Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6240 |
| ensemblid | ENSG00000167325.15 |
| hgncid | 10451 |
| symbol | RRM1 |
| name | ribonucleotide reductase catalytic subunit M1 |
| refseq_nuc | NM_001033.5 |
| refseq_prot | NP_001024.1 |
| ensembl_nuc | ENST00000300738.10 |
| ensembl_prot | ENSP00000300738.5 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 4094799 |
| end | 4138932 |
| strand | + |
| ver | v1.2 |
| region | chr11:4094799-4138932 |
| region5000 | chr11:4089799-4143932 |
| regionname0 | RRM1_chr11_4094799_4138932 |
| regionname5000 | RRM1_chr11_4089799_4143932 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 792 | 364 | 87 | 69 | 158 | 8 | 40 | 118 | RRM1_chr11_4089799_4143932 | RRM1 | MHVIK others(787): Show |
chr11 | 4089799 | 4143932 |
| a0002 | 0/0 | 792 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | MHVIK others(787): Show |
chr11 | 4089799 | 4143932 |
| a0003 | 0/0 | 792 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | MHVIK others(787): Show |
chr11 | 4089799 | 4143932 |
| a0004 | 0/0 | 792 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | MHVIK others(787): Show |
chr11 | 4089799 | 4143932 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2376 | 170 | 52 | 30 | 63 | 2 | 22 | RRM1_chr11_4089799_4143932 | RRM1 | ATGCA others(2371): Show |
chr11 | 4089799 | 4143932 | ||
| a0001c0002 | 0/0 | 2376 | 105 | 2 | 23 | 63 | 4 | 13 | RRM1_chr11_4089799_4143932 | RRM1 | ATGCA others(2371): Show |
chr11 | 4089799 | 4143932 | ||
| a0001c0003 | 1/0 | 2376 | 77 | 22 | 16 | 31 | 2 | 5 | RRM1_chr11_4089799_4143932 | RRM1 | ATGCA others(2371): Show |
chr11 | 4089799 | 4143932 | ||
| a0001c0004 | 0/0 | 2376 | 5 | 5 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | ATGCA others(2371): Show |
chr11 | 4089799 | 4143932 | ||
| a0001c0005 | 0/0 | 2376 | 3 | 3 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | ATGCA others(2371): Show |
chr11 | 4089799 | 4143932 | ||
| a0001c0006 | 0/0 | 2376 | 3 | 3 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | ATGCA others(2371): Show |
chr11 | 4089799 | 4143932 | ||
| a0001c0009 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | ATGCA others(2371): Show |
chr11 | 4089799 | 4143932 | ||
| a0002c0007 | 0/0 | 2376 | 2 | 2 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | ATGCA others(2371): Show |
chr11 | 4089799 | 4143932 | ||
| a0003c0010 | 0/0 | 2376 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | ATGCA others(2371): Show |
chr11 | 4089799 | 4143932 | ||
| a0004c0008 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | ATGCA others(2371): Show |
chr11 | 4089799 | 4143932 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3141 | 153 | 40 | 28 | 60 | 2 | 22 | RRM1_chr11_4089799_4143932 | RRM1 | CCCTT others(3136): Show |
chr11 | 4089799 | 4143932 |
| a0001c0001t0002 | 0/0 | 3142 | 2 | 0 | 0 | 2 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | CCCTT others(3137): Show |
chr11 | 4089799 | 4143932 |
| a0001c0001t0003 | 0/0 | 3140 | 13 | 12 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | CCCTT others(3135): Show |
chr11 | 4089799 | 4143932 |
| a0001c0001t0005 | 0/0 | 3141 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | CCCTT others(3136): Show |
chr11 | 4089799 | 4143932 |
| a0001c0001t0006 | 0/0 | 3141 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | CCCTT others(3136): Show |
chr11 | 4089799 | 4143932 |
| a0001c0002t0001 | 0/0 | 3141 | 105 | 2 | 23 | 63 | 4 | 13 | RRM1_chr11_4089799_4143932 | RRM1 | CCCTT others(3136): Show |
chr11 | 4089799 | 4143932 |
| a0001c0003t0002 | 1/0 | 3142 | 76 | 22 | 15 | 31 | 2 | 5 | RRM1_chr11_4089799_4143932 | RRM1 | CCCTT others(3137): Show |
chr11 | 4089799 | 4143932 |
| a0001c0003t0004 | 0/0 | 3142 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | CCCTT others(3137): Show |
chr11 | 4089799 | 4143932 |
| a0001c0004t0001 | 0/0 | 3141 | 5 | 5 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | CCCTT others(3136): Show |
chr11 | 4089799 | 4143932 |
| a0001c0005t0001 | 0/0 | 3141 | 3 | 3 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | CCCTT others(3136): Show |
chr11 | 4089799 | 4143932 |
| a0001c0006t0001 | 0/0 | 3141 | 3 | 3 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | CCCTT others(3136): Show |
chr11 | 4089799 | 4143932 |
| a0001c0009t0001 | 0/0 | 3141 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | CCCTT others(3136): Show |
chr11 | 4089799 | 4143932 |
| a0002c0007t0002 | 0/0 | 3142 | 2 | 2 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | CCCTT others(3137): Show |
chr11 | 4089799 | 4143932 |
| a0003c0010t0001 | 0/0 | 3141 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | CCCTT others(3136): Show |
chr11 | 4089799 | 4143932 |
| a0004c0008t0001 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | CCCTT others(3136): Show |
chr11 | 4089799 | 4143932 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0332 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0001 | 0/0 | 11 | 1 | 3 | 7 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0003 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0002 | 1/0 | 6 | 0 | 2 | 1 | 0 | 2 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0003t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0004t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0004t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0004t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0005t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0005t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0005t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0006t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0006t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0006t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0001c0009t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0002c0007t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0002c0007t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0003c0010t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| a0004c0008t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0117 | EUR | GBR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0199 | EUR | GBR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | CHS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | CHS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00438 | hp2 | a0001 | c0003 | t0002 | g0305 | EAS | CHS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00609 | hp1 | a0001 | c0003 | t0002 | g0172 | EAS | CHS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | CHS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00639 | hp1 | a0001 | c0003 | t0002 | g0006 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00642 | hp1 | a0001 | c0003 | t0002 | g0321 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0123 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0080 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0094 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0093 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01099 | hp1 | a0003 | c0010 | t0001 | g0217 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0078 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01192 | hp2 | a0001 | c0003 | t0002 | g0265 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0322 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01243 | hp2 | a0001 | c0003 | t0004 | g0208 | AMR | PUR | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0102 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0120 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01257 | hp2 | a0001 | c0003 | t0002 | g0002 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01258 | hp1 | a0001 | c0003 | t0002 | g0002 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01358 | hp1 | a0001 | c0003 | t0002 | g0250 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0119 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0207 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01496 | hp1 | a0001 | c0003 | t0002 | g0262 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0079 | AMR | CLM | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0122 | EUR | IBS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01516 | hp2 | a0001 | c0003 | t0002 | g0317 | EUR | IBS | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0081 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01934 | hp1 | a0001 | c0003 | t0002 | g0015 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01943 | hp2 | a0001 | c0003 | t0002 | g0263 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01978 | hp2 | a0001 | c0003 | t0002 | g0274 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01981 | hp1 | a0001 | c0003 | t0002 | g0264 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02027 | hp1 | a0001 | c0001 | t0006 | g0229 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02055 | hp1 | a0001 | c0005 | t0001 | g0299 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02071 | hp2 | a0001 | c0003 | t0002 | g0255 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02132 | hp2 | a0001 | c0003 | t0002 | g0261 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02135 | hp1 | a0001 | c0003 | t0002 | g0270 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02148 | hp2 | a0001 | c0003 | t0002 | g0243 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | CDX | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CDX | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | CDX | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02257 | hp2 | a0001 | c0006 | t0001 | g0169 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0323 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02258 | hp2 | a0001 | c0003 | t0002 | g0316 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02273 | hp1 | a0001 | c0003 | t0002 | g0278 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02273 | hp2 | a0001 | c0003 | t0002 | g0251 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02280 | hp1 | a0001 | c0003 | t0002 | g0016 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02300 | hp1 | a0001 | c0003 | t0002 | g0242 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0092 | AMR | PEL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02451 | hp2 | a0001 | c0003 | t0002 | g0313 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02523 | hp2 | a0001 | c0003 | t0002 | g0252 | EAS | KHV | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02572 | hp2 | a0001 | c0003 | t0002 | g0015 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0097 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02615 | hp2 | a0001 | c0003 | t0002 | g0253 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0016 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02630 | hp1 | a0001 | c0004 | t0001 | g0174 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02647 | hp1 | a0001 | c0005 | t0001 | g0297 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02647 | hp2 | a0002 | c0007 | t0002 | g0210 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0095 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02717 | hp1 | a0001 | c0005 | t0001 | g0301 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02717 | hp2 | a0001 | c0006 | t0001 | g0240 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02723 | hp1 | a0001 | c0003 | t0002 | g0005 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0118 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0333 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02886 | hp1 | a0002 | c0007 | t0002 | g0209 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02922 | hp1 | a0001 | c0003 | t0002 | g0005 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02922 | hp2 | a0001 | c0003 | t0002 | g0046 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0044 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0306 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03017 | hp2 | a0001 | c0003 | t0002 | g0002 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03041 | hp2 | a0001 | c0003 | t0002 | g0030 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0295 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03139 | hp1 | a0001 | c0003 | t0002 | g0307 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03139 | hp2 | a0001 | c0003 | t0002 | g0275 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0294 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03209 | hp1 | a0001 | c0003 | t0002 | g0005 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03491 | hp1 | a0001 | c0003 | t0002 | g0002 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0053 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0087 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03516 | hp1 | a0001 | c0003 | t0002 | g0273 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03540 | hp2 | a0001 | c0003 | t0002 | g0310 | AFR | GWD | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03579 | hp2 | a0001 | c0004 | t0001 | g0032 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0091 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | STU | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0109 | SAS | STU | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0065 | SAS | PJL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03831 | hp1 | a0001 | c0003 | t0002 | g0320 | SAS | BEB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03831 | hp2 | a0001 | c0003 | t0002 | g0245 | SAS | BEB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0198 | SAS | BEB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0060 | SAS | BEB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0062 | SAS | BEB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03942 | hp2 | a0001 | c0003 | t0002 | g0241 | SAS | BEB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | STU | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | STU | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | STU | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | STU | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0052 | SAS | STU | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | YRI | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18522 | hp2 | a0004 | c0008 | t0001 | g0298 | AFR | YRI | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CHB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18612 | hp2 | a0001 | c0003 | t0002 | g0268 | EAS | CHB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18747 | hp2 | a0001 | c0003 | t0002 | g0258 | EAS | CHB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18906 | hp1 | a0001 | c0003 | t0002 | g0326 | AFR | YRI | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | YRI | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18942 | hp2 | a0001 | c0003 | t0002 | g0257 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18943 | hp1 | a0001 | c0003 | t0002 | g0272 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18945 | hp1 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18945 | hp2 | a0001 | c0003 | t0002 | g0260 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18953 | hp1 | a0001 | c0003 | t0002 | g0256 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18954 | hp1 | a0001 | c0003 | t0002 | g0246 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18959 | hp1 | a0001 | c0003 | t0002 | g0269 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18963 | hp1 | a0001 | c0003 | t0002 | g0304 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18970 | hp2 | a0001 | c0003 | t0002 | g0259 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18971 | hp1 | a0001 | c0003 | t0002 | g0315 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18972 | hp1 | a0001 | c0003 | t0002 | g0254 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18981 | hp1 | a0001 | c0003 | t0002 | g0312 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18982 | hp1 | a0001 | c0003 | t0002 | g0266 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18982 | hp2 | a0001 | c0009 | t0001 | g0206 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18984 | hp1 | a0001 | c0003 | t0002 | g0244 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18992 | hp1 | a0001 | c0003 | t0002 | g0277 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18998 | hp2 | a0001 | c0003 | t0002 | g0311 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19002 | hp2 | a0001 | c0003 | t0002 | g0267 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19006 | hp2 | a0001 | c0003 | t0002 | g0276 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19007 | hp2 | a0001 | c0003 | t0002 | g0247 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19011 | hp1 | a0001 | c0003 | t0002 | g0271 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19030 | hp1 | a0001 | c0006 | t0001 | g0214 | AFR | LWK | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19030 | hp2 | a0001 | c0003 | t0002 | g0171 | AFR | LWK | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | LWK | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19062 | hp1 | a0001 | c0003 | t0002 | g0248 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19064 | hp2 | a0001 | c0003 | t0002 | g0249 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19090 | hp2 | a0001 | c0003 | t0002 | g0319 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0296 | AFR | YRI | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA19240 | hp2 | a0001 | c0004 | t0001 | g0034 | AFR | YRI | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | TSI | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0082 | EUR | TSI | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA20805 | hp1 | a0001 | c0003 | t0002 | g0318 | EUR | TSI | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | TSI | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | GIH | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | GIH | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ACB | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG03471 | hp2 | a0001 | c0003 | t0002 | g0308 | AFR | MSL | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG06807 | hp1 | a0001 | c0003 | t0002 | g0006 | AFR | USA | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | USA | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | USA | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA20300 | hp2 | a0001 | c0003 | t0002 | g0031 | AFR | USA | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA21309 | hp1 | a0001 | c0003 | t0002 | g0309 | AFR | LWK | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| NA21309 | hp2 | a0001 | c0004 | t0001 | g0043 | AFR | LWK | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0332 | REF | REF | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0002 | g0002 | REF | REF | RRM1_chr11_4089799_4143932 | RRM1 | chr11 | 4089799 | 4143932 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:4111628 | A | T | 1 | a0003 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.475A>T | p.Ile159Phe | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 6/19 | 689/3142 | 475/2379 | 159/792 | chr11 | 4111628 | |||
| chr11:4127054 | G | A | 1 | a0002 | 2 | HG02647.hp2 HG02886.hp1 |
missense_variant | MODERATE | c.1490G>A | p.Arg497His | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/19 | 1704/3142 | 1490/2379 | 497/792 | chr11 | 4127054 | |||
| chr11:4129149 | A | C | 1 | a0004 | 1 | NA18522.hp2 | missense_variant&splice_region_variant | MODERATE | c.1768A>C | p.Lys590Gln | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/19 | 1982/3142 | 1768/2379 | 590/792 | chr11 | 4129149 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:4107509 | T | C | 2 | a0001c0005 a0004c0008 |
4 | HG02055.hp1 HG02647.hp1 HG02717.hp1 others(1): Show |
synonymous_variant | LOW | c.361T>C | p.Leu121Leu | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/19 | 575/3142 | 361/2379 | 121/792 | chr11 | 4107509 | |||
| chr11:4119902 | C | A | 1 | a0001c0002 | 105 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(102): Show |
synonymous_variant | LOW | c.850C>A | p.Arg284Arg | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/19 | 1064/3142 | 850/2379 | 284/792 | chr11 | 4119902 | |||
| chr11:4122212 | A | T | 1 | a0001c0006 | 3 | HG02257.hp2 HG02717.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.1110A>T | p.Leu370Leu | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 11/19 | 1324/3142 | 1110/2379 | 370/792 | chr11 | 4122212 | |||
| chr11:4127223 | C | T | 1 | a0001c0009 | 1 | NA18982.hp2 | synonymous_variant | LOW | c.1659C>T | p.Tyr553Tyr | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/19 | 1873/3142 | 1659/2379 | 553/792 | chr11 | 4127223 | |||
| chr11:4138227 | A | G | 2 | a0001c0002 a0001c0004 |
110 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(107): Show |
synonymous_variant | LOW | c.2223A>G | p.Thr741Thr | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 19/19 | 2437/3142 | 2223/2379 | 741/792 | chr11 | 4138227 | |||
| chr11:4138236 | G | A | 8 | a0001c0001 a0001c0002 a0001c0004 others(5): Show |
288 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(285): Show |
synonymous_variant | LOW | c.2232G>A | p.Ala744Ala | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 19/19 | 2446/3142 | 2232/2379 | 744/792 | chr11 | 4138236 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:4094858 | T | G | 2 | a0001c0001t0005 a0001c0003t0004 |
2 | HG01243.hp2 HG01433.hp1 |
5_prime_UTR_variant | MODIFIER | c.-155T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/19 | 155 | chr11 | 4094858 | ||||||
| chr11:4138534 | A | T | 11 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(8): Show |
286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*151A>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 19/19 | 151 | chr11 | 4138534 | ||||||
| chr11:4138540 | AT | A | 11 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(8): Show |
286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*167delT | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 19/19 | 167 | INFO_REALIGN_3_PRIME | chr11 | 4138540 | |||||
| chr11:4138598 | GA | G | 1 | a0001c0001t0003 | 13 | HG01243.hp1 HG02258.hp1 HG02486.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*225delA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 19/19 | 225 | INFO_REALIGN_3_PRIME | chr11 | 4138598 | |||||
| chr11:4138696 | C | A | 1 | a0001c0001t0006 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*313C>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 19/19 | 313 | chr11 | 4138696 | ||||||
| chr11:4138699 | C | A | 11 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(8): Show |
286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*316C>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 19/19 | 316 | chr11 | 4138699 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:4095064 | G | T | 1 | a0001c0001t0001g0334 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.19+33G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4095064 | |||||||
| chr11:4095089 | C | T | 1 | a0001c0001t0003g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.19+58C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4095089 | |||||||
| chr11:4095105 | A | C | 256 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(253): Show |
279 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.19+74A>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4095105 | |||||||
| chr11:4095131 | C | G | 1 | a0001c0001t0002g0331 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.19+100C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4095131 | |||||||
| chr11:4095132 | G | C | 1 | a0001c0001t0002g0331 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.19+101G>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4095132 | |||||||
| chr11:4095156 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.19+125G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4095156 | |||||||
| chr11:4095183 | C | G | 1 | a0001c0001t0001g0330 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.19+152C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4095183 | |||||||
| chr11:4095259 | G | A | 1 | a0001c0001t0003g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.19+228G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4095259 | |||||||
| chr11:4095384 | AACTGACG others(20): Show |
A | 201 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(198): Show |
222 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.19+360_19+386delGC others(25): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4095384 | ||||||
| chr11:4095444 | G | A | 302 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(299): Show |
327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.19+413G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4095444 | |||||||
| chr11:4095491 | G | T | 35 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(32): Show |
37 | HG00099.hp2 HG00558.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.19+460G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4095491 | |||||||
| chr11:4095495 | G | T | 33 | a0001c0001t0001g0175 a0001c0001t0001g0279 a0001c0001t0001g0280 others(30): Show |
33 | HG01243.hp1 HG01346.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.19+464G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4095495 | |||||||
| chr11:4095499 | G | A | 15 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(12): Show |
16 | HG00639.hp1 HG02109.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.19+468G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4095499 | |||||||
| chr11:4095530 | C | T | 1 | a0001c0004t0001g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.19+499C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4095530 | |||||||
| chr11:4095634 | T | TTCCCTTC others(13): Show |
1 | a0001c0002t0001g0173 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.19+604_19+623dupTC others(18): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4095634 | ||||||
| chr11:4095827 | T | A | 1 | a0001c0001t0002g0331 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.19+796T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4095827 | |||||||
| chr11:4095873 | T | C | 1 | a0001c0004t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.19+842T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4095873 | |||||||
| chr11:4095925 | T | C | 155 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(152): Show |
175 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.19+894T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4095925 | |||||||
| chr11:4096202 | A | T | 1 | a0001c0002t0001g0173 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.19+1171A>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4096202 | |||||||
| chr11:4096272 | C | G | 1 | a0001c0004t0001g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.19+1241C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4096272 | |||||||
| chr11:4096293 | T | G | 2 | a0001c0002t0001g0007 a0001c0002t0001g0033 |
3 | HG01069.hp2 HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.19+1262T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4096293 | |||||||
| chr11:4096295 | C | T | 6 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(3): Show |
6 | HG01109.hp2 HG02145.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+1264C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4096295 | |||||||
| chr11:4096335 | T | C | 1 | a0001c0004t0001g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.19+1304T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4096335 | |||||||
| chr11:4096455 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.19+1424T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4096455 | |||||||
| chr11:4096479 | C | G | 88 | a0001c0001t0001g0072 a0001c0002t0001g0001 a0001c0002t0001g0003 others(85): Show |
106 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.19+1448C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4096479 | |||||||
| chr11:4096500 | G | C | 117 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(114): Show |
121 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.19+1469G>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4096500 | |||||||
| chr11:4096563 | T | G | 1 | a0001c0001t0001g0125 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.19+1532T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4096563 | |||||||
| chr11:4096700 | G | T | 1 | a0001c0003t0002g0278 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.19+1669G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4096700 | |||||||
| chr11:4096709 | CCCAGGCT others(9): Show |
C | 1 | a0001c0001t0002g0331 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.19+1680_19+1695del others(16): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4096709 | ||||||
| chr11:4096728 | C | T | 4 | a0001c0003t0002g0046 a0001c0003t0004g0208 a0002c0007t0002g0209 others(1): Show |
4 | HG01243.hp2 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+1697C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4096728 | |||||||
| chr11:4096889 | A | G | 2 | a0001c0003t0002g0276 a0001c0003t0002g0277 |
2 | NA18992.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.19+1858A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4096889 | |||||||
| chr11:4096977 | T | TAAAAAGT others(313): Show |
2 | a0001c0001t0003g0018 a0001c0001t0003g0041 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.19+1965_19+1966ins others(320): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4096977 | ||||||
| chr11:4096977 | T | TAAAAAGT others(314): Show |
2 | a0001c0001t0003g0039 a0001c0001t0003g0040 |
2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.19+1965_19+1966ins others(321): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4096977 | ||||||
| chr11:4096977 | T | TAAAAAGT others(324): Show |
1 | a0001c0001t0003g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.19+1965_19+1966ins others(331): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4096977 | ||||||
| chr11:4096977 | T | TAAAAAGT others(326): Show |
9 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.19+1965_19+1966ins others(333): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4096977 | ||||||
| chr11:4096977 | T | TAAAAAGT others(327): Show |
4 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+1965_19+1966ins others(334): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4096977 | ||||||
| chr11:4096977 | T | TAAAAAGT others(335): Show |
1 | a0001c0001t0003g0322 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.19+1965_19+1966ins others(342): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4096977 | ||||||
| chr11:4097240 | T | C | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01943.hp1 HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.19+2209T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4097240 | |||||||
| chr11:4097247 | C | G | 41 | a0001c0003t0002g0006 a0001c0003t0002g0031 a0001c0003t0002g0172 others(38): Show |
42 | HG00609.hp1 HG00639.hp1 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.19+2216C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4097247 | |||||||
| chr11:4097278 | C | CA | 44 | a0001c0001t0001g0042 a0001c0001t0001g0126 a0001c0001t0001g0177 others(41): Show |
44 | HG00423.hp2 HG00438.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.19+2270dupA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4097278 | ||||||
| chr11:4097278 | CA | C | 137 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(134): Show |
143 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.19+2270delA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4097278 | ||||||
| chr11:4097278 | CAA | C | 45 | a0001c0001t0001g0176 a0001c0001t0001g0197 a0001c0001t0001g0205 others(42): Show |
46 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.19+2269_19+2270del others(2): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4097278 | ||||||
| chr11:4097367 | A | G | 1 | a0001c0003t0002g0321 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.19+2336A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4097367 | |||||||
| chr11:4097378 | C | G | 1 | a0001c0003t0002g0275 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.19+2347C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4097378 | |||||||
| chr11:4097406 | T | C | 1 | a0001c0006t0001g0214 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19+2375T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4097406 | |||||||
| chr11:4097518 | T | C | 32 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(29): Show |
34 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.19+2487T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4097518 | |||||||
| chr11:4097726 | G | C | 136 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(133): Show |
140 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.19+2695G>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4097726 | |||||||
| chr11:4097966 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.19+2935A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4097966 | |||||||
| chr11:4098132 | G | T | 1 | a0001c0003t0002g0320 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.19+3101G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4098132 | |||||||
| chr11:4098201 | G | A | 4 | a0001c0004t0001g0034 a0001c0004t0001g0043 a0001c0004t0001g0044 others(1): Show |
4 | HG02630.hp1 HG02965.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+3170G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4098201 | |||||||
| chr11:4098285 | CCTTCCTT others(9): Show |
C | 5 | a0001c0003t0002g0030 a0001c0003t0002g0046 a0001c0003t0004g0208 others(2): Show |
5 | HG01243.hp2 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+3261_19+3276del others(16): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4098285 | ||||||
| chr11:4098384 | C | T | 1 | a0001c0002t0001g0173 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.19+3353C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4098384 | |||||||
| chr11:4098400 | T | C | 1 | a0001c0001t0002g0331 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.19+3369T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4098400 | |||||||
| chr11:4098448 | C | G | 1 | a0001c0001t0001g0126 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.19+3417C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4098448 | |||||||
| chr11:4098458 | TA | T | 250 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(247): Show |
274 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(271): Show |
intron_variant | MODIFIER | c.19+3429delA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4098458 | ||||||
| chr11:4098754 | T | A | 314 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(311): Show |
339 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(336): Show |
intron_variant | MODIFIER | c.20-3239T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4098754 | |||||||
| chr11:4098807 | A | G | 1 | a0001c0001t0005g0207 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.20-3186A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4098807 | |||||||
| chr11:4098853 | C | T | 3 | a0001c0001t0001g0286 a0001c0001t0001g0302 a0001c0001t0001g0303 |
3 | HG02895.hp2 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.20-3140C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4098853 | |||||||
| chr11:4098947 | AATAGT | A | 4 | a0001c0004t0001g0034 a0001c0004t0001g0043 a0001c0004t0001g0044 others(1): Show |
4 | HG02630.hp1 HG02965.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-3043_20-3039del others(5): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4098947 | ||||||
| chr11:4099037 | G | A | 6 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(3): Show |
6 | HG01109.hp2 HG02145.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-2956G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4099037 | |||||||
| chr11:4099143 | T | A | 1 | a0001c0002t0001g0173 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.20-2850T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4099143 | |||||||
| chr11:4099274 | G | A | 1 | a0001c0002t0001g0064 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.20-2719G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4099274 | |||||||
| chr11:4099295 | A | ATTTTTT | 9 | a0001c0001t0001g0197 a0001c0002t0001g0065 a0001c0002t0001g0173 others(6): Show |
9 | HG00558.hp2 HG01243.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.20-2684_20-2679dup others(6): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4099295 | ||||||
| chr11:4099295 | A | ATTTTTTT | 118 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(115): Show |
138 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.20-2685_20-2679dup others(7): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4099295 | ||||||
| chr11:4099295 | A | ATTTTTTT others(1): Show |
44 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0188 others(41): Show |
45 | HG01192.hp1 HG01256.hp2 HG01978.hp2 others(42): Show |
intron_variant | MODIFIER | c.20-2686_20-2679dup others(8): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4099295 | ||||||
| chr11:4099295 | A | ATTTTTTT others(2): Show |
19 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(16): Show |
19 | HG00099.hp1 HG00438.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.20-2687_20-2679dup others(9): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4099295 | ||||||
| chr11:4099295 | A | ATTTTTTT others(3): Show |
24 | a0001c0001t0001g0024 a0001c0001t0001g0133 a0001c0001t0001g0175 others(21): Show |
24 | HG00558.hp1 HG01346.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.20-2688_20-2679dup others(10): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4099295 | ||||||
| chr11:4099295 | A | ATTTTTTT others(4): Show |
72 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(69): Show |
76 | HG00423.hp1 HG00639.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.20-2689_20-2679dup others(11): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4099295 | ||||||
| chr11:4099295 | A | ATTTTTTT others(5): Show |
24 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0132 others(21): Show |
24 | HG00408.hp2 HG00733.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.20-2690_20-2679dup others(12): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4099295 | ||||||
| chr11:4099295 | A | ATTTTTTT others(6): Show |
3 | a0001c0001t0001g0330 a0001c0006t0001g0214 a0001c0006t0001g0240 |
3 | HG02717.hp2 NA18957.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.20-2691_20-2679dup others(13): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4099295 | ||||||
| chr11:4099565 | C | T | 40 | a0001c0003t0002g0006 a0001c0003t0002g0031 a0001c0003t0002g0172 others(37): Show |
41 | HG00609.hp1 HG00639.hp1 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.20-2428C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4099565 | |||||||
| chr11:4099619 | T | C | 40 | a0001c0003t0002g0006 a0001c0003t0002g0031 a0001c0003t0002g0172 others(37): Show |
41 | HG00609.hp1 HG00639.hp1 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.20-2374T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4099619 | |||||||
| chr11:4099711 | T | G | 1 | a0001c0002t0001g0060 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.20-2282T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4099711 | |||||||
| chr11:4099865 | C | CT | 6 | a0001c0003t0002g0030 a0001c0003t0002g0046 a0001c0003t0004g0208 others(3): Show |
6 | HG01243.hp2 HG02647.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-2116dupT | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4099865 | ||||||
| chr11:4099865 | CT | C | 53 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(50): Show |
55 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.20-2116delT | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4099865 | ||||||
| chr11:4099943 | T | TC | 126 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0042 others(123): Show |
146 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.20-2042dupC | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4099943 | ||||||
| chr11:4099949 | C | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0027 |
2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.20-2044C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4099949 | |||||||
| chr11:4099951 | C | T | 2 | a0001c0003t0002g0006 a0001c0003t0002g0031 |
3 | HG00639.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.20-2042C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4099951 | |||||||
| chr11:4100414 | C | A | 2 | a0001c0003t0002g0005 a0001c0003t0002g0310 |
4 | HG02723.hp1 HG02922.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-1579C>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4100414 | |||||||
| chr11:4100485 | C | G | 3 | a0001c0001t0001g0159 a0001c0001t0001g0170 a0001c0001t0001g0236 |
3 | HG01099.hp2 HG03688.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.20-1508C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4100485 | |||||||
| chr11:4100488 | T | G | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0066 others(2): Show |
5 | HG00423.hp2 HG02135.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-1505T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4100488 | |||||||
| chr11:4100668 | AT | A | 264 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(261): Show |
288 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.20-1316delT | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4100668 | ||||||
| chr11:4100670 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.20-1323T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4100670 | |||||||
| chr11:4100851 | CTGAT | C | 33 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(30): Show |
35 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.20-1139_20-1136del others(4): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4100851 | ||||||
| chr11:4100998 | A | T | 1 | a0001c0003t0002g0046 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.20-995A>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4100998 | |||||||
| chr11:4101070 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.20-923A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4101070 | |||||||
| chr11:4101204 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.20-789G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4101204 | |||||||
| chr11:4101315 | A | AT | 8 | a0001c0001t0001g0017 a0001c0001t0001g0126 a0001c0002t0001g0047 others(5): Show |
8 | HG02055.hp1 HG02071.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.20-663dupT | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4101315 | ||||||
| chr11:4101494 | A | G | 1 | a0001c0004t0001g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.20-499A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4101494 | |||||||
| chr11:4101554 | T | TCCA | 11 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(8): Show |
11 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.20-437_20-435dupCA others(1): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4101554 | ||||||
| chr11:4101557 | A | ACCAC | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0003g0322 |
3 | HG01243.hp1 HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.20-435_20-434insCA others(2): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4101557 | ||||||
| chr11:4101557 | A | ACCCC | 16 | a0001c0001t0001g0014 a0001c0001t0001g0215 a0001c0001t0001g0231 others(13): Show |
17 | HG00558.hp1 HG01433.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.20-435_20-434insCC others(2): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4101557 | ||||||
| chr11:4101557 | A | ACCCCC | 31 | a0001c0001t0001g0128 a0001c0001t0001g0152 a0001c0001t0001g0153 others(28): Show |
31 | HG00738.hp1 HG01346.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.20-435_20-434insCC others(3): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4101557 | ||||||
| chr11:4101557 | A | ACCCCCC | 37 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0036 others(34): Show |
39 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.20-435_20-434insCC others(4): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4101557 | ||||||
| chr11:4101557 | A | ACCCCCCC | 21 | a0001c0001t0001g0013 a0001c0001t0001g0125 a0001c0001t0001g0126 others(18): Show |
22 | HG00423.hp1 HG01069.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.20-435_20-434insCC others(5): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4101557 | ||||||
| chr11:4101557 | A | ACCCCCCC others(3): Show |
1 | a0001c0001t0001g0324 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.20-435_20-434insCC others(8): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4101557 | ||||||
| chr11:4101559 | A | C | 306 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(303): Show |
331 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(328): Show |
intron_variant | MODIFIER | c.20-434A>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4101559 | |||||||
| chr11:4101559 | A | G | 1 | a0001c0004t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.20-434A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4101559 | |||||||
| chr11:4101559 | A | T | 1 | a0001c0002t0001g0095 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.20-434A>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4101559 | |||||||
| chr11:4101561 | C | T | 2 | a0001c0003t0002g0309 a0001c0003t0002g0321 |
2 | HG00642.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.20-432C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4101561 | |||||||
| chr11:4101564 | C | A | 1 | a0001c0002t0001g0033 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.20-429C>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4101564 | |||||||
| chr11:4101564 | C | CA | 123 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(120): Show |
143 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.20-429_20-428insA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4101564 | |||||||
| chr11:4101565 | C | A | 1 | a0001c0004t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.20-428C>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4101565 | |||||||
| chr11:4101565 | C | CCCCCCCG | 14 | a0001c0003t0002g0006 a0001c0003t0002g0172 a0001c0003t0002g0247 others(11): Show |
15 | HG00609.hp1 HG00639.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.20-425_20-424insCC others(5): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 4101565 | ||||||
| chr11:4101565 | C | G | 1 | a0001c0003t0002g0046 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.20-428C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4101565 | |||||||
| chr11:4101568 | C | CCCCCCCC others(3): Show |
2 | a0001c0001t0003g0039 a0001c0001t0003g0040 |
2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.20-425_20-424insCC others(8): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4101568 | |||||||
| chr11:4101615 | A | T | 1 | a0001c0003t0002g0268 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.20-378A>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4101615 | |||||||
| chr11:4101788 | G | C | 1 | a0001c0002t0001g0069 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.20-205G>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4101788 | |||||||
| chr11:4101889 | A | T | 9 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.20-104A>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4101889 | |||||||
| chr11:4101968 | T | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG02056.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.20-25T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 1/18 | chr11 | 4101968 | |||||||
| chr11:4102115 | C | G | 263 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(260): Show |
287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.108+34C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4102115 | |||||||
| chr11:4102197 | C | G | 88 | a0001c0001t0001g0072 a0001c0002t0001g0001 a0001c0002t0001g0003 others(85): Show |
106 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.108+116C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4102197 | |||||||
| chr11:4102228 | AT | A | 33 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(30): Show |
35 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.108+156delT | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 4102228 | ||||||
| chr11:4102496 | A | G | 1 | a0001c0002t0001g0094 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.108+415A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4102496 | |||||||
| chr11:4102531 | G | T | 40 | a0001c0003t0002g0006 a0001c0003t0002g0031 a0001c0003t0002g0172 others(37): Show |
41 | HG00609.hp1 HG00639.hp1 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.108+450G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4102531 | |||||||
| chr11:4102569 | T | C | 1 | a0001c0003t0004g0208 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.108+488T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4102569 | |||||||
| chr11:4102607 | G | A | 1 | a0001c0003t0002g0030 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.108+526G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4102607 | |||||||
| chr11:4102631 | G | A | 4 | a0001c0001t0003g0018 a0001c0001t0003g0039 a0001c0001t0003g0040 others(1): Show |
4 | HG02615.hp1 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+550G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4102631 | |||||||
| chr11:4102651 | C | CA | 47 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0001g0194 others(44): Show |
48 | HG00609.hp1 HG00639.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.108+586dupA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 4102651 | ||||||
| chr11:4102714 | A | G | 2 | a0001c0003t0002g0309 a0001c0003t0002g0321 |
2 | HG00642.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.108+633A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4102714 | |||||||
| chr11:4102882 | T | C | 263 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(260): Show |
287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.108+801T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4102882 | |||||||
| chr11:4102938 | C | G | 1 | a0001c0002t0001g0093 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.108+857C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4102938 | |||||||
| chr11:4103046 | G | C | 127 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(124): Show |
147 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.108+965G>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4103046 | |||||||
| chr11:4103052 | T | G | 1 | a0001c0004t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.108+971T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4103052 | |||||||
| chr11:4103142 | G | A | 81 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(78): Show |
85 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.108+1061G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4103142 | |||||||
| chr11:4103228 | C | A | 1 | a0001c0002t0001g0063 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.108+1147C>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4103228 | |||||||
| chr11:4103501 | G | C | 33 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(30): Show |
35 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.108+1420G>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4103501 | |||||||
| chr11:4103519 | G | T | 1 | a0001c0001t0001g0230 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.108+1438G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4103519 | |||||||
| chr11:4103536 | C | T | 40 | a0001c0003t0002g0006 a0001c0003t0002g0031 a0001c0003t0002g0172 others(37): Show |
41 | HG00609.hp1 HG00639.hp1 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.108+1455C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4103536 | |||||||
| chr11:4103569 | G | A | 3 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 |
3 | HG02615.hp1 HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.108+1488G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4103569 | |||||||
| chr11:4103599 | G | T | 41 | a0001c0003t0002g0006 a0001c0003t0002g0031 a0001c0003t0002g0172 others(38): Show |
42 | HG00609.hp1 HG00639.hp1 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.108+1518G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4103599 | |||||||
| chr11:4103687 | A | G | 1 | a0001c0001t0005g0207 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.108+1606A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4103687 | |||||||
| chr11:4103696 | C | T | 19 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(16): Show |
19 | HG01243.hp1 HG02109.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.108+1615C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4103696 | |||||||
| chr11:4103781 | A | AT | 130 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(127): Show |
134 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.108+1719dupT | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 4103781 | ||||||
| chr11:4103781 | A | ATT | 19 | a0001c0001t0001g0133 a0001c0001t0001g0140 a0001c0001t0001g0150 others(16): Show |
19 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.108+1718_108+1719d others(4): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 4103781 | ||||||
| chr11:4103946 | C | CA | 7 | a0001c0001t0002g0331 a0001c0003t0002g0171 a0001c0003t0002g0245 others(4): Show |
7 | HG02135.hp1 HG03139.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.108+1887dupA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 4103946 | ||||||
| chr11:4103946 | CA | C | 25 | a0001c0001t0001g0035 a0001c0001t0001g0126 a0001c0001t0001g0129 others(22): Show |
25 | HG01243.hp2 HG01255.hp1 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.108+1887delA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 4103946 | ||||||
| chr11:4103946 | CAA | C | 211 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(208): Show |
233 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.108+1886_108+1887d others(4): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 4103946 | ||||||
| chr11:4103946 | CAAA | C | 33 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(30): Show |
35 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.108+1885_108+1887d others(5): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 4103946 | ||||||
| chr11:4103952 | A | T | 1 | a0001c0003t0002g0253 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.108+1871A>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4103952 | |||||||
| chr11:4103986 | C | T | 41 | a0001c0003t0002g0006 a0001c0003t0002g0031 a0001c0003t0002g0172 others(38): Show |
42 | HG00609.hp1 HG00639.hp1 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.108+1905C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4103986 | |||||||
| chr11:4104240 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.109-1806T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4104240 | |||||||
| chr11:4104264 | A | G | 19 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(16): Show |
19 | HG01243.hp1 HG02109.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.109-1782A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4104264 | |||||||
| chr11:4104524 | A | G | 1 | a0001c0002t0001g0114 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.109-1522A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4104524 | |||||||
| chr11:4104542 | A | G | 41 | a0001c0003t0002g0006 a0001c0003t0002g0031 a0001c0003t0002g0172 others(38): Show |
42 | HG00609.hp1 HG00639.hp1 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.109-1504A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4104542 | |||||||
| chr11:4104658 | T | C | 1 | a0001c0002t0001g0061 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.109-1388T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4104658 | |||||||
| chr11:4104779 | T | G | 34 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(31): Show |
36 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.109-1267T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4104779 | |||||||
| chr11:4105158 | A | G | 1 | a0001c0003t0002g0275 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.109-888A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4105158 | |||||||
| chr11:4105210 | A | G | 262 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(259): Show |
286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.109-836A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4105210 | |||||||
| chr11:4105288 | A | G | 1 | a0001c0001t0005g0207 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.109-758A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4105288 | |||||||
| chr11:4105312 | T | C | 1 | a0001c0003t0004g0208 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.109-734T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4105312 | |||||||
| chr11:4105369 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.109-677C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4105369 | |||||||
| chr11:4105404 | T | A | 1 | a0001c0001t0001g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109-642T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4105404 | |||||||
| chr11:4105578 | C | CT | 51 | a0001c0001t0001g0042 a0001c0001t0001g0157 a0001c0001t0001g0177 others(48): Show |
52 | HG00609.hp1 HG00639.hp1 HG01192.hp2 others(49): Show |
intron_variant | MODIFIER | c.109-448dupT | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 4105578 | ||||||
| chr11:4105578 | C | CTT | 231 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(228): Show |
255 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.109-449_109-448dup others(2): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 4105578 | ||||||
| chr11:4105578 | C | CTTT | 17 | a0001c0001t0001g0019 a0001c0001t0001g0135 a0001c0001t0001g0158 others(14): Show |
17 | HG01433.hp2 HG02071.hp1 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.109-450_109-448dup others(3): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 4105578 | ||||||
| chr11:4105578 | C | CTTTT | 8 | a0001c0002t0001g0047 a0001c0002t0001g0054 a0001c0002t0001g0055 others(5): Show |
8 | NA18942.hp1 NA18963.hp2 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.109-451_109-448dup others(4): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 4105578 | ||||||
| chr11:4105600 | A | C | 1 | a0001c0003t0002g0275 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.109-446A>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4105600 | |||||||
| chr11:4105642 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.109-404A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4105642 | |||||||
| chr11:4105856 | C | T | 1 | a0001c0003t0002g0046 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.109-190C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4105856 | |||||||
| chr11:4105920 | C | T | 1 | a0001c0003t0002g0273 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.109-126C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4105920 | |||||||
| chr11:4105931 | T | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0141 |
2 | HG01261.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.109-115T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4105931 | |||||||
| chr11:4105934 | G | A | 1 | a0001c0002t0001g0100 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.109-112G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4105934 | |||||||
| chr11:4105974 | T | C | 1 | a0001c0003t0002g0171 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.109-72T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4105974 | |||||||
| chr11:4105999 | A | G | 1 | a0001c0006t0001g0240 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.109-47A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 2/18 | chr11 | 4105999 | |||||||
| chr11:4106379 | G | A | 42 | a0001c0003t0002g0006 a0001c0003t0002g0031 a0001c0003t0002g0172 others(39): Show |
43 | HG00609.hp1 HG00639.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.286+156G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 3/18 | chr11 | 4106379 | |||||||
| chr11:4106419 | C | G | 87 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0007 others(84): Show |
105 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.286+196C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 3/18 | chr11 | 4106419 | |||||||
| chr11:4106435 | C | T | 2 | a0001c0002t0001g0062 a0001c0002t0001g0065 |
2 | HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.286+212C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 3/18 | chr11 | 4106435 | |||||||
| chr11:4106511 | G | C | 1 | a0001c0004t0001g0043 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.286+288G>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 3/18 | chr11 | 4106511 | |||||||
| chr11:4106534 | G | A | 1 | a0001c0004t0001g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.286+311G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 3/18 | chr11 | 4106534 | |||||||
| chr11:4106622 | C | T | 2 | a0001c0001t0001g0176 a0001c0004t0001g0034 |
2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.286+399C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 3/18 | chr11 | 4106622 | |||||||
| chr11:4106747 | C | CATAA | 3 | a0001c0004t0001g0043 a0001c0004t0001g0044 a0001c0004t0001g0174 |
3 | HG02630.hp1 HG02965.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.286+548_286+551dup others(4): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 4106747 | ||||||
| chr11:4106747 | CATAA | C | 3 | a0001c0001t0001g0130 a0001c0002t0001g0007 a0001c0002t0001g0033 |
4 | HG01069.hp2 HG01071.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+548_286+551del others(4): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 4106747 | ||||||
| chr11:4106816 | G | A | 2 | a0001c0001t0001g0042 a0001c0004t0001g0034 |
2 | NA18941.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.286+593G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 3/18 | chr11 | 4106816 | |||||||
| chr11:4106986 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.287-449C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 3/18 | chr11 | 4106986 | |||||||
| chr11:4107055 | G | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0045 others(5): Show |
10 | HG00558.hp2 HG02056.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.287-380G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 3/18 | chr11 | 4107055 | |||||||
| chr11:4107139 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.287-296G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 3/18 | chr11 | 4107139 | |||||||
| chr11:4107171 | C | T | 1 | a0001c0004t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.287-264C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 3/18 | chr11 | 4107171 | |||||||
| chr11:4107184 | G | A | 3 | a0001c0004t0001g0043 a0001c0004t0001g0044 a0001c0004t0001g0174 |
3 | HG02630.hp1 HG02965.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.287-251G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 3/18 | chr11 | 4107184 | |||||||
| chr11:4107256 | A | G | 146 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(143): Show |
166 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.287-179A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 3/18 | chr11 | 4107256 | |||||||
| chr11:4107381 | G | T | 1 | a0001c0003t0002g0277 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.287-54G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 3/18 | chr11 | 4107381 | |||||||
| chr11:4107382 | A | G | 1 | a0001c0003t0002g0277 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.287-53A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 3/18 | chr11 | 4107382 | |||||||
| chr11:4107388 | C | G | 2 | a0001c0001t0001g0149 a0001c0001t0001g0158 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.287-47C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 3/18 | chr11 | 4107388 | |||||||
| chr11:4107615 | G | A | 146 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(143): Show |
166 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.387+80G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4107615 | |||||||
| chr11:4107728 | C | T | 5 | a0001c0003t0002g0030 a0001c0003t0002g0046 a0001c0003t0004g0208 others(2): Show |
5 | HG01243.hp2 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+193C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4107728 | |||||||
| chr11:4107769 | C | T | 1 | a0001c0003t0002g0277 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.387+234C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4107769 | |||||||
| chr11:4107770 | T | C | 1 | a0001c0003t0002g0277 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.387+235T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4107770 | |||||||
| chr11:4107778 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.387+243G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4107778 | |||||||
| chr11:4107811 | C | G | 4 | a0001c0001t0003g0018 a0001c0001t0003g0039 a0001c0001t0003g0040 others(1): Show |
4 | HG02615.hp1 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+276C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4107811 | |||||||
| chr11:4107890 | C | T | 147 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(144): Show |
168 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.387+355C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4107890 | |||||||
| chr11:4108162 | T | A | 1 | a0001c0003t0002g0277 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.387+627T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4108162 | |||||||
| chr11:4108163 | A | T | 1 | a0001c0003t0002g0277 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.387+628A>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4108163 | |||||||
| chr11:4108408 | C | G | 10 | a0001c0001t0003g0018 a0001c0001t0003g0022 a0001c0001t0003g0028 others(7): Show |
10 | HG01243.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.387+873C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4108408 | |||||||
| chr11:4108487 | A | T | 41 | a0001c0003t0002g0006 a0001c0003t0002g0031 a0001c0003t0002g0172 others(38): Show |
42 | HG00609.hp1 HG00639.hp1 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.387+952A>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4108487 | |||||||
| chr11:4108515 | G | A | 2 | a0001c0003t0002g0005 a0001c0003t0002g0310 |
4 | HG02723.hp1 HG02922.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.387+980G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4108515 | |||||||
| chr11:4108524 | G | T | 1 | a0001c0001t0001g0286 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.387+989G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4108524 | |||||||
| chr11:4108556 | C | T | 1 | a0001c0001t0005g0207 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.387+1021C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4108556 | |||||||
| chr11:4108571 | C | A | 2 | a0001c0003t0002g0005 a0001c0003t0002g0310 |
4 | HG02723.hp1 HG02922.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.387+1036C>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4108571 | |||||||
| chr11:4108587 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.387+1052G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4108587 | |||||||
| chr11:4108597 | C | CA | 18 | a0001c0001t0001g0142 a0001c0001t0001g0150 a0001c0001t0001g0161 others(15): Show |
18 | HG00639.hp2 HG01243.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.388-1026dupA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr11 | 4108597 | ||||||
| chr11:4108597 | C | CAAAA | 113 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(110): Show |
132 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.388-1029_388-1026d others(6): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr11 | 4108597 | ||||||
| chr11:4108597 | C | CAAAAA | 18 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0178 others(15): Show |
19 | HG00423.hp2 HG01361.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.388-1030_388-1026d others(7): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr11 | 4108597 | ||||||
| chr11:4108597 | CA | C | 42 | a0001c0001t0001g0170 a0001c0001t0001g0239 a0001c0003t0002g0006 others(39): Show |
43 | HG00609.hp1 HG00639.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.388-1026delA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr11 | 4108597 | ||||||
| chr11:4108618 | A | T | 1 | a0001c0003t0002g0275 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.388-1026A>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4108618 | |||||||
| chr11:4108629 | T | C | 135 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(132): Show |
155 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.388-1015T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4108629 | |||||||
| chr11:4108660 | T | TA | 41 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(38): Show |
43 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.388-981dupA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr11 | 4108660 | ||||||
| chr11:4108697 | G | C | 1 | a0001c0003t0002g0030 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.388-947G>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4108697 | |||||||
| chr11:4108724 | T | G | 1 | a0001c0003t0002g0277 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.388-920T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4108724 | |||||||
| chr11:4108854 | T | C | 1 | a0001c0003t0002g0266 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.388-790T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4108854 | |||||||
| chr11:4108987 | G | A | 10 | a0001c0001t0003g0018 a0001c0001t0003g0022 a0001c0001t0003g0028 others(7): Show |
10 | HG01243.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.388-657G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4108987 | |||||||
| chr11:4109034 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.388-610A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4109034 | |||||||
| chr11:4109313 | C | G | 93 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0007 others(90): Show |
111 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.388-331C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4109313 | |||||||
| chr11:4109391 | A | G | 4 | a0001c0001t0001g0215 a0001c0001t0001g0218 a0001c0001t0001g0220 others(1): Show |
4 | HG00558.hp1 HG02027.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-253A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4109391 | |||||||
| chr11:4109463 | T | C | 7 | a0001c0002t0001g0050 a0001c0002t0001g0070 a0001c0002t0001g0074 others(4): Show |
7 | NA18954.hp2 NA18981.hp2 NA18988.hp2 others(4): Show |
intron_variant | MODIFIER | c.388-181T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4109463 | |||||||
| chr11:4109572 | G | C | 5 | a0001c0003t0002g0030 a0001c0003t0002g0046 a0001c0003t0004g0208 others(2): Show |
5 | HG01243.hp2 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.388-72G>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 4/18 | chr11 | 4109572 | |||||||
| chr11:4109959 | T | G | 4 | a0001c0004t0001g0034 a0001c0004t0001g0043 a0001c0004t0001g0044 others(1): Show |
4 | HG02630.hp1 HG02965.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+256T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | chr11 | 4109959 | |||||||
| chr11:4110021 | C | G | 1 | a0001c0002t0001g0068 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.447+318C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | chr11 | 4110021 | |||||||
| chr11:4110151 | TAAA | T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0045 others(5): Show |
10 | HG00558.hp2 HG02056.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.447+455_447+457del others(3): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 4110151 | ||||||
| chr11:4110220 | T | G | 1 | a0001c0003t0002g0275 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.447+517T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | chr11 | 4110220 | |||||||
| chr11:4110342 | G | A | 3 | a0001c0001t0003g0022 a0001c0001t0003g0028 a0001c0001t0003g0029 |
3 | HG02486.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.447+639G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | chr11 | 4110342 | |||||||
| chr11:4110350 | A | G | 150 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(147): Show |
170 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.447+647A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | chr11 | 4110350 | |||||||
| chr11:4110494 | A | G | 151 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(148): Show |
171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.447+791A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | chr11 | 4110494 | |||||||
| chr11:4110505 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.447+802C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | chr11 | 4110505 | |||||||
| chr11:4110552 | G | A | 4 | a0001c0002t0001g0078 a0001c0002t0001g0079 a0001c0002t0001g0123 others(1): Show |
4 | HG00735.hp1 HG01109.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+849G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | chr11 | 4110552 | |||||||
| chr11:4110597 | T | C | 308 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(305): Show |
333 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(330): Show |
intron_variant | MODIFIER | c.447+894T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | chr11 | 4110597 | |||||||
| chr11:4110768 | C | CA | 9 | a0001c0001t0001g0193 a0001c0001t0001g0220 a0001c0001t0002g0331 others(6): Show |
9 | HG02056.hp2 HG02071.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.448-813dupA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 4110768 | ||||||
| chr11:4110912 | T | C | 2 | a0001c0003t0002g0309 a0001c0003t0002g0321 |
2 | HG00642.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.448-689T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | chr11 | 4110912 | |||||||
| chr11:4110921 | T | C | 3 | a0001c0004t0001g0043 a0001c0004t0001g0044 a0001c0004t0001g0174 |
3 | HG02630.hp1 HG02965.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.448-680T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | chr11 | 4110921 | |||||||
| chr11:4110961 | G | A | 1 | a0001c0004t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.448-640G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | chr11 | 4110961 | |||||||
| chr11:4111085 | G | A | 1 | a0001c0002t0001g0080 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.448-516G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | chr11 | 4111085 | |||||||
| chr11:4111204 | A | G | 1 | a0001c0003t0002g0275 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.448-397A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | chr11 | 4111204 | |||||||
| chr11:4111303 | C | T | 2 | a0001c0003t0002g0307 a0001c0003t0002g0308 |
2 | HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.448-298C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | chr11 | 4111303 | |||||||
| chr11:4111343 | A | G | 151 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(148): Show |
171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.448-258A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | chr11 | 4111343 | |||||||
| chr11:4111398 | G | A | 5 | a0001c0003t0002g0030 a0001c0003t0002g0046 a0001c0003t0004g0208 others(2): Show |
5 | HG01243.hp2 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.448-203G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | chr11 | 4111398 | |||||||
| chr11:4111401 | A | G | 1 | a0001c0003t0002g0265 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.448-200A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | chr11 | 4111401 | |||||||
| chr11:4111410 | C | CA | 49 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(46): Show |
51 | HG00438.hp1 HG00558.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.448-175dupA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 4111410 | ||||||
| chr11:4111410 | CA | C | 10 | a0001c0001t0003g0018 a0001c0001t0003g0022 a0001c0001t0003g0028 others(7): Show |
10 | HG01243.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.448-175delA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 4111410 | ||||||
| chr11:4112087 | C | A | 260 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(257): Show |
284 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.650+25C>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4112087 | |||||||
| chr11:4112373 | T | G | 9 | a0001c0001t0001g0038 a0001c0001t0001g0279 a0001c0002t0001g0081 others(6): Show |
9 | HG01928.hp2 HG01943.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.650+311T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4112373 | |||||||
| chr11:4112426 | C | T | 6 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(3): Show |
6 | HG01109.hp2 HG02145.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.650+364C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4112426 | |||||||
| chr11:4112427 | G | A | 1 | a0001c0002t0001g0102 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.650+365G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4112427 | |||||||
| chr11:4112514 | C | T | 1 | a0001c0003t0002g0326 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.650+452C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4112514 | |||||||
| chr11:4112638 | G | A | 151 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(148): Show |
171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.650+576G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4112638 | |||||||
| chr11:4112776 | G | A | 5 | a0001c0003t0002g0030 a0001c0003t0002g0046 a0001c0003t0004g0208 others(2): Show |
5 | HG01243.hp2 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.650+714G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4112776 | |||||||
| chr11:4112842 | C | G | 1 | a0001c0001t0003g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.650+780C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4112842 | |||||||
| chr11:4112970 | T | C | 41 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(38): Show |
43 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.650+908T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4112970 | |||||||
| chr11:4113003 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.650+941A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4113003 | |||||||
| chr11:4113019 | G | A | 1 | a0001c0003t0002g0246 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.650+957G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4113019 | |||||||
| chr11:4113065 | A | C | 1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.650+1003A>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4113065 | |||||||
| chr11:4113084 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.650+1022G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4113084 | |||||||
| chr11:4113117 | TA | T | 188 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(185): Show |
209 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.650+1066delA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 4113117 | ||||||
| chr11:4113232 | C | T | 42 | a0001c0003t0002g0006 a0001c0003t0002g0031 a0001c0003t0002g0172 others(39): Show |
43 | HG00609.hp1 HG00639.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.650+1170C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4113232 | |||||||
| chr11:4113252 | T | C | 1 | a0001c0002t0001g0067 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.650+1190T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4113252 | |||||||
| chr11:4113359 | G | A | 2 | a0001c0001t0001g0200 a0001c0001t0001g0205 |
2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.650+1297G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4113359 | |||||||
| chr11:4113523 | C | A | 4 | a0001c0001t0003g0018 a0001c0001t0003g0039 a0001c0001t0003g0040 others(1): Show |
4 | HG02615.hp1 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.650+1461C>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4113523 | |||||||
| chr11:4113560 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0188 |
2 | NA19000.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.650+1498G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4113560 | |||||||
| chr11:4113590 | G | C | 6 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(3): Show |
6 | HG01109.hp2 HG02145.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.650+1528G>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4113590 | |||||||
| chr11:4113647 | A | G | 1 | a0001c0003t0002g0030 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.650+1585A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4113647 | |||||||
| chr11:4113692 | T | A | 2 | a0001c0003t0002g0309 a0001c0003t0002g0321 |
2 | HG00642.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.650+1630T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4113692 | |||||||
| chr11:4113901 | C | T | 1 | a0001c0002t0001g0090 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.650+1839C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4113901 | |||||||
| chr11:4113990 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0027 |
3 | HG02109.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.650+1928C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4113990 | |||||||
| chr11:4114090 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.650+2028G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4114090 | |||||||
| chr11:4114121 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.650+2059C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4114121 | |||||||
| chr11:4114269 | C | T | 3 | a0001c0004t0001g0043 a0001c0004t0001g0044 a0001c0004t0001g0174 |
3 | HG02630.hp1 HG02965.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.650+2207C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4114269 | |||||||
| chr11:4114363 | C | G | 1 | a0001c0001t0003g0028 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.650+2301C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4114363 | |||||||
| chr11:4114424 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.650+2362C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4114424 | |||||||
| chr11:4114550 | TA | T | 7 | a0001c0001t0001g0035 a0001c0001t0003g0028 a0001c0002t0001g0054 others(4): Show |
7 | HG01516.hp2 HG02698.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.650+2504delA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 4114550 | ||||||
| chr11:4114652 | C | A | 1 | a0001c0001t0005g0207 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.650+2590C>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4114652 | |||||||
| chr11:4114902 | G | T | 4 | a0001c0002t0001g0078 a0001c0002t0001g0079 a0001c0002t0001g0100 others(1): Show |
4 | HG00735.hp1 HG01109.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.650+2840G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4114902 | |||||||
| chr11:4114949 | G | A | 1 | a0001c0001t0003g0322 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.650+2887G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4114949 | |||||||
| chr11:4115170 | A | G | 1 | a0001c0003t0002g0309 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.650+3108A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4115170 | |||||||
| chr11:4115211 | C | G | 2 | a0001c0003t0002g0309 a0001c0003t0002g0321 |
2 | HG00642.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.651-3109C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4115211 | |||||||
| chr11:4115294 | A | G | 1 | a0001c0003t0002g0275 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.651-3026A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4115294 | |||||||
| chr11:4115507 | C | CA | 10 | a0001c0001t0001g0143 a0001c0001t0001g0168 a0001c0001t0001g0175 others(7): Show |
10 | HG01433.hp2 HG02622.hp1 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.651-2797dupA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 4115507 | ||||||
| chr11:4115507 | CA | C | 14 | a0001c0001t0003g0018 a0001c0001t0003g0022 a0001c0001t0003g0028 others(11): Show |
14 | HG01243.hp1 HG02027.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.651-2797delA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 4115507 | ||||||
| chr11:4115598 | T | C | 311 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(308): Show |
336 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(333): Show |
intron_variant | MODIFIER | c.651-2722T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4115598 | |||||||
| chr11:4115604 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.651-2716T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4115604 | |||||||
| chr11:4115610 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.651-2710G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4115610 | |||||||
| chr11:4115613 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.651-2707G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4115613 | |||||||
| chr11:4115705 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.651-2615C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4115705 | |||||||
| chr11:4115744 | A | G | 86 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0007 others(83): Show |
104 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.651-2576A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4115744 | |||||||
| chr11:4115882 | A | C | 6 | a0001c0003t0002g0244 a0001c0003t0002g0250 a0001c0003t0002g0251 others(3): Show |
6 | HG01358.hp1 HG01978.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.651-2438A>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4115882 | |||||||
| chr11:4115887 | A | G | 4 | a0001c0004t0001g0034 a0001c0004t0001g0043 a0001c0004t0001g0044 others(1): Show |
4 | HG02630.hp1 HG02965.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.651-2433A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4115887 | |||||||
| chr11:4115971 | A | G | 2 | a0001c0001t0001g0215 a0001c0001t0001g0220 |
2 | HG00558.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.651-2349A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4115971 | |||||||
| chr11:4116000 | G | A | 86 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0007 others(83): Show |
104 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.651-2320G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4116000 | |||||||
| chr11:4116007 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.651-2313G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4116007 | |||||||
| chr11:4116109 | T | C | 305 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(302): Show |
330 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(327): Show |
intron_variant | MODIFIER | c.651-2211T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4116109 | |||||||
| chr11:4116212 | G | A | 1 | a0001c0003t0002g0319 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.651-2108G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4116212 | |||||||
| chr11:4116300 | T | C | 1 | a0001c0001t0003g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.651-2020T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4116300 | |||||||
| chr11:4116352 | G | A | 1 | a0001c0002t0001g0173 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.651-1968G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4116352 | |||||||
| chr11:4116395 | C | T | 1 | a0001c0003t0002g0171 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.651-1925C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4116395 | |||||||
| chr11:4116454 | T | C | 1 | a0001c0006t0001g0214 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.651-1866T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4116454 | |||||||
| chr11:4116834 | G | T | 1 | a0001c0004t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.651-1486G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4116834 | |||||||
| chr11:4116899 | C | G | 1 | a0001c0006t0001g0169 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.651-1421C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4116899 | |||||||
| chr11:4116909 | G | T | 1 | a0001c0004t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.651-1411G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4116909 | |||||||
| chr11:4116966 | C | CA | 46 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(43): Show |
48 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.651-1345dupA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 4116966 | ||||||
| chr11:4116976 | G | A | 147 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(144): Show |
167 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.651-1344G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4116976 | |||||||
| chr11:4116981 | G | A | 2 | a0001c0004t0001g0044 a0001c0004t0001g0174 |
2 | HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.651-1339G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4116981 | |||||||
| chr11:4117074 | C | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(113): Show |
120 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.651-1246C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4117074 | |||||||
| chr11:4117093 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0026 |
2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.651-1227T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4117093 | |||||||
| chr11:4117153 | T | A | 10 | a0001c0001t0003g0018 a0001c0001t0003g0022 a0001c0001t0003g0028 others(7): Show |
10 | HG01243.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.651-1167T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4117153 | |||||||
| chr11:4117314 | A | T | 1 | a0001c0004t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.651-1006A>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4117314 | |||||||
| chr11:4117378 | G | A | 1 | a0001c0004t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.651-942G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4117378 | |||||||
| chr11:4117511 | A | T | 6 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(3): Show |
6 | HG01109.hp2 HG02145.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.651-809A>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4117511 | |||||||
| chr11:4117517 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.651-803T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4117517 | |||||||
| chr11:4117880 | A | G | 6 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(3): Show |
6 | HG01109.hp2 HG02145.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.651-440A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4117880 | |||||||
| chr11:4117895 | G | A | 268 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(265): Show |
293 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.651-425G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4117895 | |||||||
| chr11:4117897 | A | G | 1 | a0001c0004t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.651-423A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4117897 | |||||||
| chr11:4118053 | T | C | 1 | a0001c0006t0001g0214 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.651-267T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4118053 | |||||||
| chr11:4118140 | C | T | 3 | a0001c0001t0001g0224 a0001c0001t0001g0234 a0001c0001t0001g0235 |
3 | NA18940.hp2 NA18964.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.651-180C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | chr11 | 4118140 | |||||||
| chr11:4118218 | CTCTT | C | 7 | a0001c0003t0002g0242 a0001c0003t0002g0243 a0001c0003t0002g0262 others(4): Show |
7 | HG01192.hp2 HG01496.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.651-100_651-97delC others(3): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 4118218 | ||||||
| chr11:4118220 | CT | C | 117 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(114): Show |
121 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.651-86delT | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 4118220 | ||||||
| chr11:4118620 | A | C | 1 | a0001c0001t0001g0178 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.792+159A>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 8/18 | chr11 | 4118620 | |||||||
| chr11:4118748 | T | C | 42 | a0001c0002t0001g0051 a0001c0003t0002g0006 a0001c0003t0002g0031 others(39): Show |
43 | HG00609.hp1 HG00639.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.792+287T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 8/18 | chr11 | 4118748 | |||||||
| chr11:4118910 | T | G | 1 | a0001c0002t0001g0173 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.792+449T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 8/18 | chr11 | 4118910 | |||||||
| chr11:4118961 | G | T | 1 | a0001c0003t0002g0316 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.792+500G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 8/18 | chr11 | 4118961 | |||||||
| chr11:4118971 | T | A | 1 | a0001c0002t0001g0198 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.792+510T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 8/18 | chr11 | 4118971 | |||||||
| chr11:4118999 | T | C | 134 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(131): Show |
154 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.792+538T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 8/18 | chr11 | 4118999 | |||||||
| chr11:4119216 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.793-629G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 8/18 | chr11 | 4119216 | |||||||
| chr11:4119282 | G | C | 1 | a0001c0004t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.793-563G>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 8/18 | chr11 | 4119282 | |||||||
| chr11:4119358 | T | G | 4 | a0001c0004t0001g0034 a0001c0004t0001g0043 a0001c0004t0001g0044 others(1): Show |
4 | HG02630.hp1 HG02965.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.793-487T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 8/18 | chr11 | 4119358 | |||||||
| chr11:4119740 | T | C | 4 | a0001c0001t0003g0018 a0001c0001t0003g0039 a0001c0001t0003g0040 others(1): Show |
4 | HG02615.hp1 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.793-105T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 8/18 | chr11 | 4119740 | |||||||
| chr11:4120094 | A | G | 3 | a0001c0003t0002g0311 a0001c0003t0002g0312 a0001c0003t0002g0315 |
3 | NA18971.hp1 NA18981.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.876+166A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/18 | chr11 | 4120094 | |||||||
| chr11:4120282 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.876+354A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/18 | chr11 | 4120282 | |||||||
| chr11:4120292 | G | C | 1 | a0001c0005t0001g0297 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.876+364G>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/18 | chr11 | 4120292 | |||||||
| chr11:4120407 | A | C | 1 | a0001c0001t0001g0230 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.876+479A>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/18 | chr11 | 4120407 | |||||||
| chr11:4120420 | A | G | 1 | a0001c0003t0002g0171 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.876+492A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/18 | chr11 | 4120420 | |||||||
| chr11:4120444 | G | T | 1 | a0001c0002t0001g0054 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.876+516G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/18 | chr11 | 4120444 | |||||||
| chr11:4120565 | T | C | 5 | a0001c0002t0001g0082 a0001c0002t0001g0117 a0001c0002t0001g0118 others(2): Show |
5 | HG00099.hp1 HG01361.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.876+637T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/18 | chr11 | 4120565 | |||||||
| chr11:4120655 | T | A | 1 | a0001c0003t0002g0171 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.876+727T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/18 | chr11 | 4120655 | |||||||
| chr11:4120678 | A | G | 2 | a0001c0003t0002g0246 a0001c0003t0002g0261 |
2 | HG02132.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.876+750A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/18 | chr11 | 4120678 | |||||||
| chr11:4120712 | C | G | 41 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(38): Show |
43 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.876+784C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/18 | chr11 | 4120712 | |||||||
| chr11:4120786 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.877-818G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/18 | chr11 | 4120786 | |||||||
| chr11:4120839 | C | T | 83 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(80): Show |
87 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.877-765C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/18 | chr11 | 4120839 | |||||||
| chr11:4120942 | C | T | 117 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(114): Show |
121 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.877-662C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/18 | chr11 | 4120942 | |||||||
| chr11:4120999 | G | A | 58 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(55): Show |
60 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.877-605G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/18 | chr11 | 4120999 | |||||||
| chr11:4121258 | T | C | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.877-346T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/18 | chr11 | 4121258 | |||||||
| chr11:4121357 | C | T | 1 | a0001c0002t0001g0089 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.877-247C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/18 | chr11 | 4121357 | |||||||
| chr11:4121362 | T | C | 117 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(114): Show |
121 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.877-242T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/18 | chr11 | 4121362 | |||||||
| chr11:4121501 | TGTA | T | 2 | a0001c0003t0002g0005 a0001c0003t0002g0310 |
4 | HG02723.hp1 HG02922.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.877-100_877-98delA others(2): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr11 | 4121501 | ||||||
| chr11:4121559 | GTTTCATT others(26): Show |
G | 1 | a0001c0001t0001g0189 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.877-41_877-9delCAT others(30): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr11 | 4121559 | ||||||
| chr11:4121857 | T | C | 10 | a0001c0001t0003g0018 a0001c0001t0003g0022 a0001c0001t0003g0028 others(7): Show |
10 | HG01243.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1038+92T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 10/18 | chr11 | 4121857 | |||||||
| chr11:4121905 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1038+140G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 10/18 | chr11 | 4121905 | |||||||
| chr11:4121916 | C | G | 41 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(38): Show |
43 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.1038+151C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 10/18 | chr11 | 4121916 | |||||||
| chr11:4121927 | A | G | 41 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(38): Show |
43 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.1038+162A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 10/18 | chr11 | 4121927 | |||||||
| chr11:4121936 | A | C | 1 | a0001c0001t0005g0207 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1038+171A>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 10/18 | chr11 | 4121936 | |||||||
| chr11:4121971 | A | G | 4 | a0001c0004t0001g0034 a0001c0004t0001g0043 a0001c0004t0001g0044 others(1): Show |
4 | HG02630.hp1 HG02965.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-170A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 10/18 | chr11 | 4121971 | |||||||
| chr11:4122089 | A | G | 1 | a0001c0003t0002g0319 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1039-52A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 10/18 | chr11 | 4122089 | |||||||
| chr11:4122462 | T | A | 309 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(306): Show |
334 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(331): Show |
intron_variant | MODIFIER | c.1118+242T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 11/18 | chr11 | 4122462 | |||||||
| chr11:4122491 | G | T | 114 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(111): Show |
118 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.1118+271G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 11/18 | chr11 | 4122491 | |||||||
| chr11:4122561 | C | T | 1 | a0001c0006t0001g0169 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1118+341C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 11/18 | chr11 | 4122561 | |||||||
| chr11:4122567 | T | G | 1 | a0001c0001t0001g0126 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1118+347T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 11/18 | chr11 | 4122567 | |||||||
| chr11:4122594 | C | T | 27 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(24): Show |
27 | HG00741.hp2 HG02040.hp2 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.1118+374C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 11/18 | chr11 | 4122594 | |||||||
| chr11:4122656 | T | G | 117 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(114): Show |
121 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.1118+436T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 11/18 | chr11 | 4122656 | |||||||
| chr11:4122760 | C | A | 117 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(114): Show |
121 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.1119-423C>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 11/18 | chr11 | 4122760 | |||||||
| chr11:4122815 | G | A | 2 | a0001c0003t0002g0276 a0001c0003t0002g0277 |
2 | NA18992.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1119-368G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 11/18 | chr11 | 4122815 | |||||||
| chr11:4122872 | C | CA | 53 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(50): Show |
56 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.1119-298dupA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 4122872 | ||||||
| chr11:4122873 | A | G | 1 | a0001c0003t0002g0030 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1119-310A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 11/18 | chr11 | 4122873 | |||||||
| chr11:4123417 | G | T | 1 | a0001c0001t0001g0230 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1320+33G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4123417 | |||||||
| chr11:4123552 | T | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0045 others(5): Show |
10 | HG00558.hp2 HG02056.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1320+168T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4123552 | |||||||
| chr11:4123612 | A | G | 267 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(264): Show |
291 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.1320+228A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4123612 | |||||||
| chr11:4123637 | C | G | 117 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(114): Show |
121 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.1320+253C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4123637 | |||||||
| chr11:4123734 | G | T | 1 | a0001c0001t0005g0207 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1320+350G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4123734 | |||||||
| chr11:4123761 | T | C | 5 | a0001c0003t0002g0030 a0001c0003t0002g0046 a0001c0003t0004g0208 others(2): Show |
5 | HG01243.hp2 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1320+377T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4123761 | |||||||
| chr11:4123839 | A | G | 40 | a0001c0001t0002g0314 a0001c0001t0002g0331 a0001c0003t0002g0172 others(37): Show |
40 | HG00609.hp1 HG01192.hp2 HG01358.hp1 others(37): Show |
intron_variant | MODIFIER | c.1320+455A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4123839 | |||||||
| chr11:4123953 | A | G | 1 | a0001c0003t0002g0030 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1320+569A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4123953 | |||||||
| chr11:4124034 | G | A | 3 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 |
3 | HG02615.hp1 HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1320+650G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4124034 | |||||||
| chr11:4124046 | A | G | 1 | a0001c0001t0005g0207 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1320+662A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4124046 | |||||||
| chr11:4124155 | G | T | 87 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0007 others(84): Show |
105 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1320+771G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4124155 | |||||||
| chr11:4124185 | G | A | 134 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(131): Show |
154 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.1320+801G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4124185 | |||||||
| chr11:4124225 | G | T | 1 | a0001c0001t0003g0022 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1320+841G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4124225 | |||||||
| chr11:4124243 | A | G | 4 | a0001c0004t0001g0034 a0001c0004t0001g0043 a0001c0004t0001g0044 others(1): Show |
4 | HG02630.hp1 HG02965.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1320+859A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4124243 | |||||||
| chr11:4124428 | A | G | 87 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0007 others(84): Show |
105 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1320+1044A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4124428 | |||||||
| chr11:4124490 | T | C | 2 | a0001c0003t0002g0307 a0001c0003t0002g0308 |
2 | HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1320+1106T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4124490 | |||||||
| chr11:4124707 | G | A | 1 | a0001c0003t0002g0316 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1320+1323G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4124707 | |||||||
| chr11:4124759 | C | T | 1 | a0001c0004t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1320+1375C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4124759 | |||||||
| chr11:4124831 | TTTTTC | T | 144 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(141): Show |
164 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1320+1467_1320+147 others(9): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr11 | 4124831 | ||||||
| chr11:4124918 | T | TA | 91 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0007 others(88): Show |
109 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1320+1534_1320+153 others(5): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4124918 | |||||||
| chr11:4124920 | A | AT | 42 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(39): Show |
44 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.1320+1549dupT | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr11 | 4124920 | ||||||
| chr11:4124920 | A | T | 91 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0007 others(88): Show |
109 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1320+1536A>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4124920 | |||||||
| chr11:4124922 | T | A | 91 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0007 others(88): Show |
109 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1320+1538T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4124922 | |||||||
| chr11:4124924 | T | A | 1 | a0001c0001t0001g0035 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1320+1540T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4124924 | |||||||
| chr11:4125027 | G | T | 1 | a0001c0001t0001g0144 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1320+1643G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4125027 | |||||||
| chr11:4125062 | G | A | 2 | a0001c0003t0002g0246 a0001c0003t0002g0261 |
2 | HG02132.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1321-1622G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4125062 | |||||||
| chr11:4125104 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1321-1580G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4125104 | |||||||
| chr11:4125167 | C | T | 1 | a0001c0002t0001g0051 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1321-1517C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4125167 | |||||||
| chr11:4125168 | C | T | 1 | a0001c0002t0001g0051 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1321-1516C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4125168 | |||||||
| chr11:4125578 | A | G | 5 | a0001c0003t0002g0030 a0001c0003t0002g0046 a0001c0003t0004g0208 others(2): Show |
5 | HG01243.hp2 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1321-1106A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4125578 | |||||||
| chr11:4125749 | C | A | 27 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(24): Show |
27 | HG00741.hp2 HG02040.hp2 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.1321-935C>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4125749 | |||||||
| chr11:4125770 | G | A | 10 | a0001c0001t0003g0018 a0001c0001t0003g0022 a0001c0001t0003g0028 others(7): Show |
10 | HG01243.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1321-914G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4125770 | |||||||
| chr11:4125774 | T | C | 127 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(124): Show |
131 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.1321-910T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4125774 | |||||||
| chr11:4125832 | C | T | 1 | a0001c0003t0002g0030 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1321-852C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4125832 | |||||||
| chr11:4126013 | T | TA | 5 | a0001c0003t0002g0030 a0001c0003t0002g0046 a0001c0003t0004g0208 others(2): Show |
5 | HG01243.hp2 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1321-670dupA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr11 | 4126013 | ||||||
| chr11:4126148 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1321-536A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4126148 | |||||||
| chr11:4126310 | A | G | 5 | a0001c0003t0002g0030 a0001c0003t0002g0046 a0001c0003t0004g0208 others(2): Show |
5 | HG01243.hp2 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1321-374A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4126310 | |||||||
| chr11:4126374 | T | C | 4 | a0001c0001t0001g0175 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02622.hp1 HG02723.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1321-310T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | chr11 | 4126374 | |||||||
| chr11:4126444 | TTCTC | T | 3 | a0001c0001t0001g0149 a0001c0001t0001g0155 a0001c0001t0001g0158 |
3 | HG03490.hp1 HG03492.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1321-230_1321-227d others(6): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr11 | 4126444 | ||||||
| chr11:4126950 | G | A | 4 | a0001c0001t0003g0018 a0001c0001t0003g0039 a0001c0001t0003g0040 others(1): Show |
4 | HG02615.hp1 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1471-85G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 13/18 | chr11 | 4126950 | |||||||
| chr11:4126953 | A | G | 1 | a0001c0004t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1471-82A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 13/18 | chr11 | 4126953 | |||||||
| chr11:4127382 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1692+126A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | chr11 | 4127382 | |||||||
| chr11:4127383 | A | G | 1 | a0003c0010t0001g0217 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1692+127A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | chr11 | 4127383 | |||||||
| chr11:4127617 | G | A | 6 | a0001c0001t0003g0022 a0001c0001t0003g0028 a0001c0001t0003g0029 others(3): Show |
6 | HG01243.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1692+361G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | chr11 | 4127617 | |||||||
| chr11:4127718 | C | T | 87 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0007 others(84): Show |
105 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1692+462C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | chr11 | 4127718 | |||||||
| chr11:4127763 | C | G | 1 | a0001c0004t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1692+507C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | chr11 | 4127763 | |||||||
| chr11:4127809 | T | G | 4 | a0001c0004t0001g0034 a0001c0004t0001g0043 a0001c0004t0001g0044 others(1): Show |
4 | HG02630.hp1 HG02965.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1692+553T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | chr11 | 4127809 | |||||||
| chr11:4127907 | G | A | 2 | a0001c0002t0001g0007 a0001c0002t0001g0033 |
3 | HG01069.hp2 HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1692+651G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | chr11 | 4127907 | |||||||
| chr11:4127935 | G | A | 5 | a0001c0003t0002g0030 a0001c0003t0002g0046 a0001c0003t0004g0208 others(2): Show |
5 | HG01243.hp2 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1692+679G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | chr11 | 4127935 | |||||||
| chr11:4127984 | A | T | 82 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(79): Show |
86 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1692+728A>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | chr11 | 4127984 | |||||||
| chr11:4128095 | T | C | 5 | a0001c0003t0002g0030 a0001c0003t0002g0046 a0001c0003t0004g0208 others(2): Show |
5 | HG01243.hp2 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1692+839T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | chr11 | 4128095 | |||||||
| chr11:4128153 | CT | C | 3 | a0001c0001t0001g0231 a0001c0001t0001g0237 a0001c0002t0001g0083 |
3 | NA18612.hp1 NA18957.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1692+898delT | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | chr11 | 4128153 | |||||||
| chr11:4128161 | C | CT | 12 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0228 others(9): Show |
14 | HG01981.hp2 HG03579.hp2 HG03688.hp2 others(11): Show |
intron_variant | MODIFIER | c.1693-895dupT | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 4128161 | ||||||
| chr11:4128161 | CT | C | 79 | a0001c0001t0001g0152 a0001c0001t0001g0175 a0001c0001t0001g0279 others(76): Show |
80 | HG00609.hp1 HG00639.hp1 HG01192.hp2 others(77): Show |
intron_variant | MODIFIER | c.1693-895delT | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 4128161 | ||||||
| chr11:4128166 | T | C | 43 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(40): Show |
45 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.1693-908T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | chr11 | 4128166 | |||||||
| chr11:4128298 | G | C | 1 | a0001c0001t0001g0128 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1693-776G>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | chr11 | 4128298 | |||||||
| chr11:4128457 | A | G | 6 | a0001c0001t0003g0022 a0001c0001t0003g0028 a0001c0001t0003g0029 others(3): Show |
6 | HG01243.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1693-617A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | chr11 | 4128457 | |||||||
| chr11:4128465 | C | G | 1 | a0001c0004t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1693-609C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | chr11 | 4128465 | |||||||
| chr11:4128568 | A | G | 1 | a0001c0003t0002g0046 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1693-506A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | chr11 | 4128568 | |||||||
| chr11:4128615 | G | A | 1 | a0001c0002t0001g0199 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1693-459G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | chr11 | 4128615 | |||||||
| chr11:4128814 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1693-260C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | chr11 | 4128814 | |||||||
| chr11:4128871 | T | C | 42 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(39): Show |
44 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.1693-203T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | chr11 | 4128871 | |||||||
| chr11:4129008 | G | GT | 158 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(155): Show |
165 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.1693-52dupT | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 4129008 | ||||||
| chr11:4129008 | G | GTT | 7 | a0001c0001t0001g0020 a0001c0001t0001g0128 a0001c0001t0001g0159 others(4): Show |
7 | HG01099.hp2 HG01978.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1693-53_1693-52dup others(2): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 4129008 | ||||||
| chr11:4129061 | G | A | 10 | a0001c0001t0003g0018 a0001c0001t0003g0022 a0001c0001t0003g0028 others(7): Show |
10 | HG01243.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1693-13G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 14/18 | chr11 | 4129061 | |||||||
| chr11:4129401 | T | C | 2 | a0001c0003t0002g0311 a0001c0003t0002g0315 |
2 | NA18971.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1769+251T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4129401 | |||||||
| chr11:4129467 | AT | A | 50 | a0001c0001t0001g0176 a0001c0001t0002g0314 a0001c0001t0002g0331 others(47): Show |
51 | HG00609.hp1 HG00639.hp1 HG01192.hp2 others(48): Show |
intron_variant | MODIFIER | c.1769+328delT | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4129467 | ||||||
| chr11:4129479 | A | G | 1 | a0001c0006t0001g0240 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1769+329A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4129479 | |||||||
| chr11:4129482 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1769+332T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4129482 | |||||||
| chr11:4129521 | G | A | 1 | a0001c0003t0002g0275 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1769+371G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4129521 | |||||||
| chr11:4129611 | GA | G | 262 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(259): Show |
286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.1769+470delA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4129611 | ||||||
| chr11:4129639 | G | A | 87 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0007 others(84): Show |
105 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1769+489G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4129639 | |||||||
| chr11:4129663 | T | C | 43 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(40): Show |
45 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.1769+513T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4129663 | |||||||
| chr11:4129713 | A | G | 1 | a0001c0006t0001g0214 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1769+563A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4129713 | |||||||
| chr11:4129938 | T | C | 1 | a0001c0002t0001g0116 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1769+788T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4129938 | |||||||
| chr11:4129998 | C | T | 1 | a0001c0002t0001g0124 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1769+848C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4129998 | |||||||
| chr11:4130062 | G | GTATA | 52 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0008 others(49): Show |
69 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1769+915_1769+916i others(6): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130062 | ||||||
| chr11:4130062 | G | GTATATA | 13 | a0001c0002t0001g0007 a0001c0002t0001g0033 a0001c0002t0001g0066 others(10): Show |
14 | HG00609.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1769+915_1769+916i others(8): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130062 | ||||||
| chr11:4130062 | G | GTATATAT others(1): Show |
9 | a0001c0002t0001g0054 a0001c0002t0001g0055 a0001c0002t0001g0056 others(6): Show |
9 | NA18940.hp1 NA18942.hp1 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.1769+915_1769+916i others(10): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130062 | ||||||
| chr11:4130062 | G | GTATATAT others(3): Show |
8 | a0001c0002t0001g0063 a0001c0002t0001g0082 a0001c0002t0001g0091 others(5): Show |
8 | HG00735.hp2 HG01192.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.1769+915_1769+916i others(12): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130062 | ||||||
| chr11:4130062 | G | GTATATAT others(5): Show |
1 | a0001c0002t0001g0117 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1769+915_1769+916i others(14): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130062 | ||||||
| chr11:4130062 | G | GTATATAT others(7): Show |
1 | a0001c0002t0001g0047 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1769+915_1769+916i others(16): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130062 | ||||||
| chr11:4130062 | G | GTATATAT others(9): Show |
1 | a0001c0001t0001g0037 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1769+915_1769+916i others(18): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130062 | ||||||
| chr11:4130066 | T | A | 88 | a0001c0001t0001g0037 a0001c0002t0001g0001 a0001c0002t0001g0003 others(85): Show |
106 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.1769+916T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130066 | |||||||
| chr11:4130066 | T | TATATATA others(12): Show |
1 | a0001c0001t0001g0303 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1769+916_1769+917i others(21): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130066 | |||||||
| chr11:4130066 | T | TTATATAT others(1): Show |
7 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0026 others(4): Show |
9 | HG00558.hp2 HG01243.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.1769+930_1769+937d others(10): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130066 | ||||||
| chr11:4130066 | T | TTATATAT others(3): Show |
7 | a0001c0001t0001g0024 a0001c0001t0001g0183 a0001c0001t0001g0184 others(4): Show |
7 | HG02040.hp2 HG02132.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1769+928_1769+937d others(12): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130066 | ||||||
| chr11:4130066 | T | TTATATAT others(5): Show |
13 | a0001c0001t0001g0042 a0001c0001t0001g0177 a0001c0001t0001g0178 others(10): Show |
13 | HG00741.hp2 HG02083.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1769+926_1769+937d others(14): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130066 | ||||||
| chr11:4130066 | T | TTATATAT others(7): Show |
12 | a0001c0001t0001g0145 a0001c0001t0001g0200 a0001c0001t0001g0201 others(9): Show |
12 | HG01109.hp2 HG02145.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1769+924_1769+937d others(16): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130066 | ||||||
| chr11:4130066 | T | TTATATAT others(9): Show |
34 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0128 others(31): Show |
34 | HG00423.hp1 HG00639.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1769+922_1769+937d others(18): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130066 | ||||||
| chr11:4130066 | T | TTATATAT others(11): Show |
6 | a0001c0001t0001g0127 a0001c0001t0001g0283 a0001c0001t0001g0284 others(3): Show |
6 | HG01074.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1769+920_1769+937d others(20): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130066 | ||||||
| chr11:4130066 | T | TTATATAT others(13): Show |
19 | a0001c0001t0001g0017 a0001c0001t0001g0132 a0001c0001t0001g0143 others(16): Show |
19 | HG00738.hp1 HG01884.hp2 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.1769+918_1769+937d others(22): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130066 | ||||||
| chr11:4130066 | T | TTATATAT others(15): Show |
10 | a0001c0001t0001g0136 a0001c0001t0001g0147 a0001c0001t0001g0221 others(7): Show |
10 | HG01169.hp2 HG01261.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.1769+937_1769+938i others(24): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130066 | ||||||
| chr11:4130066 | T | TTATATAT others(17): Show |
14 | a0001c0001t0001g0137 a0001c0001t0001g0231 a0001c0001t0001g0237 others(11): Show |
14 | HG01978.hp2 HG01981.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.1769+937_1769+938i others(26): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130066 | ||||||
| chr11:4130066 | T | TTATATAT others(19): Show |
10 | a0001c0001t0001g0125 a0001c0001t0001g0146 a0001c0001t0001g0282 others(7): Show |
10 | HG01943.hp2 HG02083.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.1769+937_1769+938i others(28): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130066 | ||||||
| chr11:4130066 | T | TTATATAT others(21): Show |
8 | a0001c0003t0002g0172 a0001c0003t0002g0242 a0001c0003t0002g0248 others(5): Show |
8 | HG00609.hp1 HG01496.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.1769+937_1769+938i others(30): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130066 | ||||||
| chr11:4130066 | T | TTATATAT others(23): Show |
3 | a0001c0001t0001g0279 a0001c0003t0002g0245 a0001c0003t0002g0265 |
3 | HG01192.hp2 HG01943.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1769+937_1769+938i others(32): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130066 | ||||||
| chr11:4130066 | T | TTATATAT others(25): Show |
1 | a0001c0003t0002g0273 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1769+937_1769+938i others(34): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130066 | ||||||
| chr11:4130066 | T | TTATATAT others(27): Show |
2 | a0001c0001t0001g0280 a0001c0003t0002g0277 |
2 | NA18992.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1769+937_1769+938i others(36): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130066 | ||||||
| chr11:4130068 | A | T | 3 | a0001c0003t0002g0006 a0001c0003t0002g0031 a0001c0003t0002g0326 |
4 | HG00639.hp1 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1769+918A>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130068 | |||||||
| chr11:4130086 | A | AT | 8 | a0001c0001t0002g0314 a0001c0001t0002g0331 a0001c0003t0002g0002 others(5): Show |
12 | HG00438.hp2 HG01257.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1769+954dupT | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130086 | ||||||
| chr11:4130086 | A | ATATATAT others(8): Show |
2 | a0001c0001t0001g0325 a0001c0001t0003g0296 |
2 | HG03540.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1769+937_1769+938i others(17): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130086 | ||||||
| chr11:4130086 | A | ATATATAT others(10): Show |
1 | a0001c0001t0003g0294 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1769+937_1769+938i others(19): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130086 | ||||||
| chr11:4130086 | A | ATATATAT others(12): Show |
1 | a0001c0001t0003g0295 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1769+937_1769+938i others(21): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130086 | ||||||
| chr11:4130086 | A | ATATATAT others(18): Show |
2 | a0001c0001t0001g0175 a0001c0001t0001g0291 |
2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1769+937_1769+938i others(27): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130086 | ||||||
| chr11:4130086 | A | ATATATAT others(24): Show |
1 | a0001c0003t0002g0006 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1769+937_1769+938i others(33): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130086 | ||||||
| chr11:4130086 | A | ATATATAT others(26): Show |
1 | a0001c0001t0005g0207 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1769+937_1769+938i others(35): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130086 | ||||||
| chr11:4130086 | A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1769+937_1769+938i others(42): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130086 | ||||||
| chr11:4130086 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0300 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1769+937_1769+938i others(24): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130086 | ||||||
| chr11:4130086 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0134 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1769+937_1769+938i others(22): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130086 | ||||||
| chr11:4130086 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0288 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1769+937_1769+938i others(18): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130086 | ||||||
| chr11:4130086 | A | ATATATAT others(9): Show |
1 | a0001c0001t0003g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1769+937_1769+938i others(18): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130086 | ||||||
| chr11:4130086 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0045 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1769+937_1769+938i others(12): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130086 | ||||||
| chr11:4130086 | A | ATATATAT others(8): Show |
1 | a0001c0001t0003g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1769+937_1769+938i others(17): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130086 | ||||||
| chr11:4130086 | A | ATATATTT others(5): Show |
1 | a0001c0001t0003g0028 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1769+937_1769+938i others(14): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130086 | ||||||
| chr11:4130086 | A | ATATATTT others(6): Show |
3 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 |
3 | HG02615.hp1 HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1769+937_1769+938i others(15): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130086 | ||||||
| chr11:4130086 | A | ATATATTT others(7): Show |
2 | a0001c0001t0003g0022 a0001c0001t0003g0029 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1769+937_1769+938i others(16): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 4130086 | ||||||
| chr11:4130087 | T | TA | 6 | a0001c0001t0001g0303 a0001c0003t0002g0002 a0001c0003t0002g0016 others(3): Show |
7 | HG02258.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1769+937_1769+938i others(3): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130087 | |||||||
| chr11:4130087 | T | TATATATA others(4): Show |
2 | a0001c0001t0001g0019 a0001c0001t0001g0038 |
2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1769+937_1769+938i others(13): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130087 | |||||||
| chr11:4130087 | T | TATATATA others(6): Show |
4 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1769+937_1769+938i others(15): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130087 | |||||||
| chr11:4130087 | T | TATATATA others(8): Show |
18 | a0001c0001t0001g0014 a0001c0001t0001g0144 a0001c0001t0001g0211 others(15): Show |
18 | HG01099.hp1 HG02027.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.1769+937_1769+938i others(17): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130087 | |||||||
| chr11:4130087 | T | TATATATA others(10): Show |
5 | a0001c0001t0001g0014 a0001c0001t0001g0072 a0001c0001t0001g0126 others(2): Show |
5 | HG02109.hp1 NA18975.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.1769+937_1769+938i others(19): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130087 | |||||||
| chr11:4130087 | T | TATATATA others(12): Show |
6 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0167 others(3): Show |
9 | HG00408.hp2 HG00558.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.1769+937_1769+938i others(21): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130087 | |||||||
| chr11:4130087 | T | TATATATA others(14): Show |
2 | a0001c0001t0001g0281 a0001c0003t0002g0251 |
2 | HG02257.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1769+937_1769+938i others(23): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130087 | |||||||
| chr11:4130087 | T | TATATATA others(18): Show |
1 | a0001c0003t0002g0326 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1769+937_1769+938i others(27): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130087 | |||||||
| chr11:4130087 | T | TATATATA others(30): Show |
1 | a0001c0003t0002g0006 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1769+937_1769+938i others(39): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130087 | |||||||
| chr11:4130088 | T | A | 219 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(216): Show |
238 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.1769+938T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130088 | |||||||
| chr11:4130089 | T | A | 37 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0020 others(34): Show |
39 | HG00408.hp2 HG00558.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.1769+939T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130089 | |||||||
| chr11:4130090 | T | A | 155 | a0001c0001t0001g0017 a0001c0001t0001g0036 a0001c0001t0001g0042 others(152): Show |
172 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.1769+940T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130090 | |||||||
| chr11:4130091 | T | A | 11 | a0001c0001t0001g0126 a0001c0001t0001g0219 a0001c0001t0001g0293 others(8): Show |
11 | HG01099.hp1 HG02027.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1769+941T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130091 | |||||||
| chr11:4130092 | T | A | 105 | a0001c0001t0001g0042 a0001c0001t0001g0136 a0001c0001t0001g0153 others(102): Show |
112 | HG00438.hp1 HG00609.hp1 HG00733.hp2 others(109): Show |
intron_variant | MODIFIER | c.1769+942T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130092 | |||||||
| chr11:4130093 | T | A | 4 | a0001c0001t0001g0293 a0001c0002t0001g0114 a0001c0003t0002g0251 others(1): Show |
4 | HG01099.hp1 HG02109.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.1769+943T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130093 | |||||||
| chr11:4130094 | T | A | 74 | a0001c0001t0001g0042 a0001c0001t0001g0177 a0001c0001t0001g0178 others(71): Show |
76 | HG00438.hp1 HG00609.hp1 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.1769+944T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130094 | |||||||
| chr11:4130095 | T | A | 1 | a0001c0003t0002g0251 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1769+945T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130095 | |||||||
| chr11:4130096 | T | A | 39 | a0001c0002t0001g0073 a0001c0003t0002g0172 a0001c0003t0002g0241 others(36): Show |
39 | HG00609.hp1 HG01192.hp2 HG01358.hp1 others(36): Show |
intron_variant | MODIFIER | c.1769+946T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130096 | |||||||
| chr11:4130097 | T | A | 1 | a0001c0003t0002g0251 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1769+947T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130097 | |||||||
| chr11:4130098 | T | A | 34 | a0001c0003t0002g0172 a0001c0003t0002g0242 a0001c0003t0002g0243 others(31): Show |
34 | HG00609.hp1 HG01192.hp2 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.1769+948T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130098 | |||||||
| chr11:4130104 | T | C | 88 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0007 others(85): Show |
106 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.1769+954T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130104 | |||||||
| chr11:4130163 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1769+1013A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130163 | |||||||
| chr11:4130334 | A | G | 41 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(38): Show |
43 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.1769+1184A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130334 | |||||||
| chr11:4130389 | A | C | 1 | a0001c0001t0001g0279 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1769+1239A>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130389 | |||||||
| chr11:4130486 | A | G | 42 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(39): Show |
44 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.1769+1336A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130486 | |||||||
| chr11:4130496 | G | C | 1 | a0001c0006t0001g0169 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1769+1346G>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130496 | |||||||
| chr11:4130717 | G | A | 1 | a0001c0002t0001g0073 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1769+1567G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130717 | |||||||
| chr11:4130735 | T | G | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0127 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1770-1551T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130735 | |||||||
| chr11:4130951 | A | G | 1 | a0001c0003t0002g0273 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1770-1335A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130951 | |||||||
| chr11:4130965 | C | G | 1 | a0001c0003t0002g0257 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1770-1321C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4130965 | |||||||
| chr11:4131030 | C | T | 1 | a0001c0002t0001g0097 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1770-1256C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4131030 | |||||||
| chr11:4131076 | A | C | 2 | a0001c0003t0002g0030 a0001c0003t0002g0046 |
2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1770-1210A>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4131076 | |||||||
| chr11:4131183 | C | T | 266 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(263): Show |
290 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.1770-1103C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4131183 | |||||||
| chr11:4131272 | G | A | 1 | a0001c0002t0001g0062 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1770-1014G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4131272 | |||||||
| chr11:4131302 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1770-984G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4131302 | |||||||
| chr11:4131386 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1770-900G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4131386 | |||||||
| chr11:4131614 | T | G | 1 | a0001c0003t0002g0250 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1770-672T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4131614 | |||||||
| chr11:4131615 | G | A | 4 | a0001c0001t0003g0018 a0001c0001t0003g0039 a0001c0001t0003g0040 others(1): Show |
4 | HG02615.hp1 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1770-671G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4131615 | |||||||
| chr11:4131618 | A | G | 9 | a0001c0001t0003g0022 a0001c0001t0003g0028 a0001c0001t0003g0029 others(6): Show |
9 | HG01243.hp1 HG02258.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1770-668A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4131618 | |||||||
| chr11:4131669 | C | T | 3 | a0001c0002t0001g0071 a0001c0002t0001g0081 a0001c0002t0001g0120 |
3 | HG01257.hp1 HG01346.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1770-617C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4131669 | |||||||
| chr11:4131685 | G | A | 127 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(124): Show |
131 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.1770-601G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4131685 | |||||||
| chr11:4131752 | T | G | 1 | a0001c0003t0002g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1770-534T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4131752 | |||||||
| chr11:4132001 | T | C | 114 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(111): Show |
118 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.1770-285T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4132001 | |||||||
| chr11:4132008 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1770-278A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4132008 | |||||||
| chr11:4132177 | C | T | 82 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(79): Show |
86 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1770-109C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4132177 | |||||||
| chr11:4132178 | A | G | 82 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(79): Show |
86 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1770-108A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 15/18 | chr11 | 4132178 | |||||||
| chr11:4132537 | A | G | 263 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(260): Show |
287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.1905+116A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 16/18 | chr11 | 4132537 | |||||||
| chr11:4132586 | G | T | 1 | a0001c0009t0001g0206 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1905+165G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 16/18 | chr11 | 4132586 | |||||||
| chr11:4132590 | A | C | 1 | a0001c0002t0001g0064 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1905+169A>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 16/18 | chr11 | 4132590 | |||||||
| chr11:4132661 | T | C | 88 | a0001c0001t0001g0190 a0001c0002t0001g0001 a0001c0002t0001g0003 others(85): Show |
106 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.1905+240T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 16/18 | chr11 | 4132661 | |||||||
| chr11:4132959 | T | G | 1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1905+538T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 16/18 | chr11 | 4132959 | |||||||
| chr11:4133077 | T | C | 87 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0007 others(84): Show |
105 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1906-486T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 16/18 | chr11 | 4133077 | |||||||
| chr11:4133106 | A | T | 307 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(304): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.1906-457A>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 16/18 | chr11 | 4133106 | |||||||
| chr11:4133367 | CAG | C | 3 | a0001c0003t0002g0016 a0001c0003t0002g0306 a0001c0003t0002g0316 |
4 | HG02258.hp2 HG02280.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1906-194_1906-193d others(4): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 4133367 | ||||||
| chr11:4133680 | T | C | 1 | a0001c0003t0002g0319 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2001+22T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 17/18 | chr11 | 4133680 | |||||||
| chr11:4133902 | C | T | 262 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(259): Show |
286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.2001+244C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 17/18 | chr11 | 4133902 | |||||||
| chr11:4133956 | T | A | 1 | a0001c0004t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2001+298T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 17/18 | chr11 | 4133956 | |||||||
| chr11:4133980 | A | AT | 98 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0036 others(95): Show |
102 | HG00408.hp2 HG00558.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.2001+346dupT | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 4133980 | ||||||
| chr11:4133980 | A | ATT | 105 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0072 others(102): Show |
124 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.2001+345_2001+346d others(4): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 4133980 | ||||||
| chr11:4133980 | A | ATTT | 27 | a0001c0001t0001g0280 a0001c0001t0001g0282 a0001c0001t0001g0286 others(24): Show |
27 | HG00438.hp1 HG01192.hp1 HG01975.hp2 others(24): Show |
intron_variant | MODIFIER | c.2001+344_2001+346d others(5): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 4133980 | ||||||
| chr11:4133980 | A | ATTTTTT | 16 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(13): Show |
16 | HG02040.hp2 HG02083.hp2 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.2001+341_2001+346d others(8): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 4133980 | ||||||
| chr11:4133980 | A | ATTTTTTT | 9 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0024 others(6): Show |
9 | HG00741.hp2 HG02451.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2001+340_2001+346d others(9): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 4133980 | ||||||
| chr11:4133980 | A | ATTTTTTT others(1): Show |
7 | a0001c0001t0001g0011 a0001c0001t0001g0045 a0001c0001t0001g0196 others(4): Show |
8 | HG01109.hp2 HG02074.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.2001+339_2001+346d others(10): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 4133980 | ||||||
| chr11:4133980 | A | ATTTTTTT others(2): Show |
8 | a0001c0001t0001g0012 a0001c0001t0001g0126 a0001c0001t0001g0193 others(5): Show |
9 | HG00558.hp2 HG02056.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2001+338_2001+346d others(11): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 4133980 | ||||||
| chr11:4133980 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0201 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2001+337_2001+346d others(12): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 4133980 | ||||||
| chr11:4134010 | G | A | 1 | a0001c0001t0003g0028 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2001+352G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 17/18 | chr11 | 4134010 | |||||||
| chr11:4134012 | A | C | 1 | a0001c0001t0001g0325 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2001+354A>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 17/18 | chr11 | 4134012 | |||||||
| chr11:4134022 | G | A | 1 | a0001c0003t0002g0319 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2001+364G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 17/18 | chr11 | 4134022 | |||||||
| chr11:4134057 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2001+399A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 17/18 | chr11 | 4134057 | |||||||
| chr11:4134568 | CTGTG | C | 6 | a0001c0001t0003g0294 a0001c0001t0003g0295 a0001c0001t0003g0296 others(3): Show |
6 | HG01243.hp1 HG02258.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2002-510_2002-507d others(6): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 4134568 | ||||||
| chr11:4134656 | G | C | 1 | a0001c0004t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2002-426G>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 17/18 | chr11 | 4134656 | |||||||
| chr11:4134810 | T | A | 113 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(110): Show |
117 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.2002-272T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 17/18 | chr11 | 4134810 | |||||||
| chr11:4134876 | G | A | 93 | a0001c0001t0001g0176 a0001c0002t0001g0001 a0001c0002t0001g0003 others(90): Show |
111 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.2002-206G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 17/18 | chr11 | 4134876 | |||||||
| chr11:4135431 | G | A | 262 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(259): Show |
286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.2190+161G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4135431 | |||||||
| chr11:4135512 | TCCTTCCT others(3): Show |
T | 1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2190+244_2190+253d others(12): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 4135512 | ||||||
| chr11:4135621 | T | C | 126 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(123): Show |
130 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.2190+351T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4135621 | |||||||
| chr11:4135663 | C | G | 1 | a0001c0003t0002g0309 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2190+393C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4135663 | |||||||
| chr11:4135692 | C | T | 82 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(79): Show |
86 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.2190+422C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4135692 | |||||||
| chr11:4135713 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2190+443C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4135713 | |||||||
| chr11:4135716 | C | A | 1 | a0001c0001t0001g0126 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2190+446C>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4135716 | |||||||
| chr11:4135765 | G | A | 1 | a0001c0002t0001g0103 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2190+495G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4135765 | |||||||
| chr11:4136113 | A | G | 1 | a0001c0004t0001g0043 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2190+843A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136113 | |||||||
| chr11:4136177 | TA | T | 4 | a0001c0003t0002g0171 a0001c0003t0002g0308 a0001c0003t0002g0309 others(1): Show |
4 | HG00642.hp1 HG03471.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2190+914delA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 4136177 | ||||||
| chr11:4136181 | A | T | 1 | a0001c0003t0002g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2190+911A>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136181 | |||||||
| chr11:4136182 | A | G | 1 | a0001c0003t0002g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2190+912A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136182 | |||||||
| chr11:4136183 | A | G | 1 | a0001c0003t0002g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2190+913A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136183 | |||||||
| chr11:4136184 | AGTTTGAT others(786): Show |
A | 1 | a0001c0003t0002g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2190+915_2191-1218 others(3): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136184 | |||||||
| chr11:4136271 | G | T | 3 | a0001c0003t0002g0005 a0001c0003t0002g0310 a0001c0003t0002g0313 |
5 | HG02451.hp2 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2190+1001G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136271 | |||||||
| chr11:4136283 | A | G | 263 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(260): Show |
287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.2190+1013A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136283 | |||||||
| chr11:4136315 | G | T | 1 | a0001c0001t0005g0207 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2190+1045G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136315 | |||||||
| chr11:4136614 | A | G | 2 | a0001c0003t0002g0275 a0001c0004t0001g0032 |
2 | HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2190+1344A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136614 | |||||||
| chr11:4136648 | C | T | 1 | a0001c0004t0001g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2190+1378C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136648 | |||||||
| chr11:4136713 | C | A | 3 | a0001c0003t0004g0208 a0002c0007t0002g0209 a0002c0007t0002g0210 |
3 | HG01243.hp2 HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2190+1443C>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136713 | |||||||
| chr11:4136734 | TTTTG | T | 255 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(252): Show |
279 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.2191-1441_2191-143 others(8): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 4136734 | ||||||
| chr11:4136742 | G | T | 13 | a0001c0001t0003g0018 a0001c0001t0003g0022 a0001c0001t0003g0028 others(10): Show |
13 | HG01243.hp1 HG02258.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2191-1453G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136742 | |||||||
| chr11:4136754 | G | T | 7 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(4): Show |
7 | HG01943.hp1 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2191-1441G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136754 | |||||||
| chr11:4136757 | T | C | 7 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(4): Show |
7 | HG01943.hp1 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2191-1438T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136757 | |||||||
| chr11:4136761 | C | T | 7 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(4): Show |
7 | HG01943.hp1 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2191-1434C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136761 | |||||||
| chr11:4136763 | T | A | 7 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(4): Show |
7 | HG01943.hp1 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2191-1432T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136763 | |||||||
| chr11:4136765 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2191-1430T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136765 | |||||||
| chr11:4136796 | A | G | 113 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(110): Show |
117 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.2191-1399A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136796 | |||||||
| chr11:4136806 | G | A | 43 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(40): Show |
45 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.2191-1389G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136806 | |||||||
| chr11:4136900 | G | T | 262 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(259): Show |
286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.2191-1295G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136900 | |||||||
| chr11:4136915 | G | A | 262 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(259): Show |
286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.2191-1280G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136915 | |||||||
| chr11:4136922 | C | T | 262 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(259): Show |
286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.2191-1273C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136922 | |||||||
| chr11:4136977 | G | C | 262 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(259): Show |
286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.2191-1218G>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4136977 | |||||||
| chr11:4137043 | C | T | 13 | a0001c0001t0003g0018 a0001c0001t0003g0022 a0001c0001t0003g0028 others(10): Show |
13 | HG01243.hp1 HG02258.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2191-1152C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137043 | |||||||
| chr11:4137078 | G | A | 113 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(110): Show |
117 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.2191-1117G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137078 | |||||||
| chr11:4137158 | C | T | 1 | a0001c0001t0005g0207 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2191-1037C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137158 | |||||||
| chr11:4137272 | A | G | 1 | a0001c0002t0001g0104 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2191-923A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137272 | |||||||
| chr11:4137311 | A | G | 320 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(317): Show |
348 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(345): Show |
intron_variant | MODIFIER | c.2191-884A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137311 | |||||||
| chr11:4137328 | A | G | 1 | a0001c0001t0001g0330 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2191-867A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137328 | |||||||
| chr11:4137345 | G | C | 1 | a0001c0003t0002g0276 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2191-850G>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137345 | |||||||
| chr11:4137346 | C | G | 1 | a0001c0003t0002g0276 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2191-849C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137346 | |||||||
| chr11:4137346 | C | T | 1 | a0001c0003t0002g0245 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2191-849C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137346 | |||||||
| chr11:4137372 | AGACGGGG others(41): Show |
A | 43 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(40): Show |
45 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.2191-806_2191-759d others(50): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 4137372 | ||||||
| chr11:4137389 | AGGCGGGG others(41): Show |
A | 1 | a0001c0001t0005g0207 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2191-794_2191-747d others(50): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 4137389 | ||||||
| chr11:4137393 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | NA19004.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.2191-802G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137393 | |||||||
| chr11:4137436 | C | T | 126 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(123): Show |
130 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.2191-759C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137436 | |||||||
| chr11:4137456 | C | T | 13 | a0001c0001t0003g0018 a0001c0001t0003g0022 a0001c0001t0003g0028 others(10): Show |
13 | HG01243.hp1 HG02258.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2191-739C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137456 | |||||||
| chr11:4137472 | C | T | 263 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(260): Show |
287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.2191-723C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137472 | |||||||
| chr11:4137486 | GGGCCGGG others(7): Show |
G | 1 | a0001c0003t0002g0276 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2191-708_2191-695d others(16): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137486 | |||||||
| chr11:4137490 | C | G | 313 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(310): Show |
338 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(335): Show |
intron_variant | MODIFIER | c.2191-705C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137490 | |||||||
| chr11:4137509 | C | T | 262 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(259): Show |
286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.2191-686C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137509 | |||||||
| chr11:4137517 | C | T | 1 | a0001c0002t0001g0084 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2191-678C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137517 | |||||||
| chr11:4137521 | C | T | 262 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(259): Show |
286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.2191-674C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137521 | |||||||
| chr11:4137525 | G | GGGGCAGC others(9): Show |
1 | a0001c0003t0002g0276 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2191-670_2191-669i others(18): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137525 | |||||||
| chr11:4137527 | G | A | 37 | a0001c0003t0002g0172 a0001c0003t0002g0241 a0001c0003t0002g0242 others(34): Show |
37 | HG00609.hp1 HG01192.hp2 HG01358.hp1 others(34): Show |
intron_variant | MODIFIER | c.2191-668G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137527 | |||||||
| chr11:4137534 | C | A | 1 | a0001c0003t0002g0276 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2191-661C>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137534 | |||||||
| chr11:4137572 | G | A | 262 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(259): Show |
286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.2191-623G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137572 | |||||||
| chr11:4137574 | G | A | 41 | a0001c0003t0002g0006 a0001c0003t0002g0031 a0001c0003t0002g0172 others(38): Show |
42 | HG00609.hp1 HG00639.hp1 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.2191-621G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137574 | |||||||
| chr11:4137581 | G | C | 262 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(259): Show |
286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.2191-614G>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137581 | |||||||
| chr11:4137582 | G | A | 136 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(133): Show |
156 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.2191-613G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137582 | |||||||
| chr11:4137583 | C | T | 1 | a0001c0004t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2191-612C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137583 | |||||||
| chr11:4137596 | G | A | 1 | a0001c0003t0002g0030 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2191-599G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137596 | |||||||
| chr11:4137612 | C | T | 1 | a0001c0002t0001g0091 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2191-583C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137612 | |||||||
| chr11:4137617 | T | G | 262 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(259): Show |
286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.2191-578T>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137617 | |||||||
| chr11:4137618 | G | T | 261 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(258): Show |
285 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.2191-577G>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137618 | |||||||
| chr11:4137628 | T | C | 261 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(258): Show |
285 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.2191-567T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137628 | |||||||
| chr11:4137630 | CCCCCACC others(217): Show |
C | 12 | a0001c0001t0001g0045 a0001c0001t0001g0128 a0001c0001t0001g0222 others(9): Show |
12 | HG00438.hp1 HG00609.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.2191-559_2191-336d others(2): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 4137630 | ||||||
| chr11:4137634 | CACCTCCC others(218): Show |
C | 249 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(246): Show |
273 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.2191-520_2191-296d others(2): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 4137634 | ||||||
| chr11:4137638 | T | A | 1 | a0001c0002t0001g0099 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2191-557T>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137638 | |||||||
| chr11:4137677 | CCCCCCCA others(392): Show |
C | 1 | a0001c0002t0001g0099 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2191-511_2191-113d others(2): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 4137677 | ||||||
| chr11:4137684 | ACCTC | A | 42 | a0001c0003t0002g0006 a0001c0003t0002g0031 a0001c0003t0002g0172 others(39): Show |
43 | HG00609.hp1 HG00639.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.2191-504_2191-501d others(6): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 4137684 | ||||||
| chr11:4137766 | ACCTCCCG others(42): Show |
A | 5 | a0001c0003t0002g0030 a0001c0003t0002g0046 a0001c0003t0004g0208 others(2): Show |
5 | HG01243.hp2 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2191-352_2191-304d others(51): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 4137766 | ||||||
| chr11:4137794 | T | C | 2 | a0001c0003t0002g0307 a0001c0003t0002g0308 |
2 | HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2191-401T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137794 | |||||||
| chr11:4137859 | A | C | 12 | a0001c0001t0001g0045 a0001c0001t0001g0128 a0001c0001t0001g0222 others(9): Show |
12 | HG00438.hp1 HG00609.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.2191-336A>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137859 | |||||||
| chr11:4137929 | A | G | 2 | a0001c0003t0002g0030 a0001c0003t0002g0046 |
2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2191-266A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137929 | |||||||
| chr11:4137950 | A | AC | 80 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(77): Show |
84 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.2191-238dupC | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 4137950 | ||||||
| chr11:4137957 | C | G | 1 | a0001c0002t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2191-238C>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137957 | |||||||
| chr11:4137969 | A | G | 2 | a0001c0003t0002g0030 a0001c0003t0002g0046 |
2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2191-226A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137969 | |||||||
| chr11:4137972 | T | C | 261 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(258): Show |
285 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.2191-223T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137972 | |||||||
| chr11:4137981 | TGGCCGGG others(30): Show |
T | 5 | a0001c0003t0002g0030 a0001c0003t0002g0046 a0001c0003t0004g0208 others(2): Show |
5 | HG01243.hp2 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2191-200_2191-164d others(39): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 4137981 | ||||||
| chr11:4137995 | A | G | 261 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(258): Show |
285 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.2191-200A>G | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4137995 | |||||||
| chr11:4138017 | G | A | 261 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(258): Show |
285 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.2191-178G>A | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4138017 | |||||||
| chr11:4138022 | C | T | 42 | a0001c0003t0002g0006 a0001c0003t0002g0031 a0001c0003t0002g0172 others(39): Show |
43 | HG00609.hp1 HG00639.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.2191-173C>T | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4138022 | |||||||
| chr11:4138055 | T | C | 308 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(305): Show |
333 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(330): Show |
intron_variant | MODIFIER | c.2191-140T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4138055 | |||||||
| chr11:4138067 | C | CG | 39 | a0001c0001t0001g0136 a0001c0001t0001g0175 a0001c0001t0001g0279 others(36): Show |
39 | HG01243.hp2 HG01261.hp1 HG01346.hp1 others(36): Show |
intron_variant | MODIFIER | c.2191-123dupG | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 4138067 | ||||||
| chr11:4138067 | C | CGGGGGGC others(43): Show |
3 | a0001c0001t0001g0211 a0001c0001t0001g0219 a0001c0001t0001g0225 |
3 | HG02602.hp2 HG02738.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2191-123_2191-122i others(52): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 4138067 | ||||||
| chr11:4138067 | C | CGGGGGGC others(43): Show |
220 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(217): Show |
244 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.2191-123_2191-122i others(52): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 4138067 | ||||||
| chr11:4138067 | C | CGGGGGGC others(44): Show |
2 | a0001c0001t0001g0128 a0001c0001t0001g0135 |
2 | HG02738.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.2191-123_2191-122i others(53): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 4138067 | ||||||
| chr11:4138067 | C | CGGGGGGC others(43): Show |
1 | a0001c0004t0001g0043 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2191-123_2191-122i others(52): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 4138067 | ||||||
| chr11:4138076 | A | AC | 224 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(221): Show |
248 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.2191-112dupC | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 4138076 | ||||||
| chr11:4138076 | A | ACCCCCCC others(44): Show |
32 | a0001c0001t0001g0175 a0001c0001t0001g0279 a0001c0001t0001g0280 others(29): Show |
32 | HG01346.hp1 HG01884.hp2 HG01943.hp1 others(29): Show |
intron_variant | MODIFIER | c.2191-109_2191-108i others(53): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 4138076 | ||||||
| chr11:4138083 | C | CA | 3 | a0001c0001t0003g0294 a0001c0001t0003g0295 a0001c0001t0003g0296 |
3 | HG03130.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2191-111dupA | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 4138083 | ||||||
| chr11:4138083 | C | CCACCACC others(49): Show |
1 | a0001c0001t0001g0072 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2191-112_2191-111i others(58): Show |
RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4138083 | |||||||
| chr11:4138084 | A | C | 1 | a0001c0001t0001g0072 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2191-111A>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4138084 | |||||||
| chr11:4138094 | T | C | 262 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(259): Show |
286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.2191-101T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4138094 | |||||||
| chr11:4138141 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2191-54T>C | RRM1 | ENSG00000167325.15 | transcript | ENST00000300738.10 | protein_coding | 18/18 | chr11 | 4138141 |