Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MNDDP others(494): Show |
chr12 | 25047706 | 25113335 |
| a0002 | 0/0 | 499 | 100 | 41 | 31 | 19 | 0 | 9 | 15 | IRAG2_chr12_25047706_25113335 | IRAG2 | MNDDP others(494): Show |
chr12 | 25047706 | 25113335 |
| a0003 | 1/0 | 499 | 55 | 18 | 13 | 14 | 5 | 4 | 9 | IRAG2_chr12_25047706_25113335 | IRAG2 | MNDDP others(494): Show |
chr12 | 25047706 | 25113335 |
| a0004 | 0/0 | 499 | 24 | 4 | 9 | 0 | 2 | 9 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | MNDDP others(494): Show |
chr12 | 25047706 | 25113335 |
| a0005 | 0/0 | 499 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | MNDDP others(494): Show |
chr12 | 25047706 | 25113335 |
| a0006 | 0/0 | 499 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | MNDDP others(494): Show |
chr12 | 25047706 | 25113335 |
| a0007 | 0/0 | 499 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | MNDDP others(494): Show |
chr12 | 25047706 | 25113335 |
| a0008 | 0/0 | 499 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | MNDDP others(494): Show |
chr12 | 25047706 | 25113335 |
| a0009 | 0/0 | 499 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | MNDDP others(494): Show |
chr12 | 25047706 | 25113335 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1497 | 138 | 9 | 33 | 71 | 7 | 17 | IRAG2_chr12_25047706_25113335 | IRAG2 | ATGAA others(1492): Show |
chr12 | 25047706 | 25113335 | ||
| a0001c0007 | 0/0 | 1497 | 3 | 0 | 0 | 3 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | ATGAA others(1492): Show |
chr12 | 25047706 | 25113335 | ||
| a0001c0008 | 0/0 | 1497 | 2 | 0 | 0 | 2 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | ATGAA others(1492): Show |
chr12 | 25047706 | 25113335 | ||
| a0001c0010 | 0/0 | 1497 | 2 | 0 | 0 | 2 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | ATGAA others(1492): Show |
chr12 | 25047706 | 25113335 | ||
| a0002c0002 | 0/0 | 1497 | 100 | 41 | 31 | 19 | 0 | 9 | IRAG2_chr12_25047706_25113335 | IRAG2 | ATGAA others(1492): Show |
chr12 | 25047706 | 25113335 | ||
| a0003c0003 | 1/0 | 1497 | 55 | 18 | 13 | 14 | 5 | 4 | IRAG2_chr12_25047706_25113335 | IRAG2 | ATGAA others(1492): Show |
chr12 | 25047706 | 25113335 | ||
| a0004c0004 | 0/0 | 1497 | 24 | 4 | 9 | 0 | 2 | 9 | IRAG2_chr12_25047706_25113335 | IRAG2 | ATGAA others(1492): Show |
chr12 | 25047706 | 25113335 | ||
| a0005c0006 | 0/0 | 1497 | 8 | 8 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | ATGAA others(1492): Show |
chr12 | 25047706 | 25113335 | ||
| a0006c0005 | 0/0 | 1497 | 8 | 8 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | ATGAA others(1492): Show |
chr12 | 25047706 | 25113335 | ||
| a0007c0009 | 0/0 | 1497 | 2 | 2 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | ATGAA others(1492): Show |
chr12 | 25047706 | 25113335 | ||
| a0008c0012 | 0/0 | 1497 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | ATGAA others(1492): Show |
chr12 | 25047706 | 25113335 | ||
| a0009c0011 | 0/0 | 1497 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | ATGAA others(1492): Show |
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 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0001c0001t0002 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0001c0001t0006 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0001c0001t0013 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0001c0001t0014 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0001c0007t0001 | 0/0 | 2472 | 3 | 0 | 0 | 3 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0001c0008t0001 | 0/0 | 2472 | 2 | 0 | 0 | 2 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0001c0010t0001 | 0/0 | 2472 | 2 | 0 | 0 | 2 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0002c0002t0001 | 0/0 | 2472 | 95 | 39 | 31 | 16 | 0 | 9 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0002c0002t0003 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0002c0002t0006 | 0/0 | 2472 | 2 | 0 | 0 | 2 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0002c0002t0010 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0002c0002t0012 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0003c0003t0001 | 1/0 | 2472 | 8 | 6 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0003c0003t0002 | 0/0 | 2472 | 22 | 0 | 8 | 11 | 2 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0003c0003t0003 | 0/0 | 2472 | 10 | 10 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0003c0003t0004 | 0/0 | 2472 | 6 | 0 | 1 | 1 | 3 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0003c0003t0005 | 0/0 | 2472 | 4 | 0 | 3 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0003c0003t0008 | 0/0 | 2472 | 2 | 2 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0003c0003t0009 | 0/0 | 2472 | 2 | 0 | 0 | 2 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0003c0003t0010 | 0/0 | 2472 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0004c0004t0001 | 0/0 | 2472 | 23 | 4 | 9 | 0 | 2 | 8 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0004c0004t0006 | 0/0 | 2472 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0005c0006t0001 | 0/0 | 2472 | 4 | 4 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0005c0006t0007 | 0/0 | 2472 | 3 | 3 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0005c0006t0011 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0006c0005t0001 | 0/0 | 2472 | 8 | 8 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0007c0009t0001 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0007c0009t0003 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0008c0012t0001 | 0/0 | 2472 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| a0009c0011t0002 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | AGTTT others(2467): Show |
chr12 | 25047706 | 25113335 |
| actghapid | grch38/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 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0093 | 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 |
| a0001c0001t0001g0122 | 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 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0219 | 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 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0001c0001t0001g0231 | 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 |
| a0001c0001t0001g0267 | 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 |
| a0001c0008t0001g0217 | 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 |
| a0002c0002t0001g0082 | 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 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0002c0002t0001g0268 | 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 |
| a0002c0002t0006g0220 | 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 |
| a0003c0003t0002g0094 | 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 |
| 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 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0003c0003t0005g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0008c0012t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| a0009c0011t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | g0213 | 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 | g0084 | 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 | g0126 | 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 | g0321 | 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 | g0034 | 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 | g0125 | 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 | g0211 | 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 | g0212 | 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 | g0320 | 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 | g0322 | 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 | g0214 | 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 | g0127 | EAS | KHV | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0231 | 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 | g0323 | 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 | g0032 | 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 | g0083 | SAS | PJL | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0228 | 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 | g0082 | 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 | g0227 | 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 | g0033 | 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 | g0093 | SAS | STU | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| HG04204 | hp2 | a0008 | 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 | g0124 | 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 | g0217 | 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 | g0267 | 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 | g0233 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0215 | 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 | g0094 | 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 | g0122 | 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 | g0210 | 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 | g0268 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0232 | 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 | g0230 | 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 | g0229 | 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 | a0009 | 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 | g0123 | 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 | g0216 | EAS | JPT | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| NA19091 | hp1 | a0002 | c0002 | t0006 | g0220 | 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 | g0219 | 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 | a0001 | c0001 | t0001 | g0085 | REF | REF | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0001 | g0162 | REF | REF | IRAG2_chr12_25047706_25113335 | IRAG2 | chr12 | 25047706 | 25113335 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:25079438 | A | G | 2 | a0005 a0007 |
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 | a0001 a0002 a0005 others(1): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): 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 | a0001 a0004 a0008 others(1): Show |
170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): 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 | a0008 | 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 | a0009 | 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 | a0002 a0003 a0007 |
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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:25052787 | T | C | 3 | a0002c0002t0012 a0003c0003t0008 a0005c0006t0011 |
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 | a0001c0001t0006 a0002c0002t0006 a0002c0002t0010 others(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 | a0002c0002t0010 a0003c0003t0004 a0003c0003t0005 others(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 | a0005c0006t0007 a0005c0006t0011 |
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 | a0001c0001t0002 a0003c0003t0002 a0003c0003t0004 others(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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | a0001c0001t0001g0025 a0003c0003t0003g0022 a0003c0003t0003g0023 others(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 | a0001c0001t0001g0312 a0002c0002t0001g0308 a0002c0002t0001g0309 others(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 | a0003c0003t0003g0021 a0003c0003t0003g0307 |
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 | a0001c0001t0001g0305 a0001c0001t0001g0306 |
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 | a0005c0006t0001g0298 a0005c0006t0001g0299 a0005c0006t0001g0300 others(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 | a0002c0002t0001g0295 a0002c0002t0001g0296 |
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 | a0002c0002t0001g0295 a0002c0002t0001g0296 |
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 | a0001c0001t0001g0312 a0002c0002t0001g0001 a0002c0002t0001g0027 others(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 | a0002c0002t0001g0001 a0002c0002t0001g0027 |
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 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0003c0003t0003g0022 others(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 | a0001c0001t0001g0182 a0001c0001t0001g0185 a0001c0001t0001g0186 others(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 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
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 | 290 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(287): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): 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 | a0002c0002t0010g0030 a0003c0003t0004g0314 a0003c0003t0004g0315 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0002c0002t0001g0151 others(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 | a0005c0006t0007g0302 a0005c0006t0007g0304 a0005c0006t0011g0303 |
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 | a0001c0001t0001g0025 a0003c0003t0003g0022 a0003c0003t0003g0023 others(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 | a0003c0003t0003g0156 a0003c0003t0003g0158 a0006c0005t0001g0157 |
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 | a0001c0001t0001g0312 a0002c0002t0001g0308 a0002c0002t0001g0309 others(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 | a0002c0002t0010g0030 a0003c0003t0004g0314 a0003c0003t0004g0315 others(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 | 299 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(296): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): 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 | a0002c0002t0010g0030 a0003c0003t0004g0314 a0003c0003t0004g0315 others(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 | a0001c0001t0001g0182 a0002c0002t0001g0181 a0003c0003t0002g0180 |
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 | a0001c0001t0001g0290 a0002c0002t0001g0289 a0002c0002t0001g0291 others(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 | 260 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(257): Show |
274 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(271): 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 | 302 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(299): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): 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 | a0002c0002t0001g0171 a0002c0002t0001g0172 a0002c0002t0001g0174 others(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 | 302 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(299): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): 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 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0194 others(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 | 228 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(225): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): 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 | a0001c0001t0001g0035 a0001c0001t0001g0139 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0312 a0002c0002t0001g0308 a0002c0002t0001g0309 others(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 | a0001c0001t0001g0290 a0002c0002t0001g0199 a0002c0002t0001g0280 others(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 | a0002c0002t0001g0171 a0002c0002t0001g0172 a0002c0002t0001g0174 others(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 | a0002c0002t0001g0171 a0002c0002t0001g0172 a0002c0002t0001g0174 others(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 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
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 | a0002c0002t0010g0030 a0003c0003t0004g0314 a0003c0003t0004g0315 others(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 | 309 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(306): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): 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 | a0002c0002t0010g0030 a0003c0003t0009g0031 |
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 | a0002c0002t0010g0030 a0003c0003t0009g0031 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0002c0002t0010g0030 a0003c0003t0004g0314 a0003c0003t0004g0315 others(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 | 132 | a0001c0001t0001g0007 a0001c0001t0001g0080 a0001c0001t0001g0081 others(129): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(133): 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 | a0002c0002t0010g0030 a0003c0003t0004g0314 a0003c0003t0004g0315 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0002c0002t0001g0006 others(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 | a0002c0002t0010g0030 a0003c0003t0004g0314 a0003c0003t0004g0315 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0068 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
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 | a0002c0002t0001g0171 a0002c0002t0001g0172 a0002c0002t0001g0174 others(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 | a0004c0004t0001g0067 a0004c0004t0001g0140 |
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 | a0002c0002t0010g0030 a0003c0003t0004g0314 a0003c0003t0004g0315 others(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 | a0002c0002t0001g0001 a0002c0002t0001g0027 |
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 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0312 a0002c0002t0001g0308 a0002c0002t0001g0309 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0182 a0001c0001t0001g0276 a0001c0001t0001g0277 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0001t0001g0135 others(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 | a0002c0002t0010g0030 a0003c0003t0004g0314 a0003c0003t0004g0315 others(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 | a0001c0001t0001g0025 a0003c0003t0003g0022 a0003c0003t0003g0023 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0068 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
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 | a0001c0001t0001g0025 a0001c0001t0001g0068 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0068 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0068 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0068 a0001c0001t0001g0072 others(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 | a0003c0003t0003g0156 a0003c0003t0003g0158 a0006c0005t0001g0157 |
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 | 130 | a0001c0001t0001g0007 a0001c0001t0001g0080 a0001c0001t0001g0081 others(127): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): 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 | a0002c0002t0010g0030 a0003c0003t0004g0314 a0003c0003t0004g0315 others(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 | a0001c0001t0001g0312 a0002c0002t0001g0001 a0002c0002t0001g0027 others(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 | 130 | a0001c0001t0001g0007 a0001c0001t0001g0080 a0001c0001t0001g0081 others(127): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): 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 | a0003c0003t0003g0156 a0003c0003t0003g0158 a0006c0005t0001g0157 |
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 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0312 a0002c0002t0001g0001 a0002c0002t0001g0027 others(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 | a0002c0002t0001g0295 a0002c0002t0001g0296 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0045 a0001c0001t0001g0068 others(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 | 120 | a0001c0001t0001g0007 a0001c0001t0001g0080 a0001c0001t0001g0081 others(117): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): 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 | a0002c0002t0001g0063 a0003c0003t0001g0061 a0003c0003t0001g0062 others(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 | a0001c0001t0001g0312 a0002c0002t0001g0001 a0002c0002t0001g0027 others(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 | a0001c0001t0001g0025 a0002c0002t0001g0280 a0003c0003t0002g0201 others(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 | a0002c0002t0001g0171 a0002c0002t0001g0172 a0002c0002t0001g0174 others(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 | a0002c0002t0001g0308 a0002c0002t0001g0309 a0002c0002t0001g0310 others(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 | a0001c0001t0001g0025 a0002c0002t0001g0280 a0003c0003t0002g0201 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0312 a0002c0002t0001g0006 others(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 | 118 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0045 others(115): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): 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 | a0004c0004t0001g0002 a0004c0004t0001g0067 a0004c0004t0001g0140 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | 116 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0045 others(113): Show |
122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): 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 | a0002c0002t0001g0006 a0002c0002t0001g0037 a0002c0002t0001g0069 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | 175 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0039 others(172): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): 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 | 124 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0039 others(121): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): 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 | a0001c0001t0001g0072 a0001c0001t0001g0312 a0002c0002t0001g0141 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0114 others(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 | a0006c0005t0001g0065 a0006c0005t0001g0066 |
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 | 119 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0045 others(116): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): 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 | 118 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0045 others(115): Show |
126 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(123): 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 | a0003c0003t0004g0314 a0003c0003t0004g0315 a0003c0003t0004g0316 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0134 others(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 | a0003c0003t0003g0060 a0006c0005t0001g0059 |
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 | a0001c0001t0001g0072 a0001c0001t0001g0312 a0002c0002t0001g0141 others(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 | a0003c0003t0003g0156 a0003c0003t0008g0161 a0006c0005t0001g0157 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0248 a0001c0001t0001g0249 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0312 a0002c0002t0001g0141 others(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 | a0002c0002t0001g0295 a0002c0002t0001g0296 |
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 | 129 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0039 others(126): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): 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 | 299 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(296): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): 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 | a0002c0002t0001g0308 a0002c0002t0001g0309 |
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 | a0001c0001t0001g0025 a0002c0002t0001g0280 a0003c0003t0001g0159 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | a0001c0001t0001g0198 a0001c0001t0001g0277 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0045 a0002c0002t0001g0043 others(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 | a0002c0002t0001g0295 a0002c0002t0001g0296 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0045 a0002c0002t0001g0043 others(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 | a0002c0002t0001g0308 a0002c0002t0001g0309 a0002c0002t0001g0310 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | a0002c0002t0001g0308 a0002c0002t0001g0309 a0002c0002t0001g0310 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0134 others(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 | 296 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(293): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): 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 | a0002c0002t0001g0308 a0002c0002t0001g0309 a0002c0002t0001g0310 others(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 | a0002c0002t0001g0006 a0002c0002t0001g0037 a0002c0002t0001g0038 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | 123 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0039 others(120): Show |
126 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(123): 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 | a0002c0002t0001g0308 a0002c0002t0001g0309 a0002c0002t0001g0310 others(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 | 113 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0045 others(110): Show |
118 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(115): 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 | a0002c0002t0001g0295 a0002c0002t0001g0296 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0025 a0002c0002t0001g0280 a0003c0003t0002g0203 others(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 | 262 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(259): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): 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 | a0005c0006t0001g0298 a0005c0006t0001g0299 a0005c0006t0001g0300 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | 114 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0045 others(111): Show |
119 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(116): 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 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0039 others(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 | a0001c0001t0001g0025 a0002c0002t0001g0280 a0003c0003t0002g0203 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0002c0002t0001g0295 a0002c0002t0001g0296 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0134 others(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 | a0005c0006t0007g0302 a0005c0006t0007g0304 a0005c0006t0011g0303 |
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 | 114 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0045 others(111): Show |
119 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(116): 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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0134 others(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 | 116 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0045 others(113): Show |
121 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.24+2948A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25072379 | |||||||
| chr12:25072401 | G | A | 114 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0045 others(111): Show |
119 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(116): 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 | a0001c0001t0001g0025 a0002c0002t0001g0280 a0003c0003t0002g0203 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | |||||||
| chr12:25072789 | 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 | a0002c0002t0001g0171 a0002c0002t0001g0172 a0002c0002t0001g0176 |
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 | a0002c0002t0001g0171 a0002c0002t0001g0172 a0002c0002t0001g0176 others(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 | 164 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0025 others(161): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): 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 | a0003c0003t0001g0243 a0006c0005t0001g0244 |
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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | a0002c0002t0001g0171 a0002c0002t0001g0172 a0002c0002t0001g0176 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0025 a0002c0002t0001g0280 a0003c0003t0002g0203 others(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 | 110 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0042 others(107): Show |
114 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(111): 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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0320 others(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 | a0002c0002t0001g0295 a0002c0002t0001g0296 |
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 | a0002c0002t0001g0295 a0002c0002t0001g0296 |
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 | 129 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0025 others(126): Show |
134 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(131): 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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0134 others(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 | 111 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0042 others(108): Show |
116 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(113): 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 | a0002c0002t0001g0295 a0002c0002t0001g0296 |
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 | 257 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(254): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): 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 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0237 others(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 | a0001c0001t0001g0025 a0002c0002t0001g0280 a0003c0003t0002g0203 others(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 | a0002c0002t0001g0047 a0002c0002t0001g0048 |
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 | 112 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0042 others(109): Show |
117 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(114): 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 | a0002c0002t0001g0295 a0002c0002t0001g0296 |
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 | a0005c0006t0001g0298 a0005c0006t0001g0299 a0005c0006t0001g0300 others(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 | a0004c0004t0001g0002 a0004c0004t0001g0040 a0004c0004t0001g0067 others(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 | 154 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0039 others(151): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): 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 | a0005c0006t0001g0298 a0005c0006t0001g0299 a0005c0006t0001g0300 others(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 | a0002c0002t0001g0295 a0002c0002t0001g0296 |
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 | 103 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(100): Show |
110 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(107): 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 | a0001c0001t0001g0084 a0001c0001t0001g0112 a0001c0001t0001g0224 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0045 a0002c0002t0001g0160 a0002c0002t0001g0226 |
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 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0263 others(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 | a0001c0001t0001g0253 a0002c0002t0001g0052 a0003c0003t0003g0049 others(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 | a0002c0002t0001g0001 a0002c0002t0001g0027 |
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 | a0005c0006t0001g0298 a0005c0006t0001g0299 a0005c0006t0001g0300 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0002c0002t0010g0030 others(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 | a0001c0001t0001g0122 a0003c0003t0002g0079 a0003c0003t0002g0125 others(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 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0138 others(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 | 97 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0039 others(94): Show |
99 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(96): 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 | a0005c0006t0007g0302 a0005c0006t0007g0304 a0005c0006t0011g0303 |
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 | 111 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0042 others(108): Show |
116 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(113): 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 | a0002c0002t0001g0308 a0002c0002t0001g0309 a0002c0002t0001g0310 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | 256 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(253): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): 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 | a0003c0003t0002g0079 a0003c0003t0005g0032 a0003c0003t0005g0033 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(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 | a0002c0002t0001g0308 a0002c0002t0001g0309 a0002c0002t0001g0310 others(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 | a0001c0001t0001g0112 a0001c0001t0001g0251 |
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 | a0002c0002t0001g0308 a0002c0002t0001g0309 a0002c0002t0001g0310 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0093 a0003c0003t0002g0079 a0003c0003t0002g0201 others(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 | a0001c0001t0001g0093 a0003c0003t0002g0079 a0003c0003t0002g0201 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0092 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0093 a0003c0003t0002g0079 a0003c0003t0002g0201 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 |
88 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0042 others(85): Show |
91 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(88): 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 | a0001c0001t0001g0112 a0001c0001t0001g0251 |
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 | a0003c0003t0002g0201 a0003c0003t0002g0202 a0003c0003t0004g0314 others(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 | a0001c0001t0001g0093 a0001c0001t0001g0210 a0001c0001t0001g0284 others(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 | a0002c0002t0001g0308 a0002c0002t0001g0309 a0002c0002t0001g0310 |
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 | a0001c0001t0001g0093 a0001c0001t0001g0210 a0001c0001t0001g0284 others(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 | a0003c0003t0002g0079 a0003c0003t0005g0033 a0003c0003t0005g0034 |
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 | a0001c0001t0001g0093 a0001c0001t0001g0210 a0001c0001t0001g0284 others(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 | a0003c0003t0002g0079 a0003c0003t0005g0033 a0003c0003t0005g0034 |
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 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0253 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0253 others(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 | a0001c0001t0001g0210 | 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 | a0001c0001t0001g0092 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0112 a0001c0001t0001g0251 |
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 | a0001c0001t0001g0112 a0001c0001t0001g0251 |
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 | a0001c0001t0001g0112 a0001c0001t0001g0251 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0002c0002t0001g0043 a0002c0002t0001g0044 |
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 | a0002c0002t0001g0183 a0002c0002t0001g0229 |
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 | a0004c0004t0001g0002 a0004c0004t0001g0140 |
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 | a0001c0001t0001g0206 a0001c0001t0001g0267 |
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 | a0001c0001t0001g0186 a0001c0001t0001g0194 a0001c0001t0001g0223 |
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 | a0001c0001t0001g0185 a0001c0001t0001g0293 a0008c0012t0001g0193 |
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 | a0001c0001t0001g0192 a0002c0002t0001g0245 a0003c0003t0003g0021 |
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 | a0001c0001t0001g0198 a0001c0001t0001g0277 |
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 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(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 | a0001c0001t0001g0230 a0002c0002t0001g0199 |
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 | a0002c0002t0001g0227 | 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 | a0001c0001t0001g0231 | 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 | a0002c0002t0001g0207 a0004c0004t0001g0004 |
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 | a0001c0008t0001g0217 | 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 | a0001c0001t0001g0204 a0001c0001t0001g0218 a0001c0001t0001g0246 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0214 a0001c0001t0001g0215 others(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 | a0001c0001t0001g0306 a0002c0002t0001g0235 a0003c0003t0003g0158 |
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 | a0001c0001t0001g0068 a0006c0005t0001g0244 |
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 | a0001c0001t0001g0219 | 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 | a0001c0001t0001g0248 a0002c0002t0006g0220 |
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 | a0002c0002t0001g0160 a0002c0002t0001g0174 |
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 | a0001c0001t0001g0042 a0001c0001t0001g0083 |
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 |
1 | a0002c0002t0001g0082 | 1 | HG03669.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 | a0001c0001t0001g0081 a0001c0001t0001g0084 |
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 | a0001c0001t0001g0080 a0001c0001t0001g0225 a0002c0002t0001g0008 |
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 | a0001c0001t0002g0281 a0001c0007t0001g0129 a0001c0007t0001g0130 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
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 | a0002c0002t0001g0308 a0002c0002t0001g0309 a0002c0002t0001g0310 others(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 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
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 | a0001c0001t0001g0112 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0003c0003t0002g0079 a0003c0003t0005g0033 a0003c0003t0005g0034 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | a0001c0001t0001g0322 | 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 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0083 a0001c0001t0001g0206 others(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 | 112 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0042 others(109): Show |
115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): 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 | a0003c0003t0002g0201 a0003c0003t0002g0202 a0003c0003t0004g0314 others(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 | a0001c0001t0001g0039 a0002c0002t0001g0043 a0002c0002t0001g0044 |
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 | a0001c0001t0001g0005 a0002c0002t0001g0308 a0002c0002t0001g0309 others(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 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0112 others(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 | a0003c0003t0002g0079 a0003c0003t0005g0033 a0003c0003t0005g0034 |
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 | a0003c0003t0002g0094 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0002c0002t0001g0108 others(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 | a0002c0002t0001g0063 a0003c0003t0001g0062 a0006c0005t0001g0019 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0134 others(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 | a0002c0002t0001g0308 a0002c0002t0001g0309 a0002c0002t0001g0310 others(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 | a0001c0001t0001g0214 a0002c0002t0001g0199 a0002c0002t0001g0308 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | a0001c0001t0001g0323 a0002c0002t0001g0160 a0002c0002t0001g0174 |
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 | a0001c0001t0001g0323 a0002c0002t0001g0160 a0002c0002t0001g0174 |
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 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0185 others(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 | 84 | a0001c0001t0001g0007 a0001c0001t0001g0042 a0001c0001t0001g0068 others(81): Show |
87 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(84): 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 | a0001c0001t0001g0039 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0003c0003t0002g0201 a0003c0003t0002g0202 a0003c0003t0004g0314 others(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 | a0001c0001t0001g0191 a0002c0002t0001g0175 a0004c0004t0001g0254 others(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 | a0001c0001t0001g0263 a0002c0002t0001g0017 a0002c0002t0001g0255 others(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 | a0004c0004t0001g0016 a0004c0004t0001g0264 a0004c0004t0001g0273 others(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 | a0001c0001t0001g0253 a0002c0002t0001g0288 a0004c0004t0001g0265 others(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 | a0003c0003t0003g0049 a0005c0006t0007g0051 |
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 | a0001c0001t0001g0153 a0002c0002t0001g0151 a0002c0002t0001g0152 others(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 | a0001c0001t0006g0195 a0003c0003t0009g0031 |
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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0134 others(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 | 88 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0042 others(85): Show |
91 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.25-1934T>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 6/21 | chr12 | 25077310 | |||||||
| chr12:25077316 | T | TATATGA | 85 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0042 others(82): Show |
88 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(85): 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 | a0001c0001t0001g0089 a0001c0001t0001g0185 a0001c0001t0001g0186 others(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 | a0003c0003t0002g0079 a0003c0003t0005g0033 a0003c0003t0005g0034 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0185 a0001c0001t0001g0186 others(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 | a0001c0001t0001g0045 a0002c0002t0001g0046 a0002c0002t0001g0308 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0322 a0005c0006t0007g0302 a0005c0006t0007g0304 others(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 | a0003c0003t0009g0031 a0004c0004t0001g0209 |
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 | a0003c0003t0002g0079 a0003c0003t0005g0033 a0003c0003t0005g0034 |
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 | a0001c0008t0001g0217 | 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 | a0001c0008t0001g0217 | 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 | a0003c0003t0002g0079 a0003c0003t0005g0033 a0003c0003t0005g0034 others(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 | a0003c0003t0002g0201 a0003c0003t0002g0202 a0003c0003t0004g0314 others(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 | a0001c0001t0001g0323 a0002c0002t0001g0160 a0002c0002t0001g0174 |
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 | a0003c0003t0002g0079 a0003c0003t0005g0033 a0003c0003t0005g0034 others(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 | a0001c0001t0001g0191 a0001c0001t0001g0198 a0001c0001t0001g0277 others(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 | a0001c0001t0001g0322 a0002c0002t0001g0308 a0002c0002t0001g0309 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | 90 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0042 others(87): Show |
93 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(90): 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 | a0003c0003t0002g0201 a0003c0003t0002g0202 a0003c0003t0004g0314 others(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 | a0003c0003t0002g0201 a0003c0003t0002g0202 a0003c0003t0004g0314 others(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 | a0005c0006t0007g0302 a0005c0006t0007g0304 a0005c0006t0011g0303 |
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 | a0005c0006t0007g0302 a0005c0006t0007g0304 a0005c0006t0011g0303 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | a0003c0003t0002g0201 a0003c0003t0002g0202 a0003c0003t0004g0314 others(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 | a0001c0001t0001g0323 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | 83 | a0001c0001t0001g0007 a0001c0001t0001g0042 a0001c0001t0001g0068 others(80): Show |
86 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(83): 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 | a0003c0003t0002g0079 a0003c0003t0005g0033 a0003c0003t0005g0034 |
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 | a0004c0004t0001g0067 a0004c0004t0001g0140 |
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 | a0001c0001t0001g0219 | 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 | a0001c0001t0001g0197 a0002c0002t0001g0245 |
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 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0192 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0138 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0198 a0001c0001t0001g0277 others(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 | a0001c0001t0001g0092 a0001c0001t0001g0146 |
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 | a0002c0002t0001g0047 a0002c0002t0001g0048 |
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 |
81 | a0001c0001t0001g0042 a0001c0001t0001g0068 a0001c0001t0001g0080 others(78): Show |
83 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(80): 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 | a0001c0001t0001g0039 a0002c0002t0001g0043 a0002c0002t0001g0044 |
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 | a0002c0002t0001g0308 a0002c0002t0001g0309 a0002c0002t0001g0310 others(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 | a0001c0001t0001g0045 a0001c0008t0001g0217 a0002c0002t0001g0046 others(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 | a0002c0002t0001g0171 a0002c0002t0001g0172 a0002c0002t0001g0176 others(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 | a0003c0003t0002g0201 a0003c0003t0002g0202 a0003c0003t0004g0314 others(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 | a0003c0003t0002g0201 a0003c0003t0002g0202 a0003c0003t0004g0314 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0045 a0001c0001t0001g0191 others(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 | a0001c0001t0001g0092 a0001c0001t0001g0146 a0001c0001t0001g0252 others(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 | a0003c0003t0002g0201 a0003c0003t0002g0202 a0003c0003t0004g0314 others(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 | a0002c0002t0001g0171 a0002c0002t0001g0172 a0002c0002t0001g0176 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0002c0002t0001g0295 a0002c0002t0001g0296 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0045 a0002c0002t0001g0043 others(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 | a0002c0002t0001g0171 a0002c0002t0001g0172 a0002c0002t0001g0176 others(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 | 111 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0042 others(108): Show |
116 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(113): 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 | a0005c0006t0001g0298 a0005c0006t0001g0299 a0005c0006t0001g0300 others(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 | a0002c0002t0001g0295 a0002c0002t0001g0296 |
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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0134 others(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 | 130 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0039 others(127): Show |
135 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(132): 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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0134 a0003c0003t0002g0128 |
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 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0253 others(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 | a0004c0004t0001g0002 a0004c0004t0001g0040 a0004c0004t0001g0067 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | a0002c0002t0001g0295 a0002c0002t0001g0296 |
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 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0253 others(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 | a0005c0006t0001g0298 a0005c0006t0001g0299 a0005c0006t0001g0300 others(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 | a0002c0002t0001g0199 a0002c0002t0001g0289 a0002c0002t0001g0294 others(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 | a0004c0004t0001g0002 a0004c0004t0001g0040 a0004c0004t0001g0067 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0136 a0001c0001t0001g0320 others(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 | a0004c0004t0001g0002 a0004c0004t0001g0040 a0004c0004t0001g0067 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0253 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0269 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0253 others(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 | a0001c0001t0001g0095 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0007t0001g0129 a0001c0007t0001g0130 a0001c0007t0001g0131 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0111 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | 298 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(295): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): 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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0134 others(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 | a0002c0002t0001g0295 a0002c0002t0001g0296 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0320 a0001c0001t0001g0321 others(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 | a0002c0002t0001g0295 a0002c0002t0001g0296 a0002c0002t0001g0308 others(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 | a0002c0002t0001g0295 a0002c0002t0001g0296 |
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 | 284 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(281): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): 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 | a0002c0002t0001g0308 a0002c0002t0001g0309 a0002c0002t0001g0310 others(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 | a0001c0001t0001g0025 a0002c0002t0001g0280 a0003c0003t0002g0203 others(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 | a0001c0001t0001g0095 a0001c0001t0001g0107 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0134 others(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 | 231 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(228): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): 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 | 53 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0042 others(50): Show |
55 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(52): 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 | a0002c0002t0001g0006 a0002c0002t0001g0037 a0002c0002t0001g0038 others(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 | a0002c0002t0001g0001 a0002c0002t0001g0027 a0004c0004t0001g0002 others(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 | 276 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(273): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): 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 | |||||||
| chr12:25083979 | G | A | 16 | a0002c0002t0001g0280 a0002c0002t0001g0308 a0002c0002t0001g0309 others(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 | 221 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(218): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): 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 | a0002c0002t0001g0262 a0003c0003t0002g0286 |
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 | a0002c0002t0001g0295 a0002c0002t0001g0296 a0003c0003t0001g0173 |
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 | a0002c0002t0001g0280 a0002c0002t0001g0308 a0002c0002t0001g0309 others(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 | a0001c0001t0001g0191 a0001c0001t0006g0195 |
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 | 146 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0029 others(143): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): 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 | a0001c0001t0001g0042 a0001c0001t0001g0050 a0001c0001t0001g0225 others(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 | a0002c0002t0001g0294 a0002c0002t0001g0308 a0002c0002t0001g0309 others(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 | a0002c0002t0001g0280 a0003c0003t0002g0203 a0004c0004t0001g0103 others(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 | 121 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0029 others(118): Show |
124 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(121): 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 | a0002c0002t0001g0308 a0002c0002t0001g0309 a0002c0002t0001g0310 others(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 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
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 | a0002c0002t0001g0047 a0002c0002t0001g0048 a0002c0002t0001g0063 others(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 | a0001c0001t0001g0218 a0002c0002t0001g0280 a0002c0002t0001g0291 others(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 | a0004c0004t0001g0016 a0004c0004t0001g0254 a0004c0004t0001g0264 others(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 | a0005c0006t0007g0051 a0007c0009t0001g0200 |
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 | a0002c0002t0001g0047 a0002c0002t0001g0048 a0002c0002t0001g0160 others(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 | a0002c0002t0001g0063 a0002c0002t0001g0175 a0002c0002t0001g0311 others(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 | a0005c0006t0007g0302 a0005c0006t0011g0303 |
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 | a0002c0002t0001g0047 a0002c0002t0001g0048 a0002c0002t0001g0063 others(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 | a0001c0001t0001g0025 a0003c0003t0001g0170 a0003c0003t0003g0156 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0134 a0003c0003t0002g0079 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0002c0002t0001g0047 a0002c0002t0001g0048 a0002c0002t0001g0063 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0002c0002t0001g0152 a0002c0002t0001g0280 a0002c0002t0001g0291 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0253 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0084 a0001c0001t0001g0138 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0205 others(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 | a0001c0001t0001g0122 a0002c0002t0001g0006 a0002c0002t0001g0038 others(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 | a0001c0001t0001g0134 a0002c0002t0001g0037 a0002c0002t0001g0052 others(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 | a0001c0001t0001g0025 a0002c0002t0001g0152 a0002c0002t0001g0308 others(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 | a0002c0002t0001g0047 a0002c0002t0001g0048 a0002c0002t0001g0160 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0096 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0091 a0001c0001t0001g0102 others(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 | a0006c0005t0001g0064 a0006c0005t0001g0065 a0006c0005t0001g0066 |
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 | a0003c0003t0001g0062 a0005c0006t0007g0304 a0005c0006t0011g0303 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0134 a0003c0003t0002g0079 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0253 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0002c0002t0001g0280 a0002c0002t0001g0291 a0002c0002t0001g0292 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0253 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0253 others(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 | a0002c0002t0001g0199 a0002c0002t0001g0294 a0003c0003t0003g0057 others(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 | a0002c0002t0001g0152 a0002c0002t0001g0280 a0002c0002t0001g0291 others(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 | a0002c0002t0001g0047 a0002c0002t0001g0048 a0002c0002t0001g0063 others(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 | a0003c0003t0004g0315 a0003c0003t0004g0317 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0253 a0002c0002t0001g0001 a0002c0002t0001g0027 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0134 a0001c0001t0001g0253 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0002c0002t0001g0232 | 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 | a0003c0003t0002g0079 a0003c0003t0002g0201 a0003c0003t0002g0202 others(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 | a0003c0003t0002g0079 a0003c0003t0005g0032 a0003c0003t0005g0033 others(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 | a0002c0002t0001g0160 a0003c0003t0001g0061 |
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 | a0002c0002t0001g0152 a0002c0002t0001g0174 a0002c0002t0001g0175 others(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 | 150 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(147): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): 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 | a0004c0004t0001g0002 a0004c0004t0001g0004 a0004c0004t0001g0016 others(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 | a0004c0004t0001g0002 a0004c0004t0001g0004 a0004c0004t0001g0016 others(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 | 238 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(235): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): 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 | a0002c0002t0001g0001 a0002c0002t0001g0027 |
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 | a0001c0001t0001g0210 | 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 | a0003c0003t0002g0123 | 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 | 185 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(182): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): 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 | a0003c0003t0001g0028 a0003c0003t0001g0159 a0003c0003t0003g0021 others(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 | a0001c0001t0002g0281 a0003c0003t0001g0173 a0003c0003t0002g0079 others(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 | 234 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(231): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): 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 | a0001c0001t0001g0039 a0001c0001t0001g0045 a0001c0001t0001g0153 others(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 | 238 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(235): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): 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 | a0001c0001t0001g0143 a0001c0001t0001g0251 |
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 | a0002c0002t0001g0038 a0002c0002t0001g0073 |
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 | a0004c0004t0001g0002 a0004c0004t0001g0004 a0004c0004t0001g0016 others(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 | a0002c0002t0003g0283 a0003c0003t0001g0028 a0003c0003t0003g0021 others(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 | a0001c0001t0001g0213 | 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 | a0001c0001t0001g0270 a0002c0002t0001g0001 a0002c0002t0001g0003 others(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 | a0001c0001t0001g0270 a0002c0002t0001g0001 a0002c0002t0001g0003 others(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 | 293 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(290): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): 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 | a0001c0001t0001g0270 a0002c0002t0001g0001 a0002c0002t0001g0003 others(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 | a0003c0003t0001g0243 a0006c0005t0001g0019 a0006c0005t0001g0059 others(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 | 287 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(284): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.606+1907C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25092104 | |||||||
| chr12:25092131 | A | G | 287 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(284): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.606+1934A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25092131 | |||||||
| chr12:25092133 | C | T | 155 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(152): Show |
165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.606+1936C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25092133 | |||||||
| chr12:25092186 | A | G | 287 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(284): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.606+1989A>G | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25092186 | |||||||
| chr12:25092272 | C | T | 154 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(151): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): 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 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0013 others(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 | a0001c0001t0001g0270 a0002c0002t0001g0008 a0002c0002t0001g0017 others(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 | a0002c0002t0001g0001 a0002c0002t0001g0027 a0002c0002t0001g0056 others(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 | a0001c0001t0001g0090 a0003c0003t0002g0079 a0003c0003t0002g0094 others(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 | a0003c0003t0002g0126 | 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 | a0003c0003t0002g0094 a0003c0003t0002g0123 a0003c0003t0002g0124 others(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 | a0002c0002t0001g0063 a0002c0002t0001g0076 a0002c0002t0001g0142 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0045 a0001c0001t0001g0153 others(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 | a0002c0002t0001g0046 a0004c0004t0001g0002 a0004c0004t0001g0004 others(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 | 133 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(130): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): 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 | a0001c0001t0001g0039 a0001c0001t0001g0045 a0001c0001t0001g0153 others(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 | a0003c0003t0002g0079 a0003c0003t0002g0094 a0003c0003t0002g0113 others(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 | 318 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(315): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): 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 | a0001c0001t0001g0270 a0002c0002t0001g0001 a0002c0002t0001g0003 others(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 | 155 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(152): Show |
165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): 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 | a0003c0003t0002g0079 a0003c0003t0002g0094 a0003c0003t0002g0113 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0251 |
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 | a0001c0001t0001g0270 a0002c0002t0001g0001 a0002c0002t0001g0003 others(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 | a0003c0003t0001g0243 a0006c0005t0001g0019 a0006c0005t0001g0059 others(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 | 195 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(192): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): 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 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0014 others(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 | 196 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(193): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.607-3157C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25093753 | |||||||
| chr12:25093756 | C | T | 196 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(193): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): 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 | a0003c0003t0002g0079 a0003c0003t0002g0184 a0003c0003t0002g0201 others(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 | 141 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(138): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): 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 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0006 others(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 | a0002c0002t0003g0283 a0003c0003t0001g0028 a0003c0003t0003g0021 others(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 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0017 others(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 | a0004c0004t0001g0002 a0004c0004t0001g0004 a0004c0004t0001g0016 others(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 | a0003c0003t0001g0243 a0006c0005t0001g0064 a0006c0005t0001g0244 |
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 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0006 others(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 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0006 others(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 | 238 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(235): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): 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 | a0004c0004t0001g0002 a0004c0004t0001g0004 a0004c0004t0001g0016 others(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 | a0004c0004t0001g0002 a0004c0004t0001g0004 a0004c0004t0001g0016 others(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 | a0004c0004t0001g0002 a0004c0004t0001g0004 a0004c0004t0001g0016 others(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 | a0004c0004t0001g0002 a0004c0004t0001g0004 a0004c0004t0001g0016 others(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 | a0004c0004t0001g0002 a0004c0004t0001g0004 a0004c0004t0001g0016 others(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 | 161 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(158): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): 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 | 161 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(158): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): 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 | a0002c0002t0001g0227 | 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 | a0003c0003t0002g0079 a0003c0003t0002g0094 a0003c0003t0002g0113 others(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 | a0003c0003t0002g0079 a0003c0003t0002g0094 a0003c0003t0002g0113 others(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 | 293 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(290): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): 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 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0284 |
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 | a0002c0002t0001g0175 a0002c0002t0001g0308 a0002c0002t0001g0309 others(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 | a0003c0003t0002g0079 a0003c0003t0002g0094 a0003c0003t0002g0113 others(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 | 176 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(173): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.607-101T>C | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 14/21 | chr12 | 25096809 | |||||||
| chr12:25096851 | T | C | 197 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(194): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): 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 | a0003c0003t0002g0079 a0003c0003t0005g0032 a0003c0003t0005g0033 others(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 | a0003c0003t0002g0079 a0003c0003t0002g0094 a0003c0003t0002g0113 others(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 | 196 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(193): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): 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 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0006 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0111 others(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 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0014 others(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 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0017 others(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 | a0003c0003t0002g0079 a0003c0003t0002g0094 a0003c0003t0002g0113 others(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 | 156 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(153): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): 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 | 318 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(315): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): 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 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
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 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0008 others(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 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0017 others(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 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0008 others(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 | a0002c0002t0001g0175 a0002c0002t0001g0308 a0002c0002t0001g0309 |
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 | a0002c0002t0001g0046 a0002c0002t0001g0063 a0002c0002t0001g0160 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0248 |
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 | a0002c0002t0001g0006 a0002c0002t0001g0037 a0002c0002t0001g0038 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0117 a0001c0001t0001g0186 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 |
35 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0041 others(32): Show |
40 | HG00423.hp1 HG00609.hp1 HG00621.hp1 others(37): 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 | a0001c0001t0001g0084 a0001c0001t0001g0225 a0001c0001t0001g0248 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0039 a0003c0003t0001g0173 a0003c0003t0003g0060 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0223 a0004c0004t0001g0002 others(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 | a0003c0003t0002g0094 a0003c0003t0002g0113 a0003c0003t0002g0123 others(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 | a0003c0003t0002g0079 a0003c0003t0002g0184 a0003c0003t0002g0201 others(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 | a0003c0003t0002g0079 a0003c0003t0002g0094 a0003c0003t0002g0113 others(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 | 229 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(226): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): 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 | a0003c0003t0003g0021 a0003c0003t0003g0022 a0003c0003t0003g0023 others(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 | a0001c0001t0002g0281 a0002c0002t0001g0006 a0002c0002t0001g0037 others(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 | a0001c0001t0001g0216 a0001c0001t0001g0267 a0001c0001t0001g0269 others(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 | a0002c0002t0001g0046 a0002c0002t0001g0160 a0003c0003t0001g0159 others(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 | a0002c0002t0001g0001 a0002c0002t0001g0027 a0002c0002t0001g0056 others(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 | a0001c0001t0001g0216 a0001c0001t0001g0267 a0001c0001t0001g0269 others(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 | a0003c0003t0002g0125 | 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 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0014 others(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 | a0002c0002t0001g0038 a0002c0002t0001g0073 a0002c0002t0001g0074 others(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 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0014 others(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 | a0002c0002t0001g0046 a0002c0002t0001g0160 a0003c0003t0001g0159 others(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 | 276 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(273): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): 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 | a0001c0001t0001g0216 a0001c0001t0001g0267 a0001c0001t0001g0269 others(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 | a0003c0003t0002g0113 a0003c0003t0002g0180 |
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 | a0001c0001t0001g0216 a0001c0001t0001g0267 a0001c0001t0001g0269 others(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 | a0001c0001t0001g0216 a0001c0001t0001g0267 a0001c0001t0001g0269 others(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 | 321 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(318): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): 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 | a0002c0002t0001g0046 a0002c0002t0001g0160 a0003c0003t0001g0159 others(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 | a0001c0001t0001g0312 a0003c0003t0001g0173 |
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 | a0001c0001t0001g0216 a0001c0001t0001g0267 a0001c0001t0001g0269 others(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 | a0001c0001t0001g0216 a0001c0001t0001g0267 a0001c0001t0001g0269 others(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 | a0001c0001t0001g0216 a0001c0001t0001g0267 a0001c0001t0001g0269 others(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 | a0002c0002t0001g0006 a0002c0002t0001g0037 a0002c0002t0001g0038 others(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 | a0001c0001t0001g0186 a0001c0001t0001g0194 |
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 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0210 |
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 | a0002c0002t0001g0046 a0002c0002t0001g0160 a0003c0003t0001g0159 others(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 | a0001c0001t0001g0312 a0003c0003t0001g0173 |
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 | 133 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(130): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1047-129T>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 19/21 | chr12 | 25104232 | |||||||
| chr12:25104248 | GA | G | 236 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(233): Show |
251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): 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 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0014 others(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 | a0001c0001t0001g0216 a0001c0001t0001g0267 a0001c0001t0001g0269 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0248 |
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 | 133 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(130): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): 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 | a0001c0001t0002g0281 a0003c0003t0002g0079 a0003c0003t0002g0094 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0045 a0001c0001t0001g0154 others(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 | 130 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(127): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): 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 | a0001c0001t0001g0053 a0001c0001t0001g0211 a0001c0001t0001g0216 others(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 | a0002c0002t0001g0175 a0002c0002t0001g0308 a0002c0002t0001g0309 others(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 | a0004c0004t0001g0002 a0004c0004t0001g0004 a0004c0004t0001g0016 others(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 | a0001c0001t0002g0281 a0003c0003t0002g0079 a0003c0003t0002g0094 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0102 a0001c0001t0001g0106 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0219 |
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 | a0002c0002t0001g0229 | 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 | a0001c0001t0001g0039 a0001c0001t0001g0045 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0312 a0003c0003t0001g0173 |
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 | a0001c0001t0002g0281 a0003c0003t0002g0094 a0003c0003t0002g0113 others(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 | a0006c0005t0001g0019 a0006c0005t0001g0059 a0006c0005t0001g0064 others(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 | 321 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(318): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): 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 | a0002c0002t0001g0046 a0002c0002t0001g0160 a0003c0003t0001g0159 others(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 | a0003c0003t0001g0062 a0003c0003t0001g0170 |
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 | a0002c0002t0001g0227 a0002c0002t0001g0228 a0002c0002t0001g0240 others(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 | a0002c0002t0001g0046 a0002c0002t0001g0160 a0003c0003t0001g0159 others(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 | a0001c0001t0001g0216 a0001c0001t0001g0267 a0001c0001t0001g0269 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0020 others(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 | a0002c0002t0001g0046 a0002c0002t0001g0160 a0003c0003t0001g0159 others(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 | a0003c0003t0001g0062 a0003c0003t0001g0170 |
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 |
138 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(135): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0020 others(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 | 146 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(143): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0020 others(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 | 146 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(143): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): 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 | a0001c0001t0001g0312 a0003c0003t0001g0173 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0020 others(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 | 148 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(145): Show |
152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0020 others(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 | 148 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(145): Show |
152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.1149-406C>T | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106537 | |||||||
| chr12:25106538 | A | T | 217 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(214): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0020 others(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 | 148 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(145): Show |
152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): 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 | 148 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(145): Show |
152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0020 others(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 | a0001c0001t0013g0087 a0002c0002t0001g0003 a0002c0002t0001g0013 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0020 others(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 | a0002c0002t0001g0295 a0002c0002t0001g0296 a0003c0003t0001g0028 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0020 others(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 |
66 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(63): Show |
69 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(66): 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 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0132 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0143 a0001c0001t0002g0281 others(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 | a0002c0002t0001g0046 a0003c0003t0002g0150 a0003c0003t0002g0187 others(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 | a0003c0003t0002g0123 a0003c0003t0002g0126 a0003c0003t0002g0127 others(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 | a0001c0001t0001g0270 a0003c0003t0009g0031 a0003c0003t0009g0078 others(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 | a0003c0003t0002g0094 a0003c0003t0002g0125 a0006c0005t0001g0064 others(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 | a0003c0003t0002g0128 a0006c0005t0001g0019 |
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 | a0003c0003t0002g0124 | 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 | a0001c0001t0001g0312 a0003c0003t0001g0173 |
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 | a0004c0004t0001g0190 a0004c0004t0001g0209 |
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 | 217 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(214): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): 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 | 217 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(214): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1149-389C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106554 | |||||||
| chr12:25106556 | C | A | 217 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(214): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1149-387C>A | IRAG2 | ENSG00000118308.16 | transcript | ENST00000556887.6 | protein_coding | 20/21 | chr12 | 25106556 | |||||||
| chr12:25106558 | G | A | 217 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(214): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): 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 | 218 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(215): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): 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 | a0003c0003t0001g0062 a0003c0003t0001g0170 |
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 | a0002c0002t0001g0259 a0003c0003t0002g0260 a0003c0003t0002g0261 others(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 | 218 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(215): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): 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 | a0001c0001t0001g0216 a0001c0001t0001g0267 a0001c0001t0001g0269 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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 |