0024t0024g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2695-968G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160055456 | ||||||
| chr6:160055913
|
C | T | 81 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(78): Show | 81 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.2695-511C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160055913 | ||||||
| chr6:160055952
|
A | G | 13 | a0001c0004t0044g0153a0006c0010t0002g0010a0006c0010t0011g0122others(10): Show | 13 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.2695-472A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160055952 | ||||||
| chr6:160056017
|
C | T | 1 | a0003c0007t0022g0108 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2695-407C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160056017 | ||||||
| chr6:160056296
|
C | T | 1 | a0032c0065t0041g0283 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2695-128C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160056296 | ||||||
| chr6:160056322
|
C | G | 3 | a0001c0005t0004g0024a0001c0005t0004g0026a0001c0005t0092g0025 | 3 | NA18945.hp1 NA18980.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.2695-102C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160056322 | ||||||
| chr6:160056354
|
C | T | 1 | a0006c0010t0072g0196 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2695-70C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 19/47 | chr6 | 160056354 | ||||||
| chr6:160056776
|
C | T | 1 | a0001c0036t0047g0248 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2796+251C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 20/47 | chr6 | 160056776 | ||||||
| chr6:160056853
|
G | A | 27 | a0001c0001t0002g0062a0001c0001t0002g0141a0001c0001t0002g0293others(24): Show | 27 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.2796+328G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 20/47 | chr6 | 160056853 | ||||||
| chr6:160056875
|
C | T | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2796+350C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 20/47 | chr6 | 160056875 | ||||||
| chr6:160056885
|
G | T | 1 | a0001c0004t0020g0253 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2796+360G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 20/47 | chr6 | 160056885 | ||||||
| chr6:160056891
|
C | T | 3 | a0010c0016t0016g0150a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2796+366C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 20/47 | chr6 | 160056891 | ||||||
| chr6:160057007
|
A | G | 2 | a0002c0003t0008g0136a0002c0003t0077g0134 | 2 | NA18994.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.2796+482A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 20/47 | chr6 | 160057007 | ||||||
| chr6:160057038
|
T | C | 3 | a0001c0024t0070g0282a0003c0007t0075g0147a0036c0067t0034g0110 | 3 | HG03195.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2796+513T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 20/47 | chr6 | 160057038 | ||||||
| chr6:160057055
|
T | TTGTGTGT others(69): Show |
3 | a0010c0016t0016g0150a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2796+555_2796+630d others(78): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 20/47 | INFO_REALIGN_3_PRIME | chr6 | 160057055 | |||||
| chr6:160057354
|
A | G | 1 | a0002c0003t0014g0173 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2797-669A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 20/47 | chr6 | 160057354 | ||||||
| chr6:160057420
|
C | G | 9 | a0006c0010t0002g0010a0006c0010t0011g0122a0006c0010t0011g0123others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2797-603C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 20/47 | chr6 | 160057420 | ||||||
| chr6:160057440
|
C | T | 2 | a0001c0002t0002g0030a0001c0002t0080g0054 | 2 | HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.2797-583C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 20/47 | chr6 | 160057440 | ||||||
| chr6:160057496
|
C | A | 1 | a0036c0067t0034g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2797-527C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 20/47 | chr6 | 160057496 | ||||||
| chr6:160057732
|
T | C | 2 | a0001c0001t0026g0268a0001c0001t0026g0269 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2797-291T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 20/47 | chr6 | 160057732 | ||||||
| chr6:160057757
|
A | G | 62 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(59): Show | 62 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.2797-266A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 20/47 | chr6 | 160057757 | ||||||
| chr6:160058128
|
A | G | 3 | a0006c0025t0059g0288a0007c0018t0019g0238a0007c0018t0019g0239 | 3 | HG02280.hp2 HG03041.hp1 NA19240.hp2 |
splice_region_variant&intron_variant | LOW | c.2898+4A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 21/47 | chr6 | 160058128 | ||||||
| chr6:160058177
|
A | G | 1 | a0001c0001t0006g0308 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2898+53A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 21/47 | chr6 | 160058177 | ||||||
| chr6:160058446
|
G | A | 97 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(94): Show | 98 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.2898+322G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 21/47 | chr6 | 160058446 | ||||||
| chr6:160058480
|
A | G | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2898+356A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 21/47 | chr6 | 160058480 | ||||||
| chr6:160058538
|
G | A | 4 | a0001c0046t0054g0281a0001c0069t0052g0164a0021c0044t0074g0111others(1): Show | 4 | HG02965.hp1 HG02976.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2899-368G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 21/47 | chr6 | 160058538 | ||||||
| chr6:160058635
|
A | G | 1 | a0003c0007t0003g0254 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2899-271A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 21/47 | chr6 | 160058635 | ||||||
| chr6:160058658
|
A | T | 1 | a0001c0001t0069g0232 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2899-248A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 21/47 | chr6 | 160058658 | ||||||
| chr6:160058669
|
C | T | 3 | a0001c0002t0071g0194a0001c0004t0034g0126a0001c0004t0044g0153 | 3 | HG02055.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2899-237C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 21/47 | chr6 | 160058669 | ||||||
| chr6:160058757
|
A | G | 97 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(94): Show | 98 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.2899-149A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 21/47 | chr6 | 160058757 | ||||||
| chr6:160058850
|
G | A | 97 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(94): Show | 98 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.2899-56G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 21/47 | chr6 | 160058850 | ||||||
| chr6:160058881
|
A | G | 1 | a0002c0003t0064g0213 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2899-25A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 21/47 | chr6 | 160058881 | ||||||
| chr6:160058892
|
C | T | 1 | a0004c0006t0002g0084 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2899-14C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 21/47 | chr6 | 160058892 | ||||||
| chr6:160059288
|
C | CTGTGTGA others(7): Show |
3 | a0010c0016t0016g0150a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3091+190_3091+191i others(16): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 22/47 | chr6 | 160059288 | ||||||
| chr6:160059288
|
C | T | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3091+190C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 22/47 | chr6 | 160059288 | ||||||
| chr6:160059814
|
G | T | 2 | a0001c0002t0071g0194a0001c0004t0034g0126 | 2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3091+716G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 22/47 | chr6 | 160059814 | ||||||
| chr6:160059911
|
A | G | 11 | a0001c0001t0002g0043a0001c0001t0002g0142a0001c0001t0003g0246others(8): Show | 11 | HG00280.hp1 HG00642.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.3092-636A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 22/47 | chr6 | 160059911 | ||||||
| chr6:160059981
|
T | C | 9 | a0006c0010t0002g0010a0006c0010t0011g0122a0006c0010t0011g0123others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3092-566T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 22/47 | chr6 | 160059981 | ||||||
| chr6:160059985
|
G | A | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3092-562G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 22/47 | chr6 | 160059985 | ||||||
| chr6:160060169
|
G | A | 1 | a0001c0004t0020g0253 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3092-378G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 22/47 | chr6 | 160060169 | ||||||
| chr6:160060313
|
G | A | 1 | a0032c0065t0041g0283 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3092-234G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 22/47 | chr6 | 160060313 | ||||||
| chr6:160060412
|
C | T | 1 | a0001c0004t0081g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3092-135C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 22/47 | chr6 | 160060412 | ||||||
| chr6:160060505
|
T | C | 99 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(96): Show | 100 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.3092-42T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 22/47 | chr6 | 160060505 | ||||||
| chr6:160060530
|
G | A | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3092-17G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 22/47 | chr6 | 160060530 | ||||||
| chr6:160060851
|
T | C | 2 | a0013c0026t0029g0149a0013c0026t0029g0297 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.3262+134T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 23/47 | chr6 | 160060851 | ||||||
| chr6:160060912
|
A | G | 1 | a0001c0046t0054g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3262+195A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 23/47 | chr6 | 160060912 | ||||||
| chr6:160060987
|
G | A | 3 | a0010c0016t0016g0150a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3262+270G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 23/47 | chr6 | 160060987 | ||||||
| chr6:160061012
|
C | G | 1 | a0001c0004t0044g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3262+295C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 23/47 | chr6 | 160061012 | ||||||
| chr6:160061316
|
G | A | 1 | a0002c0003t0001g0191 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3263-187G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 23/47 | chr6 | 160061316 | ||||||
| chr6:160061343
|
T | G | 1 | a0032c0065t0041g0283 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3263-160T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 23/47 | chr6 | 160061343 | ||||||
| chr6:160061974
|
A | G | 3 | a0001c0002t0071g0194a0001c0004t0034g0126a0001c0004t0044g0153 | 3 | HG02055.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3582+46A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 25/47 | chr6 | 160061974 | ||||||
| chr6:160061990
|
G | T | 1 | a0003c0030t0025g0257 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3582+62G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 25/47 | chr6 | 160061990 | ||||||
| chr6:160062007
|
A | G | 2 | a0001c0046t0054g0281a0001c0069t0052g0164 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3582+79A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 25/47 | chr6 | 160062007 | ||||||
| chr6:160062111
|
C | T | 1 | a0003c0007t0075g0147 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3582+183C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 25/47 | chr6 | 160062111 | ||||||
| chr6:160062112
|
G | A | 51 | a0002c0003t0001g0001a0002c0003t0001g0002a0002c0003t0001g0175others(48): Show | 52 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.3582+184G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 25/47 | chr6 | 160062112 | ||||||
| chr6:160062133
|
A | G | 22 | a0001c0002t0010g0168a0001c0005t0004g0012a0001c0005t0004g0014others(19): Show | 22 | HG00423.hp1 HG01109.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.3582+205A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 25/47 | chr6 | 160062133 | ||||||
| chr6:160062168
|
A | AT | 29 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(26): Show | 29 | HG00140.hp2 HG00423.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.3582+263dupT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 25/47 | INFO_REALIGN_3_PRIME | chr6 | 160062168 | |||||
| chr6:160062168
|
AT | A | 106 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(103): Show | 107 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.3582+263delT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 25/47 | INFO_REALIGN_3_PRIME | chr6 | 160062168 | |||||
| chr6:160062168
|
ATT | A | 11 | a0001c0004t0002g0132a0001c0024t0024g0201a0001c0024t0070g0282others(8): Show | 11 | HG01168.hp1 HG01884.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.3582+262_3582+263d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 25/47 | INFO_REALIGN_3_PRIME | chr6 | 160062168 | |||||
| chr6:160062168
|
ATTT | A | 10 | a0002c0003t0064g0213a0006c0010t0002g0010a0006c0010t0011g0122others(7): Show | 10 | HG01891.hp2 HG02145.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.3582+261_3582+263d others(5): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 25/47 | INFO_REALIGN_3_PRIME | chr6 | 160062168 | |||||
| chr6:160062238
|
A | G | 9 | a0006c0010t0002g0010a0006c0010t0011g0122a0006c0010t0011g0123others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3583-294A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 25/47 | chr6 | 160062238 | ||||||
| chr6:160062467
|
C | T | 1 | a0012c0031t0089g0067 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3583-65C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 25/47 | chr6 | 160062467 | ||||||
| chr6:160062701
|
G | A | 9 | a0006c0010t0002g0010a0006c0010t0011g0122a0006c0010t0011g0123others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3670+82G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 26/47 | chr6 | 160062701 | ||||||
| chr6:160062868
|
A | T | 1 | a0032c0065t0041g0283 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3670+249A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 26/47 | chr6 | 160062868 | ||||||
| chr6:160062913
|
C | T | 2 | a0001c0002t0007g0060a0001c0002t0007g0061 | 2 | HG00733.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.3670+294C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 26/47 | chr6 | 160062913 | ||||||
| chr6:160062977
|
A | C | 2 | a0001c0046t0054g0281a0001c0069t0052g0164 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3670+358A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 26/47 | chr6 | 160062977 | ||||||
| chr6:160062978
|
T | TGTGGAAA others(310): Show |
2 | a0001c0004t0003g0192a0003c0007t0006g0272 | 2 | NA18963.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.3670+374_3670+375i others(319): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr6 | 160062978 | |||||
| chr6:160062978
|
T | TGTGGAAA others(315): Show |
7 | a0001c0002t0028g0034a0001c0002t0067g0247a0001c0002t0090g0133others(4): Show | 7 | HG00408.hp2 HG00597.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.3670+374_3670+375i others(324): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr6 | 160062978 | |||||
| chr6:160062978
|
T | TGTGGAAA others(316): Show |
29 | a0001c0002t0002g0020a0001c0002t0003g0302a0001c0002t0003g0303others(26): Show | 29 | HG00544.hp2 HG00621.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.3670+374_3670+375i others(325): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr6 | 160062978 | |||||
| chr6:160062978
|
T | TGTGGAAA others(317): Show |
15 | a0001c0002t0002g0030a0001c0002t0015g0127a0001c0002t0027g0052others(12): Show | 15 | HG00741.hp2 HG01175.hp2 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.3670+374_3670+375i others(326): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr6 | 160062978 | |||||
| chr6:160062978
|
T | TGTGGAAA others(318): Show |
2 | a0001c0002t0002g0299a0001c0056t0003g0154 | 2 | HG02602.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.3670+374_3670+375i others(327): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr6 | 160062978 | |||||
| chr6:160062978
|
T | TGTGGAAA others(319): Show |
1 | a0001c0001t0003g0249 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3670+374_3670+375i others(328): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr6 | 160062978 | |||||
| chr6:160063039
|
G | GT | 13 | a0001c0001t0003g0231a0001c0002t0071g0194a0001c0004t0002g0132others(10): Show | 13 | HG00423.hp1 HG01109.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.3671-359dupT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr6 | 160063039 | |||||
| chr6:160063289
|
A | G | 184 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(181): Show | 185 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.3671-126A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 26/47 | chr6 | 160063289 | ||||||
| chr6:160063332
|
C | T | 3 | a0002c0003t0001g0002a0002c0003t0001g0179a0002c0052t0008g0023 | 3 | HG00438.hp2 NA18960.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.3671-83C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 26/47 | chr6 | 160063332 | ||||||
| chr6:160063336
|
C | G | 1 | a0002c0003t0008g0148 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3671-79C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 26/47 | chr6 | 160063336 | ||||||
| chr6:160063715
|
G | A | 12 | a0006c0010t0002g0010a0006c0010t0011g0122a0006c0010t0011g0123others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.3886+85G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 27/47 | chr6 | 160063715 | ||||||
| chr6:160063741
|
T | TA | 8 | a0001c0001t0002g0043a0001c0001t0002g0142a0001c0001t0003g0246others(5): Show | 8 | HG00642.hp2 HG01081.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3886+125dupA | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 27/47 | INFO_REALIGN_3_PRIME | chr6 | 160063741 | |||||
| chr6:160063741
|
TA | T | 12 | a0001c0001t0021g0045a0001c0002t0071g0194a0001c0002t0090g0133others(9): Show | 12 | HG00408.hp2 HG01515.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.3886+125delA | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 27/47 | INFO_REALIGN_3_PRIME | chr6 | 160063741 | |||||
| chr6:160063742
|
A | G | 1 | a0001c0001t0030g0105 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3886+112A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 27/47 | chr6 | 160063742 | ||||||
| chr6:160063806
|
T | A | 1 | a0001c0001t0010g0157 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3886+176T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 27/47 | chr6 | 160063806 | ||||||
| chr6:160064028
|
G | A | 22 | a0001c0002t0010g0168a0001c0005t0004g0012a0001c0005t0004g0014others(19): Show | 22 | HG00423.hp1 HG01109.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.3887-373G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 27/47 | chr6 | 160064028 | ||||||
| chr6:160064162
|
A | G | 13 | a0001c0002t0023g0101a0001c0002t0028g0034a0001c0002t0067g0247others(10): Show | 13 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.3887-239A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 27/47 | chr6 | 160064162 | ||||||
| chr6:160064338
|
A | G | 1 | a0003c0007t0075g0147 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3887-63A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 27/47 | chr6 | 160064338 | ||||||
| chr6:160064611
|
C | T | 1 | a0003c0007t0075g0147 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4017+80C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 28/47 | chr6 | 160064611 | ||||||
| chr6:160065051
|
A | G | 21 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(18): Show | 21 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.4115+150A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065051 | ||||||
| chr6:160065053
|
G | A | 3 | a0001c0046t0054g0281a0001c0069t0052g0164a0032c0065t0041g0283 | 3 | HG02965.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.4115+152G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065053 | ||||||
| chr6:160065233
|
C | T | 3 | a0010c0016t0016g0150a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4115+332C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065233 | ||||||
| chr6:160065253
|
A | G | 2 | a0001c0001t0002g0141a0001c0001t0003g0256 | 2 | HG01243.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.4115+352A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065253 | ||||||
| chr6:160065437
|
G | C | 1 | a0001c0001t0043g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4115+536G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065437 | ||||||
| chr6:160065460
|
G | A | 5 | a0001c0002t0067g0247a0001c0004t0003g0223a0001c0004t0027g0287others(2): Show | 5 | HG00738.hp2 HG01243.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.4115+559G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065460 | ||||||
| chr6:160065568
|
C | G | 4 | a0001c0046t0054g0281a0001c0069t0052g0164a0021c0044t0074g0111others(1): Show | 4 | HG02965.hp1 HG02976.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.4115+667C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065568 | ||||||
| chr6:160065639
|
A | T | 1 | a0001c0001t0002g0293 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4115+738A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065639 | ||||||
| chr6:160065713
|
A | C | 1 | a0001c0001t0043g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4115+812A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065713 | ||||||
| chr6:160065776
|
A | G | 2 | a0001c0001t0026g0268a0001c0001t0026g0269 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.4115+875A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065776 | ||||||
| chr6:160065782
|
A | ATG | 7 | a0001c0005t0012g0258a0001c0046t0054g0281a0001c0069t0052g0164others(4): Show | 7 | HG00438.hp1 HG02965.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.4115+913_4115+914d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065782 | |||||
| chr6:160065782
|
A | G | 40 | a0001c0001t0002g0062a0001c0001t0002g0141a0001c0001t0002g0293others(37): Show | 40 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.4115+881A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065782 | ||||||
| chr6:160065782
|
ATGTGTG | A | 3 | a0001c0024t0024g0201a0007c0018t0019g0238a0007c0018t0019g0239 | 3 | HG02280.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4115+909_4115+914d others(8): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065782 | |||||
| chr6:160065786
|
G | A | 1 | a0001c0004t0003g0203 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.4115+885G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065786 | ||||||
| chr6:160065794
|
G | T | 2 | a0018c0032t0033g0086a0018c0032t0033g0087 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.4115+893G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065794 | ||||||
| chr6:160065802
|
G | A | 1 | a0001c0001t0085g0294 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4115+901G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065802 | ||||||
| chr6:160065804
|
G | A | 1 | a0001c0001t0085g0294 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4115+903G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065804 | ||||||
| chr6:160065804
|
GTGTGTGT others(5): Show |
G | 1 | a0002c0003t0063g0207 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.4115+905_4115+916d others(14): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065804 | |||||
| chr6:160065804
|
GTGTGTGT others(7): Show |
G | 3 | a0007c0014t0011g0092a0007c0014t0011g0093a0007c0014t0011g0094 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4115+905_4115+918d others(16): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065804 | |||||
| chr6:160065804
|
GTGTGTGT others(9): Show |
G | 4 | a0006c0010t0011g0122a0006c0010t0011g0123a0006c0010t0011g0125others(1): Show | 4 | HG02630.hp2 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4115+905_4115+920d others(18): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065804 | |||||
| chr6:160065804
|
GTGTGTGT others(11): Show |
G | 2 | a0006c0010t0002g0010a0006c0025t0009g0139 | 2 | HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.4115+905_4115+922d others(20): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065804 | |||||
| chr6:160065806
|
G | A | 1 | a0001c0001t0085g0294 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4115+905G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065806 | ||||||
| chr6:160065807
|
T | C | 1 | a0001c0001t0026g0269 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4115+906T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065807 | ||||||
| chr6:160065808
|
G | A | 1 | a0001c0001t0085g0294 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4115+907G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065808 | ||||||
| chr6:160065810
|
G | A | 2 | a0001c0001t0085g0294a0001c0024t0024g0201 | 2 | HG00140.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4115+909G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065810 | ||||||
| chr6:160065812
|
G | A | 4 | a0001c0001t0085g0294a0001c0002t0071g0194a0001c0024t0024g0201others(1): Show | 4 | HG00140.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.4115+911G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065812 | ||||||
| chr6:160065812
|
G | GTA | 3 | a0001c0004t0034g0126a0001c0004t0044g0153a0005c0008t0002g0029 | 3 | HG01361.hp1 HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4115+912_4115+913i others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065812 | |||||
| chr6:160065814
|
G | A | 12 | a0001c0001t0085g0294a0001c0002t0071g0194a0001c0004t0034g0126others(9): Show | 12 | HG00140.hp1 HG01361.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.4115+913G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065814 | ||||||
| chr6:160065814
|
G | GTA | 4 | a0001c0001t0013g0145a0001c0001t0013g0146a0004c0006t0087g0081others(1): Show | 4 | HG00642.hp2 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.4115+943_4115+944d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTATATAT others(5): Show |
4 | a0001c0001t0002g0141a0001c0001t0003g0256a0001c0001t0005g0028others(1): Show | 4 | HG01243.hp2 HG01934.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.4115+933_4115+944d others(14): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTATATAT others(7): Show |
1 | a0001c0001t0008g0042 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4115+931_4115+944d others(16): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTATATAT others(9): Show |
1 | a0001c0002t0050g0242 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4115+929_4115+944d others(18): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTATATAT others(15): Show |
1 | a0016c0019t0005g0118 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.4115+923_4115+944d others(24): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTA | 3 | a0002c0003t0001g0220a0002c0028t0001g0263a0004c0029t0003g0180 | 3 | NA18982.hp1 NA18983.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.4115+914_4115+915i others(6): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTATAT others(3): Show |
2 | a0001c0001t0035g0053a0010c0016t0016g0170 | 2 | HG01934.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.4115+914_4115+915i others(12): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTATAT others(5): Show |
4 | a0009c0013t0010g0158a0009c0013t0010g0159a0009c0013t0010g0160others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.4115+914_4115+915i others(14): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTATAT others(7): Show |
6 | a0001c0001t0005g0115a0001c0001t0005g0117a0001c0001t0069g0232others(3): Show | 6 | HG01981.hp2 HG02293.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.4115+914_4115+915i others(16): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTATAT others(9): Show |
3 | a0001c0001t0005g0121a0008c0011t0017g0152a0016c0019t0005g0138 | 3 | HG01943.hp2 HG02723.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.4115+914_4115+915i others(18): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTATAT others(11): Show |
2 | a0001c0001t0003g0037a0001c0001t0005g0116 | 2 | HG02683.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4115+914_4115+915i others(20): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTATAT others(15): Show |
2 | a0001c0001t0005g0119a0008c0043t0017g0038 | 2 | HG00323.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4115+914_4115+915i others(24): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTATAT others(25): Show |
1 | a0001c0009t0005g0143 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4115+914_4115+915i others(34): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTATGT others(25): Show |
1 | a0029c0038t0003g0286 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4115+914_4115+915i others(34): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTAT others(5): Show |
1 | a0001c0001t0021g0044 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.4115+914_4115+915i others(14): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTAT others(7): Show |
2 | a0001c0001t0005g0114a0001c0001t0035g0113 | 2 | HG00735.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.4115+914_4115+915i others(16): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTAT others(9): Show |
1 | a0001c0001t0005g0120 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4115+914_4115+915i others(18): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTAT others(11): Show |
4 | a0001c0001t0021g0045a0001c0001t0021g0046a0001c0009t0002g0068others(1): Show | 4 | HG01515.hp1 HG01517.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.4115+914_4115+915i others(20): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTAT others(13): Show |
1 | a0001c0039t0045g0228 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4115+914_4115+915i others(22): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTGT others(3): Show |
1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4115+914_4115+915i others(12): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTGT others(9): Show |
5 | a0001c0002t0009g0102a0001c0002t0009g0103a0020c0041t0002g0013others(2): Show | 5 | HG00639.hp1 HG02976.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.4115+914_4115+915i others(18): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTGT others(11): Show |
6 | a0001c0001t0001g0187a0001c0001t0001g0305a0001c0001t0014g0300others(3): Show | 6 | HG00280.hp2 HG01192.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.4115+914_4115+915i others(20): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTGT others(13): Show |
1 | a0001c0001t0001g0301 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4115+914_4115+915i others(22): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTGT others(15): Show |
2 | a0001c0001t0002g0293a0001c0001t0003g0307 | 2 | HG03834.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.4115+914_4115+915i others(24): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTGT others(13): Show |
1 | a0001c0009t0001g0181 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.4115+914_4115+915i others(22): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTGT others(13): Show |
1 | a0001c0002t0006g0197 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.4115+914_4115+915i others(22): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTGT others(19): Show |
1 | a0001c0002t0006g0198 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4115+914_4115+915i others(28): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTGT others(11): Show |
1 | a0003c0012t0009g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4115+914_4115+915i others(20): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTGT others(13): Show |
3 | a0001c0001t0003g0230a0001c0001t0003g0231a0001c0001t0006g0308 | 3 | HG03490.hp2 HG04115.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.4115+914_4115+915i others(22): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTGT others(15): Show |
7 | a0001c0001t0001g0304a0001c0001t0006g0219a0001c0001t0006g0274others(4): Show | 7 | HG00323.hp2 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.4115+914_4115+915i others(24): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTGT others(17): Show |
1 | a0003c0012t0006g0285 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4115+914_4115+915i others(26): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTGT others(19): Show |
1 | a0001c0009t0008g0011 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.4115+914_4115+915i others(28): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTGT others(11): Show |
1 | a0001c0034t0006g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4115+914_4115+915i others(20): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTGT others(13): Show |
1 | a0003c0012t0009g0095 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4115+914_4115+915i others(22): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTGT others(15): Show |
1 | a0001c0009t0023g0131 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.4115+914_4115+915i others(24): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTGT others(17): Show |
3 | a0001c0001t0026g0268a0001c0001t0026g0269a0001c0009t0001g0211 | 3 | HG02630.hp1 HG02886.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.4115+914_4115+915i others(26): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTGT others(17): Show |
2 | a0001c0001t0006g0244a0001c0009t0028g0229 | 2 | HG00544.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.4115+914_4115+915i others(26): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
G | GTGTGTGT others(19): Show |
1 | a0001c0001t0006g0264 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.4115+914_4115+915i others(28): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
GTA | G | 23 | a0001c0049t0004g0090a0002c0003t0001g0175a0002c0003t0001g0188others(20): Show | 23 | HG00423.hp2 HG00621.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.4115+943_4115+944d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
GTATA | G | 6 | a0001c0005t0004g0014a0001c0005t0004g0021a0001c0005t0004g0022others(3): Show | 6 | HG00423.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4115+941_4115+944d others(6): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
GTATATA | G | 12 | a0001c0005t0004g0012a0001c0005t0004g0018a0001c0005t0004g0019others(9): Show | 12 | HG03942.hp1 NA18942.hp1 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.4115+939_4115+944d others(8): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
GTATATAT others(1): Show |
G | 3 | a0001c0001t0005g0100a0035c0060t0042g0267a0036c0067t0034g0110 | 3 | HG01346.hp2 HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4115+937_4115+944d others(10): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
GTATATAT others(3): Show |
G | 15 | a0001c0002t0010g0168a0001c0002t0023g0101a0001c0002t0028g0034others(12): Show | 15 | HG00738.hp1 HG01081.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.4115+935_4115+944d others(12): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
GTATATAT others(5): Show |
G | 55 | a0001c0001t0002g0062a0001c0001t0003g0249a0001c0002t0002g0020others(52): Show | 55 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.4115+933_4115+944d others(14): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
GTATATAT others(7): Show |
G | 12 | a0001c0002t0015g0009a0001c0002t0015g0163a0001c0002t0018g0235others(9): Show | 12 | HG02109.hp1 HG02258.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.4115+931_4115+944d others(16): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065814
|
GTATATAT others(9): Show |
G | 3 | a0013c0026t0029g0149a0013c0026t0029g0297a0015c0023t0037g0309 | 3 | HG02055.hp1 HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4115+929_4115+944d others(18): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160065814 | |||||
| chr6:160065816
|
A | G | 29 | a0001c0001t0002g0043a0001c0001t0002g0142a0001c0001t0003g0246others(26): Show | 30 | HG00408.hp1 HG01081.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.4115+915A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065816 | ||||||
| chr6:160065818
|
A | G | 8 | a0001c0005t0012g0258a0001c0046t0054g0281a0001c0049t0004g0090others(5): Show | 8 | HG00408.hp1 HG02965.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.4115+917A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065818 | ||||||
| chr6:160065820
|
A | G | 10 | a0001c0005t0004g0014a0001c0005t0004g0021a0001c0005t0004g0022others(7): Show | 10 | HG00423.hp1 HG02258.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.4115+919A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065820 | ||||||
| chr6:160065822
|
A | G | 20 | a0001c0005t0004g0012a0001c0005t0004g0014a0001c0005t0004g0018others(17): Show | 20 | HG00423.hp1 HG02258.hp1 HG02965.hp1 others(17): Show |
intron_variant | MODIFIER | c.4115+921A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065822 | ||||||
| chr6:160065824
|
A | G | 20 | a0001c0005t0004g0012a0001c0005t0004g0014a0001c0005t0004g0018others(17): Show | 20 | HG00423.hp1 HG02258.hp1 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.4115+923A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065824 | ||||||
| chr6:160065826
|
A | G | 32 | a0001c0002t0010g0168a0001c0002t0023g0101a0001c0002t0028g0034others(29): Show | 32 | HG00423.hp1 HG00738.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.4115+925A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065826 | ||||||
| chr6:160065828
|
A | G | 74 | a0001c0001t0002g0062a0001c0001t0003g0249a0001c0002t0002g0020others(71): Show | 74 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.4115+927A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065828 | ||||||
| chr6:160065830
|
A | G | 66 | a0001c0001t0002g0062a0001c0001t0003g0249a0001c0002t0002g0020others(63): Show | 66 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.4115+929A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065830 | ||||||
| chr6:160065832
|
A | G | 55 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(52): Show | 55 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.4115+931A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065832 | ||||||
| chr6:160065836
|
A | G | 1 | a0003c0007t0075g0147 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4115+935A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065836 | ||||||
| chr6:160065899
|
C | T | 16 | a0001c0001t0005g0028a0001c0001t0005g0100a0001c0001t0005g0114others(13): Show | 16 | HG00323.hp1 HG00735.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.4115+998C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160065899 | ||||||
| chr6:160066001
|
A | G | 9 | a0006c0010t0002g0010a0006c0010t0011g0122a0006c0010t0011g0123others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.4115+1100A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160066001 | ||||||
| chr6:160066012
|
G | GT | 15 | a0001c0001t0010g0157a0001c0002t0036g0289a0001c0005t0004g0024others(12): Show | 15 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.4115+1128dupT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160066012 | |||||
| chr6:160066083
|
C | T | 12 | a0006c0010t0002g0010a0006c0010t0011g0122a0006c0010t0011g0123others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.4115+1182C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160066083 | ||||||
| chr6:160066101
|
G | A | 2 | a0001c0009t0005g0143a0001c0009t0005g0144 | 2 | HG01884.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.4115+1200G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160066101 | ||||||
| chr6:160066129
|
C | T | 2 | a0001c0046t0054g0281a0001c0069t0052g0164 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4115+1228C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160066129 | ||||||
| chr6:160066140
|
G | C | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4115+1239G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160066140 | ||||||
| chr6:160066164
|
G | A | 22 | a0001c0002t0010g0168a0001c0005t0004g0012a0001c0005t0004g0014others(19): Show | 22 | HG00423.hp1 HG01109.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.4115+1263G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160066164 | ||||||
| chr6:160066250
|
C | T | 2 | a0001c0046t0054g0281a0001c0069t0052g0164 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4115+1349C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160066250 | ||||||
| chr6:160066395
|
C | T | 1 | a0011c0017t0086g0016 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4115+1494C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160066395 | ||||||
| chr6:160066445
|
G | A | 1 | a0003c0066t0053g0162 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4115+1544G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160066445 | ||||||
| chr6:160066448
|
C | T | 2 | a0004c0006t0002g0128a0004c0006t0002g0130 | 2 | HG02738.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.4115+1547C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160066448 | ||||||
| chr6:160067198
|
G | A | 1 | a0001c0002t0023g0101 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.4116-1051G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160067198 | ||||||
| chr6:160067212
|
C | T | 3 | a0010c0016t0016g0150a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4116-1037C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160067212 | ||||||
| chr6:160067303
|
C | T | 1 | a0005c0008t0002g0029 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.4116-946C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160067303 | ||||||
| chr6:160067322
|
C | T | 1 | a0001c0001t0006g0274 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4116-927C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160067322 | ||||||
| chr6:160067385
|
C | G | 1 | a0031c0048t0002g0069 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.4116-864C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160067385 | ||||||
| chr6:160067395
|
G | C | 1 | a0001c0002t0007g0058 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4116-854G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160067395 | ||||||
| chr6:160067640
|
G | A | 3 | a0001c0002t0003g0303a0001c0002t0003g0306a0036c0067t0034g0110 | 3 | HG03195.hp1 NA18982.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.4116-609G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160067640 | ||||||
| chr6:160067646
|
G | A | 1 | a0004c0006t0002g0071 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4116-603G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160067646 | ||||||
| chr6:160067672
|
C | T | 3 | a0007c0014t0011g0092a0007c0014t0011g0093a0007c0014t0011g0094 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4116-577C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160067672 | ||||||
| chr6:160067789
|
A | AT | 3 | a0007c0014t0011g0092a0007c0014t0011g0093a0007c0014t0011g0094 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4116-457dupT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160067789 | |||||
| chr6:160067839
|
G | A | 51 | a0002c0003t0001g0001a0002c0003t0001g0002a0002c0003t0001g0175others(48): Show | 52 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.4116-410G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160067839 | ||||||
| chr6:160067944
|
C | T | 2 | a0001c0001t0013g0145a0001c0001t0013g0146 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.4116-305C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160067944 | ||||||
| chr6:160068023
|
A | G | 2 | a0001c0002t0028g0034a0003c0007t0023g0109 | 2 | HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4116-226A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160068023 | ||||||
| chr6:160068060
|
TGG | T | 81 | a0001c0001t0001g0187a0001c0001t0001g0304a0001c0001t0001g0305others(78): Show | 81 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.4116-184_4116-183d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160068060 | |||||
| chr6:160068063
|
G | GGT | 11 | a0001c0001t0002g0043a0001c0001t0005g0028a0001c0001t0005g0117others(8): Show | 11 | HG01081.hp2 HG01884.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.4116-185_4116-184i others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160068063 | |||||
| chr6:160068063
|
G | GGTGTGTG others(3): Show |
2 | a0013c0026t0029g0149a0013c0026t0029g0297 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.4116-185_4116-184i others(12): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160068063 | |||||
| chr6:160068063
|
GGGGT | G | 27 | a0001c0001t0003g0037a0001c0001t0010g0157a0001c0002t0009g0047others(24): Show | 27 | HG00597.hp2 HG01891.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.4116-184_4116-181d others(6): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160068063 | |||||
| chr6:160068063
|
GGGGTGT | G | 43 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(40): Show | 43 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.4116-184_4116-179d others(8): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160068063 | |||||
| chr6:160068063
|
GGGGTGTG others(1): Show |
G | 23 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(20): Show | 23 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.4116-184_4116-177d others(10): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160068063 | |||||
| chr6:160068063
|
GGGGTGTG others(3): Show |
G | 3 | a0001c0002t0080g0054a0001c0004t0003g0190a0010c0016t0016g0150 | 3 | HG01175.hp2 HG02280.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.4116-184_4116-175d others(12): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160068063 | |||||
| chr6:160068063
|
GGGGTGTG others(5): Show |
G | 2 | a0010c0016t0016g0169a0010c0016t0016g0170 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4116-184_4116-173d others(14): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160068063 | |||||
| chr6:160068065
|
G | T | 44 | a0001c0001t0001g0301a0001c0001t0002g0043a0001c0001t0005g0028others(41): Show | 44 | HG00323.hp1 HG00544.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.4116-184G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160068065 | ||||||
| chr6:160068065
|
GGT | G | 26 | a0004c0006t0002g0071a0004c0006t0002g0072a0004c0006t0002g0073others(23): Show | 26 | HG00597.hp1 HG00733.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.4116-142_4116-141d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160068065 | |||||
| chr6:160068065
|
GGTGTGTG others(1): Show |
G | 47 | a0002c0003t0001g0001a0002c0003t0001g0002a0002c0003t0001g0175others(44): Show | 48 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.4116-148_4116-141d others(10): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160068065 | |||||
| chr6:160068065
|
GGTGTGTG others(9): Show |
G | 2 | a0004c0006t0002g0082a0005c0027t0003g0003 | 2 | NA18960.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.4116-156_4116-141d others(18): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160068065 | |||||
| chr6:160068066
|
GTGTGTGT others(4): Show |
G | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4116-182_4116-172d others(13): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160068066 | ||||||
| chr6:160068067
|
T | G | 2 | a0004c0006t0002g0075a0005c0008t0083g0039 | 2 | HG00639.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.4116-182T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160068067 | ||||||
| chr6:160068073
|
T | G | 1 | a0002c0003t0001g0208 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.4116-176T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160068073 | ||||||
| chr6:160068082
|
G | T | 3 | a0001c0005t0004g0014a0001c0005t0004g0022a0001c0005t0012g0184 | 3 | NA18943.hp2 NA18948.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.4116-167G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160068082 | ||||||
| chr6:160068103
|
T | TGTGA | 3 | a0001c0002t0071g0194a0001c0004t0034g0126a0001c0004t0044g0153 | 3 | HG02055.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4116-143_4116-142i others(6): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160068103 | |||||
| chr6:160068183
|
CAG | C | 80 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(77): Show | 80 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.4116-63_4116-62del others(2): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr6 | 160068183 | |||||
| chr6:160068191
|
C | G | 1 | a0002c0003t0008g0085 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4116-58C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160068191 | ||||||
| chr6:160068194
|
A | G | 3 | a0001c0001t0006g0274a0001c0001t0026g0268a0001c0001t0026g0269 | 3 | HG02630.hp1 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4116-55A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 29/47 | chr6 | 160068194 | ||||||
| chr6:160068615
|
GGCTGGCA others(53): Show |
G | 1 | a0001c0004t0027g0287 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4252+251_4252+310d others(62): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 30/47 | INFO_REALIGN_3_PRIME | chr6 | 160068615 | |||||
| chr6:160068682
|
A | T | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4252+297A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 30/47 | chr6 | 160068682 | ||||||
| chr6:160068691
|
A | G | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4252+306A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 30/47 | chr6 | 160068691 | ||||||
| chr6:160068712
|
G | C | 104 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(101): Show | 104 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.4252+327G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 30/47 | chr6 | 160068712 | ||||||
| chr6:160068906
|
G | A | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4252+521G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 30/47 | chr6 | 160068906 | ||||||
| chr6:160069063
|
G | A | 56 | a0001c0024t0024g0201a0002c0003t0001g0001a0002c0003t0001g0002others(53): Show | 57 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.4252+678G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 30/47 | chr6 | 160069063 | ||||||
| chr6:160069066
|
T | C | 3 | a0010c0016t0016g0150a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4252+681T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 30/47 | chr6 | 160069066 | ||||||
| chr6:160069142
|
G | A | 182 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(179): Show | 183 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.4253-726G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 30/47 | chr6 | 160069142 | ||||||
| chr6:160069282
|
C | T | 101 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(98): Show | 101 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.4253-586C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 30/47 | chr6 | 160069282 | ||||||
| chr6:160069319
|
T | C | 1 | a0001c0002t0015g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4253-549T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 30/47 | chr6 | 160069319 | ||||||
| chr6:160069530
|
C | T | 1 | a0001c0005t0012g0258 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.4253-338C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 30/47 | chr6 | 160069530 | ||||||
| chr6:160069561
|
A | C | 2 | a0001c0024t0070g0282a0032c0065t0041g0283 | 2 | NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.4253-307A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 30/47 | chr6 | 160069561 | ||||||
| chr6:160069616
|
C | T | 16 | a0001c0001t0002g0062a0001c0001t0002g0293a0001c0001t0003g0230others(13): Show | 16 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.4253-252C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 30/47 | chr6 | 160069616 | ||||||
| chr6:160069782
|
C | T | 2 | a0001c0034t0006g0035a0003c0012t0009g0088 | 2 | HG02145.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.4253-86C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 30/47 | chr6 | 160069782 | ||||||
| chr6:160069785
|
G | C | 2 | a0004c0029t0003g0180a0004c0029t0003g0185 | 2 | NA18983.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.4253-83G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 30/47 | chr6 | 160069785 | ||||||
| chr6:160069848
|
T | C | 2 | a0005c0008t0002g0032a0005c0008t0013g0104 | 2 | HG00733.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.4253-20T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 30/47 | chr6 | 160069848 | ||||||
| chr6:160070115
|
G | T | 1 | a0036c0067t0034g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4443+57G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160070115 | ||||||
| chr6:160070234
|
C | T | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4443+176C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160070234 | ||||||
| chr6:160070277
|
G | A | 5 | a0004c0006t0002g0071a0004c0006t0002g0072a0004c0006t0002g0073others(2): Show | 5 | HG00597.hp1 HG03654.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.4443+219G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160070277 | ||||||
| chr6:160070407
|
G | A | 2 | a0022c0042t0024g0151a0037c0033t0073g0140 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.4443+349G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160070407 | ||||||
| chr6:160070421
|
G | A | 2 | a0001c0001t0006g0308a0001c0009t0023g0131 | 2 | NA18974.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.4443+363G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160070421 | ||||||
| chr6:160070525
|
G | A | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4443+467G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160070525 | ||||||
| chr6:160070709
|
A | G | 183 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(180): Show | 184 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.4443+651A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160070709 | ||||||
| chr6:160070711
|
G | A | 9 | a0006c0010t0002g0010a0006c0010t0011g0122a0006c0010t0011g0123others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.4443+653G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160070711 | ||||||
| chr6:160070814
|
C | G | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4443+756C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160070814 | ||||||
| chr6:160070864
|
G | A | 2 | a0007c0018t0019g0238a0007c0018t0019g0239 | 2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4443+806G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160070864 | ||||||
| chr6:160070970
|
G | A | 3 | a0010c0016t0016g0150a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4443+912G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160070970 | ||||||
| chr6:160070996
|
G | T | 5 | a0001c0024t0024g0201a0014c0022t0038g0275a0014c0022t0040g0270others(2): Show | 5 | HG02109.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.4444-914G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160070996 | ||||||
| chr6:160071012
|
A | G | 1 | a0036c0067t0034g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4444-898A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071012 | ||||||
| chr6:160071043
|
A | G | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4444-867A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071043 | ||||||
| chr6:160071045
|
A | T | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4444-865A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071045 | ||||||
| chr6:160071062
|
G | A | 1 | a0032c0065t0041g0283 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4444-848G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071062 | ||||||
| chr6:160071063
|
TGAAGGGG others(213): Show |
T | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4444-846_4444-627d others(2): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071063 | ||||||
| chr6:160071118
|
A | G | 1 | a0002c0015t0014g0298 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4444-792A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071118 | ||||||
| chr6:160071125
|
T | G | 1 | a0002c0015t0014g0298 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4444-785T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071125 | ||||||
| chr6:160071133
|
G | C | 1 | a0002c0015t0014g0298 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4444-777G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071133 | ||||||
| chr6:160071135
|
G | A | 1 | a0002c0015t0014g0298 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4444-775G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071135 | ||||||
| chr6:160071138
|
C | A | 1 | a0021c0044t0074g0111 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4444-772C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071138 | ||||||
| chr6:160071140
|
T | C | 1 | a0002c0015t0014g0298 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4444-770T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071140 | ||||||
| chr6:160071149
|
C | A | 186 | a0001c0001t0003g0249a0001c0001t0005g0114a0001c0001t0005g0115others(183): Show | 187 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.4444-761C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071149 | ||||||
| chr6:160071150
|
A | G | 186 | a0001c0001t0003g0249a0001c0001t0005g0114a0001c0001t0005g0115others(183): Show | 187 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.4444-760A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071150 | ||||||
| chr6:160071152
|
A | G | 1 | a0002c0015t0014g0298 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4444-758A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071152 | ||||||
| chr6:160071156
|
A | G | 1 | a0002c0015t0014g0298 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4444-754A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071156 | ||||||
| chr6:160071158
|
G | T | 1 | a0002c0015t0014g0298 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4444-752G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071158 | ||||||
| chr6:160071173
|
A | G | 1 | a0002c0015t0014g0298 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4444-737A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071173 | ||||||
| chr6:160071177
|
G | C | 1 | a0002c0015t0014g0298 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4444-733G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071177 | ||||||
| chr6:160071178
|
A | G | 1 | a0002c0015t0014g0298 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4444-732A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071178 | ||||||
| chr6:160071179
|
A | G | 1 | a0002c0015t0014g0298 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4444-731A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071179 | ||||||
| chr6:160071194
|
C | T | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4444-716C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071194 | ||||||
| chr6:160071203
|
C | A | 1 | a0002c0015t0014g0298 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4444-707C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071203 | ||||||
| chr6:160071204
|
A | G | 1 | a0002c0015t0014g0298 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4444-706A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071204 | ||||||
| chr6:160071206
|
A | ACCCAGGA others(101): Show |
1 | a0004c0029t0003g0185 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.4444-701_4444-594d others(110): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr6 | 160071206 | |||||
| chr6:160071206
|
A | G | 1 | a0002c0015t0014g0298 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4444-704A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071206 | ||||||
| chr6:160071206
|
ACCCAGGA others(47): Show |
A | 51 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(48): Show | 51 | HG00544.hp2 HG00738.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.4444-647_4444-594d others(56): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr6 | 160071206 | |||||
| chr6:160071210
|
A | G | 1 | a0002c0015t0014g0298 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4444-700A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071210 | ||||||
| chr6:160071212
|
G | T | 1 | a0002c0015t0014g0298 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4444-698G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071212 | ||||||
| chr6:160071230
|
T | TCGGGGGT others(49): Show |
1 | a0002c0015t0014g0298 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4444-680_4444-679i others(58): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071230 | ||||||
| chr6:160071230
|
T | TGGGGGGT others(158): Show |
1 | a0002c0003t0001g0265 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.4444-675_4444-674i others(167): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr6 | 160071230 | |||||
| chr6:160071241
|
C | CGAGGCCC others(48): Show |
1 | a0029c0038t0003g0286 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4444-626_4444-625i others(57): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr6 | 160071241 | |||||
| chr6:160071257
|
A | C | 62 | a0001c0002t0023g0101a0001c0002t0028g0034a0001c0002t0067g0247others(59): Show | 63 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.4444-653A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071257 | ||||||
| chr6:160071258
|
G | A | 62 | a0001c0002t0023g0101a0001c0002t0028g0034a0001c0002t0067g0247others(59): Show | 63 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.4444-652G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071258 | ||||||
| chr6:160071259
|
G | A | 20 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(17): Show | 20 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.4444-651G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071259 | ||||||
| chr6:160071260
|
G | A | 62 | a0001c0002t0023g0101a0001c0002t0028g0034a0001c0002t0067g0247others(59): Show | 63 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.4444-650G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071260 | ||||||
| chr6:160071263
|
C | T | 2 | a0002c0003t0001g0265a0002c0015t0014g0298 | 2 | HG02155.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.4444-647C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071263 | ||||||
| chr6:160071264
|
A | G | 65 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(62): Show | 65 | HG00140.hp2 HG00423.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.4444-646A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071264 | ||||||
| chr6:160071266
|
G | T | 63 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(60): Show | 63 | HG00140.hp2 HG00423.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.4444-644G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071266 | ||||||
| chr6:160071284
|
T | C | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4444-626T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071284 | ||||||
| chr6:160071284
|
T | TC | 59 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(56): Show | 59 | HG00140.hp2 HG00423.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.4444-626_4444-625i others(3): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071284 | ||||||
| chr6:160071284
|
T | TCGGGGGT others(49): Show |
1 | a0032c0065t0041g0283 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4444-626_4444-625i others(58): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071284 | ||||||
| chr6:160071284
|
T | TGGGGGGT others(104): Show |
1 | a0002c0047t0008g0135 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.4444-621_4444-620i others(113): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr6 | 160071284 | |||||
| chr6:160071284
|
T | TGGGGGTG others(48): Show |
1 | a0002c0003t0001g0002 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.4444-594_4444-593i others(57): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr6 | 160071284 | |||||
| chr6:160071284
|
T | TGGGGGTG others(103): Show |
1 | a0037c0033t0073g0140 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4444-616_4444-615i others(112): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr6 | 160071284 | |||||
| chr6:160071295
|
C | CGAGGCCC others(430): Show |
1 | a0001c0004t0044g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4444-594_4444-593i others(439): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr6 | 160071295 | |||||
| chr6:160071295
|
C | CGAGGCCC others(484): Show |
2 | a0001c0002t0071g0194a0001c0004t0034g0126 | 2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.4444-594_4444-593i others(493): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr6 | 160071295 | |||||
| chr6:160071295
|
C | CGAGGCCC others(158): Show |
1 | a0002c0003t0014g0177 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4444-594_4444-593i others(167): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr6 | 160071295 | |||||
| chr6:160071295
|
C | CGAGGCCC others(103): Show |
17 | a0002c0003t0001g0175a0002c0003t0001g0179a0002c0003t0001g0188others(14): Show | 17 | HG00438.hp2 HG01168.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.4444-594_4444-593i others(112): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr6 | 160071295 | |||||
| chr6:160071295
|
C | CGAGGCCC others(158): Show |
20 | a0002c0003t0001g0186a0002c0003t0001g0241a0002c0003t0001g0255others(17): Show | 20 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.4444-594_4444-593i others(167): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr6 | 160071295 | |||||
| chr6:160071295
|
C | CGAGGCCC others(377): Show |
1 | a0002c0003t0001g0206 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.4444-594_4444-593i others(386): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr6 | 160071295 | |||||
| chr6:160071295
|
C | CGAGGCCC others(158): Show |
1 | a0002c0003t0001g0220 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.4444-591_4444-590i others(167): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr6 | 160071295 | |||||
| chr6:160071295
|
C | CGAGGCCC others(158): Show |
3 | a0002c0003t0001g0202a0002c0003t0001g0204a0002c0003t0001g0208 | 3 | NA18952.hp2 NA18974.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.4444-583_4444-582i others(167): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr6 | 160071295 | |||||
| chr6:160071295
|
C | CGAGGCCC others(212): Show |
3 | a0002c0003t0001g0001a0002c0003t0001g0212a0002c0003t0001g0218 | 4 | HG01258.hp2 HG01358.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.4444-600_4444-599i others(221): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr6 | 160071295 | |||||
| chr6:160071295
|
C | G | 45 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(42): Show | 45 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.4444-615C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071295 | ||||||
| chr6:160071317
|
T | C | 16 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(13): Show | 16 | HG00140.hp2 HG00733.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.4444-593T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071317 | ||||||
| chr6:160071318
|
G | A | 16 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(13): Show | 16 | HG00140.hp2 HG00733.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.4444-592G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071318 | ||||||
| chr6:160071431
|
C | T | 1 | a0001c0001t0003g0249 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4444-479C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071431 | ||||||
| chr6:160071581
|
T | C | 22 | a0001c0005t0004g0012a0001c0005t0004g0014a0001c0005t0004g0018others(19): Show | 22 | HG00423.hp1 HG01109.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.4444-329T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071581 | ||||||
| chr6:160071728
|
A | C | 1 | a0036c0067t0034g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4444-182A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071728 | ||||||
| chr6:160071768
|
C | T | 2 | a0001c0046t0054g0281a0001c0069t0052g0164 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4444-142C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 31/47 | chr6 | 160071768 | ||||||
| chr6:160072085
|
C | T | 23 | a0001c0005t0004g0012a0001c0005t0004g0014a0001c0005t0004g0018others(20): Show | 23 | HG00423.hp1 HG01109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.4570+49C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 32/47 | chr6 | 160072085 | ||||||
| chr6:160072339
|
TC | T | 12 | a0006c0010t0002g0010a0006c0010t0011g0122a0006c0010t0011g0123others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.4570+305delC | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 32/47 | INFO_REALIGN_3_PRIME | chr6 | 160072339 | |||||
| chr6:160072402
|
G | A | 1 | a0001c0001t0008g0042 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4571-363G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 32/47 | chr6 | 160072402 | ||||||
| chr6:160072696
|
G | A | 1 | a0036c0067t0034g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4571-69G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 32/47 | chr6 | 160072696 | ||||||
| chr6:160072936
|
T | C | 1 | a0032c0065t0041g0283 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4690+52T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 33/47 | chr6 | 160072936 | ||||||
| chr6:160073036
|
C | T | 20 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(17): Show | 20 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.4690+152C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 33/47 | chr6 | 160073036 | ||||||
| chr6:160073086
|
G | A | 1 | a0002c0003t0001g0208 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.4691-127G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 33/47 | chr6 | 160073086 | ||||||
| chr6:160073209
|
G | A | 2 | a0008c0011t0017g0152a0008c0043t0017g0038 | 2 | HG02723.hp2 HG03471.hp1 |
splice_region_variant&intron_variant | LOW | c.4691-4G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 33/47 | chr6 | 160073209 | ||||||
| chr6:160073489
|
C | T | 58 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(55): Show | 58 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.4947+20C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 34/47 | chr6 | 160073489 | ||||||
| chr6:160074023
|
A | C | 27 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(24): Show | 27 | HG00323.hp2 HG00544.hp1 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.5166+48A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160074023 | ||||||
| chr6:160074035
|
T | G | 2 | a0001c0002t0071g0194a0001c0004t0034g0126 | 2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.5166+60T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160074035 | ||||||
| chr6:160074041
|
G | A | 2 | a0001c0046t0054g0281a0001c0069t0052g0164 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5166+66G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160074041 | ||||||
| chr6:160074064
|
T | G | 1 | a0001c0001t0002g0062 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.5166+89T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160074064 | ||||||
| chr6:160074158
|
G | A | 2 | a0013c0026t0029g0149a0013c0026t0029g0297 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.5166+183G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160074158 | ||||||
| chr6:160074213
|
G | T | 21 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(18): Show | 21 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.5166+238G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160074213 | ||||||
| chr6:160074274
|
G | A | 1 | a0001c0001t0069g0232 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.5166+299G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160074274 | ||||||
| chr6:160074313
|
G | A | 56 | a0001c0024t0024g0201a0002c0003t0001g0001a0002c0003t0001g0002others(53): Show | 57 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.5166+338G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160074313 | ||||||
| chr6:160074343
|
G | A | 1 | a0014c0022t0040g0270 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5166+368G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160074343 | ||||||
| chr6:160074365
|
C | G | 1 | a0001c0024t0024g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5166+390C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160074365 | ||||||
| chr6:160074444
|
T | A | 9 | a0006c0010t0002g0010a0006c0010t0011g0122a0006c0010t0011g0123others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.5166+469T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160074444 | ||||||
| chr6:160074575
|
A | G | 121 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(118): Show | 122 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.5166+600A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160074575 | ||||||
| chr6:160074776
|
A | G | 3 | a0001c0001t0021g0044a0001c0001t0021g0045a0001c0001t0021g0046 | 3 | HG01515.hp1 HG01517.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.5166+801A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160074776 | ||||||
| chr6:160074887
|
C | T | 1 | a0021c0044t0074g0111 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5166+912C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160074887 | ||||||
| chr6:160074929
|
C | T | 1 | a0020c0041t0002g0013 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5167-918C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160074929 | ||||||
| chr6:160075023
|
G | A | 44 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(41): Show | 44 | HG00140.hp2 HG00423.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.5167-824G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160075023 | ||||||
| chr6:160075033
|
C | T | 1 | a0003c0007t0022g0106 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.5167-814C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160075033 | ||||||
| chr6:160075107
|
C | T | 1 | a0001c0069t0052g0164 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5167-740C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160075107 | ||||||
| chr6:160075111
|
C | T | 1 | a0001c0069t0052g0164 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5167-736C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160075111 | ||||||
| chr6:160075142
|
ACATT | A | 24 | a0001c0001t0003g0037a0001c0001t0005g0028a0001c0001t0005g0100others(21): Show | 24 | HG00323.hp1 HG00735.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.5167-701_5167-698d others(6): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | INFO_REALIGN_3_PRIME | chr6 | 160075142 | |||||
| chr6:160075169
|
C | T | 3 | a0010c0016t0016g0150a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.5167-678C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160075169 | ||||||
| chr6:160075211
|
T | G | 182 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(179): Show | 183 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.5167-636T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160075211 | ||||||
| chr6:160075400
|
C | T | 10 | a0001c0001t0002g0043a0001c0001t0002g0142a0001c0001t0003g0246others(7): Show | 10 | HG00280.hp1 HG00642.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.5167-447C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160075400 | ||||||
| chr6:160075493
|
G | A | 2 | a0002c0003t0001g0175a0002c0003t0008g0148 | 2 | HG01192.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.5167-354G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160075493 | ||||||
| chr6:160075507
|
C | T | 2 | a0001c0001t0002g0141a0001c0001t0003g0256 | 2 | HG01243.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.5167-340C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160075507 | ||||||
| chr6:160075673
|
C | T | 3 | a0010c0016t0016g0150a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.5167-174C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160075673 | ||||||
| chr6:160075706
|
A | G | 1 | a0001c0009t0005g0143 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5167-141A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160075706 | ||||||
| chr6:160075744
|
C | T | 2 | a0001c0002t0006g0197a0001c0002t0006g0198 | 2 | HG01433.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.5167-103C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160075744 | ||||||
| chr6:160075785
|
T | C | 23 | a0001c0005t0004g0012a0001c0005t0004g0014a0001c0005t0004g0018others(20): Show | 23 | HG00423.hp1 HG01109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.5167-62T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 35/47 | chr6 | 160075785 | ||||||
| chr6:160076070
|
C | T | 3 | a0001c0002t0071g0194a0001c0004t0034g0126a0001c0004t0044g0153 | 3 | HG02055.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.5316+74C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160076070 | ||||||
| chr6:160076183
|
G | A | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5316+187G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160076183 | ||||||
| chr6:160076210
|
G | A | 1 | a0001c0001t0002g0142 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.5316+214G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160076210 | ||||||
| chr6:160076280
|
A | T | 5 | a0001c0024t0024g0201a0014c0022t0038g0275a0014c0022t0040g0270others(2): Show | 5 | HG02109.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.5316+284A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160076280 | ||||||
| chr6:160076510
|
C | T | 23 | a0001c0005t0004g0012a0001c0005t0004g0014a0001c0005t0004g0018others(20): Show | 23 | HG00423.hp1 HG01109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.5316+514C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160076510 | ||||||
| chr6:160076604
|
A | C | 1 | a0001c0004t0003g0203 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.5316+608A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160076604 | ||||||
| chr6:160076607
|
A | T | 2 | a0015c0023t0037g0309a0015c0023t0094g0096 | 2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.5316+611A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160076607 | ||||||
| chr6:160076690
|
G | A | 1 | a0001c0001t0030g0105 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5316+694G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160076690 | ||||||
| chr6:160076814
|
AAT | A | 13 | a0001c0001t0005g0028a0001c0001t0005g0100a0001c0001t0005g0114others(10): Show | 13 | HG00323.hp1 HG00735.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.5316+821_5316+822d others(4): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr6 | 160076814 | |||||
| chr6:160076858
|
C | T | 51 | a0002c0003t0001g0001a0002c0003t0001g0002a0002c0003t0001g0175others(48): Show | 52 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.5316+862C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160076858 | ||||||
| chr6:160077017
|
G | A | 61 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(58): Show | 61 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.5316+1021G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160077017 | ||||||
| chr6:160077045
|
C | T | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5316+1049C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160077045 | ||||||
| chr6:160077111
|
G | C | 1 | a0001c0004t0051g0178 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.5317-1090G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160077111 | ||||||
| chr6:160077224
|
C | T | 1 | a0004c0006t0003g0176 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.5317-977C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160077224 | ||||||
| chr6:160077245
|
C | A | 1 | a0036c0067t0034g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5317-956C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160077245 | ||||||
| chr6:160077386
|
A | G | 3 | a0001c0002t0071g0194a0001c0004t0034g0126a0001c0004t0044g0153 | 3 | HG02055.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.5317-815A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160077386 | ||||||
| chr6:160077424
|
G | C | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5317-777G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160077424 | ||||||
| chr6:160077454
|
G | T | 1 | a0001c0024t0024g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5317-747G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160077454 | ||||||
| chr6:160077686
|
A | G | 1 | a0002c0003t0001g0218 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.5317-515A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160077686 | ||||||
| chr6:160077832
|
C | T | 2 | a0004c0029t0003g0180a0004c0029t0003g0185 | 2 | NA18983.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.5317-369C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160077832 | ||||||
| chr6:160077933
|
C | T | 56 | a0001c0024t0024g0201a0002c0003t0001g0001a0002c0003t0001g0002others(53): Show | 57 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.5317-268C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160077933 | ||||||
| chr6:160078101
|
C | T | 2 | a0001c0046t0054g0281a0001c0069t0052g0164 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5317-100C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160078101 | ||||||
| chr6:160078149
|
A | G | 1 | a0003c0007t0079g0137 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5317-52A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160078149 | ||||||
| chr6:160078181
|
C | T | 2 | a0001c0002t0071g0194a0001c0004t0034g0126 | 2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.5317-20C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 36/47 | chr6 | 160078181 | ||||||
| chr6:160078369
|
C | T | 2 | a0001c0046t0054g0281a0001c0069t0052g0164 | 2 | HG02965.hp1 HG03453.hp2 |
splice_region_variant&intron_variant | LOW | c.5478+7C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 37/47 | chr6 | 160078369 | ||||||
| chr6:160078533
|
T | C | 98 | a0001c0005t0004g0012a0001c0005t0004g0014a0001c0005t0004g0018others(95): Show | 99 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.5478+171T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 37/47 | chr6 | 160078533 | ||||||
| chr6:160078637
|
G | A | 3 | a0001c0002t0071g0194a0001c0004t0034g0126a0001c0004t0044g0153 | 3 | HG02055.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.5478+275G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 37/47 | chr6 | 160078637 | ||||||
| chr6:160078674
|
C | G | 1 | a0036c0067t0034g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5478+312C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 37/47 | chr6 | 160078674 | ||||||
| chr6:160078704
|
A | G | 182 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(179): Show | 183 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.5478+342A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 37/47 | chr6 | 160078704 | ||||||
| chr6:160078845
|
T | C | 1 | a0032c0065t0041g0283 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5478+483T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 37/47 | chr6 | 160078845 | ||||||
| chr6:160078864
|
C | T | 1 | a0008c0011t0017g0195 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5478+502C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 37/47 | chr6 | 160078864 | ||||||
| chr6:160079089
|
T | A | 2 | a0018c0032t0033g0086a0018c0032t0033g0087 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.5479-491T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 37/47 | chr6 | 160079089 | ||||||
| chr6:160079205
|
G | A | 2 | a0003c0012t0006g0284a0003c0012t0006g0285 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.5479-375G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 37/47 | chr6 | 160079205 | ||||||
| chr6:160079295
|
T | G | 1 | a0022c0042t0024g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5479-285T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 37/47 | chr6 | 160079295 | ||||||
| chr6:160079348
|
C | T | 1 | a0013c0026t0029g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5479-232C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 37/47 | chr6 | 160079348 | ||||||
| chr6:160079360
|
C | G | 1 | a0021c0044t0074g0111 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5479-220C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 37/47 | chr6 | 160079360 | ||||||
| chr6:160079554
|
G | A | 3 | a0010c0016t0016g0150a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.5479-26G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 37/47 | chr6 | 160079554 | ||||||
| chr6:160079563
|
G | T | 4 | a0013c0026t0029g0149a0013c0026t0029g0297a0015c0023t0037g0309others(1): Show | 4 | HG02055.hp1 HG02486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.5479-17G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 37/47 | chr6 | 160079563 | ||||||
| chr6:160079867
|
G | A | 1 | a0008c0011t0078g0008 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.5686+80G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 38/47 | chr6 | 160079867 | ||||||
| chr6:160079925
|
C | G | 1 | a0021c0044t0074g0111 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5686+138C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 38/47 | chr6 | 160079925 | ||||||
| chr6:160079957
|
G | A | 1 | a0004c0006t0002g0075 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5686+170G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 38/47 | chr6 | 160079957 | ||||||
| chr6:160080090
|
G | A | 1 | a0001c0004t0001g0222 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.5687-39G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 38/47 | chr6 | 160080090 | ||||||
| chr6:160080466
|
C | A | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5833+191C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160080466 | ||||||
| chr6:160080489
|
G | A | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5833+214G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160080489 | ||||||
| chr6:160080522
|
A | G | 1 | a0002c0003t0001g0193 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.5833+247A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160080522 | ||||||
| chr6:160080608
|
A | G | 1 | a0001c0004t0044g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5833+333A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160080608 | ||||||
| chr6:160080644
|
G | A | 1 | a0001c0046t0054g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5833+369G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160080644 | ||||||
| chr6:160080675
|
C | T | 167 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(164): Show | 168 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.5833+400C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160080675 | ||||||
| chr6:160080733
|
TG | T | 22 | a0001c0005t0004g0012a0001c0005t0004g0014a0001c0005t0004g0018others(19): Show | 22 | HG00423.hp1 HG01109.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.5833+459delG | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160080733 | ||||||
| chr6:160080793
|
G | A | 4 | a0001c0001t0013g0006a0001c0001t0013g0145a0001c0001t0013g0146others(1): Show | 4 | HG00280.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.5833+518G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160080793 | ||||||
| chr6:160080794
|
G | A | 1 | a0004c0006t0002g0072 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.5833+519G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160080794 | ||||||
| chr6:160080857
|
C | A | 1 | a0001c0002t0007g0066 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.5833+582C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160080857 | ||||||
| chr6:160080902
|
G | A | 1 | a0001c0046t0054g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5833+627G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160080902 | ||||||
| chr6:160080961
|
CA | C | 180 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(177): Show | 181 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.5833+701delA | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | INFO_REALIGN_3_PRIME | chr6 | 160080961 | |||||
| chr6:160080987
|
G | A | 2 | a0001c0009t0005g0143a0001c0009t0005g0144 | 2 | HG01884.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.5833+712G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160080987 | ||||||
| chr6:160080994
|
C | T | 1 | a0032c0065t0041g0283 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5833+719C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160080994 | ||||||
| chr6:160080997
|
G | A | 56 | a0001c0024t0024g0201a0002c0003t0001g0001a0002c0003t0001g0002others(53): Show | 57 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.5833+722G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160080997 | ||||||
| chr6:160081009
|
C | T | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5833+734C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160081009 | ||||||
| chr6:160081041
|
G | T | 1 | a0005c0008t0083g0039 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5833+766G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160081041 | ||||||
| chr6:160081077
|
G | A | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5833+802G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160081077 | ||||||
| chr6:160081120
|
G | A | 1 | a0001c0001t0006g0274 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5833+845G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160081120 | ||||||
| chr6:160081125
|
CA | C | 180 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(177): Show | 181 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.5833+864delA | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | INFO_REALIGN_3_PRIME | chr6 | 160081125 | |||||
| chr6:160081152
|
A | G | 4 | a0013c0026t0029g0149a0013c0026t0029g0297a0015c0023t0037g0309others(1): Show | 4 | HG02055.hp1 HG02486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.5833+877A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160081152 | ||||||
| chr6:160081199
|
A | G | 1 | a0003c0030t0004g0049 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5833+924A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160081199 | ||||||
| chr6:160081233
|
C | T | 2 | a0002c0028t0001g0262a0002c0028t0001g0263 | 2 | HG00438.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.5833+958C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160081233 | ||||||
| chr6:160081234
|
G | A | 1 | a0027c0055t0020g0183 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.5833+959G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160081234 | ||||||
| chr6:160081258
|
T | C | 1 | a0001c0004t0003g0223 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.5833+983T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160081258 | ||||||
| chr6:160081428
|
A | T | 61 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(58): Show | 61 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.5833+1153A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160081428 | ||||||
| chr6:160081695
|
T | C | 182 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(179): Show | 183 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.5833+1420T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160081695 | ||||||
| chr6:160081697
|
C | T | 1 | a0001c0001t0043g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5833+1422C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160081697 | ||||||
| chr6:160081731
|
A | C | 48 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(45): Show | 48 | HG00140.hp2 HG00423.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.5833+1456A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160081731 | ||||||
| chr6:160081752
|
A | G | 2 | a0006c0010t0011g0122a0006c0010t0072g0196 | 2 | HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.5833+1477A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160081752 | ||||||
| chr6:160081778
|
C | T | 5 | a0008c0011t0017g0152a0008c0011t0017g0195a0008c0011t0030g0124others(2): Show | 5 | HG02723.hp2 HG02895.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.5833+1503C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160081778 | ||||||
| chr6:160081806
|
C | T | 1 | a0002c0003t0001g0276 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.5833+1531C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160081806 | ||||||
| chr6:160081816
|
C | T | 1 | a0001c0001t0085g0294 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5833+1541C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160081816 | ||||||
| chr6:160081884
|
T | G | 4 | a0013c0026t0029g0149a0013c0026t0029g0297a0015c0023t0037g0309others(1): Show | 4 | HG02055.hp1 HG02486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.5833+1609T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160081884 | ||||||
| chr6:160081903
|
A | C | 1 | a0003c0007t0001g0205 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.5833+1628A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160081903 | ||||||
| chr6:160081970
|
C | G | 13 | a0001c0002t0023g0101a0001c0002t0028g0034a0001c0002t0067g0247others(10): Show | 13 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.5833+1695C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160081970 | ||||||
| chr6:160082039
|
A | G | 2 | a0001c0046t0054g0281a0001c0069t0052g0164 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5833+1764A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160082039 | ||||||
| chr6:160082168
|
A | T | 1 | a0001c0036t0047g0248 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.5834-1782A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160082168 | ||||||
| chr6:160082278
|
T | A | 2 | a0001c0046t0054g0281a0001c0069t0052g0164 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5834-1672T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160082278 | ||||||
| chr6:160082312
|
A | AT | 28 | a0001c0005t0004g0012a0001c0005t0004g0014a0001c0005t0004g0018others(25): Show | 28 | HG00423.hp1 HG01109.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.5834-1624dupT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | INFO_REALIGN_3_PRIME | chr6 | 160082312 | |||||
| chr6:160082356
|
C | T | 2 | a0001c0046t0054g0281a0001c0069t0052g0164 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5834-1594C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160082356 | ||||||
| chr6:160082431
|
T | G | 1 | a0027c0055t0020g0183 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.5834-1519T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160082431 | ||||||
| chr6:160082574
|
T | G | 1 | a0002c0003t0001g0206 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.5834-1376T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160082574 | ||||||
| chr6:160082587
|
G | A | 3 | a0001c0002t0071g0194a0001c0004t0034g0126a0001c0004t0044g0153 | 3 | HG02055.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.5834-1363G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160082587 | ||||||
| chr6:160082590
|
G | A | 182 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(179): Show | 183 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.5834-1360G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160082590 | ||||||
| chr6:160082591
|
T | A | 182 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(179): Show | 183 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.5834-1359T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160082591 | ||||||
| chr6:160082615
|
A | AT | 68 | a0001c0024t0024g0201a0002c0003t0001g0001a0002c0003t0001g0002others(65): Show | 69 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.5834-1327dupT | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | INFO_REALIGN_3_PRIME | chr6 | 160082615 | |||||
| chr6:160082624
|
C | T | 97 | a0001c0005t0004g0012a0001c0005t0004g0014a0001c0005t0004g0018others(94): Show | 98 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.5834-1326C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160082624 | ||||||
| chr6:160082625
|
G | A | 1 | a0003c0012t0009g0095 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5834-1325G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160082625 | ||||||
| chr6:160082703
|
G | A | 19 | a0002c0003t0001g0001a0002c0003t0001g0186a0002c0003t0001g0199others(16): Show | 20 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(17): Show |
intron_variant | MODIFIER | c.5834-1247G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160082703 | ||||||
| chr6:160082813
|
A | T | 20 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(17): Show | 20 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.5834-1137A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160082813 | ||||||
| chr6:160082814
|
T | C | 1 | a0036c0067t0034g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5834-1136T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160082814 | ||||||
| chr6:160082862
|
C | T | 61 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(58): Show | 61 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.5834-1088C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160082862 | ||||||
| chr6:160082863
|
G | A | 1 | a0036c0067t0034g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5834-1087G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160082863 | ||||||
| chr6:160082871
|
G | C | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5834-1079G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160082871 | ||||||
| chr6:160082879
|
C | T | 9 | a0006c0010t0002g0010a0006c0010t0011g0122a0006c0010t0011g0123others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.5834-1071C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160082879 | ||||||
| chr6:160082997
|
A | C | 5 | a0008c0011t0017g0152a0008c0011t0017g0195a0008c0011t0030g0124others(2): Show | 5 | HG02723.hp2 HG02895.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.5834-953A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160082997 | ||||||
| chr6:160083377
|
G | A | 3 | a0001c0005t0004g0012a0001c0005t0004g0018a0001c0005t0004g0019 | 3 | NA18950.hp2 NA18998.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.5834-573G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160083377 | ||||||
| chr6:160083583
|
G | C | 182 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(179): Show | 183 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.5834-367G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160083583 | ||||||
| chr6:160083612
|
C | T | 4 | a0001c0005t0012g0167a0012c0031t0019g0165a0012c0031t0089g0067others(1): Show | 4 | HG01109.hp1 HG02257.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.5834-338C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160083612 | ||||||
| chr6:160083752
|
C | T | 22 | a0001c0005t0004g0012a0001c0005t0004g0014a0001c0005t0004g0018others(19): Show | 22 | HG00423.hp1 HG01109.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.5834-198C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160083752 | ||||||
| chr6:160083853
|
G | A | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5834-97G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 39/47 | chr6 | 160083853 | ||||||
| chr6:160084220
|
C | T | 3 | a0001c0004t0084g0098a0015c0023t0037g0309a0015c0023t0094g0096 | 3 | HG06807.hp2 NA18906.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.6068+36C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 40/47 | chr6 | 160084220 | ||||||
| chr6:160084280
|
G | C | 17 | a0001c0005t0004g0012a0001c0005t0004g0014a0001c0005t0004g0018others(14): Show | 17 | HG00423.hp1 HG03942.hp1 HG04204.hp1 others(14): Show |
intron_variant | MODIFIER | c.6068+96G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 40/47 | chr6 | 160084280 | ||||||
| chr6:160084330
|
T | C | 1 | a0036c0067t0034g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.6068+146T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 40/47 | chr6 | 160084330 | ||||||
| chr6:160084469
|
C | T | 1 | a0001c0002t0002g0030 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.6068+285C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 40/47 | chr6 | 160084469 | ||||||
| chr6:160084499
|
G | A | 21 | a0001c0005t0004g0012a0001c0005t0004g0014a0001c0005t0004g0018others(18): Show | 21 | HG00423.hp1 HG01109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.6068+315G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 40/47 | chr6 | 160084499 | ||||||
| chr6:160084512
|
C | T | 1 | a0001c0001t0005g0028 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.6068+328C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 40/47 | chr6 | 160084512 | ||||||
| chr6:160084739
|
G | A | 2 | a0001c0046t0054g0281a0001c0069t0052g0164 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6069-256G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 40/47 | chr6 | 160084739 | ||||||
| chr6:160084779
|
G | A | 1 | a0036c0067t0034g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.6069-216G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 40/47 | chr6 | 160084779 | ||||||
| chr6:160084847
|
A | G | 1 | a0004c0061t0003g0266 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.6069-148A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 40/47 | chr6 | 160084847 | ||||||
| chr6:160084890
|
T | C | 2 | a0001c0046t0054g0281a0001c0069t0052g0164 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6069-105T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 40/47 | chr6 | 160084890 | ||||||
| chr6:160085218
|
G | T | 1 | a0005c0008t0083g0039 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6205+87G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160085218 | ||||||
| chr6:160085244
|
A | AGATATGA others(6): Show |
1 | a0001c0024t0024g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.6205+115_6205+127d others(15): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | INFO_REALIGN_3_PRIME | chr6 | 160085244 | |||||
| chr6:160085380
|
G | A | 2 | a0018c0032t0033g0086a0018c0032t0033g0087 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.6205+249G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160085380 | ||||||
| chr6:160085430
|
G | A | 60 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(57): Show | 60 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.6205+299G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160085430 | ||||||
| chr6:160085479
|
T | C | 13 | a0001c0002t0023g0101a0001c0002t0028g0034a0001c0002t0067g0247others(10): Show | 13 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.6205+348T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160085479 | ||||||
| chr6:160085496
|
G | A | 12 | a0006c0010t0002g0010a0006c0010t0011g0122a0006c0010t0011g0123others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.6205+365G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160085496 | ||||||
| chr6:160085555
|
A | G | 2 | a0018c0032t0033g0086a0018c0032t0033g0087 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.6205+424A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160085555 | ||||||
| chr6:160085612
|
A | G | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6205+481A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160085612 | ||||||
| chr6:160085708
|
CTGGAGTG others(3): Show |
C | 2 | a0001c0001t0021g0045a0001c0001t0021g0046 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.6205+579_6205+588d others(12): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | INFO_REALIGN_3_PRIME | chr6 | 160085708 | |||||
| chr6:160085719
|
T | A | 2 | a0001c0001t0021g0045a0001c0001t0021g0046 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.6205+588T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160085719 | ||||||
| chr6:160085720
|
T | A | 2 | a0001c0001t0021g0045a0001c0001t0021g0046 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.6205+589T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160085720 | ||||||
| chr6:160085723
|
C | T | 56 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(53): Show | 56 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.6205+592C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160085723 | ||||||
| chr6:160085850
|
A | T | 1 | a0005c0008t0083g0039 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6205+719A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160085850 | ||||||
| chr6:160085871
|
A | T | 2 | a0014c0022t0038g0275a0014c0022t0040g0270 | 2 | HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6205+740A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160085871 | ||||||
| chr6:160085891
|
C | T | 2 | a0003c0012t0006g0284a0003c0012t0006g0285 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.6205+760C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160085891 | ||||||
| chr6:160085892
|
G | T | 1 | a0036c0067t0034g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.6205+761G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160085892 | ||||||
| chr6:160085906
|
C | T | 1 | a0001c0001t0002g0293 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.6205+775C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160085906 | ||||||
| chr6:160085975
|
G | T | 1 | a0001c0004t0051g0178 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.6205+844G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160085975 | ||||||
| chr6:160086070
|
C | T | 3 | a0001c0002t0071g0194a0001c0004t0034g0126a0001c0004t0044g0153 | 3 | HG02055.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.6205+939C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160086070 | ||||||
| chr6:160086093
|
G | C | 1 | a0001c0002t0007g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.6205+962G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160086093 | ||||||
| chr6:160086266
|
A | G | 182 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(179): Show | 183 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.6205+1135A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160086266 | ||||||
| chr6:160086402
|
G | A | 2 | a0017c0021t0031g0004a0017c0021t0031g0005 | 2 | HG03688.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.6205+1271G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160086402 | ||||||
| chr6:160086405
|
A | G | 4 | a0001c0002t0036g0289a0001c0002t0036g0290a0001c0002t0056g0156others(1): Show | 4 | HG00642.hp1 HG01433.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.6205+1274A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160086405 | ||||||
| chr6:160086446
|
A | G | 170 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(167): Show | 171 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.6205+1315A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160086446 | ||||||
| chr6:160086464
|
G | T | 1 | a0001c0001t0043g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.6205+1333G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160086464 | ||||||
| chr6:160086832
|
T | G | 1 | a0002c0003t0061g0182 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6206-1201T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160086832 | ||||||
| chr6:160086840
|
T | C | 1 | a0001c0002t0007g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.6206-1193T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160086840 | ||||||
| chr6:160086855
|
A | G | 56 | a0001c0024t0024g0201a0002c0003t0001g0001a0002c0003t0001g0002others(53): Show | 57 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.6206-1178A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160086855 | ||||||
| chr6:160086927
|
G | A | 3 | a0010c0016t0016g0150a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.6206-1106G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160086927 | ||||||
| chr6:160086971
|
C | T | 2 | a0015c0023t0037g0309a0015c0023t0094g0096 | 2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.6206-1062C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160086971 | ||||||
| chr6:160087025
|
G | A | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6206-1008G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160087025 | ||||||
| chr6:160087081
|
G | A | 23 | a0001c0005t0004g0012a0001c0005t0004g0014a0001c0005t0004g0018others(20): Show | 23 | HG00423.hp1 HG01109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.6206-952G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160087081 | ||||||
| chr6:160087089
|
T | C | 3 | a0010c0016t0016g0150a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.6206-944T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160087089 | ||||||
| chr6:160087117
|
G | A | 1 | a0001c0046t0054g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.6206-916G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160087117 | ||||||
| chr6:160087140
|
T | C | 180 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(177): Show | 181 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.6206-893T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160087140 | ||||||
| chr6:160087312
|
A | G | 3 | a0006c0025t0059g0288a0007c0018t0019g0238a0007c0018t0019g0239 | 3 | HG02280.hp2 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.6206-721A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160087312 | ||||||
| chr6:160087589
|
C | T | 21 | a0001c0005t0004g0012a0001c0005t0004g0014a0001c0005t0004g0018others(18): Show | 21 | HG00423.hp1 HG01109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.6206-444C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160087589 | ||||||
| chr6:160087696
|
T | G | 3 | a0010c0016t0016g0150a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.6206-337T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160087696 | ||||||
| chr6:160087767
|
C | T | 3 | a0014c0022t0038g0275a0014c0022t0040g0270a0037c0033t0073g0140 | 3 | HG02109.hp2 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6206-266C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 41/47 | chr6 | 160087767 | ||||||
| chr6:160088761
|
T | C | 1 | a0021c0044t0074g0111 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6321-346T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 42/47 | chr6 | 160088761 | ||||||
| chr6:160088876
|
T | C | 3 | a0001c0046t0054g0281a0001c0069t0052g0164a0021c0044t0074g0111 | 3 | HG02965.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.6321-231T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 42/47 | chr6 | 160088876 | ||||||
| chr6:160088965
|
C | A | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6321-142C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 42/47 | chr6 | 160088965 | ||||||
| chr6:160089029
|
C | T | 3 | a0010c0016t0016g0150a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.6321-78C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 42/47 | chr6 | 160089029 | ||||||
| chr6:160089070
|
G | A | 4 | a0001c0005t0012g0167a0012c0031t0019g0165a0012c0031t0089g0067others(1): Show | 4 | HG01109.hp1 HG02257.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.6321-37G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 42/47 | chr6 | 160089070 | ||||||
| chr6:160089264
|
C | T | 1 | a0021c0044t0074g0111 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6467+11C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 43/47 | chr6 | 160089264 | ||||||
| chr6:160089327
|
C | T | 3 | a0002c0003t0001g0224a0002c0003t0001g0225a0002c0015t0001g0280 | 3 | NA18999.hp1 NA19062.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.6467+74C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 43/47 | chr6 | 160089327 | ||||||
| chr6:160089476
|
C | T | 1 | a0004c0006t0003g0217 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.6467+223C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 43/47 | chr6 | 160089476 | ||||||
| chr6:160089741
|
T | C | 2 | a0001c0046t0054g0281a0001c0069t0052g0164 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6468-175T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 43/47 | chr6 | 160089741 | ||||||
| chr6:160089789
|
C | T | 1 | a0003c0007t0003g0172 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.6468-127C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 43/47 | chr6 | 160089789 | ||||||
| chr6:160089792
|
G | C | 9 | a0006c0010t0002g0010a0006c0010t0011g0122a0006c0010t0011g0123others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.6468-124G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 43/47 | chr6 | 160089792 | ||||||
| chr6:160089824
|
G | T | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6468-92G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 43/47 | chr6 | 160089824 | ||||||
| chr6:160090217
|
C | T | 12 | a0006c0010t0002g0010a0006c0010t0011g0122a0006c0010t0011g0123others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.6655+114C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160090217 | ||||||
| chr6:160090218
|
T | A | 182 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(179): Show | 183 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.6655+115T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160090218 | ||||||
| chr6:160090232
|
T | G | 9 | a0006c0010t0002g0010a0006c0010t0011g0122a0006c0010t0011g0123others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.6655+129T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160090232 | ||||||
| chr6:160090322
|
G | A | 60 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(57): Show | 60 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.6655+219G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160090322 | ||||||
| chr6:160090365
|
C | G | 1 | a0003c0012t0009g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.6655+262C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160090365 | ||||||
| chr6:160090387
|
C | T | 1 | a0021c0044t0074g0111 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6655+284C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160090387 | ||||||
| chr6:160090523
|
G | A | 4 | a0013c0026t0029g0149a0013c0026t0029g0297a0015c0023t0037g0309others(1): Show | 4 | HG02055.hp1 HG02486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.6655+420G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160090523 | ||||||
| chr6:160090578
|
G | A | 2 | a0001c0002t0090g0133a0033c0064t0068g0221 | 2 | HG00408.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.6655+475G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160090578 | ||||||
| chr6:160090595
|
A | G | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6655+492A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160090595 | ||||||
| chr6:160090620
|
C | T | 1 | a0003c0012t0009g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.6655+517C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160090620 | ||||||
| chr6:160090839
|
T | C | 1 | a0001c0001t0006g0274 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.6655+736T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160090839 | ||||||
| chr6:160090848
|
G | T | 3 | a0001c0002t0007g0060a0001c0002t0007g0061a0001c0002t0007g0091 | 3 | HG00140.hp2 HG00733.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.6655+745G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160090848 | ||||||
| chr6:160090901
|
TCATCGCC others(336): Show |
T | 3 | a0001c0002t0071g0194a0001c0004t0034g0126a0001c0004t0044g0153 | 3 | HG02055.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.6655+860_6655+1202 others(3): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | INFO_REALIGN_3_PRIME | chr6 | 160090901 | |||||
| chr6:160090918
|
C | G | 1 | a0004c0006t0049g0226 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.6655+815C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160090918 | ||||||
| chr6:160090919
|
A | AGGTGCTC others(37): Show |
1 | a0001c0004t0081g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.6655+823_6655+824i others(46): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | INFO_REALIGN_3_PRIME | chr6 | 160090919 | |||||
| chr6:160090927
|
C | T | 1 | a0001c0004t0081g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.6655+824C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160090927 | ||||||
| chr6:160090952
|
C | T | 1 | a0001c0004t0081g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.6655+849C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160090952 | ||||||
| chr6:160090952
|
CGAGAAGG others(37): Show |
C | 1 | a0005c0008t0002g0029 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.6655+925_6655+968d others(46): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | INFO_REALIGN_3_PRIME | chr6 | 160090952 | |||||
| chr6:160091037
|
C | T | 2 | a0001c0002t0002g0020a0001c0004t0001g0222 | 2 | HG00544.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.6655+934C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160091037 | ||||||
| chr6:160091049
|
G | A | 1 | a0037c0033t0073g0140 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.6655+946G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160091049 | ||||||
| chr6:160091050
|
C | T | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6655+947C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160091050 | ||||||
| chr6:160091079
|
A | G | 1 | a0037c0033t0073g0140 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.6655+976A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160091079 | ||||||
| chr6:160091119
|
C | T | 1 | a0003c0030t0004g0049 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.6655+1016C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160091119 | ||||||
| chr6:160091156
|
A | ACATCGCC others(37): Show |
2 | a0001c0046t0054g0281a0001c0069t0052g0164 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6655+1211_6655+125 others(48): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | INFO_REALIGN_3_PRIME | chr6 | 160091156 | |||||
| chr6:160091156
|
A | G | 1 | a0001c0009t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.6655+1053A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160091156 | ||||||
| chr6:160091164
|
G | A | 1 | a0001c0002t0015g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.6655+1061G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160091164 | ||||||
| chr6:160091199
|
C | T | 1 | a0012c0031t0019g0165 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.6655+1096C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160091199 | ||||||
| chr6:160091288
|
G | T | 3 | a0001c0002t0071g0194a0001c0004t0034g0126a0001c0004t0044g0153 | 3 | HG02055.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.6655+1185G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160091288 | ||||||
| chr6:160091332
|
G | A | 56 | a0001c0024t0024g0201a0002c0003t0001g0001a0002c0003t0001g0002others(53): Show | 57 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.6655+1229G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160091332 | ||||||
| chr6:160091358
|
T | C | 19 | a0001c0001t0005g0028a0001c0001t0005g0100a0001c0001t0005g0114others(16): Show | 19 | HG00323.hp1 HG00735.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.6655+1255T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160091358 | ||||||
| chr6:160091383
|
C | T | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6655+1280C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160091383 | ||||||
| chr6:160091463
|
G | T | 1 | a0001c0001t0069g0232 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.6655+1360G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160091463 | ||||||
| chr6:160091496
|
C | T | 2 | a0002c0028t0001g0262a0002c0028t0001g0263 | 2 | HG00438.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.6655+1393C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160091496 | ||||||
| chr6:160091640
|
G | C | 1 | a0002c0015t0001g0280 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.6655+1537G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160091640 | ||||||
| chr6:160091716
|
G | A | 22 | a0001c0005t0004g0012a0001c0005t0004g0014a0001c0005t0004g0018others(19): Show | 22 | HG00423.hp1 HG01109.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.6655+1613G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160091716 | ||||||
| chr6:160091738
|
C | G | 2 | a0004c0006t0003g0216a0004c0006t0003g0217 | 2 | HG02040.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.6655+1635C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160091738 | ||||||
| chr6:160091754
|
G | T | 1 | a0001c0005t0004g0022 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.6655+1651G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160091754 | ||||||
| chr6:160091792
|
C | G | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6655+1689C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160091792 | ||||||
| chr6:160091815
|
A | T | 8 | a0002c0003t0001g0175a0002c0003t0001g0188a0002c0003t0001g0189others(5): Show | 8 | HG01168.hp1 HG01192.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.6655+1712A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160091815 | ||||||
| chr6:160091846
|
A | G | 1 | a0011c0017t0086g0016 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.6655+1743A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160091846 | ||||||
| chr6:160092038
|
TAGTGCCC others(73): Show |
T | 56 | a0001c0024t0024g0201a0002c0003t0001g0001a0002c0003t0001g0002others(53): Show | 57 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.6655+2134_6655+221 others(84): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | INFO_REALIGN_3_PRIME | chr6 | 160092038 | |||||
| chr6:160092245
|
G | T | 1 | a0036c0067t0034g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.6655+2142G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160092245 | ||||||
| chr6:160092251
|
G | C | 85 | a0001c0005t0004g0012a0001c0005t0004g0014a0001c0005t0004g0018others(82): Show | 86 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.6655+2148G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160092251 | ||||||
| chr6:160092380
|
G | C | 22 | a0001c0005t0004g0012a0001c0005t0004g0014a0001c0005t0004g0018others(19): Show | 22 | HG00423.hp1 HG01109.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.6655+2277G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160092380 | ||||||
| chr6:160092410
|
T | G | 1 | a0003c0007t0003g0254 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.6655+2307T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160092410 | ||||||
| chr6:160092611
|
T | A | 24 | a0001c0005t0004g0012a0001c0005t0004g0014a0001c0005t0004g0018others(21): Show | 24 | HG00423.hp1 HG01109.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.6655+2508T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160092611 | ||||||
| chr6:160092761
|
G | A | 61 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(58): Show | 61 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.6655+2658G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160092761 | ||||||
| chr6:160092867
|
T | C | 2 | a0001c0046t0054g0281a0001c0069t0052g0164 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6655+2764T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160092867 | ||||||
| chr6:160093214
|
A | G | 182 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(179): Show | 183 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.6655+3111A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160093214 | ||||||
| chr6:160093240
|
G | A | 1 | a0001c0005t0092g0025 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.6655+3137G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160093240 | ||||||
| chr6:160093251
|
A | G | 6 | a0001c0001t0013g0006a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG00280.hp1 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.6655+3148A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160093251 | ||||||
| chr6:160093450
|
G | A | 5 | a0001c0001t0002g0062a0001c0001t0003g0230a0001c0001t0003g0231others(2): Show | 5 | HG02698.hp2 HG02735.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.6656-2989G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160093450 | ||||||
| chr6:160093509
|
T | C | 184 | a0001c0001t0003g0249a0001c0001t0003g0307a0001c0002t0002g0020others(181): Show | 185 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.6656-2930T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160093509 | ||||||
| chr6:160093529
|
A | G | 2 | a0003c0012t0006g0284a0003c0012t0006g0285 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.6656-2910A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160093529 | ||||||
| chr6:160093613
|
C | T | 1 | a0003c0007t0006g0272 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.6656-2826C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160093613 | ||||||
| chr6:160093809
|
C | G | 1 | a0004c0006t0002g0073 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.6656-2630C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160093809 | ||||||
| chr6:160093871
|
C | T | 2 | a0001c0002t0002g0020a0001c0004t0001g0222 | 2 | HG00544.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.6656-2568C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160093871 | ||||||
| chr6:160093909
|
A | G | 1 | a0001c0004t0046g0273 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.6656-2530A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160093909 | ||||||
| chr6:160094113
|
G | A | 16 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(13): Show | 16 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.6656-2326G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160094113 | ||||||
| chr6:160094220
|
A | G | 1 | a0032c0065t0041g0283 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6656-2219A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160094220 | ||||||
| chr6:160094360
|
C | T | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6656-2079C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160094360 | ||||||
| chr6:160094512
|
C | G | 3 | a0010c0016t0016g0150a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.6656-1927C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160094512 | ||||||
| chr6:160094568
|
C | T | 15 | a0006c0010t0002g0010a0006c0010t0011g0122a0006c0010t0011g0123others(12): Show | 15 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.6656-1871C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160094568 | ||||||
| chr6:160094767
|
G | A | 1 | a0032c0065t0041g0283 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6656-1672G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160094767 | ||||||
| chr6:160094862
|
C | T | 51 | a0002c0003t0001g0001a0002c0003t0001g0002a0002c0003t0001g0175others(48): Show | 52 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.6656-1577C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160094862 | ||||||
| chr6:160094884
|
C | T | 2 | a0013c0026t0029g0149a0013c0026t0029g0297 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.6656-1555C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160094884 | ||||||
| chr6:160094897
|
C | CA | 68 | a0001c0001t0003g0249a0001c0001t0003g0307a0001c0001t0032g0041others(65): Show | 68 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.6656-1523dupA | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | INFO_REALIGN_3_PRIME | chr6 | 160094897 | |||||
| chr6:160094897
|
C | CAA | 50 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(47): Show | 50 | HG00140.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.6656-1524_6656-152 others(6): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | INFO_REALIGN_3_PRIME | chr6 | 160094897 | |||||
| chr6:160094897
|
C | CAAA | 65 | a0001c0002t0007g0061a0001c0002t0071g0194a0001c0004t0034g0126others(62): Show | 66 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.6656-1525_6656-152 others(7): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | INFO_REALIGN_3_PRIME | chr6 | 160094897 | |||||
| chr6:160094897
|
C | CAAAA | 6 | a0002c0003t0001g0175a0002c0003t0001g0224a0002c0003t0001g0255others(3): Show | 6 | HG00438.hp2 HG01981.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.6656-1526_6656-152 others(8): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | INFO_REALIGN_3_PRIME | chr6 | 160094897 | |||||
| chr6:160094953
|
G | A | 1 | a0012c0031t0089g0067 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6656-1486G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160094953 | ||||||
| chr6:160095111
|
C | A | 2 | a0001c0046t0054g0281a0001c0069t0052g0164 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6656-1328C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160095111 | ||||||
| chr6:160095119
|
C | T | 1 | a0001c0004t0001g0222 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.6656-1320C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160095119 | ||||||
| chr6:160095176
|
G | A | 3 | a0010c0016t0016g0150a0010c0016t0016g0169a0010c0016t0016g0170 | 3 | HG01884.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.6656-1263G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160095176 | ||||||
| chr6:160095358
|
C | T | 1 | a0018c0032t0033g0086 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.6656-1081C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160095358 | ||||||
| chr6:160095416
|
C | G | 1 | a0032c0065t0041g0283 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6656-1023C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160095416 | ||||||
| chr6:160095521
|
G | A | 1 | a0032c0065t0041g0283 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6656-918G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160095521 | ||||||
| chr6:160095543
|
G | A | 2 | a0001c0001t0002g0141a0001c0001t0003g0256 | 2 | HG01243.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.6656-896G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160095543 | ||||||
| chr6:160095590
|
C | T | 1 | a0001c0004t0002g0129 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.6656-849C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160095590 | ||||||
| chr6:160095659
|
A | G | 1 | a0001c0002t0002g0030 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.6656-780A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160095659 | ||||||
| chr6:160096062
|
C | T | 56 | a0001c0024t0024g0201a0002c0003t0001g0001a0002c0003t0001g0002others(53): Show | 57 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.6656-377C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160096062 | ||||||
| chr6:160096097
|
C | T | 1 | a0005c0020t0002g0031 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6656-342C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160096097 | ||||||
| chr6:160096133
|
G | T | 1 | a0001c0001t0005g0028 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.6656-306G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160096133 | ||||||
| chr6:160096207
|
G | A | 1 | a0003c0058t0076g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6656-232G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 44/47 | chr6 | 160096207 | ||||||
| chr6:160096812
|
A | G | 3 | a0006c0025t0059g0288a0007c0018t0019g0238a0007c0018t0019g0239 | 3 | HG02280.hp2 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.6842+187A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160096812 | ||||||
| chr6:160096856
|
C | T | 178 | a0001c0001t0003g0249a0001c0002t0002g0020a0001c0002t0002g0030others(175): Show | 179 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.6842+231C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160096856 | ||||||
| chr6:160096925
|
G | C | 2 | a0001c0001t0001g0304a0001c0009t0001g0211 | 2 | NA18987.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.6842+300G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160096925 | ||||||
| chr6:160096937
|
T | C | 3 | a0001c0002t0036g0289a0001c0002t0036g0290a0001c0002t0056g0156 | 3 | HG00642.hp1 HG01433.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.6842+312T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160096937 | ||||||
| chr6:160097263
|
A | C | 2 | a0013c0026t0029g0149a0013c0026t0029g0297 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.6842+638A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160097263 | ||||||
| chr6:160097296
|
T | C | 2 | a0001c0001t0010g0157a0001c0002t0010g0168 | 2 | HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.6842+671T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160097296 | ||||||
| chr6:160097335
|
T | C | 62 | a0001c0001t0001g0301a0001c0002t0007g0055a0001c0002t0007g0056others(59): Show | 62 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.6842+710T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160097335 | ||||||
| chr6:160097336
|
T | G | 9 | a0006c0010t0002g0010a0006c0010t0011g0122a0006c0010t0011g0123others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.6842+711T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160097336 | ||||||
| chr6:160097393
|
C | T | 3 | a0001c0001t0026g0268a0001c0001t0026g0269a0001c0001t0030g0105 | 3 | HG02630.hp1 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.6842+768C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160097393 | ||||||
| chr6:160097494
|
T | C | 39 | a0001c0001t0003g0249a0001c0001t0003g0307a0001c0002t0002g0020others(36): Show | 39 | HG00544.hp2 HG00738.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.6842+869T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160097494 | ||||||
| chr6:160097541
|
G | A | 1 | a0001c0004t0020g0253 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.6842+916G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160097541 | ||||||
| chr6:160097561
|
C | T | 1 | a0022c0042t0024g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6842+936C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160097561 | ||||||
| chr6:160097817
|
C | G | 8 | a0001c0001t0010g0157a0001c0002t0015g0009a0001c0002t0018g0237others(5): Show | 8 | HG02258.hp2 HG02559.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.6842+1192C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160097817 | ||||||
| chr6:160098110
|
A | G | 3 | a0006c0025t0059g0288a0007c0018t0019g0238a0007c0018t0019g0239 | 3 | HG02280.hp2 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.6842+1485A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160098110 | ||||||
| chr6:160098196
|
G | A | 7 | a0001c0002t0007g0055a0001c0002t0007g0056a0001c0002t0007g0057others(4): Show | 7 | HG00140.hp2 HG00733.hp2 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.6842+1571G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160098196 | ||||||
| chr6:160098244
|
T | C | 279 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(276): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.6842+1619T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160098244 | ||||||
| chr6:160098305
|
G | A | 2 | a0001c0046t0054g0281a0001c0069t0052g0164 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6842+1680G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160098305 | ||||||
| chr6:160098447
|
G | T | 1 | a0001c0002t0039g0233 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.6842+1822G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160098447 | ||||||
| chr6:160098491
|
T | G | 1 | a0001c0005t0012g0258 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.6842+1866T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160098491 | ||||||
| chr6:160098547
|
G | A | 1 | a0001c0001t0002g0293 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.6842+1922G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160098547 | ||||||
| chr6:160098553
|
T | G | 4 | a0002c0003t0008g0085a0002c0003t0020g0278a0002c0003t0063g0207others(1): Show | 4 | HG00621.hp2 HG02040.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.6842+1928T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160098553 | ||||||
| chr6:160098703
|
C | T | 1 | a0001c0005t0004g0083 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.6842+2078C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160098703 | ||||||
| chr6:160098768
|
G | A | 2 | a0001c0009t0028g0229a0030c0040t0002g0291 | 2 | HG00544.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.6842+2143G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160098768 | ||||||
| chr6:160098843
|
A | T | 1 | a0002c0015t0001g0280 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.6842+2218A>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160098843 | ||||||
| chr6:160099331
|
T | TTTATG | 54 | a0001c0001t0001g0301a0001c0001t0002g0062a0001c0001t0003g0231others(51): Show | 54 | HG00597.hp2 HG00621.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.6842+2751_6842+275 others(9): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | INFO_REALIGN_3_PRIME | chr6 | 160099331 | |||||
| chr6:160099331
|
T | TTTATGTT others(3): Show |
15 | a0001c0001t0002g0293a0001c0001t0003g0256a0001c0001t0003g0307others(12): Show | 15 | HG00408.hp1 HG01934.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.6842+2746_6842+275 others(14): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | INFO_REALIGN_3_PRIME | chr6 | 160099331 | |||||
| chr6:160099331
|
T | TTTATGTT others(8): Show |
5 | a0001c0001t0002g0141a0001c0002t0003g0302a0001c0002t0003g0303others(2): Show | 5 | HG01243.hp2 NA18982.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.6842+2741_6842+275 others(19): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | INFO_REALIGN_3_PRIME | chr6 | 160099331 | |||||
| chr6:160099331
|
TTTATG | T | 41 | a0001c0001t0005g0028a0001c0001t0013g0006a0001c0002t0007g0055others(38): Show | 42 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.6842+2751_6842+275 others(9): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | INFO_REALIGN_3_PRIME | chr6 | 160099331 | |||||
| chr6:160099331
|
TTTATGTT others(3): Show |
T | 13 | a0001c0034t0006g0035a0003c0012t0006g0284a0003c0012t0006g0285others(10): Show | 13 | HG01109.hp1 HG02145.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.6842+2746_6842+275 others(14): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | INFO_REALIGN_3_PRIME | chr6 | 160099331 | |||||
| chr6:160099435
|
C | T | 2 | a0022c0042t0024g0151a0037c0033t0073g0140 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.6842+2810C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160099435 | ||||||
| chr6:160099606
|
A | G | 1 | a0001c0034t0006g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6843-2913A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160099606 | ||||||
| chr6:160099620
|
G | A | 1 | a0001c0001t0003g0246 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.6843-2899G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160099620 | ||||||
| chr6:160099713
|
G | A | 7 | a0001c0002t0039g0233a0001c0024t0024g0201a0014c0022t0038g0275others(4): Show | 7 | HG02109.hp2 HG02647.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.6843-2806G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160099713 | ||||||
| chr6:160099736
|
C | T | 34 | a0001c0002t0039g0233a0001c0002t0071g0194a0001c0004t0034g0126others(31): Show | 34 | HG00408.hp1 HG00423.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.6843-2783C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160099736 | ||||||
| chr6:160099774
|
A | G | 20 | a0001c0002t0015g0009a0001c0002t0015g0127a0001c0002t0015g0163others(17): Show | 20 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.6843-2745A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160099774 | ||||||
| chr6:160099813
|
T | A | 1 | a0001c0001t0013g0006 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.6843-2706T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160099813 | ||||||
| chr6:160099855
|
G | A | 2 | a0006c0010t0002g0010a0006c0025t0009g0139 | 2 | HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.6843-2664G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160099855 | ||||||
| chr6:160099977
|
G | A | 1 | a0001c0024t0024g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.6843-2542G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160099977 | ||||||
| chr6:160100010
|
T | G | 1 | a0001c0001t0006g0244 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.6843-2509T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100010 | ||||||
| chr6:160100108
|
C | G | 1 | a0006c0010t0002g0010 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6843-2411C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100108 | ||||||
| chr6:160100306
|
A | G | 1 | a0001c0004t0044g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.6843-2213A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100306 | ||||||
| chr6:160100398
|
G | T | 5 | a0001c0004t0046g0273a0003c0007t0022g0107a0003c0007t0022g0108others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.6843-2121G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100398 | ||||||
| chr6:160100609
|
C | T | 1 | a0001c0004t0048g0259 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.6843-1910C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100609 | ||||||
| chr6:160100646
|
T | C | 4 | a0001c0002t0071g0194a0001c0004t0034g0126a0001c0004t0044g0153others(1): Show | 4 | HG02055.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.6843-1873T>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100646 | ||||||
| chr6:160100674
|
A | G | 1 | a0031c0048t0002g0069 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.6843-1845A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100674 | ||||||
| chr6:160100723
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0006g0244 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.6843-1796_6843-179 others(21): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(8): Show |
C | 1 | a0002c0003t0014g0173 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.6843-1795_6843-178 others(19): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(13): Show |
C | 2 | a0001c0002t0018g0236a0005c0020t0002g0031 | 2 | HG01175.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.6843-1795_6843-177 others(24): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(14): Show |
C | 1 | a0001c0004t0003g0190 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.6843-1795_6843-177 others(25): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(15): Show |
C | 2 | a0001c0001t0006g0264a0001c0002t0088g0063 | 2 | HG01258.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.6843-1795_6843-177 others(26): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(17): Show |
C | 2 | a0001c0004t0003g0223a0005c0008t0002g0033 | 2 | HG01261.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.6843-1795_6843-177 others(28): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(18): Show |
C | 3 | a0004c0029t0003g0185a0005c0008t0002g0029a0029c0038t0003g0286 | 3 | HG01361.hp1 HG06807.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.6843-1795_6843-177 others(29): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(19): Show |
C | 2 | a0001c0004t0001g0222a0004c0006t0003g0216 | 2 | HG02040.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.6843-1795_6843-177 others(30): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(21): Show |
C | 1 | a0001c0001t0002g0142 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.6843-1795_6843-176 others(32): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(23): Show |
C | 9 | a0001c0002t0007g0057a0001c0004t0003g0192a0001c0004t0003g0210others(6): Show | 9 | HG01255.hp1 HG02738.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.6843-1795_6843-176 others(34): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(24): Show |
C | 1 | a0002c0028t0001g0262 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.6843-1795_6843-176 others(35): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(25): Show |
C | 4 | a0001c0002t0002g0030a0001c0002t0007g0061a0002c0003t0008g0148others(1): Show | 4 | HG00735.hp1 HG00741.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.6843-1795_6843-176 others(36): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(26): Show |
C | 5 | a0001c0002t0006g0198a0001c0002t0007g0060a0003c0012t0006g0285others(2): Show | 5 | HG00733.hp2 HG01433.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.6843-1795_6843-176 others(37): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(27): Show |
C | 2 | a0002c0003t0001g0224a0003c0012t0006g0284 | 2 | HG02451.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.6843-1795_6843-176 others(38): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(28): Show |
C | 4 | a0001c0002t0002g0020a0001c0002t0018g0237a0001c0024t0024g0201others(1): Show | 4 | HG00544.hp2 HG02055.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.6843-1795_6843-176 others(39): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(29): Show |
C | 6 | a0001c0002t0009g0103a0001c0004t0002g0129a0002c0003t0001g0251others(3): Show | 6 | HG02683.hp2 HG03492.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.6843-1795_6843-176 others(40): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(30): Show |
C | 5 | a0001c0001t0026g0268a0001c0001t0026g0269a0001c0002t0009g0102others(2): Show | 5 | HG02486.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.6843-1795_6843-175 others(41): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(31): Show |
C | 1 | a0002c0003t0001g0225 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.6843-1795_6843-175 others(42): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(32): Show |
C | 1 | a0001c0056t0003g0154 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.6843-1795_6843-175 others(43): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(33): Show |
C | 4 | a0001c0002t0006g0197a0004c0061t0003g0266a0006c0025t0009g0139others(1): Show | 4 | HG00642.hp2 HG01517.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.6843-1795_6843-175 others(44): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(34): Show |
C | 8 | a0001c0002t0007g0091a0002c0003t0001g0241a0002c0003t0064g0213others(5): Show | 8 | HG00140.hp2 HG00438.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.6843-1795_6843-175 others(45): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(35): Show |
C | 12 | a0001c0001t0001g0304a0001c0002t0007g0055a0001c0002t0039g0233others(9): Show | 12 | HG01891.hp1 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.6843-1795_6843-175 others(46): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(36): Show |
C | 13 | a0001c0001t0001g0305a0001c0004t0001g0240a0001c0004t0051g0178others(10): Show | 13 | HG00423.hp2 HG01943.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.6843-1795_6843-175 others(47): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(37): Show |
C | 13 | a0001c0001t0001g0187a0001c0001t0003g0230a0001c0001t0003g0307others(10): Show | 13 | HG00597.hp1 HG01168.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.6843-1795_6843-175 others(48): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(38): Show |
C | 17 | a0001c0001t0001g0301a0001c0001t0008g0042a0001c0001t0014g0300others(14): Show | 17 | HG00408.hp1 HG00423.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.6843-1795_6843-175 others(49): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(39): Show |
C | 17 | a0001c0001t0013g0006a0001c0005t0004g0012a0001c0005t0004g0014others(14): Show | 17 | HG00280.hp1 HG00621.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.6843-1795_6843-175 others(50): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(40): Show |
C | 20 | a0001c0001t0006g0274a0001c0005t0004g0018a0001c0005t0004g0022others(17): Show | 20 | HG00741.hp1 HG02040.hp2 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.6843-1795_6843-174 others(51): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(41): Show |
C | 8 | a0001c0001t0002g0043a0001c0002t0007g0058a0001c0005t0012g0184others(5): Show | 8 | HG01081.hp2 HG02257.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.6843-1795_6843-174 others(52): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(42): Show |
C | 5 | a0001c0001t0013g0145a0001c0001t0013g0146a0001c0002t0018g0235others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.6843-1795_6843-174 others(53): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(43): Show |
C | 4 | a0001c0002t0091g0292a0001c0004t0066g0174a0004c0006t0002g0075others(1): Show | 4 | HG00639.hp2 HG02165.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.6843-1795_6843-174 others(54): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(45): Show |
C | 5 | a0001c0001t0005g0116a0001c0002t0023g0101a0001c0002t0090g0133others(2): Show | 5 | HG00408.hp2 HG00544.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.6843-1795_6843-174 others(56): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(46): Show |
C | 7 | a0001c0001t0006g0308a0001c0002t0015g0127a0001c0002t0015g0163others(4): Show | 7 | HG00597.hp2 HG00621.hp1 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.6843-1795_6843-174 others(57): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(47): Show |
C | 12 | a0001c0001t0005g0028a0001c0001t0005g0100a0001c0001t0005g0117others(9): Show | 12 | HG00323.hp1 HG00323.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.6843-1795_6843-174 others(58): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(48): Show |
C | 12 | a0001c0001t0005g0114a0001c0001t0005g0115a0001c0001t0005g0120others(9): Show | 12 | HG00735.hp2 HG01169.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.6843-1795_6843-174 others(59): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(49): Show |
C | 11 | a0001c0001t0030g0105a0001c0004t0002g0064a0001c0004t0002g0065others(8): Show | 11 | HG00738.hp1 HG01081.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.6843-1795_6843-174 others(60): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(50): Show |
C | 11 | a0001c0001t0003g0037a0001c0002t0009g0047a0001c0002t0080g0054others(8): Show | 11 | HG01175.hp2 HG02165.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.6843-1795_6843-173 others(61): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(51): Show |
C | 14 | a0001c0005t0012g0167a0001c0046t0054g0281a0001c0069t0052g0164others(11): Show | 14 | HG02257.hp1 HG02896.hp1 HG02897.hp2 others(11): Show |
intron_variant | MODIFIER | c.6843-1795_6843-173 others(62): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(52): Show |
C | 7 | a0001c0001t0003g0246a0001c0004t0084g0098a0006c0010t0011g0122others(4): Show | 7 | HG01109.hp2 HG02630.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.6843-1795_6843-173 others(63): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(53): Show |
C | 3 | a0001c0001t0085g0294a0007c0014t0011g0092a0032c0065t0041g0283 | 3 | HG00140.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.6843-1795_6843-173 others(64): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(54): Show |
C | 2 | a0001c0002t0002g0299a0001c0002t0050g0242 | 2 | HG02602.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.6843-1795_6843-173 others(65): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(55): Show |
C | 7 | a0001c0001t0002g0293a0001c0001t0003g0249a0001c0001t0003g0256others(4): Show | 8 | HG01258.hp2 HG01358.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.6843-1795_6843-173 others(66): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(56): Show |
C | 18 | a0001c0001t0002g0062a0001c0001t0002g0141a0001c0001t0003g0231others(15): Show | 18 | HG00280.hp2 HG00639.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.6843-1795_6843-173 others(67): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(57): Show |
C | 2 | a0001c0001t0021g0044a0002c0003t0001g0189 | 2 | HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.6843-1795_6843-173 others(68): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(58): Show |
C | 6 | a0001c0002t0007g0066a0001c0002t0036g0289a0001c0002t0036g0290others(3): Show | 6 | HG00642.hp1 HG01433.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.6843-1795_6843-173 others(69): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(61): Show |
C | 1 | a0005c0008t0002g0032 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.6843-1795_6843-172 others(72): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(63): Show |
C | 2 | a0001c0004t0003g0203a0018c0032t0033g0087 | 2 | HG02818.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.6843-1795_6843-172 others(74): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(64): Show |
C | 3 | a0001c0024t0070g0282a0004c0006t0002g0071a0018c0032t0033g0086 | 3 | HG02572.hp1 HG03654.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.6843-1795_6843-172 others(75): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100723
|
CCTTTTTT others(67): Show |
C | 9 | a0001c0002t0071g0194a0001c0004t0034g0126a0001c0004t0044g0153others(6): Show | 9 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.6843-1795_6843-172 others(78): Show |
IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100723 | ||||||
| chr6:160100724
|
C | T | 1 | a0001c0001t0006g0244 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.6843-1795C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100724 | ||||||
| chr6:160100842
|
G | A | 2 | a0001c0005t0004g0024a0001c0005t0004g0026 | 2 | NA18945.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.6843-1677G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100842 | ||||||
| chr6:160100844
|
G | A | 22 | a0001c0005t0004g0012a0001c0005t0004g0014a0001c0005t0004g0018others(19): Show | 22 | HG00408.hp1 HG00423.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.6843-1675G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100844 | ||||||
| chr6:160100853
|
C | T | 5 | a0001c0001t0013g0006a0001c0001t0013g0145a0001c0001t0013g0146others(2): Show | 5 | HG00280.hp1 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.6843-1666C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100853 | ||||||
| chr6:160100866
|
C | A | 1 | a0029c0038t0003g0286 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.6843-1653C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160100866 | ||||||
| chr6:160101304
|
C | T | 7 | a0001c0002t0039g0233a0001c0024t0024g0201a0014c0022t0038g0275others(4): Show | 7 | HG02109.hp2 HG02647.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.6843-1215C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160101304 | ||||||
| chr6:160101542
|
G | A | 1 | a0001c0002t0018g0235 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6843-977G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160101542 | ||||||
| chr6:160101965
|
G | T | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6843-554G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160101965 | ||||||
| chr6:160102019
|
C | T | 1 | a0001c0001t0006g0308 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.6843-500C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160102019 | ||||||
| chr6:160102139
|
C | G | 65 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(62): Show | 66 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.6843-380C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160102139 | ||||||
| chr6:160102223
|
C | T | 24 | a0001c0002t0015g0009a0001c0002t0015g0127a0001c0002t0015g0163others(21): Show | 24 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.6843-296C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160102223 | ||||||
| chr6:160102224
|
G | A | 1 | a0002c0003t0001g0255 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.6843-295G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160102224 | ||||||
| chr6:160102283
|
C | T | 1 | a0003c0007t0009g0048 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.6843-236C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160102283 | ||||||
| chr6:160102379
|
T | G | 3 | a0006c0025t0059g0288a0007c0018t0019g0238a0007c0018t0019g0239 | 3 | HG02280.hp2 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.6843-140T>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160102379 | ||||||
| chr6:160102388
|
G | T | 11 | a0001c0001t0003g0230a0004c0006t0002g0071a0004c0006t0002g0072others(8): Show | 11 | HG00597.hp1 HG02738.hp2 HG03490.hp2 others(8): Show |
intron_variant | MODIFIER | c.6843-131G>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160102388 | ||||||
| chr6:160102491
|
C | T | 1 | a0001c0004t0020g0253 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.6843-28C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 45/47 | chr6 | 160102491 | ||||||
| chr6:160102677
|
C | T | 24 | a0001c0002t0015g0009a0001c0002t0015g0127a0001c0002t0015g0163others(21): Show | 24 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(21): Show |
splice_region_variant&intron_variant | LOW | c.6995+6C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 46/47 | chr6 | 160102677 | ||||||
| chr6:160102872
|
G | A | 9 | a0001c0046t0054g0281a0001c0069t0052g0164a0006c0010t0011g0122others(6): Show | 9 | HG02630.hp2 HG02895.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.6995+201G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 46/47 | chr6 | 160102872 | ||||||
| chr6:160103110
|
A | C | 1 | a0001c0005t0004g0083 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.6995+439A>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 46/47 | chr6 | 160103110 | ||||||
| chr6:160103122
|
C | T | 1 | a0001c0024t0070g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6995+451C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 46/47 | chr6 | 160103122 | ||||||
| chr6:160103123
|
G | A | 4 | a0003c0007t0075g0147a0010c0016t0016g0150a0010c0016t0016g0169others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.6995+452G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 46/47 | chr6 | 160103123 | ||||||
| chr6:160103130
|
G | A | 5 | a0006c0025t0059g0288a0007c0018t0019g0238a0007c0018t0019g0239others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.6995+459G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 46/47 | chr6 | 160103130 | ||||||
| chr6:160103304
|
C | G | 111 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(108): Show | 112 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.6996-442C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 46/47 | chr6 | 160103304 | ||||||
| chr6:160103340
|
G | A | 1 | a0001c0024t0024g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.6996-406G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 46/47 | chr6 | 160103340 | ||||||
| chr6:160103546
|
C | G | 159 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(156): Show | 160 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.6996-200C>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 46/47 | chr6 | 160103546 | ||||||
| chr6:160103639
|
A | G | 165 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(162): Show | 166 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.6996-107A>G | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 46/47 | chr6 | 160103639 | ||||||
| chr6:160103741
|
T | A | 82 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(79): Show | 83 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
splice_region_variant&intron_variant | LOW | c.6996-5T>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 46/47 | chr6 | 160103741 | ||||||
| chr6:160103844
|
G | A | 5 | a0001c0002t0015g0009a0001c0002t0015g0127a0001c0002t0015g0163others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.7065+29G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 47/47 | chr6 | 160103844 | ||||||
| chr6:160103950
|
C | T | 1 | a0014c0022t0038g0275 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.7065+135C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 47/47 | chr6 | 160103950 | ||||||
| chr6:160104012
|
G | A | 5 | a0001c0001t0002g0141a0001c0001t0003g0256a0001c0001t0010g0157others(2): Show | 5 | HG01243.hp2 HG01934.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.7065+197G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 47/47 | chr6 | 160104012 | ||||||
| chr6:160104148
|
C | A | 1 | a0017c0021t0031g0004 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.7065+333C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 47/47 | chr6 | 160104148 | ||||||
| chr6:160104155
|
G | A | 82 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(79): Show | 83 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.7065+340G>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 47/47 | chr6 | 160104155 | ||||||
| chr6:160104255
|
G | C | 159 | a0001c0001t0001g0187a0001c0001t0001g0301a0001c0001t0001g0304others(156): Show | 160 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.7066-419G>C | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 47/47 | chr6 | 160104255 | ||||||
| chr6:160104339
|
C | A | 1 | a0001c0037t0002g0079 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.7066-335C>A | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 47/47 | chr6 | 160104339 | ||||||
| chr6:160104371
|
C | T | 5 | a0001c0004t0001g0222a0001c0009t0001g0181a0002c0003t0001g0251others(2): Show | 5 | HG02155.hp2 NA18951.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.7066-303C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 47/47 | chr6 | 160104371 | ||||||
| chr6:160104503
|
C | T | 1 | a0002c0003t0001g0191 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.7066-171C>T | IGF2R | ENSG00000197081.16 | transcript | ENST00000356956.6 | protein_coding | 47/47 | chr6 | 160104503 |