Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 144715 |
| ensemblid | ENSG00000151164.19 |
| hgncid | 21700 |
| symbol | RAD9B |
| name | RAD9 checkpoint clamp component B |
| refseq_nuc | NM_001286535.2 |
| refseq_prot | NP_001273464.1 |
| ensembl_nuc | ENST00000409300.6 |
| ensembl_prot | ENSP00000386434.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 110502331 |
| end | 110533556 |
| strand | + |
| ver | v1.2 |
| region | chr12:110502331-110533556 |
| region5000 | chr12:110497331-110538556 |
| regionname0 | RAD9B_chr12_110502331_110533556 |
| regionname5000 | RAD9B_chr12_110497331_110538556 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 417 | 243 | 71 | 51 | 75 | 14 | 30 | 60 | RAD9B_chr12_110497331_110538556 | RAD9B | MAAML others(412): Show |
chr12 | 110497331 | 110538556 |
| a0002 | 0/0 | 417 | 36 | 14 | 0 | 18 | 0 | 4 | 15 | RAD9B_chr12_110497331_110538556 | RAD9B | MAAML others(412): Show |
chr12 | 110497331 | 110538556 |
| a0003 | 0/0 | 417 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | MAAML others(412): Show |
chr12 | 110497331 | 110538556 |
| a0004 | 0/0 | 417 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | MAAML others(412): Show |
chr12 | 110497331 | 110538556 |
| a0005 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | MAAML others(412): Show |
chr12 | 110497331 | 110538556 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1251 | 238 | 67 | 51 | 74 | 14 | 30 | RAD9B_chr12_110497331_110538556 | RAD9B | ATGGC others(1246): Show |
chr12 | 110497331 | 110538556 | ||
| a0001c0003 | 0/0 | 1251 | 4 | 3 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | ATGGC others(1246): Show |
chr12 | 110497331 | 110538556 | ||
| a0001c0007 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | ATGGC others(1246): Show |
chr12 | 110497331 | 110538556 | ||
| a0002c0002 | 0/0 | 1251 | 36 | 14 | 0 | 18 | 0 | 4 | RAD9B_chr12_110497331_110538556 | RAD9B | ATGGC others(1246): Show |
chr12 | 110497331 | 110538556 | ||
| a0003c0004 | 0/0 | 1251 | 2 | 1 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | ATGGC others(1246): Show |
chr12 | 110497331 | 110538556 | ||
| a0004c0005 | 0/0 | 1251 | 2 | 2 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | ATGGC others(1246): Show |
chr12 | 110497331 | 110538556 | ||
| a0005c0006 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | ATGGC others(1246): Show |
chr12 | 110497331 | 110538556 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4164 | 185 | 37 | 44 | 65 | 12 | 25 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0001c0001t0002 | 0/0 | 4164 | 31 | 18 | 3 | 6 | 1 | 3 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0001c0001t0003 | 0/0 | 4160 | 5 | 5 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4155): Show |
chr12 | 110497331 | 110538556 |
| a0001c0001t0004 | 0/0 | 4162 | 3 | 3 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4157): Show |
chr12 | 110497331 | 110538556 |
| a0001c0001t0005 | 0/0 | 4164 | 2 | 1 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0001c0001t0008 | 0/0 | 4164 | 2 | 0 | 2 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0001c0001t0009 | 0/0 | 4164 | 2 | 0 | 0 | 2 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0001c0001t0010 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0001c0001t0011 | 0/0 | 4164 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0001c0001t0012 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0001c0001t0014 | 0/0 | 4164 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0001c0001t0015 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0001c0001t0016 | 0/0 | 4164 | 1 | 0 | 0 | 0 | 1 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0001c0001t0017 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0001c0001t0018 | 0/0 | 4164 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0001c0003t0001 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0001c0003t0002 | 0/0 | 4164 | 3 | 3 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0001c0007t0001 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0002c0002t0001 | 0/0 | 4164 | 31 | 11 | 0 | 16 | 0 | 4 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0002c0002t0006 | 0/0 | 4164 | 2 | 0 | 0 | 2 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0002c0002t0007 | 0/0 | 4164 | 2 | 2 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0002c0002t0013 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0003c0004t0001 | 0/0 | 4164 | 2 | 1 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0004c0005t0001 | 0/0 | 4164 | 2 | 2 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| a0005c0006t0001 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | AGGGC others(4159): Show |
chr12 | 110497331 | 110538556 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 0 | 9 | 0 | 1 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0014 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0015 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0101 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0005 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0005g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0008g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0009g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0009g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0010g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0011g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0012g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0014g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0015g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0016g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0017g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0001t0018g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0003t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0003t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0001c0007t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0006g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0002c0002t0013g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0003c0004t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0004c0005t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| a0005c0006t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | GBR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | FIN | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | FIN | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00323 | hp1 | a0001 | c0001 | t0016 | g0107 | EUR | FIN | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0181 | EUR | FIN | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00423 | hp2 | a0002 | c0002 | t0006 | g0021 | EAS | CHS | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00738 | hp1 | a0001 | c0001 | t0008 | g0017 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01069 | hp2 | a0001 | c0001 | t0008 | g0017 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01099 | hp2 | a0003 | c0004 | t0001 | g0032 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0024 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01346 | hp2 | a0001 | c0001 | t0014 | g0001 | AMR | CLM | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | CLM | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | IBS | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01891 | hp1 | a0001 | c0003 | t0002 | g0192 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02055 | hp1 | a0004 | c0005 | t0001 | g0031 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02071 | hp2 | a0002 | c0002 | t0006 | g0021 | EAS | KHV | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02145 | hp2 | a0003 | c0004 | t0001 | g0032 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0020 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02258 | hp1 | a0001 | c0007 | t0001 | g0106 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02280 | hp2 | a0001 | c0001 | t0012 | g0133 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0116 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02647 | hp1 | a0001 | c0001 | t0015 | g0014 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0052 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0115 | SAS | PJL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02886 | hp1 | a0002 | c0002 | t0007 | g0113 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02922 | hp1 | a0001 | c0003 | t0002 | g0036 | AFR | ESN | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02965 | hp1 | a0002 | c0002 | t0013 | g0059 | AFR | ESN | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | ESN | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | ESN | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | ESN | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | ESN | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03098 | hp1 | a0002 | c0002 | t0007 | g0111 | AFR | MSL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | ESN | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03195 | hp2 | a0001 | c0003 | t0002 | g0036 | AFR | ESN | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | MSL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | MSL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0188 | SAS | PJL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | PJL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | ESN | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | STU | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | STU | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03927 | hp2 | a0001 | c0001 | t0011 | g0197 | SAS | BEB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG04115 | hp1 | a0001 | c0001 | t0018 | g0119 | SAS | STU | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0162 | SAS | STU | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | BEB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0090 | SAS | STU | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | STU | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0114 | SAS | STU | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | STU | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | STU | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0091 | AFR | YRI | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | YRI | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | YRI | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | YRI | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18943 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18946 | hp2 | a0005 | c0006 | t0001 | g0002 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18991 | hp2 | a0001 | c0003 | t0001 | g0080 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19010 | hp2 | a0001 | c0001 | t0009 | g0078 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | LWK | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0191 | AFR | LWK | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | LWK | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19085 | hp2 | a0001 | c0001 | t0017 | g0011 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | YRI | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | YRI | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ASW | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ASW | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | TSI | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | TSI | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | GIH | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | GIH | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02486 | hp2 | a0004 | c0005 | t0001 | g0031 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | MSL | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | USA | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | USA | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | LWK | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0101 | REF | REF | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0015 | REF | REF | RAD9B_chr12_110497331_110538556 | RAD9B | chr12 | 110497331 | 110538556 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110512830 | T | C | 1 | a0005 | 1 | NA18946.hp2 | missense_variant | MODERATE | c.440T>C | p.Val147Ala | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/11 | 447/4164 | 440/1254 | 147/417 | chr12 | 110512830 | |||
| chr12:110512860 | C | T | 1 | a0004 | 2 | HG02055.hp1 HG02486.hp2 |
missense_variant | MODERATE | c.470C>T | p.Thr157Met | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/11 | 477/4164 | 470/1254 | 157/417 | chr12 | 110512860 | |||
| chr12:110519858 | G | A | 1 | a0004 | 2 | HG02055.hp1 HG02486.hp2 |
missense_variant | MODERATE | c.832G>A | p.Asp278Asn | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/11 | 839/4164 | 832/1254 | 278/417 | chr12 | 110519858 | |||
| chr12:110522236 | T | C | 1 | a0003 | 2 | HG01099.hp2 HG02145.hp2 |
missense_variant | MODERATE | c.950T>C | p.Ile317Thr | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/11 | 957/4164 | 950/1254 | 317/417 | chr12 | 110522236 | |||
| chr12:110522391 | G | A | 1 | a0002 | 36 | HG00423.hp2 HG00558.hp2 HG01884.hp1 others(33): Show |
missense_variant | MODERATE | c.1105G>A | p.Gly369Arg | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/11 | 1112/4164 | 1105/1254 | 369/417 | chr12 | 110522391 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110503846 | C | T | 1 | a0001c0003 | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
synonymous_variant | LOW | c.87C>T | p.Asp29Asp | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 2/11 | 94/4164 | 87/1254 | 29/417 | chr12 | 110503846 | |||
| chr12:110506636 | A | C | 1 | a0001c0007 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.331A>C | p.Arg111Arg | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/11 | 338/4164 | 331/1254 | 111/417 | chr12 | 110506636 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110530920 | T | G | 1 | a0001c0001t0005 | 2 | HG01109.hp1 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*267T>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 11/11 | 267 | chr12 | 110530920 | ||||||
| chr12:110530993 | G | T | 1 | a0001c0001t0018 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*340G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 11/11 | 340 | chr12 | 110530993 | ||||||
| chr12:110531254 | G | A | 1 | a0002c0002t0006 | 2 | HG00423.hp2 HG02071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*601G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 11/11 | 601 | chr12 | 110531254 | ||||||
| chr12:110531389 | G | A | 1 | a0002c0002t0007 | 2 | HG02886.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*736G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 11/11 | 736 | chr12 | 110531389 | ||||||
| chr12:110531575 | G | A | 1 | a0001c0001t0010 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*922G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 11/11 | 922 | chr12 | 110531575 | ||||||
| chr12:110531583 | GGAAA | G | 1 | a0001c0001t0003 | 5 | HG02647.hp2 HG03516.hp2 NA18522.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*934_*937delAGAA | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 11/11 | 934 | INFO_REALIGN_3_PRIME | chr12 | 110531583 | |||||
| chr12:110531798 | T | C | 1 | a0001c0001t0008 | 2 | HG00738.hp1 HG01069.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1145T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 11/11 | 1145 | chr12 | 110531798 | ||||||
| chr12:110531858 | A | G | 1 | a0001c0001t0017 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1205A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 11/11 | 1205 | chr12 | 110531858 | ||||||
| chr12:110531893 | G | A | 1 | a0001c0001t0011 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1240G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 11/11 | 1240 | chr12 | 110531893 | ||||||
| chr12:110532214 | T | G | 1 | a0001c0001t0012 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1561T>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 11/11 | 1561 | chr12 | 110532214 | ||||||
| chr12:110532265 | C | T | 1 | a0001c0001t0008 | 2 | HG00738.hp1 HG01069.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1612C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 11/11 | 1612 | chr12 | 110532265 | ||||||
| chr12:110532290 | ACT | A | 1 | a0001c0001t0004 | 3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1640_*1641delCT | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 11/11 | 1640 | INFO_REALIGN_3_PRIME | chr12 | 110532290 | |||||
| chr12:110532352 | G | A | 1 | a0001c0001t0009 | 2 | NA18943.hp2 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1699G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 11/11 | 1699 | chr12 | 110532352 | ||||||
| chr12:110532623 | C | T | 1 | a0001c0001t0011 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1970C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 11/11 | 1970 | chr12 | 110532623 | ||||||
| chr12:110532652 | A | G | 3 | a0001c0001t0002 a0001c0001t0010 a0001c0003t0002 |
35 | HG00323.hp2 HG01167.hp2 HG01175.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1999A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 11/11 | 1999 | chr12 | 110532652 | ||||||
| chr12:110532774 | C | A | 1 | a0002c0002t0013 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2121C>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 11/11 | 2121 | chr12 | 110532774 | ||||||
| chr12:110532987 | A | G | 1 | a0001c0001t0016 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2334A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 11/11 | 2334 | chr12 | 110532987 | ||||||
| chr12:110532995 | C | T | 2 | a0001c0001t0008 a0001c0001t0015 |
3 | HG00738.hp1 HG01069.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2342C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 11/11 | 2342 | chr12 | 110532995 | ||||||
| chr12:110533147 | G | C | 1 | a0001c0001t0014 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2494G>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 11/11 | 2494 | chr12 | 110533147 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110502388 | A | C | 1 | a0001c0001t0011g0197 | 1 | HG03927.hp2 | splice_region_variant&intron_variant | LOW | c.46+5A>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 1/10 | chr12 | 110502388 | |||||||
| chr12:110502625 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.46+242T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 1/10 | chr12 | 110502625 | |||||||
| chr12:110502698 | A | G | 5 | a0001c0001t0002g0005 a0001c0001t0002g0193 a0001c0001t0002g0194 others(2): Show |
10 | HG01167.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.46+315A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 1/10 | chr12 | 110502698 | |||||||
| chr12:110502744 | T | C | 4 | a0001c0001t0001g0038 a0001c0001t0004g0039 a0001c0001t0004g0040 others(1): Show |
4 | HG02630.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.46+361T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 1/10 | chr12 | 110502744 | |||||||
| chr12:110502835 | A | G | 2 | a0001c0003t0002g0036 a0001c0003t0002g0192 |
3 | HG01891.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.46+452A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 1/10 | chr12 | 110502835 | |||||||
| chr12:110502943 | C | T | 25 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0034 others(22): Show |
35 | HG00323.hp2 HG01167.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.46+560C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 1/10 | chr12 | 110502943 | |||||||
| chr12:110503112 | G | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0174 others(3): Show |
9 | HG01081.hp1 HG01943.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.47-694G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 1/10 | chr12 | 110503112 | |||||||
| chr12:110503253 | AT | A | 2 | a0001c0001t0002g0177 a0001c0001t0008g0017 |
3 | HG00738.hp1 HG01069.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.47-552delT | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 1/10 | chr12 | 110503253 | |||||||
| chr12:110503254 | T | A | 30 | a0001c0001t0001g0173 a0001c0001t0002g0005 a0001c0001t0002g0016 others(27): Show |
42 | HG00323.hp2 HG01099.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.47-552T>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 1/10 | chr12 | 110503254 | |||||||
| chr12:110503257 | A | T | 6 | a0001c0001t0001g0173 a0001c0001t0004g0039 a0001c0001t0004g0040 others(3): Show |
8 | HG01099.hp2 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.47-549A>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 1/10 | chr12 | 110503257 | |||||||
| chr12:110503383 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.47-423A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 1/10 | chr12 | 110503383 | |||||||
| chr12:110503534 | G | GC | 32 | a0001c0001t0001g0173 a0001c0001t0002g0005 a0001c0001t0002g0016 others(29): Show |
45 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.47-271dupC | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 110503534 | ||||||
| chr12:110503605 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.47-201C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 1/10 | chr12 | 110503605 | |||||||
| chr12:110503723 | C | T | 1 | a0001c0001t0003g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.47-83C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 1/10 | chr12 | 110503723 | |||||||
| chr12:110503920 | A | T | 1 | a0001c0001t0001g0008 | 5 | HG01069.hp1 HG01071.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+44A>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 2/10 | chr12 | 110503920 | |||||||
| chr12:110504074 | G | C | 1 | a0001c0001t0001g0042 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.117+198G>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 2/10 | chr12 | 110504074 | |||||||
| chr12:110504106 | A | G | 3 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.117+230A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 2/10 | chr12 | 110504106 | |||||||
| chr12:110504246 | A | G | 1 | a0001c0001t0010g0191 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.117+370A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 2/10 | chr12 | 110504246 | |||||||
| chr12:110504400 | T | C | 16 | a0001c0001t0002g0016 a0001c0001t0002g0034 a0001c0001t0002g0035 others(13): Show |
20 | HG00323.hp2 HG01175.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.117+524T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 2/10 | chr12 | 110504400 | |||||||
| chr12:110504449 | G | A | 1 | a0001c0003t0002g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.117+573G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 2/10 | chr12 | 110504449 | |||||||
| chr12:110504478 | C | CA | 15 | a0001c0001t0001g0018 a0001c0001t0001g0043 a0001c0001t0001g0044 others(12): Show |
17 | HG00738.hp1 HG01069.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.117+622dupA | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 110504478 | ||||||
| chr12:110504800 | C | T | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.118-817C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 2/10 | chr12 | 110504800 | |||||||
| chr12:110504867 | A | G | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.118-750A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 2/10 | chr12 | 110504867 | |||||||
| chr12:110504872 | G | A | 8 | a0001c0001t0002g0005 a0001c0001t0002g0190 a0001c0001t0002g0193 others(5): Show |
14 | HG01167.hp2 HG01891.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.118-745G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 2/10 | chr12 | 110504872 | |||||||
| chr12:110505026 | A | C | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.118-591A>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 2/10 | chr12 | 110505026 | |||||||
| chr12:110505196 | G | T | 31 | a0001c0001t0001g0173 a0001c0001t0002g0005 a0001c0001t0002g0016 others(28): Show |
43 | HG00323.hp2 HG01099.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.118-421G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 2/10 | chr12 | 110505196 | |||||||
| chr12:110505279 | T | C | 1 | a0001c0001t0002g0181 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.118-338T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 2/10 | chr12 | 110505279 | |||||||
| chr12:110505294 | G | A | 2 | a0001c0001t0003g0052 a0001c0001t0003g0170 |
2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.118-323G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 2/10 | chr12 | 110505294 | |||||||
| chr12:110505395 | C | G | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.118-222C>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 2/10 | chr12 | 110505395 | |||||||
| chr12:110505579 | G | A | 4 | a0002c0002t0001g0053 a0002c0002t0001g0054 a0002c0002t0001g0055 others(1): Show |
4 | NA18946.hp1 NA18959.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-38G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 2/10 | chr12 | 110505579 | |||||||
| chr12:110505827 | G | A | 1 | a0001c0001t0010g0191 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.273+55G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 3/10 | chr12 | 110505827 | |||||||
| chr12:110505862 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.273+90T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 3/10 | chr12 | 110505862 | |||||||
| chr12:110505915 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.273+143C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 3/10 | chr12 | 110505915 | |||||||
| chr12:110505926 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.273+154C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 3/10 | chr12 | 110505926 | |||||||
| chr12:110506166 | G | A | 4 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0058 others(1): Show |
6 | HG01884.hp2 HG02257.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+394G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 3/10 | chr12 | 110506166 | |||||||
| chr12:110506333 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.274-246C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 3/10 | chr12 | 110506333 | |||||||
| chr12:110506424 | G | A | 1 | a0002c0002t0006g0021 | 2 | HG00423.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.274-155G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 3/10 | chr12 | 110506424 | |||||||
| chr12:110506434 | C | T | 3 | a0001c0001t0001g0173 a0003c0004t0001g0032 a0004c0005t0001g0031 |
5 | HG01099.hp2 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-145C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 3/10 | chr12 | 110506434 | |||||||
| chr12:110506494 | G | C | 39 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(36): Show |
52 | HG00099.hp2 HG00621.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.274-85G>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 3/10 | chr12 | 110506494 | |||||||
| chr12:110506780 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.388+87T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110506780 | |||||||
| chr12:110506843 | CT | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0173 a0001c0001t0008g0017 |
8 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.388+164delT | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 110506843 | ||||||
| chr12:110506952 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.388+259G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110506952 | |||||||
| chr12:110507096 | G | A | 3 | a0001c0001t0001g0173 a0003c0004t0001g0032 a0004c0005t0001g0031 |
5 | HG01099.hp2 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.388+403G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110507096 | |||||||
| chr12:110507347 | TTA | T | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.388+663_388+664del others(2): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 110507347 | ||||||
| chr12:110507366 | TATATATA others(18): Show |
T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02451.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.388+693_388+717del others(25): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 110507366 | ||||||
| chr12:110507382 | A | C | 2 | a0001c0001t0003g0052 a0001c0001t0003g0170 |
2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.388+689A>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110507382 | |||||||
| chr12:110507386 | T | A | 1 | a0002c0002t0001g0090 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.388+693T>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110507386 | |||||||
| chr12:110507393 | TATATA | T | 3 | a0001c0001t0001g0166 a0001c0001t0002g0016 a0001c0001t0002g0177 |
5 | HG01361.hp1 NA18948.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.388+706_388+710del others(5): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 110507393 | ||||||
| chr12:110507411 | A | T | 5 | a0001c0001t0002g0005 a0001c0001t0002g0193 a0001c0001t0002g0194 others(2): Show |
10 | HG01167.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.388+718A>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110507411 | |||||||
| chr12:110507436 | TAAATA | T | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG02004.hp1 NA19082.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.388+744_388+748del others(5): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110507436 | |||||||
| chr12:110507441 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.388+748A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110507441 | |||||||
| chr12:110507455 | G | A | 1 | a0002c0002t0001g0091 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.388+762G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110507455 | |||||||
| chr12:110507468 | T | TATATATG others(18): Show |
2 | a0001c0001t0001g0044 a0001c0001t0001g0092 |
2 | HG01358.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.388+844_388+868dup others(25): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 110507468 | ||||||
| chr12:110507468 | TATATATG others(18): Show |
T | 48 | a0001c0001t0001g0025 a0001c0001t0001g0060 a0001c0001t0001g0112 others(45): Show |
72 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.388+844_388+868del others(25): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 110507468 | ||||||
| chr12:110507468 | TATATATG others(43): Show |
T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(118): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.388+819_388+868del others(50): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 110507468 | ||||||
| chr12:110507470 | TATATGTA others(41): Show |
T | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.388+782_388+829del others(48): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 110507470 | ||||||
| chr12:110507493 | AATATATG others(58): Show |
A | 1 | a0001c0001t0001g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.388+813_388+877del others(65): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 110507493 | ||||||
| chr12:110507504 | TAAATATA others(44): Show |
T | 1 | a0001c0001t0001g0097 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.388+814_388+864del others(51): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 110507504 | ||||||
| chr12:110507540 | C | T | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.388+847C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110507540 | |||||||
| chr12:110507571 | T | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG00738.hp2 HG01175.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.388+878T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110507571 | |||||||
| chr12:110507596 | A | G | 1 | a0002c0002t0001g0116 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.388+903A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110507596 | |||||||
| chr12:110507761 | C | T | 19 | a0002c0002t0001g0004 a0002c0002t0001g0010 a0002c0002t0001g0026 others(16): Show |
30 | HG00423.hp2 HG00558.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.388+1068C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110507761 | |||||||
| chr12:110507812 | G | A | 9 | a0001c0001t0001g0037 a0001c0001t0001g0061 a0001c0001t0001g0062 others(6): Show |
9 | HG00738.hp2 HG01074.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.388+1119G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110507812 | |||||||
| chr12:110507863 | A | T | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.388+1170A>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110507863 | |||||||
| chr12:110508117 | G | C | 1 | a0001c0001t0001g0174 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.388+1424G>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110508117 | |||||||
| chr12:110508219 | G | A | 5 | a0001c0001t0002g0005 a0001c0001t0002g0193 a0001c0001t0002g0194 others(2): Show |
10 | HG01167.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.388+1526G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110508219 | |||||||
| chr12:110508316 | G | A | 31 | a0001c0001t0001g0173 a0001c0001t0002g0005 a0001c0001t0002g0016 others(28): Show |
43 | HG00323.hp2 HG01099.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.388+1623G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110508316 | |||||||
| chr12:110508983 | A | G | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.388+2290A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110508983 | |||||||
| chr12:110509194 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.388+2501T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110509194 | |||||||
| chr12:110509380 | T | C | 32 | a0001c0001t0001g0173 a0001c0001t0002g0005 a0001c0001t0002g0016 others(29): Show |
45 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.388+2687T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110509380 | |||||||
| chr12:110509643 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.388+2950T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110509643 | |||||||
| chr12:110509674 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.388+2981A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110509674 | |||||||
| chr12:110509806 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.389-2973G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110509806 | |||||||
| chr12:110509978 | G | A | 31 | a0001c0001t0001g0173 a0001c0001t0002g0005 a0001c0001t0002g0016 others(28): Show |
43 | HG00323.hp2 HG01099.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.389-2801G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110509978 | |||||||
| chr12:110510370 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.389-2409C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110510370 | |||||||
| chr12:110510470 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.389-2309C>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110510470 | |||||||
| chr12:110510630 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.389-2149C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110510630 | |||||||
| chr12:110510639 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.389-2140C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110510639 | |||||||
| chr12:110510764 | G | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 |
3 | NA18954.hp2 NA18961.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.389-2015G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110510764 | |||||||
| chr12:110510826 | C | T | 4 | a0001c0001t0001g0165 a0001c0001t0004g0039 a0001c0001t0004g0040 others(1): Show |
4 | HG02004.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.389-1953C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110510826 | |||||||
| chr12:110511005 | GAGAAA | G | 3 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.389-1759_389-1755d others(7): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 110511005 | ||||||
| chr12:110511022 | G | T | 2 | a0001c0001t0001g0173 a0003c0004t0001g0032 |
3 | HG01099.hp2 HG02145.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.389-1757G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110511022 | |||||||
| chr12:110511101 | A | G | 3 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0189 |
3 | HG00323.hp2 HG01175.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.389-1678A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110511101 | |||||||
| chr12:110511105 | A | T | 1 | a0001c0001t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.389-1674A>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110511105 | |||||||
| chr12:110511118 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.389-1661C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110511118 | |||||||
| chr12:110511245 | G | GA | 4 | a0001c0001t0001g0028 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
5 | HG01167.hp1 HG03688.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.389-1525dupA | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 110511245 | ||||||
| chr12:110511318 | G | A | 1 | a0002c0002t0001g0058 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.389-1461G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110511318 | |||||||
| chr12:110512404 | C | T | 1 | a0002c0002t0013g0059 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.389-375C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110512404 | |||||||
| chr12:110512513 | C | G | 4 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 others(1): Show |
5 | HG00738.hp1 HG01069.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.389-266C>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110512513 | |||||||
| chr12:110512571 | T | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(103): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.389-208T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110512571 | |||||||
| chr12:110512655 | A | G | 3 | a0001c0001t0001g0057 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | NA18964.hp1 NA19002.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.389-124A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 4/10 | chr12 | 110512655 | |||||||
| chr12:110512967 | C | T | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.488+89C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | chr12 | 110512967 | |||||||
| chr12:110513110 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.488+232C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | chr12 | 110513110 | |||||||
| chr12:110513273 | AT | A | 33 | a0001c0001t0001g0029 a0001c0001t0001g0173 a0001c0001t0002g0005 others(30): Show |
47 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.488+407delT | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 110513273 | ||||||
| chr12:110513428 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.488+550A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | chr12 | 110513428 | |||||||
| chr12:110513494 | A | G | 6 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0174 others(3): Show |
9 | HG01081.hp1 HG01943.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.488+616A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | chr12 | 110513494 | |||||||
| chr12:110513692 | ATAT | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0042 others(21): Show |
38 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.488+858_488+860del others(3): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 110513692 | ||||||
| chr12:110513692 | ATATTAT | A | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0038 others(18): Show |
31 | HG00099.hp1 HG00280.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.488+855_488+860del others(6): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 110513692 | ||||||
| chr12:110513692 | ATATTATT others(2): Show |
A | 56 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(53): Show |
81 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.488+852_488+860del others(9): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 110513692 | ||||||
| chr12:110513692 | ATATTATT others(5): Show |
A | 68 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(65): Show |
92 | HG00323.hp2 HG00597.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.488+849_488+860del others(12): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 110513692 | ||||||
| chr12:110513692 | ATATTATT others(8): Show |
A | 9 | a0001c0001t0001g0014 a0001c0001t0001g0068 a0001c0001t0001g0069 others(6): Show |
11 | HG00733.hp1 HG01081.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.488+846_488+860del others(15): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 110513692 | ||||||
| chr12:110513692 | ATATTATT others(11): Show |
A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG01167.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.488+843_488+860del others(18): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 110513692 | ||||||
| chr12:110513715 | ATTATTAT others(4): Show |
A | 1 | a0001c0001t0001g0122 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.488+838_488+848del others(11): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | chr12 | 110513715 | |||||||
| chr12:110513736 | A | T | 1 | a0001c0001t0001g0129 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.488+858A>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | chr12 | 110513736 | |||||||
| chr12:110513880 | T | C | 1 | a0001c0001t0002g0182 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.488+1002T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | chr12 | 110513880 | |||||||
| chr12:110513906 | A | G | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.488+1028A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | chr12 | 110513906 | |||||||
| chr12:110514027 | C | CCCTT | 13 | a0001c0001t0001g0006 a0001c0001t0001g0072 a0001c0001t0001g0073 others(10): Show |
17 | HG00621.hp1 HG00621.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.489-994_489-991dup others(4): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 110514027 | ||||||
| chr12:110514027 | CCCTT | C | 40 | a0001c0001t0001g0013 a0001c0001t0002g0016 a0001c0001t0002g0034 others(37): Show |
60 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.489-994_489-991del others(4): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 110514027 | ||||||
| chr12:110514070 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.489-980T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | chr12 | 110514070 | |||||||
| chr12:110514269 | C | T | 1 | a0001c0001t0002g0179 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.489-781C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | chr12 | 110514269 | |||||||
| chr12:110514280 | A | AT | 32 | a0001c0001t0001g0173 a0001c0001t0002g0005 a0001c0001t0002g0016 others(29): Show |
45 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.489-766dupT | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 110514280 | ||||||
| chr12:110514475 | G | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0174 others(3): Show |
9 | HG01081.hp1 HG01943.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.489-575G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | chr12 | 110514475 | |||||||
| chr12:110514578 | A | G | 8 | a0001c0001t0001g0037 a0001c0001t0001g0061 a0001c0001t0001g0062 others(5): Show |
8 | HG00738.hp2 HG01175.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.489-472A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | chr12 | 110514578 | |||||||
| chr12:110514702 | C | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0051 others(3): Show |
9 | HG00438.hp1 HG00558.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.489-348C>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | chr12 | 110514702 | |||||||
| chr12:110515037 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.489-13T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 5/10 | chr12 | 110515037 | |||||||
| chr12:110515415 | T | C | 32 | a0001c0001t0001g0173 a0001c0001t0002g0005 a0001c0001t0002g0016 others(29): Show |
45 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.595+259T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110515415 | |||||||
| chr12:110515604 | T | C | 1 | a0001c0001t0010g0191 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.595+448T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110515604 | |||||||
| chr12:110515638 | G | C | 1 | a0001c0001t0001g0151 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.595+482G>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110515638 | |||||||
| chr12:110516056 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.595+900A>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110516056 | |||||||
| chr12:110516121 | G | A | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.595+965G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110516121 | |||||||
| chr12:110516192 | A | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0174 others(3): Show |
9 | HG01081.hp1 HG01943.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.595+1036A>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110516192 | |||||||
| chr12:110516216 | G | A | 31 | a0001c0001t0001g0173 a0001c0001t0002g0005 a0001c0001t0002g0016 others(28): Show |
43 | HG00323.hp2 HG01099.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.595+1060G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110516216 | |||||||
| chr12:110516401 | G | T | 3 | a0001c0001t0001g0045 a0001c0001t0016g0107 a0001c0007t0001g0106 |
3 | HG00323.hp1 HG02258.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.595+1245G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110516401 | |||||||
| chr12:110516522 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.595+1366T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110516522 | |||||||
| chr12:110516769 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0174 others(3): Show |
9 | HG01081.hp1 HG01943.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.595+1613C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110516769 | |||||||
| chr12:110516790 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0159 |
2 | HG03471.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.595+1634C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110516790 | |||||||
| chr12:110516858 | G | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0132 |
2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.595+1702G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110516858 | |||||||
| chr12:110516914 | A | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0098 a0001c0001t0001g0104 |
4 | HG02717.hp2 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.595+1758A>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110516914 | |||||||
| chr12:110517384 | G | A | 1 | a0002c0002t0001g0026 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.596-1292G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110517384 | |||||||
| chr12:110517751 | G | GAC | 43 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(40): Show |
64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.596-887_596-886dup others(2): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 110517751 | ||||||
| chr12:110517751 | G | GACAC | 43 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0018 others(40): Show |
62 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.596-889_596-886dup others(4): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 110517751 | ||||||
| chr12:110517751 | G | GACACAC | 14 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0048 others(11): Show |
14 | HG01255.hp2 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.596-891_596-886dup others(6): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 110517751 | ||||||
| chr12:110517751 | G | GACACACA others(1): Show |
5 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0004g0040 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.596-893_596-886dup others(8): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 110517751 | ||||||
| chr12:110517751 | G | GACACACA others(3): Show |
1 | a0001c0001t0004g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.596-895_596-886dup others(10): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 110517751 | ||||||
| chr12:110517751 | GAC | G | 13 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0044 others(10): Show |
16 | HG01167.hp1 HG01358.hp2 HG02717.hp2 others(13): Show |
intron_variant | MODIFIER | c.596-887_596-886del others(2): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 110517751 | ||||||
| chr12:110517751 | GACAC | G | 32 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0033 others(29): Show |
48 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.596-889_596-886del others(4): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 110517751 | ||||||
| chr12:110517751 | GACACAC | G | 8 | a0001c0001t0001g0159 a0002c0002t0001g0010 a0002c0002t0001g0046 others(5): Show |
12 | HG02055.hp1 HG02486.hp2 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.596-891_596-886del others(6): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 110517751 | ||||||
| chr12:110517751 | GACACACA others(3): Show |
G | 5 | a0001c0001t0008g0017 a0002c0002t0001g0019 a0002c0002t0001g0026 others(2): Show |
8 | HG00738.hp1 HG01069.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.596-895_596-886del others(10): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 110517751 | ||||||
| chr12:110517751 | GACACACA others(5): Show |
G | 1 | a0001c0001t0001g0079 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.596-897_596-886del others(12): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 110517751 | ||||||
| chr12:110517751 | GACACACA others(7): Show |
G | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 |
3 | NA18942.hp1 NA18973.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.596-899_596-886del others(14): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 110517751 | ||||||
| chr12:110517790 | A | ACAC | 4 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0126 others(1): Show |
4 | HG00099.hp1 HG02080.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.596-886_596-885ins others(3): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110517790 | |||||||
| chr12:110517879 | G | A | 5 | a0001c0001t0002g0005 a0001c0001t0002g0193 a0001c0001t0002g0194 others(2): Show |
10 | HG01167.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.596-797G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110517879 | |||||||
| chr12:110517984 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.596-692C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110517984 | |||||||
| chr12:110518033 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.596-643T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110518033 | |||||||
| chr12:110518047 | C | T | 3 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.596-629C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110518047 | |||||||
| chr12:110518052 | G | A | 1 | a0002c0002t0001g0047 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.596-624G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110518052 | |||||||
| chr12:110518079 | A | T | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(171): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.596-597A>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110518079 | |||||||
| chr12:110518097 | A | G | 13 | a0002c0002t0001g0004 a0002c0002t0001g0010 a0002c0002t0001g0046 others(10): Show |
22 | HG00423.hp2 HG00558.hp2 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.596-579A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110518097 | |||||||
| chr12:110518195 | G | GA | 43 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(40): Show |
57 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.596-468dupA | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 110518195 | ||||||
| chr12:110518204 | A | C | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.596-472A>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110518204 | |||||||
| chr12:110518561 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.596-115G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110518561 | |||||||
| chr12:110518565 | G | A | 31 | a0001c0001t0001g0173 a0001c0001t0002g0005 a0001c0001t0002g0016 others(28): Show |
43 | HG00323.hp2 HG01099.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.596-111G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 6/10 | chr12 | 110518565 | |||||||
| chr12:110519094 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0155 |
2 | HG00597.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.767+156G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 8/10 | chr12 | 110519094 | |||||||
| chr12:110519109 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.767+171T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 8/10 | chr12 | 110519109 | |||||||
| chr12:110519244 | C | T | 6 | a0001c0001t0002g0005 a0001c0001t0002g0190 a0001c0001t0002g0193 others(3): Show |
11 | HG01167.hp2 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.767+306C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 8/10 | chr12 | 110519244 | |||||||
| chr12:110519355 | C | T | 31 | a0001c0001t0001g0173 a0001c0001t0002g0005 a0001c0001t0002g0016 others(28): Show |
43 | HG00323.hp2 HG01099.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.767+417C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 8/10 | chr12 | 110519355 | |||||||
| chr12:110519409 | T | TTTG | 9 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(6): Show |
14 | HG00741.hp1 HG01175.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.768-348_768-346dup others(3): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 110519409 | ||||||
| chr12:110519409 | TTTG | T | 8 | a0001c0001t0001g0158 a0001c0001t0001g0173 a0001c0001t0004g0039 others(5): Show |
10 | HG01099.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.768-348_768-346del others(3): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 110519409 | ||||||
| chr12:110519409 | TTTGTTG | T | 27 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0112 others(24): Show |
37 | HG00323.hp2 HG01167.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.768-351_768-346del others(6): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 110519409 | ||||||
| chr12:110519415 | G | T | 7 | a0001c0001t0001g0173 a0001c0001t0004g0039 a0001c0001t0004g0040 others(4): Show |
9 | HG01099.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.768-379G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 8/10 | chr12 | 110519415 | |||||||
| chr12:110519418 | G | T | 24 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0034 others(21): Show |
34 | HG00323.hp2 HG01167.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.768-376G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 8/10 | chr12 | 110519418 | |||||||
| chr12:110519626 | G | C | 1 | a0001c0001t0001g0099 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.768-168G>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 8/10 | chr12 | 110519626 | |||||||
| chr12:110519661 | C | T | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG02004.hp1 NA19082.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.768-133C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 8/10 | chr12 | 110519661 | |||||||
| chr12:110519662 | G | T | 1 | a0001c0001t0001g0138 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.768-132G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 8/10 | chr12 | 110519662 | |||||||
| chr12:110519683 | G | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 |
3 | NA18954.hp2 NA18961.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.768-111G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 8/10 | chr12 | 110519683 | |||||||
| chr12:110520092 | A | C | 1 | a0001c0001t0001g0065 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.890+176A>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | chr12 | 110520092 | |||||||
| chr12:110520194 | T | G | 1 | a0001c0001t0002g0183 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.890+278T>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | chr12 | 110520194 | |||||||
| chr12:110520194 | T | TTTG | 31 | a0001c0001t0001g0173 a0001c0001t0002g0005 a0001c0001t0002g0016 others(28): Show |
44 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.890+299_890+301dup others(3): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 110520194 | ||||||
| chr12:110520366 | C | T | 1 | a0001c0001t0001g0022 | 2 | HG00099.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.890+450C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | chr12 | 110520366 | |||||||
| chr12:110520610 | C | T | 2 | a0001c0001t0003g0052 a0001c0001t0003g0170 |
2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.890+694C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | chr12 | 110520610 | |||||||
| chr12:110520627 | T | G | 1 | a0001c0001t0001g0141 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.890+711T>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | chr12 | 110520627 | |||||||
| chr12:110520628 | C | CT | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(131): Show |
188 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.890+730dupT | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 110520628 | ||||||
| chr12:110520628 | C | CTT | 34 | a0001c0001t0001g0071 a0001c0001t0001g0077 a0001c0001t0001g0123 others(31): Show |
44 | HG00323.hp2 HG01099.hp2 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.890+729_890+730dup others(2): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 110520628 | ||||||
| chr12:110520629 | TTTTTTTT others(14): Show |
T | 1 | a0001c0001t0001g0092 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.890+724_890+744del others(21): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 110520629 | ||||||
| chr12:110520641 | T | G | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.890+725T>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | chr12 | 110520641 | |||||||
| chr12:110520642 | T | G | 2 | a0001c0001t0002g0035 a0001c0001t0002g0182 |
3 | HG02055.hp2 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.890+726T>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | chr12 | 110520642 | |||||||
| chr12:110520644 | T | G | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.890+728T>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | chr12 | 110520644 | |||||||
| chr12:110520645 | T | G | 2 | a0001c0001t0002g0035 a0001c0001t0002g0182 |
3 | HG02055.hp2 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.890+729T>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | chr12 | 110520645 | |||||||
| chr12:110520646 | TGTTG | T | 2 | a0001c0001t0002g0035 a0001c0001t0002g0182 |
3 | HG02055.hp2 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.890+731_890+734del others(4): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | chr12 | 110520646 | |||||||
| chr12:110520647 | G | T | 1 | a0001c0001t0002g0177 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.890+731G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | chr12 | 110520647 | |||||||
| chr12:110520650 | G | GT | 16 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0002g0016 others(13): Show |
20 | HG00323.hp2 HG00735.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.890+744dupT | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 110520650 | ||||||
| chr12:110521161 | T | C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG02258.hp2 HG02572.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.891-1016T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | chr12 | 110521161 | |||||||
| chr12:110521162 | A | T | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.891-1015A>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | chr12 | 110521162 | |||||||
| chr12:110521182 | G | T | 3 | a0001c0001t0001g0057 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | NA18964.hp1 NA19002.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.891-995G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | chr12 | 110521182 | |||||||
| chr12:110521320 | T | G | 1 | a0001c0001t0001g0134 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.891-857T>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | chr12 | 110521320 | |||||||
| chr12:110521473 | A | G | 1 | a0004c0005t0001g0031 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.891-704A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | chr12 | 110521473 | |||||||
| chr12:110521555 | C | CT | 6 | a0001c0001t0001g0070 a0001c0001t0001g0130 a0002c0002t0001g0019 others(3): Show |
8 | HG01884.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.891-603dupT | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 110521555 | ||||||
| chr12:110521555 | CT | C | 29 | a0001c0001t0001g0122 a0001c0001t0001g0173 a0001c0001t0002g0005 others(26): Show |
42 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.891-603delT | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 110521555 | ||||||
| chr12:110521599 | C | T | 1 | a0001c0003t0001g0080 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.891-578C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | chr12 | 110521599 | |||||||
| chr12:110521845 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0174 others(3): Show |
9 | HG01081.hp1 HG01943.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.891-332C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | chr12 | 110521845 | |||||||
| chr12:110521904 | T | G | 1 | a0001c0001t0001g0075 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.891-273T>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 9/10 | chr12 | 110521904 | |||||||
| chr12:110522626 | T | C | 2 | a0002c0002t0007g0111 a0002c0002t0007g0113 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1125+215T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110522626 | |||||||
| chr12:110522634 | C | A | 1 | a0001c0001t0001g0075 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1125+223C>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110522634 | |||||||
| chr12:110523226 | C | T | 1 | a0001c0001t0001g0008 | 5 | HG01069.hp1 HG01071.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1125+815C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110523226 | |||||||
| chr12:110523227 | G | T | 1 | a0002c0002t0001g0056 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1125+816G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110523227 | |||||||
| chr12:110523260 | C | A | 1 | a0001c0001t0005g0024 | 2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1125+849C>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110523260 | |||||||
| chr12:110523277 | C | T | 40 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0033 others(37): Show |
60 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.1125+866C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110523277 | |||||||
| chr12:110523318 | T | C | 31 | a0001c0001t0001g0173 a0001c0001t0002g0005 a0001c0001t0002g0016 others(28): Show |
43 | HG00323.hp2 HG01099.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.1125+907T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110523318 | |||||||
| chr12:110523456 | G | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0033 others(5): Show |
15 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1125+1045G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110523456 | |||||||
| chr12:110523679 | C | T | 1 | a0001c0001t0011g0197 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1125+1268C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110523679 | |||||||
| chr12:110523751 | G | A | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1125+1340G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110523751 | |||||||
| chr12:110523805 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1125+1394C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110523805 | |||||||
| chr12:110523814 | A | C | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1125+1403A>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110523814 | |||||||
| chr12:110524109 | A | G | 1 | a0001c0001t0002g0190 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1125+1698A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110524109 | |||||||
| chr12:110524264 | G | T | 1 | a0001c0001t0001g0008 | 5 | HG01069.hp1 HG01071.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1125+1853G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110524264 | |||||||
| chr12:110524378 | T | C | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1125+1967T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110524378 | |||||||
| chr12:110524485 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1125+2074C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110524485 | |||||||
| chr12:110524635 | C | T | 1 | a0004c0005t0001g0031 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1125+2224C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110524635 | |||||||
| chr12:110524897 | C | A | 31 | a0001c0001t0001g0173 a0001c0001t0002g0005 a0001c0001t0002g0016 others(28): Show |
43 | HG00323.hp2 HG01099.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.1125+2486C>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110524897 | |||||||
| chr12:110525134 | T | C | 40 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0033 others(37): Show |
60 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.1125+2723T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110525134 | |||||||
| chr12:110525179 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1125+2768C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110525179 | |||||||
| chr12:110525218 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1125+2807C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110525218 | |||||||
| chr12:110525292 | G | A | 32 | a0001c0001t0001g0173 a0001c0001t0002g0005 a0001c0001t0002g0016 others(29): Show |
45 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1125+2881G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110525292 | |||||||
| chr12:110525544 | G | A | 1 | a0001c0001t0002g0184 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1125+3133G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110525544 | |||||||
| chr12:110525643 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1125+3232G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110525643 | |||||||
| chr12:110525650 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0098 a0001c0001t0001g0104 |
4 | HG02717.hp2 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+3239A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110525650 | |||||||
| chr12:110525791 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0018g0119 |
3 | HG03688.hp1 HG03834.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1125+3380A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110525791 | |||||||
| chr12:110525803 | A | G | 32 | a0001c0001t0001g0173 a0001c0001t0002g0005 a0001c0001t0002g0016 others(29): Show |
45 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1125+3392A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110525803 | |||||||
| chr12:110525907 | G | T | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1125+3496G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110525907 | |||||||
| chr12:110526036 | T | G | 25 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0034 others(22): Show |
35 | HG00323.hp2 HG01167.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.1125+3625T>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110526036 | |||||||
| chr12:110526126 | C | G | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1125+3715C>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110526126 | |||||||
| chr12:110526219 | TA | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0174 others(4): Show |
11 | HG01081.hp1 HG01099.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.1125+3819delA | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 110526219 | ||||||
| chr12:110526371 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1125+3960T>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110526371 | |||||||
| chr12:110526401 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1125+3990A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110526401 | |||||||
| chr12:110526457 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1125+4046C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110526457 | |||||||
| chr12:110526509 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1126-4016C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110526509 | |||||||
| chr12:110526647 | T | C | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1126-3878T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110526647 | |||||||
| chr12:110526781 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0174 others(3): Show |
9 | HG01081.hp1 HG01943.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1126-3744C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110526781 | |||||||
| chr12:110526882 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1126-3643C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110526882 | |||||||
| chr12:110527044 | C | A | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1126-3481C>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110527044 | |||||||
| chr12:110527410 | A | G | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1126-3115A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110527410 | |||||||
| chr12:110527455 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1126-3070C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110527455 | |||||||
| chr12:110527683 | G | T | 1 | a0001c0001t0001g0157 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1126-2842G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110527683 | |||||||
| chr12:110527746 | G | A | 3 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1126-2779G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110527746 | |||||||
| chr12:110527782 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1126-2743G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110527782 | |||||||
| chr12:110527904 | C | T | 1 | a0001c0001t0004g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1126-2621C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110527904 | |||||||
| chr12:110527922 | C | A | 1 | a0001c0001t0001g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1126-2603C>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110527922 | |||||||
| chr12:110527923 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1126-2602A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110527923 | |||||||
| chr12:110527943 | G | T | 4 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0058 others(1): Show |
6 | HG01884.hp2 HG02257.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1126-2582G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110527943 | |||||||
| chr12:110528247 | GGA | G | 8 | a0001c0001t0002g0005 a0001c0001t0002g0190 a0001c0001t0002g0193 others(5): Show |
14 | HG01167.hp2 HG01891.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1126-2272_1126-227 others(6): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 110528247 | ||||||
| chr12:110528249 | A | G | 1 | a0001c0001t0001g0025 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1126-2276A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110528249 | |||||||
| chr12:110528372 | G | T | 16 | a0001c0001t0002g0016 a0001c0001t0002g0034 a0001c0001t0002g0035 others(13): Show |
20 | HG00323.hp2 HG01175.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.1126-2153G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110528372 | |||||||
| chr12:110528465 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1126-2060C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110528465 | |||||||
| chr12:110528482 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1126-2043C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110528482 | |||||||
| chr12:110528483 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1126-2042T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110528483 | |||||||
| chr12:110528589 | A | T | 1 | a0001c0001t0001g0049 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1126-1936A>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110528589 | |||||||
| chr12:110528598 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1126-1927C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110528598 | |||||||
| chr12:110528623 | A | G | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1126-1902A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110528623 | |||||||
| chr12:110528734 | GT | G | 2 | a0002c0002t0001g0004 a0002c0002t0001g0047 |
7 | HG00558.hp2 NA18947.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.1126-1786delT | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 110528734 | ||||||
| chr12:110528925 | A | T | 25 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0034 others(22): Show |
35 | HG00323.hp2 HG01167.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.1126-1600A>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110528925 | |||||||
| chr12:110529106 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1126-1419A>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110529106 | |||||||
| chr12:110529144 | G | C | 1 | a0002c0002t0001g0114 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1126-1381G>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110529144 | |||||||
| chr12:110529286 | G | A | 31 | a0001c0001t0001g0173 a0001c0001t0002g0005 a0001c0001t0002g0016 others(28): Show |
43 | HG00323.hp2 HG01099.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.1126-1239G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110529286 | |||||||
| chr12:110529375 | C | A | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1126-1150C>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110529375 | |||||||
| chr12:110529435 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0135 |
2 | HG03579.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1126-1090G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110529435 | |||||||
| chr12:110529543 | G | C | 1 | a0001c0001t0002g0187 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1126-982G>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110529543 | |||||||
| chr12:110529589 | G | GA | 16 | a0001c0001t0001g0051 a0001c0001t0001g0061 a0001c0001t0001g0076 others(13): Show |
16 | HG00280.hp2 HG01175.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.1126-923dupA | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 110529589 | ||||||
| chr12:110529607 | G | T | 1 | a0001c0001t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1126-918G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110529607 | |||||||
| chr12:110529685 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1126-840G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110529685 | |||||||
| chr12:110529739 | A | G | 4 | a0001c0001t0001g0050 a0001c0001t0001g0140 a0001c0001t0001g0143 others(1): Show |
4 | HG01109.hp2 HG01346.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1126-786A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110529739 | |||||||
| chr12:110529847 | G | T | 25 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0034 others(22): Show |
35 | HG00323.hp2 HG01167.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.1126-678G>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110529847 | |||||||
| chr12:110530042 | T | G | 31 | a0001c0001t0001g0173 a0001c0001t0002g0005 a0001c0001t0002g0016 others(28): Show |
44 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.1126-483T>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110530042 | |||||||
| chr12:110530078 | C | G | 1 | a0002c0002t0001g0026 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1126-447C>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110530078 | |||||||
| chr12:110530152 | C | A | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1126-373C>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110530152 | |||||||
| chr12:110530209 | A | T | 2 | a0001c0001t0002g0179 a0001c0001t0002g0186 |
2 | HG03491.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1126-316A>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110530209 | |||||||
| chr12:110530314 | A | G | 32 | a0001c0001t0001g0173 a0001c0001t0002g0005 a0001c0001t0002g0016 others(29): Show |
45 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1126-211A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110530314 | |||||||
| chr12:110530325 | G | A | 1 | a0001c0001t0002g0187 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1126-200G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110530325 | |||||||
| chr12:110530335 | A | G | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1126-190A>G | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110530335 | |||||||
| chr12:110530340 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1126-185C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110530340 | |||||||
| chr12:110530341 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0161 |
6 | HG01069.hp1 HG01071.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1126-184G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110530341 | |||||||
| chr12:110530375 | TAATG | T | 31 | a0001c0001t0001g0173 a0001c0001t0002g0005 a0001c0001t0002g0016 others(28): Show |
43 | HG00323.hp2 HG01099.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.1126-147_1126-144d others(6): Show |
RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 110530375 | ||||||
| chr12:110530403 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1126-122C>T | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110530403 | |||||||
| chr12:110530405 | T | C | 1 | a0001c0001t0008g0017 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1126-120T>C | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110530405 | |||||||
| chr12:110530465 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1126-60G>A | RAD9B | ENSG00000151164.19 | transcript | ENST00000409300.6 | protein_coding | 10/10 | chr12 | 110530465 |