Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4033 |
|---|---|
| ensemblid | ENSG00000118308.16 |
| hgncid | 6690 |
| symbol | IRAG2 |
| name | inositol 1,4,5-triphosphate receptor associated 2 |
| refseq_nuc | NM_001366544.2 |
| refseq_prot | NP_001353473.1 |
| ensembl_nuc | ENST00000556887.6 |
| ensembl_prot | ENSP00000451048.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 25052706 |
| end | 25108335 |
| strand | + |
| ver | v1.2 |
| region | chr12:25052706-25108335 |
| region5000 | chr12:25047706-25113335 |
| regionname0 | IRAG2_chr12_25052706_25108335 |
| regionname5000 | IRAG2_chr12_25047706_25113335 |
| 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 | 499 | 145 | 9 | 33 | 78 | 7 | 17 | 49 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0002 | 0/0 | 499 | 100 | 41 | 31 | 19 | 0 | 9 | 15 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0003 | 1/0 | 499 | 55 | 18 | 13 | 14 | 5 | 4 | 9 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0004 | 0/0 | 499 | 24 | 4 | 9 | 0 | 2 | 9 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0005 | 0/0 | 499 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0006 | 0/0 | 499 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0007 | 0/0 | 499 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0008 | 0/0 | 499 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0009 | 0/0 | 499 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| 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 | 0/1 | 1500 | 138 | 9 | 33 | 71 | 7 | 17 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| c0002 | 0/0 | 1500 | 100 | 41 | 31 | 19 | 0 | 9 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| c0003 | 1/0 | 1500 | 55 | 18 | 13 | 14 | 5 | 4 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| c0004 | 0/0 | 1500 | 24 | 4 | 9 | 0 | 2 | 9 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| c0005 | 0/0 | 1500 | 8 | 8 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| c0006 | 0/0 | 1500 | 8 | 8 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| c0007 | 0/0 | 1500 | 3 | 0 | 0 | 3 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| c0008 | 0/0 | 1500 | 2 | 0 | 0 | 2 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| c0009 | 0/0 | 1500 | 2 | 2 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| c0010 | 0/0 | 1500 | 2 | 0 | 0 | 2 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| c0011 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| c0012 | 0/0 | 1500 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| 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 | 1/1 | 973 | 281 | 71 | 73 | 91 | 9 | 35 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| t0002 | 0/0 | 973 | 24 | 0 | 8 | 13 | 2 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| t0003 | 0/0 | 973 | 12 | 12 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| t0004 | 0/0 | 973 | 6 | 0 | 1 | 1 | 3 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| t0005 | 0/0 | 973 | 4 | 0 | 3 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| t0006 | 0/0 | 973 | 4 | 0 | 0 | 3 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| t0007 | 0/0 | 973 | 3 | 3 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| t0008 | 0/0 | 973 | 2 | 2 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| t0009 | 0/0 | 973 | 2 | 0 | 0 | 2 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| t0010 | 0/0 | 973 | 2 | 0 | 0 | 1 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| t0011 | 0/0 | 973 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| t0012 | 0/0 | 973 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| t0013 | 0/0 | 973 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| t0014 | 0/0 | 973 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| 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 | 3 | 3 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0002 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| 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 | 0/1 | 1500 | 138 | 9 | 33 | 71 | 7 | 17 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0001c0007 | 0/0 | 1500 | 3 | 0 | 0 | 3 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0001c0008 | 0/0 | 1500 | 2 | 0 | 0 | 2 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0001c0010 | 0/0 | 1500 | 2 | 0 | 0 | 2 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0002c0002 | 0/0 | 1500 | 100 | 41 | 31 | 19 | 0 | 9 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0003c0003 | 1/0 | 1500 | 55 | 18 | 13 | 14 | 5 | 4 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0004c0004 | 0/0 | 1500 | 24 | 4 | 9 | 0 | 2 | 9 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0005c0006 | 0/0 | 1500 | 8 | 8 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0006c0005 | 0/0 | 1500 | 8 | 8 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0007c0009 | 0/0 | 1500 | 2 | 2 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0008c0011 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0009c0012 | 0/0 | 1500 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2472 | 134 | 9 | 32 | 68 | 7 | 17 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0001c0001t0002 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0001c0001t0006 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0001c0001t0013 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0001c0001t0014 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0001c0007t0001 | 0/0 | 2472 | 3 | 0 | 0 | 3 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0001c0008t0001 | 0/0 | 2472 | 2 | 0 | 0 | 2 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0001c0010t0001 | 0/0 | 2472 | 2 | 0 | 0 | 2 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0002c0002t0001 | 0/0 | 2472 | 95 | 39 | 31 | 16 | 0 | 9 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0002c0002t0003 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0002c0002t0006 | 0/0 | 2472 | 2 | 0 | 0 | 2 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0002c0002t0010 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0002c0002t0012 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0003c0003t0001 | 1/0 | 2472 | 8 | 6 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0003c0003t0002 | 0/0 | 2472 | 22 | 0 | 8 | 11 | 2 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0003c0003t0003 | 0/0 | 2472 | 10 | 10 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0003c0003t0004 | 0/0 | 2472 | 6 | 0 | 1 | 1 | 3 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0003c0003t0005 | 0/0 | 2472 | 4 | 0 | 3 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0003c0003t0008 | 0/0 | 2472 | 2 | 2 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0003c0003t0009 | 0/0 | 2472 | 2 | 0 | 0 | 2 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0003c0003t0010 | 0/0 | 2472 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0004c0004t0001 | 0/0 | 2472 | 23 | 4 | 9 | 0 | 2 | 8 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0004c0004t0006 | 0/0 | 2472 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0005c0006t0001 | 0/0 | 2472 | 4 | 4 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0005c0006t0007 | 0/0 | 2472 | 3 | 3 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0005c0006t0011 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0006c0005t0001 | 0/0 | 2472 | 8 | 8 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0007c0009t0001 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0007c0009t0003 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0008c0011t0002 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| a0009c0012t0001 | 0/0 | 2472 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | copy fasta | chr12 | 25047706 | 25113335 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0013g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0014g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0007t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0007t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0007t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0008t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0008t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0010t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0010t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0010g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0012g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0001g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0004g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0004g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0004g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0004g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0004g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0005g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0005g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0005g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0008g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0009g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0009g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0010g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0004c0004t0001g0002 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0004c0004t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0004c0004t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0004c0004t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0004c0004t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0004c0004t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0004c0004t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0004c0004t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0004c0004t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0004c0004t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0004c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0004c0004t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0004c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0004c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0004c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0004c0004t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0004c0004t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0004c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0004c0004t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0004c0004t0006g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0005c0006t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0005c0006t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0005c0006t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0005c0006t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0005c0006t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0005c0006t0007g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0005c0006t0007g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0005c0006t0011g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0006c0005t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0006c0005t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0006c0005t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0006c0005t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0006c0005t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0006c0005t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0006c0005t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0006c0005t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0007c0009t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0007c0009t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0008c0011t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0009c0012t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0002 | g0079 | EUR | GBR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00099 | hp2 | a0003 | c0003 | t0004 | g0319 | EUR | GBR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | GBR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | GBR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | FIN | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00280 | hp2 | a0004 | c0004 | t0001 | g0016 | EUR | FIN | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00323 | hp1 | a0003 | c0003 | t0004 | g0317 | EUR | FIN | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | FIN | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00408 | hp2 | a0003 | c0003 | t0002 | g0124 | EAS | CHS | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | CHS | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00639 | hp1 | a0003 | c0003 | t0004 | g0315 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00642 | hp2 | a0004 | c0004 | t0001 | g0254 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0052 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00735 | hp1 | a0004 | c0004 | t0001 | g0105 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0070 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0142 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0288 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0294 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01081 | hp2 | a0004 | c0004 | t0001 | g0004 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01099 | hp1 | a0004 | c0004 | t0001 | g0016 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01099 | hp2 | a0003 | c0003 | t0005 | g0033 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01106 | hp1 | a0004 | c0004 | t0001 | g0004 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0075 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01109 | hp2 | a0003 | c0003 | t0002 | g0150 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0259 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01168 | hp1 | a0004 | c0004 | t0001 | g0002 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01169 | hp2 | a0004 | c0004 | t0001 | g0002 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01175 | hp1 | a0003 | c0003 | t0002 | g0184 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0056 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01192 | hp1 | a0003 | c0003 | t0001 | g0061 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01256 | hp1 | a0003 | c0003 | t0005 | g0036 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01256 | hp2 | a0003 | c0003 | t0002 | g0202 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01258 | hp1 | a0003 | c0003 | t0002 | g0201 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0141 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0257 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01346 | hp2 | a0003 | c0003 | t0002 | g0127 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01358 | hp1 | a0001 | c0001 | t0014 | g0018 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0071 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01361 | hp2 | a0004 | c0004 | t0001 | g0190 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0076 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0291 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0241 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | IBS | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01515 | hp2 | a0003 | c0003 | t0004 | g0316 | EUR | IBS | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | IBS | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01517 | hp2 | a0003 | c0003 | t0002 | g0260 | EUR | IBS | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0168 | AFR | ACB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0207 | AFR | ACB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01891 | hp1 | a0005 | c0006 | t0011 | g0303 | AFR | ACB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01891 | hp2 | a0003 | c0003 | t0008 | g0166 | AFR | ACB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0199 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0240 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0258 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01981 | hp2 | a0003 | c0003 | t0002 | g0261 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0255 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02004 | hp1 | a0003 | c0003 | t0002 | g0266 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0208 | EAS | KHV | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | KHV | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | KHV | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02055 | hp1 | a0005 | c0006 | t0001 | g0299 | AFR | ACB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02074 | hp2 | a0002 | c0002 | t0006 | g0234 | EAS | KHV | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02083 | hp2 | a0003 | c0003 | t0002 | g0125 | EAS | KHV | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02135 | hp1 | a0001 | c0001 | t0006 | g0195 | EAS | KHV | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02135 | hp2 | a0003 | c0003 | t0004 | g0314 | EAS | KHV | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02145 | hp1 | a0003 | c0003 | t0003 | g0156 | AFR | ACB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0285 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0074 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CDX | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CDX | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CDX | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0171 | AFR | ACB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02257 | hp2 | a0003 | c0003 | t0008 | g0161 | AFR | ACB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02258 | hp1 | a0003 | c0003 | t0001 | g0159 | AFR | ACB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0164 | AFR | ACB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02293 | hp1 | a0003 | c0003 | t0005 | g0034 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0262 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0048 | AFR | ACB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02451 | hp2 | a0003 | c0003 | t0003 | g0023 | AFR | ACB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02523 | hp1 | a0003 | c0003 | t0009 | g0031 | EAS | KHV | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0163 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02572 | hp2 | a0007 | c0009 | t0001 | g0200 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02602 | hp2 | a0003 | c0003 | t0002 | g0203 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02615 | hp1 | a0003 | c0003 | t0001 | g0062 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02615 | hp2 | a0006 | c0005 | t0001 | g0065 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0311 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02647 | hp1 | a0003 | c0003 | t0001 | g0170 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02647 | hp2 | a0004 | c0004 | t0001 | g0002 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02683 | hp2 | a0004 | c0004 | t0001 | g0287 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02698 | hp1 | a0004 | c0004 | t0001 | g0273 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02717 | hp1 | a0005 | c0006 | t0001 | g0301 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0063 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02723 | hp1 | a0006 | c0005 | t0001 | g0165 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0173 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0073 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02738 | hp1 | a0004 | c0004 | t0001 | g0209 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02738 | hp2 | a0003 | c0003 | t0010 | g0313 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0239 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02809 | hp2 | a0005 | c0006 | t0001 | g0298 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02818 | hp1 | a0004 | c0004 | t0001 | g0067 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02818 | hp2 | a0006 | c0005 | t0001 | g0019 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02895 | hp1 | a0006 | c0005 | t0001 | g0064 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0043 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02896 | hp1 | a0007 | c0009 | t0003 | g0297 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0044 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02965 | hp1 | a0004 | c0004 | t0001 | g0040 | AFR | ESN | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0172 | AFR | ESN | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02970 | hp1 | a0003 | c0003 | t0003 | g0057 | AFR | ESN | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02970 | hp2 | a0002 | c0002 | t0003 | g0283 | AFR | ESN | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02976 | hp1 | a0003 | c0003 | t0001 | g0028 | AFR | ESN | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0152 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0174 | AFR | ESN | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03130 | hp2 | a0003 | c0003 | t0003 | g0049 | AFR | ESN | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0309 | AFR | ESN | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | MSL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03225 | hp1 | a0005 | c0006 | t0007 | g0302 | AFR | MSL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03225 | hp2 | a0003 | c0003 | t0003 | g0022 | AFR | MSL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0232 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03453 | hp1 | a0006 | c0005 | t0001 | g0066 | AFR | MSL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0027 | AFR | MSL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0155 | AFR | MSL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0046 | AFR | MSL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03491 | hp2 | a0004 | c0004 | t0001 | g0271 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0289 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03492 | hp2 | a0004 | c0004 | t0001 | g0272 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03516 | hp1 | a0005 | c0006 | t0007 | g0304 | AFR | ESN | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0176 | AFR | ESN | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03540 | hp1 | a0003 | c0003 | t0003 | g0060 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03540 | hp2 | a0006 | c0005 | t0001 | g0244 | AFR | GWD | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03579 | hp1 | a0003 | c0003 | t0003 | g0024 | AFR | MSL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03579 | hp2 | a0002 | c0002 | t0012 | g0167 | AFR | MSL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03654 | hp1 | a0004 | c0004 | t0001 | g0264 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0083 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0231 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03710 | hp2 | a0004 | c0004 | t0001 | g0278 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0280 | SAS | BEB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03834 | hp2 | a0003 | c0003 | t0004 | g0318 | SAS | BEB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0275 | SAS | BEB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0037 | SAS | BEB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | STU | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG04115 | hp2 | a0004 | c0004 | t0006 | g0147 | SAS | STU | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0247 | SAS | BEB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG04184 | hp2 | a0003 | c0003 | t0005 | g0032 | SAS | BEB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | STU | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG04204 | hp2 | a0009 | c0012 | t0001 | g0193 | SAS | STU | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18522 | hp1 | a0004 | c0004 | t0001 | g0140 | AFR | YRI | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0295 | AFR | YRI | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18612 | hp1 | a0003 | c0003 | t0002 | g0123 | EAS | CHB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18906 | hp1 | a0003 | c0003 | t0003 | g0307 | AFR | YRI | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0151 | AFR | YRI | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18949 | hp1 | a0003 | c0003 | t0002 | g0113 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18950 | hp1 | a0003 | c0003 | t0002 | g0188 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18954 | hp2 | a0001 | c0010 | t0001 | g0115 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18957 | hp1 | a0001 | c0008 | t0001 | g0219 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18960 | hp1 | a0001 | c0007 | t0001 | g0130 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18960 | hp2 | a0003 | c0003 | t0002 | g0189 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18964 | hp1 | a0001 | c0010 | t0001 | g0116 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18968 | hp1 | a0001 | c0007 | t0001 | g0131 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18970 | hp1 | a0001 | c0008 | t0001 | g0274 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18981 | hp2 | a0003 | c0003 | t0002 | g0093 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18982 | hp2 | a0003 | c0003 | t0009 | g0078 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18988 | hp2 | a0001 | c0007 | t0001 | g0129 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18989 | hp2 | a0003 | c0003 | t0002 | g0128 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0296 | AFR | LWK | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19030 | hp2 | a0003 | c0003 | t0003 | g0021 | AFR | LWK | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19054 | hp1 | a0003 | c0003 | t0002 | g0180 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19070 | hp2 | a0008 | c0011 | t0002 | g0077 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19074 | hp1 | a0003 | c0003 | t0002 | g0187 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19074 | hp2 | a0003 | c0003 | t0002 | g0122 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19077 | hp1 | a0002 | c0002 | t0010 | g0030 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19077 | hp2 | a0001 | c0001 | t0013 | g0087 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19091 | hp1 | a0002 | c0002 | t0006 | g0210 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19240 | hp1 | a0006 | c0005 | t0001 | g0157 | AFR | YRI | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0308 | AFR | YRI | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA20129 | hp1 | a0003 | c0003 | t0001 | g0243 | AFR | ASW | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0047 | AFR | ASW | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | TSI | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA20752 | hp2 | a0004 | c0004 | t0001 | g0103 | EUR | TSI | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | GIH | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA20905 | hp2 | a0004 | c0004 | t0001 | g0265 | SAS | GIH | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01123 | hp1 | a0003 | c0003 | t0002 | g0286 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG01123 | hp2 | a0004 | c0004 | t0001 | g0104 | AMR | CLM | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02109 | hp2 | a0006 | c0005 | t0001 | g0059 | AFR | ACB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02486 | hp2 | a0005 | c0006 | t0001 | g0300 | AFR | ACB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0292 | AFR | ACB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | MSL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0310 | AFR | MSL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG06807 | hp1 | a0005 | c0006 | t0007 | g0051 | AFR | USA | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG06807 | hp2 | a0003 | c0003 | t0003 | g0158 | AFR | USA | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0160 | AFR | USA | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0256 | AFR | USA | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | LWK | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | LWK | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0082 | REF | REF | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| homoSapiens_grch38 | hp1 | a0003 | c0003 | t0001 | g0162 | REF | REF | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:25079438
|
A | G | 2 | a0005a0007 | 10 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
missense_variant | MODERATE | c.112A>G | p.Thr38Ala | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 8/22 | 809/2472 | 112/1500 | 38/499 | chr12 | 25079438 | ||
| chr12:25089661
|
C | G | 4 | a0001a0002a0005others(1): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
missense_variant | MODERATE | c.421C>G | p.Leu141Val | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 12/22 | 1118/2472 | 421/1500 | 141/499 | chr12 | 25089661 | ||
| chr12:25090181
|
G | C | 4 | a0001a0004a0008others(1): Show | 171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
missense_variant | MODERATE | c.590G>C | p.Cys197Ser | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/22 | 1287/2472 | 590/1500 | 197/499 | chr12 | 25090181 | ||
| chr12:25102198
|
A | G | 1 | a0009 | 1 | HG04204.hp2 | missense_variant&splice_region_variant | MODERATE | c.890A>G | p.Asp297Gly | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 17/22 | 1587/2472 | 890/1500 | 297/499 | chr12 | 25102198 | ||
| chr12:25104034
|
G | A | 1 | a0008 | 1 | NA19070.hp2 | missense_variant | MODERATE | c.1022G>A | p.Arg341Gln | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 19/22 | 1719/2472 | 1022/1500 | 341/499 | chr12 | 25104034 | ||
| chr12:25107016
|
A | G | 1 | a0006 | 8 | HG02109.hp2 HG02615.hp2 HG02723.hp1 others(5): Show |
missense_variant | MODERATE | c.1222A>G | p.Lys408Glu | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 21/22 | 1919/2472 | 1222/1500 | 408/499 | chr12 | 25107016 | ||
| chr12:25108334
|
C | G | 3 | a0002a0003a0007 | 14 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(11): Show |
splice_region_variant | LOW | c.*274C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 22/22 | chr12 | 25108334 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:25079261
|
C | T | 1 | a0001c0010 | 2 | NA18954.hp2 NA18964.hp1 |
synonymous_variant | LOW | c.42C>T | p.Arg14Arg | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 7/22 | 739/2472 | 42/1500 | 14/499 | chr12 | 25079261 | ||
| chr12:25101219
|
C | T | 1 | a0001c0007 | 3 | NA18960.hp1 NA18968.hp1 NA18988.hp2 |
synonymous_variant | LOW | c.783C>T | p.His261His | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 16/22 | 1480/2472 | 783/1500 | 261/499 | chr12 | 25101219 | ||
| chr12:25101255
|
C | T | 1 | a0001c0008 | 2 | NA18957.hp1 NA18970.hp1 |
synonymous_variant | LOW | c.819C>T | p.His273His | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 16/22 | 1516/2472 | 819/1500 | 273/499 | chr12 | 25101255 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:25052787
|
T | C | 3 | a0002c0002t0012a0003c0003t0008a0005c0006t0011 | 4 | HG01891.hp1 HG01891.hp2 HG02257.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-616T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/22 | 16621 | chr12 | 25052787 | |||||
| chr12:25052867
|
C | T | 7 | a0001c0001t0006a0002c0002t0006a0002c0002t0010others(4): Show | 14 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-536C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/22 | 16541 | chr12 | 25052867 | |||||
| chr12:25052910
|
A | C | 1 | a0001c0001t0014 | 1 | HG01358.hp1 | 5_prime_UTR_variant | MODIFIER | c.-493A>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/22 | 16498 | chr12 | 25052910 | |||||
| chr12:25062831
|
T | C | 1 | a0001c0001t0013 | 1 | NA19077.hp2 | 5_prime_UTR_variant | MODIFIER | c.-373T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 3/22 | 6577 | chr12 | 25062831 | |||||
| chr12:25063777
|
C | T | 4 | a0002c0002t0010a0003c0003t0004a0003c0003t0005others(1): Show | 12 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(9): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-246C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/22 | chr12 | 25063777 | ||||||
| chr12:25069386
|
G | A | 2 | a0005c0006t0007a0005c0006t0011 | 4 | HG01891.hp1 HG03225.hp1 HG03516.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-22G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/22 | 22 | chr12 | 25069386 | |||||
| chr12:25108231
|
A | G | 6 | a0001c0001t0002a0003c0003t0002a0003c0003t0004others(3): Show | 36 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*171A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 22/22 | 171 | chr12 | 25108231 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:25052972
|
T | C | 1 | a0001c0001t0014g0018 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-447+16T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25052972 | ||||||
| chr12:25053054
|
T | C | 1 | a0001c0001t0014g0018 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-447+98T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25053054 | ||||||
| chr12:25053074
|
A | G | 1 | a0001c0001t0014g0018 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-447+118A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25053074 | ||||||
| chr12:25053152
|
T | A | 1 | a0006c0005t0001g0019 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-447+196T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25053152 | ||||||
| chr12:25053209
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-447+253T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25053209 | ||||||
| chr12:25053222
|
T | A | 1 | a0006c0005t0001g0019 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-447+266T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25053222 | ||||||
| chr12:25053300
|
A | G | 13 | a0001c0001t0001g0020a0001c0001t0001g0320a0001c0001t0001g0321others(10): Show | 13 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.-447+344A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25053300 | ||||||
| chr12:25053321
|
T | C | 1 | a0003c0003t0003g0021 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-447+365T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25053321 | ||||||
| chr12:25053626
|
T | C | 5 | a0001c0001t0001g0025a0003c0003t0003g0022a0003c0003t0003g0023others(2): Show | 6 | HG01081.hp2 HG01106.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-447+670T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25053626 | ||||||
| chr12:25053698
|
C | A | 1 | a0001c0001t0001g0026 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-447+742C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25053698 | ||||||
| chr12:25053717
|
TATAA | T | 5 | a0001c0001t0001g0312a0002c0002t0001g0308a0002c0002t0001g0309others(2): Show | 5 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-447+765_-447+768d others(6): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 25053717 | |||||
| chr12:25053789
|
A | C | 2 | a0003c0003t0003g0021a0003c0003t0003g0307 | 2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-447+833A>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25053789 | ||||||
| chr12:25053878
|
C | T | 2 | a0001c0001t0001g0305a0001c0001t0001g0306 | 2 | HG02040.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-447+922C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25053878 | ||||||
| chr12:25053997
|
C | T | 8 | a0005c0006t0001g0298a0005c0006t0001g0299a0005c0006t0001g0300others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-447+1041C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25053997 | ||||||
| chr12:25054311
|
G | T | 2 | a0002c0002t0001g0295a0002c0002t0001g0296 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-447+1355G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25054311 | ||||||
| chr12:25054312
|
C | G | 2 | a0002c0002t0001g0295a0002c0002t0001g0296 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-447+1356C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25054312 | ||||||
| chr12:25054458
|
T | C | 7 | a0001c0001t0001g0312a0002c0002t0001g0001a0002c0002t0001g0027others(4): Show | 9 | HG02109.hp1 HG02630.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.-447+1502T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25054458 | ||||||
| chr12:25054462
|
T | C | 1 | a0003c0003t0001g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-447+1506T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25054462 | ||||||
| chr12:25054619
|
T | C | 2 | a0002c0002t0001g0001a0002c0002t0001g0027 | 4 | HG02109.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-447+1663T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25054619 | ||||||
| chr12:25054647
|
G | A | 6 | a0001c0001t0001g0025a0001c0001t0001g0029a0003c0003t0003g0022others(3): Show | 7 | HG00741.hp2 HG01081.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.-447+1691G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25054647 | ||||||
| chr12:25054719
|
A | G | 122 | a0001c0001t0001g0182a0001c0001t0001g0185a0001c0001t0001g0186others(119): Show | 124 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-447+1763A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25054719 | ||||||
| chr12:25054918
|
A | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG01081.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.-447+1962A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25054918 | ||||||
| chr12:25054977
|
T | G | 291 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(288): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.-447+2021T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25054977 | ||||||
| chr12:25055024
|
A | T | 1 | a0002c0002t0001g0294 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-447+2068A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25055024 | ||||||
| chr12:25055028
|
C | T | 1 | a0001c0001t0001g0293 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-447+2072C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25055028 | ||||||
| chr12:25055206
|
T | G | 1 | a0002c0002t0001g0179 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-447+2250T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25055206 | ||||||
| chr12:25055611
|
C | A | 12 | a0002c0002t0010g0030a0003c0003t0004g0314a0003c0003t0004g0315others(9): Show | 12 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-447+2655C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25055611 | ||||||
| chr12:25055723
|
G | T | 6 | a0001c0001t0001g0153a0001c0001t0001g0154a0002c0002t0001g0151others(3): Show | 6 | HG00738.hp2 HG01243.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-447+2767G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25055723 | ||||||
| chr12:25055795
|
A | G | 3 | a0005c0006t0007g0302a0005c0006t0007g0304a0005c0006t0011g0303 | 3 | HG01891.hp1 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-447+2839A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25055795 | ||||||
| chr12:25055823
|
G | A | 5 | a0001c0001t0001g0025a0003c0003t0003g0022a0003c0003t0003g0023others(2): Show | 6 | HG01081.hp2 HG01106.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-447+2867G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25055823 | ||||||
| chr12:25055831
|
CATATT | C | 3 | a0003c0003t0003g0156a0003c0003t0003g0158a0006c0005t0001g0157 | 3 | HG02145.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-447+2877_-447+288 others(9): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 25055831 | |||||
| chr12:25055863
|
T | C | 5 | a0001c0001t0001g0312a0002c0002t0001g0308a0002c0002t0001g0309others(2): Show | 5 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-447+2907T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25055863 | ||||||
| chr12:25056062
|
C | T | 12 | a0002c0002t0010g0030a0003c0003t0004g0314a0003c0003t0004g0315others(9): Show | 12 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-447+3106C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25056062 | ||||||
| chr12:25056102
|
A | G | 300 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(297): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-447+3146A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25056102 | ||||||
| chr12:25056210
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-447+3254G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25056210 | ||||||
| chr12:25056291
|
G | C | 12 | a0002c0002t0010g0030a0003c0003t0004g0314a0003c0003t0004g0315others(9): Show | 12 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-447+3335G>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25056291 | ||||||
| chr12:25056312
|
G | A | 1 | a0003c0003t0001g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-447+3356G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25056312 | ||||||
| chr12:25056413
|
T | G | 3 | a0001c0001t0001g0182a0002c0002t0001g0181a0003c0003t0002g0180 | 3 | HG00408.hp1 NA18952.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-447+3457T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25056413 | ||||||
| chr12:25056738
|
C | T | 4 | a0001c0001t0001g0290a0002c0002t0001g0289a0002c0002t0001g0291others(1): Show | 4 | HG01243.hp1 HG01433.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-447+3782C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25056738 | ||||||
| chr12:25056830
|
G | A | 261 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(258): Show | 275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.-447+3874G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25056830 | ||||||
| chr12:25056848
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-447+3892G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25056848 | ||||||
| chr12:25056918
|
A | G | 1 | a0002c0002t0001g0288 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-447+3962A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25056918 | ||||||
| chr12:25056936
|
T | C | 303 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(300): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.-447+3980T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25056936 | ||||||
| chr12:25057082
|
A | G | 7 | a0002c0002t0001g0171a0002c0002t0001g0172a0002c0002t0001g0174others(4): Show | 7 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-447+4126A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25057082 | ||||||
| chr12:25057241
|
C | T | 303 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(300): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.-447+4285C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25057241 | ||||||
| chr12:25057252
|
A | AT | 31 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0194others(28): Show | 31 | HG01256.hp1 HG01361.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.-446-4316dupT | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 25057252 | |||||
| chr12:25057252
|
A | ATT | 229 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(226): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.-446-4317_-446-431 others(6): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 25057252 | |||||
| chr12:25057252
|
A | ATTT | 27 | a0001c0001t0001g0035a0001c0001t0001g0139a0001c0001t0001g0143others(24): Show | 27 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.-447+4318_-446-431 others(7): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 25057252 | |||||
| chr12:25057404
|
G | A | 5 | a0001c0001t0001g0312a0002c0002t0001g0308a0002c0002t0001g0309others(2): Show | 5 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-446-4188G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25057404 | ||||||
| chr12:25057528
|
G | A | 11 | a0001c0001t0001g0290a0002c0002t0001g0199a0002c0002t0001g0280others(8): Show | 11 | HG01070.hp1 HG01243.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.-446-4064G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25057528 | ||||||
| chr12:25057591
|
C | T | 6 | a0002c0002t0001g0171a0002c0002t0001g0172a0002c0002t0001g0174others(3): Show | 6 | HG02257.hp1 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-446-4001C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25057591 | ||||||
| chr12:25057847
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-446-3745A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25057847 | ||||||
| chr12:25057862
|
A | G | 6 | a0002c0002t0001g0171a0002c0002t0001g0172a0002c0002t0001g0174others(3): Show | 6 | HG02257.hp1 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-446-3730A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25057862 | ||||||
| chr12:25057876
|
G | T | 1 | a0001c0001t0001g0279 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-446-3716G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25057876 | ||||||
| chr12:25058053
|
A | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | HG00544.hp1 HG00609.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.-446-3539A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25058053 | ||||||
| chr12:25058131
|
A | T | 12 | a0002c0002t0010g0030a0003c0003t0004g0314a0003c0003t0004g0315others(9): Show | 12 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-446-3461A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25058131 | ||||||
| chr12:25058174
|
T | C | 310 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(307): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-446-3418T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25058174 | ||||||
| chr12:25058838
|
A | G | 2 | a0002c0002t0010g0030a0003c0003t0009g0031 | 2 | HG02523.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-446-2754A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25058838 | ||||||
| chr12:25058849
|
A | G | 2 | a0002c0002t0010g0030a0003c0003t0009g0031 | 2 | HG02523.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-446-2743A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25058849 | ||||||
| chr12:25059107
|
C | T | 70 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(67): Show | 74 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.-446-2485C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25059107 | ||||||
| chr12:25059178
|
C | T | 12 | a0002c0002t0010g0030a0003c0003t0004g0314a0003c0003t0004g0315others(9): Show | 12 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-446-2414C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25059178 | ||||||
| chr12:25059269
|
A | AT | 133 | a0001c0001t0001g0007a0001c0001t0001g0080a0001c0001t0001g0081others(130): Show | 137 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.-446-2317dupT | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 25059269 | |||||
| chr12:25059444
|
C | T | 12 | a0002c0002t0010g0030a0003c0003t0004g0314a0003c0003t0004g0315others(9): Show | 12 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-446-2148C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25059444 | ||||||
| chr12:25059539
|
A | C | 14 | a0001c0001t0001g0068a0001c0001t0001g0072a0002c0002t0001g0006others(11): Show | 15 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.-446-2053A>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25059539 | ||||||
| chr12:25059577
|
C | T | 1 | a0004c0004t0001g0278 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-446-2015C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25059577 | ||||||
| chr12:25059598
|
T | C | 12 | a0002c0002t0010g0030a0003c0003t0004g0314a0003c0003t0004g0315others(9): Show | 12 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-446-1994T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25059598 | ||||||
| chr12:25059605
|
C | T | 31 | a0001c0001t0001g0025a0001c0001t0001g0068a0001c0001t0001g0072others(28): Show | 35 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.-446-1987C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25059605 | ||||||
| chr12:25059832
|
C | T | 1 | a0003c0003t0001g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-446-1760C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25059832 | ||||||
| chr12:25060069
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | NA18948.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.-446-1523G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25060069 | ||||||
| chr12:25060146
|
A | G | 6 | a0002c0002t0001g0171a0002c0002t0001g0172a0002c0002t0001g0174others(3): Show | 6 | HG02257.hp1 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-446-1446A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25060146 | ||||||
| chr12:25060158
|
T | A | 2 | a0004c0004t0001g0067a0004c0004t0001g0140 | 2 | HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-446-1434T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25060158 | ||||||
| chr12:25060212
|
AAT | A | 12 | a0002c0002t0010g0030a0003c0003t0004g0314a0003c0003t0004g0315others(9): Show | 12 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-446-1378_-446-137 others(6): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 25060212 | |||||
| chr12:25060245
|
T | G | 1 | a0002c0002t0001g0171 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-446-1347T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25060245 | ||||||
| chr12:25060271
|
C | A | 2 | a0002c0002t0001g0001a0002c0002t0001g0027 | 4 | HG02109.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-446-1321C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25060271 | ||||||
| chr12:25060349
|
A | T | 7 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(4): Show | 7 | HG02083.hp1 NA18947.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.-446-1243A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25060349 | ||||||
| chr12:25060517
|
G | A | 5 | a0001c0001t0001g0312a0002c0002t0001g0308a0002c0002t0001g0309others(2): Show | 5 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-446-1075G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25060517 | ||||||
| chr12:25060648
|
T | C | 116 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 123 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.-446-944T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25060648 | ||||||
| chr12:25060668
|
C | CT | 7 | a0001c0001t0001g0182a0001c0001t0001g0276a0001c0001t0001g0277others(4): Show | 7 | HG00408.hp1 HG02165.hp2 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.-446-902dupT | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 25060668 | |||||
| chr12:25060668
|
CT | C | 154 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(151): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.-446-902delT | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 25060668 | |||||
| chr12:25060668
|
CTT | C | 10 | a0001c0001t0001g0039a0001c0001t0001g0086a0001c0001t0001g0135others(7): Show | 10 | HG00609.hp2 HG02630.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-446-903_-446-902d others(4): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 25060668 | |||||
| chr12:25060675
|
T | C | 12 | a0002c0002t0010g0030a0003c0003t0004g0314a0003c0003t0004g0315others(9): Show | 12 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-446-917T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25060675 | ||||||
| chr12:25060700
|
T | G | 1 | a0001c0001t0013g0087 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-446-892T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25060700 | ||||||
| chr12:25060703
|
C | T | 1 | a0005c0006t0001g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-446-889C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25060703 | ||||||
| chr12:25060742
|
C | A | 1 | a0003c0003t0002g0128 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-446-850C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25060742 | ||||||
| chr12:25060803
|
G | A | 5 | a0001c0001t0001g0025a0003c0003t0003g0022a0003c0003t0003g0023others(2): Show | 6 | HG01081.hp2 HG01106.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-446-789G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25060803 | ||||||
| chr12:25060810
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-446-782G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25060810 | ||||||
| chr12:25060835
|
AT | A | 39 | a0001c0001t0001g0025a0001c0001t0001g0068a0001c0001t0001g0072others(36): Show | 43 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.-446-745delT | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr12 | 25060835 | |||||
| chr12:25060856
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG02602.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-446-736T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25060856 | ||||||
| chr12:25060886
|
C | T | 40 | a0001c0001t0001g0025a0001c0001t0001g0068a0001c0001t0001g0072others(37): Show | 44 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.-446-706C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25060886 | ||||||
| chr12:25060937
|
A | G | 40 | a0001c0001t0001g0025a0001c0001t0001g0068a0001c0001t0001g0072others(37): Show | 44 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.-446-655A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25060937 | ||||||
| chr12:25061108
|
C | T | 23 | a0001c0001t0001g0025a0001c0001t0001g0068a0001c0001t0001g0072others(20): Show | 27 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.-446-484C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25061108 | ||||||
| chr12:25061166
|
G | C | 47 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0045others(44): Show | 51 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.-446-426G>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25061166 | ||||||
| chr12:25061197
|
T | A | 40 | a0001c0001t0001g0025a0001c0001t0001g0068a0001c0001t0001g0072others(37): Show | 44 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.-446-395T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25061197 | ||||||
| chr12:25061365
|
A | G | 3 | a0003c0003t0003g0156a0003c0003t0003g0158a0006c0005t0001g0157 | 3 | HG02145.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-446-227A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25061365 | ||||||
| chr12:25061572
|
G | T | 1 | a0003c0003t0001g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-446-20G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 1/21 | chr12 | 25061572 | ||||||
| chr12:25061686
|
T | C | 131 | a0001c0001t0001g0007a0001c0001t0001g0080a0001c0001t0001g0081others(128): Show | 135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.-385+33T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 2/21 | chr12 | 25061686 | ||||||
| chr12:25061712
|
G | A | 12 | a0002c0002t0010g0030a0003c0003t0004g0314a0003c0003t0004g0315others(9): Show | 12 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-385+59G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 2/21 | chr12 | 25061712 | ||||||
| chr12:25062035
|
T | G | 7 | a0001c0001t0001g0312a0002c0002t0001g0001a0002c0002t0001g0027others(4): Show | 9 | HG02109.hp1 HG02630.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.-385+382T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 2/21 | chr12 | 25062035 | ||||||
| chr12:25062257
|
G | T | 131 | a0001c0001t0001g0007a0001c0001t0001g0080a0001c0001t0001g0081others(128): Show | 135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.-384-563G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 2/21 | chr12 | 25062257 | ||||||
| chr12:25062478
|
C | A | 1 | a0003c0003t0003g0049 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-384-342C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 2/21 | chr12 | 25062478 | ||||||
| chr12:25062589
|
C | G | 3 | a0003c0003t0003g0156a0003c0003t0003g0158a0006c0005t0001g0157 | 3 | HG02145.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-384-231C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 2/21 | chr12 | 25062589 | ||||||
| chr12:25062741
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-384-79A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 2/21 | chr12 | 25062741 | ||||||
| chr12:25063049
|
G | C | 47 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0045others(44): Show | 50 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.-304+149G>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 3/21 | chr12 | 25063049 | ||||||
| chr12:25063089
|
T | C | 1 | a0005c0006t0007g0302 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-304+189T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 3/21 | chr12 | 25063089 | ||||||
| chr12:25063165
|
A | C | 7 | a0001c0001t0001g0312a0002c0002t0001g0001a0002c0002t0001g0027others(4): Show | 9 | HG02109.hp1 HG02630.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.-304+265A>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 3/21 | chr12 | 25063165 | ||||||
| chr12:25063397
|
A | G | 2 | a0002c0002t0001g0295a0002c0002t0001g0296 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-303-323A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 3/21 | chr12 | 25063397 | ||||||
| chr12:25063432
|
C | G | 33 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0068others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.-303-288C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 3/21 | chr12 | 25063432 | ||||||
| chr12:25063471
|
G | A | 121 | a0001c0001t0001g0007a0001c0001t0001g0080a0001c0001t0001g0081others(118): Show | 125 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-303-249G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 3/21 | chr12 | 25063471 | ||||||
| chr12:25063521
|
A | T | 8 | a0002c0002t0001g0063a0003c0003t0001g0061a0003c0003t0001g0062others(5): Show | 10 | HG01168.hp1 HG01169.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.-303-199A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 3/21 | chr12 | 25063521 | ||||||
| chr12:25063583
|
T | A | 7 | a0001c0001t0001g0312a0002c0002t0001g0001a0002c0002t0001g0027others(4): Show | 9 | HG02109.hp1 HG02630.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.-303-137T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 3/21 | chr12 | 25063583 | ||||||
| chr12:25063684
|
C | CT | 17 | a0001c0001t0001g0025a0002c0002t0001g0280a0003c0003t0002g0201others(14): Show | 18 | HG01081.hp2 HG01106.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.-303-33dupT | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr12 | 25063684 | |||||
| chr12:25063690
|
A | C | 6 | a0002c0002t0001g0171a0002c0002t0001g0172a0002c0002t0001g0174others(3): Show | 6 | HG02257.hp1 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-303-30A>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 3/21 | chr12 | 25063690 | ||||||
| chr12:25063856
|
G | A | 1 | a0002c0002t0001g0207 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-207+40G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25063856 | ||||||
| chr12:25064029
|
G | A | 5 | a0002c0002t0001g0308a0002c0002t0001g0309a0002c0002t0001g0310others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-207+213G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25064029 | ||||||
| chr12:25064040
|
C | T | 9 | a0001c0001t0001g0025a0002c0002t0001g0280a0003c0003t0002g0201others(6): Show | 10 | HG01081.hp2 HG01106.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.-207+224C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25064040 | ||||||
| chr12:25064351
|
C | G | 16 | a0001c0001t0001g0072a0001c0001t0001g0312a0002c0002t0001g0006others(13): Show | 17 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-207+535C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25064351 | ||||||
| chr12:25064415
|
T | C | 119 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0045others(116): Show | 125 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-207+599T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25064415 | ||||||
| chr12:25064507
|
C | T | 3 | a0004c0004t0001g0002a0004c0004t0001g0067a0004c0004t0001g0140 | 5 | HG01168.hp1 HG01169.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-207+691C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25064507 | ||||||
| chr12:25064618
|
T | G | 119 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(116): Show | 126 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.-207+802T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25064618 | ||||||
| chr12:25064719
|
G | A | 117 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0045others(114): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.-207+903G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25064719 | ||||||
| chr12:25064822
|
G | A | 5 | a0002c0002t0001g0006a0002c0002t0001g0037a0002c0002t0001g0069others(2): Show | 6 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.-207+1006G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25064822 | ||||||
| chr12:25064828
|
G | A | 11 | a0001c0001t0001g0020a0001c0001t0001g0320a0001c0001t0001g0321others(8): Show | 11 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.-207+1012G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25064828 | ||||||
| chr12:25064840
|
T | A | 176 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0039others(173): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.-207+1024T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25064840 | ||||||
| chr12:25064963
|
A | G | 1 | a0003c0003t0009g0031 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-207+1147A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25064963 | ||||||
| chr12:25065026
|
G | C | 1 | a0004c0004t0001g0016 | 2 | HG00280.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.-207+1210G>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25065026 | ||||||
| chr12:25065089
|
C | CA | 125 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0039others(122): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.-206-1264dupA | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 25065089 | |||||
| chr12:25065100
|
A | G | 4 | a0001c0001t0001g0072a0001c0001t0001g0312a0002c0002t0001g0141others(1): Show | 4 | HG01261.hp1 HG02258.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-206-1265A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25065100 | ||||||
| chr12:25065135
|
CACAGTTC others(1): Show |
C | 12 | a0001c0001t0001g0012a0001c0001t0001g0029a0001c0001t0001g0114others(9): Show | 13 | HG00673.hp1 HG00741.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-206-1228_-206-122 others(12): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr12 | 25065135 | |||||
| chr12:25065243
|
C | T | 2 | a0006c0005t0001g0065a0006c0005t0001g0066 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-206-1122C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25065243 | ||||||
| chr12:25065406
|
A | G | 120 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0045others(117): Show | 128 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.-206-959A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25065406 | ||||||
| chr12:25065590
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-206-775T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25065590 | ||||||
| chr12:25065594
|
T | G | 119 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0045others(116): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.-206-771T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25065594 | ||||||
| chr12:25065640
|
A | G | 7 | a0003c0003t0004g0314a0003c0003t0004g0315a0003c0003t0004g0316others(4): Show | 7 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(4): Show |
intron_variant | MODIFIER | c.-206-725A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25065640 | ||||||
| chr12:25065949
|
C | T | 29 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0001g0134others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.-206-416C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25065949 | ||||||
| chr12:25066012
|
C | T | 2 | a0003c0003t0003g0060a0006c0005t0001g0059 | 2 | HG02109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-206-353C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25066012 | ||||||
| chr12:25066014
|
C | T | 4 | a0001c0001t0001g0072a0001c0001t0001g0312a0002c0002t0001g0141others(1): Show | 4 | HG01261.hp1 HG02258.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-206-351C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25066014 | ||||||
| chr12:25066260
|
T | C | 3 | a0003c0003t0003g0156a0003c0003t0008g0161a0006c0005t0001g0157 | 3 | HG02145.hp1 HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-206-105T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 4/21 | chr12 | 25066260 | ||||||
| chr12:25066665
|
C | CT | 7 | a0001c0001t0001g0089a0001c0001t0001g0248a0001c0001t0001g0249others(4): Show | 7 | HG00544.hp2 HG01255.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.-59+168dupT | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr12 | 25066665 | |||||
| chr12:25066742
|
C | T | 1 | a0007c0009t0001g0200 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-59+230C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25066742 | ||||||
| chr12:25066794
|
C | T | 4 | a0001c0001t0001g0072a0001c0001t0001g0312a0002c0002t0001g0141others(1): Show | 4 | HG01261.hp1 HG02258.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-59+282C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25066794 | ||||||
| chr12:25066894
|
C | T | 2 | a0002c0002t0001g0295a0002c0002t0001g0296 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-59+382C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25066894 | ||||||
| chr12:25066922
|
T | C | 130 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0039others(127): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-59+410T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25066922 | ||||||
| chr12:25066941
|
C | T | 1 | a0002c0002t0001g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-59+429C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25066941 | ||||||
| chr12:25066995
|
A | G | 300 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-59+483A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25066995 | ||||||
| chr12:25067096
|
G | A | 2 | a0002c0002t0001g0308a0002c0002t0001g0309 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-59+584G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25067096 | ||||||
| chr12:25067317
|
G | A | 16 | a0001c0001t0001g0025a0002c0002t0001g0280a0003c0003t0001g0159others(13): Show | 16 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-59+805G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25067317 | ||||||
| chr12:25067388
|
G | A | 12 | a0001c0001t0001g0020a0001c0001t0001g0320a0001c0001t0001g0321others(9): Show | 12 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.-59+876G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25067388 | ||||||
| chr12:25067404
|
C | T | 2 | a0001c0001t0001g0198a0001c0001t0001g0277 | 2 | HG02056.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-59+892C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25067404 | ||||||
| chr12:25067438
|
G | A | 8 | a0001c0001t0001g0039a0001c0001t0001g0045a0002c0002t0001g0043others(5): Show | 10 | HG01168.hp1 HG01169.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-59+926G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25067438 | ||||||
| chr12:25067465
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-59+953A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25067465 | ||||||
| chr12:25067498
|
A | G | 2 | a0002c0002t0001g0295a0002c0002t0001g0296 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-59+986A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25067498 | ||||||
| chr12:25067530
|
A | G | 8 | a0001c0001t0001g0039a0001c0001t0001g0045a0002c0002t0001g0043others(5): Show | 10 | HG01168.hp1 HG01169.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-59+1018A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25067530 | ||||||
| chr12:25067703
|
TCTGTCAC others(1): Show |
T | 4 | a0002c0002t0001g0308a0002c0002t0001g0309a0002c0002t0001g0310others(1): Show | 4 | HG02630.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-59+1193_-59+1200d others(10): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr12 | 25067703 | |||||
| chr12:25067895
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-59+1383C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25067895 | ||||||
| chr12:25068162
|
G | A | 8 | a0001c0001t0001g0020a0001c0001t0001g0320a0001c0001t0001g0321others(5): Show | 8 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58-1188G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25068162 | ||||||
| chr12:25068323
|
G | A | 1 | a0001c0001t0002g0281 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-58-1027G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25068323 | ||||||
| chr12:25068331
|
T | C | 1 | a0005c0006t0007g0302 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-58-1019T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25068331 | ||||||
| chr12:25068638
|
G | A | 4 | a0002c0002t0001g0308a0002c0002t0001g0309a0002c0002t0001g0310others(1): Show | 4 | HG02630.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58-712G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25068638 | ||||||
| chr12:25068640
|
G | A | 31 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0001g0134others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.-58-710G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25068640 | ||||||
| chr12:25068934
|
C | A | 1 | a0003c0003t0001g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-58-416C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25068934 | ||||||
| chr12:25069090
|
A | G | 297 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(294): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.-58-260A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25069090 | ||||||
| chr12:25069267
|
G | A | 4 | a0002c0002t0001g0308a0002c0002t0001g0309a0002c0002t0001g0310others(1): Show | 4 | HG02630.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58-83G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25069267 | ||||||
| chr12:25069335
|
A | G | 11 | a0002c0002t0001g0006a0002c0002t0001g0037a0002c0002t0001g0038others(8): Show | 12 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.-58-15A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 5/21 | chr12 | 25069335 | ||||||
| chr12:25069809
|
A | T | 1 | a0002c0002t0001g0247 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.24+378A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25069809 | ||||||
| chr12:25069854
|
C | T | 12 | a0001c0001t0001g0020a0001c0001t0001g0320a0001c0001t0001g0321others(9): Show | 12 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.24+423C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25069854 | ||||||
| chr12:25069866
|
T | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0320a0001c0001t0001g0321others(5): Show | 8 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.24+435T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25069866 | ||||||
| chr12:25069894
|
A | G | 124 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0039others(121): Show | 127 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.24+463A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25069894 | ||||||
| chr12:25069903
|
C | T | 4 | a0002c0002t0001g0308a0002c0002t0001g0309a0002c0002t0001g0310others(1): Show | 4 | HG02630.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.24+472C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25069903 | ||||||
| chr12:25070156
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.24+725T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25070156 | ||||||
| chr12:25070342
|
G | T | 1 | a0003c0003t0001g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.24+911G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25070342 | ||||||
| chr12:25070416
|
T | A | 114 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0045others(111): Show | 119 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.24+985T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25070416 | ||||||
| chr12:25070442
|
A | C | 2 | a0002c0002t0001g0295a0002c0002t0001g0296 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.24+1011A>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25070442 | ||||||
| chr12:25070740
|
C | G | 1 | a0002c0002t0001g0071 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.24+1309C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25070740 | ||||||
| chr12:25070784
|
G | C | 85 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(82): Show | 90 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.24+1353G>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25070784 | ||||||
| chr12:25070895
|
C | G | 1 | a0003c0003t0003g0049 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.24+1464C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25070895 | ||||||
| chr12:25071057
|
A | T | 31 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0001g0134others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.24+1626A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25071057 | ||||||
| chr12:25071152
|
C | G | 136 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(133): Show | 144 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.24+1721C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25071152 | ||||||
| chr12:25071200
|
C | CAAAA | 7 | a0001c0001t0001g0025a0002c0002t0001g0280a0003c0003t0002g0203others(4): Show | 8 | HG01081.hp2 HG01106.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.24+1771_24+1774dup others(4): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25071200 | |||||
| chr12:25071317
|
G | A | 1 | a0004c0004t0001g0209 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.24+1886G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25071317 | ||||||
| chr12:25071332
|
A | C | 263 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(260): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.24+1901A>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25071332 | ||||||
| chr12:25071546
|
G | T | 9 | a0005c0006t0001g0298a0005c0006t0001g0299a0005c0006t0001g0300others(6): Show | 9 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.24+2115G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25071546 | ||||||
| chr12:25071549
|
C | T | 12 | a0001c0001t0001g0020a0001c0001t0001g0320a0001c0001t0001g0321others(9): Show | 12 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.24+2118C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25071549 | ||||||
| chr12:25071740
|
T | G | 115 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0045others(112): Show | 120 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.24+2309T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25071740 | ||||||
| chr12:25071792
|
A | AT | 77 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0039others(74): Show | 80 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.24+2376dupT | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25071792 | |||||
| chr12:25071879
|
G | A | 7 | a0001c0001t0001g0025a0002c0002t0001g0280a0003c0003t0002g0203others(4): Show | 8 | HG01081.hp2 HG01106.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.24+2448G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25071879 | ||||||
| chr12:25071929
|
C | T | 82 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(79): Show | 87 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.24+2498C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25071929 | ||||||
| chr12:25071941
|
C | T | 2 | a0002c0002t0001g0295a0002c0002t0001g0296 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.24+2510C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25071941 | ||||||
| chr12:25071969
|
C | T | 12 | a0001c0001t0001g0020a0001c0001t0001g0320a0001c0001t0001g0321others(9): Show | 12 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.24+2538C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25071969 | ||||||
| chr12:25072108
|
G | C | 32 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0001g0134others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.24+2677G>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25072108 | ||||||
| chr12:25072130
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.24+2699G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25072130 | ||||||
| chr12:25072159
|
G | A | 3 | a0005c0006t0007g0302a0005c0006t0007g0304a0005c0006t0011g0303 | 3 | HG01891.hp1 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.24+2728G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25072159 | ||||||
| chr12:25072197
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.24+2766T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25072197 | ||||||
| chr12:25072241
|
A | G | 115 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0045others(112): Show | 120 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.24+2810A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25072241 | ||||||
| chr12:25072245
|
G | A | 32 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0001g0134others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.24+2814G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25072245 | ||||||
| chr12:25072379
|
A | G | 117 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0045others(114): Show | 122 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.24+2948A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25072379 | ||||||
| chr12:25072401
|
G | A | 115 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0045others(112): Show | 120 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.24+2970G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25072401 | ||||||
| chr12:25072462
|
G | T | 1 | a0001c0001t0001g0146 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.24+3031G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25072462 | ||||||
| chr12:25072528
|
C | G | 1 | a0001c0001t0001g0137 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.24+3097C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25072528 | ||||||
| chr12:25072561
|
A | G | 7 | a0001c0001t0001g0025a0002c0002t0001g0280a0003c0003t0002g0203others(4): Show | 8 | HG01081.hp2 HG01106.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.24+3130A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25072561 | ||||||
| chr12:25072585
|
G | A | 32 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0001g0134others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.24+3154G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25072585 | ||||||
| chr12:25072600
|
T | C | 8 | a0001c0001t0001g0020a0001c0001t0001g0320a0001c0001t0001g0321others(5): Show | 8 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.24+3169T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25072600 | ||||||
| chr12:25072647
|
A | C | 323 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(320): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.24+3216A>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25072647 | ||||||
| chr12:25072789
|
C | T | 1 | a0003c0003t0002g0189 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.24+3358C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25072789 | ||||||
| chr12:25072805
|
G | C | 3 | a0002c0002t0001g0171a0002c0002t0001g0172a0002c0002t0001g0176 | 3 | HG02257.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.24+3374G>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25072805 | ||||||
| chr12:25073037
|
T | C | 4 | a0002c0002t0001g0171a0002c0002t0001g0172a0002c0002t0001g0176others(1): Show | 4 | HG02257.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.24+3606T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25073037 | ||||||
| chr12:25073083
|
G | C | 165 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0025others(162): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.24+3652G>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25073083 | ||||||
| chr12:25073126
|
A | G | 2 | a0003c0003t0001g0243a0006c0005t0001g0244 | 2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.24+3695A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25073126 | ||||||
| chr12:25073156
|
C | T | 32 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0001g0134others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.24+3725C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25073156 | ||||||
| chr12:25073370
|
C | T | 8 | a0001c0001t0001g0020a0001c0001t0001g0320a0001c0001t0001g0321others(5): Show | 8 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.24+3939C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25073370 | ||||||
| chr12:25073382
|
G | T | 4 | a0002c0002t0001g0171a0002c0002t0001g0172a0002c0002t0001g0176others(1): Show | 4 | HG02257.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.24+3951G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25073382 | ||||||
| chr12:25073399
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.24+3968G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25073399 | ||||||
| chr12:25073454
|
T | C | 84 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(81): Show | 89 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.24+4023T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25073454 | ||||||
| chr12:25073564
|
A | G | 7 | a0001c0001t0001g0025a0002c0002t0001g0280a0003c0003t0002g0203others(4): Show | 8 | HG01081.hp2 HG01106.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.24+4133A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25073564 | ||||||
| chr12:25073611
|
C | G | 111 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0042others(108): Show | 115 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.24+4180C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25073611 | ||||||
| chr12:25073643
|
C | T | 1 | a0002c0002t0001g0001 | 3 | HG02109.hp1 HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.24+4212C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25073643 | ||||||
| chr12:25073762
|
CAA | C | 84 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(81): Show | 89 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.24+4333_24+4334del others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25073762 | |||||
| chr12:25073811
|
C | T | 94 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(91): Show | 99 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.24+4380C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25073811 | ||||||
| chr12:25073896
|
G | C | 32 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0001g0134others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.24+4465G>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25073896 | ||||||
| chr12:25074104
|
A | G | 19 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0320others(16): Show | 20 | HG00733.hp2 HG01081.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.24+4673A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25074104 | ||||||
| chr12:25074181
|
T | C | 2 | a0002c0002t0001g0295a0002c0002t0001g0296 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.24+4750T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25074181 | ||||||
| chr12:25074355
|
C | T | 2 | a0002c0002t0001g0295a0002c0002t0001g0296 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.25-4889C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25074355 | ||||||
| chr12:25074368
|
T | C | 130 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0025others(127): Show | 135 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.25-4876T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25074368 | ||||||
| chr12:25074415
|
C | T | 84 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(81): Show | 89 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.25-4829C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25074415 | ||||||
| chr12:25074433
|
C | A | 32 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0001g0134others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.25-4811C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25074433 | ||||||
| chr12:25074481
|
C | G | 112 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0042others(109): Show | 117 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.25-4763C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25074481 | ||||||
| chr12:25074507
|
G | A | 2 | a0002c0002t0001g0295a0002c0002t0001g0296 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.25-4737G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25074507 | ||||||
| chr12:25074539
|
G | A | 258 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(255): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.25-4705G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25074539 | ||||||
| chr12:25074604
|
C | T | 27 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0237others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.25-4640C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25074604 | ||||||
| chr12:25074672
|
A | G | 1 | a0005c0006t0007g0302 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.25-4572A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25074672 | ||||||
| chr12:25074694
|
G | A | 7 | a0001c0001t0001g0025a0002c0002t0001g0280a0003c0003t0002g0203others(4): Show | 8 | HG01081.hp2 HG01106.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.25-4550G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25074694 | ||||||
| chr12:25074768
|
A | G | 2 | a0002c0002t0001g0047a0002c0002t0001g0048 | 2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.25-4476A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25074768 | ||||||
| chr12:25074783
|
A | C | 113 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0042others(110): Show | 118 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.25-4461A>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25074783 | ||||||
| chr12:25074800
|
T | A | 2 | a0002c0002t0001g0295a0002c0002t0001g0296 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.25-4444T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25074800 | ||||||
| chr12:25074803
|
G | A | 1 | a0002c0002t0001g0174 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.25-4441G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25074803 | ||||||
| chr12:25075017
|
T | C | 10 | a0005c0006t0001g0298a0005c0006t0001g0299a0005c0006t0001g0300others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.25-4227T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25075017 | ||||||
| chr12:25075058
|
G | A | 4 | a0004c0004t0001g0002a0004c0004t0001g0040a0004c0004t0001g0067others(1): Show | 6 | HG01168.hp1 HG01169.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.25-4186G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25075058 | ||||||
| chr12:25075218
|
G | A | 155 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0039others(152): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.25-4026G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25075218 | ||||||
| chr12:25075274
|
C | A | 10 | a0005c0006t0001g0298a0005c0006t0001g0299a0005c0006t0001g0300others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.25-3970C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25075274 | ||||||
| chr12:25075521
|
C | CATGTGTG others(5): Show |
2 | a0002c0002t0001g0295a0002c0002t0001g0296 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.25-3723_25-3722ins others(12): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25075521 | ||||||
| chr12:25075521
|
C | CGT | 104 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(101): Show | 111 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.25-3688_25-3687dup others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25075521 | |||||
| chr12:25075521
|
C | CGTGT | 9 | a0001c0001t0001g0085a0001c0001t0001g0112a0001c0001t0001g0224others(6): Show | 10 | HG00280.hp1 HG01175.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.25-3690_25-3687dup others(4): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25075521 | |||||
| chr12:25075521
|
C | CGTGTGT | 7 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0143others(4): Show | 7 | HG00621.hp1 HG01261.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.25-3692_25-3687dup others(6): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25075521 | |||||
| chr12:25075521
|
C | CGTGTGTG others(1): Show |
3 | a0001c0001t0001g0045a0002c0002t0001g0160a0002c0002t0001g0226 | 3 | HG02922.hp2 NA18949.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.25-3694_25-3687dup others(8): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25075521 | |||||
| chr12:25075521
|
C | CGTGTGTG others(3): Show |
1 | a0002c0002t0001g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.25-3696_25-3687dup others(10): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25075521 | |||||
| chr12:25075521
|
CGT | C | 32 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0263others(29): Show | 34 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.25-3688_25-3687del others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25075521 | |||||
| chr12:25075521
|
CGTGT | C | 6 | a0001c0001t0001g0253a0002c0002t0001g0052a0003c0003t0003g0049others(3): Show | 6 | HG00733.hp1 HG02109.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.25-3690_25-3687del others(4): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25075521 | |||||
| chr12:25075521
|
CGTGTGT | C | 2 | a0002c0002t0001g0001a0002c0002t0001g0027 | 4 | HG02109.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.25-3692_25-3687del others(6): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25075521 | |||||
| chr12:25075521
|
CGTGTGTG others(1): Show |
C | 10 | a0005c0006t0001g0298a0005c0006t0001g0299a0005c0006t0001g0300others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.25-3694_25-3687del others(8): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25075521 | |||||
| chr12:25075548
|
GTGTGTGT others(3): Show |
G | 1 | a0002c0002t0001g0179 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.25-3688_25-3679del others(10): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25075548 | |||||
| chr12:25075550
|
GTGTGTGT others(1): Show |
G | 14 | a0001c0001t0001g0121a0001c0001t0001g0134a0002c0002t0010g0030others(11): Show | 14 | HG00408.hp2 HG00609.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.25-3686_25-3679del others(8): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25075550 | |||||
| chr12:25075552
|
GTGTGTA | G | 22 | a0001c0001t0001g0126a0003c0003t0002g0079a0003c0003t0002g0127others(19): Show | 24 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.25-3686_25-3681del others(6): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25075552 | |||||
| chr12:25075556
|
GTA | G | 20 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0138others(17): Show | 20 | HG00323.hp2 HG01361.hp2 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.25-3686_25-3685del others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25075556 | |||||
| chr12:25075558
|
A | G | 98 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0039others(95): Show | 100 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.25-3686A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25075558 | ||||||
| chr12:25075841
|
CTTTA | C | 3 | a0005c0006t0007g0302a0005c0006t0007g0304a0005c0006t0011g0303 | 3 | HG01891.hp1 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.25-3399_25-3396del others(4): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25075841 | |||||
| chr12:25075927
|
T | C | 1 | a0002c0002t0001g0289 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.25-3317T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25075927 | ||||||
| chr12:25075966
|
T | C | 112 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0042others(109): Show | 117 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.25-3278T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25075966 | ||||||
| chr12:25076041
|
G | T | 4 | a0002c0002t0001g0308a0002c0002t0001g0309a0002c0002t0001g0310others(1): Show | 4 | HG02630.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-3203G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25076041 | ||||||
| chr12:25076078
|
C | CA | 18 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0001g0134others(15): Show | 18 | HG00408.hp2 HG00609.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.25-3156dupA | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25076078 | |||||
| chr12:25076078
|
C | T | 14 | a0001c0001t0001g0020a0001c0001t0001g0320a0001c0001t0001g0321others(11): Show | 14 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.25-3166C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25076078 | ||||||
| chr12:25076099
|
T | C | 32 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0001g0134others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.25-3145T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25076099 | ||||||
| chr12:25076371
|
A | G | 91 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(88): Show | 97 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.25-2873A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25076371 | ||||||
| chr12:25076388
|
G | A | 8 | a0001c0001t0001g0020a0001c0001t0001g0320a0001c0001t0001g0321others(5): Show | 8 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.25-2856G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25076388 | ||||||
| chr12:25076406
|
C | A | 1 | a0001c0001t0001g0290 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.25-2838C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25076406 | ||||||
| chr12:25076671
|
G | A | 257 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(254): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.25-2573G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25076671 | ||||||
| chr12:25076898
|
C | T | 1 | a0001c0001t0001g0306 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.25-2346C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25076898 | ||||||
| chr12:25077048
|
T | C | 5 | a0003c0003t0002g0079a0003c0003t0005g0032a0003c0003t0005g0033others(2): Show | 5 | HG00099.hp1 HG01099.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-2196T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077048 | ||||||
| chr12:25077148
|
C | T | 8 | a0001c0001t0001g0020a0001c0001t0001g0320a0001c0001t0001g0321others(5): Show | 8 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.25-2096C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077148 | ||||||
| chr12:25077155
|
C | T | 12 | a0001c0001t0001g0020a0001c0001t0001g0320a0001c0001t0001g0321others(9): Show | 12 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.25-2089C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077155 | ||||||
| chr12:25077161
|
G | A | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | NA18948.hp2 NA18954.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-2083G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077161 | ||||||
| chr12:25077174
|
C | CATATATA others(17): Show |
1 | a0001c0001t0001g0138 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.25-2050_25-2027dup others(24): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077174 | |||||
| chr12:25077184
|
T | TCA | 4 | a0002c0002t0001g0308a0002c0002t0001g0309a0002c0002t0001g0310others(1): Show | 4 | HG02630.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-2060_25-2059ins others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077184 | ||||||
| chr12:25077185
|
G | GATATATA others(48): Show |
2 | a0001c0001t0001g0112a0001c0001t0001g0251 | 2 | NA18955.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.25-2051_25-2050ins others(55): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077185 | |||||
| chr12:25077185
|
G | T | 4 | a0002c0002t0001g0308a0002c0002t0001g0309a0002c0002t0001g0310others(1): Show | 4 | HG02630.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-2059G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077185 | ||||||
| chr12:25077185
|
GAT | G | 80 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(77): Show | 85 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.25-2050_25-2049del others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077185 | |||||
| chr12:25077187
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.25-2057T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077187 | ||||||
| chr12:25077187
|
T | TATATATG others(140): Show |
1 | a0001c0001t0001g0094 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.25-2051_25-2050ins others(147): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077187 | |||||
| chr12:25077198
|
A | T | 1 | a0001c0001t0001g0094 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.25-2046A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077198 | ||||||
| chr12:25077198
|
AAT | A | 82 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(79): Show | 87 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.25-2037_25-2036del others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077198 | |||||
| chr12:25077207
|
A | G | 15 | a0001c0001t0001g0094a0003c0003t0002g0079a0003c0003t0002g0201others(12): Show | 15 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.25-2037A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077207 | ||||||
| chr12:25077208
|
T | A | 15 | a0001c0001t0001g0094a0003c0003t0002g0079a0003c0003t0002g0201others(12): Show | 15 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.25-2036T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077208 | ||||||
| chr12:25077209
|
G | GAT | 29 | a0001c0001t0001g0020a0001c0001t0001g0092a0001c0001t0001g0121others(26): Show | 29 | HG00408.hp2 HG00609.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.25-2028_25-2027dup others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077209 | |||||
| chr12:25077209
|
G | T | 15 | a0001c0001t0001g0094a0003c0003t0002g0079a0003c0003t0002g0201others(12): Show | 15 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.25-2035G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077209 | ||||||
| chr12:25077220
|
A | AAT | 101 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(98): Show | 108 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.25-2017_25-2016dup others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077220 | |||||
| chr12:25077220
|
A | AATATATA others(17): Show |
89 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0042others(86): Show | 92 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.25-2016_25-2015ins others(24): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077220 | |||||
| chr12:25077220
|
A | AATATATA others(269): Show |
1 | a0004c0004t0001g0209 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.25-2016_25-2015ins others(276): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077220 | |||||
| chr12:25077220
|
A | AATATATA others(311): Show |
1 | a0001c0001t0001g0221 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.25-2016_25-2015ins others(318): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077220 | |||||
| chr12:25077220
|
A | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0251 | 2 | NA18955.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.25-2024A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077220 | ||||||
| chr12:25077220
|
AATATATA others(2): Show |
A | 11 | a0003c0003t0002g0201a0003c0003t0002g0202a0003c0003t0004g0314others(8): Show | 11 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.25-2015_25-2007del others(9): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077220 | |||||
| chr12:25077229
|
G | A | 5 | a0001c0001t0001g0094a0001c0001t0001g0211a0001c0001t0001g0284others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-2015G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077229 | ||||||
| chr12:25077229
|
GAT | G | 3 | a0002c0002t0001g0308a0002c0002t0001g0309a0002c0002t0001g0310 | 3 | HG03195.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.25-2006_25-2005del others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077229 | |||||
| chr12:25077230
|
A | T | 5 | a0001c0001t0001g0094a0001c0001t0001g0211a0001c0001t0001g0284others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-2014A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077230 | ||||||
| chr12:25077231
|
T | A | 3 | a0003c0003t0002g0079a0003c0003t0005g0032a0003c0003t0005g0033 | 3 | HG00099.hp1 HG01099.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.25-2013T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077231 | ||||||
| chr12:25077231
|
T | G | 5 | a0001c0001t0001g0094a0001c0001t0001g0211a0001c0001t0001g0284others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-2013T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077231 | ||||||
| chr12:25077231
|
T | TATATATG others(11): Show |
1 | a0002c0002t0001g0311 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.25-2007_25-2006ins others(18): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077231 | |||||
| chr12:25077240
|
GAA | G | 3 | a0003c0003t0002g0079a0003c0003t0005g0032a0003c0003t0005g0033 | 3 | HG00099.hp1 HG01099.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.25-2002_25-2001del others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077240 | |||||
| chr12:25077242
|
A | T | 35 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0253others(32): Show | 37 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.25-2002A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077242 | ||||||
| chr12:25077242
|
AAT | A | 17 | a0001c0001t0001g0020a0001c0001t0001g0322a0001c0001t0001g0323others(14): Show | 17 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.25-1993_25-1992del others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077242 | |||||
| chr12:25077244
|
T | TATATGAA | 34 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0253others(31): Show | 36 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.25-1996_25-1995ins others(7): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077244 | |||||
| chr12:25077244
|
T | TATATGAA others(57): Show |
1 | a0004c0004t0001g0254 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.25-1996_25-1995ins others(64): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077244 | |||||
| chr12:25077252
|
T | TCATATAT others(324): Show |
1 | a0001c0001t0001g0211 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.25-1992_25-1991ins others(331): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077252 | ||||||
| chr12:25077253
|
G | C | 1 | a0001c0001t0001g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.25-1991G>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077253 | ||||||
| chr12:25077253
|
G | GATATATA others(298): Show |
1 | a0004c0004t0001g0067 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25-1983_25-1982ins others(305): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077253 | |||||
| chr12:25077255
|
T | A | 22 | a0001c0001t0001g0092a0001c0001t0001g0121a0001c0001t0001g0126others(19): Show | 22 | HG00408.hp2 HG00609.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.25-1989T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077255 | ||||||
| chr12:25077262
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0251 | 2 | NA18955.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.25-1982A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077262 | ||||||
| chr12:25077263
|
T | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0251 | 2 | NA18955.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.25-1981T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077263 | ||||||
| chr12:25077264
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0251 | 2 | NA18955.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.25-1980G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077264 | ||||||
| chr12:25077266
|
A | AAT | 120 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(117): Show | 126 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.25-1971_25-1970dup others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(529): Show |
2 | a0002c0002t0001g0043a0002c0002t0001g0044 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(536): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(293): Show |
1 | a0002c0002t0001g0196 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(300): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(350): Show |
1 | a0001c0001t0001g0250 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(357): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(293): Show |
2 | a0002c0002t0001g0183a0002c0002t0001g0233 | 2 | NA18984.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(300): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(324): Show |
2 | a0004c0004t0001g0002a0004c0004t0001g0140 | 4 | HG01168.hp1 HG01169.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(331): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(324): Show |
1 | a0004c0004t0001g0040 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(331): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(306): Show |
1 | a0002c0002t0003g0283 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(313): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(243): Show |
1 | a0001c0001t0001g0138 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(250): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(278): Show |
2 | a0001c0001t0001g0206a0001c0001t0001g0268 | 2 | NA18954.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(285): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(302): Show |
1 | a0001c0001t0001g0222 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(309): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(350): Show |
1 | a0001c0001t0001g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(357): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(286): Show |
1 | a0003c0003t0001g0243 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(293): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(138): Show |
3 | a0001c0001t0001g0186a0001c0001t0001g0194a0001c0001t0001g0223 | 3 | HG00639.hp2 HG01943.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(145): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(162): Show |
1 | a0004c0004t0001g0190 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(169): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(186): Show |
3 | a0001c0001t0001g0185a0001c0001t0001g0293a0009c0012t0001g0193 | 3 | HG04204.hp2 NA18950.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(193): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(199): Show |
1 | a0001c0001t0001g0191 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(206): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(210): Show |
3 | a0001c0001t0001g0192a0002c0002t0001g0245a0003c0003t0003g0021 | 3 | NA18941.hp2 NA19004.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(217): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(223): Show |
2 | a0001c0001t0001g0198a0001c0001t0001g0277 | 2 | HG02056.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(230): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(234): Show |
9 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(6): Show | 9 | HG00140.hp1 HG01070.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(241): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(258): Show |
2 | a0001c0001t0001g0227a0002c0002t0001g0199 | 2 | HG01934.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(265): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(282): Show |
1 | a0002c0002t0001g0231 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(289): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(306): Show |
1 | a0003c0003t0002g0184 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(313): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(258): Show |
1 | a0001c0001t0001g0228 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(265): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(206): Show |
2 | a0002c0002t0001g0207a0004c0004t0001g0004 | 3 | HG01081.hp2 HG01106.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(213): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(182): Show |
1 | a0001c0001t0001g0089 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(189): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(206): Show |
1 | a0001c0001t0006g0195 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(213): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(230): Show |
1 | a0001c0008t0001g0219 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(237): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(254): Show |
6 | a0001c0001t0001g0204a0001c0001t0001g0218a0001c0001t0001g0246others(3): Show | 6 | HG00423.hp2 HG01074.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(261): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(278): Show |
15 | a0001c0001t0001g0143a0001c0001t0001g0215a0001c0001t0001g0216others(12): Show | 15 | HG00544.hp2 HG00621.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(285): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(302): Show |
3 | a0001c0001t0001g0306a0002c0002t0001g0235a0003c0003t0003g0158 | 3 | HG02040.hp1 HG06807.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(309): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(326): Show |
1 | a0002c0002t0006g0234 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(333): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(350): Show |
2 | a0001c0001t0001g0068a0006c0005t0001g0244 | 2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(357): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(202): Show |
1 | a0001c0001t0001g0220 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(209): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(274): Show |
1 | a0001c0001t0001g0205 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(281): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(276): Show |
2 | a0001c0001t0001g0248a0002c0002t0006g0210 | 2 | HG02080.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(283): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(260): Show |
1 | a0001c0001t0001g0224 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(267): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(232): Show |
1 | a0002c0002t0001g0179 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(239): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(250): Show |
1 | a0002c0002t0001g0226 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(257): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(278): Show |
1 | a0001c0001t0001g0242 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(285): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(230): Show |
1 | a0001c0001t0001g0269 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(237): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(4): Show |
2 | a0002c0002t0001g0160a0002c0002t0001g0174 | 2 | HG03130.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(11): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(19): Show |
1 | a0001c0001t0001g0252 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(26): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(57): Show |
1 | a0004c0004t0001g0278 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(64): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(6): Show |
1 | a0001c0001t0001g0221 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(13): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(368): Show |
1 | a0001c0001t0001g0045 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(375): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(529): Show |
1 | a0001c0001t0001g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(536): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(258): Show |
1 | a0006c0005t0001g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(265): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(226): Show |
1 | a0001c0001t0001g0007 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(233): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(186): Show |
1 | a0001c0001t0001g0197 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(193): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(254): Show |
2 | a0001c0001t0001g0042a0001c0001t0001g0084 | 2 | HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(261): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(278): Show |
2 | a0001c0001t0001g0082a0002c0002t0001g0083 | 2 | HG03669.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(285): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(230): Show |
2 | a0001c0001t0001g0081a0001c0001t0001g0085 | 2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(237): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(254): Show |
3 | a0001c0001t0001g0080a0001c0001t0001g0225a0002c0002t0001g0008 | 4 | HG01257.hp1 HG01258.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(261): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(278): Show |
4 | a0001c0001t0002g0281a0001c0007t0001g0129a0001c0007t0001g0130others(1): Show | 4 | NA18960.hp1 NA18968.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(285): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(274): Show |
2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | NA18947.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(281): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(118): Show |
1 | a0006c0005t0001g0064 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(125): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(280): Show |
1 | a0001c0001t0001g0284 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(287): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(374): Show |
1 | a0002c0002t0001g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.25-1970_25-1969ins others(381): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(54): Show |
4 | a0002c0002t0001g0308a0002c0002t0001g0309a0002c0002t0001g0310others(1): Show | 4 | HG02630.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(61): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATA others(232): Show |
2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG00673.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(239): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATG others(114): Show |
1 | a0002c0002t0001g0295 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.25-1972_25-1971ins others(121): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | AATATATG others(138): Show |
1 | a0002c0002t0001g0296 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.25-1972_25-1971ins others(145): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077266
|
A | T | 36 | a0001c0001t0001g0112a0001c0001t0001g0121a0001c0001t0001g0126others(33): Show | 36 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.25-1978A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077266 | ||||||
| chr12:25077266
|
AAT | A | 3 | a0003c0003t0002g0079a0003c0003t0005g0032a0003c0003t0005g0033 | 3 | HG00099.hp1 HG01099.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.25-1971_25-1970del others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077266 | |||||
| chr12:25077273
|
A | ATATGATA others(516): Show |
4 | a0001c0001t0001g0020a0001c0001t0001g0322a0001c0001t0001g0323others(1): Show | 4 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-1970_25-1969ins others(523): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077273 | |||||
| chr12:25077275
|
G | GATATATA others(472): Show |
1 | a0001c0001t0001g0320 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.25-1968_25-1967ins others(479): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077275 | |||||
| chr12:25077277
|
A | AAT | 22 | a0001c0001t0001g0045a0001c0001t0001g0089a0001c0001t0001g0185others(19): Show | 24 | HG00639.hp2 HG01168.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.25-1960_25-1959dup others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077277 | |||||
| chr12:25077277
|
A | AATATATA others(13): Show |
1 | a0002c0002t0001g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.25-1950_25-1949ins others(20): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077277 | |||||
| chr12:25077277
|
A | G | 15 | a0001c0001t0001g0068a0001c0001t0001g0084a0001c0001t0001g0206others(12): Show | 15 | HG01070.hp1 HG01934.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.25-1967A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077277 | ||||||
| chr12:25077277
|
A | T | 113 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0042others(110): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.25-1967A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077277 | ||||||
| chr12:25077277
|
AAT | A | 11 | a0003c0003t0002g0201a0003c0003t0002g0202a0003c0003t0004g0314others(8): Show | 11 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.25-1960_25-1959del others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077277 | |||||
| chr12:25077285
|
T | TATGAAAT others(109): Show |
1 | a0001c0001t0001g0005 | 2 | HG01106.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.25-1959_25-1958ins others(116): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077285 | ||||||
| chr12:25077285
|
T | TGA | 3 | a0001c0001t0001g0039a0002c0002t0001g0043a0002c0002t0001g0044 | 3 | HG02895.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.25-1958_25-1957dup others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077285 | |||||
| chr12:25077286
|
G | A | 5 | a0001c0001t0001g0005a0002c0002t0001g0308a0002c0002t0001g0309others(2): Show | 6 | HG01106.hp2 HG01192.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.25-1958G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077286 | ||||||
| chr12:25077286
|
G | GAA | 12 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0112others(9): Show | 12 | HG02074.hp1 HG02451.hp1 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.25-1957_25-1956ins others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077286 | |||||
| chr12:25077286
|
G | GAAAT | 3 | a0003c0003t0002g0079a0003c0003t0005g0032a0003c0003t0005g0033 | 3 | HG00099.hp1 HG01099.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.25-1957_25-1956ins others(4): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077286 | |||||
| chr12:25077286
|
G | GAAATATA others(109): Show |
1 | a0003c0003t0002g0093 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.25-1957_25-1956ins others(116): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077286 | |||||
| chr12:25077286
|
G | GAAATATA others(120): Show |
61 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(58): Show | 65 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.25-1957_25-1956ins others(127): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077286 | |||||
| chr12:25077286
|
G | GAAATATA others(109): Show |
1 | a0002c0002t0001g0056 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.25-1957_25-1956ins others(116): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077286 | |||||
| chr12:25077286
|
G | GAAATATA others(127): Show |
5 | a0001c0001t0001g0106a0001c0001t0001g0107a0002c0002t0001g0108others(2): Show | 5 | HG02523.hp2 NA18952.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-1957_25-1956ins others(134): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077286 | |||||
| chr12:25077286
|
G | GAAATATA others(114): Show |
1 | a0001c0001t0001g0111 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.25-1957_25-1956ins others(121): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077286 | |||||
| chr12:25077286
|
G | GAAATATA others(83): Show |
5 | a0002c0002t0001g0063a0003c0003t0001g0062a0006c0005t0001g0019others(2): Show | 5 | HG02615.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-1957_25-1956ins others(90): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077286 | |||||
| chr12:25077286
|
G | GATATATA others(6): Show |
1 | a0006c0005t0001g0064 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.25-1949_25-1937dup others(13): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077286 | |||||
| chr12:25077286
|
GAT | G | 26 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0001g0134others(23): Show | 26 | HG00408.hp2 HG00609.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.25-1949_25-1948del others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077286 | |||||
| chr12:25077287
|
A | T | 4 | a0002c0002t0001g0308a0002c0002t0001g0309a0002c0002t0001g0310others(1): Show | 4 | HG02630.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-1957A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077287 | ||||||
| chr12:25077288
|
T | G | 8 | a0001c0001t0001g0215a0002c0002t0001g0199a0002c0002t0001g0308others(5): Show | 8 | HG01175.hp1 HG01934.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.25-1956T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077288 | ||||||
| chr12:25077290
|
T | A | 18 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0001g0134others(15): Show | 18 | HG00408.hp2 HG00609.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.25-1954T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077290 | ||||||
| chr12:25077295
|
A | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0320a0001c0001t0001g0321others(5): Show | 8 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.25-1949A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077295 | ||||||
| chr12:25077296
|
T | A | 3 | a0001c0001t0001g0321a0002c0002t0001g0160a0002c0002t0001g0174 | 3 | HG02273.hp1 HG03130.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.25-1948T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077296 | ||||||
| chr12:25077297
|
G | A | 3 | a0001c0001t0001g0321a0002c0002t0001g0160a0002c0002t0001g0174 | 3 | HG02273.hp1 HG03130.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.25-1947G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077297 | ||||||
| chr12:25077299
|
A | AAT | 18 | a0001c0001t0001g0045a0001c0001t0001g0089a0001c0001t0001g0185others(15): Show | 20 | HG00639.hp2 HG01168.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.25-1938_25-1937dup others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077299 | |||||
| chr12:25077299
|
A | G | 85 | a0001c0001t0001g0007a0001c0001t0001g0042a0001c0001t0001g0068others(82): Show | 88 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.25-1945A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077299 | ||||||
| chr12:25077299
|
A | T | 43 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0126others(40): Show | 43 | HG00099.hp1 HG00408.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.25-1945A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077299 | ||||||
| chr12:25077299
|
AAT | A | 11 | a0003c0003t0002g0201a0003c0003t0002g0202a0003c0003t0004g0314others(8): Show | 11 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.25-1938_25-1937del others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077299 | |||||
| chr12:25077306
|
A | G | 1 | a0003c0003t0009g0031 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.25-1938A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077306 | ||||||
| chr12:25077307
|
T | A | 1 | a0003c0003t0009g0031 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.25-1937T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077307 | ||||||
| chr12:25077308
|
G | GAT | 7 | a0001c0001t0001g0191a0002c0002t0001g0175a0004c0004t0001g0254others(4): Show | 7 | HG00642.hp2 HG01891.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.25-1929_25-1928dup others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077308 | |||||
| chr12:25077308
|
G | GATATATA others(37): Show |
12 | a0001c0001t0001g0263a0002c0002t0001g0017a0002c0002t0001g0255others(9): Show | 13 | HG01074.hp1 HG01123.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.25-1928_25-1927ins others(44): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077308 | |||||
| chr12:25077308
|
G | GATATATA others(48): Show |
4 | a0004c0004t0001g0016a0004c0004t0001g0264a0004c0004t0001g0273others(1): Show | 5 | HG00280.hp2 HG01099.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-1928_25-1927ins others(55): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077308 | |||||
| chr12:25077308
|
G | GATATATA others(59): Show |
5 | a0001c0001t0001g0253a0002c0002t0001g0288a0004c0004t0001g0265others(2): Show | 5 | HG01069.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-1928_25-1927ins others(66): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077308 | |||||
| chr12:25077308
|
G | GATATATA others(70): Show |
1 | a0004c0004t0006g0147 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.25-1928_25-1927ins others(77): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077308 | |||||
| chr12:25077308
|
G | GATATATA others(26): Show |
2 | a0003c0003t0003g0049a0005c0006t0007g0051 | 2 | HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.25-1904_25-1903ins others(33): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077308 | |||||
| chr12:25077308
|
G | GATATATA others(37): Show |
8 | a0001c0001t0001g0153a0002c0002t0001g0151a0002c0002t0001g0152others(5): Show | 8 | HG00738.hp2 HG02109.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.25-1904_25-1903ins others(44): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077308 | |||||
| chr12:25077308
|
G | GATATATA others(35): Show |
1 | a0001c0001t0001g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.25-1904_25-1903ins others(42): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077308 | |||||
| chr12:25077308
|
G | T | 2 | a0001c0001t0006g0195a0003c0003t0009g0031 | 2 | HG02135.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.25-1936G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077308 | ||||||
| chr12:25077310
|
T | A | 20 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0001g0134others(17): Show | 20 | HG00099.hp1 HG00408.hp2 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.25-1934T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077310 | ||||||
| chr12:25077310
|
T | G | 89 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0042others(86): Show | 92 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.25-1934T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077310 | ||||||
| chr12:25077316
|
T | TATATGA | 86 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0042others(83): Show | 89 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.25-1928_25-1927ins others(6): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077316 | ||||||
| chr12:25077316
|
T | TATGA | 15 | a0001c0001t0001g0089a0001c0001t0001g0185a0001c0001t0001g0186others(12): Show | 15 | HG00639.hp2 HG01255.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.25-1928_25-1927ins others(4): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077316 | ||||||
| chr12:25077316
|
TG | T | 3 | a0003c0003t0002g0079a0003c0003t0005g0032a0003c0003t0005g0033 | 3 | HG00099.hp1 HG01099.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.25-1927delG | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077316 | ||||||
| chr12:25077317
|
G | A | 12 | a0001c0001t0001g0089a0001c0001t0001g0185a0001c0001t0001g0186others(9): Show | 12 | HG00639.hp2 HG01255.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.25-1927G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077317 | ||||||
| chr12:25077317
|
G | GAA | 10 | a0001c0001t0001g0045a0002c0002t0001g0046a0002c0002t0001g0308others(7): Show | 12 | HG01168.hp1 HG01169.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.25-1926_25-1925ins others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077317 | |||||
| chr12:25077317
|
GAT | G | 33 | a0001c0001t0001g0020a0001c0001t0001g0121a0001c0001t0001g0126others(30): Show | 34 | HG00408.hp2 HG00609.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.25-1918_25-1917del others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077317 | |||||
| chr12:25077319
|
T | A | 4 | a0001c0001t0001g0320a0005c0006t0007g0302a0005c0006t0007g0304others(1): Show | 4 | HG01891.hp1 HG02004.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.25-1925T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077319 | ||||||
| chr12:25077319
|
T | G | 2 | a0003c0003t0009g0031a0004c0004t0001g0209 | 2 | HG02523.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.25-1925T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077319 | ||||||
| chr12:25077321
|
T | TG | 3 | a0003c0003t0002g0079a0003c0003t0005g0032a0003c0003t0005g0033 | 3 | HG00099.hp1 HG01099.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.25-1923_25-1922ins others(1): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077321 | ||||||
| chr12:25077326
|
A | G | 1 | a0001c0008t0001g0219 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.25-1918A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077326 | ||||||
| chr12:25077327
|
T | A | 1 | a0001c0008t0001g0219 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.25-1917T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077327 | ||||||
| chr12:25077328
|
G | A | 6 | a0003c0003t0002g0079a0003c0003t0005g0032a0003c0003t0005g0033others(3): Show | 6 | HG00099.hp1 HG01099.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.25-1916G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077328 | ||||||
| chr12:25077328
|
G | GAA | 11 | a0003c0003t0002g0201a0003c0003t0002g0202a0003c0003t0004g0314others(8): Show | 11 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.25-1915_25-1914ins others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077328 | |||||
| chr12:25077328
|
GAT | G | 3 | a0001c0001t0001g0321a0002c0002t0001g0160a0002c0002t0001g0174 | 3 | HG02273.hp1 HG03130.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.25-1907_25-1906del others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077328 | |||||
| chr12:25077329
|
A | T | 6 | a0003c0003t0002g0079a0003c0003t0005g0032a0003c0003t0005g0033others(3): Show | 6 | HG00099.hp1 HG01099.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.25-1915A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077329 | ||||||
| chr12:25077330
|
T | G | 9 | a0001c0001t0001g0191a0001c0001t0001g0198a0001c0001t0001g0277others(6): Show | 9 | HG00099.hp1 HG01099.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.25-1914T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077330 | ||||||
| chr12:25077330
|
T | TATATATA others(24): Show |
1 | a0001c0001t0001g0169 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.25-1883_25-1853dup others(31): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077330 | |||||
| chr12:25077337
|
A | G | 5 | a0001c0001t0001g0320a0002c0002t0001g0308a0002c0002t0001g0309others(2): Show | 5 | HG02004.hp2 HG02630.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-1907A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077337 | ||||||
| chr12:25077339
|
GAA | G | 4 | a0001c0001t0001g0020a0001c0001t0001g0322a0001c0001t0001g0323others(1): Show | 4 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-1903_25-1902del others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077339 | |||||
| chr12:25077341
|
A | G | 91 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0042others(88): Show | 94 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.25-1903A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077341 | ||||||
| chr12:25077341
|
A | T | 15 | a0003c0003t0002g0201a0003c0003t0002g0202a0003c0003t0004g0314others(12): Show | 15 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.25-1903A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077341 | ||||||
| chr12:25077343
|
T | TATATG | 11 | a0003c0003t0002g0201a0003c0003t0002g0202a0003c0003t0004g0314others(8): Show | 11 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.25-1897_25-1896ins others(5): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077343 | |||||
| chr12:25077348
|
A | G | 3 | a0005c0006t0007g0302a0005c0006t0007g0304a0005c0006t0011g0303 | 3 | HG01891.hp1 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.25-1896A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077348 | ||||||
| chr12:25077349
|
T | A | 3 | a0005c0006t0007g0302a0005c0006t0007g0304a0005c0006t0011g0303 | 3 | HG01891.hp1 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.25-1895T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077349 | ||||||
| chr12:25077350
|
A | G | 5 | a0001c0001t0001g0020a0001c0001t0001g0322a0001c0001t0001g0323others(2): Show | 5 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-1894A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077350 | ||||||
| chr12:25077351
|
T | A | 8 | a0001c0001t0001g0020a0001c0001t0001g0322a0001c0001t0001g0323others(5): Show | 8 | HG00733.hp2 HG01891.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.25-1893T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077351 | ||||||
| chr12:25077352
|
G | GAAAT | 11 | a0003c0003t0002g0201a0003c0003t0002g0202a0003c0003t0004g0314others(8): Show | 11 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.25-1891_25-1890ins others(4): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077352 | |||||
| chr12:25077352
|
G | GATATATA others(499): Show |
1 | a0001c0001t0001g0321 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.25-1875_25-1874ins others(506): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077352 | |||||
| chr12:25077352
|
G | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0322a0001c0001t0001g0323others(4): Show | 7 | HG00733.hp2 HG01891.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.25-1892G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077352 | ||||||
| chr12:25077354
|
T | A | 84 | a0001c0001t0001g0007a0001c0001t0001g0042a0001c0001t0001g0068others(81): Show | 87 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.25-1890T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077354 | ||||||
| chr12:25077354
|
TATATATG | T | 3 | a0003c0003t0002g0079a0003c0003t0005g0032a0003c0003t0005g0033 | 3 | HG00099.hp1 HG01099.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.25-1883_25-1877del others(7): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077354 | |||||
| chr12:25077360
|
T | TATGAAAT others(213): Show |
1 | a0002c0002t0001g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.25-1884_25-1883ins others(220): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077360 | ||||||
| chr12:25077360
|
T | TATGAAAT others(167): Show |
1 | a0004c0004t0001g0002 | 3 | HG01168.hp1 HG01169.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.25-1884_25-1883ins others(174): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077360 | ||||||
| chr12:25077360
|
T | TATGAAAT others(191): Show |
2 | a0004c0004t0001g0067a0004c0004t0001g0140 | 2 | HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.25-1884_25-1883ins others(198): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077360 | ||||||
| chr12:25077360
|
T | TATGAAAT others(189): Show |
1 | a0001c0001t0001g0045 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.25-1884_25-1883ins others(196): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077360 | ||||||
| chr12:25077360
|
T | TATGAAAT others(189): Show |
1 | a0004c0004t0001g0040 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.25-1884_25-1883ins others(196): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077360 | ||||||
| chr12:25077360
|
T | TATGAGAT others(78): Show |
1 | a0001c0001t0001g0220 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.25-1884_25-1883ins others(85): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077360 | ||||||
| chr12:25077360
|
T | TATGAGAT others(82): Show |
2 | a0001c0001t0001g0197a0002c0002t0001g0245 | 2 | NA18971.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.25-1884_25-1883ins others(89): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077360 | ||||||
| chr12:25077360
|
T | TATGATAT others(146): Show |
1 | a0001c0001t0001g0089 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.25-1884_25-1883ins others(153): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077360 | ||||||
| chr12:25077360
|
T | TATGATAT others(56): Show |
1 | a0001c0001t0006g0195 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.25-1884_25-1883ins others(63): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077360 | ||||||
| chr12:25077360
|
T | TATGATAT others(128): Show |
1 | a0001c0001t0001g0138 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.25-1884_25-1883ins others(135): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077360 | ||||||
| chr12:25077360
|
T | TATGATAT others(104): Show |
7 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0192others(4): Show | 7 | HG00639.hp2 HG01361.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.25-1884_25-1883ins others(111): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077360 | ||||||
| chr12:25077360
|
T | TATGATAT others(98): Show |
1 | a0001c0001t0001g0223 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.25-1884_25-1883ins others(105): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077360 | ||||||
| chr12:25077361
|
G | A | 15 | a0001c0001t0001g0089a0001c0001t0001g0138a0001c0001t0001g0185others(12): Show | 15 | HG00639.hp2 HG01255.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.25-1883G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077361 | ||||||
| chr12:25077361
|
G | GAA | 4 | a0001c0001t0001g0007a0001c0001t0001g0198a0001c0001t0001g0277others(1): Show | 5 | HG01070.hp2 HG01071.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-1882_25-1881ins others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077361 | |||||
| chr12:25077361
|
G | GAAATATA others(118): Show |
2 | a0001c0001t0001g0092a0001c0001t0001g0146 | 2 | HG02698.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.25-1882_25-1881ins others(125): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077361 | |||||
| chr12:25077361
|
G | GAAATATA others(116): Show |
1 | a0001c0001t0001g0252 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.25-1882_25-1881ins others(123): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077361 | |||||
| chr12:25077361
|
G | GAAATATA others(114): Show |
2 | a0002c0002t0001g0047a0002c0002t0001g0048 | 2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.25-1882_25-1881ins others(121): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077361 | |||||
| chr12:25077361
|
G | GAAATATA others(6): Show |
82 | a0001c0001t0001g0042a0001c0001t0001g0068a0001c0001t0001g0080others(79): Show | 84 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.25-1882_25-1881ins others(13): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077361 | |||||
| chr12:25077361
|
G | GAGATATA others(8): Show |
3 | a0001c0001t0001g0039a0002c0002t0001g0043a0002c0002t0001g0044 | 3 | HG02895.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.25-1882_25-1881ins others(15): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077361 | |||||
| chr12:25077361
|
G | GATATATA others(549): Show |
1 | a0002c0002t0001g0160 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.25-1875_25-1874ins others(556): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077361 | |||||
| chr12:25077361
|
G | GATATATA others(525): Show |
1 | a0002c0002t0001g0174 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.25-1875_25-1874ins others(532): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077361 | |||||
| chr12:25077361
|
G | GTGAAATA others(443): Show |
4 | a0002c0002t0001g0308a0002c0002t0001g0309a0002c0002t0001g0310others(1): Show | 4 | HG02630.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-1883_25-1882ins others(450): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077361 | ||||||
| chr12:25077361
|
G | T | 7 | a0001c0001t0001g0045a0001c0008t0001g0219a0002c0002t0001g0046others(4): Show | 9 | HG01168.hp1 HG01169.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.25-1883G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077361 | ||||||
| chr12:25077365
|
T | C | 4 | a0002c0002t0001g0171a0002c0002t0001g0172a0002c0002t0001g0176others(1): Show | 4 | HG02257.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-1879T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077365 | ||||||
| chr12:25077370
|
G | A | 14 | a0003c0003t0002g0201a0003c0003t0002g0202a0003c0003t0004g0314others(11): Show | 14 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.25-1874G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077370 | ||||||
| chr12:25077371
|
A | T | 14 | a0003c0003t0002g0201a0003c0003t0002g0202a0003c0003t0004g0314others(11): Show | 14 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.25-1873A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077371 | ||||||
| chr12:25077372
|
A | AATATATA others(15): Show |
1 | a0003c0003t0001g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.25-1870_25-1849dup others(22): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077372 | |||||
| chr12:25077372
|
A | G | 30 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0191others(27): Show | 32 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.25-1872A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077372 | ||||||
| chr12:25077372
|
AAT | A | 8 | a0001c0001t0001g0092a0001c0001t0001g0146a0001c0001t0001g0252others(5): Show | 8 | HG00099.hp1 HG01099.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.25-1863_25-1862del others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077372 | |||||
| chr12:25077374
|
T | A | 14 | a0003c0003t0002g0201a0003c0003t0002g0202a0003c0003t0004g0314others(11): Show | 14 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.25-1870T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077374 | ||||||
| chr12:25077374
|
T | TATATATA others(355): Show |
4 | a0002c0002t0001g0171a0002c0002t0001g0172a0002c0002t0001g0176others(1): Show | 4 | HG02257.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-1862_25-1861ins others(362): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077374 | |||||
| chr12:25077374
|
T | TATATATA others(15): Show |
145 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(142): Show | 154 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.25-1861_25-1840dup others(22): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077374 | |||||
| chr12:25077374
|
T | TATATATG others(13): Show |
1 | a0001c0001t0001g0134 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.25-1864_25-1863ins others(20): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077374 | |||||
| chr12:25077374
|
T | TATATATG others(44): Show |
2 | a0002c0002t0001g0295a0002c0002t0001g0296 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.25-1864_25-1863ins others(51): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr12 | 25077374 | |||||
| chr12:25077396
|
A | G | 9 | a0001c0001t0001g0039a0001c0001t0001g0045a0002c0002t0001g0043others(6): Show | 11 | HG01168.hp1 HG01169.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.25-1848A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077396 | ||||||
| chr12:25077445
|
T | C | 6 | a0002c0002t0001g0171a0002c0002t0001g0172a0002c0002t0001g0176others(3): Show | 6 | HG02257.hp1 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.25-1799T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077445 | ||||||
| chr12:25077484
|
C | T | 112 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0042others(109): Show | 117 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.25-1760C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077484 | ||||||
| chr12:25077631
|
T | C | 1 | a0002c0002t0001g0179 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.25-1613T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077631 | ||||||
| chr12:25077637
|
G | T | 9 | a0005c0006t0001g0298a0005c0006t0001g0299a0005c0006t0001g0300others(6): Show | 9 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.25-1607G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077637 | ||||||
| chr12:25077810
|
C | G | 2 | a0002c0002t0001g0295a0002c0002t0001g0296 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.25-1434C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077810 | ||||||
| chr12:25077907
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.25-1337A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077907 | ||||||
| chr12:25078190
|
A | T | 32 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0001g0134others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.25-1054A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25078190 | ||||||
| chr12:25078301
|
T | C | 131 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0039others(128): Show | 136 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.25-943T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25078301 | ||||||
| chr12:25078518
|
T | C | 18 | a0001c0001t0001g0020a0001c0001t0001g0320a0001c0001t0001g0321others(15): Show | 18 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.25-726T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25078518 | ||||||
| chr12:25078587
|
T | C | 31 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0001g0134others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.25-657T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25078587 | ||||||
| chr12:25078650
|
T | C | 2 | a0001c0001t0001g0134a0003c0003t0002g0128 | 2 | HG02083.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.25-594T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25078650 | ||||||
| chr12:25078824
|
A | T | 1 | a0001c0001t0001g0068 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.25-420A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25078824 | ||||||
| chr12:25079186
|
T | A | 34 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0253others(31): Show | 36 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.25-58T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25079186 | ||||||
| chr12:25079195
|
T | A | 4 | a0004c0004t0001g0002a0004c0004t0001g0040a0004c0004t0001g0067others(1): Show | 6 | HG01168.hp1 HG01169.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.25-49T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25079195 | ||||||
| chr12:25079517
|
C | G | 12 | a0001c0001t0001g0020a0001c0001t0001g0320a0001c0001t0001g0321others(9): Show | 12 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.136+55C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 8/21 | chr12 | 25079517 | ||||||
| chr12:25079606
|
T | C | 2 | a0002c0002t0001g0295a0002c0002t0001g0296 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.137-50T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 8/21 | chr12 | 25079606 | ||||||
| chr12:25080063
|
TG | T | 33 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0253others(30): Show | 35 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.244+303delG | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 25080063 | |||||
| chr12:25080161
|
A | G | 10 | a0005c0006t0001g0298a0005c0006t0001g0299a0005c0006t0001g0300others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.244+398A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25080161 | ||||||
| chr12:25080218
|
AC | A | 7 | a0002c0002t0001g0199a0002c0002t0001g0289a0002c0002t0001g0294others(4): Show | 7 | HG01070.hp1 HG01934.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.244+456delC | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25080218 | ||||||
| chr12:25080254
|
T | A | 4 | a0004c0004t0001g0002a0004c0004t0001g0040a0004c0004t0001g0067others(1): Show | 6 | HG01168.hp1 HG01169.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.244+491T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25080254 | ||||||
| chr12:25080312
|
T | TA | 15 | a0001c0001t0001g0020a0001c0001t0001g0136a0001c0001t0001g0320others(12): Show | 15 | HG00544.hp1 HG00733.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.244+558dupA | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 25080312 | |||||
| chr12:25080312
|
TA | T | 4 | a0004c0004t0001g0002a0004c0004t0001g0040a0004c0004t0001g0067others(1): Show | 6 | HG01168.hp1 HG01169.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.244+558delA | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 25080312 | |||||
| chr12:25080313
|
A | T | 33 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0253others(30): Show | 35 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.244+550A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25080313 | ||||||
| chr12:25080355
|
C | CT | 45 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0269others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.244+606dupT | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 25080355 | |||||
| chr12:25080355
|
C | CTT | 36 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0253others(33): Show | 38 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.244+605_244+606dup others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 25080355 | |||||
| chr12:25080383
|
G | A | 33 | a0001c0001t0001g0095a0001c0001t0001g0121a0001c0001t0001g0126others(30): Show | 33 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.244+620G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25080383 | ||||||
| chr12:25080438
|
G | A | 4 | a0001c0007t0001g0129a0001c0007t0001g0130a0001c0007t0001g0131others(1): Show | 4 | HG03130.hp2 NA18960.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+675G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25080438 | ||||||
| chr12:25080590
|
G | C | 1 | a0001c0001t0001g0206 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.244+827G>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25080590 | ||||||
| chr12:25080599
|
T | G | 184 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(181): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.244+836T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25080599 | ||||||
| chr12:25080684
|
G | A | 184 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(181): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.244+921G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25080684 | ||||||
| chr12:25080847
|
A | G | 137 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(134): Show | 146 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.244+1084A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25080847 | ||||||
| chr12:25080848
|
T | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0111 | 2 | HG02155.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.244+1085T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25080848 | ||||||
| chr12:25080876
|
C | T | 12 | a0001c0001t0001g0020a0001c0001t0001g0320a0001c0001t0001g0321others(9): Show | 12 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.244+1113C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25080876 | ||||||
| chr12:25080895
|
A | T | 1 | a0001c0001t0001g0095 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.244+1132A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25080895 | ||||||
| chr12:25080923
|
C | G | 299 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(296): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.244+1160C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25080923 | ||||||
| chr12:25081016
|
T | C | 1 | a0003c0003t0001g0173 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.244+1253T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25081016 | ||||||
| chr12:25081053
|
C | T | 136 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(133): Show | 145 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.244+1290C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25081053 | ||||||
| chr12:25081086
|
G | A | 184 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(181): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.244+1323G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25081086 | ||||||
| chr12:25081112
|
A | G | 12 | a0001c0001t0001g0020a0001c0001t0001g0320a0001c0001t0001g0321others(9): Show | 12 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.244+1349A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25081112 | ||||||
| chr12:25081128
|
G | A | 1 | a0002c0002t0001g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.244+1365G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25081128 | ||||||
| chr12:25081151
|
G | GTC | 137 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(134): Show | 146 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.244+1401_244+1402d others(4): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 25081151 | |||||
| chr12:25081189
|
G | A | 32 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0001g0134others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.244+1426G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25081189 | ||||||
| chr12:25081356
|
C | G | 2 | a0002c0002t0001g0295a0002c0002t0001g0296 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.244+1593C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25081356 | ||||||
| chr12:25081396
|
G | A | 14 | a0001c0001t0001g0020a0001c0001t0001g0320a0001c0001t0001g0321others(11): Show | 14 | HG00733.hp2 HG01928.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.244+1633G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25081396 | ||||||
| chr12:25081459
|
G | A | 1 | a0003c0003t0001g0173 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.244+1696G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25081459 | ||||||
| chr12:25081712
|
T | C | 7 | a0002c0002t0001g0295a0002c0002t0001g0296a0002c0002t0001g0308others(4): Show | 7 | HG02630.hp2 HG02723.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.245-1711T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25081712 | ||||||
| chr12:25081808
|
C | T | 2 | a0002c0002t0001g0295a0002c0002t0001g0296 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.245-1615C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25081808 | ||||||
| chr12:25081834
|
G | A | 285 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(282): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.245-1589G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25081834 | ||||||
| chr12:25081838
|
A | G | 4 | a0002c0002t0001g0308a0002c0002t0001g0309a0002c0002t0001g0310others(1): Show | 4 | HG02630.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-1585A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25081838 | ||||||
| chr12:25082046
|
C | T | 9 | a0001c0001t0001g0025a0002c0002t0001g0280a0003c0003t0002g0203others(6): Show | 9 | HG00735.hp1 HG01123.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.245-1377C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25082046 | ||||||
| chr12:25082211
|
C | T | 1 | a0004c0004t0001g0190 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.245-1212C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25082211 | ||||||
| chr12:25082315
|
A | G | 1 | a0002c0002t0001g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.245-1108A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25082315 | ||||||
| chr12:25082330
|
T | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0107 | 2 | NA18973.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.245-1093T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25082330 | ||||||
| chr12:25082428
|
G | A | 79 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(76): Show | 84 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.245-995G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25082428 | ||||||
| chr12:25082449
|
A | C | 1 | a0003c0003t0001g0062 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.245-974A>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25082449 | ||||||
| chr12:25082491
|
T | C | 79 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(76): Show | 84 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.245-932T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25082491 | ||||||
| chr12:25082599
|
C | CA | 32 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0001g0134others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.245-814dupA | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 25082599 | |||||
| chr12:25082609
|
A | AC | 232 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(229): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.245-813dupC | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 25082609 | |||||
| chr12:25082623
|
C | CAAACA | 54 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0042others(51): Show | 56 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.245-781_245-777dup others(5): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr12 | 25082623 | |||||
| chr12:25082648
|
A | C | 1 | a0002c0002t0001g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.245-775A>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25082648 | ||||||
| chr12:25082713
|
T | C | 13 | a0002c0002t0001g0006a0002c0002t0001g0037a0002c0002t0001g0038others(10): Show | 14 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.245-710T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25082713 | ||||||
| chr12:25083258
|
T | A | 6 | a0002c0002t0001g0001a0002c0002t0001g0027a0004c0004t0001g0002others(3): Show | 10 | HG01168.hp1 HG01169.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.245-165T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25083258 | ||||||
| chr12:25083384
|
G | T | 1 | a0001c0001t0001g0178 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.245-39G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 9/21 | chr12 | 25083384 | ||||||
| chr12:25083575
|
G | A | 1 | a0002c0002t0001g0006 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.315+82G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25083575 | ||||||
| chr12:25083609
|
C | A | 277 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(274): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.315+116C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25083609 | ||||||
| chr12:25083705
|
G | C | 1 | a0002c0002t0001g0208 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.315+212G>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25083705 | ||||||
| chr12:25083905
|
C | T | 323 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(320): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.315+412C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25083905 | ||||||
| chr12:25083979
|
G | A | 16 | a0002c0002t0001g0280a0002c0002t0001g0308a0002c0002t0001g0309others(13): Show | 16 | HG00735.hp1 HG01123.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.315+486G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25083979 | ||||||
| chr12:25084036
|
T | TA | 222 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(219): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.315+546dupA | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25084036 | |||||
| chr12:25084076
|
A | G | 2 | a0002c0002t0001g0262a0003c0003t0002g0286 | 2 | HG01123.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.315+583A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25084076 | ||||||
| chr12:25084126
|
G | A | 3 | a0002c0002t0001g0295a0002c0002t0001g0296a0003c0003t0001g0173 | 3 | HG02723.hp2 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.315+633G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25084126 | ||||||
| chr12:25084172
|
G | A | 1 | a0002c0002t0001g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.315+679G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25084172 | ||||||
| chr12:25084354
|
C | T | 15 | a0002c0002t0001g0280a0002c0002t0001g0308a0002c0002t0001g0309others(12): Show | 15 | HG00735.hp1 HG01123.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.315+861C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25084354 | ||||||
| chr12:25084489
|
A | G | 2 | a0001c0001t0001g0191a0001c0001t0006g0195 | 2 | HG02135.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.315+996A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25084489 | ||||||
| chr12:25084540
|
G | GGT | 147 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0029others(144): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.315+1074_315+1075d others(4): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25084540 | |||||
| chr12:25084540
|
G | GGTGT | 16 | a0001c0001t0001g0042a0001c0001t0001g0050a0001c0001t0001g0225others(13): Show | 17 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.315+1072_315+1075d others(6): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25084540 | |||||
| chr12:25084540
|
GGTGT | G | 11 | a0002c0002t0001g0294a0002c0002t0001g0308a0002c0002t0001g0309others(8): Show | 11 | HG01070.hp1 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.315+1072_315+1075d others(6): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25084540 | |||||
| chr12:25084565
|
GTGTA | G | 5 | a0002c0002t0001g0280a0003c0003t0002g0203a0004c0004t0001g0103others(2): Show | 5 | HG00735.hp1 HG01123.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.315+1074_315+1077d others(6): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25084565 | |||||
| chr12:25084642
|
T | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0029others(119): Show | 125 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.315+1149T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25084642 | ||||||
| chr12:25084652
|
C | G | 1 | a0002c0002t0001g0280 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.315+1159C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25084652 | ||||||
| chr12:25084828
|
C | T | 4 | a0002c0002t0001g0308a0002c0002t0001g0309a0002c0002t0001g0310others(1): Show | 4 | HG02630.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.315+1335C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25084828 | ||||||
| chr12:25084858
|
T | C | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.315+1365T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25084858 | ||||||
| chr12:25084871
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.315+1378G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25084871 | ||||||
| chr12:25085089
|
G | A | 1 | a0003c0003t0001g0173 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.315+1596G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25085089 | ||||||
| chr12:25085151
|
T | C | 1 | a0003c0003t0001g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.315+1658T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25085151 | ||||||
| chr12:25085155
|
C | T | 1 | a0002c0002t0001g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.315+1662C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25085155 | ||||||
| chr12:25085245
|
C | T | 20 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0063others(17): Show | 20 | HG01192.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.315+1752C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25085245 | ||||||
| chr12:25085327
|
GATGGAGT others(11): Show |
G | 18 | a0001c0001t0001g0218a0002c0002t0001g0280a0002c0002t0001g0291others(15): Show | 18 | HG00735.hp1 HG01074.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.315+1840_315+1857d others(20): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25085327 | |||||
| chr12:25085333
|
GTGGGAAG others(11): Show |
G | 4 | a0004c0004t0001g0016a0004c0004t0001g0254a0004c0004t0001g0264others(1): Show | 5 | HG00280.hp2 HG00642.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.315+1849_315+1866d others(20): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25085333 | |||||
| chr12:25085708
|
C | A | 1 | a0003c0003t0001g0173 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.315+2215C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25085708 | ||||||
| chr12:25085739
|
T | TCCCATAT others(36): Show |
2 | a0005c0006t0007g0051a0007c0009t0001g0200 | 2 | HG02572.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.315+2260_315+2261i others(45): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25085739 | |||||
| chr12:25085739
|
T | TCCCATAT others(42): Show |
7 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0160others(4): Show | 7 | HG01192.hp1 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.315+2260_315+2261i others(51): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25085739 | |||||
| chr12:25085739
|
T | TCCCATAT others(48): Show |
9 | a0002c0002t0001g0063a0002c0002t0001g0175a0002c0002t0001g0311others(6): Show | 9 | HG02615.hp1 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.315+2260_315+2261i others(57): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25085739 | |||||
| chr12:25085739
|
T | TCCCATAT others(54): Show |
2 | a0005c0006t0007g0302a0005c0006t0011g0303 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.315+2260_315+2261i others(63): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25085739 | |||||
| chr12:25085917
|
G | A | 20 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0063others(17): Show | 20 | HG01192.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.316-2183G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25085917 | ||||||
| chr12:25086035
|
T | C | 9 | a0001c0001t0001g0025a0003c0003t0001g0170a0003c0003t0003g0156others(6): Show | 11 | HG01168.hp1 HG01169.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.316-2065T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25086035 | ||||||
| chr12:25086137
|
T | C | 1 | a0001c0001t0001g0005 | 2 | HG01106.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.316-1963T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25086137 | ||||||
| chr12:25086146
|
G | A | 1 | a0003c0003t0003g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.316-1954G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25086146 | ||||||
| chr12:25086271
|
A | G | 33 | a0001c0001t0001g0126a0001c0001t0001g0134a0003c0003t0002g0079others(30): Show | 33 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.316-1829A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25086271 | ||||||
| chr12:25086277
|
CA | C | 137 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(134): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.316-1822delA | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25086277 | ||||||
| chr12:25086446
|
G | A | 17 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0063others(14): Show | 17 | HG01192.hp1 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.316-1654G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25086446 | ||||||
| chr12:25086488
|
C | T | 63 | a0001c0001t0001g0025a0001c0001t0001g0153a0001c0001t0001g0154others(60): Show | 67 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.316-1612C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25086488 | ||||||
| chr12:25086494
|
C | T | 1 | a0003c0003t0003g0057 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.316-1606C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25086494 | ||||||
| chr12:25086694
|
G | A | 1 | a0002c0002t0001g0262 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316-1406G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25086694 | ||||||
| chr12:25086760
|
G | T | 15 | a0002c0002t0001g0152a0002c0002t0001g0280a0002c0002t0001g0291others(12): Show | 15 | HG01433.hp2 HG02451.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.316-1340G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25086760 | ||||||
| chr12:25086930
|
T | C | 37 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0253others(34): Show | 39 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.316-1170T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25086930 | ||||||
| chr12:25086940
|
C | T | 120 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(117): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.316-1160C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25086940 | ||||||
| chr12:25087036
|
C | T | 87 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(84): Show | 92 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.316-1064C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087036 | ||||||
| chr12:25087153
|
C | CT | 32 | a0001c0001t0001g0029a0001c0001t0001g0085a0001c0001t0001g0138others(29): Show | 36 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.316-918dupT | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25087153 | |||||
| chr12:25087153
|
C | CTT | 46 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0205others(43): Show | 48 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.316-919_316-918dup others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25087153 | |||||
| chr12:25087153
|
C | CTTT | 36 | a0001c0001t0001g0126a0002c0002t0001g0006a0002c0002t0001g0038others(33): Show | 37 | HG00408.hp2 HG00642.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.316-920_316-918dup others(3): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25087153 | |||||
| chr12:25087153
|
C | CTTTT | 9 | a0001c0001t0001g0134a0002c0002t0001g0037a0002c0002t0001g0052others(6): Show | 9 | HG00733.hp1 HG01109.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.316-921_316-918dup others(4): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25087153 | |||||
| chr12:25087153
|
CT | C | 12 | a0001c0001t0001g0025a0002c0002t0001g0152a0002c0002t0001g0308others(9): Show | 14 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.316-918delT | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25087153 | |||||
| chr12:25087153
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0290 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.316-930_316-918del others(13): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25087153 | |||||
| chr12:25087177
|
T | TTG | 7 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0160others(4): Show | 7 | HG01192.hp1 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.316-922_316-921ins others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25087177 | |||||
| chr12:25087180
|
T | G | 21 | a0001c0001t0001g0025a0001c0001t0001g0096a0001c0001t0001g0097others(18): Show | 23 | HG00423.hp1 HG01168.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.316-920T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087180 | ||||||
| chr12:25087180
|
T | TG | 57 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(54): Show | 62 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.316-920_316-919ins others(1): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087180 | ||||||
| chr12:25087180
|
T | TTG | 9 | a0001c0001t0001g0058a0001c0001t0001g0091a0001c0001t0001g0102others(6): Show | 9 | HG00609.hp2 HG00621.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.316-919_316-918ins others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25087180 | |||||
| chr12:25087180
|
T | TTTTTTTG others(3): Show |
3 | a0006c0005t0001g0064a0006c0005t0001g0065a0006c0005t0001g0066 | 3 | HG02615.hp2 HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.316-918_316-917ins others(10): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25087180 | |||||
| chr12:25087180
|
T | TTTTTTTT others(4): Show |
4 | a0003c0003t0001g0062a0005c0006t0007g0304a0005c0006t0011g0303others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-918_316-917ins others(11): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25087180 | |||||
| chr12:25087258
|
C | G | 33 | a0001c0001t0001g0126a0001c0001t0001g0134a0003c0003t0002g0079others(30): Show | 33 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.316-842C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087258 | ||||||
| chr12:25087293
|
G | A | 1 | a0001c0001t0001g0221 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.316-807G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087293 | ||||||
| chr12:25087313
|
C | A | 1 | a0001c0001t0001g0223 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.316-787C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087313 | ||||||
| chr12:25087313
|
C | T | 1 | a0002c0002t0001g0015 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.316-787C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087313 | ||||||
| chr12:25087314
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.316-786T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087314 | ||||||
| chr12:25087315
|
G | C | 1 | a0001c0001t0001g0223 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.316-785G>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087315 | ||||||
| chr12:25087377
|
A | G | 39 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0253others(36): Show | 41 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.316-723A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087377 | ||||||
| chr12:25087404
|
G | A | 1 | a0002c0002t0001g0280 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.316-696G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087404 | ||||||
| chr12:25087413
|
C | T | 87 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(84): Show | 92 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.316-687C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087413 | ||||||
| chr12:25087464
|
T | A | 183 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(180): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.316-636T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087464 | ||||||
| chr12:25087502
|
C | T | 11 | a0002c0002t0001g0280a0002c0002t0001g0291a0002c0002t0001g0292others(8): Show | 11 | HG01433.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.316-598C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087502 | ||||||
| chr12:25087546
|
A | G | 203 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(200): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.316-554A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087546 | ||||||
| chr12:25087597
|
A | T | 28 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0253others(25): Show | 29 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.316-503A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087597 | ||||||
| chr12:25087606
|
G | A | 26 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0253others(23): Show | 27 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.316-494G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087606 | ||||||
| chr12:25087629
|
CT | C | 5 | a0002c0002t0001g0199a0002c0002t0001g0294a0003c0003t0003g0057others(2): Show | 5 | HG01070.hp1 HG01934.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.316-469delT | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr12 | 25087629 | |||||
| chr12:25087722
|
G | A | 16 | a0002c0002t0001g0152a0002c0002t0001g0280a0002c0002t0001g0291others(13): Show | 16 | HG01433.hp2 HG02451.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.316-378G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087722 | ||||||
| chr12:25087740
|
G | A | 1 | a0003c0003t0001g0173 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.316-360G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087740 | ||||||
| chr12:25087821
|
G | T | 16 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0063others(13): Show | 16 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.316-279G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087821 | ||||||
| chr12:25087930
|
C | T | 2 | a0003c0003t0004g0315a0003c0003t0004g0317 | 2 | HG00323.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.316-170C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087930 | ||||||
| chr12:25087978
|
T | C | 1 | a0002c0002t0001g0179 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.316-122T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25087978 | ||||||
| chr12:25088030
|
G | C | 92 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(89): Show | 97 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.316-70G>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25088030 | ||||||
| chr12:25088054
|
G | T | 23 | a0001c0001t0001g0253a0002c0002t0001g0001a0002c0002t0001g0027others(20): Show | 27 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.316-46G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 10/21 | chr12 | 25088054 | ||||||
| chr12:25088290
|
G | A | 167 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(164): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.373+133G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 11/21 | chr12 | 25088290 | ||||||
| chr12:25088363
|
C | T | 165 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(162): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.373+206C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 11/21 | chr12 | 25088363 | ||||||
| chr12:25088426
|
C | T | 73 | a0001c0001t0001g0126a0001c0001t0001g0134a0001c0001t0001g0253others(70): Show | 77 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.373+269C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 11/21 | chr12 | 25088426 | ||||||
| chr12:25088455
|
A | G | 1 | a0006c0005t0001g0064 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.373+298A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 11/21 | chr12 | 25088455 | ||||||
| chr12:25088594
|
C | G | 1 | a0004c0004t0001g0209 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.373+437C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 11/21 | chr12 | 25088594 | ||||||
| chr12:25088709
|
C | T | 85 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(82): Show | 89 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.373+552C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 11/21 | chr12 | 25088709 | ||||||
| chr12:25088825
|
T | G | 1 | a0002c0002t0001g0229 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.373+668T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 11/21 | chr12 | 25088825 | ||||||
| chr12:25088933
|
TGATAA | T | 17 | a0003c0003t0002g0079a0003c0003t0002g0201a0003c0003t0002g0202others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.374-676_374-672del others(5): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr12 | 25088933 | |||||
| chr12:25089005
|
T | G | 5 | a0003c0003t0002g0079a0003c0003t0005g0032a0003c0003t0005g0033others(2): Show | 5 | HG00099.hp1 HG01099.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.374-609T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 11/21 | chr12 | 25089005 | ||||||
| chr12:25089064
|
A | G | 2 | a0002c0002t0001g0160a0003c0003t0001g0061 | 2 | HG01192.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.374-550A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 11/21 | chr12 | 25089064 | ||||||
| chr12:25089316
|
A | G | 30 | a0002c0002t0001g0152a0002c0002t0001g0174a0002c0002t0001g0175others(27): Show | 30 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.374-298A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 11/21 | chr12 | 25089316 | ||||||
| chr12:25089399
|
C | CA | 151 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(148): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.374-214dupA | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr12 | 25089399 | |||||
| chr12:25089494
|
G | A | 20 | a0004c0004t0001g0002a0004c0004t0001g0004a0004c0004t0001g0016others(17): Show | 24 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.374-120G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 11/21 | chr12 | 25089494 | ||||||
| chr12:25089824
|
A | G | 20 | a0004c0004t0001g0002a0004c0004t0001g0004a0004c0004t0001g0016others(17): Show | 24 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.465+34A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 13/21 | chr12 | 25089824 | ||||||
| chr12:25089842
|
C | T | 239 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(236): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.465+52C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 13/21 | chr12 | 25089842 | ||||||
| chr12:25089899
|
C | T | 2 | a0002c0002t0001g0001a0002c0002t0001g0027 | 4 | HG02109.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+109C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 13/21 | chr12 | 25089899 | ||||||
| chr12:25089917
|
C | A | 1 | a0001c0001t0001g0211 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.465+127C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 13/21 | chr12 | 25089917 | ||||||
| chr12:25089951
|
T | C | 1 | a0003c0003t0002g0122 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.466-106T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 13/21 | chr12 | 25089951 | ||||||
| chr12:25090336
|
G | T | 186 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(183): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.606+139G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25090336 | ||||||
| chr12:25090379
|
C | CA | 32 | a0003c0003t0001g0028a0003c0003t0001g0159a0003c0003t0003g0021others(29): Show | 34 | HG00280.hp2 HG00642.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.606+198dupA | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 25090379 | |||||
| chr12:25090379
|
CA | C | 35 | a0001c0001t0002g0281a0003c0003t0001g0173a0003c0003t0002g0079others(32): Show | 35 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.606+198delA | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 25090379 | |||||
| chr12:25090379
|
CAA | C | 235 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(232): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.606+197_606+198del others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 25090379 | |||||
| chr12:25090528
|
G | C | 5 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0153others(2): Show | 5 | HG00738.hp2 HG01243.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.606+331G>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25090528 | ||||||
| chr12:25090604
|
A | G | 239 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(236): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.606+407A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25090604 | ||||||
| chr12:25090612
|
A | C | 1 | a0002c0002t0001g0236 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.606+415A>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25090612 | ||||||
| chr12:25090624
|
T | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0251 | 2 | HG00621.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.606+427T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25090624 | ||||||
| chr12:25090737
|
T | A | 2 | a0002c0002t0001g0038a0002c0002t0001g0073 | 2 | HG01993.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.606+540T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25090737 | ||||||
| chr12:25090884
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.606+687C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25090884 | ||||||
| chr12:25090959
|
C | T | 20 | a0004c0004t0001g0002a0004c0004t0001g0004a0004c0004t0001g0016others(17): Show | 24 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.606+762C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25090959 | ||||||
| chr12:25091162
|
T | G | 15 | a0002c0002t0003g0283a0003c0003t0001g0028a0003c0003t0003g0021others(12): Show | 15 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.606+965T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25091162 | ||||||
| chr12:25091229
|
C | G | 1 | a0001c0001t0001g0214 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.606+1032C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25091229 | ||||||
| chr12:25091245
|
T | C | 98 | a0001c0001t0001g0270a0002c0002t0001g0001a0002c0002t0001g0003others(95): Show | 108 | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(105): Show |
intron_variant | MODIFIER | c.606+1048T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25091245 | ||||||
| chr12:25091449
|
A | G | 98 | a0001c0001t0001g0270a0002c0002t0001g0001a0002c0002t0001g0003others(95): Show | 108 | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(105): Show |
intron_variant | MODIFIER | c.606+1252A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25091449 | ||||||
| chr12:25091492
|
A | T | 294 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(291): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.606+1295A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25091492 | ||||||
| chr12:25091650
|
G | GTAATTAT others(1): Show |
98 | a0001c0001t0001g0270a0002c0002t0001g0001a0002c0002t0001g0003others(95): Show | 108 | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(105): Show |
intron_variant | MODIFIER | c.606+1455_606+1462d others(10): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 25091650 | |||||
| chr12:25091867
|
G | A | 9 | a0003c0003t0001g0243a0006c0005t0001g0019a0006c0005t0001g0059others(6): Show | 9 | HG02109.hp2 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.606+1670G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25091867 | ||||||
| chr12:25091999
|
G | A | 1 | a0003c0003t0001g0173 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.606+1802G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25091999 | ||||||
| chr12:25092085
|
CGAAACAC others(128): Show |
C | 1 | a0001c0001t0001g0097 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.606+1907_606+2041d others(2): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 25092085 | |||||
| chr12:25092104
|
C | A | 288 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(285): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.606+1907C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25092104 | ||||||
| chr12:25092131
|
A | G | 288 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(285): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.606+1934A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25092131 | ||||||
| chr12:25092133
|
C | T | 156 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(153): Show | 166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.606+1936C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25092133 | ||||||
| chr12:25092186
|
A | G | 288 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(285): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.606+1989A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25092186 | ||||||
| chr12:25092272
|
C | T | 155 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(152): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.606+2075C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25092272 | ||||||
| chr12:25092274
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.606+2077C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25092274 | ||||||
| chr12:25092400
|
C | CA | 38 | a0002c0002t0001g0003a0002c0002t0001g0006a0002c0002t0001g0013others(35): Show | 44 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.606+2218dupA | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 25092400 | |||||
| chr12:25092400
|
C | CAA | 47 | a0001c0001t0001g0270a0002c0002t0001g0008a0002c0002t0001g0017others(44): Show | 49 | HG00423.hp2 HG01069.hp1 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.606+2217_606+2218d others(4): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 25092400 | |||||
| chr12:25092400
|
C | CAAA | 13 | a0002c0002t0001g0001a0002c0002t0001g0027a0002c0002t0001g0056others(10): Show | 15 | HG01070.hp1 HG01175.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.606+2216_606+2218d others(5): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 25092400 | |||||
| chr12:25092400
|
CA | C | 36 | a0001c0001t0001g0090a0003c0003t0002g0079a0003c0003t0002g0093others(33): Show | 36 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.606+2218delA | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 25092400 | |||||
| chr12:25092461
|
A | G | 1 | a0003c0003t0002g0124 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.606+2264A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25092461 | ||||||
| chr12:25092466
|
G | A | 1 | a0002c0002t0006g0234 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.606+2269G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25092466 | ||||||
| chr12:25092564
|
CA | C | 17 | a0003c0003t0002g0093a0003c0003t0002g0122a0003c0003t0002g0123others(14): Show | 17 | HG00323.hp1 HG00408.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.606+2390delA | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 25092564 | |||||
| chr12:25092564
|
CAA | C | 31 | a0002c0002t0001g0063a0002c0002t0001g0076a0002c0002t0001g0142others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.606+2389_606+2390d others(4): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 25092564 | |||||
| chr12:25092564
|
CAAA | C | 116 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0153others(113): Show | 126 | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(123): Show |
intron_variant | MODIFIER | c.606+2388_606+2390d others(5): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 25092564 | |||||
| chr12:25092564
|
CAAAA | C | 19 | a0002c0002t0001g0046a0004c0004t0001g0002a0004c0004t0001g0004others(16): Show | 23 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.606+2387_606+2390d others(6): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 25092564 | |||||
| chr12:25092564
|
CAAAAAA | C | 134 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(131): Show | 140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.606+2385_606+2390d others(8): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 25092564 | |||||
| chr12:25092581
|
A | G | 20 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0153others(17): Show | 20 | HG00738.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.606+2384A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25092581 | ||||||
| chr12:25092590
|
A | ACAGTTT | 35 | a0003c0003t0002g0079a0003c0003t0002g0093a0003c0003t0002g0113others(32): Show | 35 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.606+2397_606+2402d others(8): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 25092590 | |||||
| chr12:25092654
|
A | G | 319 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(316): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.606+2457A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25092654 | ||||||
| chr12:25092670
|
T | C | 98 | a0001c0001t0001g0270a0002c0002t0001g0001a0002c0002t0001g0003others(95): Show | 108 | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(105): Show |
intron_variant | MODIFIER | c.606+2473T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25092670 | ||||||
| chr12:25092819
|
G | A | 156 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(153): Show | 166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.606+2622G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25092819 | ||||||
| chr12:25092960
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.606+2763C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25092960 | ||||||
| chr12:25093094
|
C | T | 35 | a0003c0003t0002g0079a0003c0003t0002g0093a0003c0003t0002g0113others(32): Show | 35 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.606+2897C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25093094 | ||||||
| chr12:25093110
|
T | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0251 | 2 | HG00621.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.606+2913T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25093110 | ||||||
| chr12:25093114
|
A | G | 98 | a0001c0001t0001g0270a0002c0002t0001g0001a0002c0002t0001g0003others(95): Show | 108 | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(105): Show |
intron_variant | MODIFIER | c.606+2917A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25093114 | ||||||
| chr12:25093212
|
C | T | 9 | a0003c0003t0001g0243a0006c0005t0001g0019a0006c0005t0001g0059others(6): Show | 9 | HG02109.hp2 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.606+3015C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25093212 | ||||||
| chr12:25093237
|
T | G | 196 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(193): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.606+3040T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25093237 | ||||||
| chr12:25093371
|
G | C | 1 | a0001c0001t0002g0281 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.606+3174G>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25093371 | ||||||
| chr12:25093434
|
T | C | 34 | a0002c0002t0001g0003a0002c0002t0001g0013a0002c0002t0001g0014others(31): Show | 39 | HG01167.hp2 HG01169.hp1 HG01261.hp1 others(36): Show |
intron_variant | MODIFIER | c.606+3237T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25093434 | ||||||
| chr12:25093626
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.607-3284G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25093626 | ||||||
| chr12:25093753
|
C | T | 197 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(194): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.607-3157C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25093753 | ||||||
| chr12:25093756
|
C | T | 197 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(194): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.607-3154C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25093756 | ||||||
| chr12:25093895
|
G | A | 19 | a0003c0003t0002g0079a0003c0003t0002g0184a0003c0003t0002g0201others(16): Show | 19 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.607-3015G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25093895 | ||||||
| chr12:25093926
|
ATTGAG | A | 142 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(139): Show | 148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.607-2981_607-2977d others(7): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 25093926 | |||||
| chr12:25094055
|
G | C | 1 | a0001c0001t0001g0138 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.607-2855G>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25094055 | ||||||
| chr12:25094089
|
TGTA | T | 97 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0006others(94): Show | 107 | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(104): Show |
intron_variant | MODIFIER | c.607-2818_607-2816d others(5): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 25094089 | |||||
| chr12:25094142
|
T | G | 16 | a0002c0002t0003g0283a0003c0003t0001g0028a0003c0003t0003g0021others(13): Show | 16 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.607-2768T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25094142 | ||||||
| chr12:25094154
|
T | C | 51 | a0002c0002t0001g0001a0002c0002t0001g0008a0002c0002t0001g0017others(48): Show | 55 | HG00423.hp2 HG01069.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.607-2756T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25094154 | ||||||
| chr12:25094188
|
T | C | 1 | a0003c0003t0001g0243 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.607-2722T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25094188 | ||||||
| chr12:25094229
|
A | G | 20 | a0004c0004t0001g0002a0004c0004t0001g0004a0004c0004t0001g0016others(17): Show | 24 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.607-2681A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25094229 | ||||||
| chr12:25094332
|
T | C | 3 | a0003c0003t0001g0243a0006c0005t0001g0064a0006c0005t0001g0244 | 3 | HG02895.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.607-2578T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25094332 | ||||||
| chr12:25094425
|
C | T | 97 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0006others(94): Show | 107 | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(104): Show |
intron_variant | MODIFIER | c.607-2485C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25094425 | ||||||
| chr12:25094685
|
G | A | 1 | a0002c0002t0001g0141 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.607-2225G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25094685 | ||||||
| chr12:25094706
|
A | G | 97 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0006others(94): Show | 107 | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(104): Show |
intron_variant | MODIFIER | c.607-2204A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25094706 | ||||||
| chr12:25094731
|
C | CTTCT | 239 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(236): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.607-2177_607-2176i others(6): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 25094731 | |||||
| chr12:25094734
|
G | C | 20 | a0004c0004t0001g0002a0004c0004t0001g0004a0004c0004t0001g0016others(17): Show | 24 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.607-2176G>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25094734 | ||||||
| chr12:25094736
|
C | T | 20 | a0004c0004t0001g0002a0004c0004t0001g0004a0004c0004t0001g0016others(17): Show | 24 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.607-2174C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25094736 | ||||||
| chr12:25094738
|
T | G | 20 | a0004c0004t0001g0002a0004c0004t0001g0004a0004c0004t0001g0016others(17): Show | 24 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.607-2172T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25094738 | ||||||
| chr12:25094739
|
C | T | 20 | a0004c0004t0001g0002a0004c0004t0001g0004a0004c0004t0001g0016others(17): Show | 24 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.607-2171C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25094739 | ||||||
| chr12:25094740
|
T | C | 20 | a0004c0004t0001g0002a0004c0004t0001g0004a0004c0004t0001g0016others(17): Show | 24 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.607-2170T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25094740 | ||||||
| chr12:25094772
|
C | T | 162 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(159): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.607-2138C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25094772 | ||||||
| chr12:25094773
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.607-2137G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25094773 | ||||||
| chr12:25094925
|
C | G | 162 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(159): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.607-1985C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25094925 | ||||||
| chr12:25094951
|
A | G | 1 | a0002c0002t0001g0231 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.607-1959A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25094951 | ||||||
| chr12:25095236
|
T | C | 35 | a0003c0003t0002g0079a0003c0003t0002g0093a0003c0003t0002g0113others(32): Show | 35 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.607-1674T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25095236 | ||||||
| chr12:25095461
|
T | C | 1 | a0002c0002t0001g0207 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.607-1449T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25095461 | ||||||
| chr12:25095890
|
C | T | 35 | a0003c0003t0002g0079a0003c0003t0002g0093a0003c0003t0002g0113others(32): Show | 35 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.607-1020C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25095890 | ||||||
| chr12:25095929
|
A | G | 1 | a0007c0009t0001g0200 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.607-981A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25095929 | ||||||
| chr12:25096133
|
G | GA | 294 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(291): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.607-775dupA | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 25096133 | |||||
| chr12:25096155
|
A | AT | 13 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0095others(10): Show | 14 | HG00673.hp1 HG01257.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.607-747dupT | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr12 | 25096155 | |||||
| chr12:25096166
|
A | T | 3 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0284 | 3 | HG00673.hp2 NA18982.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.607-744A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25096166 | ||||||
| chr12:25096520
|
T | A | 4 | a0002c0002t0001g0175a0002c0002t0001g0308a0002c0002t0001g0309others(1): Show | 4 | HG03041.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.607-390T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25096520 | ||||||
| chr12:25096530
|
T | C | 1 | a0002c0002t0001g0155 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.607-380T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25096530 | ||||||
| chr12:25096611
|
A | G | 35 | a0003c0003t0002g0079a0003c0003t0002g0093a0003c0003t0002g0113others(32): Show | 35 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.607-299A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25096611 | ||||||
| chr12:25096809
|
T | C | 177 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(174): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.607-101T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25096809 | ||||||
| chr12:25096851
|
T | C | 198 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(195): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.607-59T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25096851 | ||||||
| chr12:25097166
|
A | G | 1 | a0005c0006t0007g0051 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.741+122A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25097166 | ||||||
| chr12:25097170
|
G | A | 5 | a0003c0003t0002g0079a0003c0003t0005g0032a0003c0003t0005g0033others(2): Show | 5 | HG00099.hp1 HG01099.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.741+126G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25097170 | ||||||
| chr12:25097225
|
TAAAA | T | 35 | a0003c0003t0002g0079a0003c0003t0002g0093a0003c0003t0002g0113others(32): Show | 35 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.741+185_741+188del others(4): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 25097225 | |||||
| chr12:25097238
|
T | C | 197 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(194): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.741+194T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25097238 | ||||||
| chr12:25097238
|
T | TAAC | 125 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0006others(122): Show | 135 | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(132): Show |
intron_variant | MODIFIER | c.741+195_741+196ins others(3): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 25097238 | |||||
| chr12:25097411
|
G | A | 12 | a0001c0001t0001g0091a0001c0001t0001g0098a0001c0001t0001g0111others(9): Show | 12 | HG00544.hp1 HG00544.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.741+367G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25097411 | ||||||
| chr12:25097419
|
C | G | 1 | a0002c0002t0001g0074 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.741+375C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25097419 | ||||||
| chr12:25097808
|
C | T | 1 | a0002c0002t0001g0199 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.741+764C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25097808 | ||||||
| chr12:25097819
|
T | C | 1 | a0003c0003t0001g0173 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.741+775T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25097819 | ||||||
| chr12:25097826
|
T | C | 28 | a0002c0002t0001g0003a0002c0002t0001g0013a0002c0002t0001g0014others(25): Show | 33 | HG01167.hp2 HG01169.hp1 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.741+782T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25097826 | ||||||
| chr12:25098162
|
G | C | 53 | a0002c0002t0001g0001a0002c0002t0001g0008a0002c0002t0001g0017others(50): Show | 57 | HG00423.hp2 HG01069.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.741+1118G>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25098162 | ||||||
| chr12:25098170
|
G | A | 35 | a0003c0003t0002g0079a0003c0003t0002g0093a0003c0003t0002g0113others(32): Show | 35 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.741+1126G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25098170 | ||||||
| chr12:25098311
|
A | G | 1 | a0001c0001t0001g0097 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.741+1267A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25098311 | ||||||
| chr12:25098374
|
C | T | 1 | a0001c0001t0014g0018 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.741+1330C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25098374 | ||||||
| chr12:25098447
|
G | A | 157 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(154): Show | 167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.741+1403G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25098447 | ||||||
| chr12:25098448
|
C | T | 1 | a0003c0003t0001g0243 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.741+1404C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25098448 | ||||||
| chr12:25099184
|
G | C | 319 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(316): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.742-1994G>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25099184 | ||||||
| chr12:25099205
|
T | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG01081.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.742-1973T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25099205 | ||||||
| chr12:25099244
|
C | A | 101 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0008others(98): Show | 114 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(111): Show |
intron_variant | MODIFIER | c.742-1934C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25099244 | ||||||
| chr12:25099256
|
G | A | 1 | a0003c0003t0003g0158 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.742-1922G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25099256 | ||||||
| chr12:25099354
|
G | A | 50 | a0002c0002t0001g0001a0002c0002t0001g0008a0002c0002t0001g0017others(47): Show | 54 | HG00423.hp2 HG01069.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.742-1824G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25099354 | ||||||
| chr12:25099476
|
T | C | 81 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0008others(78): Show | 90 | HG00423.hp2 HG01069.hp1 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.742-1702T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25099476 | ||||||
| chr12:25099538
|
T | G | 1 | a0001c0001t0006g0195 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.742-1640T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25099538 | ||||||
| chr12:25099682
|
T | G | 3 | a0002c0002t0001g0175a0002c0002t0001g0308a0002c0002t0001g0309 | 3 | HG03041.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.742-1496T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25099682 | ||||||
| chr12:25099691
|
A | G | 4 | a0002c0002t0001g0046a0002c0002t0001g0063a0002c0002t0001g0160others(1): Show | 4 | HG02717.hp2 HG03486.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.742-1487A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25099691 | ||||||
| chr12:25099717
|
T | G | 2 | a0001c0001t0001g0138a0001c0001t0001g0248 | 2 | HG02080.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.742-1461T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25099717 | ||||||
| chr12:25100000
|
G | GA | 12 | a0002c0002t0001g0006a0002c0002t0001g0037a0002c0002t0001g0038others(9): Show | 13 | HG00642.hp1 HG00733.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.742-1153dupA | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 25100000 | |||||
| chr12:25100000
|
G | GAAAAAAA others(2): Show |
31 | a0001c0001t0001g0035a0001c0001t0001g0117a0001c0001t0001g0186others(28): Show | 34 | HG00639.hp2 HG01070.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.742-1161_742-1153d others(11): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 25100000 | |||||
| chr12:25100000
|
G | GAAAAAAA others(3): Show |
61 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0053others(58): Show | 64 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.742-1162_742-1153d others(12): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 25100000 | |||||
| chr12:25100000
|
G | GAAAAAAA others(4): Show |
72 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(69): Show | 75 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.742-1163_742-1153d others(13): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 25100000 | |||||
| chr12:25100000
|
G | GAAAAAAA others(5): Show |
36 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0041others(33): Show | 41 | HG00423.hp1 HG00609.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.742-1164_742-1153d others(14): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 25100000 | |||||
| chr12:25100000
|
G | GAAAAAAA others(6): Show |
18 | a0001c0001t0001g0085a0001c0001t0001g0225a0001c0001t0001g0248others(15): Show | 19 | HG00280.hp1 HG01261.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.742-1165_742-1153d others(15): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 25100000 | |||||
| chr12:25100000
|
G | GAAAAAAA others(7): Show |
15 | a0001c0001t0001g0045a0001c0001t0001g0153a0001c0001t0001g0154others(12): Show | 15 | HG00738.hp2 HG01243.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.742-1166_742-1153d others(16): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 25100000 | |||||
| chr12:25100000
|
G | GAAAAAAA others(8): Show |
4 | a0001c0001t0001g0039a0003c0003t0001g0173a0003c0003t0003g0060others(1): Show | 4 | HG02257.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.742-1167_742-1153d others(17): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 25100000 | |||||
| chr12:25100000
|
GAA | G | 21 | a0001c0001t0001g0107a0001c0001t0001g0223a0004c0004t0001g0002others(18): Show | 25 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.742-1154_742-1153d others(4): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 25100000 | |||||
| chr12:25100000
|
GAAAA | G | 16 | a0003c0003t0002g0093a0003c0003t0002g0113a0003c0003t0002g0122others(13): Show | 16 | HG00408.hp2 HG01109.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.742-1156_742-1153d others(6): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 25100000 | |||||
| chr12:25100000
|
GAAAAA | G | 19 | a0003c0003t0002g0079a0003c0003t0002g0184a0003c0003t0002g0201others(16): Show | 19 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.742-1157_742-1153d others(7): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 25100000 | |||||
| chr12:25100026
|
T | A | 1 | a0007c0009t0001g0200 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.742-1152T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25100026 | ||||||
| chr12:25100105
|
C | T | 1 | a0003c0003t0001g0173 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.742-1073C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25100105 | ||||||
| chr12:25100325
|
A | C | 34 | a0003c0003t0002g0079a0003c0003t0002g0093a0003c0003t0002g0113others(31): Show | 34 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.742-853A>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25100325 | ||||||
| chr12:25100390
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.742-788G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25100390 | ||||||
| chr12:25100702
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.742-476C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25100702 | ||||||
| chr12:25100825
|
C | CT | 230 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(227): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.742-338dupT | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 25100825 | |||||
| chr12:25100881
|
A | G | 1 | a0002c0002t0001g0280 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.742-297A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25100881 | ||||||
| chr12:25100990
|
G | A | 1 | a0002c0002t0012g0167 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.742-188G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25100990 | ||||||
| chr12:25101044
|
CT | C | 9 | a0003c0003t0003g0021a0003c0003t0003g0022a0003c0003t0003g0023others(6): Show | 9 | HG01891.hp2 HG02451.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.742-129delT | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr12 | 25101044 | |||||
| chr12:25101049
|
T | A | 82 | a0001c0001t0002g0281a0002c0002t0001g0006a0002c0002t0001g0037others(79): Show | 87 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.742-129T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25101049 | ||||||
| chr12:25101050
|
A | T | 56 | a0001c0001t0001g0217a0001c0001t0001g0268a0001c0001t0001g0269others(53): Show | 60 | HG00423.hp2 HG01069.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.742-128A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 15/21 | chr12 | 25101050 | ||||||
| chr12:25101410
|
A | G | 4 | a0002c0002t0001g0046a0002c0002t0001g0160a0003c0003t0001g0159others(1): Show | 4 | HG02258.hp1 HG03486.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.889+85A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 16/21 | chr12 | 25101410 | ||||||
| chr12:25101496
|
T | C | 1 | a0005c0006t0001g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.889+171T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 16/21 | chr12 | 25101496 | ||||||
| chr12:25101623
|
A | G | 12 | a0002c0002t0001g0001a0002c0002t0001g0027a0002c0002t0001g0056others(9): Show | 14 | HG01070.hp1 HG01175.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.889+298A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 16/21 | chr12 | 25101623 | ||||||
| chr12:25101642
|
C | T | 53 | a0001c0001t0001g0217a0001c0001t0001g0268a0001c0001t0001g0269others(50): Show | 57 | HG00423.hp2 HG01069.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.889+317C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 16/21 | chr12 | 25101642 | ||||||
| chr12:25101773
|
G | A | 1 | a0003c0003t0002g0127 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.890-425G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 16/21 | chr12 | 25101773 | ||||||
| chr12:25101776
|
G | C | 44 | a0002c0002t0001g0003a0002c0002t0001g0013a0002c0002t0001g0014others(41): Show | 49 | HG01167.hp2 HG01169.hp1 HG01261.hp1 others(46): Show |
intron_variant | MODIFIER | c.890-422G>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 16/21 | chr12 | 25101776 | ||||||
| chr12:25101798
|
A | G | 5 | a0002c0002t0001g0038a0002c0002t0001g0073a0002c0002t0001g0074others(2): Show | 5 | HG00738.hp1 HG01433.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.890-400A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 16/21 | chr12 | 25101798 | ||||||
| chr12:25101856
|
T | C | 32 | a0002c0002t0001g0003a0002c0002t0001g0013a0002c0002t0001g0014others(29): Show | 37 | HG01167.hp2 HG01169.hp1 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.890-342T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 16/21 | chr12 | 25101856 | ||||||
| chr12:25101868
|
G | A | 1 | a0002c0002t0001g0151 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.890-330G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 16/21 | chr12 | 25101868 | ||||||
| chr12:25101917
|
C | T | 12 | a0002c0002t0001g0046a0002c0002t0001g0160a0003c0003t0001g0159others(9): Show | 12 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.890-281C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 16/21 | chr12 | 25101917 | ||||||
| chr12:25102030
|
T | A | 1 | a0001c0001t0001g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.890-168T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 16/21 | chr12 | 25102030 | ||||||
| chr12:25102041
|
A | C | 277 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(274): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.890-157A>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 16/21 | chr12 | 25102041 | ||||||
| chr12:25102100
|
C | T | 53 | a0001c0001t0001g0217a0001c0001t0001g0268a0001c0001t0001g0269others(50): Show | 57 | HG00423.hp2 HG01069.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.890-98C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 16/21 | chr12 | 25102100 | ||||||
| chr12:25102357
|
T | C | 1 | a0002c0002t0001g0155 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.933+116T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 17/21 | chr12 | 25102357 | ||||||
| chr12:25102441
|
A | T | 1 | a0002c0002t0001g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.933+200A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 17/21 | chr12 | 25102441 | ||||||
| chr12:25102452
|
C | G | 2 | a0003c0003t0002g0113a0003c0003t0002g0180 | 2 | NA18949.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.933+211C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 17/21 | chr12 | 25102452 | ||||||
| chr12:25102501
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.933+260G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 17/21 | chr12 | 25102501 | ||||||
| chr12:25102574
|
C | T | 53 | a0001c0001t0001g0217a0001c0001t0001g0268a0001c0001t0001g0269others(50): Show | 57 | HG00423.hp2 HG01069.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.933+333C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 17/21 | chr12 | 25102574 | ||||||
| chr12:25102770
|
C | T | 101 | a0001c0001t0001g0217a0001c0001t0001g0268a0001c0001t0001g0269others(98): Show | 110 | HG00423.hp2 HG01069.hp1 HG01070.hp1 others(107): Show |
intron_variant | MODIFIER | c.933+529C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 17/21 | chr12 | 25102770 | ||||||
| chr12:25102790
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.933+549T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 17/21 | chr12 | 25102790 | ||||||
| chr12:25103012
|
A | G | 322 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(319): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.933+771A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 17/21 | chr12 | 25103012 | ||||||
| chr12:25103042
|
C | T | 12 | a0002c0002t0001g0046a0002c0002t0001g0160a0003c0003t0001g0159others(9): Show | 12 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.934-795C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 17/21 | chr12 | 25103042 | ||||||
| chr12:25103126
|
C | T | 2 | a0001c0001t0001g0312a0003c0003t0001g0173 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.934-711C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 17/21 | chr12 | 25103126 | ||||||
| chr12:25103252
|
A | C | 1 | a0001c0001t0001g0086 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.934-585A>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 17/21 | chr12 | 25103252 | ||||||
| chr12:25103371
|
C | T | 53 | a0001c0001t0001g0217a0001c0001t0001g0268a0001c0001t0001g0269others(50): Show | 57 | HG00423.hp2 HG01069.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.934-466C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 17/21 | chr12 | 25103371 | ||||||
| chr12:25103376
|
G | A | 53 | a0001c0001t0001g0217a0001c0001t0001g0268a0001c0001t0001g0269others(50): Show | 57 | HG00423.hp2 HG01069.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.934-461G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 17/21 | chr12 | 25103376 | ||||||
| chr12:25103420
|
C | T | 101 | a0001c0001t0001g0217a0001c0001t0001g0268a0001c0001t0001g0269others(98): Show | 110 | HG00423.hp2 HG01069.hp1 HG01070.hp1 others(107): Show |
intron_variant | MODIFIER | c.934-417C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 17/21 | chr12 | 25103420 | ||||||
| chr12:25103490
|
C | A | 12 | a0002c0002t0001g0006a0002c0002t0001g0037a0002c0002t0001g0038others(9): Show | 13 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.934-347C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 17/21 | chr12 | 25103490 | ||||||
| chr12:25103652
|
G | A | 2 | a0001c0001t0001g0186a0001c0001t0001g0194 | 2 | HG00639.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.934-185G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 17/21 | chr12 | 25103652 | ||||||
| chr12:25103673
|
T | A | 1 | a0001c0001t0001g0253 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.934-164T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 17/21 | chr12 | 25103673 | ||||||
| chr12:25103809
|
T | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0211 | 3 | NA18948.hp2 NA18954.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.934-28T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 17/21 | chr12 | 25103809 | ||||||
| chr12:25103966
|
G | A | 4 | a0002c0002t0001g0046a0002c0002t0001g0160a0003c0003t0001g0159others(1): Show | 4 | HG02258.hp1 HG03486.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.997-43G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 18/21 | chr12 | 25103966 | ||||||
| chr12:25104123
|
G | T | 2 | a0001c0001t0001g0312a0003c0003t0001g0173 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1046+65G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 19/21 | chr12 | 25104123 | ||||||
| chr12:25104232
|
T | A | 134 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(131): Show | 140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1047-129T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 19/21 | chr12 | 25104232 | ||||||
| chr12:25104248
|
GA | G | 237 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(234): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1047-106delA | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr12 | 25104248 | |||||
| chr12:25104354
|
T | C | 1 | a0007c0009t0001g0200 | 1 | HG02572.hp2 | splice_region_variant&intron_variant | LOW | c.1047-7T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 19/21 | chr12 | 25104354 | ||||||
| chr12:25104495
|
C | T | 46 | a0002c0002t0001g0003a0002c0002t0001g0013a0002c0002t0001g0014others(43): Show | 51 | HG01167.hp2 HG01169.hp1 HG01261.hp1 others(48): Show |
intron_variant | MODIFIER | c.1148+33C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25104495 | ||||||
| chr12:25104874
|
CATCT | C | 53 | a0001c0001t0001g0217a0001c0001t0001g0268a0001c0001t0001g0269others(50): Show | 57 | HG00423.hp2 HG01069.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.1148+421_1148+424d others(6): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25104874 | |||||
| chr12:25105050
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0248 | 2 | HG02080.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1148+588G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25105050 | ||||||
| chr12:25105056
|
C | A | 134 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(131): Show | 140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1148+594C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25105056 | ||||||
| chr12:25105056
|
CCTTA | C | 36 | a0001c0001t0002g0281a0003c0003t0002g0079a0003c0003t0002g0093others(33): Show | 36 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.1148+598_1148+601d others(6): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25105056 | |||||
| chr12:25105071
|
G | GT | 17 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0154others(14): Show | 17 | HG00738.hp1 HG01099.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1148+632dupT | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25105071 | |||||
| chr12:25105071
|
GT | G | 131 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(128): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.1148+632delT | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25105071 | |||||
| chr12:25105071
|
GTT | G | 89 | a0001c0001t0001g0053a0001c0001t0001g0212a0001c0001t0001g0217others(86): Show | 98 | HG00423.hp2 HG01069.hp1 HG01070.hp1 others(95): Show |
intron_variant | MODIFIER | c.1148+631_1148+632d others(4): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25105071 | |||||
| chr12:25105079
|
T | G | 1 | a0001c0010t0001g0115 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1148+617T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25105079 | ||||||
| chr12:25105138
|
G | A | 4 | a0002c0002t0001g0175a0002c0002t0001g0308a0002c0002t0001g0309others(1): Show | 4 | HG03041.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1148+676G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25105138 | ||||||
| chr12:25105139
|
C | T | 18 | a0004c0004t0001g0002a0004c0004t0001g0004a0004c0004t0001g0016others(15): Show | 22 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.1148+677C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25105139 | ||||||
| chr12:25105181
|
A | G | 36 | a0001c0001t0002g0281a0003c0003t0002g0079a0003c0003t0002g0093others(33): Show | 36 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.1148+719A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25105181 | ||||||
| chr12:25105318
|
C | T | 11 | a0001c0001t0001g0010a0001c0001t0001g0102a0001c0001t0001g0106others(8): Show | 12 | HG00621.hp2 HG00673.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1148+856C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25105318 | ||||||
| chr12:25105323
|
G | A | 1 | a0002c0002t0001g0142 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1148+861G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25105323 | ||||||
| chr12:25105524
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0220 | 2 | HG02486.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1148+1062A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25105524 | ||||||
| chr12:25105563
|
A | T | 1 | a0002c0002t0003g0283 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1148+1101A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25105563 | ||||||
| chr12:25105567
|
T | G | 1 | a0002c0002t0001g0233 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1148+1105T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25105567 | ||||||
| chr12:25105640
|
G | GA | 85 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0153others(82): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.1148+1187dupA | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25105640 | |||||
| chr12:25105793
|
G | A | 2 | a0001c0001t0001g0312a0003c0003t0001g0173 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1149-1150G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25105793 | ||||||
| chr12:25105842
|
T | C | 18 | a0001c0001t0002g0281a0003c0003t0002g0093a0003c0003t0002g0113others(15): Show | 18 | HG00408.hp2 HG01109.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.1149-1101T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25105842 | ||||||
| chr12:25105966
|
AT | A | 8 | a0006c0005t0001g0019a0006c0005t0001g0059a0006c0005t0001g0064others(5): Show | 8 | HG02109.hp2 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1149-976delT | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25105966 | ||||||
| chr12:25105984
|
A | G | 322 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(319): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1149-959A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25105984 | ||||||
| chr12:25106055
|
ATACTAAT others(1): Show |
A | 4 | a0002c0002t0001g0046a0002c0002t0001g0160a0003c0003t0001g0159others(1): Show | 4 | HG02258.hp1 HG03486.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1149-885_1149-878d others(10): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25106055 | |||||
| chr12:25106085
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1149-858G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106085 | ||||||
| chr12:25106145
|
T | C | 2 | a0003c0003t0001g0062a0003c0003t0001g0170 | 2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1149-798T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106145 | ||||||
| chr12:25106223
|
T | C | 6 | a0002c0002t0001g0231a0002c0002t0001g0232a0002c0002t0001g0240others(3): Show | 6 | HG01496.hp1 HG01934.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1149-720T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106223 | ||||||
| chr12:25106290
|
C | T | 1 | a0003c0003t0001g0173 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1149-653C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106290 | ||||||
| chr12:25106328
|
A | G | 4 | a0002c0002t0001g0046a0002c0002t0001g0160a0003c0003t0001g0159others(1): Show | 4 | HG02258.hp1 HG03486.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1149-615A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106328 | ||||||
| chr12:25106340
|
TATAC | T | 54 | a0001c0001t0001g0217a0001c0001t0001g0268a0001c0001t0001g0269others(51): Show | 58 | HG00423.hp2 HG01069.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.1149-595_1149-592d others(6): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25106340 | |||||
| chr12:25106527
|
G | GTCAGACT others(213): Show |
1 | a0005c0006t0001g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1149-415_1149-414i others(222): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25106527 | |||||
| chr12:25106528
|
T | TCAGA | 69 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(66): Show | 76 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1149-415_1149-414i others(6): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106528 | ||||||
| chr12:25106528
|
T | TCAGACTC others(230): Show |
4 | a0002c0002t0001g0046a0002c0002t0001g0160a0003c0003t0001g0159others(1): Show | 4 | HG02258.hp1 HG03486.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1149-415_1149-414i others(239): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106528 | ||||||
| chr12:25106528
|
T | TCAGACTC others(233): Show |
2 | a0003c0003t0001g0062a0003c0003t0001g0170 | 2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1149-415_1149-414i others(242): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106528 | ||||||
| chr12:25106528
|
T | TCAGACTC others(227): Show |
1 | a0003c0003t0002g0184 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1149-415_1149-414i others(236): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106528 | ||||||
| chr12:25106528
|
T | TCAGACTC others(231): Show |
139 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(136): Show | 142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1149-415_1149-414i others(240): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106528 | ||||||
| chr12:25106528
|
T | TCAGACTC others(229): Show |
1 | a0001c0001t0001g0005 | 2 | HG01106.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1149-415_1149-414i others(238): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106528 | ||||||
| chr12:25106529
|
T | A | 1 | a0005c0006t0001g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1149-414T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106529 | ||||||
| chr12:25106529
|
T | C | 71 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(68): Show | 78 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1149-414T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106529 | ||||||
| chr12:25106529
|
T | G | 147 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(144): Show | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1149-414T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106529 | ||||||
| chr12:25106531
|
C | T | 1 | a0005c0006t0001g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1149-412C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106531 | ||||||
| chr12:25106532
|
T | TG | 69 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(66): Show | 76 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1149-411_1149-410i others(3): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106532 | ||||||
| chr12:25106532
|
T | TGAC | 147 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(144): Show | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1149-411_1149-410i others(5): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106532 | ||||||
| chr12:25106532
|
T | TTAAATAT others(224): Show |
2 | a0001c0001t0001g0312a0003c0003t0001g0173 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1149-410_1149-409i others(233): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25106532 | |||||
| chr12:25106534
|
C | T | 1 | a0005c0006t0001g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1149-409C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106534 | ||||||
| chr12:25106536
|
C | CTTAAATA others(461): Show |
69 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(66): Show | 76 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1149-407_1149-406i others(470): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106536 | ||||||
| chr12:25106536
|
C | G | 149 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(146): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.1149-407C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106536 | ||||||
| chr12:25106536
|
C | T | 1 | a0005c0006t0001g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1149-407C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106536 | ||||||
| chr12:25106537
|
C | A | 70 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(67): Show | 77 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1149-406C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106537 | ||||||
| chr12:25106537
|
C | T | 149 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(146): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.1149-406C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106537 | ||||||
| chr12:25106538
|
A | T | 218 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(215): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1149-405A>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106538 | ||||||
| chr12:25106541
|
C | A | 69 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(66): Show | 76 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1149-402C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106541 | ||||||
| chr12:25106544
|
G | T | 69 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(66): Show | 76 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1149-399G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106544 | ||||||
| chr12:25106545
|
G | A | 70 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(67): Show | 77 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1149-398G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106545 | ||||||
| chr12:25106546
|
C | CT | 149 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(146): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.1149-397_1149-396i others(3): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106546 | ||||||
| chr12:25106547
|
A | G | 149 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(146): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.1149-396A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106547 | ||||||
| chr12:25106548
|
G | T | 69 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(66): Show | 76 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1149-395G>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106548 | ||||||
| chr12:25106549
|
A | AT | 18 | a0001c0001t0013g0087a0002c0002t0001g0003a0002c0002t0001g0013others(15): Show | 23 | HG01167.hp2 HG01169.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.1149-394_1149-393i others(3): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106549 | ||||||
| chr12:25106549
|
A | ATAT | 47 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(44): Show | 49 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1149-394_1149-393i others(5): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106549 | ||||||
| chr12:25106549
|
AG | A | 4 | a0002c0002t0001g0295a0002c0002t0001g0296a0003c0003t0001g0028others(1): Show | 4 | HG00099.hp1 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1149-393delG | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106549 | ||||||
| chr12:25106550
|
G | A | 65 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(62): Show | 72 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.1149-393G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106550 | ||||||
| chr12:25106550
|
G | GTACAGTA others(230): Show |
1 | a0001c0001t0001g0097 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1149-392_1149-391i others(239): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25106550 | |||||
| chr12:25106550
|
G | GTACAGTA others(229): Show |
67 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(64): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1149-392_1149-391i others(238): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25106550 | |||||
| chr12:25106550
|
G | GTACAGTA others(231): Show |
22 | a0001c0001t0001g0009a0001c0001t0001g0045a0001c0001t0001g0089others(19): Show | 23 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1149-392_1149-391i others(240): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25106550 | |||||
| chr12:25106550
|
G | GTACAGTA others(233): Show |
21 | a0001c0001t0001g0025a0001c0001t0001g0132a0001c0001t0001g0133others(18): Show | 21 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.1149-392_1149-391i others(242): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25106550 | |||||
| chr12:25106550
|
G | GTACAGTA others(235): Show |
8 | a0001c0001t0001g0121a0001c0001t0001g0143a0001c0001t0002g0281others(5): Show | 8 | HG00609.hp1 HG00621.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1149-392_1149-391i others(244): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25106550 | |||||
| chr12:25106550
|
G | GTACAGTA others(237): Show |
5 | a0002c0002t0001g0046a0003c0003t0002g0150a0003c0003t0002g0187others(2): Show | 5 | HG01109.hp2 HG03486.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.1149-392_1149-391i others(246): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25106550 | |||||
| chr12:25106550
|
G | GTACAGTA others(239): Show |
5 | a0003c0003t0002g0122a0003c0003t0002g0124a0003c0003t0002g0125others(2): Show | 5 | HG00408.hp2 HG02004.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.1149-392_1149-391i others(248): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25106550 | |||||
| chr12:25106550
|
G | GTACAGTA others(241): Show |
7 | a0001c0001t0001g0270a0003c0003t0009g0031a0003c0003t0009g0078others(4): Show | 7 | HG02109.hp2 HG02523.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1149-392_1149-391i others(250): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25106550 | |||||
| chr12:25106550
|
G | GTACAGTA others(243): Show |
5 | a0003c0003t0002g0093a0003c0003t0002g0127a0006c0005t0001g0064others(2): Show | 5 | HG01346.hp2 HG02895.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1149-392_1149-391i others(252): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25106550 | |||||
| chr12:25106550
|
G | GTACAGTA others(245): Show |
2 | a0003c0003t0002g0128a0006c0005t0001g0019 | 2 | HG02818.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1149-392_1149-391i others(254): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25106550 | |||||
| chr12:25106550
|
G | GTACAGTA others(247): Show |
1 | a0003c0003t0002g0123 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1149-392_1149-391i others(256): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25106550 | |||||
| chr12:25106550
|
G | GTACAGTA others(249): Show |
1 | a0006c0005t0001g0065 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1149-392_1149-391i others(258): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25106550 | |||||
| chr12:25106551
|
T | TACAGTAG others(213): Show |
2 | a0001c0001t0001g0312a0003c0003t0001g0173 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1149-392_1149-391i others(222): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106551 | ||||||
| chr12:25106551
|
T | TACAGTAG others(219): Show |
2 | a0004c0004t0001g0190a0004c0004t0001g0209 | 2 | HG01361.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1149-392_1149-391i others(228): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106551 | ||||||
| chr12:25106552
|
T | A | 218 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(215): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1149-391T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106552 | ||||||
| chr12:25106552
|
T | C | 1 | a0005c0006t0001g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1149-391T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106552 | ||||||
| chr12:25106554
|
C | A | 218 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(215): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1149-389C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106554 | ||||||
| chr12:25106556
|
C | A | 218 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(215): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1149-387C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106556 | ||||||
| chr12:25106558
|
G | A | 218 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(215): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1149-385G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106558 | ||||||
| chr12:25106558
|
G | GTTGCCTA others(240): Show |
1 | a0005c0006t0001g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1149-385_1149-384i others(249): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106558 | ||||||
| chr12:25106559
|
C | T | 219 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(216): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1149-384C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106559 | ||||||
| chr12:25106596
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1149-347A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106596 | ||||||
| chr12:25106647
|
T | TTTGTATA others(18): Show |
2 | a0003c0003t0001g0062a0003c0003t0001g0170 | 2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1149-270_1149-246d others(27): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25106647 | |||||
| chr12:25106647
|
TTTGTATA others(18): Show |
T | 1 | a0001c0001t0014g0018 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1149-270_1149-246d others(27): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25106647 | |||||
| chr12:25106694
|
TCTAA | T | 4 | a0002c0002t0001g0259a0003c0003t0002g0260a0003c0003t0002g0261others(1): Show | 4 | HG01167.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1149-242_1149-239d others(6): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25106694 | |||||
| chr12:25106742
|
A | AT | 219 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(216): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1149-196dupT | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr12 | 25106742 | |||||
| chr12:25106816
|
G | A | 56 | a0001c0001t0001g0217a0001c0001t0001g0268a0001c0001t0001g0269others(53): Show | 60 | HG00423.hp2 HG01069.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.1149-127G>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106816 | ||||||
| chr12:25107155
|
T | TTGTTGTA others(7): Show |
1 | a0001c0001t0001g0143 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1256+108_1256+121d others(16): Show |
IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr12 | 25107155 | |||||
| chr12:25107741
|
C | G | 14 | a0001c0001t0001g0020a0001c0001t0001g0053a0001c0001t0001g0054others(11): Show | 14 | HG00140.hp2 HG00733.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1257-76C>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 21/21 | chr12 | 25107741 |